Careers

iBio is a global leader in plant-based biologics manufacturing. Our FastPharming System combines vertical farming, automated hydroponics, and glycan engineering technologies to rapidly deliver gram quantities of high-quality monoclonal antibodies, vaccines, bioinks and other proteins. We accomplish all of this via our CGMP 130,000 square foot facility in Bryan, TX.  

Just imagine what we can do together!  We know great things happen when talent and opportunity cross paths. We are looking to hire exceptional people who have demonstrated track records of success.  Our greatest scientific solution is bringing talented people together who have a passion for advancing plant-based biologics for our customers and the world.

Apply now for our Agronomy Supervisor position!

MISSION OF THE POSITION

The Agronomy Supervisor is responsible for assisting in the planning, directing and coordinating of the activities of personnel engaged in seeding, germination, transplant, and growth of horticultural species in pilot and manufacturing scale production. The Agronomy Supervisor is also responsible for improving existing procedures and optimizing processes.

ESSENTIAL DUTIES & RESPONSIBILITES

• Oversee and provide leadership to the Upstream Manufacturing/Agronomy operations
• Coordinate seeding, transplant, and plant monitoring operations
• Collaborate with other departments to coordinate product development activities
• Contribute to increase throughput, efficacy, and capabilities i.e. increase capacity and workflow
• Coordinate production activities and monitoring during seeding, transplant, and post-infiltration plant growth
• Define data reporting on plant growth and plant growth systems. Reviews data and provide comment
• Develop timelines and budgets to accomplish activities
• Help establish priorities and assure adequate resources to complete projects in a timely manner
• Select and qualify vendors for materials and equipment for Agronomy plant production following cGMP supply chain requirements
• Develop and oversee execution of methods to evaluate materials, equipment, and growth protocols (photoperiod, irrigation frequency, nutrient solution attributes, environmental conditions, and disease control)
• Develop Standard Operating Procedures, Master Batch Records, and other quality documentation
• Prepare necessary reports and record keeping documents
• Review batch documentation for completeness and accuracy; Resolve document execution issues
• Proficiency with compliance; adherence to standard operating procedures, batch record, and good documentation practices
• Maintain an effective working relationship with others.
• Provide training and technical coaching to junior staff members.
• Monitor critical process parameters.
• Champion area specific initiatives associated with work safety and operational improvements.
• Help build, maintain and motivate the upstream team to achieve productivity targets and output requirements measured by KPI’s (key performance indicators).
• Engage in and support culture of continual improvement through ownership of improvement for work processes, equipment, and safe work environment.
• Advise executive management on improvements which may optimize work processes

 KNOWLEDGE, SKILLS, & ABILITIES

• Experience working in a regulated environment, familiarity with FDA a plus
• Collaborative team player.
• Ability to coordinate, facilitate and organize resources.
• Ability to hire, train, and develop employees to grow within the organization.
• Ability to work effectively under extreme pressure to meet deadlines.
• Well organized with ability to handle multiple activities simultaneously.
• Good interpersonal skills with an understanding of diverse backgrounds and an emphasis on communication: training, team building, negotiation skills, interdepartmental interactions, leadership and supervision (motivating, directing) and management (planning, budgeting, etc.)

EDUCATION & EXPERIENCE

• High School Diploma with a minimum of twelve (12) years of experience in Agronomy, Plant Biotechnology, Horticulture or related field or;
• Bachelor’s degree and minimum of six (6) years of experience in Agronomy, Plant Biotechnology, Horticulture or related field
• Three (3) to five-(5) years of supervision experience is required
• Experience and ability to work in warm and humid conditions

iBio is a global leader in plant-based biologics manufacturing. Our FastPharming System combines vertical farming, automated hydroponics, and glycan engineering technologies to rapidly deliver gram quantities of high-quality monoclonal antibodies, vaccines, bioinks and other proteins. We accomplish all of this via our CGMP 130,000 square foot facility in Bryan, TX.  

Just imagine what we can do together!  We know great things happen when talent and opportunity cross paths. We are looking to hire exceptional people who have demonstrated track records of success.  Our greatest scientific solution is bringing talented people together who have a passion for advancing plant-based biologics for our customers and the world.

Apply now for our Agronomy Technician II position!

MISSION OF THE POSITION

The Agronomy Technician II performs a variety of hydroponic plant production tasks and experiments. This position works with the Agronomy team to manage and maintain a healthy plant lifecycle and partners with manufacturing to ensure alignment. 

ESSENTIAL DUTIES & RESPONSIBILITES

• Produce hydroponic plant materials under controlled conditions in the Pilot Production Resource
• Seed, transplant, and manage plant lifecycle in pre-infiltration and post-infiltration environments
• Assist with managing seed stock and seed bank
• Maintain nutrient solution by preparing nutrient stocks and sample nutrient solution for proper fertility and pH levels
• Directly monitor and maintain irrigation delivery system, including but not limited to plumbing, pumps, irrigation controllers, valves, emitters and makes repairs as needed
• Perform tasks related to disease and pest prevention such as monitoring, sanitization, and data collection
• Handle the disposal of pilot plant production waste materials, including BSL-1 waste from genetically modified plant materials
• Perform support function for Agronomy Supervisor; adherence to standard operating procedures, batch record, and good documentation practices
• Assist the Production team in manufacturing activities as necessary
• Maintain effective working relationships with others
• Other duties as assigned 

KNOWLEDGE, SKILLS, & ABILITIES

• Ability to learn new techniques/skills in proficiency
• Working knowledge of hydroponics and plant nutrition and growth needs
• Must be skilled in keeping excellent scientific records, cGMP experience is a plus
• Ability to work independently; creative problem-solving is a plus

EDUCATION & EXPERIENCE

• Associates degree with a minimum of two (2) years’ relevant greenhouse/ plant production experience; Or
• High School Diploma/GED with a minimum of four (4) years relevant greenhouse/plant production experience
• Experience in automation, particularly greenhouse automation technologies is a plus
• Experience and ability to work in warm, humid conditions

iBio is a global leader in plant-based biologics manufacturing. Our FastPharming System combines vertical farming, automated hydroponics, and glycan engineering technologies to rapidly deliver gram quantities of high-quality monoclonal antibodies, vaccines, bioinks and other proteins. We accomplish all of this via our CGMP 130,000 square foot facility in Bryan, TX.  

Just imagine what we can do together!  We know great things happen when talent and opportunity cross paths. We are looking to hire exceptional people who have demonstrated track records of success.  Our greatest scientific solution is bringing talented people together who have a passion for advancing plant-based biologics for our customers and the world.

Apply now for our Assay Development Research Associate position!

MISSION OF THE POSITION

The Assay Development Research Associate will be part of the assay development group at iBio and is responsible for assisting with the development, design, execution, and transfer of biological, biochemical, and molecular assays to support product development, process characterization, and early stage production of biotherapeutic molecules.

ESSENTIAL DUTIES & RESPONSIBILITES

• Work in the laboratory setting (BSL-1 and BSL-2)
• Assist scientific staff with assay development and execution
• Maintain detailed laboratory notebooks
• Grow and maintain cell cultures
• Capability and interest in learning multiple analytical methods
• Assist with document preparation as required
• Perform reagent and sample preparation
• Perform analytical methods with minimal supervision
• Maintain laboratory equipment
• Place orders for supplies as necessary
• General laboratory maintenance
• Perform data analysis with limited supervision

 KNOWLEDGE, SKILLS, & ABILITIES

• Understanding of laboratory safety
• Maintain professionalism with personnel and management
• Collaborative team player
• Working knowledge of multiple computer programs (e.g. Microsoft office)
• Experience with one or more analytical assays such as SDS-PAGE
• Must be capability of and driven to learn multiple new methods
• Strong communication skills both verbal and written
• Well organized with effective time management
• Energetic and detail oriented 

EDUCATION & EXPERIENCE

• Bachelor’s degree in Molecular Biology or related field required
• Tissue culture experience is a strong plus
• Experience with one of more relevant analytical methods (e.g. ELISA)
• Experience in a cGMP regulated environment is a plus

iBio is a global leader in plant-based biologics manufacturing. Our FastPharming System combines vertical farming, automated hydroponics, and glycan engineering technologies to rapidly deliver gram quantities of high-quality monoclonal antibodies, vaccines, bioinks and other proteins. We accomplish all of this via our CGMP 130,000 square foot facility in Bryan, TX.  

Just imagine what we can do together!  We know great things happen when talent and opportunity cross paths. We are looking to hire exceptional people who have demonstrated track records of success.  Our greatest scientific solution is bringing talented people together who have a passion for advancing plant-based biologics for our customers and the world.

Apply now for our Assay Development Technician position!

MISSION OF THE POSITION

The Assay Development Technician will be part of the assay development group at iBio and is responsible for assisting with the development, design, execution, and transfer of biological, biochemical, and molecular assays to support product development, process characterization, and early stage production of biotherapeutic molecules.

ESSENTIAL DUTIES & RESPONSIBILITES

• Maintain laboratory equipment
• Maintain laboratory logbooks
• General maintenance of the process development lab
• Keep an organized, detailed lab notebook
• Order supplies as necessary
• Prepare buffers and reagents
• Train on multiple analytical methods
• Perform analytical methods with general supervision
• Assist with analytical development activities

 KNOWLEDGE, SKILLS, & ABILITIES

• Maintain professionalism with personnel and management
• Collaborative team player
• Working knowledge of common computer programs (e.g. Microsoft office)
• Understanding of one or more analytical assays such as SDS-PAGE
• Must be capable and interested in learning new methods
• Strong communication skills both verbal and written
• Well organized with effective time management
• Energetic and detail oriented

 EDUCATION & EXPERIENCE

• Associate degree in Molecular Biology or related field required; Bachelor’s degree preferred
• Tissue culture experience is a strong plus
• Experience in a laboratory setting

iBio is a global leader in plant-based biologics manufacturing. Our FastPharming System combines vertical farming, automated hydroponics, and glycan engineering technologies to rapidly deliver gram quantities of high-quality monoclonal antibodies, vaccines, bioinks and other proteins. We accomplish all of this via our CGMP 130,000 square foot facility in Bryan, TX.  

Just imagine what we can do together!  We know great things happen when talent and opportunity cross paths. We are looking to hire exceptional people who have demonstrated track records of success.  Our greatest scientific solution is bringing talented people together who have a passion for advancing plant-based biologics for our customers and the world.

Apply now for our Buyer/Planner position!

MISSION OF THE POSITION

The Buyer/Planner is responsible for the overall ordering process to support demand planning and inventory management by optimizing inventory to meet production / forecasting and scheduling efficiencies. This position will develop a schedule for procuring new and existing devices in support of inventory objectives and facility goals.

 POSITION SUMMARY

This position will create, prepare, distribute, monitor and follow-up on purchasing actions based upon orders that have been placed, and historical parts usage based upon RMA activity. The Buyer/Planner will be a subject matter expert in inventory management and purchasing. 

ESSENTIAL DUTIES & RESPONSIBILITIES

• Consistently maintain proper inventory levels; manage all inventories and forecast accurate inventory targets and allocations
• Identify potential supply risks and inventory exposures by aligning supply chain and forecast models
• Support physical inventory counts, reconcile inventory variances
• Interact with suppliers to maintain delivery scheduling
• Monitor supplier performance by ensuring product deliveries as scheduled and meets specifications
• Perform physical inventory checks
• Maintain appropriate inventory levels consistent with targeted inventory goals
• Maintain accuracy within Purchasing ERP system regarding Orders and Inventory
• Coordinate with Materials Technician to ensure what is captured as part of Shipping & Receiving aligns with order receipt and inventory and following Standard Operating Procedures and Forms
• Participate in regular Site Supply Chain / Planning meetings (e.g. S&OP and LRP) to evaluate manufacturing plans to ensure inventory coverage and supply readiness
• Maintain system planning parameters (e.g. lot size, lead-time, and safety stock levels) within the site ERP
• Work closely with Sr. Manager, Procurement to manage assigned Strategic / Preferred Suppliers
• Assist identification and qualification of new sources of supply to support the business strategies
• Review, approve, and coordinate change to specifications as required
• Demonstrate project management skills, including project chartering, timeline development and management of deliverables
• Issue purchase orders using ERP system and ensure suppliers confirm receipt of PO
• Collaborate with Facilities, Quality, Engineering, and EMS groups to understand their sourcing needs and issuing purchase orders while meeting the appropriate need-by-date
• Review open Purchase Order List and follow up on updated delivery time with suppliers to ensure assurance of supply 

KNOWLEDGE, SKILLS, & ABILITIES

• Competent and knowledgeable in utilizing best practices in inventory management
• Strong analytical skills and attention to detail
• Advanced level Microsoft Excel and reporting skills
• Ability to identify and  evaluate key supply issues for the company and develop alternative solutions
• Strong verbal and written communication skills
• Ability to be a team player and work with various areas of the organization 

EDUCATION & EXPERIENCE

• BS/BA degree with concentration in Supply Chain, Operations, Purchasing, or related
• Minimum 2-3 years of buying and/or planning experience in similar or equivalent role 
• Buyer and/or Supply Planning experience in SAP
• Warehouse experience
• APICS or ISM Certification, preferred
• Life science experience or regulated industry experience, beneficial

iBio is a global leader in plant-based biologics manufacturing. Our FastPharming System combines vertical farming, automated hydroponics, and glycan engineering technologies to rapidly deliver gram quantities of high-quality monoclonal antibodies, vaccines, bioinks and other proteins. We accomplish all of this via our CGMP 130,000 square foot facility in Bryan, TX.  

Just imagine what we can do together!  We know great things happen when talent and opportunity cross paths. We are looking to hire exceptional people who have demonstrated track records of success.  Our greatest scientific solution is bringing talented people together who have a passion for advancing plant-based biologics for our customers and the world.

Apply now for our Controller position!

MISSION OF THE POSITION
We are seeking a highly motivated individual to join us as the iBio Controller. This position is responsible for safeguarding the assets of the company and for all required financial reporting. The Controller will be the subject matter expert on SEC regulations and provisions of the Sarbanes-Oxley Act that apply to iBio as a publicly traded company.

POSITION SUMMARY

This position ensures the effectiveness of the financial control environment and also the accounting policies, processes and procedures of the organization. This position will ensure that the accounting for all transactions is performed in an accurate, efficient and timely manner in conformity with GAAP. The Controller will work cross-functionally with leaders, including in operations, and reports directly to the Chief Financial Officer.

ESSENTIAL DUTIES & RESPONSIBILITES

• All accounting operations and full cycle transactional responsibilities including, but not limited to, the following:
  • Cash Management
  • Accounts Receivables / Customer Maintenance
  • Prepaids
  • Fixed Assets
  • Capital Leasing
  • Accounts Payable / Vendor Maintenance
  • Purchasing and Requisitioning
  • Intercompanies
  • General Ledger / Chart of Accounts / Journal Entries
  • Invoicing/Billing
  • Revenue recognition in conformity with ASC 606
  • Expenses
• Responsible for supervising and signing off on the semi-monthly payrolls for all employees
• Ownership over the monthly, quarterly and annual close cycle (close, consolidation and reporting), including the preparation or review of all supporting documentation, schedules, reconciliations and other requirements
• Has primary ownership of the annual audit and interim reviews, coordinates with outside auditors and manages internal resources to complete on an accurate and timely basis.
• Coordinates the timely filing of the Company tax returns prepared by outside tax advisors and ensures proper maintenance of accounting records and documentation in compliance with statutory requirements and Company policies.
• Directs the preparation and analysis of monthly financial statements for review by Company management
• Oversees company sub-contractors, consultants and vendors relative to invoices, purchase orders and certificates of insurance.
• Support the business and management with accurate cost accounting and department profit & loss statements
• Pricing, cost and other strategic modeling and analytics
• Perform other duties as assigned and / or required

KNOWLEDGE, SKILLS, & ABILITIES

• Collaborative team player
• High level verbal and written communications skills
• Ability to gather and analyze information skillfully
• Thorough and high attention to detail
• Expertise in accounting in accordance with GAAP
• Exemplary planning and time management skills
• Ability to multitask and prioritize daily workload
• Discretion and confidentiality
• Ability to work with cross-functional teams and senior finance management
• Demonstrated ability to mentor and train personnel 

EDUCATION & EXPERIENCE

• Bachelor’s degree in Accounting required
• Master of Business Administration with a concentration in Accounting and Finance preferred
• CPA certification required
• Minimum of 3+ years’ experience in public accounting
• Minimum 2 years’ experience working in the finance department of a publicly traded company
• Sarbanes-Oxley and understanding of SEC reporting requirements
• Experience with stock-based compensation and equity
• Experience in biotechnology / pharmaceutical industry preferred
• Working knowledge of SAP (FICO) preferred

iBio is a global leader in plant-based biologics manufacturing. Our FastPharming System combines vertical farming, automated hydroponics, and glycan engineering technologies to rapidly deliver gram quantities of high-quality monoclonal antibodies, vaccines, bioinks and other proteins. We accomplish all of this via our CGMP 130,000 square foot facility in Bryan, TX.  

Just imagine what we can do together!  We know great things happen when talent and opportunity cross paths. We are looking to hire exceptional people who have demonstrated track records of success.  Our greatest scientific solution is bringing talented people together who have a passion for advancing plant-based biologics for our customers and the world.

Apply now for our Director of Analytical Sciences position!

MISSION OF THE POSITION

The Director of Analytical Sciences is responsible for the strategic planning and management of all analytical and bioassay development, qualification, and testing activities at both internal and external testing laboratories in support of products (research-use, for further manufacturing, preclinical, clinical and commercial.) 

POSITION SUMMARY

The Director of Analytical Sciences directs all analytical laboratory activities including analytical development, bioassays, and transfer of assays to the Quality Control group. This position will ensure that analytical methods are developed and qualified/validated as required and that all laboratory activities, both internal and at external contract testing laboratories, are conducted in accordance with required regulatory requirements to ensure ongoing supply of product to meet clinical and commercial demand. 

ESSENTIAL DUTIES & RESPONSIBILITES

• Review and approve documents as required, including specifications, SOPs, protocols, technical reports, test methods, change requests, technical transfers, OOS/OOT investigations, regulatory submissions, and deviations
• Ensure that appropriate Quality Management Systems for internal and external contract manufacturers/laboratories are developed, implemented, and managed in collaboration with Quality Assurance
• Ensure phase-appropriate development, change control, and qualification/validation of test methods and associated equipment/instrumentation
• Remain current with USP, EP, BP, JP and ICH requirements, as applicable
• Ensure the establishment of product specifications and appropriate acceptance criteria for the stage of the product development in collaboration with Process Development.
• Ensure a robust and globally compliant Stability Program is established and maintained for all iBio and iBio CDMO services client products (research-use, for further manufacturing, preclinical, clinical and commercial)
• Track and trend product test data including the evaluation and approval of data received from external contract laboratories
• Compile and report data with appropriate interpretations for internal Management Reviews, Product Reviews, Client Reviews and Audits, and all other product quality assessments
• Mentor staff on scientific innovation, regulatory guidelines, and project management
• Coordinate and prioritize resources ensuring that quality, time to market, performance, and budgetary goals are met
• Prepare presentations for executive management to provide updates and facilitate decision-making
• Participate in proposal development and defining scopes of work for iBio and iBio CDMO services clients
• Author iBio and iBio CDMO services client reports and papers for journal submission and peer review

KNOWLEDGE, SKILLS, & ABILITIES

• Working knowledge and ability to apply cGMP in conformance to U.S., EU, ROW and ICH Standards
• Expertise in protein, biological, cell-based, and analytical technologies and laboratory operations
• Ability to multi-task and prioritize complex daily workload
• Ability to effectively negotiate internally and externally at all levels within an organization and build collaboration among individuals
• Demonstrated ability to develop, coach, and mentor employees
• Strong written and verbal communication skills
• Proficient with Microsoft Office Suite
• Able to proactively identify issues and address with solutions-oriented approaches 

EDUCATION & EXPERIENCE

• Bachelor’s degree in Genetics, Pharmacology, Cellular and Molecular Biology, Biochemistry or related field required; higher education (MS or PhD) strongly preferred
• 7-15 years of industry experience strongly preferred
• 5+ years progressive cGMP experience in a pharmaceutical or biologics operation
• 2+ years of management/leadership experience
• Experience with global regulatory requirements and inspections

iBio is a global leader in plant-based biologics manufacturing. Our FastPharming™ System combines vertical farming, automated hydroponics, and glycan engineering technologies to rapidly deliver gram quantities of high-quality monoclonal antibodies, vaccines, bioinks and other proteins. We accomplish all of this via our CGMP 130,000 square foot facility in Bryan, TX.  

Just imagine what we can do together!  We know great things happen when talent and opportunity cross paths. We are looking to hire exceptional people who have demonstrated track records of success.  Our greatest scientific solution is bringing talented people together who have a passion for advancing plant-based biologics for our customers and the world.

Apply now for our Lead Manufacturing Technician – Fill Finish position!

MISSION OF THE POSITION

Based in Bryan, Texas, this position will perform basic to complex activities on the fill finish line for production and will work in accordance with regulations, detailed protocols, batch records, SOPs, and work instructions. The Lead Manufacturing Technician – Fill Finish will be expected to be a subject matter expertise cGMP manufacturing.

POSITION SUMMARY

The Lead Manufacturing Technician focus will be to provide operational and technical support for all fill finish operations with adherence to cGMP compliance. This position requires proficiency in aseptic technique, and deliberate movements inside isolators. The candidate for this position will be working in close association with Process Development, Quality Assurance, Quality Control, Project Management, and Supply Chain to ensure conformance to the manufacturing schedule.

ESSENTIAL DUTIES & RESPONSIBILITES

• Daily Aseptic processing within a controlled isolator environment and within a BSC.
• Perform legible, clear, and concise data entry into batch records, logbooks, and all other controlled forms used in a cGMP process.
• Follows verbal and written procedures in operating production equipment and performing processing steps.
• Identifies, escalates and documents events and variances that deviate from normal operation; participate as needed in investigations.
• Monitor assigned processes using automated production systems and controls with limited supervision.
• Equipment preparation activities including, parts cleaning, autoclaving, and room clearance.
• Demonstrates ability to troubleshoot basic mechanical operations.
• Post-Fill tasks will include visual inspection, secondary packaging, and environmental monitoring.
• Performs batch record review, procedure revisions, and work order generation.
• Fulfills role of lead trainer on numerous operations and is an area SME.
• Work in accordance with site and company EHS programs.
• Prepare and process components, materials and equipment for aseptic fill finish activities, operate filling equipment and perform aseptic manipulations, able to inspect finished vials and perform labeling activities to support shipment.

KNOWLEDGE, SKILLS, & ABILITIES

• A strong attention to detail
• Must be able to work in a fast-paced environment.
• Team Player
• Excellent verbal and written communication skills
• Ability to aseptically gown and/or sterile gown as needed.
• Effectively utilizes Microsoft office applications.
• Work towards solutions to given problems and operate under cGMP requirements.
• Work cross-functionally with support groups such as Facilities, Supply Chain, Quality Control and Quality Assurance.
• Qualify to work in aseptic environments to complete required production activities.

EDUCATION & EXPERIENCE

• BS – Chemistry, Biology or related field – preferred. A combination of education and experience will be considered.
• 3+ years industry related experience of on-the-floor leadership or “subject matter expertise”.
• Subject matter expertise in cGMP manufacturing.

iBio is a global leader in plant-based biologics manufacturing. Our FastPharming System combines vertical farming, automated hydroponics, and glycan engineering technologies to rapidly deliver gram quantities of high-quality monoclonal antibodies, vaccines, bioinks and other proteins. We accomplish all of this via our CGMP 130,000 square foot facility in Bryan, TX.  

Just imagine what we can do together!  We know great things happen when talent and opportunity cross paths. We are looking to hire exceptional people who have demonstrated track records of success.  Our greatest scientific solution is bringing talented people together who have a passion for advancing plant-based biologics for our customers and the world.

Apply now for our Materials Technician position!

MISSION OF THE POSITION

We are seeking a highly motivated individual to join us as the iBio Materials Technician. This position is will be responsible for all daily activities related to shipping, receiving, delivery, monitoring and stocking. This position will also work in support of the Buyer / Planner and will be responsible for ensuring the smooth and efficient operations of shipping, receiving and inventory. 

ESSENTIAL DUTIES & RESPONSIBILITES

• Responsible for all for incoming materials (GMP / Non-GMP / Facilities, etc)
• Manage the dock operating a forklift, verify and sign Incoming Delivery Bill of Lading
• Oversee incoming and outgoing shipping activities to ensure accuracy, completeness, and conditions of shipments
• Inspect incoming materials and notify appropriate staff of potential quality issues
• Examine, stock, and distribute materials to inventory and appropriate departments
• Inspect loading operations to ensure compliance with specifications
  Process Receiving / Returns Transactions
• Maintain spreadsheets or ERP system in support of inventory management
  Follow SOP’s regarding processing of incoming GMP and non-GMP materials
• File all Shipping / Receiving / Returns documents accordingly
• Maintain close lines of communication with the Buyer / Planner on delivery of materials and inventory
• Responsible for Inventory Racks, floor location organization and overall cleanliness of the stocking areas
• Maintain inventory by identifying, labeling, and placing materials and supplies in stock, recording location of inventory
• Process incoming receipts
• Deliver original packing slips to Accounts Payable
• Responsible for maintaining quality and regulatory compliance in the job duties and following appropriate procedures
• Communicate often with the Buyer / Planner for effective and accurate inventory and ordering
• Immediately report all delivery shortages to the Buyer / Planner
• Must be responsible in maintaining receiving and shipping accuracy
• Other duties as assigned

 KNOWLEDGE, SKILLS, & ABILITIES

• Basic skillset in Microsoft Office products/Google Drive (Excel, Word, PowerPoint, etc.)
• Self-directed with high energy and motivation
• Ability to work independently with limited oversight
• Excellent verbal and written communication skills; Presentation skills are a plus
• Position has physical requirements and must be able to lift 70lbs boxes on a routine basis
• Must be able to routinely stand between 75%-100% per working day
• Ability to successfully interact and coordinate with different teams within the organization
• Ability to work in a high paced environment 

EDUCATION & EXPERIENCE

• High School Diploma or GED
• Two years warehouse work experience in Receiving, Shipping, Returns
• Experience operating a forklift is a plus
• Experience using an ERP system is a plus.

iBio is a global leader in plant-based biologics manufacturing. Our FastPharming System combines vertical farming, automated hydroponics, and glycan engineering technologies to rapidly deliver gram quantities of high-quality monoclonal antibodies, vaccines, bioinks and other proteins. We accomplish all of this via our CGMP 130,000 square foot facility in Bryan, TX.  

Just imagine what we can do together!  We know great things happen when talent and opportunity cross paths. We are looking to hire exceptional people who have demonstrated track records of success.  Our greatest scientific solution is bringing talented people together who have a passion for advancing plant-based biologics for our customers and the world.

Apply now for our Molecular Biology Research Associate position!

MISSION OF THE POSITION

The Molecular Biology Research Associate is expected to assist in the generation of expressions systems including, but not limited to, cloning of expression vectors, plant infiltration, and extraction and yield analysis of recombinant proteins.

POSITION SUMMARY

This position will perform experiments and interpret results, subject to verification by the Scientist of Molecular Biology, according to applicable SOPs and business/biological deadlines. The Molecular Biology Research Associate will be familiar with cGMP regulations and a subject matter expert in standard molecular biology techniques.

ESSENTIAL DUTIES & RESPONSIBILITES

• Help construct and analyze accuracy of expression vectors using routine molecular biology techniques
• Transform bacteria, amplify and isolate expression vectors, and generate plasmid and bacterial clone stocks
• Prepare media, reagents, culture flasks and bioreactors for the culture of bacteria
• Run and harvest bacterial cultures
• Perform infiltration of plant material for the expression of recombinant proteins
• Clean and autoclave BSL1 biohazard material as required
• Responsible for the culture of inoculum including agrobacteria in a culture flask and bioreactor format
• Perform plant infiltration
• Harvest plant biomass and organize its storage
• Perform recombinant protein extraction and analyze recombinant protein expression levels
• Assist in the organization and maintenance of plasmids and bacterial clone stocks
• Comply with government and company health and safety policies and regulations, especially with respect to biohazardous materials
• Assist the Lab Manager in maintaining the stock of lab supplies, chemicals, and reagents
• Assist in the organization of the lab
• Record the results of technical experiments according to data collection guidelines and policies
• Assist in creating and updating official documents including, but not limited to, Standard Operating Procedures (SOPs)

KNOWLEDGE, SKILLS, & ABILITIES

• Knowledge in standard molecular biology techniques including cloning, Polymerase Chain Reaction (PCR), gel electrophoresis, bacteria transformation, DNA isolation and sequence analysis
• Knowledge of protein characterization techniques including Enzyme- Linked Immuno Assay (ELISA), western blot and SDS-PAGE
• Skill in documentation and attention to detail
• Skill in basic computer functions such as word processors, spreadsheets and presentation applications
• Familiarity with current good manufacturing practice (cGMP) regulations for pharmaceutical manufacturing
• Familiarity with protocol writing
• Collaborative team player
• Must be able to communicate effectively through oral and written communication
• Must be able to gather and analyze information skillfully

 EDUCATION & EXPERIENCE

• Associate degree in Molecular Biology, Biological Sciences or other related discipline required; Bachelor’s degree preferred
• Working experience in general laboratory techniques and laboratory maintenance

iBio is a global leader in plant-based biologics manufacturing. Our FastPharming System combines vertical farming, automated hydroponics, and glycan engineering technologies to rapidly deliver gram quantities of high-quality monoclonal antibodies, vaccines, bioinks and other proteins. We accomplish all of this via our CGMP 130,000 square foot facility in Bryan, TX.  

Just imagine what we can do together!  We know great things happen when talent and opportunity cross paths. We are looking to hire exceptional people who have demonstrated track records of success.  Our greatest scientific solution is bringing talented people together who have a passion for advancing plant-based biologics for our customers and the world.

Apply now for our Principal Engineer, Manufacturing Science & Technology (MSAT) position!

MISSION OF THE POSITION

As the Principal Engineer of Manufacturing Science & Technology (MSAT) you will have responsibilities for providing scientific and technical support to downstream bioprocess manufacturing operations. This role is responsible for managing tech transfer packages from Process Development to support the design, installation, commissioning, and validation of GMP processes and equipment. 

POSITION SUMMARY

The Principal Engineer, MSAT will be responsible for performing process monitoring and analysis, process performance troubleshooting, as well as establishment and maintenance of the process validated state and ongoing process improvement.

ESSENTIAL DUTIES & RESPONSIBILITES

• Manage team responsible for facility fit activities; including process flow diagram generation, scale-up calculations, defining equipment and solution requirements, generation bill of materials (BOM) and new specifications while ensuring safety and quality standards are maintained.
• Provide technical expertise to lead process tech transfers through budget development, schedule development, resource planning, design, construction, commissioning, and qualification activities.
• Provide technical expertise to lead the commissioning and validation of processes, process equipment and utilities.
• Partner with Manufacturing, Process Development, Engineering, QA, QC, and Project Management to support the process transfer and project timelines.
• Lead gap analyses and risk assessments to support the tech transfers.
• Author tech transfer related projects plans, assessments, and process validation protocols
• Authors and reviews process descriptions, formulations, batch records, bill of material, change controls.
• Generate controlled documents to support the start-up, operation, validation and maintenance of equipment and complex systems.
• Works closely with manufacturing to provide on-the-floor technical oversight before and during GMP runs.
• Review and approve vendor information packages, including drawings and specifications.
• Provide key input into the validation of process equipment and associated utilities. Direct manufacturing and operations staff in the execution of validation protocols.
• Assess all major deviations, identify potential root causes using a systematic approach. Expertise in use and application of variety of problem-solving tools. Able to identify potential solutions and lead multidisciplinary teams in developing and implementing solutions.
• Recommends improvements for MSAT practices and procedures. Leads the compilation of process data, including communicating project status, and delivering presentations.

KNOWLEDGE, SKILLS, & ABILITIES

• Excellent organization and time management skills.
• Excellent communication skills, both written and verbal.
• Use creativity and innovation to address urgent and/or complex problems and propose solutions.
• Solid technical understanding of downstream processes (harvest, chromatography, TFF, and/or UF/DF)
• Thorough knowledge of biopharmaceutical manufacturing, process equipment and supporting utility systems, especially those related to sterile operations
• Process troubleshooting and experimental design
• Prior experience in biologics manufacturing facility
• Perform, understand, and interpret all types of complex data analysis such as multiple linear regression analysis, ANOVA, multivariate analysis and identify applications.
• Thorough knowledge of cGMP guidelines, experience in generation of controlled documents and extensive experience in equipment start-up and validation. 

EDUCATION & EXPERIENCE

• BS/MS/PhD in engineering discipline – Chemical Engineering, Biochemical Engineering, Biotechnology, Biochemistry, or related field.
• 8+ years’ experience in downstream biologics process development, technology transfer, pilot plant, or manufacturing support.
• 8+ years applicable equipment and process system experience.
• Extensive experience in biotech industry in process development, process scale up, tech transfer and manufacturing.
• Experience in the design, installation, and operations of GMP processes and equipment.

iBio is a global leader in plant-based biologics manufacturing. Our FastPharming System combines vertical farming, automated hydroponics, and glycan engineering technologies to rapidly deliver gram quantities of high-quality monoclonal antibodies, vaccines, bioinks and other proteins. We accomplish all of this via our CGMP 130,000 square foot facility in Bryan, TX.  

Just imagine what we can do together!  We know great things happen when talent and opportunity cross paths. We are looking to hire exceptional people who have demonstrated track records of success.  Our greatest scientific solution is bringing talented people together who have a passion for advancing plant-based biologics for our customers and the world.

Apply now for our Process Development Research Associate II position!

MISSION OF THE POSITION

The Process Development (PD) Research Associate II will follow protocols and execute experiments as delineated by senior personnel. These protocols may range from small-scale to at scale experiments for downstream protein purification and may include helping in the execution of characterization assays to meet or exceed internal and/or client expectations. Duties include buffer preparation, plant tissue homogenization, product extraction, tangential flow filtration, chromatographic purification, and sterile filtration.

POSITION SUMMARY

The successful candidate will be expected to work cross functionally with colleagues in other departments (Molecular Biology, Agronomy, Quality Control, Analytical Development). The employee is also responsible for training on, understanding, and following documented procedures that apply to his/her position. This position reports to  the Director of Downstream Process Development.  

ESSENTIAL DUTIES & RESPONSIBILITES

• Executes biomass homogenization and clarification, and assists in protein purification protocols
• Performs buffer filtration, depth, micro-, and ultra- filtration
• Provides support during protein purifications by helping set up buffers for column chromatography on FPLCs
• Performs analyses such as: SDS-PAGE, concentration determination, Western blot, ELISA, assists on setting up HPLC
• Operates centrifugation equipment with the supervision of senior personnel
• Is expected to record data and maintain records of experiments performed in company provided laboratory notebooks. Maintains records of experiments performed
• Assists with day to day maintenance and cleaning of the laboratory and its equipment, which include but is not limited to performing calibrations of laboratory equipment, autoclaving of glassware, and helps stock and order supplies
• Should be able to provide research or information for use in presentations

KNOWLEDGE, SKILLS, & ABILITIES

• Collaborative team player
• Attention to detail and organization
• Must be able to communicate effectively (oral and written)
• Ability to follow oral and written guidance
• Computer skills must include proficiency in MS Office 

EDUCATION & EXPERIENCE

• BS/BA, associate degree in biomedical sciences and 2-4 years of research and/or biotech wet lab experience

iBio is a global leader in plant-based biologics manufacturing. Our FastPharming System combines vertical farming, automated hydroponics, and glycan engineering technologies to rapidly deliver gram quantities of high-quality monoclonal antibodies, vaccines, bioinks and other proteins. We accomplish all of this via our CGMP 130,000 square foot facility in Bryan, TX.  

Just imagine what we can do together!  We know great things happen when talent and opportunity cross paths. We are looking to hire exceptional people who have demonstrated track records of success.  Our greatest scientific solution is bringing talented people together who have a passion for advancing plant-based biologics for our customers and the world.

Apply now for our Process Development Scientist position!

MISSION OF THE POSITION 

The Process Development (PD) Scientist will assist senior personnel in the development and optimization of scalable purification processes and will execute small-scale and at-scale experiments for downstream protein purification to meet or exceed internal and/or client expectations. He/She will be an expert in a range of purification technologies including filtration technologies (depth and TFF), chromatographic separations (including affinity, IEX, HIC, etc), and basic laboratory analytical techniques. The PD Scientist will be able to troubleshoot experimental and instrumental issues related to downstream protein purification.

POSITION SUMMARY 

The successful candidate will be expected to effectively collaborate with colleagues in other departments (Molecular Biology, Agronomy, Quality Control, Analytical Development) and participate in discussion of data analysis and process development/optimization. The employee is also responsible for training on, understanding, and following documented procedures that apply to his/her position. This position reports to the Director of Downstream Process Development.

ESSENTIAL DUTIES & RESPONSIBILITES

• Assists in the development, optimization, and scale-up of purification protocols
• May be assigned as a lead on individual projects
• Executes biomass homogenization, clarification, and protein purification
• Operates filtration (depth, micro-, and ultra- filtration) equipment
• Expert operator of chromatographic systems (GE AKTA, and other Unicorn based equipment), which includes column packing experience
• Operates HPLC equipment
• Performs analyses such as: SDS-PAGE, concentration determination, Western blot, ELISA, assists on setting up HPLC
• Authors reports detailing experimental work, summarizes and provides critical analysis of results and next steps that should be taken in company provided laboratory notebooks and does so in a timely manner
• Troubleshoots challenging technical, experimental, and instrumental issues with little to no supervision
• Trains junior staff (Research Associates I, II, and III) in the execution of downstream processes

KNOWLEDGE, SKILLS, & ABILITIES 

• Understanding of biochemical and biophysical principles involved in purification and analysis of biological macromolecules
• Experience in downstream processing and process development in biopharmaceutical industry
• Hands-on experience with preparative chromatography and membrane separations
• Strong technical communication skills for creation of documents, articulation of ideas,
• Experience in protein characterization (SDS-PAGE, Western blotting, protein quantification)
• Strong work ethic, attention to detail, and ability to work within timelines
• Must be able to communicate effectively (oral and written)
• Ability to work both independently and in close coordination with others in a highly collaborative, fast-paced, cross-functional environment
• Must be proficient in MS Office

EDUCATION & EXPERIENCE

• BS/BA in biomedical sciences or related field and 7-8 years in the biotechnology industry; OR
• MS in biomedical sciences or related field and 4-5 years in the biotechnology industry; OR
• PhD in biomedical sciences or related field and 2-3 years in the biotechnology industry
• Demonstrated and documented ability to perform all job requirements listed under duties and responsibilities

iBio is a global leader in plant-based biologics manufacturing. Our FastPharming System combines vertical farming, automated hydroponics, and glycan engineering technologies to rapidly deliver gram quantities of high-quality monoclonal antibodies, vaccines, bioinks and other proteins. We accomplish all of this via our CGMP 130,000 square foot facility in Bryan, TX.  

Just imagine what we can do together!  We know great things happen when talent and opportunity cross paths. We are looking to hire exceptional people who have demonstrated track records of success.  Our greatest scientific solution is bringing talented people together who have a passion for advancing plant-based biologics for our customers and the world.

Apply now for our PMO Director position!

MISSION OF THE POSITION

This position will be based in Bryan, Texas and will oversee iBio’s overall project management function, providing leadership, integration, and management of PMO process and functions to improve the consistency and efficiency of the company’s project delivery. 

POSITION SUMMARY

The PMO Director will be responsible for leading the development and execution of program/project plans for all company projects, including vaccine & therapeutic development, customer projects, R&D, etc. This position applies a combination of life sciences strategy, leadership, and managerial experience to identify opportunities and proactively identify and facilitate risks, mitigations, resolution and escalation of issues, and will track and communicate status to internal/external stakeholders.

ESSENTIAL DUTIES & RESPONSIBILITES

• Assess, propose, and implement project management automation software
• Develop strategy and operating model for the Project Management office
• Define and execute the mission, vision, strategy and direction of the PMO in alignment with company goals
• As a member of the leadership team, evaluate and prioritize capability and innovation initiatives
• Lead the development of business plans, capital appropriation requests, and business cases for initiatives under the direction of PMO
• Responsible for decisions regarding prioritization, resource allocation, and budget for the PMO
• Anticipate obstacles and develop contingency plans to address them; taking necessary corrective actions to keep program on schedule
• Represent the PMO confidently in interactions with key internal and external stakeholders
• Identify and manage PMO team KPIs as well as KPIs for projects and programs under management; measure quality and opportunities for improvement
• Standardize project management best practices to improve overall efficiency, accuracy, and compliance while overseeing multiple customer product portfolios
• Ensure the generation and maintenance of integrated project plans (options development, opportunities identification, timing) that reflect the approved balance of scope, time, and resources
• Act as the central liaison to clients, providing clear, concise, actionable messages that benefit all aspects of the project/program (technical, programmatic, regulatory, contractual, etc.)
• Facilitate and manage productive team communication and collaboration, both internally and externally
• Knowledgeable of changes with international guidance and regulation impacting PMO initiatives
• Track workstream initiatives, develop reporting dashboards, standardize report configurations, and build executive briefings

KNOWLEDGE, SKILLS, & ABILITIES

• Demonstrated project management skills, with proven track record of leading broad, complex and/or strategic programs combined with the ability to execute at tactical project level activites and tasks
• Experience successfully leading matrix teams of subject matter experts from diverse disciplines
• Experience leading large-scale initiatives involving technology, business process, and change management in a pharmaceutical research and development setting
• Demonstrated experience in US Government-supported contract management
• Excellent leadership and negotiation skills to manage programs and develop new business
• Strong creative, analytical, and problem-solving skills
• Strong interpersonal, leadership, and presentation skills for interacting with and influencing team members, clients, leaders, and subject matter experts
• Strong written communication and presentation skills 

EDUCATION & EXPERIENCE

• Master’s level degree (or bachelor’s degree with relevant experience) in life sciences, business, or a combination of relevant education or professional experience
• Project Management Professional (PMP) Certification strongly preferred
• Ten (10) – Fifteen (15) years of practical program/project management experience in biotechnology-related work, preferably a mix of industry and government contract experience
• Experience working with automated project management tools, has implemented software automation systems in previous work experience

PROJECT MANAGER

iBio is a global leader in plant-based biologics manufacturing. Our FastPharming System combines vertical farming, automated hydroponics, and glycan engineering technologies to rapidly deliver gram quantities of high quality monoclonal antibodies, vaccines, bioinks and other proteins. We accomplish all of this via our CGMP 130,000 square foot facility in Bryan, TX.  

Just imagine what we can do together!  We know great things happen when talent and opportunity cross paths. We are looking to hire exceptional people who have demonstrated track records of success.  Our greatest scientific solution is bringing talented people together who have a passion for advancing plant-based biologics for our customers and the world.

Apply now for our Project Manager position!

MISSION OF THE POSITION

The Project Manager is primarily responsible for ensuring projects at iBio are completed within budget and within the proposed schedule, while meeting quality and customer expectations. This position requires experience in the biotechnology industry within project management and will play an important role in helping the CDMO team manage projects and communicate with iBio customers.

POSITION SUMMARY

This position will work closely with the Project Management Lead to communicate with the internal team and external customers regarding project progress and will provide recommendations on resource evaluation and allotment. The Project Manager will be involved in all phases of the Project Management process and will maintain project tracking tools to ensure expectations, responsibilities, and accountability are clear for all parties.

ESSENTIAL DUTIES & RESPONSIBILITIES

• Regular interactions with customers to evaluate the project process & review applicable documents
• Track and ensure project activities are on time, on budget, and ensure that projects are effectively managed. This includes monitoring invoices and project study protocols, statements of work, work orders, etc.
• Interact daily with iBio team on product development activities and related project deliverables
• Provide recommendations on resource evaluation and allotment
• Clarify areas such as outsourcing opportunities, customer set-up, logistics, and due diligence for each customer
• Assist in the management of project budgets and forecasts
• Monitor and control expenditures and communicate variances to leadership
• Assist with creating and maintaining project tracking tools to ensure all parties are clear on expectations and responsibilities
• Help establish product and portfolio development processes to deliver clarity at the appropriate inflection points of project strategy phases
• Integrate knowledge and set up program requirements for each project assigned
• Provide expertise and guidance when identifying and mitigating risk for projects
• Effectively present project goals and updates to the leadership team
• Provide technical assessment/recommendation of potential project opportunities to the commercial, R&D, operations and process team leads.
• Act as the liaison between the technical team and the customer.
• May attend trade shows and technical conferences to represent the company, as needed 
• Assist with standardizing templates for typical proposal documents
• Complete proposals and grants for review and submission

KNOWLEDGE, SKILLS, & ABILITIES

• Excellent written and verbal communication skills
• Highly proficient in Word, Power Point, Excel,
• Experience with MS Project preferred
• Problem solving, prioritization and time management skills
• Fundamental understanding of Biologics / Biologics manufacturing is required
• Extremely detail oriented
• Excellent organizational and time management skills
• Relevant skill set in program management, sales, business or technical experience is highly valued for consideration.
• Required - ability to travel (≤ 25%) and work non-standard hours (flexible management)
• Strong customer-facing interpersonal skills

EDUCATION & EXPERIENCE

• Bachelor’s Degree in a scientific discipline, biologics preferred
• 5-7 years in bio/pharmaceutical industry experience, CDMO preferred
• 3-5 years of project management experience preferred
• Previous experience in grant writing preferred
• Previous customer facing interaction required

iBio is a global leader in plant-based biologics manufacturing. Our FastPharming™ System combines vertical farming, automated hydroponics, and glycan engineering technologies to rapidly deliver gram quantities of high-quality monoclonal antibodies, vaccines, bioinks and other proteins. We accomplish all of this via our CGMP 130,000 square foot facility in Bryan, TX.  

Just imagine what we can do together!  We know great things happen when talent and opportunity cross paths. We are looking to hire exceptional people who have demonstrated track records of success.  Our greatest scientific solution is bringing talented people together who have a passion for advancing plant-based biologics for our customers and the world.

Apply now for our Senior Manager of Facilities and Maintenance position!

MISSION OF THE POSITION

The Senior Manager of Facilities and Maintenance will be based in Bryan, Texas. The position will have responsibility for ensuring all facilities and equipment are maintained to the highest standards and will support the design, development and installation for new and modified equipment and utilities to satisfy plant operational requirements.

POSITION SUMMARY

The Senior Manager of Facilities and Maintenance will utilize thorough organization and planning skills to strategically coordinate the activities of the equipment maintenance programs and assist with development of site capital plan. The position will specify and implement process control procedures and introduce new processes/practices to improve plant efficiencies, address energy inefficiencies, and resolve complex operational challenges and use proven problem-solving methodologies to provide technical support to Facilities.

ESSENTIAL DUTIES & RESPONSIBILITES

• Lead, develop and guide the work of facility and maintenance technicians including contract staff.
• Responsible for implementing/managing maintenance and spare parts programs and ensuring the reliability of site wide systems and equipment.
• Drive reliability improvement initiatives for cGMP and non-cGMP equipment systems.
• Support the overall design, development, construction, startup, optimization and operation of the company's manufacturing plant.
• Develop and approve documents related to site SOP's, Work Plans, and Job Aides.
• Ensure timely completion of all work activities including scheduled and emergency.
• Develop and maintains PM and Reliability programs, as well as address short-term equipment operation issues.
• Implement Predictive Maintenance Technologies.
• Solve problems to root cause and implement effective corrective actions.
• Utilize failure modes and effects analysis (FMEA) and root cause analysis (RCFA) to minimize risk and eliminate failures, perform criticality assessments of equipment and establish the best spare part strategy, educate staff on Reliability Centered Maintenance (RCM) and other Operational Excellence efforts centered on reliability.
• Interface daily with multiple functions to identify/resolve problems, implement solutions including diagnosing, troubleshooting, and resolving equipment issues.
• Author and drive Change Controls and GMP related investigations from creation through approval.
• Oversee the functioning of building systems including mechanical, electrical, fire/life safety, and plumbing. 

KNOWLEDGE, SKILLS, & ABILITIES

• Excellent management skills with demonstrated organizational, administrative, interpersonal, communication and supervisory skills with the demonstrated ability to work with a wide variety of people
• Ability to read and interpret architectural prints, job specifications
• Pharmaceutical GMP and GLP expertise
• Project Management skills
• Knowledge of Facilities Management
• Strong knowledge of HVAC balancing, mechanical and electrical systems.
• Familiar with FDA and EU regulations and GMP standards.
• Knowledge of OSHA guidelines, and other federal, state and local regulations

EDUCATION & EXPERIENCE

• Bachelor's degree in engineering; Master’s degree preferred
• Minimum of 10 years of pharmaceutical industry experience
• Minimum of 5 years of managerial experience
• Prior experience with agency filings and inspections a must
• Experienced in the operations and management of facility and utility systems in a GMP and Laboratory environment
• Extensive experience in troubleshooting temperature, air flow, differential pressure and humidity and dehumidification problems related to the HVAC system in ISO classified environments
• Significant experience with Asset and Maintenance Management Systems
• Must have experience in maintenance and construction projects and service vendor management
• Strong experience implementing reliability and predictive maintenance programs
• Experience with HVAC, electrical, plumbing and emergency power systems, clean water such as RO and WFI systems and preventive and predictive maintenance and technologies practices