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\n\t\t\t\tPay Grade: 33E
Context of the Job:
Major Responsibilities
- Demonstrate NIIMBL’s Core Values in daily conduct and ensures all decisions, actions, and teamwork practices align with the organization’s Business Principles.
- Serve as a lead technical scientist on multiple projects involving downstream purification unit operations for the manufacture of industrially relevant products and related activities.
- Evaluate and introduce new technologies and analytical tools to existing processes.
- Adhere to 21CFR58 GxP guidelines in execution of work.
- Set-up, operate, troubleshoot, maintain, and clean downstream bioprocessing equipment.
- Use manufacturing experience to identify process parameters and define their setpoints.
- Perform DoE studies to confirm the impact of process parameters on impurity levels, product recovery, and potency.
- Characterize performance of existing purification and formulation unit operations, including column chromatography (e.g., ProA, SEC, CEX, AEX), filtration, TFF, and bulk filling.
- Develop new filtration unit operations such as tangential-flow filtration (TFF), virus filtration, and depth filtration.
- Develop new chromatography unit operations, from screening and characterization to optimization and initial scale-up.
- Optimize buffer compositions to improve the stability and solubility of target molecules.
- Collaborate with an analytical team to adapt and troubleshoot research analytical methods such as HPLC, SDS-PAGE, enzyme activity and endotoxin assays to quantify yield, activity, and purity at various stages of the manufacturing process.
- Document all work and analyses in an electronic lab notebook. Perform tracking and trend analysis of method performance.
- Analyze process performance trends, perform statistical data analysis, and present data to teams.
- Partner with Informatics Infrastructure team on deploying structured data capture systems.
- Draft and revise SOPs and batch records.
- Maintain detailed documentation of lab activities and tabulation of data.
- Compile data generated to present and discuss at team meetings.
- Author, review and edit technical reports and manuscripts intended for publication.
- Stay current with relevant technologies and scientific literature.
- Perform other job-related duties as assigned.
Qualifications:
- A Masters and 5+ years or PhD and 2+ years in chemical engineering or relevant life science discipline.
- Industrially relevant downstream purification experience is required with preference for experience in a 21CFR58-compliant GxP environment.
- Hands-on experience with a range of downstream unit operations and control systems, experience with DeltaV preferred.
- Operates chromatography skids and other bioprocess equipment for purification of industrially relevant materials.
- Knowledge of biotech manufacturing process and equipment including depth and tangential flow filtration, column chromatography, protein purification and formulation and/or buffer and media operations.
- Possess a contribution mindset fueled by an inner drive to take initiative without being directed.
- Excellent interpersonal and managing skills with the desire to work collaboratively and effectively in a team environment.
- Ability to demonstrate effective leadership through communication, respect, influence, persuasion, and trust.
- Excellent problem solving and critical thinking skills.
- Excellent writing, communication, and presentation skills.
- Strong MS Excel, PowerPoint, and Word skills. Microsoft Project skills.
- Excellent organization and planning skills.
- Strong attention to detail and ability to adhere to standards procedures.
- Ability to function in a rapidly changing environment.
Applications close: Open until filled
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