Associate Principal Scientist, Analytical R&D
About The Position
Our Manufacturing Operations teams are the people that make our products. We work in the manufacturing plants with a “Safety First, Quality Always” mindset striving for continuous improvement. We work in the local plant connected to our global manufacturing network to ensure the highest quality of raw materials, intermediates and finished goods. Global Quality Large Molecule Analytical Sciences (GQ- LMAS), in our Manufacturing Division, is accountable for the commercialization of large molecule, vaccines and biologics, analytical techniques from Phase III through launch and transfer to supply. This team is highly motivated, fast-paced and focused on the rapid advancement of our Company's large molecule pipeline, plus growth of existing products. This position will involve oversight of late-stage method development, validation, and life-cycle management of methods but mainly global method transfer activities. Within the Global Quality Large Molecule Analytical Sciences (GQ- LMAS) organization, this Analytical Transfer Team include activities interfacing with a global network of product manufacturing and testing sites, collaborating with product development groups within our manufacturing division and our Research Laboratories division, continuous improvement of analytical methodology, assay validation, analytical technical transfer, and Biologics License Application preparation.
Requirements
- Bachelor’s degree in biology, chemistry, biochemistry, or related science with six years of relevant industry knowledge in systematic development, validation, and/or quality control (QC) or
- Master’s degree in biology, chemistry, biochemistry, or related science with four years of relevant industry knowledge in systematic development, validation, and/or quality control (QC) or
- PhD in biology, chemistry, biochemistry, or related science with one year of relevant industry knowledge in systematic development, validation, and/or quality control (QC)
- Knowledge of ICH, USP and other compendial chapters required for method transfer and validation.
- Knowledge with late-stage method development, validation, and transfer
- Minimum two years working knowledge in a current Good Manufacturing Practices (cGMP) laboratory environment in large molecules (vaccines, biologics)
- Development and management of project timelines and deliverables
- Participation in cross-functional project teams
- Authoring and review of technical documents
- Ability to work objectively and within a cross-functional team
- Ability to learn new techniques
- Technical, verbal, and written communications, stakeholder management, and teamwork skills
- Self-motivated with a positive attitude and proven performance record
- Knowledge with drug substance and drug product release, stability, and extended characterization testing for vaccines and biologics
- Strong organizational and project management skills
- Ability to effectively identify and express risks
Nice To Haves
- Deviation management and change control processes
- Authoring and/or reviewing technical documents to support Process Performance Qualification (PPQ)
- Global launch or supply experiences
- Supporting/writing regulatory filings (IND, MAA, BLA) and inspections with multiple agencies (FDA, EMA, JNDA)
- Continuous improvement or lean six sigma methodology
Responsibilities
- Lead complex analytical transfers for the team including ADCs, mAbs and Vaccines
- Lead method transfers and/or validations across vaccine and biologics programs including quality risk assessments/gap analysis.
- Provide sponsorship of both in-line and pipeline analytical methods. The candidate will interface across our Company network and external partners to ensure the successful commercialization of assays promoting our pipeline programs
- Involvement in development, troubleshooting and optimization of analytical methods
- Continuous improvement using laboratory standardization, lean laboratory, and six sigma methodology
- Assay Life Cycle activities across various large molecule franchises and analytical platforms
- Promote various vaccine and/or biologics registrations, launches, and troubleshooting activities external to the US, including documentation preparation
- Direct strategic initiatives within departmental and cross-functional teams representing Global Quality Large Molecule Analytical Sciences (GQ- LMAS).
- Manage global registration and test on importation (TOI) activities
- Collaborating with commercial manufacturing teams to support facility start-up activities, New Product Introduction and provide analytical support both within our Company network and at contract manufacturing organizations (CMOs) or contract testing laboratories
Benefits
- medical, dental, vision healthcare and other insurance benefits (for employee and family)
- retirement benefits, including 401(k)
- paid holidays, vacation, and compassionate and sick days
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What This Job Offers
Job Type
Full-time
Career Level
Principal
