Principal Scientist/Director – Biologics Drug Substance Commercialization
Job in
Hamilton, Atlantic County, New Jersey, USA
Listed on 2026-09-16
Listing for:
Jobtailor
Full Time
position Listed on 2026-09-16
Job specializations:
-
Pharmaceutical
Regulatory Compliance Specialist, Pharmaceutical Manufacturing, Validation Engineer
Job Description & How to Apply Below
- Lead downstream and/or integrated drug substance teams for late-stage clinical and commercial programs
- Provide technical leadership for laboratory-scale and manufacturing-scale studies involving process characterization, validation, investigations, and continued process verification
- Serve as a downstream subject matter expert across core unit operations and upstream, analytical, and GMP manufacturing interdependencies
- Ensure process and product knowledge are developed, documented, and transferred according to company standards and regulatory expectations
- Support technology transfer to internal and external manufacturing sites, including scale-up, process validation, and manufacturing readiness
- Contribute to manufacturing investigations and lifecycle management for commercial processes
- Author and review technical and regulatory documentation, including regulatory submission sections
- Drive division-wide biologics manufacturing and commercialization initiatives
- Influence multi-year planning for capability needs, digital systems, and platform evolution
- Represent BDSC on cross-functional and cross-divisional teams
- Collaborate with internal stakeholders and external partners, including contract development and manufacturing organizations
- Lead, coach, and mentor downstream scientists
- Promote innovation, continuous improvement, and operational excellence in the laboratory
- Support resource planning, staffing strategies, hiring decisions, and talent development
- BS, MS, or PhD in Chemical Engineering, Biological Engineering, Chemistry, or a related discipline
- Fourteen (14) years of industry experience with a BS, twelve (12) years with an MS, or six (6) years with a PhD
- Deep technical expertise in downstream processing of biologics
- Ability to independently design, direct, execute, analyze, and document all stages of process development
- Experience supporting biologics commercialization, including late-stage development and/or commercial manufacturing
- Ability to prioritize and deliver complex objectives in fast-paced, dynamic environments
- Strong leadership and collaboration skills within cross-functional, matrixed organizations
- Action-oriented problem-solving mindset with a track record of innovation and continuous improvement
- Commitment to coaching and mentoring scientific staff
- Excellent written and verbal communication skills
- Preferred: leadership experience on drug substance working groups or program teams
- Preferred: direct people management experience
- Preferred: hands-on experience with technology transfer, scale-up, and validation of biologics processes
- Preferred: in-depth knowledge of preparative chromatography, tangential flow filtration, and virus retentive filtration
- Preferred: experience developing or supporting multi-specific antibody therapeutics
- Preferred: experience with process characterization, viral clearance studies, PPQ, and validation
- Preferred: experience authoring regulatory submission content and/or working with external development or manufacturing partners
- Preferred: working knowledge of analytical characterization of biologics, cGMPs, and U.S./EU regulatory expectations
- Preferred: experience applying lean leadership and operational excellence principles
- Willingness to travel 10%
Demonstrates deep technical expertise in downstream processing of biologics, with a strong focus on process development, technology transfer, and regulatory compliance. Proven leadership in managing cross-functional teams and driving innovation in biologics manufacturing and commercialization.
Highest-signal resume keywords- Downstream Processing of Biologics
- Process Development and Validation
- Regulatory Submission Authoring
- Leadership in Cross-Functional Teams
- Technology Transfer and Scale-Up
- Process Characterization
- Viral Clearance Studies
- Preparative Chromatography
- Tangential Flow Filtration
- Virus Retentive Filtration
- Multi-Specific Antibody Therapeutics
- PPQ
- CGMP Compliance
- Analytical Characterization of Biologics
- Lean Leadership Principles
- Strong Leadership Skills
- Collaboration Skills
- Action-Oriented Problem Solving
- Coaching and Mentoring
- Excellent Communication Skills
- Biologics Manufacturing
- Commercialization
- GMP Manufacturing
- Regulatory Expectations
- Process Verification
- Lifecycle Management
- Innovation
- Operational Excellence
- Cross-Functional Collaboration
- Talent Development
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