Production Specialist III Cell Therapy Cell Culture - Berkeley, CA

Bayer; Berkeley (CA); On-site; USD 78,000 - 117,000; Full time

Benefits offered by this job

Health care

Vision

Dental

Retirement

PTO

Sick leave

Job summary

Bayer in Berkeley, CA, seeks a Production Specialist III CT-MOD to manufacture clinical cell therapy products and partner with BD and MSAT for new product introductions, ensuring GMP compliance across solution prep, expansion, culture, and fill/finish.

The role requires a bachelor’s in biotech or related field and 4–6 years of cGMP biologics/cell therapy experience, with strong documentation, cross‑functional collaboration, and hands‑on experience with single‑use systems.

Qualifications

• Bachelor’s degree in Biotechnology, Biology, Biochemistry, Chemical Engineering, or related field.
• 4–6 years of cGMP biologics or cell therapy manufacturing experience.
• Proficiency with single‑use technology systems.
• Working knowledge of phase‑appropriate cGMP practices and documentation from clinical through launch.
• Experience monitoring and controlling processes using data trending and/or statistical process control.
• Experience authoring, redlining, and reviewing controlled documents and SOPs.

Responsibilities

• Perform clinical manufacturing operations across Solution Preparation, Cell Expansion, Cell Culture, and Final Fill and freezing.
• Participate in new product introductions into CT-MOD with BD and MSAT support.
• Manufacture products across multiple phases from clinical through launch and document accordingly.
• Handle and troubleshoot single-use technology and monitor processes with data trends.
• Author and review SOPs and change controls; assess impact of material/equipment changes.
• Develop and maintain training curricula; deliver training and promote continuous improvement.

Skills

cGMP Biologics

Cell culture

Single-use tech

Documentation

Data trending

Cross-functional

Quality systems

Education

Bachelor’s degree in Biotechnology

Master’s degree in Biotechnology

Tools

JMP

Minitab

Spotfire

EBR

MES

Job description

At Bayer we’re visionaries, driven to solve the world’s toughest challenges and striving for a world where 'Health for all Hunger for none’ is no longer a dream, but a real possibility. We’re doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our capabilities and redefining ‘impossible’. There are so many reasons to join us. If you’re hungry to build a varied and meaningful career in a community of brilliant and diverse minds to make a real difference, there’s only one choice.

Production Specialist III Cell Therapy Cell Culture - Berkeley, CA

Production Specialist III, CT-MOD – Cell Therapy Manufacturing

Responsible for clinical manufacturing of novel cell therapy drug substance within the Cell Therapy Module (CT-MOD); collaborate closely with Biological Development (BD) and Manufacturing Science and Technology (MSAT) for new product introductions and ensure platform alignment; contribute to bringing transformative cell therapies to patients by operating at the interface of development and GMP manufacturing within a highly cross-functional, science-driven environment.

Your Tasks And Responsibilities

The primary responsibilities of this role, Production Specialist III, CT-MOD, are to:

• Perform clinical manufacturing operations across Solution Preparation, Cell Expansion, Cell Culture, and Final Fill and freezing, executing seamlessly across all areas and acting as a delegate to the Sr. Production Specialist;
• Participate in new product introductions into CT-MOD with BD and MSAT support, ensuring activities are performed according to schedule and aligned with platform processes, equipment, raw materials, and automation for at least one area;
• Manufacture products across multiple phases of the product life cycle from clinical through launch and clearly communicate phase-appropriate differences in documentation, sample handling, automation, and cGMP expectations;
• Handle and troubleshoot single-use technology, monitor and control processes using data trending and/or statistical process control, and work cross-functionally to ensure process control, escalation, and investigation of issues;
• Author, redline, and review controlled documents for equipment and processes, ensure alignment with cell therapy platform philosophy, and assess documentation impact of changes in materials and equipment to provide sound recommendations;
• Create, own, and drive business processes of moderate complexity in CT-MOD to ensure operational readiness and efficient manufacturing, including raising and supporting deviation investigations, partnering on root cause and product impact, and implementing effective corrective actions;
• Perform commissioning and IOPQ of CT-MOD equipment and execute C&Q documentation under supervision, participate in regulatory and internal audits, and support safety investigations while promoting safe behaviors and implementing corrective actions;
• Support development of training curricula and materials for the CT-MOD team, deliver training as a subject matter expert, maintain personal training compliance, and drive a culture of continuous improvement by challenging the status quo, proposing solutions, and encouraging innovation in others.

WHO YOU ARE

Bayer seeks an incumbent who possesses the following:

Required Qualifications

• Bachelor’s degree in Biotechnology, Biology, Biochemistry, Chemical Engineering, or a related field;
• 4–6 years of cGMP biologics or cell therapy manufacturing experience with hands‑on work in solution preparation, cell expansion/culture, and aseptic fill/finish;
• Proficiency with single‑use technology systems, including setup, operation, and troubleshooting;
• Working knowledge of phase‑appropriate cGMP practices and documentation from clinical through launch, including sampling, automation, batch records, and change control;
• Experience monitoring and controlling processes using data trending and/or statistical process control, with the ability to upscale issues and support investigations;
• Demonstrated ability to author, redline, and review controlled documents and SOPs for equipment and processes;
• Experience supporting deviations, conducting root cause analyses, and implementing effective CAPA to prevent recurrence;
• Familiarity with commissioning and qualification activities, including IOPQ and executing C&Q documentation under supervision;
• Strong cross‑functional collaboration skills partnering with Development and MSAT to align on process, equipment, materials, and automation;
• Excellent oral, written, and presentation communication skills to ensure effective knowledge transfer across shifts and to leadership;
• Proven ability to create, own, and drive business processes of moderate complexity to achieve operational readiness;
• Demonstrated commitment to safety, including participation in safety investigations and regulatory/internal audits;
• Willingness to work across CT‑MOD areas and shifts as business needs require.

Preferred Qualifications

• Master’s degree in Biotechnology, Biology, Biochemistry, Chemical Engineering, or a related discipline;
• 6+ years of cGMP experience in cell therapy, gene therapy, or biologics manufacturing, including late‑stage and launch products;
• Direct experience in a clinical cell therapy environment (e.g., autologous or allogeneic cell therapies) using single‑use technologies;
• Hands‑on experience with end‑to‑end cell therapy processes, including cell expansion, differentiation, and fill/finish for a single cell line or platform;
• Experience leading or acting as a subject matter expert in regulatory inspections and internal audits;
• Advanced experience with statistical process control tools and data analytics (e.g., JMP, Minitab, Spotfire, or similar);
• Demonstrated experience driving continuous improvement or operational excellence initiatives (e.g., Lean, Six Sigma, Kaizen);
• Prior experience mentoring or training operators or associates and developing training curricula or materials;
• Experience with electronic batch records (EBR), MES, and automation platforms commonly used in cell therapy manufacturing;
• Familiarity with commissioning, qualification, and validation (CQV) for cell therapy equipment and single‑use systems.

Employees can expect to be paid a salary between $77,760.00 to $116,640.00. Additional compensation may include a bonus or incentive compensation (if relevant). Additional benefits include health care, vision, dental, retirement, PTO, sick leave, etc.

This salary range is merely an estimate and may vary based on an applicant’s location, market data/ranges, an applicant’s skills and prior relevant experience, certain degrees and certifications, and other relevant factors.

This posting will be available for application until at least 9/4/26.

Bayer is an Equal Opportunity Employer/Disabled/Veterans

Bayer is committed to providing access and reasonable accommodations in its application process for individuals with disabilities and encourages applicants with disabilities to request any needed accommodation(s) using the contact information below.

Equal Opportunity Employer Statement: Notice for U.S. Visitors: All information on this site is subject to compliance with local rule and regulations as they may vary from time to time and across different geographies, including, without limitation, U.S. Executive Orders.

Bayer is an E-Verify Employer.

Location

United States : California : Berkeley

Division

Pharmaceuticals

Reference Code

881884

Contact Us

Email: [e-mail]