Posted 10 July, 2026

Job Id: 628994

Senior Project Manager, Technical Operations


Location: San Diego, California
Category: Scientific
Salary: Apply for details
Country: United States
Employment: Direct Hire/Perm
Worksite: On-Site
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Job Description

Responsibilities:

  • Execute CMC strategies aligned with corporate objectives for biologics program(s).
  • Develop and maintain integrated project plans, timelines, and resource forecasts.
  • Ensure effective communication of project status, risks, and opportunities; improve operational efficiency.
  • Facilitate team meetings, prepare agenda, publish meeting minutes, and ensure accountability for deliverables.
  • Monitor project progress and proactively identify, assess, and mitigate risks.
  • Coordinate CMC initiatives and activities, and partner with cross-functional teams to ensure readiness and timely delivery of technical documentation and regulatory commitments, and other CMC deliverables.
  • Align with internal and external stakeholders to support production schedules, supply planning, and inventory management to ensure uninterrupted product availability.
  • Additional duties assigned as needed.

 

Education/Experience Requirements:  

  • Bachelor’s degree in Life Sciences, Chemistry, Pharmaceutical Sciences, Biology, Biochemistry, Chemical Engineering, or a related discipline required.  Equivalent combination of education and applicable job experience may be considered
  • MS, MBA, PhD, PharmD, or other advanced degree in a related discipline preferred
  • 7+ years of relevant experience in biotechnology, pharmaceutical development, manufacturing, or technical operations
  • 4+ years of project management experience supporting CMC, Technical Operations, Manufacturing, or Product Development programs
  • Direct experience supporting biologic drug products, including CMC development, manufacturing, and lifecycle management activities
  • Demonstrated experience managing complex cross-functional projects through clinical development and commercialization
  • Experience supporting Biologics License Application (BLA) submissions and post-approval commitments is preferred
  • Familiarity with GMP regulations, quality systems, and biologics manufacturing operations
  • Knowledge of process validation, technology transfer, and commercial manufacturing operations for biologics

Equal Opportunity Employer

We are proud to be an equal opportunity employer. We welcome and encourage applications from all qualified candidates regardless of race, sex, gender identity or expression, disability, age, religion or belief, sexual orientation, or any other characteristic protected by applicable laws and regulations. It is our policy not to discriminate against any applicant or employee, and we are committed to fostering a diverse, inclusive, and respectful work environment across all locations in which we operate. We believe that diversity, equity, and inclusion are fundamental to our mission and enhance our ability to serve clients globally. If you have a disability or require any reasonable accommodations during the application or interview process, please inform your recruiter or contact us directly so that we can explore the appropriate arrangements.

Fraud Alert

Candidate safety is a top priority at Planet Pharma. The industry has seen an increase in people falsely representing themselves as recruiters to gather personal information from job seekers. For your safety, do not provide sensitive data to anyone you have not spoken with thoroughly, never provide banking information during the application process and always double check the email address of the Recruiter to ensure it’s from an official Planet Pharma domain (@planet-pharma.com, @planet-pharma.co.uk, and @ppgadvisorypartners.com) and not a domain with an alternative extension like .net, .org or .jobs.

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