Associate Production Scientist - Torrance
About The Position
PolyPeptide is seeking an Associate Production Scientist to play a key role in translating process development into GMP manufacturing at scale. This is a highly technical, hands-on role where you will bridge development and production, drive process improvements, and ensure successful execution of complex manufacturing campaigns. In this role, you will support the scale-up of peptide manufacturing processes, ensuring they are robust, efficient, and compliant with cGMP standards. You will work closely with cross-functional teams to oversee production activities, analyze process performance, and drive continuous improvement from development through commercial manufacturing.
Requirements
- Bachelor’s degree in Chemistry, Biochemistry, Engineering, or related field
- 3+ years of experience in GMP pharmaceutical manufacturing or MS&T
- Experience with process scale-up, investigations, and data analysis
- Experience with HPLC and cGMP processes
Nice To Haves
- Familiarity with SPPS or peptide manufacturing preferred
- Strong problem-solving and analytical mindset
- Ability to manage multiple projects in a fast-paced environment
- Excellent technical writing and communication skills
- Collaborative approach across cross-functional teams
- Detail-oriented with a strong focus on quality and compliance
Responsibilities
- Create and refine Master Batch Production Records (MBPRs) for large-scale manufacturing
- Support technology transfer from development to GMP production
- Provide on-floor technical support during manufacturing campaigns
- Analyze process data to drive yield improvements and optimization
- Lead and support investigations (OOS, OOT, deviations, CAPA) using root cause analysis
- Author and review technical and quality documents (MBPRs, SOPs, risk assessments, PPQ protocols)
- Collaborate with Production, QA, QC, Development, and Supply Chain teams
- Present project updates to internal and external stakeholders
- Identify process bottlenecks and support continuous improvement initiatives
- Train operators and support process knowledge transfer
Benefits
- Work at the intersection of process development and GMP manufacturing
- Gain hands-on experience with large-scale peptide production
- Contribute to high-impact pharmaceutical programs
- Be part of a collaborative, science-driven environment
- Opportunity to grow within a global organization
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
