Manufacturing Process Specialist
Quick Summary
Manufacturing Process Specialist Location: San Diego, CA | Employment Type: Full-Time Be the technical expert behind high-impact peptide manufacturing. PolyPeptide is a global leader in peptide development and manufacturing, supporting some of the most advanced therapies in the industry.
Provide hands-on support for SPPS, Cleavage, Purification, and Lyophilization processes Lead and support deviation investigations, root cause analysis, and CAPA Drive technology transfers between Development and Manufacturing Support PPQ execution…
Bachelor’s degree in Chemistry, Biochemistry, Engineering, or related field 3+ years of experience in pharmaceutical manufacturing or cGMP environment Peptide manufacturing experience preferred Technical Strengths Knowledge of cGMP manufacturing,…
PolyPeptide is a global leader in peptide development and manufacturing, supporting some of the most advanced therapies in the industry. We are looking for a Manufacturing Process Specialist to bridge process development and manufacturing, ensuring our processes are robust, scalable, and consistently deliver high-quality results.
If you enjoy solving complex problems, working hands-on in a GMP environment, and driving process improvements, this role offers strong technical exposure and growth.
The Manufacturing Process Specialist provides floor-side technical support and drives process excellence across peptide manufacturing operations. You will play a key role in technology transfer, process validation (PPQ/CPV), equipment qualification, and investigations, helping ensure reliable and compliant production from development through commercial manufacturing.
Responsibilities
~1 min read- →
Provide hands-on support for SPPS, Cleavage, Purification, and Lyophilization processes
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Lead and support deviation investigations, root cause analysis, and CAPA
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Drive technology transfers between Development and Manufacturing
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Support PPQ execution and CPV monitoring, including data analysis and reporting
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Lead equipment qualification (IQ/OQ/PQ) and introduce new manufacturing systems
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Improve batch documentation and workflows to enhance efficiency and data integrity
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Collaborate cross-functionally with MFG, PD, QC, and QA
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Serve as a technical SME for internal teams and external stakeholders
Requirements
~1 min readBachelor’s degree in Chemistry, Biochemistry, Engineering, or related field
3+ years of experience in pharmaceutical manufacturing or cGMP environment
Peptide manufacturing experience preferred
Knowledge of cGMP manufacturing, process validation, and equipment qualification
Experience with SPPS, purification, and lyophilization processes
Strong background in GMP documentation, investigations, and change control
Strong problem-solving and analytical mindset
Ability to work hands-on in manufacturing environments
Clear communication across technical and non-technical teams
Collaborative approach with confidence in client-facing situations
What We Offer
~1 min readSalary: $33-$37/hr
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law.
Location & Eligibility
Listing Details
- Posted
- April 14, 2026
- First seen
- May 6, 2026
- Last seen
- May 8, 2026
Posting Health
- Days active
- 0
- Repost count
- 0
- Trust Level
- 14%
- Scored at
- May 6, 2026
Signal breakdown
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