QC Chemist - San Diego
Listed on 2025-11-06
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Quality Assurance - QA/QC
Quality Technician/ Inspector, Quality Control / Manager, QA Specialist / Manager
Job Summary
The Quality Control Chemist performs analytical testing on raw materials, intermediates, and finished peptide products using a range of laboratory instruments to ensure compliance with quality standards and GMP guidelines. This role prepares samples, calibrates equipment, documents results, and identifies potential quality issues, supporting the development of corrective actions as needed. The chemist also contributes to SOP development and maintains a clean, compliant laboratory environment.
This role contributes directly to Poly Peptide’s commitment to delivering exceptional quality and on-time delivery to our customers.
- Required
Education:- BS degree in Chemistry or Biochemistry or equivalent
- Experience:
- 1+ years experience in a cGMP pharmaceutical/biotechnology laboratory
- Technical Skills:
- Proficient use of analytical techniques/instruments such as:
- HPLC/UPLC - Analytical, GC, MS, pH Meter, Balance, Hand Tools, FTIR, Polarimeter, LC/MS, Elemental (Nitrogen) Analyzer, Karl-Fischer Titrator
- Proficient use of Microsoft Office suite of applications (Outlook, Excel, Word, PowerPoint, Teams, etc.)
- Proficient use of analytical techniques/instruments such as:
- Soft Skills:
- Ability to rapidly change focus during times of shifting or changing priorities
- Impeccable technical writing skills with extreme attention to detail, specifically the lexicology and grammatology of written English text as applied to technical writing
- Excellent organizational, multitasking, and communication skills
- Ability to work as part of a team and also independently with minimal to no supervision
- Competencies:
- Technical Proficiency in Analytical Testing
- cGMP Compliance & Documentation Accuracy
- Problem Solving & Quality Issue Resolution
- Attention to Detail & Data Integrity
- Collaboration & Communication
This role may be based in an office, laboratory, or GMP manufacturing environment, depending on the position. Office-based employees primarily work at a computer in a standard office setting, while lab and manufacturing roles may require work in controlled environments with appropriate gowning and PPE.
Physical demands may include:
- Prolonged sitting or standing, depending on the role.
- Frequent movement between work areas and occasional lifting of up to 25 pounds.
- Performing repetitive tasks, including pipetting, weighing, and data entry.
- Use of hands for data entry, equipment operation, or laboratory tasks.
- Exposure to chemicals, equipment noise, or temperature-controlled environments in lab or production settings.
- Occasional evening, weekend, or overtime hours to meet production or testing deadlines.
- Reasonable accommodations will be made as needed.
$26-$29/hr
Equal Opportunity EmployerWe 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.
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