PolyPeptide Group
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 PolyPeptide’s commitment to delivering exceptional quality and on-time delivery to our customers.
Key Responsibilities
Uses basic to moderately complex test and measurement equipment and instruments to complete quality control tasks for raw materials, intermediates, in-process and finished products.
Calibrates test and measurement equipment and devices to ensure accuracy.
Prepares samples and solutions for tests in accordance with established methodologies and protocols.
Identifies material, product and/or methodology issues impacting quality and reports them to senior QC personnel or management.
Documents all tests and measurements according to GMP guidelines.
Assists in developing corrective measures and actions to resolve quality issues.
Performs basic troubleshooting of tests and measurement equipment.
Maintains high housekeeping and cleanliness standards.
Supports development of SOPs and protocols for proper testing and measurement.
Performs any additional duties as required.
Qualifications Education & Experience
Required Education:
BS degree in Chemistry or Biochemistry or equivalent.
Experience:
1+ years experience in a cGMP pharmaceutical/biotechnology laboratory.
Skills & Competencies Technical Skills
Proficient use of analytical techniques/instruments such as HPLC/UPLC, GC, MS, pH Meter, Balance, Hand Tools, FTIR, Polarimeter, LC/MS, Elemental (Nitrogen) Analyzer, Karl-Fischer Titrator.
Proficient use of Microsoft Office suite (Outlook, Excel, Word, PowerPoint, Teams, etc.).
Soft Skills
Ability to rapidly shift focus during changing priorities.
Impeccable technical writing skills with extreme attention to detail.
Excellent organizational, multitasking, and communication skills.
Ability to work independently or as part of a team with minimal supervision.
Competencies
Technical Proficiency in Analytical Testing.
cGMP Compliance & Documentation Accuracy.
Problem Solving & Quality Issue Resolution.
Attention to Detail & Data Integrity.
Collaboration & Communication.
Work Environment & Physical Demands 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, while lab and manufacturing roles may require work in controlled environments with appropriate gowning and PPE.
Physical Demands May Include
Prolonged sitting or standing as required.
Frequent movement between work areas and occasional lifting of up to 25 pounds.
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.
Occasional evening, weekend, or overtime hours to meet deadlines.
Reasonable accommodations will be made as needed.
Salary:
$26-$29/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.
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Key Responsibilities
Uses basic to moderately complex test and measurement equipment and instruments to complete quality control tasks for raw materials, intermediates, in-process and finished products.
Calibrates test and measurement equipment and devices to ensure accuracy.
Prepares samples and solutions for tests in accordance with established methodologies and protocols.
Identifies material, product and/or methodology issues impacting quality and reports them to senior QC personnel or management.
Documents all tests and measurements according to GMP guidelines.
Assists in developing corrective measures and actions to resolve quality issues.
Performs basic troubleshooting of tests and measurement equipment.
Maintains high housekeeping and cleanliness standards.
Supports development of SOPs and protocols for proper testing and measurement.
Performs any additional duties as required.
Qualifications Education & Experience
Required Education:
BS degree in Chemistry or Biochemistry or equivalent.
Experience:
1+ years experience in a cGMP pharmaceutical/biotechnology laboratory.
Skills & Competencies Technical Skills
Proficient use of analytical techniques/instruments such as HPLC/UPLC, GC, MS, pH Meter, Balance, Hand Tools, FTIR, Polarimeter, LC/MS, Elemental (Nitrogen) Analyzer, Karl-Fischer Titrator.
Proficient use of Microsoft Office suite (Outlook, Excel, Word, PowerPoint, Teams, etc.).
Soft Skills
Ability to rapidly shift focus during changing priorities.
Impeccable technical writing skills with extreme attention to detail.
Excellent organizational, multitasking, and communication skills.
Ability to work independently or as part of a team with minimal supervision.
Competencies
Technical Proficiency in Analytical Testing.
cGMP Compliance & Documentation Accuracy.
Problem Solving & Quality Issue Resolution.
Attention to Detail & Data Integrity.
Collaboration & Communication.
Work Environment & Physical Demands 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, while lab and manufacturing roles may require work in controlled environments with appropriate gowning and PPE.
Physical Demands May Include
Prolonged sitting or standing as required.
Frequent movement between work areas and occasional lifting of up to 25 pounds.
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.
Occasional evening, weekend, or overtime hours to meet deadlines.
Reasonable accommodations will be made as needed.
Salary:
$26-$29/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.
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