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Job Description
Ready to Take Your Analytical Chemistry Career to the Next Level? PrideStaff is recruiting on behalf of our client, a premier, fast-growing Contract Development and Manufacturing Organization (CDMO) . We are seeking a dynamic, detail-oriented, and driven QC Analytical Chemist II to join a high-performing Quality Control team. If you are a skilled chemist who thrives in a regulated environment, loves solving technical puzzles, and is ready to mentor the next generation of lab talent, this is the impactful role you've been looking for! ##
Position Overview Job Title:
QC Analytical Chemist II Department:
Quality Control Reports To:
QC Lab Supervisor Employment Type:
Full-Time, Non-Exempt ## Why This Role Matters As a QC Analytical Chemist II, you won't just be running routine tests—you will be a vital technical resource. You will independently execute routine and non-routine laboratory testing using cutting-edge compendial and validated analytical methods. Your work directly ensures the quality, safety, and compliance of raw materials, in-process materials, and finished products in a thriving cGMP manufacturing operation. Beyond the bench, you will drive continuous improvement, lead laboratory investigations, support method validation, and serve as a mentor to junior laboratory personnel. ##
Key Responsibilities Precision Testing:
Perform chemical and physical testing of raw materials, finished products, stability samples, and cleaning verifications in strict compliance with cGMP, GDP, and data integrity principles.
Instrumentation & Troubleshooting:
Operate, maintain, and troubleshoot advanced laboratory equipment and support qualification activities.
Investigations & Compliance:
Participate in out-of-specification (OOS) and out-of-trend (OOT) investigations, supporting root cause analysis and implementing corrective actions.
Method & Lifecycle Support:
Support HPLC method development, validation, verification, and transfer activities through protocol writing, execution, and technical reporting.
Leadership & Collaboration:
Train and mentor junior lab staff, assist with internal/external audits, and collaborate across departments (QA, Manufacturing, R D) to keep operations running seamlessly. ## What You Bring to the
Table Education & Experience:
Degree:
Bachelor's Degree in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, Biochemistry, or a related scientific discipline.
Experience:
Minimum of three (3) years of analytical laboratory experience in a GMP-regulated manufacturing environment (Pharmaceutical, Veterinary, Nutraceutical, Food Supplement, or Cosmetics industries).
Technical Edge:
Proven experience with HPLC method development and validation .
Bonus Points:
Experience supporting FDA or third-party audits, stability programs, and laboratory investigations is highly preferred!
Technical Knowledge & Skills:
Strong understanding of analytical chemistry principles and cGMP compliance requirements. Solid working knowledge of USP compendial testing requirements and Data Integrity principles (21 CFR Part 211, 21 CFR Part 507). Exceptional troubleshooting and data analysis abilities. Superb organizational skills with the ability to manage multiple projects simultaneously.
Computer & Software Literacy:
Proficiency in MS Office (Word, Excel, PowerPoint, Teams) and SharePoint.
Bonus Points:
Experience with ERP Systems (SAP) and Electronic Quality Management Systems (eQMS) is a major plus. ## Ready to Apply? If you are looking for a position where your expertise is valued, your growth is supported, and your work makes a tangible impact every day, we want to hear from you. Apply today through PrideStaff and catalyze your career growth!
