QC Chemist & Documentation Specialist

Location: Philadelphia
Posted on: June 23, 2025

Job Description:

QC Chemist & Documentation Specialist - Hiring ASAP! This Jobot Job is hosted by: Jenner Wiggins Are you a fit? Easy Apply now by clicking the "Apply Now" button and sending us your resume. Salary: $55,000 - $65,000 per year A bit about us: We are a family-owned contract manufacturer specializing in human and veterinary pharmaceuticals, nutritional, and cosmetic products. We offer comprehensive services including R&D, manufacturing, packaging, and regulatory support, serving clients from startups to Fortune 20 companies with a commitment to high-quality, affordable products. Why join us? Reputation for high-quality manufacturing. Family owned and a very collaborative team environment. Make an impact in the Pharmaceutical industry. Job Details MUST HAVES: Analytical hands-on experience in running quality control lab tests on pharmaceutical products using instruments like HPLC, GC, UV-Vis etc. Hands-on experience in running Method Validations on pharmaceutical products using instruments like HPLC, GC, UV-Vis etc. Hands-on experience in preparing method validation protocols, reports, lab investigations, specifications, analytical procedures and other QC documents. DUTIES/RESPONSIBILITIES Gather and review data from chemists in accordance with internal Standard Operating Procedures (SOPs) and current Good Manufacturing Practices (cGMP). Develop specifications for raw materials, finished products, and stability studies. Draft analytical procedures, method validation protocols, stability protocols, and expiration memos. Prepare Certificates of Analysis (COA) and Certificates of Conformance (COC). Represent the Quality department in meetings, providing input and recommendations as needed. Ensure compliance with all safety protocols. Familiarity with GMPs, ICH guidelines, FDA regulations, and other relevant regulatory requirements is preferred. Initiate action or deviation reports for any identified nonconformances. Conduct testing of raw materials, finished products, and additional samples as required. Perform other duties as assigned by management. EDUCATION/EXPERIENCE: Minimum 3 years of quality control or quality assurance experience BS or BA Biology, Chemistry, Biochemistry, or relevant related field, or sufficient technical/professional experience Experience in quality systems including validation, documentation, and compliance HPLC analytical experience is a plus Interested in hearing more? Easy Apply now by clicking the "Apply Now" button. Jobot is an Equal Opportunity Employer. We provide an inclusive work environment that celebrates diversity and all qualified candidates receive consideration for employment without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. Sometimes Jobot is required to perform background checks with your authorization. Jobot will consider qualified candidates with criminal histories in a manner consistent with any applicable federal, state, or local law regarding criminal backgrounds, including but not limited to the Los Angeles Fair Chance Initiative for Hiring and the San Francisco Fair Chance Ordinance.

Keywords: , West Orange , QC Chemist & Documentation Specialist, Science, Research & Development , Philadelphia, New Jersey