QC Chemist & Documentation Specialist Position Available In Philadelphia, Pennsylvania

Job Description:

QC Chemist & Documentation Specialist – Hiring ASAP!

This JobotJob is hosted by:

Jenner Wiggins Are you a fit? Easy Apply now byclicking the “Apply Now” button and sending us your resume.

Salary:

$55,000 – $65,000 per year A bit about us: We are a family-ownedcontract manufacturer specializing in human and veterinarypharmaceuticals, nutritional, and cosmetic products. We offercomprehensive services including R D, manufacturing, packaging,and regulatory support, serving clients from startups to Fortune 20companies with a commitment to high-quality, affordable products.

Why join us? Reputation for high-quality manufacturing. Familyowned and a very collaborative team environment. Make an impact inthe Pharmaceutical industry. Job Details

MUST HAVES

Analyticalhands-on experience in running quality control lab tests onpharmaceutical products using instruments like HPLC, GC, UV-Visetc. Hands-on experience in running Method Validations onpharmaceutical products using instruments like HPLC, GC, UV-Visetc. Hands-on experience in preparing method validation protocols,reports, lab investigations, specifications, analytical proceduresand other QC documents.

DUTIES/RESPONSIBILITIES

Gather and reviewdata from chemists in accordance with internal Standard OperatingProcedures (SOPs) and current Good Manufacturing Practices (cGMP).Develop specifications for raw materials, finished products, andstability studies. Draft analytical procedures, method validationprotocols, stability protocols, and expiration memos. PrepareCertificates of Analysis (COA) and Certificates of Conformance(COC). Represent the Quality department in meetings, providinginput and recommendations as needed. Ensure compliance with allsafety protocols. Familiarity with GMPs, ICH guidelines, FDAregulations, and other relevant regulatory requirements ispreferred. Initiate action or deviation reports for any identifiednonconformances. Conduct testing of raw materials, finishedproducts, and additional samples as required. Perform other dutiesas assigned by management.

EDUCATION/EXPERIENCE

Minimum 3 years ofquality control or quality assurance experience BS or BA Biology,Chemistry, Biochemistry, or relevant related field, or sufficienttechnical/professional experience Experience in quality systemsincluding validation, documentation, and compliance HPLC analyticalexperience is a plus Interested in hearing more? Easy Apply now byclicking the “Apply Now” button. Jobot is an Equal OpportunityEmployer. We provide an inclusive work environment that celebratesdiversity and all qualified candidates receive consideration foremployment without regard to race, color, religion, age, sex,national origin, disability status, genetics, protected veteranstatus, sexual orientation, gender identity or expression, or anyother characteristic protected by federal, state or local laws.

Sometimes Jobot is required to perform background checks with yourauthorization. Jobot will consider qualified candidates withcriminal histories in a manner consistent with any applicablefederal, state, or local law regarding criminal backgrounds,including but not limited to the Los Angeles Fair Chance Initiativefor Hiring and the San Francisco Fair Chance Ordinance.