Jobot
QC Chemist & Documentation Specialist
Jobot, Phila, Pennsylvania, United States, 19117
QC Chemist & Documentation Specialist - Hiring ASAP!This Jobot Job is hosted by: Jake BenyshekAre you a fit? Easy Apply now by clicking the "Apply" buttonand sending us your resume.Salary: $55,000 - $65,000 per yearA bit about us:We are a family-owned contract manufacturer based in Philadelphia, PA, with over 90 years of experience. Our expertise lies in manufacturing pharmaceutical, nutritional, and cosmetic products for both human and veterinary use. We prioritize our employees and clients, ensuring exceptional experiences and attracting a diverse range of customers, from start-ups to Fortune 20 companies worldwide. Choose us for quality, reliability, and innovation.If you are a QC Chemist & Documentation Specialist from the pharmaceutical manufacturing industry, then please apply!Why join us?Do you want to work with a company who are helping people around the world? We do too! Meaningful Work! Competitive Compensation Package! Complete Benefits Package! Accelerated Career Growth! Fun Company Activities! Many More!Job DetailsEDUCATION/EXPERIENCE REQUIREMENTS 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 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.This is an onsite position (no hybrid or remote flexibility).Interested in hearing more? Easy Apply now by clicking the "Apply" button.
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 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.This is an onsite position (no hybrid or remote flexibility).Interested in hearing more? Easy Apply now by clicking the "Apply" button.