QC Chemist & Documentation Specialist at Jobot
Philadelphia, PA 19115
About the Job
QC Chemist & Documentation Specialist - Hiring ASAP!
This Jobot Job is hosted by: Jenner Wiggins
Are you a fit? Easy Apply now by clicking the "Quick Apply" 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?
Job Details
MUST HAVES:
DUTIES/RESPONSIBILITIES
EDUCATION/EXPERIENCE:
Interested in hearing more? Easy Apply now by clicking the "Quick Apply" button.
This Jobot Job is hosted by: Jenner Wiggins
Are you a fit? Easy Apply now by clicking the "Quick Apply" 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 "Quick Apply" button.
Salary
55,000 - 65,000 /year
