QC Chemist & Documentation Specialist job at Jobot Philadelphia, PA, US

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" button and sending us your resume.
Salary: $55,000 - $65,000 per year
A 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 Details
EDUCATION/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.

Job Tags

Contract work, Immediate start, Worldwide,

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