What are the responsibilities and job description for the Quality Control Associate position at RxSource?
At RxSource, our passion drives us to be the bridge between pharma and patient. With offices in Canada, USA and Ireland we provide bespoke global clinical trial supply management services to pharma, biotech and CROs. Whether it’s employing demand-led packaging, a local sourcing model or another flexible option, we guarantee on-time delivery without compromising quality. Our clients are our partners; success for them = success for us.
We currently have an opening for a Quality Control Associate at our West Deptford, New Jersey facility. This role is a key position within our global Quality Assurance team and will be responsible for performing on-site quality activities. If you are a personable and proactive Quality professional with experience in clinical trial packaging and labelling, pharma manufacturing or pharma distribution , we would like to hear from you.
What you will do :
- Release incoming goods
- Perform in-process and finished good quality inspections
- Initiate Quality Management System documentation (i.e. Deviation, CAPA, Change Control, etc.)
- Review batch records pre- and post-execution
- Perform periodic quality walkthrough inspections to verify compliance with SOPs
- Participate in process improvement initiatives
- Manage all controlled GMP documentation and document archives
- Assist with supplier and customer verification / qualification and approval
- Provide support for customer and regulatory inspections
- Review daily / weekly checks (e.g., temperature, sanitation, etc.) and facility maintenance reports
- Assist with facility qualification activities
Your qualifications, skills and experience include :
No matter your role at RxSource, successful team members are :