Summary
One of the largest global pharmaceutical companies focused on pediatrics, cardiovascular, anti-infectives, diabetology, asthma and anti-tuberculosis is looking to bring on an experienced Quality Engineer Consultant to support the team based in Somerset, New Jersey. The Quality Engineer Consultant will be responsible for revision of SOPs, revision of master batch records, issuance and execution of protocols, and assist with any other actions necessary to enable closure of open/overdue change controls, in Manufacturing, Packaging, Engineering, Warehouse and Laboratory areas.
Responsibilities
- Duties will include taking up existing change control and CAPAs and driving them to closure.
- Revising SOPs, Forms, maintenance records, and writing equipment specific instructions based on maintenance manuals and other source material.
- Other duties as assigned by leadership
Qualifications
- 4+ years working in a pharmaceutical GMP environment.
- A B.S. in engineering.
- Experience with maintenance management systems or facilities experience in either a contributor role, design role, supervision, or QA oversight.
*This is an onsite, contract-to-hire role.
Send resumes for immediate consideration.
W-2 only.