What are the responsibilities and job description for the QC Inspection - Incoming & In-Process (Pharma) position at JMD Technologies Inc.?
Title: QC Incoming Inspector (2nd Shift)
Location: Greater Bedford Area, MA (Onsite 5 days)
Employment Type: Contract
Status: Accepting Candidates
About the role
This role supports quality operations by ensuring incoming raw materials and in-process products meet defined specifications before use in manufacturing. The position plays a key role in maintaining compliance within a regulated (cGMP) environment.
Key Responsibilities
- Perform incoming material inspection, including labeling, lot assignment, and release/rejection
- Conduct in-process inspections and line clearance checks per SOP requirements
- Complete and maintain GMP documentation, including approval forms and inspection records
- Support OOS investigations and participate in material review processes for rejected items
- Monitor and perform retain inspections and coordinate required retesting activities
- Review inspection records (MPS) and support training of personnel as needed
Qualifications
- ~1 year of experience in QC/QA or inspection within a cGMP or regulated environment (internship acceptable)
- Experience with incoming inspection and/or in-process quality checks
- Familiarity with cleanroom environments and related procedures
- Strong experience with GMP documentation practices
- Proficiency with Microsoft Office or ERP systems
- Associate degree in Life Sciences or relevant experience preferred
Compensation (MA Pay Transparency):
- Estimated hourly range: $28–$30/hr (W-2)
- Final rate within this range will be based on skills, experience, and interview results.
Salary : $28 - $30