Specialist, Quality Assurance Incoming Material Disposition, Cell Therapy
Job in
Harvard, Worcester County, Massachusetts, 01451, USA
Listed on 2026-07-04
Listing for:
Dormont Manufacturing Co
Full Time
position Listed on 2026-07-04
Job specializations:
-
Quality Assurance - QA/QC
Production QC/QA, Quality Control - QC Analysts/Managers, Regulatory Compliance Specialist
Job Description & How to Apply Below
Position Summary
The Quality Assurance Incoming Material Disposition Specialist is responsible for supporting the incoming inspection and disposition of consumables and raw materials at the Devens Cell Therapy Facility. This role performs inspections, reviews disposition deliverables, and ensures materials comply with BMS policies, standards, and global SOPs.
Duties/Responsibilities- Work closely with supply chain and manufacturing to address discrepancies with nonconforming material and support the incoming material process.
- Inspect incoming materials such as consumables, packaging, and raw materials per SOPs and specification requirements.
- Review disposition deliverables for materials and batches within inventory management systems.
- Ensure materials comply with all BMS policies, standards, network, and global SOPs.
- Review documentation supporting disposition of incoming materials.
- Use electronic systems such as SAP, learning management, and document management systems.
- Contribute to drafting, reviewing, or approving procedural documents.
- Perform assignments of simple to moderate complexity, exercise judgment to resolve problems and make routine recommendations.
- Perform other duties as required.
- Experience in a laboratory, manufacturing, quality, or warehouse environment desired.
- Evidence of successful participation on work/study teams with combined contribution, collaboration, and time‑bound results.
- Proficiency in common computer tools (word processing, spreadsheet, web‑based applications) and ERP solutions such as SAP.
- Previous work/academic experience requiring attention to detail and personal accountability.
- Strong communication skills and ability to follow written and verbal instructions.
- B.S. in science, engineering, biochemistry or related discipline, or equivalent.
- 0–2 years of directly relevant experience in a regulated cGMP environment.
- Any combination of education, experience, and military service considered in line with the above recommendations.
- Work is generally performed seated in a warehouse or laboratory setting, with standing and walking required up to 10% of the time.
- Work in cGMP laboratory or manufacturing environments with high attention to detail.
- Appropriate PPE and gowning used for restricted areas; aseptic processing and chemical handling performed in general office environment.
Devens – MA – US: $40.16 – $48.67 per hour (full‑time employee). Additional incentive cash and stock opportunities may be available. Final compensation is based on demonstrated experience.
Benefits- Health Coverage
:
Medical, pharmacy, dental, and vision care. - Well‑being Support
:
Programs such as BMS Well‑Being Account and Employee Assistance Programs. - Financial Well‑being and Protection
: 401(k) plan, disability, life insurance, and supplemental health benefits. - Work‑life Benefits
:
Paid Time Off (including unlimited flexible time for exempt employees), paid sick time, volunteer days, summer hours flexibility, and a global shutdown period.
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