Senior QC Incoming Inspector
Anika
August 10, 2026
Remote friendly (Bedford, MA)
United States
$28 - $35 USD yearly
Operations
Senior QC Incoming Inspector
What You’ll Do
- Supports quality control activities for inspection, approval, and release of raw materials and components used in product manufacturing, including in-process manufacturing and packaging inspections.
- Serves as a subject matter expert in material inspection, material disposition, documentation review, and quality system compliance to ensure materials and records meet quality and regulatory requirements.
How You’ll Contribute
- Reviews and approves material inspection documentation and Manufacturing Process Specifications (MPS) for material release.
- Supports and mentors QC Materials Inspectors I and II with technical guidance and training.
- Coordinates annual retain inspections, facilitates retesting, and ensures associated documentation completion (electronic and paper).
- Performs reverification for returned products per approved procedures.
- Reviews source inspection documentation, including third-party Device History Records (DHRs).
- Participates in out-of-specification (OOS) investigations; supports material rejection investigations.
- Provides training for new employees, contractors, and Quality personnel.
- Authors, revises, and performs periodic reviews of SOPs, MPS, and controlled documents.
- Initiates and completes Document Change Requests.
- Maintains accurate records in accordance with Good Documentation Practices (GDP).
- Maintains training compliance for assigned procedures/systems/quality processes.
- Supports internal, customer, and regulatory audits/inspections.
- Participates in cross-functional projects and continuous improvement initiatives.
What It Takes (Required)
- High school diploma or equivalent.
- Minimum 4 years in a cGMP-regulated manufacturing environment or prior QA/QC experience.
- Experience reviewing quality documentation and supporting material inspection/disposition/release.
- Working knowledge of cGMP, GDP, and quality system processes.
- Microsoft Office (Word, Excel, Outlook).
- ERP experience for inventory movement transactions and material records.
- Strong attention to detail and excellent written/verbal communication.
Nice to Have (Preferred)
- Cleanroom/controlled environment experience.
- Experience supporting regulatory inspections, customer audits, quality system assessments.
- Knowledge of OOS investigations, material rejection, corrective actions.
- Experience authoring/revising controlled documents (SOPs, manufacturing specifications).
- Ability to work independently and manage competing priorities.
- Experience training/mentoring quality personnel.
Benefits (if explicitly stated)
- Discretionary bonus program; comprehensive healthcare benefits; HSA; 401(k) with up to 5% company match; employee stock purchase plan; accrued paid time off; long-term incentives including stock awards.
Schedule
- M–F 8:00am–4:30pm
What You’ll Do
- Supports quality control activities for inspection, approval, and release of raw materials and components used in product manufacturing, including in-process manufacturing and packaging inspections.
- Serves as a subject matter expert in material inspection, material disposition, documentation review, and quality system compliance to ensure materials and records meet quality and regulatory requirements.
How You’ll Contribute
- Reviews and approves material inspection documentation and Manufacturing Process Specifications (MPS) for material release.
- Supports and mentors QC Materials Inspectors I and II with technical guidance and training.
- Coordinates annual retain inspections, facilitates retesting, and ensures associated documentation completion (electronic and paper).
- Performs reverification for returned products per approved procedures.
- Reviews source inspection documentation, including third-party Device History Records (DHRs).
- Participates in out-of-specification (OOS) investigations; supports material rejection investigations.
- Provides training for new employees, contractors, and Quality personnel.
- Authors, revises, and performs periodic reviews of SOPs, MPS, and controlled documents.
- Initiates and completes Document Change Requests.
- Maintains accurate records in accordance with Good Documentation Practices (GDP).
- Maintains training compliance for assigned procedures/systems/quality processes.
- Supports internal, customer, and regulatory audits/inspections.
- Participates in cross-functional projects and continuous improvement initiatives.
What It Takes (Required)
- High school diploma or equivalent.
- Minimum 4 years in a cGMP-regulated manufacturing environment or prior QA/QC experience.
- Experience reviewing quality documentation and supporting material inspection/disposition/release.
- Working knowledge of cGMP, GDP, and quality system processes.
- Microsoft Office (Word, Excel, Outlook).
- ERP experience for inventory movement transactions and material records.
- Strong attention to detail and excellent written/verbal communication.
Nice to Have (Preferred)
- Cleanroom/controlled environment experience.
- Experience supporting regulatory inspections, customer audits, quality system assessments.
- Knowledge of OOS investigations, material rejection, corrective actions.
- Experience authoring/revising controlled documents (SOPs, manufacturing specifications).
- Ability to work independently and manage competing priorities.
- Experience training/mentoring quality personnel.
Benefits (if explicitly stated)
- Discretionary bonus program; comprehensive healthcare benefits; HSA; 401(k) with up to 5% company match; employee stock purchase plan; accrued paid time off; long-term incentives including stock awards.
Schedule
- M–F 8:00am–4:30pm