×
Register Here to Apply for Jobs or Post Jobs. X

QAV Engineer

Job in Springfield, Hampden County, Massachusetts, 01101, USA
Listing for: United Pharma Technologies Inc
Full Time position
Listed on 2026-10-27
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering, Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 45 USD Hourly USD 45.00 HOUR
Job Description & How to Apply Below
Industry: Pharmaceutical / Biopharmaceutical

Job Description:

We are seeking an experienced QAV Engineer to support a pharmaceutical client in Boston, MA. The ideal candidate will have a strong background in Quality Assurance, equipment qualification, and validation within a GMP-regulated manufacturing environment.

Key Responsibilities:
  • Perform quality engineering activities and remediate compliance gaps within GMP facilities.
  • Initiate, manage, and own CAPAs to address quality and compliance issues.
  • Execute installation verification, functional testing, equipment qualification, and performance qualification (PQ).
  • Support validation activities for cold storage, autoclaves, and warehouse operations.
  • Develop, execute, revise, and review validation protocols, plans, SOPs, and reports.
  • Review lifecycle documentation, including URS, design documents, risk assessments, impact assessments, Part 11 assessments, and traceability matrices.
  • Investigate and remediate quality events related to qualified equipment.
  • Assess change controls for validation impact and support decommissioning activities.
  • Review and approve validation plans, protocols, and reports.
  • Collaborate with engineering teams, SMEs, and cross-functional stakeholders to maintain GMP compliance and documentation.
Required Qualifications:
  • Bachelor’s degree in Engineering, Science, or a related discipline.
  • Minimum 3 years of experience in GMP manufacturing facilities.
  • Mandatory experience in Oral Solid Dosage (OSD).
  • Hands-on experience with commissioning, qualification, and validation (CQV) of facilities, utilities, production, laboratory, or support equipment.
  • Strong knowledge of validation lifecycle management, risk-based validation, and cGxP requirements.
  • Experience with equipment qualification, process validation, computer systems validation, cleaning validation, or sterilization.
  • Knowledge of FDA, cGMP, ICH, ISO, EMA, ISPE, and PDA guidelines.
  • Strong communication, documentation, and cross-functional collaboration skills.
Pay Rate:$45/hr on W2

Employees hired into this position are eligible for the following benefits, subject to applicable plan terms and eligibility requirements:

Health Insurance:

Medical, dental, and vision insurance options are available through a third-party provider. Employees are responsible for paying the full cost of their insurance premiums.

Retirement Benefits:

A 401(k) retirement savings plan is available. No employer matching or other employer contributions are provided.

Paid Time Off (PTO):

No PTO is provided other than that required by applicable state and local laws.

To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)
0
200
Filters
Education Level
Experience Level (years)
Posted in last:
Salary