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

ATLCQV Engineer Fill​/Finish and Analytical Equipment; PA

Job in Spring House, Montgomery County, Pennsylvania, 19477, USA
Listing for: Pinnaql
Full Time position
Listed on 2026-02-27
Job specializations:
  • Engineering
    Quality Engineering, Process Engineer
  • Quality Assurance - QA/QC
    Quality Engineering
Salary/Wage Range or Industry Benchmark: 80000 - 100000 USD Yearly USD 80000.00 100000.00 YEAR
Job Description & How to Apply Below
Position: ATL02-062425 CQV Engineer  Fill/Finish and Analytical Equipment (PA)
Location: Spring House

Current job opportunities are posted here as they become available.

ATL
02-062425 CQV Engineer – Fill/Finish and Analytical Equipment (PA)

Validation & Engineering Group, Inc. (V&EG) is a leading services supplier providing solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the areas of Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other technical services.

We are currently seeking a CQV Engineer with expertise in laboratory systems, QC modules, and aseptic fill/finish equipment to support commissioning and qualification activities in support of GMP operations. The selected candidate must be available to work in cleanroom, laboratory, and classified areas, complying with all safety, gowning, and documentation standards.

Location: Spring House, PA

Responsibilities:

  • Author, review, and execute risk-based qualification protocols (IQ, OQ, PQ) for:
    • QC modules:
      Flow Cytometry, Cell Count, Reagent Fill, Ambient and Cold Storage.
    • Laboratory equipment:
      Biosafety cabinets, isolators, centrifuges, balances, peristaltic pumps, air samplers.
    • Aseptic fill/finish systems:
      Vial filling modules, isolators, cappers, crimpers, inspection systems.
  • Lead system walkdowns, protocol execution, and traceability matrix development.
  • Coordinate FAT/SAT support and ensure test readiness for system turnover.
  • Collaborate with automation, operations, and quality stakeholders to align timelines and mitigate issues.
  • Support deviation documentation and protocol closure per project requirements.

Qualifications:

  • Bachelor’s degree in life sciences, engineering, or related field.
  • Minimum 5 years of CQV experience in a GMP lab, QC, or aseptic fill/finish setting.
  • Strong knowledge of qualification strategies for lab, QC, and drug product systems.
  • Experience with barrier systems, inspection technologies, and integrated QC modules.
  • Excellent documentation, troubleshooting, and cross-functional coordination skills.
#J-18808-Ljbffr
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)

Job Posting Language
Employment Category
Education (minimum level)
Filters
Education Level
Experience Level (years)
Posted in last:
Salary