Process Validation Engineer (Medical or Pharma Manufacturing exp req)
Location: Albany GA
Salary: $95000 - $% Annual Bonus Amazing Benefits
Benefits: Fully Paid Health Insurance (employee and dependents) 401k w/ match 3 weeks PTO
Job Type: Full-Time
Typical Hours: M-F 8 AM - 5 PM
Start Date: ASAP
Sponsorship is not available
Relocation assistance available
Process Validation Engineer (Medical or Pharma Manufacturing exp req) Description
Our client a trailblazer in pharmaceutical manufacturing is seeking a Process Validation Engineer to join their team in Albany this role you will be responsible for developing and executing validation protocol documentation for equipment and manufacturing processes while ensuring compliance with regulatory and GMP standards. You will evaluate and optimize production processes support technology transfers and address non-conformance issues. Working closely with cross-functional teams you will play a pivotal role in ensuring product quality and operational efficiency. This position is ideal for a detail-oriented professional who thrives in a dynamic environment and is eager to make an impact on product integrity and process improvement. This is an exciting opportunity to join an international leader in healthcare that offers amazing benefits and prides itself on work-life balance.
Why move to Albany GA Albany is beautifully positioned on the banks of the Flint River. It is the hub of Southwest Georgia for culture shopping education healthcare and recreation. Albany is a great place to live work and play. Albanys housing costs are half as much as the state of Georgia and the national average.
Process Validation Engineer (Medical or Pharma Manufacturing exp req) Responsibilities
Spearhead qualification protocols for next-generation manufacturing processes
Drive manufacturing investigations and implement innovative solutions
Design validation strategies for new product launches and technology transfers
Lead comprehensive IQ/OQ/PQ validation activities across multiple projects
Create robust standard operating procedures for manufacturing excellence
Ensure continuous process verification for robust manufacturing operations
Coordinate cross-functional initiatives for equipment and facility optimization
Champion continuous improvement through data-driven decision making
Process Validation Engineer (Medical or Pharma Manufacturing exp req) Qualifications
Bachelors degree required
3 years of experience in a GMP-regulated environment required
Experience supporting manufacturing in the pharma or medical devices industry required
Experience with process validation documentation and execution required
Experience with IQ/OQ/PQ processes and validation protocols required
QMS experience required