What are the responsibilities and job description for the Process Validation Engineer (Medical or Pharma Manufacturing exp req) position at Rhodes Wolfe?
Process Validation Engineer (Medical or Pharma Manufacturing exp req)
Location: Albany, GA
Salary: $95,000 - $115,000 10% 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, GA. In 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. Albany’s 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
• Bachelor’s 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
Salary : $95,000 - $115,000
