Sr. Validation Engineer

Davita Inc.; Rockford (IL); On-site; USD 97,000 - 108,000; Full time

Job summary

A leading company is searching for a Senior Validation Engineer to oversee the validation of medical device assembly lines within a dynamic CDMO environment. The successful candidate will lead essential validation activities to ensure compliance with FDA and ISO standards, while collaborating with cross-functional teams for successful new product introductions and sustaining operations.

Benefits

Paid time off

Health insurance coverage (including dental and vision)

Flexible spending account

401(k)

Qualifications

• 5-8 years of validation experience in medical device or biotech.
• Hands-on experience with equipment and process validation.
• Experience in risk-based approaches and statistical tools.

Responsibilities

• Lead validation lifecycle activities including IQ/OQ/PQ.
• Develop and execute validation master plans and protocols.
• Support regulatory and customer audits as validation SME.

Skills

FDA regulations

ISO 13485

Statistical tools

Risk management

Technical writing

Communication skills

Education

Bachelor's degree in Engineering or Life Sciences

Advanced degree preferred

Tools

Minitab

JMP

Job description

Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients.

We are PCI.

Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.

Job Title: Senior Validation Engineer - Medical Device Assembly (CDMO)
Location: [Rockford]
Department: Quality
Reports To: Director of Quality

Position Summary:

We are seeking a highly skilled Senior Validation Engineer to support the validation activities associated with medical device assembly lines within a fast-paced Contract Development and Manufacturing Organization (CDMO). The ideal candidate will lead equipment, process, and cleaning validation efforts to ensure compliance with FDA, ISO 13485, and other applicable regulatory standards. This role is critical in supporting new product introductions, technology transfers, and sustaining operations for both clinical and commercial manufacturing.

Key Responsibilities:

• Lead and execute validation lifecycle activities including IQ/OQ/PQ for manufacturing equipment, utilities, and automated assembly lines.
• Develop and execute validation master plans, protocols, and reports in compliance with internal procedures and regulatory expectations.
• Provide validation support for process changes, new product introductions (NPIs), and customer tech transfers.
• Apply risk-based approaches (e.g., per ISO 14971) to validation strategy and justification.
• Utilize statistical methods to define sampling plans and acceptance criteria for validation studies.
• Support cleaning validation and verification activities for equipment used in medical device production.
• Collaborate with cross-functional teams, including Manufacturing, Quality, Engineering, and Regulatory Affairs.
• Review and approve equipment specifications, process FMEAs, URS, and validation documentation.
• Conduct gap assessments and remediation planning for existing validation documentation when required.
• Ensure all validation activities meet the standards set by FDA 21 CFR Part 820, ISO 13485, and customer requirements.
• Support regulatory and customer audits as the validation SME.

Qualifications:

• Bachelor's degree in Engineering, Life Sciences, or a related technical discipline; advanced degree preferred.
• Minimum of 5-8 years of validation experience in the medical device, pharmaceutical, or biotech industry.
• Strong knowledge of FDA regulations, ISO 13485, ISO 14971, and GAMP 5 principles.
• Hands-on experience with equipment and process validation on assembly lines (manual, semi-automated, or fully automated).
• Proficient in risk management and statistical tools (e.g., Minitab, JMP).
• Excellent technical writing and communication skills.
• Ability to manage multiple projects and timelines in a dynamic manufacturing environment.

Preferred Qualifications:

• Experience with vision systems, leak testers, ultrasonic welding, and other medical device assembly technologies.
• Familiarity with software validation and PLC-based control systems.
• Six Sigma certification or formal training in statistical process control (SPC).

For candidates in Illinois:This position's base salary hiring rangeis $97,280-$107,008, plus a 5% MBP annual performance bonus eligibility. Final offer amounts are determined by multiple factors, including but not limited to specific and relevant experience, education, credentials, geography, and subject matter expertise. PCI offers full-time employees a competitive benefits package that includes paid time off, health insurance coverage (including dental and vision), flexible spending account, and 401(k.

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Equal Employment Opportunity (EEO) Statement:
PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.

At PCI, Equity and Inclusion are at the core of our company's purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity - at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture.