More jobs:
Process Validation Engineer; Life Sciences
Job in
Tucson, Pima County, Arizona, 85718, USA
Listed on 2026-01-02
Listing for:
Dawar Consulting
Full Time
position Listed on 2026-01-02
Job specializations:
-
Engineering
Quality Engineering -
Quality Assurance - QA/QC
Quality Engineering
Job Description & How to Apply Below
Job Description :
Our client, a world leader in diagnostics and life sciences, is looking for a “Process Validation Engineer” based out of Tucson, AZ. Please review the details below:
Job Duration:
Long Term Contract (Possibility Of Further Extension)
Company Benefits:
Medical, Dental, Vision, Paid Sick leave, 401K Responsible for developing and executing process validation and/or process verification protocols and reports to ensure that manufacturing processes are compliant with regulatory requirements and company standards. This role involves collaborating with cross- functional teams to support continuous improvement and maintenance of validated processes.
- Develop, write, review, and execute process validation/process verification protocols and reports.
- Conduct risk assessments and develop validation strategies for new and existing processes.
- Analyze and interpret process validation data, ensuring accuracy, completeness, and adherence to regulatory and internal requirements.
- Collaborate with Manufacturing, Quality, Design Transfer Operations, and other departments to resolve validation issues and implement corrective actions.
- Participate in process optimization and continuous improvement initiatives to enhance quality and efficiency.
- Ensure compliance with FDA, ISO, and other relevant regulatory guidelines, as well as adherence to internal requirements.
- Provide training and guidance to manufacturing and quality personnel on validation processes and procedures.
- Maintain process validation documentation and ensure traceability and accessibility for audits and inspections.
- Bachelor’s degree in Engineering, Life Sciences, or a related field.
- Experience in process validation within a regulated industry (pharmaceutical, medical device, biotechnology, etc.)
- Strong understanding of process validation principles, techniques, and industry standards.
- Familiarity with regulatory requirements (FDA, ISO) and Good Manufacturing Practices (GMP).
- Proficient in Microsoft Office Suite (Word and Excel), Google Workspace
- Experience with statistical analysis software (e.g., Minitab, JMP) is preferred.
- Knowledge of Six Sigma or Lean methodologies is preferred.
If interested, kindly share your updated resume at /
Dawar Consulting
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