What are the responsibilities and job description for the Process Engineer / CQV Engineer position at Stark Pharma Solutions Inc?
About The Company
Stark Pharma Solutions Inc. is a global consulting and staffing partner serving the Pharmaceutical, Medical Device, Biotech, and IT industries across the USA, Canada, and India.
Position: Process Engineer / CQV Engineer
Location: North Carolina
Duration: Long Term
Job Overview
We are seeking a Process Engineer / CQV Engineer to support Commissioning & Qualification activities within a pharmaceutical manufacturing environment.
Key Responsibilities
Support Commissioning and Qualification (C&Q) activities.
Author and review engineering and qualification specifications.
Develop and review qualification plans and protocols.
Perform and document risk assessments.
Support execution of qualification activities.
Prepare and review qualification reports.
Support change controls and deviation investigations.
Collaborate with Engineering, Quality, Manufacturing, and Validation teams.
Ensure qualification activities are completed in accordance with applicable procedures and requirements.
Required Qualifications
Experience in pharmaceutical or biotechnology manufacturing environments.
Hands-on experience with Commissioning & Qualification (C&Q) activities.
Experience authoring and reviewing qualification protocols and reports.
Experience with risk assessments and qualification planning.
Experience with change controls and deviations.
Strong technical writing and documentation skills.
Strong understanding of GMP and regulated manufacturing environments.
Strong communication and collaboration skills.
Bachelor s degree in Engineering, Life Sciences, or a related field preferred.
How To Apply
Apply Now: Submit your updated resume to Stark Pharma Solutions Inc. for consideration.
Stark Pharma is an Equal Opportunity Employer and welcomes qualified candidates from diverse backgrounds.
Stark Pharma Solutions Inc. is a global consulting and staffing partner serving the Pharmaceutical, Medical Device, Biotech, and IT industries across the USA, Canada, and India.
Position: Process Engineer / CQV Engineer
Location: North Carolina
Duration: Long Term
Job Overview
We are seeking a Process Engineer / CQV Engineer to support Commissioning & Qualification activities within a pharmaceutical manufacturing environment.
Key Responsibilities
Support Commissioning and Qualification (C&Q) activities.
Author and review engineering and qualification specifications.
Develop and review qualification plans and protocols.
Perform and document risk assessments.
Support execution of qualification activities.
Prepare and review qualification reports.
Support change controls and deviation investigations.
Collaborate with Engineering, Quality, Manufacturing, and Validation teams.
Ensure qualification activities are completed in accordance with applicable procedures and requirements.
Required Qualifications
Experience in pharmaceutical or biotechnology manufacturing environments.
Hands-on experience with Commissioning & Qualification (C&Q) activities.
Experience authoring and reviewing qualification protocols and reports.
Experience with risk assessments and qualification planning.
Experience with change controls and deviations.
Strong technical writing and documentation skills.
Strong understanding of GMP and regulated manufacturing environments.
Strong communication and collaboration skills.
Bachelor s degree in Engineering, Life Sciences, or a related field preferred.
How To Apply
Apply Now: Submit your updated resume to Stark Pharma Solutions Inc. for consideration.
Stark Pharma is an Equal Opportunity Employer and welcomes qualified candidates from diverse backgrounds.