Demo

QC/LAB Equipment Validation Engineer-Pharma/BioPharma

Process Engineering Specialists
Cincinnati, OH Full Time
POSTED ON 1/12/2025
AVAILABLE BEFORE 2/7/2025

PES is an international services company providing Project Management, Construction Management, Commissioning & Qualification and Automation services to our clients in the pharmaceutical, nutritional and related sectors.


With offices across Europe, Asia and US, our core focus is on consistently delivering high quality outcomes for our multinational clients.


This focus, and our people's experience in delivering consistent quality results for our clients over the past 20 years has been key to our success to date.


We are currently looking for QC/LAB Equipment Validation Engineers to join us on a long term project to help us deliver various projects in the Life Sciences Industry.


Key Attributes/Responsibilities:

  • Looking for candidates with 5-7 years QC/Lab Equipment Validation experience.
  • Provide technical support to run and validate necessary test methods on lab equipment and in developing method transfer/validation protocols and reports.
  • Perform qualification and validation for in process, release and stability equipment (HPLC, UV, TOC, pH, etc).
  • Manage day-to-day Quality Control/LAB Validation activities in accordance with approved Project Plans and Policies for a fast-paced brownfield project.
  • Help with lab system validation, develop and oversea system qualification
  • Review and Approve C&Q plans/protocols/reports and GxP SOPs/records
  • Review validation life-cycle documents during the commissioning, qualification (IQ/OQ), and validation (PQ) phase e.g., pre and post-execution commissioning/ qualification plans and test specifications, validation summary reports & etc.
  • Ensure that documents are in compliance with quality standards and applicable regulatory requirements
  • Review engineering change control to evaluate the validation/quality impact(s).
  • Support in the resolution of validation deviations and approval.
  • Participate in the qualification coordination meeting to ensure correct event sequence in compliance


We are currently looking for candidates who can be on site or travel to site for this project.


If you'd like to find out about this opportunity, please forward your CV to Nelson Anthony (careers@pes-international.com).


If you would like to find out about the latest Jobs and Projects we are involved in then do follow us on LinkedIn: https://www.linkedin.com/company/processengineeringspecialists/mycompany/


PES International operates as an equal opportunity employer. No terminology in this advert is intended to discriminate on the grounds of age, race, religion, sexual orientation or any other factors with no bearing to employment skills and we confirm that we are happy to accept applications from persons of any background for this role.

Salary : $150,000 - $200,000

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