A mid-size Pharmaceutical company is seeking to hire a highly skilled validation engineer. The ideal candidate will be responsible for performing IQ/OQ/PQ and commissioning activities while using general engineering principles to develop capital projects that reduce costs, improve operating efficiency and progress quality.
The Validation Engineer will be responsible for the following...
-IQ OQ PQ Protocols - Writing protocols specifically designed for qualification events like Installation Qualification (IQ), Operational Qualification (OQ) Performance Testing(PV)
-FAT & SAT Commissioning Activities - Performing Factory Acceptance Tests(FATs)and Site acceptance tests(SATs).
-General Engineering Principles - Using sound judgment when implementing new processes/operations with regards to safety measures which have been put into place by engineers through time-tested methods proven effective over many years.
-SOP Development- Developing Standard Operating Procedures specific equipment maintenance procedures system upkeep guidelines ensuring compliance at all times.
-DCR System Usage - Actively utilizing Document Change Request(DCR)sytem efficiently adding removing documents depending on requirements without compromising any regulations set forth by governing bodies
The Validation Engineer should have the following qualifications...
- Bachelor's degree in Engineering or equivalent field
- Minimum of 3 years' experience as a Validation Engineer within the Medical Device industry
- Strong knowledge of Quality Assurance standards and practices
- Health Care
- Vision & Dental
- Relocation Package
Don't miss out on this amazing opportunity! Apply now if you're ready to take your career as a validation engineer further!