- Singapore Singapore
Kerja Sepenuh Masa Validation Engineer, Gaji tinggi SGD 7,000 di ORION PROJECT SERVICES PTE. LTD. - Maukerja
Validation Engineer
ORION PROJECT SERVICES PTE. LTD.
Kongsi
Simpan
Lokasi Kerja
Penerangan Kerja
Tanggungjawab
Location:
Tuas
Contract:
Initial 12-month contract with potential to extend
Industry:
Biopharmaceutical
Orion Group Life Sciences are currently recruiting a
Validation Engineer
on behalf of our multinational biopharmaceutical client based in Tuas.
This is an initial
12-month contract with potential to extend
.
Key Responsibilities
Develop and execute validation protocols, including IQ, OQ, PQ, process validation and cleaning validation.
Author validation documentation and final validation reports.
Lead validation risk assessments and ensure compliance with GMP and GAMP requirements.
Investigate validation-related deviations and support CAPA implementation.
Coordinate validation activities with cross-functional teams, including Quality Assurance, Engineering and Manufacturing.
Maintain and update Validation Master Plans.
Support continuous improvement of validation activities and documentation as required.
Requirements
Degree in Engineering, Life Sciences or a related discipline.
3+ years' validation experience within the pharmaceutical or biotechnology manufacturing industry.
Strong knowledge of GMP and GAMP requirements.
Experience with equipment qualification, process validation and cleaning validation.
Strong communication and stakeholder management skills.
Ability to work effectively within cross-functional teams.
Orion Group provides specialist life science recruitment support across pharmaceuticals, biotechnology, medical devices, agri science, and R&D organisations worldwide. Across a variety of disciplines, we connect businesses with skilled scientific, engineering, manufacturing, quality, and technical professionals who help drive innovation in highly regulated industries.
Tuas
Contract:
Initial 12-month contract with potential to extend
Industry:
Biopharmaceutical
Orion Group Life Sciences are currently recruiting a
Validation Engineer
on behalf of our multinational biopharmaceutical client based in Tuas.
This is an initial
12-month contract with potential to extend
.
Key Responsibilities
Develop and execute validation protocols, including IQ, OQ, PQ, process validation and cleaning validation.
Author validation documentation and final validation reports.
Lead validation risk assessments and ensure compliance with GMP and GAMP requirements.
Investigate validation-related deviations and support CAPA implementation.
Coordinate validation activities with cross-functional teams, including Quality Assurance, Engineering and Manufacturing.
Maintain and update Validation Master Plans.
Support continuous improvement of validation activities and documentation as required.
Requirements
Degree in Engineering, Life Sciences or a related discipline.
3+ years' validation experience within the pharmaceutical or biotechnology manufacturing industry.
Strong knowledge of GMP and GAMP requirements.
Experience with equipment qualification, process validation and cleaning validation.
Strong communication and stakeholder management skills.
Ability to work effectively within cross-functional teams.
Orion Group provides specialist life science recruitment support across pharmaceuticals, biotechnology, medical devices, agri science, and R&D organisations worldwide. Across a variety of disciplines, we connect businesses with skilled scientific, engineering, manufacturing, quality, and technical professionals who help drive innovation in highly regulated industries.
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