Overview
QA Validation Lead- BioPharma Jobs in Singapore, Singapore at EFOR (formerly Process Engineering Specialists)
Title: QA Validation Lead- BioPharma
Company: EFOR (formerly Process Engineering Specialists)
Location: Singapore, Singapore
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 QA Validation Lead to join us on a permanent basis to help us deliver various projects in the Life Sciences Industry.
Key Attributes/Responsibilities:
- Lead QA oversight of validation and qualification activities across manufacturing, utilities, facilities, equipment and computerised systems.
- Review and approve validation protocols, reports and supporting documentation to ensure compliance with cGMP and regulatory requirements.
- Provide quality oversight for IQ, OQ, PQ, Process Validation, Cleaning Validation and Computer System Validation (CSV) activities.
- Review and approve validation-related deviations, investigations, CAPAs and change controls.
- Ensure all validation activities comply with company Quality Management System (QMS), Data Integrity and Good Documentation Practices (GDP).
- Partner with Engineering, Manufacturing, MSAT, QC and other cross-functional teams to support validation projects and product lifecycle activities.
- Support regulatory inspections and customer audits by providing validation documentation and quality expertise.
- Identify compliance risks and drive continuous improvement initiatives to strengthen validation and quality systems.
- Mentor and provide technical guidance to validation and quality teams on GMP and validation best practices.
- Stay current with global regulatory requirements and industry guidelines to ensure ongoing compliance and inspection readiness.
If you’d like to find out about this opportunity, please forward your CV to Nelson Anthony ([email protected]).
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.
