QA Site Head – Pharmaceutical Manufacturing - Singapore
Summary
Oversee quality operations at a pharmaceutical manufacturing site, ensuring GMP compliance and regulatory adherence while leading quality teams and audits.
A well-established pharmaceutical manufacturing organization, is seeking an experienced QA Site Head to lead site-wide quality operations.
The QA Site Head will:
- Own site quality performance, ensuring products consistently meet client and regulatory expectations
- Build, optimize, and maintain the site's quality management system in line with GMP and regulatory standards
- Review and approve quality procedures, manuals, and periodic quality reviews
- Drive CAPA effectiveness through deviation investigations, incident handling, self-inspections, and external audits
- Serve as the key quality contact for clients, hosting audits and following through on corrective actions
- Review and approve validation master plans (VMP) and validation documentation
- Lead quality training and champion a strong quality culture across the site
- Escalate quality risks and trends to top management in a timely manner
- Ensure compliance with EHS laws, SOPs, and actively support EHS culture-building (training, drills, working groups)
To be shortlisted for the role, you will come with:
- Degree in Pharmacy, Chemistry, or a related field
- Strong understanding of pharmaceutical production, testing, and quality management; solid grasp of GMP regulations
- Strong spoken and written communication skills, with the ability to communicate effectively with clients, auditors, site teams, and senior management.
- Strong computer/IT skills
- A minimum of 8+ years of quality management experience in a pharmaceutical manufacturing environment
- Strong coordination, communication, and scientific problem-solving skills
- Proven leadership ability, with experience in leading, assigning, and developing quality teams.
AM
Reg. No. R1110770
BeathChapman Pte Ltd
Licence no. 16S8112