QA Site Head – Pharmaceutical Manufacturing - Singapore

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

See also