Site Quality Head Singapore

thermo fisher biopharma services pte. ltd.; Singapore; On-site; SGD 210,000 - 320,000; Full time

Job summary

Thermo Fisher Biopharma Services Pte. Ltd. in Singapore is seeking a Site Quality Director to lead the CDMO Quality and Regulatory teams, ensuring outstanding quality and regulatory compliance across aseptic operations.

This role champions a culture of excellence in line with regulatory guidelines and GXP requirements. You will oversee the Site Quality and Regulatory team, drive continuous improvement of quality systems, and build top-tier leadership and talent across the organization, while

Qualifications

• Minimum 15+ years in the pharmaceutical industry, including sterile products and aseptic operations.
• Experience with CDMO, biotech, and vaccine production preferred.
• 5+ years acting as a Qualified Person is preferred.
• 10+ years of leadership experience building high-performing teams.
• Outstanding communication and presentation skills for engaging senior executives.
• Strong ability to attract, hire, and develop diverse talent.
• Proactive and strategic approach with attention to detail.
• Proven ability to make high-impact quality decisions and deliver results.

Responsibilities

• Lead and manage the Site Quality and Regulatory team to maintain flawless quality and compliance.
• Maintain and continuously improve site quality systems and processes.
• Foster a collaborative, inclusive culture prioritizing quality and compliance.
• Develop and maintain proactive relationships with regulatory authorities and clients.
• Act as a role model and drive change aligned with Thermo Fisher values.
• Coordinate with DPD EU & APAC QLT and partner with sister sites and global functions.

Skills

Leadership

Regulatory knowledge

Communication

Talent development

Strategic thinking

Quality management

Job description

Business Job Title: Site Quality Director Singapore

Group/Division: Pharma Services Group / Drug Product Division - Singapore Site

Position Summary:

As the Site Quality Director, you lead the CDMO Quality and Regulatory team, ensuring outstanding quality standards and compliance across our aseptic operations. This outstanding opportunity allows you to champion a culture of excellence and innovation, strictly adhering to regulatory guidelines and GXP compliance requirements.

Key Responsibilities:

• Lead and manage the Site Quality and Regulatory team, establishing and maintaining flawless quality and compliance levels.

• Maintain and continuously improve the site quality systems and processes.

• Identify, develop, and retain top-tier talent, ensuring a strong succession plan.

• Foster a collaborative and inclusive culture that prioritizes quality and compliance.

• Develop and maintain proactive relationships with regulatory authorities and clients.

• Maintain an independent authority for any decision impacting Quality

• Act as a role model, embodying Thermo Fisher values and driving groundbreaking change.

• Act as a member of the DPD EU & APAC QLT and partner across the organization with sister sites and global functions

How You Can Make an Impact:

• Proven track record of 15+ years in the pharmaceutical industry including sterile drug products and aseptic operations. Preferred experience with CDMO, biotech, and vaccine production.

• 5+ years actings a Qualified Person is preferred.

• Extensive knowledge of quality structures and regulatory bodies.

• 10+ years of leadership experience, successfully developing high-performing teams.

• Outstanding communication and presentation skills, capable of engaging senior executives.

• Strong ability to attract, hire, and develop diverse talent.

• Proactive and strategic approach, skilled at moving between details and the “big picture.”

• Learning agility with attention to detail

• Demonstrated ability to make calculated, high-impact quality decisions and get results.

Join us to craft the future of our Quality function and make a tangible impact on global health initiatives!