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Wood

QC Analytical Chemist

1d

Wood

Singapore, SG · Full-time · S$70,000 – S$120,000

About this role

Wood has an opportunity for an experienced QC Analytical Chemist for an initial 12-month contract based in Singapore. The role drives laboratory protocol quality improvements, ensuring compliance, efficiency, and data integrity across QC operations. It includes a secondment with a key client for hands-on exposure in a regulated laboratory environment.

The position involves close collaboration with cross-functional stakeholders in a GMP-regulated setting. Daily work focuses on investigations from laboratory incidents, data accuracy for issue resolution, and monitoring product quality anomalies. Highlight issues to manufacturing and higher management for timely action.

Operate within a dynamic team committed to diversity and inclusion, with employee networks giving all a voice. Engage in a professional environment shaping standards in renewable and emerging energy sectors. Collaborate effectively across laboratory, quality, and client stakeholders.

Gain meaningful projects delivered to industry leaders. Access tailored development plans for continued professional growth. Join global experts at the leading edge of the profession.

Requirements

  • Science-based tertiary qualification, with preference for Chemistry or related disciplines
  • 5–12 years of relevant working experience within a pharmaceutical or GMP-regulated environment
  • Strong technical competency in analytical chemistry techniques and laboratory practices
  • Proven problem-solving capability with ability to apply scientific judgement to complex analytical issues
  • Well-developed influencing and interpersonal skills for effective collaboration across stakeholders
  • Prior experience of GMP work environment
  • Data Integrity knowledge
  • DMAIC knowledge

Responsibilities

  • Lead or participate in investigations arising from laboratory incidents and assess impact to recommend remedial actions
  • Ensure all data supporting resolution of process and method issues has sufficient accuracy for correct actions
  • Contribute to formulation and development of plans for implementing new testing technologies and methods
  • Approve changes impacting product quality, validation, and cGMP compliance, including assessment and closure
  • Draft, compile, review, and update laboratory documents such as testing protocols, procedures, and guidelines
  • Ensure regulatory compliance, perform Client's Management Monitoring audits, and support external audits
  • Constantly monitor product quality and highlight anomalies to manufacturing group and higher management

Benefits

  • Meaningful and interesting projects delivered to leaders of industry across renewable and emerging energy sectors
  • Commitment to Diversity and Inclusion with employee networks committed to giving all employees a voice
  • Commitment to continued professional development with tailored development plans
  • Global connections: join experts around the world at the leading edge of the industry