Job Description
Remarkable people, trusted by clients to design and advance the world.
Wood has an opportunity for an experienced QC Analytical Chemist for an initial 12 ‑ month contract based in Singapore.
The Role
The QC Analytical Chemist is accountable for driving laboratory protocol quality improvements, ensuring compliance, efficiency, and data integrity across QC operations. The position includes a secondment with a key client, offering hands-on exposure within a regulated laboratory environment and close collaboration with cross ‑ functional stakeholders.
What We Can Offer
Meaningful and interesting projects delivered to leaders of industry across renewable and emerging energy sectors
Commitment to Diversity and Inclusion; we are an organization actively committed to diversity and inclusion across our business with employee networks committed to giving all employees a voice
Competitive salary with regular salary reviews to ensure we are rewarding at the right level in line with the market
Commitment to continued professional development; development plans that are tailored to your individual needs and interests
Global connections: join experts around the world who are at the leading edge of our industry, shaping the standards of our profession
Responsibilities
- Lead or participate in investigation arising from laboratory investigation, incidents and accurately assess the impact of the failure to make appropriate recommendations remedial actions for follow-up.
- Ensure that all data supporting the resolution of process and method issues have sufficient accuracy to allow for the correct actions to be taken to address the issue.
- Contribute to the formulation and development of the plans for the implementation of new testing technologies and methods.
- Involve in the approving change that may have an impact on product quality, validation and/or cGMP compliance. This may require assessment of testing requirement, co-ordinate testing of samples and comment on change documentation and ensure closure of change. Upon completion, review and ensure closure of changes.
- Draft, compile, review and update appropriate laboratory documents such as testing protocol, procedures and guidelines relating to GMP and operational framework of the laboratory.
- Ensure regulatory compliance, perform Client's Management Monitoring audit and support Independent Business Monitoring (IBM) and external audits.
- Constantly monitor product quality and highlight the anomalies to the manufacturing group and higher management.
- Other preferences: prior experience of GMP work environment, Data Integrity knowledge, DMAIC.
Qualifications
- 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 the ability to apply scientific judgement to complex analytical issues
- Well ‑ developed influencing and interpersonal skills, with the ability to collaborate effectively across laboratory, quality, and client stakeholder
If you are an experienced QC Analytical Chemist, ready for your next challenge - apply today!
Shortlisting will commence immediately.
