ABOUT YOU
As a Senior Scientist, Intertek are currently recruiting for an experienced and self-sufficient scientist to join their growing team in Melbourn. As part of continued investment in our cGMP laboratories, this role is key to strengthening technical capability and investigation leadership within the site.
This position is suited to someone who thrives on ownership, enjoys solving complex analytical challenges and is confident making sound decisions within a regulated GMP environment.
Clear pathways for progression are available based on capability and impact.
Required skills and experience:
1. IT literate
2. Strong numeracy skills with the ability to trend, interpret and critically evaluate analytical data
3. Clear and confident written and verbal communication skills, including technical discussions with internal stakeholders and clients
4. Strong working knowledge of scientific methodologies, GMP standards and Quality Management Systems
5. Proven experience within a cGMP pharmaceutical laboratory, including leading deviations and investigations
6. Sound knowledge of laboratory safety standards, chemical handling and COSHH
7. Degree level qualification within a relevant scientific discipline or significant experience within a regulated pharmaceutical environment
8. Customer focused, comfortable engaging with clients when required
9. Extensive experience in chromatography techniques such as HPLC and/or GC, including method development, validation and troubleshooting
ABOUT THE OPPORTUNITY
On a daily basis, you will lead analytical activities within a GMP laboratory environment. This role requires a confident decision-maker who can independently manage investigations, interpret data and ensure high-quality scientific delivery.
You will play an important role in enhancing investigation standards and strengthening the technical capability of the wider team.
Key activities:
10. Operate as a subject matter expert across multiple analytical techniques
11. Lead OOS/OOT investigations, perform root cause analysis and author/close deviations and change controls within the QMS
12. Interpret complex methods and justify deviations where appropriate in line with GMP
13. Manage analytical projects from initiation through to reporting, ensuring compliance, timelines and quality standards are met
14. Provide technical guidance and informal mentoring to less experienced colleagues
15. Communicate confidently with clients regarding technical matters
16. Demonstrate strong ownership and accountability when analytical challenges arise
17. Work priorities agreed with Laboratory Manager and Team Leader, with significant autonomy in organising and delivering work
WHAT WE OFFER
Join Intertek and become part of our global network of inspiring and entrepreneurial colleagues. We are a global family that values diversity and we thrive working together with precision, pace, and passion. We are working to make the world Ever Better, ensuring the quality, safety and sustainability of products and services used by millions of people around the world.
18. Competitive salary/benefits
19. Development and career opportunities around the Globe
20. Working in a highly motivated team and dynamic working environment
We are an Equal Opportunity Employer who do not discriminate against applicants. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex or national origin.
Intertek operates a preferred supplier arrangement, and we do not accept unsolicited approaches from agencies