Analytical Scientist

TN United Kingdom; Liverpool; On-site; GBP 25,000 - 35,000; Full time

Job summary

An established industry player is seeking a dedicated individual for a permanent full-time position focused on stability testing of pharmaceutical products. This role involves performing both routine and non-routine analyses using advanced analytical techniques, ensuring compliance with GMP standards, and documenting results meticulously. The company values growth and innovation, offering a supportive environment where employees can thrive. With a commitment to sustainability and diversity, this innovative firm provides various benefits, including health plans and global career opportunities. Join a team that celebrates achievements and fosters continuous improvement.

Benefits

Health Cash Plan

Life Assurance (4x annual salary)

Company Pension Plan

Employee Assistance Programme

Free parking

Global career opportunities

Access to Perkbox for discounts

Qualifications

• Degree in Chemistry or related discipline required.
• 1+ year of relevant experience in pharmaceutical testing.
• Experience with HPLC and analytical techniques essential.

Responsibilities

• Perform routine and non-routine analysis using analytical techniques.
• Document data according to client policies and procedures.
• Handle client queries regarding test results.

Skills

HPLC

Dissolution

Karl Fischer determination

GMP compliance

Data interpretation

Chromatographic techniques

MS Office proficiency

Analytical techniques

Education

Degree in Chemistry

Tools

Electronic Lab Notebooks

LIMS

Job description

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This is a permanent full-time position, working a 35-hour week, 7 hours per day, flexibly between 7am & 7pm, 5 days a week as per business needs.

The purpose of this job is to perform stability testing of finished pharmaceutical products and produce accurate results within an acceptable timeframe.

1. To perform routine and non-routine analysis using traditional and modern analytical techniques (primarily: HPLC, Dissolution, and Karl Fisher determination), as required by the client’s representative.
2. To perform technology transfers on new products entering the team.
3. To review analytical data for GMP compliance.
4. To initiate and follow-up on OOS results and action limits as per client procedures.
5. To document data according to current client policies and procedures.
6. To collect and measure productivity through metrics such as tests performed, cycle times, lab/product issues, hours worked per project, etc.
7. To prepare and approve results for tests in which they have received training and are deemed competent.
8. To handle client queries and communicate with designated personnel, with support from onsite leadership, regarding test results or service issues.
9. To stay updated with technological or methodological revisions, complete necessary training, and adjust work as needed with approval from the Lead Analyst.
10. To support local audits as required.
11. To perform testing of QC samples following client procedures.
12. To revise SOPs as necessary.
13. To adhere to all client standards concerning safety, housekeeping, and quality, notifying management of discrepancies.

Qualifications

• A degree in Chemistry or a related discipline is required.
• A solid fundamental knowledge of Chemistry is essential.
• At least 1 year of relevant experience in analysis within a pharmaceutical testing laboratory or equivalent is desired.
• Experience with traditional analytical techniques and modern instrumental equipment (HPLC, Karl Fischer, Dissolution, UV spectroscopy) is required.
• Experience in technology transfers is desirable but not essential.
• Ability to interpret raw data and troubleshoot analyses, instruments, and methods.
• Thorough understanding of chromatographic techniques.
• Understanding of GMP environment requirements.
• Ability to learn new processes quickly.
• Proactive in suggesting improvements to existing processes.
• Experience with paperless systems like Electronic Lab Notebooks and LIMS.
• Proficiency with MS Office applications.
• Strong ability to build working relationships with colleagues.
• Ability to work independently and develop solutions collaboratively.
• Willingness to operate flexibly and switch priorities quickly.
• Continuous improvement mindset within own area of control.

Additional Information

At Eurofins, we value growth, innovation, and learning. We celebrate employee achievements through awards, recognize life events, and support charitable activities.

Benefits include:

• Reward and Recognition programs.
• Health Cash Plan.
• Life Assurance (4x annual salary).
• Company Pension Plan.
• Employee Assistance Programme – 24/7 support.
• Free parking.
• Global career opportunities.
• Access to Perkbox for discounts and savings.

What Happens Next

We seek the right individuals to join our team. Selected candidates will be invited for assessment centers or staged interviews to showcase skills and learn about Eurofins.

Your data

We are committed to transparency regarding personal data collection and processing during recruitment, complying with data protection laws.

We embrace diversity!

Eurofins promotes diversity and is an Equal Opportunity Employer, prohibiting discrimination based on gender, race, age, religion, sexual orientation, disability, or other characteristics.

Sustainability matters to us

We aim for carbon neutrality by 2025 through emission reduction and offset initiatives, encouraging sustainable practices at all levels.