Pharmaceutical Analyst

Eurofins UK PSS; Liverpool; On-site; GBP 30,000 - 40,000; Full time

Job summary

A leading pharmaceutical analysis company in Liverpool is seeking a Laboratory Analyst to perform analytical testing of raw materials and finished products. This permanent full-time position requires a degree in Chemistry and knowledge of modern analytical techniques. Responsibilities include testing in a GMP environment, reviewing data, and ensuring compliance. The role offers opportunities for growth and a supportive work environment with numerous employee benefits, including health plans and a pension scheme.

Benefits

Reward and Recognition

Health Cash Plan

Life Assurance

Company Pension Plan

Employee Assistance Programme

Free car parking

Worldwide career opportunities

Access to Perkbox

Qualifications

• A degree in Chemistry or a related discipline is required.
• Sound knowledge of pharmaceuticals is essential.
• Experience in pharmaceutical testing laboratory is required.

Responsibilities

• Perform routine and non-routine analysis using analytical techniques.
• Review analytical data for GMP compliance.
• Document data as dictated by client policies.

Skills

Fundamental knowledge of pharmaceuticals

Experience with HPLC

Competent with MS Office

Ability to interpret raw data

Strong working relationships

Education

Degree in Chemistry or related discipline

Tools

HPLC

Dissolution

Karl Fischer

UV spectroscopy

Gas chromatography

Job description

Unfortunately, we are unable to offer visa sponsorship for this role.

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

The purpose of this job is to perform analysis of pharmaceutical raw materials, drug substance, and finished product and produce accurate results within an acceptable timeframe.

Job Responsibilities

• To perform routine and non-routine analysis using traditional and modern analytical techniques (primarily: HPLC, Dissolution, and Karl Fisher determination) within a GMP framework, as required by the client’s representative.
• To review analytical data for GMP compliance.
• To initiate and follow-up OOS results and action limits as per client procedures.
• To document data as dictated by current client policies and procedures.
• To collect and measure productivity through agreed metrics such as number of tests performed, cycle times, lab/product issues, number of hours worked per project, etc.
• To prepare and approve results for tests in which they have received the appropriate training and are deemed competent.
• To deal with client queries and contact designated personnel, with appropriate support from onsite leadership, with any relevant information or issues relating to test results or the service in general.
• To keep up to date with any technological or method revisions in their area, ensuring their training is complete and adjusting their work as required with approval from the Lead Analyst.
• Support local audits as required.
• To perform testing of samples in accordance with client procedures.
• To adhere to all client standards in the areas of safety, housekeeping and quality, notifying management of any discrepancies.

Qualifications

• A degree in Chemistry or a related discipline is required.
• A sound, fundamental knowledge of pharmaceuticals is essential, with knowledge of modern analytical techniques.
• Relevant experience of analysis in a pharmaceutical testing laboratory (preferably with exposure to solid dose products) , or equivalent, is required.
• A thorough understanding of requirements for working in a GMP environment are essential.
• The candidate should be experienced and competent with traditional analytical techniques as well as modern instrumental equipment (HPLC, Dissolution, Karl Fischer and UV spectroscopy). Knowledge of gas chromatography and/or mass spectrometry (either standalone or as a detection method), would be highly advantageous.
• Experience in technology transfers desirable but not essential.
• Must be able to interpret raw data and draw conclusions regarding troubleshooting of analyses, instruments and methods.
• Have a thorough understanding of chromatographic techniques.
• Must possess experience of, or have a thorough understanding of validation activities in a GMP environment.
• Must possess the ability to quickly learn new processes.
• Be capable of working proactively to offer suggestions for new ways to improve existing processes.
• Should have the ability to work using paperless systems such as Electronic laboratory notebooks and LIMS.
• Must be competent with MS Office suite of applications.
• Requires the ability to form strong working relationships with colleagues.
• Must have the ability to work on their own initiative and be capable of developing solutions to problems as part of a team.
• Must be willing to operate in a flexible manner and be able to switch priorities at short notice.
• Should seek new ideas to make improvements within own area of control.

Additional Information

At Eurofins we are growing, innovating and always learning. We celebrate the achievements of our employees through annual long service awards, recognise our colleagues special life events, and we are committed to charitable causes through global fundraising activities.

As a Eurofins employee you will benefit from:

• Reward and Recognition
• Health Cash Plan
• Life Assurance (4 times annual salary).
• Company Pension Plan
• Employee Assistance Programme – 24/7 confidential support.
• Free car parking
• Worldwide career opportunities
• Everyone who joins our team also gets access to Perkbox, allowing you to save money all year round. Whether its supermarket savings or days out, the daily coffee or a summer holiday – there’s something to suit everyone’s lifestyle.

What Happens Next

Our people are the backbone of what we do, so it's incredibly important we find the right individuals to join us. As a potential new recruit you'll be invited to meet the team in the form of an assessment centre or a staged interview process dependent on the role and it's requirements, this will give you the opportunity to see what working for Eurofins is really like and enable us to get you know your key skills and strengths.

Your data

As part of any recruitment process, the company collects and processes personal data relating to job applicants. The company is committed to being transparent about how it collects and uses that data and to meeting its data protection obligations.

We embrace diversity!

Eurofins network of companies believe in strength and innovation through diversity, being an Equal Opportunity Employer. We prohibit discrimination against employees or applications based on gender identity and/or expression, race, nationality, age, religion, sexual orientation, disability, and everything else that makes employees of Eurofins companies unique.

Sustainability matters to us

We are well on our way to achieving our objective of carbon neutrality by 2025, through a combination of emission reduction and compensation initiatives. We encourage our laboratory leaders to make sustainable changes at their local level, and in addition to their initiatives we also count on our dedicated carbon reduction team to help us to achieve this goal!

Find out more in our career page: https://careers.eurofins.com/