Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic, and labelling is accurate.
Eurofins is dedicated to delivering testing services that contribute to the health and safety of society and the planet, and to its corporate responsibility to protect the environment and ensure diversity, equity, and inclusion across the entire network of Eurofins companies.
Eurofins PSS Insourcing Solutions® is a global, award-winning insourcing solution. We place our skilled team directly at the client site, managing operations seamlessly and eliminating complexities. We ensure a strategic, long-term service commitment that delivers value directly at the client’ site, utilising their facilities, equipment, and methodologies, while maintaining the same service, expertise, and cGMP compliance available at the Eurofins facility. If you're an employee seeking an exceptional career journey, Eurofins PSS Insourcing Solutions® is your gateway to a future where innovation, collaboration, and success converge. Join us in a world where excellence knows no boundaries!
Job Description
This role is a permanent full-time position, working a 35 hour week, flexibly between Monday – Friday 07:00 – 19:00
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.
* To perform routine and non-routine analysis using traditional and modern analytical techniques, as required by the Lead Analyst or customer representative.
* To review analytical data for GMP compliance.
* To initiate and follow-up OOS results and action limits as per customer procedures.
* To participate in the preparation of reports.
* 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.
* Ensure that the customer gets the best possible service by continually reviewing best practice in relation to both commercial and quality issues and ensuring 100% ethical work standards and GMP compliance.
* To prepare and approve results for tests in which they have received the appropriate training and are deemed competent.
* To understand and be constantly aware of the customer’s requirements and strive to meet or exceed those requirements keeping in mind the customer process end points.
* To deal with customer 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.
* Support local audits as required,
* To perform QC samples in accordance with customer procedures.
* To revise SOPs as required by the Lead Analyst.
* To keep the laboratory area clean and tidy in both ‘seen’ and ‘unseen’ areas.
* To provide cover for other members of staff as required and for taking part in the customer’s weekend rota and/or overtime schedule.
* To ensure that all documentation is carried out on time, is accurate and legible and conforms to the relevant quality standards. Must be able to mentor junior members of the team with this regard.
* To ensure that the customer’s requirements are fully met or exceeded and in so doing will be flexible to work in any area of the business as is required.
Qualifications
* A degree in Chemistry or a related discipline is required.
* A sound, fundamental knowledge of Chemistry is essential.
* 3 to 7 years’ relevant experience of pharmaceutical analysis in a development laboratory, or equivalent, is desired.
* Experienced and competent with traditional analytical techniques as well as modern instrumental equipment (HPLC, Karl Fischer, Dissolution, and UV spectroscopy). Able interpret raw data and draw conclusions regarding troubleshooting of instruments and methods.
* Thorough understanding of chromatographic techniques.
* Thorough understanding of requirements for working in a GMP environment.
* Ability to quickly learn new processes. Works proactively to offer suggestions for new ways to improve existing processes.
* Ability to work using fully electronic media, including MS Office.
* Ability to form strong working relationships with colleagues.
* Ability to work on own initiative and be capable of developing solutions to problems as part of a team.
* Willing to operate in a flexible manner and be able to switch priorities at short notice. Seeks new ideas to make improvements within own area of control.
Additional Information
Site Specific Benefits
* Working a 35 hour week, flexibly between 07:00 - 19:00, Monday - Friday.
* On site parking with access to EV charging points.
* Easy access to the transport network, (Bus and train stops within 2 minutes of site, with access to Liverpool city centre within 20 minutes)
* Free Gym facilities
Benefits
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!
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