At a Glance
- Tasks: Support quality management in pharmaceuticals, handle IT systems, and manage quality metrics.
- Company: Join Eurofins, a global leader in life sciences dedicated to safety and sustainability.
- Benefits: Enjoy enhanced leave, pension plans, healthcare, and worldwide career opportunities.
- Why this job: Be part of a mission-driven team focused on health, safety, and environmental responsibility.
- Qualifications: Experience in GMP environments, CSV knowledge, and strong communication skills required.
- Other info: Assessment centre interviews provide insight into Eurofins' culture and values.
The predicted salary is between 36000 - 60000 Β£ per year.
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.
Working Hours: 39 Hours per week. Monday - Friday. 9am - 5pm.
You will be supporting the operation and development of the Quality Management System within pharmaceutical finished products, API and raw materials:
- Administration of internal IT systems.
- Approval of procedures, protocols, reports and further approval of certificates of analysis.
- Support the resolution of quality issues.
- Management of quality KPI and metrics.
- Management of site communications on quality topics.
- Review and approval of calibration and qualification data.
- Support activities related to Metrology.
- Support activities related to stability studies.
- Completion of self-inspections.
- Support the compilation of information for client audits and regulatory inspections.
- Providing information to clients.
- Coordination of quality technical agreements.
- Administration and control of external documentation.
- Support the controlled substance process.
- Responsibility for CSV activities including computer system validation, validation plans, creation/review of validation protocols and reports, ERES assessments and the validation life-cycle.
Qualifications:
- Proven experience in a GMP-regulated environment.
- Some CSV experience.
- Deep knowledge of QMS.
- Excellent understanding of GMP.
- Ability to work independently or as part of a team.
- Able to demonstrate leadership skills, good judgement, and the ability to motivate others.
- Excellent report writing and organisational skills.
- Quality consciousness with the ability to consistently work to industry standards.
- Positive, methodical, tenacious, and innovative approach to work.
- Passionate about quality and customer service.
- Excellent communication skills. Ability to understand client requirements and able to devise and articulate the most appropriate solutions.
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:
- Enhanced Annual Leave Entitlement
- Additional Annual Leave Purchase scheme
- Annual Leave Sellback Scheme
- Additional Annual Leave at Employees set service dates
- Company Pension Plan
- Life Assurance Scheme (4 times annual salary)
- Healthcare Cash Plan (6+ months service)
- Enhanced Maternity, Adoption and Paternity Schemes
- Employee Assistance Programme β 24/7 confidential
- Health and Wellbeing Programmes
- Free parking
- Worldwide career opportunities
We also have in place rewards recognising the great work our employees deliver, their dedicated service and celebrating special life events.
What Happens Next: Our people are the backbone of what we do, so itβs incredibly important we find the right individuals to join us. As a potential new recruit youβll be invited to meet the team in the form of an assessment centre or a staged interview process dependent on the role and its requirements. This will give you the opportunity to see what working for Eurofins is really like and enable us to get to 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.
Closing Date: We reserve the right to close or extend this position depending on application numbers. Therefore we would urge candidates to submit an application as early as possible. Due to the high volume of applications we receive please be aware that if you do not receive a response within 4 weeks of the vacancy expiry date, unfortunately, on this occasion your application has been unsuccessful.
Quality and CSV Specialist employer: Stoneburgh Properties LLC
Contact Detail:
Stoneburgh Properties LLC Recruiting Team
StudySmarter Expert Advice π€«
We think this is how you could land Quality and CSV Specialist
β¨Tip Number 1
Familiarise yourself with Eurofins' core values and mission. Understanding their commitment to quality, safety, and sustainability will help you align your responses during interviews and demonstrate your passion for the role.
β¨Tip Number 2
Network with current or former employees of Eurofins on platforms like LinkedIn. They can provide valuable insights into the company culture and expectations, which can be beneficial when preparing for interviews.
β¨Tip Number 3
Brush up on your knowledge of Quality Management Systems (QMS) and Computer System Validation (CSV). Being able to discuss specific methodologies or experiences related to these areas will set you apart from other candidates.
β¨Tip Number 4
Prepare for potential assessment centre activities by practising teamwork and leadership scenarios. Eurofins values collaboration, so showcasing your ability to work well in a team will be crucial during the selection process.
We think you need these skills to ace Quality and CSV Specialist
Some tips for your application π«‘
Understand the Role: Before applying, make sure you thoroughly understand the responsibilities and qualifications required for the Quality and CSV Specialist position at Eurofins. Tailor your application to highlight relevant experience in GMP-regulated environments and your knowledge of Quality Management Systems.
Craft a Strong CV: Your CV should clearly outline your experience in quality management and computer system validation. Use specific examples to demonstrate your leadership skills, attention to detail, and ability to work independently or as part of a team.
Write a Compelling Cover Letter: In your cover letter, express your passion for quality and customer service. Highlight how your skills align with Eurofins' commitment to health, safety, and sustainability. Be sure to mention any relevant achievements that showcase your problem-solving abilities.
Proofread Your Application: Before submitting your application, take the time to proofread your CV and cover letter. Check for any grammatical errors or typos, and ensure that all information is accurate and presented professionally. A polished application reflects your attention to detail.
How to prepare for a job interview at Stoneburgh Properties LLC
β¨Understand Quality Management Systems (QMS)
Make sure you have a solid grasp of Quality Management Systems, as this role heavily involves their operation and development. Be prepared to discuss your previous experiences with QMS and how they relate to the pharmaceutical industry.
β¨Showcase Your GMP Knowledge
Since the position requires proven experience in a GMP-regulated environment, be ready to highlight your understanding of Good Manufacturing Practices. Share specific examples of how you've applied these principles in past roles.
β¨Demonstrate Leadership Skills
This role calls for leadership abilities, so think of instances where you've successfully led a team or project. Discuss how you motivated others and made decisions that positively impacted quality outcomes.
β¨Prepare for Technical Questions
Expect technical questions related to computer system validation (CSV) and quality metrics. Brush up on your knowledge of validation plans, protocols, and reports, and be ready to explain your approach to managing quality issues.