At a Glance
- Tasks: Join a dynamic team ensuring top-notch quality in pharmaceutical production.
- Company: Leading European contract manufacturer in the healthcare sector.
- Benefits: Competitive salary, flexible hours, and opportunities for growth.
- Other info: Fast-paced environment with room for personal and professional development.
- Why this job: Make a real impact in healthcare while developing your skills.
- Qualifications: Experience in analytical techniques and a passion for quality control.
The predicted salary is between 31500 - 38500 £ per year.
We are one of the leading European contract manufacturers in the pharmaceutical, biotech and healthcare sectors, with some 2,300 employees in Germany, France, Finland, UK and Norway. For us, the next step is always the one that matters most. Our fast pace drives us forward, fills our working environment with life and spurs our growth. Our winning formula for shared success: room for passion. Because we know that passion is the best medicine when it comes to excellent service around the world. Welcome to NextPharma.
Job Purpose: To support the production of both development and market finished products under GMP conditions in all areas of quality control and calibration.
Key responsibilities and accountabilities:
- Work as part of a team alongside Production and other analytical departments including development and stability.
- Actively involved in performing analytical activities to determine fitness for purpose of starting materials, intermediate and finished products.
- Technically competent in analytical activities (e.g., pharmacopeial wet chemistry, HPLC, GC, Dissolution) for QC testing of raw materials, packaging components and finished products.
- All activities to be performed under current cGMP, In house SOP’s and/or pharmacopoeia.
- Perform sampling of starting materials, packaging components and finished products.
- Perform cleaning verification analysis to assure suitability of Production equipment for subsequent use.
- Support calibration of key analytical equipment and measuring devices used in or on production equipment.
- Comply with company health and safety procedures.
Personality: Results oriented with a positive outlook and clear focus on high quality output; Solid planning and organizational ability; Reliable, tolerant, and dependable; Comfortable dealing with senior managers and customers; Enjoy working in a fast, stimulating environment. Goal-oriented; Able to work under pressure and meet deadlines; Excellent communication/ presentation skills. Able to get on with others and be a team player but equally comfortable working independently.
Personal Situation: Flexible and able to work extended hours when required.
Specific Job Skills:
- An understanding of drug development and manufacturing processes.
- Demonstrated technical competence of the technical and practical skills involved in analytical activities to prescribed quality standards.
- Skilled in analytical techniques e.g., HPLC, Dissolution, Gas Chromatography, and wet chemistry techniques.
- Able to communicate well with others, both laboratory and non-laboratory based.
- Able to work with minimal supervision.
- Good understanding of quality control, SOP and GMP adherence.
- Have a broad knowledge with and experience of working within a cGMP/GLP environment.
- Experience of working within a pharmaceutical or biotechnology industry.
- Ability to work to key regulatory and compliance requirements.
- Experience of quality control within a pharmaceutical environment.
- Experience of Chromeleon software.
- Experience of data reporting and checking data within a QC environment.
- Understand and demonstrate a pragmatic approach to problem solving with GMP constraints.
Computer skills: Must be competent in the use of MS Office, particularly Excel and Word, e-mail and internet. Previous use of chromatographic acquisition software is desired but not essential.
Literacy and Numeracy: Must be competent in writing reports both for internal use and for customers. Must be competent in the interpretation of analytical data.
Business Presentation Skills: Must be an excellent face-to-face and telephone communicator.
It's time for your next chapter: We look forward to receiving your application.
Specialist Quality Control employer: NextPharma Technologies Holding Ltd
NextPharma Technologies Holding Ltd is an exceptional employer that fosters a collaborative and innovative work culture in East Calder. Employees benefit from comprehensive professional development opportunities, competitive remuneration, and a commitment to maintaining high standards in drug formulation. Joining our team means being part of a forward-thinking company dedicated to making a meaningful impact in the pharmaceutical industry.
Contact Details:
NextPharma Technologies Holding Ltd Recruitment Team
StudySmarter Expert Advice🤫
We think this is how you could land Specialist Quality Control
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We think you need these skills to ace Specialist Quality Control
Some tips for your application 🫡
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✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at NextPharma Technologies Holding Ltd that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
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