At a Glance
- Tasks: Join a dynamic team ensuring top-notch quality control in pharmaceutical production.
- Company: Leading European contract manufacturer in the healthcare sector with a vibrant culture.
- Benefits: Private medical insurance, generous holiday entitlement, and free parking.
- Other info: Flexible hours and excellent career growth opportunities await you!
- Why this job: Make a real impact in healthcare while developing your skills in a fast-paced environment.
- Qualifications: Relevant science qualification and experience in analytical techniques like HPLC and GC.
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 2,250 employees in Germany, France, Finland, Norway and the UK.
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 Next Pharma.
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 c GMP, 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.
- Required
- Specific Job Skills
- Relevant qualification, HNC/HND/Science Degree or Equivalent
- 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
- Desired
- Have a broad knowledge with and experience of working within a c GMP/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.
Please note: Only candidates with continuing Right to Work in the UK will be considered.
Next Pharma is an equal opportunities employer and positively encourages applications from suitably qualified and eligible candidates regardless of sex, race, disability, age, sexual orientation, marriage or civil partnership, pregnancy or maternity, religion or belief.
- Private Medical Insurance
- EAP
- Health Cash Plan
- Group Pension
- Free Parking
- Generous Holiday Emtitlememnt
- #J-18808-Ljbffr
Specialist Quality Control employer: NextPharma
NextPharma is an excellent employer that fosters a collaborative and innovative work culture in Livingston, Scotland. Employees benefit from ongoing professional development opportunities, competitive compensation, and a commitment to regulatory excellence, making it a rewarding place for those passionate about pharmaceutical sciences and formulation development.