At a Glance
- Tasks: Join a dynamic team to ensure the quality of pharmaceutical products through rigorous testing.
- Company: Leading European contract manufacturer in the pharmaceutical and biotech sectors.
- Benefits: Competitive salary, private medical insurance, health cash plan, and pension scheme.
- Other info: Flexible hours and opportunities for career growth in a supportive workplace.
- Why this job: Make a real impact in healthcare while developing your skills in a fast-paced environment.
- Qualifications: HNC/HND/Science Degree or equivalent with experience in analytical techniques.
The predicted salary is between 33837 - 41357 £ per year.
Relevant qualification, HNC/HND/Science Degree or Equivalent.
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. Our fast pace drives us forward, fills our working environment with life and spurs our growth.
Job Purpose
To support the on-going stability program for commercial, clinical and technical products. In addition, support of quality control testing of both development and market finished products under GMP conditions.
Key Responsibilities And Accountabilities
- Work as part of a team alongside quality control and micro departments.
- Actively involved in performing analytical activities for stability analysis of drug products.
- Must be technically competent in analytical activities (e.g. pharmacopoeial wet chemistry, HPLC, GC, Dissolution, KF) for stability testing of finished products.
- All activities to be performed under current cGMP, In house SOP’s and/or pharmacopoeia.
- Writing of stability summaries, protocols and reports.
- Performing set down of new stability studies, receipt of stability samples being returned from storage facility and disposal of samples following reporting of analysis.
- Checking of data for stability, QC and micro departments.
- Ordering of lab supplies to ensure continued availability of materials for timely analysis.
- Comply with company health and safety procedures.
Person Profile: Quality Control Analyst (Stability)
- 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 is equally comfortable working independently.
Personal Situation
Flexible and able to work extended hours when required. Must be eligible to work in the UK.
Required Specific Job Skills:
- Relevant qualification, HNC/HND/Science Degree or Equivalent.
- An understanding of drug development and stability processes.
- Demonstrated technical competence of the technical and practical skills involved in analytical activities to prescribed quality standards.
- Must be skilled in analytical techniques e.g. HPLC, Dissolution, Gas Chromatography, KF 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 cGMP/GLP environment.
- 2-3 years experience of working within a pharmaceutical or biotechnology industry.
- Ability to work to key regulatory and compliance requirements.
- Experience of quality control/Stability 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.
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.
Remuneration Package
Basic Salary: £DOE
Private Medical Insurance
Health Cash Plan
Contributory pension scheme
Life Insurance
Please note: Only candidates with continuing Right to Work in the UK will be considered. NextPharma 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.
Specialist Quality Control in Livingston employer: NextPharma
NextPharma is an exceptional employer, offering a dynamic work environment that fosters passion and growth within the pharmaceutical, biotech, and healthcare sectors. With a commitment to employee development, competitive benefits including private medical insurance and a contributory pension scheme, and a culture that values teamwork and high-quality output, we provide our employees with the tools and support they need to thrive in their careers. Join us in the UK, where your contributions will directly impact our mission of delivering excellent service worldwide.
