Quality Control Advanced Analyst
Your new company
At SFI Health, we believe we have the responsibility to bring proven natural health solutions to people’s healthcare needs. We are a global natural health company committed to sourcing and producing natural medicines to the highest standards. Backed by evidence of effectiveness, quality and safety, our products are marketed around the world using our international community of leading life sciences companies and distributor networks.
To find out more, please visit https://www.sfihealth.com/
Your new role
As a Quality control Advanced Analyst at SFI Health, Wigan, you will be responsible for supporting the site to ensure the Quality Control laboratory can deliver testing in line with current regulatory guidelines:
Key responsibilities and accountabilities:
- Perform physical/chemical/analytical analyses on samples received within defined lead times.
- Perform testing of stability samples in line with the site schedule and procedures
- Responsible for routine calibration and maintaining laboratory equipment and devices before usage.
- Generate and complete appropriate paperwork for various stages of processing, monitored in compliance with specifications and regulations.
- Adhere to Good laboratory practices and Data Integrity.
- Perform sampling and routine testing of raw materials (including packaging materials), intermediate bulks, and finished products in accordance with GLP/GMP requirements, ensuring strict adherence to Good Documentation Practices and Data Integrity principles.
- Conduct testing of stability samples in line with approved ICH stability programs, reporting any compliance issues. Support the preparation of stability protocols and coordinate stability testing schedules as defined in stability procedures.
- Support the coordination, shipment, and follow‑up of external analytical, microbiological, and chemical testing for raw materials, intermediate bulks, and finished products.
- Write and revise standard QC operating procedures in alignment with organisational quality standards.
- Must have a degree in a scientific subject, preferably chemistry related discipline.
- Minimum 2 to 3 years’ experience post qualification experience in a relevant scientific role.
- Experience of working in a highly regulated environment, such as Pharmaceutical or Food manufacturing, and possessing the associated level of attention to detail is essential.
- Knowledge of pharma or food lab environments preferably under GMP environment.
- Experience with general physical and chemical testing, plus HPLC.
- Excellent attention to detail, self\-driven, bright, positive and motivated personality
- Experience of interpreting data and writing reports
- Supportive work culture
- Company pension
- Referral programme incentives
- Company sick pay
- Birthday Holiday
- Long service bonus
- Company performance\-based bonus
- Access to LinkedIn Learning
- Reward \& recognition programme.
You will be part of many activities and celebrations, working with diverse cultures in a growing organisation.
Schedule:
- Day shift
- Monday to Friday (5 days on\-Site)
Apply now with your resume and cover letter detailing your relevant experience and why you are the perfect fit for this role.
We thank you in advance for your interest in this position, however, only shortlisted candidates will be contacted for an interview.
Job Types: Full\-time, Permanent
Pay: £28,000\.00\-£30,000\.00 per year
Benefits:
- Additional leave
- Company events
- Company pension
- Employee discount
- Free parking
- Health \& wellbeing programme
- On\-site parking
- Referral programme
- Sick pay
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