Job Overview
We are seeking a meticulous and dedicated Quality Assurance Officer to uphold the highest standards of product and service quality within our organisation. The successful candidate will be responsible for implementing quality assurance procedures, conducting inspections, and ensuring compliance with industry regulations. This role offers an excellent opportunity for individuals passionate about maintaining excellence and continuous improvement in a dynamic environment.
Responsibilities
- Support manufacture of products by making QA decisions during batch manufacturing and ensuring GMP is adhered to at all times
- Execute documentation and batch reviews as required
- Inspect and release final products as per Company policies
- Investigate complaints and monitor CAPAs related to production
- Support delivery of product release targets, including ensuring timely batch review activities and batch disposition of any deviations with impact to product release
- Lead and support the execution of timely deviations and complaints investigations
- Ensure timely completion of all Quality System commitments
- Support the preparation and development of Annual Product Quality reviews
- Support validation programs and change control as required
- Proactively identify and support implementation of continuous improvement opportunities in QA and Operations
- Ensure that all measuring equipment that may have an impact on product quality is calibrated to traceable standards through its life cycle, using the electronic equipment management systems and related tracking sheets
- Ensure timely completion of all GMP commitments
- Ensure timely communication of significant GMP and product quality issues to QA Management
- Comply with EHS/GMP/GDP/Company and Corporate policies and external regulatory requirements;
- Ensure facility and process compliance through attendance of activities (e.g. Gemba), identifying actions and facilitate implementation
- Support QC Officer with raw material testing, release and Quarantine area issues, where required
- Support supplier complaints, managing samples for evaluation and investigation results, and liaise with Central Supplier Management teams to address and resolve issues
- Facilitate the implementation of an ‘Audit Ready’ compliant site which is always ready for MHRA, ISO9001, FEMAS, UFAS, FSSC and other internal or 3rd party audits
- Support the completion of audit findings and fully investigate to find the root cause and actions to address the audit findings are carried out in a timely manner
Requirements
- Degree or BTEC (or equivalent) in Pharmaceutical or Science related subject
- At least 2 years experience in a quality role within a GMP environment
- Strong work ethic and able to work flexibly to meet the needs of the business
Your Future Perspective
- Challenging tasks, short decision-making processes and a high level of personal responsibility in a modern work environment with flexible work time models
- Room for innovative thinking and growth with the possibility to manage your own career path.
- A company culture which promotes continuous learning and diversity.
- Excellent career opportunities in a world leading nutrition company.
- An attractive remuneration including a variety of social benefits like subsidized health & fitness offers.
Standard working hours are 14.00 – 22.10 Monday – Thursday, 14.00 – 20.20 Friday.
Salary around 28K.
Apply today.
INDYE
Job Types: Full-time, Permanent
Pay: £28,000.00 per year
Benefits:
Work Location: In person
