These are permanent position, paying a competitive salary depending on your experience plus benefits. The role will be site based 5 days a week in Worthing.
The Company
A pioneering Europe-based Pharmaceutical organisation specialising in the treatment and prevention of allergies. Their unique focus is on the vaccination and prevention of conditions such as hay fever and their products are fascinating, complex, and ever-changing. The company employs around 300 people in Worthing and has an excellent reputation for providing career development opportunities, challenging, and engaging work and a pleasant, vibrant working environment.
The Role
You will join a busy QA department that supports all company activities with close links to Manufacturing, Packaging, Validation, QC and Product Development, Sales & Marketing and Regulatory Affairs. This role is focuses on all aspects of the Quality Management System. Using your skills to the full, you will process customer complaints (using Trackwise or other system), maintain systems compliance, support change control, non-conformances, CAPA, process Product Quality Reviews, analyse data, support the Documentation Control and undertake a range of other responsibilities relating to continuous improvement. In addition, you will have the opportunity to expand into other areas of Quality Assurance activities.
This is a broad, challenging role that requires meticulous attention to detail, strong communication skills and the ability to multitask. Full details will be provided on application.
Benefits
In addition to a competitive salary, the company offers excellent career development opportunities and the following benefits:
- 25 days' holiday
- Stakeholder pension plan
- Private medical cover
- Life insurance scheme
- Non-contractual, discretionary annual bonus
- Cycle to Work Scheme
- Discounted GYM membership
Experience
The successful candidate will have a strong scientific/ technical background with experience gained in Pharmaceutical Manufacturing, testing or Quality Assurance environment paired with knowledge of GxP and GMP for at least 2 years or more. You will demonstrate the ability to multitask, use basic statistical tools and methods plus have proven abilities in Word, Excel and/or Access to process and display data graphically. Experience of using Trackwise would be advantageous to your application though can consider experience with other eQMS. In addition, you will need a strong and enthusiastic work ethic, excellent communication skills and attention to detail and enjoy a closely-knit team environment.