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 with flexibility working from home 1- or 2-days max.
The Company
A pioneering Europe-based pharmaceutical organisation specializing 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 to provide support for production and manufacturing areas. You will act as an SME and will be the first point of contact for operations. You will be responsible for streamlining batch review and batch release processes and provide a link between Operations and Batch Release Team, which will enable you to use your communication skills. Day to day duties will involve non-conformances, CAPA, Investiagtions (including GEMBA), change controls and 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 scientific degree paired with strong QA experience in pharmaceutical manufacturing working in aseptic/ sterile cleanroom areas following GxP regulations. 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 software as well. 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.