Senior Quality Manager - Nottingham
An exciting opportunity has become available for an experienced Quality Manager with expertise within the Pharmaceutical industry to join a global and leading UK based pharmaceutical and consumer goods manufacturer. On offer is a competitive salary, car allowance, an excellent and flexible benefits package which includes a company pension scheme (ratio of 2:1 employer: employee contribution), childcare vouchers, cycle to work schemes, flexible working, 25 days holiday plus bank holidays and more.
The Company: My client has over 100 years' experience of manufacturing health and beauty products and produces products that are sold globally.
Location: The role is based at their location in Nottingham, easily commutable from main transport links. With a dynamic culture, rich history and sporting glory - Nottinghamshire is one of the UK's top destinations.
Job Summary: To support their growth ambitions, this would be an exciting opportunity for a Senior Quality Manager to join their Specials department. This role will set the quality agenda for the business and be responsible for driving continuous improvement and ensuring the business remains MHRA compliant.
Define the GMP requirements and Quality Standards within the area of responsibility, act as a deputy Responsible Person (RP) and ensure GDP requirements fulfilled.
Primary point of contact for both customers and regulatory authorities on quality issues and host all customer/regulatory audits.
Ensure all licences and accreditations necessary to operate our business are maintained.
- Chemistry, Biology or Pharmacy or suitable scientific equivalent with industry experience in a Pharmaceutical/FMCG environment.
In depth knowledge of medicinal products and processes (ideally within the manufacture of sterile products).
Eligible to perform the duties of a Qualified Person under the provision of Directive 2001/83/EC and Directive 2001/82/EC; OR be a suitable candidate to undergo such training.
In depth knowledge of pharmaceutical legislation and processing including the manufacture of sterile products and Investigational Medicinal Products for clinical trials.- Successful track record of initiating and driving quality improvement.
Apply: For more information or to apply for this position, please contact Naynesh Mistry on 01246 457703 or email email@example.com. Alternatively, please click on the link below to apply online now. Please note that your CV should show exact dates of employment (month and year) and any gaps of a month or more should be explained.
CK Group is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria.
If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote reference 44300 in all correspondence.