Director of Quality
- Employer
- Planet Pharma Staffing Limited
- Location
- Buckinghamshire (GB)
- Salary
- £90K + 20% bonus
- Start date
- 28 Mar 2021
- Closing date
- 27 Apr 2021
View more
- Discipline
- Quality, Project Management, Quality Project Management
- Hours
- Full Time
- Contract Type
- Permanent
- Experience Level
- Director/Executive
Job Details
Location – Buckinghamshire
Salary – £90K + 20% bonus
Type- Permanent (Flexible Working)
Company summary:
Exciting opportunity for a Director of Quality to join a leading clinical trials company based in Buckinghamshire. With an international reach, offering services across all major clinical research countries. Working with some of the largest Biotech, Pharma and CRO companies globally, giving the Quality Director a varied and exciting role from day one!
Role summary:
As the Director of Quality, you will ensure quality remains high profile globally within the company. Covering a broad Quality Management System (QMS), focused on ensuring conformance to requirements throughout the organisation by following a defined methodology, as well as specific compliance with regulations relating to GXP and clinical trials in general.
Responsibilities:
- Input to and implement the Quality Management strategy for the company
- Input to and implement the Quality strategy across the broader organisation as governed by the QMS
- Oversee resource management for the Quality Group, including utilisation & demand
- Support and mentor the Quality Group to ensure delivery, including line management of immediate reports
- Support the Quality Group in identifying, managing and mitigating risk using appropriate methodologies and reporting tools
- Integration with other functional groups including Project Management, Nursing, Pharmacy, Vendor Management and Training
- Liaise with internal and external regulatory experts
- To lead Continuous Improvement projects directly relating to or impacting the Quality Group
- Lead and deliver projects sponsored by the board based on personal expertise
- Lead and deliver projects sponsored by other functions based on technical and regulatory expertise
- Attend regular CAPA and associated operational meetings
- Present risk-based Quality Management information and data to the Board.
Role requirements:
- Degree in a Scientific discipline is desirable.
- At least 5 years multidisciplinary activity in Pharma R&D
- 2 years’ experience of QMS implementation
- Experience of QMS applied outside of GXP / regulatory compliance areas
- GCP mandatory, GXP desirable, medical/nursing/pharmacy insight, QMS methodology knowledge
To apply
If you would like to discuss this vacancy further or to discuss your career options in confidence, please telephone on +44 (0)204 542 4275 or e-mail on jwilson@planet-pharma.co.uk
If this role isn’t suitable for you, please let us know if you can refer anyone – any recommendations are much appreciated! Planet Pharma offers a competitive referral scheme so you will be rewarded for your help!
Company
Planet Pharma was founded by a dedicated team of professionals with extensive experience supporting the pharmaceutical, biotechnology, and device industries.
Our goal is to create an organization that strengthens the employer-employee dynamic by connecting clients with talent. This results in making staffing more personal and creating enduring, valuable relationships. We value communication with our clients and make it our priority to have the hiring process be as fast and successful as possible.
We leverage cutting-edge technology and flexible service delivery models that provide efficient, personalized solutions for your business.
Our global headquarters is in Northbrook, IL and branch offices are based across the United States and Europe.
- Website
- http://www.planet-pharma.co.uk/
- Telephone
- +44 203 868 1000
- Location
-
10 Greycoat Place
London
England
SW1P 1SB
United Kingdom
Get job alerts
Create a job alert and receive personalised job recommendations straight to your inbox.
Create alert