Jobs

Intertek Pharmaceutical Services Manchester - Project Manager / Study Director - GMP, GLP, GCP

Job Title:
Project Manager / Study Director - GMP, GLP, GCP
Category:
Technical roles
Closing Date:
29/09/2019

Do you have previous knowledge and experience as a Project Manager in a Good Practice (GxP) regulatory laboratory within the chemical, pharmaceutical, biopharmaceutical industry?

Do you have specialist expertise in method development & validation of methods?

Are you looking for your next challenge in Manchester, where you can strive to deliver projects on time, on budget whilst maintaining excellent working relationship both internally and externally?

PROJECT MANAGER, MANCHESTER 

ABOUT THE ROLE:
Intertek Pharma Services Manchester (IPSM) has an extensive range of analytical instrumentation and provides analytical services to customers in the pharmaceutical, biopharmaceutical, personal care and speciality chemical sectors in a GLP, GCP and GMP regulated laboratory. The Project Manager role is an integral part of the Laboratory team and will be accountable for leading, managing and driving our Total Quality Assurance customer promise every day.

You will act as a GLP Study Director, GCP Responsible Scientist and/or GMP Project Manager for regulatory studies conducted on behalf of customer businesses.  The role will require the ability to demonstrate both project management and technical skills by acting as a direct liaison in terms of delivery and quality between both colleagues and clients.

The role will be based at Hexagon Tower, Blackley, North Manchester where the site offers a variety of on-site amenities including a gym and restaurant. In addition to generous paid annual holidays we proactively support work life balance for all our employees by operating flexible working opportunities.

ABOUT YOU:

  • BSc / MSc/ PhD in Chemistry (or related scientific discipline)
  • Excel at managing scientific projects within a Good X Practice (GxP) regulated environment
  • Understanding of the regulatory requirements or ‘Good Working Practices’ which apply to the pharmaceutical Industry
  • Experience and good working knowledge of the Chemical and Pharmaceutical Industry with good commercial understanding and natural business acumen
  • Good experience of preparing documents with technical support or guidance across multiple projects

ABOUT INTERTEK:

  • Global pioneers in the Quality Assurance industry, they are the only company in the world that delivers – on a truly global scale – a fully integrated portfolio of Assurance, Testing, Inspection and Certification services.
  • Over 44,000 employees located in 1,000+ laboratories and offices across the world.
  • Our innovation-led, end-to-end Total Quality Assurance (‘TQA’) proposition helps organisations operate safely, effectively and with complete peace of mind in an increasingly complex, fast-changing world across all industries.
  • A focused strategy and culture that gives employees the right platform to grow and develop their careersThrough our network of over 42,000 people in 1,000 laboratories and offices in 100 countries, Intertek provides quality and safety solutions to a wide range of industries around the world.

Apply at www.intertek.com/careers or email luke.williams@intertek.com 

 

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