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Quality Assurance Senior Manager - GCP Focus, Rare Disease

Employer
NonStop Consulting
Location
Hertfordshire
Salary
£70000 - £90000 per annum + 15% Bonus and £6000 Car Allowance
Closing date
Aug 20, 2019

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Sector
Science, Life Sciences, Genetics
Contract Type
Employee
Hours
Full Time
Organization Type
Clinical Practice
Jobseeker Type
Professional

Job Details

The senior Clinical QA Manager will be responsible for ensuring compliance of Pharma Clinical activities with global regulatory requirements and regulations.

Probably the best thing about this role is the chance to report straight to the Senior Director in a small, cutting edge company.

Working with rare disease and oncology products, this is great chance to be involved with a really exciting portfolio.

The Clinical QA Manager will also be the leader of continuous improvement projects, agency regulations, GxP, Industry Guidelines, local regulations, along with policies and procedures for the conduct of clinical trials.

This involves working closely with Clinical Operations, Supply Chain, Regulatory, and other supporting areas/development teams, to help ensure active participation in continuous quality improvement activities.

Requirements

  • A minimum of a Bachelor of Science degree.
  • A minimum of 8 years of relevant experience in GCP/clinical quality assurance with a minimum of 2 years of Good Clinical Practices (GCP) auditing
  • In‐depth knowledge and clear understanding of GCP regulations and industry standards, covering EU and FDA regulations, ICH guidelines, other relevant global requirements in the post market and clinical trial environment required.
  • Knowledge of other Health Authority requirements highly desired.
  • Must be able to interpret and apply regulations and guidances
  • Maintains professional expertise and knowledge of local and international regulations related to Quality.
  • Strong organizational skills/attention to details, and ability to adapt in a fast paced constantly changing environment required.
  • Clear, effective written and verbal communication skills required.
  • Ability to work under pressure in order to meet tight deadlines is required as is good interpersonal skills (i.e., team player).
  • The successful candidate is required to have strong analytical/judgment capabilities to understand/analyse/synergise and communicate.
  • A broad knowledge of Pharmaceutical regulatory compliance best practices is preferred. Project management skills including management of both time and priority constraints.
  • Good knowledge of medical terminology highly desirable.
  • Flexibility to work with colleagues in a global setting

Able to engage in work-related travel when required (potential travel to the US and Europe (approximately 1/month).

For a confidential discussion about this, please contact Edward Little on 0207 940 2749 (EXT: 7168) or send your updated CV in a word document to E.Little@nonstop-recruitment.com

NonStop is one of the largest and fastest growing specialised life sciences recruitment companies in Europe. We are proud members of the APSCo life sciences group who ensure we meet the highest quality standards within the recruitment industry. Our offices are located in the UK, Switzerland and the Czech Republic and we hold labour leasing licences across Europe. Please visit our website for a full list of the niche markets we cover.

Company

Our Consultants are trained to deliver an exceptional standard of recruitment services to clients across the life sciences, chemical, care, educations, technical, digital and finance industries. 

Our clients – and bottom line profits - tell us that we do a great many things very well. Complacency, however, is the last word you would associate with us. We work incredibly hard to deliver better and better results, based on stronger and stronger service delivery.  Which is why we believe the best is yet to come – for us, our clients and for the people who have what it takes to join us on the journey.

The result? We’re expanding (in the UK and across Europe and even to Boston, US) and continue to post impressive performances in all our niche sectors. 

Company info
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