Similar posts
QA Specialist
- Contract
- Good Clinical Practice (GCP)
- United Kingdom
This vacancy has now expired. Please see similar roles below...
An international health care organisation is advertising a vacancy for a QA Specialist, based in their London office. This establishment is known for helping people with chronic, complex, and rare diseases whilst working with world-leading healthcare providers and pharmaceutical companies. This is an exciting opportunity to work with a growing team and help shape regulatory and quality management systems.
Job Responsibilities:
- Prepare the regulatory strategy for new submissions.
- Submit new products in agreement with the yearly target.
- Obtain a number of marketing authorizations in accordance with the yearly target.
- Drive product maintenance to ensure regulatory compliance.
- Provide close regulatory support to the product launch work stream.
- Act as a strategic business partner to Business Development, Quality Assurance, Supply Chain as well as for other Global Regulatory Groups (RCCs).
- Follow trends in the regulatory environment and legislation and assure awareness and alignment within the department, in order to meet future requirements on time always work in accordance with Good Regulatory Practice.
- Strategic business partner to Business Development, Quality Assurance and Supply Chain.
- Organisation of new submissions and product maintenance in due time.
Skills and Requirements:
- Demonstrable multitasking, project management, and execution skills.
- Good interpersonal skills, including communication, presentation, persuasion, and influence.
- Good organisational skills, including efficiency, punctuality, and collaboration in a team environment.
- Proficiency with computer skills, such as MS Office.
To Apply:
Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.
In case you have difficulty in applying or if you have any questions, please contact Steven Fuller at +44 203 854 2630 or upload your CV on our website - www.proclinical.com.
A full job description is available on request.
Proclinical Staffing is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
Proclinical Staffing is an equal opportunity employer.
#LI-SF1
#Compliance/Quality
Related jobs
US$65 - US$77 per hour
New York, USA
Are you looking to make an impact with your innovation? We are working with a well-established pharmaceutical company to recruit for a manager of Global Development Quality!
Highly Competitive
Risch-Rotkreuz, Switzerland
Driving precision from sample to solution-where every biospecimen tells a story of innovation.
US$180000 - US$190000 per annum
Cambridge, USA
Ready to engineer precision in the world of biotech? Join our client's cutting-edge team and play a vital role in developing the instrumentation that powers tomorrow's breakthroughs.
US$270000.00 - US$290000.00 per annum
Cambridge, USA
Are you ready to make a groundbreaking impact in the world of biotechnology? Join a growing company that's shaping the future of healthcare and science.
Highly Competitive Salary
Basel, Switzerland
Proclinical is seeking a Supplier Lifecycle Management Specialist to support global vendor change notifications and ensure seamless coordination across multiple sites.