QA GCP Manager for leading international Pharma

1 post / 0 new
Amar Annamalai
Amar Annamalai's picture
QA GCP Manager for leading international Pharma

Please contact Caroline Yeboah on +44 7779 391196  or email eval(unescape('%64%6f%63%75%6d%65%6e%74%2e%77%72%69%74%65%28%27%3c%61%20%68%72%65%66%3d%22%6d%61%69%6c%74%6f%3a%63%61%72%6f%6c%69%6e%65%40%70%65%6f%70%6c%65%77%69%74%68%63%68%65%6d%69%73%74%72%79%2e%63%6f%6d%22%3e%63%61%72%6f%6c%69%6e%65%40%70%65%6f%70%6c%65%77%69%74%68%63%68%65%6d%69%73%74%72%79%2e%63%6f%6d%3c%2f%61%3e%27%29%3b')) if you would like to know more about this opportunity. All are conversations are treated in strict confidence.
                REQUIREMENTS FOR THIS ROLE:

  • BS/BA degree required.
  • MD or PharmD is a plus.
  • Strong GCP Experience
  • 3+ years experience in clinical research, including 2 years in quality assurance
  • Effective communication and organizational skills.
  • Ability to multi-task.
  • Excellent computer skills and advanced knowledge of Microsoft Office including Word, Excel and Outlook.
  • Ability to work hard under pressure and face challenges

RESPONSIBILITIES WITHIN THIS ROLE
                Primary responsibility for:

  • interacting with project teams with regards to internal study audits, including onsite, in-house, and clinical trials database audits.
  • Shared responsibility for interacting with vendors with regard to vendor qualification audits
  • Shared responsibility for interacting with company departments and offices with regard to internal systems and location audits.
  • Primary responsibility for the preparation for, conduct and reporting of quality assurance study audits, and vendor qualification audits.
  • Shared responsibility for the preparation for, conduct, and reporting of internal systems and location audits.
  • May be involved in the training of Operations staff in quality management issues.

My client offers excellent opportunities for growth and development within the GCP/ GMP arena.
For more information and a full job description contact Caroline Yeboah on +44 7779 391196  or email eval(unescape('%64%6f%63%75%6d%65%6e%74%2e%77%72%69%74%65%28%27%3c%61%20%68%72%65%66%3d%22%6d%61%69%6c%74%6f%3a%63%61%72%6f%6c%69%6e%65%40%70%65%6f%70%6c%65%77%69%74%68%63%68%65%6d%69%73%74%72%79%2e%63%6f%6d%22%3e%63%61%72%6f%6c%69%6e%65%40%70%65%6f%70%6c%65%77%69%74%68%63%68%65%6d%69%73%74%72%79%2e%63%6f%6d%3c%2f%61%3e%27%29%3b')) if you would like to know more about this opportunity. All are conversations are treated in strict confidence.

Find out more about us at www.peoplewithchemistry.com
 
Meet is a European wide recruitment agency who specialise purely in the pharmaceutical sector. We work in a number of regions across Europe placing both permanent and freelance candidates into Clinical, Regulatory and Data management teams within CRO’s, Pharmaceutical, Generic and Biotech companies.
 If you are interested in finding a new opportunity however the one shown in this advert is not suitable for you please do not hesitate to contact us! Our number is 0203 178 7488 or visit our website - www.peoplewithchemistry.com to upload your CV.
Key Words
Clinical Project Manager, CPM, Senior CPM, Lead CPM, Clinical study manager, GCP, clinical operations manager, Pharmaceutical, CRO, Auditing, biotech, clinical trials, Germany, Clinical Project Manager, CPM, Senior CPM, Lead CPM, Clinical study manager, Munich, Frankfurt, Berlin, Koln, Dussledorf, Projekt Manager, CPM, Klinischer, München, home based, GMP

Deadline: 10 January 2014

For more details