Quality Assurance Specialist
- Permanent
- Good Manufacturing Practice (GMP)
- United States
This vacancy has now expired. Please see similar roles below...
Proclinical is currently recruiting for a Quality Assurance Specialist with a global pharmaceutical company located in Boston, MA. Successful candidate will ensure all inspection and on-site audit related documentation is completed and filed accordingly and that are associated records are up to date.
Job Responsibilities:
- Work with team on inspection readiness activities, enabling proactive inspection readiness.
- Helps to support inspection strategy.
- Compliance and Systems and assure inspection planning across enabling ongoing efforts to maintain a steady state of inspection readiness.
- Support on site business partner audits.
- Partner with R&D Quality Compliance and Systems and stakeholders for internal audits.
- Host audits from business partners conducted on site.
- Ensure all inspection and on-site audit related documentation is completed and filed accordingly and that are associated records are up to date.
Skills and Requirements:
- Bachelor's Degree required; Advanced Degree preferred.
- Minimum 3 years of increasing responsibility in pharmaceutical GMP environment.
- Experience in managing complex organizational compliance issues and in identifying and implementing organization-wide compliance initiatives.
- Skilled in managing global, cross-functional projects.
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 call Mary Jacobs at (+1) 312-291-4181 or upload your resume on our website - www.proclinical.com.
A full job description is available on request.
Proclinical 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-MJ1
#Compliance/Quality
Related jobs
Highly Competitive
Philadelphia, USA
Play a crucial role in advancing life-changing cell and gene therapies by ensuring GMP production environments remain audit-ready and contamination-free.
Highly Competitive
Aargau, Switzerland
Be the driving force behind seamless logistics for a global CMO, where precision and efficiency for quality are key to supporting world-class manufacturing.
Highly Competitive
Bristol, USA
Join a team transforming the future of medicine through cutting-edge bioconjugation and gene therapy manufacturing.
Highly Competitive
Bern, Switzerland
Do you thrive on solving complex quality challenges and turning investigations into lasting improvements?
Highly Competitive
Mansfield, USA
Join a team where precision, quality, and scientific excellence come together to help deliver safe and effective pharmaceutical products.
Highly Competitive
Norton, USA
Passionate about quality and compliance? Join a team where your expertise helps ensure every biopharmaceutical product meets the highest standards of safety and excellence.
Highly Competitive
Paris, France
Notre client recherche un Coordinateur QHSE Prestataires pour rejoindre leur équipe et intervenir sur le site de l'un de leurs clients majeurs en pharmaceutique.
Highly Competitive
Hatfield, England
Lead the quality agenda, shape compliance excellence, and make a lasting impact on the delivery of safe, high-quality pharmaceutical products.