Similar posts
Quality Assurance Specialist III
- Contract
- 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 III for a leading pharmaceutical company located in Worcester, MA. Successful candidate will assure the quality of manufactured products and processes per Standard Operating Processes and GMP compliances.
Job Responsibilities:
- Assure the quality of manufactured products and processes per standard operating processes (SOP'S) and GMP (Good Manufacturing Practices).
- Review manufacturing documentation such as batch records and worksheets for accuracy and data integrity in real time.
- This data reviewer position requires immediate identification of GMP documentation errors and corresponding path for resolution.
- Position utilizes both a manual tracking sheet for corrections as well as use of Microsoft Excel worksheets.
- Candidate must be able to work independently and with minimal direct supervision on second shift.
Skills and Requirements:
- Familiar with GMP documentation and data entry requirements
- Ability to identify documentation errors and work with various departments to resolve
- Communication skills to work with peers for error resolution and elevate to management as necessary
- Required to appropriately gown to enter classified manufacturing environment
- Minimal supervision, ability to work independently
- SAP and Trackwise computer systems is a plus
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 Nadine Rucci at (+1) 215-531-5281 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-NR2
#Compliance/Quality
Related jobs
Highly Competitive Salary
Wilmington, USA
Proclinical is seeking a dedicated Senior Quality Specialist to provide leadership and oversight on GMP operations related to clinical manufacturing.
Highly Competitive Salary
Maidenhead, England
Proclinical is seeking a dedicated QA Associate for our Supply Chain Quality Assurance team. This is a permanent position located in Maidenhead, England.
Highly Competitive Salary
Rochester, USA
Proclinical is seeking a proactive and dedicated individual for a Customer Quality Specialist for a leading pharmaceutical company. This is a permanent position located in Rochester, NY
Highly Competitive
Brussel, België
Proclinical has been retained by a cutting edge, biopharmaceutical company to appoint a Global Head of Quality for their commercial manufacturing sites.
Highly Competitive Salary
Waltham, USA
Proclinical is seeking a Senior Quality Product Manager to join a leading pharmaceutical company. This is a permanent position located in Waltham, MA.
Highly Competitive Salary
Pearl River, USA
Proclinical is seeking a QA Manager-Site Compliance for a global mid-sized consumer healthcare and medical devices company.
US$220000 - US$250000 per annum + Highly Competitive Salary
Mountain View, USA
Proclinical Staffing is seeking a VP Quality to join a cutting-edge biotech company.
Highly Competitive Salary
Zebulon, USA
Proclinical Staffing is seeking a QC Chemist to join an ambitious pharmaceutical company.
Up to US$115000 per annum + Highly Competitive Salary
Philadelphia, USA
Proclinical Staffing is seeking a Quality Control Supervisor to join a cutting-edge biopharmaceutical company.
Highly Competitive Salary
Marietta, USA
Proclinical Staffing is seeking a QC Laboratory Technician to join a cutting-edge biopharmaceutical company.