Similar posts
QA Specialist
- Permanent
- Good Manufacturing Practice (GMP), Good Clinical Practice (GCP), Good Laboratory Practice (GLP)
- United States
This vacancy has now expired. Please see similar roles below...
Proclinical is currently recruiting for a QA Specialist with a biotechnology company located in Marietta, PA. The candidate will ensure all cGMPs, validation, quality, safety and environmental regulations are met and adhere to all safety guidelines and procedures.
Job Responsibilities:
- Perform technical review of cGMP documentation and Batch Records for completeness and compliance to cGMPs as outlined by governmental regulations and internal procedures
- Provide advice and counsel on cGMP and related quality assurance issues to the value stream
- Demonstrate sound decision making relating to quality issues
- Provide on the floor QA support and perform QA Operations activities
- Take initiative to resolve quality documentation concerns
- Perform review and support regarding discrepancies and/or anomalies noted during QA review of associated processes
- React to and escalate production issues
- Routinely communicate and report deviations from procedures/processes to Quality Assurance Management and initiate appropriate action as necessary
- Write and/or revise controlled documents in support of job responsibilities
Skills and Requirements:
- BS/BA in biology, chemical engineering, life sciences. Degree in other discipline if sufficient technical depth has been achieved from professional experience
- QA experience preferred. Minimum 1 year also preferred.
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 Zachary Hines at 215-531-6914 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-ZH1
#Compliance/Quality
Related jobs
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 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.
Highly Competitive Salary
Raritan, USA
Proclinical Staffing is seeking a QC Investigation Specialist (Level 1, 2, 3, & Senior) to join a global biotech company.
Highly Competitive Salary
Cambridge, USA
Proclinical is seeking a QA Specialist - Equipment and Computer Systems to join a global biopharmaceutical company.
Up to US$44 per hour + Highly Competitive Salary
Philadelphia, USA
Proclinical Staffing is seeking a Quality Control Analyst: Cell Therapy to join a cutting-edge biotech company.