What are the responsibilities and job description for the Quality Assurance Specialist- US Pharmaceutical / Medical device GMP / GDP position at Verbatim Pharma?
Quality Assurance Specialist- US Pharmaceutical / Medical device GMP / GDP
Verbatim Pharma are currently working with a Clinical Trial Service company who are looking for a Quality Assurance Specialist to join the team on permanent basis.
This is a great opportunity to further develop your career within quality in the clinical trial sector and further expand your experience and knowledge.
The ideal candidate will have high attention to detail, problem solving skills and good understanding of GMP / GDP environment and familiarity with clinical trial industry.
This role is full time based on their site in Pennsylvania.
You must be fluent in English.
Key duties include :
- Review of quality documentation
- Provide QMS support and improve quality processes
- Investigating and solving quality related problems
- Sampling and inspecting packaging components and supplies
Relevant job titles :
QA specialist / QA associate / QC Associate / QA inspector / QC inspector