Qa Specialist(Qa Review,Change Request,Document Creation,Quality Regulations)

Job Description:
Responsibilities:
Assist with proper integration and support of quality regulations: drug, biologics, device and/or combination products.
Assist with audits of documentation, facilities and equipment.
Complete and route change requests for process document creation, maintenance, and implementation.
Support project teams in planning, preparation, review and approval of quality documentation.
Collect and compile key quality metric data.
Perform QA review for product release.
Participate in training and education programs for various aspects of quality assurance.
Requirements:
Bachelor's Degree (Chemistry, Pharmacy, Biology, Microbiology, Engineering or other technical/ scientific area preferred) or equivalent experience.
0-2 years' experience in quality assurance, quality oversight or relevant experience.
Knowledge and familiarity with product, process, equipment, and facilities of pharmaceutical, biological and medical device products preferred.
Strong oral and written communication skills needed.
Excellent interpersonal skills a plus.
Delivers tactical results to support the quality system.
Job Types: Full-time, Contract
Pay: $29.64 per hour
Expected hours: 40.00 per week
Work Location: In person