Sr QA Technician (Records Specialist)

VARITE is looking for qualified Sr QA Technician (Records Specialist) in Greenville, NC 27834 (Onsite)
 
WHAT THE CLIENT DOES?
An American-headquartered life science and clinical research company. It is a global supplier of analytical instruments, clinical development solutions, specialty diagnostics, laboratory, pharmaceutical and biotechnology services.
 
WHAT WE DO?
Established in the Year 2000, VARITE is an award-winning minority business enterprise providing global consulting & staffing services to Fortune 1000 companies and government agencies. With 850+ global consultants, VARITE is committed to delivering excellence to its customers by leveraging its global experience and expertise in providing comprehensive scientific, engineering, technical, and non-technical staff augmentation and talent acquisition services.
 
Job Title: Sr QA Technician (Records Specialist)
Location: Greenville, NC 27834 (Onsite)
Schedule: Monday through Friday, day shift. 8-5pm fully onsite
Contract Duration: 12 months with possible extension.
Pay Rate Range: $18.00 - $25.45/hr. on W2
 
HERE’S WHAT YOU’LL DO
Position Summary:

• The Sr. Quality Technician, Provides direct quality support to ensure compliance with regulations that govern pharmaceuticals.
• Ensures the site operates in compliance with regulatory standards that ensures product quality, avoids stoppages and reinforces customer satisfaction.

Key Responsibilities

• Follow all job-related safety, quality, compliance, and training requirements.
• Review electronic manufacturing and quality data, including audit trails and associated records, to ensure completeness, accuracy, compliance with procedures, and adherence to data integrity requirements.
• Identify and assess discrepancies, atypical events, data integrity concerns, and potential compliance issues identified during review.
• Communicate and coordinate with Manufacturing, Quality, Engineering, and other departments to resolve issues identified during review.
• Apply risk-based decision-making to ensure appropriate controls are in place for product quality, patient safety, sterility assurance, and data integrity.
• Escalate deviations, discrepancies, and compliance concerns to the appropriate functional area and Quality management.
• Perform review activities of moderate complexity with limited supervision while ensuring compliance with GMP requirements and current procedures.

 
Education

• High school diploma or equivalent required.
• Associates degree or higher in Science or Technology is preferred

 
BENEFITS:
We offer a comprehensive benefits package designed to support the health, well-being, and financial security of our employees and their families. Eligible employees may receive:

• Health Insurance: Medical, dental, and vision coverage
• Retirement Plans: Participation in a company-sponsored retirement savings plan.
• Legal Service Plans: Offering access to attorneys for legal advice and representation.

 
If this opportunity interests you, please respond by clicking on EasyApply.
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VARITE is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.