Sr QA Records Specialist

Indotronix International Corporation • Greenville, NC

4d • Onsite

About The Position

Join a dynamic and growing team as a Sr QA Records Specialist. Play a pivotal part in ensuring GMP compliance and quality standards are met for high-impact pharmaceutical products. Collaborate with cross-functional professionals, take the lead in batch review improvements, and elevate your career in a supportive and safety-focused environment.

Requirements

• 2-5 years of relevant experience as a Records Specialist
• Strong understanding of GMP compliance and documentation practices
• Exceptional attention to detail and organizational skills
• Effective communication and teamwork abilities
• High School diploma or equivalent

Nice To Haves

• Associate’s degree or higher in Science or Technology
• Experience with electronic batch records and audit preparation
• Leadership in process improvement initiatives

Responsibilities

• Review complex and high-risk production records for strict GMP compliance
• Collaborate with Manufacturing and QC teams to ensure on-time batch release
• Provide hands-on guidance and training for new technicians
• Support preparation activities for regulatory and client audits
• Lead initiatives to streamline batch review and implement electronic systems
• Maintain adherence to all safety protocols and required training

Benefits

• Opportunity for career advancement in a growing industry
• Collaborative, professional work environment
• Hands-on training and mentorship
• Exposure to regulatory and client audit processes

What This Job Offers

• Job Type: Full-time
• Career Level: Senior
• Education Level: High school or GED