Quality Release Specialist at Astrix Technology Group
Edison, NJ 08837, USA -
Full Time


Start Date

Immediate

Expiry Date

02 Oct, 25

Salary

32.0

Posted On

03 Jul, 25

Experience

3 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Regulated Industry, Management Skills, Excel, Microsoft Outlook, Manufacturing

Industry

Pharmaceuticals

Description

Our Client, a global nonprofit organization on the forefront of saving and healing lives through innovations in tissue and organ donation, transplantation, and research is seeking a Quality Release Specialist to join their growing team.

QUALIFICATIONS

  • Bachelor’s degree
  • 3 years in Quality Assurance or manufacturing in GMP-regulated industry
  • Proficiency in Microsoft Outlook, Word, Excel, and data entry
  • Strong attention to detail, organizational, and people management skills
    This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!
Responsibilities
  • Conduct final review of critical documentation and testing per procedures to ensure high-quality, safe material and medical devices.
  • Approve release of processed material or medical devices for use, ensuring all non-conformances are resolved.
  • Review charts related to non-conformance issues, coordinating with other departments to complete necessary documentation.
  • Oversee special requests, matching, and non-routine releases.
  • Prioritize reviews according to business needs and lead best practices for regulatory compliance.
  • Mentor and train QA staff, update procedures, and review Quality Analysts’ work.
  • Support special projects and assist with additional duties.
Loading...