Quality Assurance Specialist

2 days ago


Cumberland, Rhode Island, United States NEUROTECH U S A Full time
Job Title: Quality Operations Specialist II

We are seeking a highly skilled Quality Operations Specialist II to join our team at Neurotech Pharmaceuticals. This role will provide full-time oversight to the validation program, including providing validation program expertise, documentation review, validation strategy, and more.

Key Responsibilities:
  • Provide technical expertise and guidance in validation approach and documentation relating to expectations from NT Quality Assurance.
  • Perform regular quality assessments of facility, personnel, and documentation to uncover errors or deficiencies and assure quality and compliance.
  • Develop and implement quality culture and environment by aiding personnel in understanding application of policies and controls.
  • Participate in rapid response and provide quality guidance for deviation events.
  • Perform quality review and approval of procedures, training documents, deviations, CAPAs, and change control.
Requirements:
  • Bachelor of Science or Engineering and 5-7 years relevant work experience within the cGMP Biotechnology and Medical Device industry.
  • Experience in medical device and biotechnology field, preferably in the Quality and validation discipline.
  • Knowledge in QMS management and support as well as significant GDP efficiency.
What We Offer:

Neurotech Pharmaceuticals provides competitive compensation, benefits, and a 401(k) plan. We also offer generous vacation time and company holidays. Our team is passionate and dedicated to our mission, and we are committed to providing a positive and inclusive work environment.

Apply now through our Neurotech Career Center to join our team and contribute to our mission to develop innovative treatments for retinal disorders.



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