Document Control Specialist (Fixed Term Contractor)

CooperCompaniesVictor, NY
$23 - $30Onsite

About The Position

At CooperVision, a business unit of CooperCompanies (Nasdaq: COO), we’re driven by a unified purpose of helping people experience life’s beautiful moments. We are connected through our shared values - dedicated, innovative, friendly, partners, and do the right thing. As a leading global manufacturer of contact lenses, we are committed to helping improve the way people see each day. Through our diverse lens portfolio, we tackle the toughest vision challenges – including astigmatism, presbyopia, and childhood myopia. We offer the most complete collection of spherical, toric, and multifocal products available, enabling us to fit 99% of all contact wearers. Learn more at www.coopervision.com. This role is not eligible for employer-sponsored work authorization now or in the future. Applicants must be authorized to work in the United States on a permanent and ongoing basis without the need for future sponsorship (i.e., H1B, STEM OPT extensions, TN, etc.). This position requires full-time onsite work (5 days per week) in Victor, NY and is not eligible for relocation assistance.

Requirements

  • Must be authorized to work in the United States on a permanent and ongoing basis without the need for future sponsorship (i.e., H1B, STEM OPT extensions, TN, etc.).

Responsibilities

  • Executing required QA review activities for change control elements associated with local and global departments in support of the Quality Management System.
  • Revising and creating Standard Operating Procedures (SOP’s), Work Instructions (WI's) and other controlled documents in collaboration with process owners and subject matter experts.
  • Utilizing the Agile electronic Quality Management System (eQMS) to process these documents and obtain approvals.
  • Reviewing Change Orders and supporting training.
  • Participating in establishing procedures for local and global review of change packages as well as engineering changes, engineering studies, and validations when necessary.
  • Assisting with the investigation of Quality Feedback (QFB’s), and Non-Conformance Reports (NCR’s) or other sources of quality data.
  • Participating with packaging verifications and validations when necessary.
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