Specialist, QMS – Document Control
Amylyx Pharmaceuticals · Cambridge, MA
Posted about a month ago · Previously reposted
or apply directly on Amylyx Pharmaceuticals's site. We never take the application ourselves.
Is this posting real?
- This role has been open
- 33 days Amylyx Pharmaceuticals's roles stay open a median of 45 days
- Reposted
- Yes taken down and listed again at least once
- Salary listed
- No 0% of Amylyx Pharmaceuticals's roles list one
- Ghost-job risk at Amylyx Pharmaceuticals
- high 17 stale, 3 reposted of 29 open
- Hiring momentum
- 42 roles opened in the last 90 days ↑ up vs. the prior 90 days
- Last confirmed on the employer's board
- 2026-09-17
Measured from postings appearing on and disappearing from Amylyx Pharmaceuticals's own greenhouse board since 2026-08-03. Full hiring picture for Amylyx Pharmaceuticals.
About this role
The Specialist, QMS – Document Control is responsible for managing the document control processes within the Quality Management System at Amylyx. This includes ensuring compliance with GxP regulations, supporting cross-functional teams in document lifecycle management, and maintaining inspection readiness. The role also involves training management, continuous improvement of document management functionality, and monitoring document control performance.
- benefits
- 1/5
- freshness
- 3/5
- career value
- 3/5
- role clarity
- 4/5
- pay transparency
- 0/5
Scored from the posting itself — how clearly the role is described, how much it says about pay and benefits, and how recently it was listed. Not a judgement of Amylyx Pharmaceuticals as an employer.
What you need
- Bachelor's degree
- 1-3 years in pharmaceutical/biotech Quality (GMP environment)
- Experience managing controlled documents and records within an electronic Quality Management System (eQMS), including experience with Veeva Vault Quality Docs/Veeva Vault Quality
- Working knowledge of Quality Management Systems (QMS), document control principles, records management, and Good Documentation Practices (GDocP)
- Understanding of GxP regulations, data integrity requirements, and industry standards applicable to biopharmaceutical organizations
- Experience supporting quality audits, regulatory inspections, and compliance activities in a regulated environment
Nice to have
- Certification in Quality, Records Management, or a related discipline
- Experience supporting eQMS implementation, validation, system administration, or continuous improvement initiatives
Worth weighing
- Remote work opportunities available, but not open to applicants from certain states (Alaska, Arizona, Hawaii, Michigan, Tennessee)
- Travel to Cambridge, MA several times a year is required
- Pay range is estimated and may vary based on experience and qualifications
Summarised from Amylyx Pharmaceuticals's posting. Read the full original.
Listed by Amylyx Pharmaceuticals on their greenhouse job board, last confirmed open on 2026-09-17. PitchMeAI is not the employer.
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