Compliance Specialist (Manufacturing)
Job Description
Temp - Compliance Specialist (Manufacturing - Onsite)
We’re looking for a Compliance Specialist (Temp) to support External Manufacturing. In this role, you’ll play a key part in ensuring quality and compliance across clinical and commercial manufacturing operations.
What you’ll do:
- Manage External Manufacturing items within the Quality System (Change Control, change notifications, CAPAs, SCARs)
- Partner with External Manufacturing Operations leads and collaborate cross-functionally
- Facilitate meetings to track priorities and provide timely updates
- Contribute to process improvements and SOP updates for the External Manufacturing department
- Support and potentially lead SOP reviews, audits, and compliance checks
What we’re looking for:
- BS degree (minimum)
- 5+ years of experience in the pharmaceutical industry
- Strong communication and technical writing skills
- Experience working with CMOs or external partners (External Manufacturing or QA preferred)
- Background in authoring, reviewing, or auditing against SOPs is a plus
Why apply?
This is an excellent opportunity to apply your compliance expertise in a collaborative, fast-paced environment, while contributing to high-quality manufacturing outcomes.
📍 Location: Rensellear, NY
⏱️ Type: Full-time, Temporary (1 Year Contract)
Pay: $40-50+/hour (No C2C or Sponsorships are able to be accepted for this position)
If you’re ready to bring your compliance expertise to external manufacturing operations, we’d love to connect. Apply today!