Alphanumeric Systems Inc.

Compliance Specialist

Collegeville, PennsylvaniaContract
$41.50 - $45.20 hourly
About the Job

Compliance Specialist

Location: Collegeville, PA
Pay Range: $41.50 – $45.20/hour

Please Note: We are unable to accept applications from third-party vendors, and we do not offer sponsorship. Applicants must be eligible to work on our W2 without requiring sponsorship now or in the future.

Alphanumeric is hiring a COMPLIANCE SPECIALIST to work in Collegeville, PA with our client of 20 years, a global leader committed to improving lives through medical and pharmaceutical advancements.

We are seeking a detail-oriented Compliance Specialist to support Quality and Engineering documentation activities within a regulated pharmaceutical environment. This position will help manage the end-to-end documentation lifecycle, coordinate reviews and approvals, maintain document control and traceability, and support ongoing audit readiness.

Key Responsibilities

  • Partner with Quality team members to support the end-to-end lifecycle of engineering documentation, ensuring required records and artifacts are created, reviewed, approved, finalized, and retained in accordance with established quality processes.
  • Coordinate with contributors and cross-functional stakeholders to advance draft documentation, facilitate reviews, resolve outstanding actions, and obtain required approvals.
  • Review documentation from a technical writing and documentation-quality perspective, identifying inconsistencies, gaps, or potential compliance concerns and escalating issues to the appropriate Quality team member.
  • Maintain controlled documentation repositories and appropriate version-control practices, supporting traceability, document integrity, and audit readiness.
  • Support compliance with internal policies and procedures related to risk, issue, and record management, including follow-up on outstanding or overdue documentation.
  • Track documentation status, outstanding actions, approvals, and other deliverables and provide timely updates to Quality stakeholders.
  • Manage document routing and administrative finalization, including uploads, version tracking, approval coordination, and sign-offs.
  • Collaborate with Quality, Engineering, and other stakeholders to help ensure documentation is accurate, complete, appropriately controlled, and inspection-ready.


Qualifications

  • Bachelor's degree in a scientific discipline required.
  • Experience supporting Quality, Compliance, Engineering, or controlled documentation within a regulated environment strongly preferred.
  • Experience in the pharmaceutical, biotechnology, life sciences, or other GxP-regulated industry preferred.
  • Understanding of document lifecycle management, document control, version control, and approval workflows.
  • Strong technical writing, proofreading, and documentation-review skills.
  • Excellent organizational skills with the ability to manage multiple documents, deadlines, and stakeholders simultaneously.
  • Strong attention to detail and ability to identify documentation inconsistencies or potential compliance issues.
  • Effective written and verbal communication skills with the ability to work cross-functionally.
  • Experience maintaining documentation in an electronic document management or quality management system is preferred.

Ideal Candidate

The ideal candidate combines strong documentation and organizational skills with experience working in a regulated Quality environment. They should be comfortable coordinating across Quality and Engineering teams, following up on outstanding documentation, maintaining accurate version control, and ensuring records remain complete, traceable, and audit-ready.