What are the responsibilities and job description for the Contract LIMS & Empower QA Specialist position at AL Solutions?
George Higginson is currently supporting a rapidly growing biologics-focused CDMO with the search for a Document Control & QA Specialist to support key LIMS and Empower implementation projects.
This position sits at the intersection of Quality Systems, Document Control and QC laboratory support, supporting GMP operations across QC documentation, sample management, stability programs, and laboratory workflows.
The team is specifically looking for someone who understands QC laboratory environments and can provide hands-on QA oversight while supporting SOP revisions, document lifecycle management, and eQMS-driven processes.
Contract Details
- Part-time contract (~9 months initial duration)
- Start: Early July
- Up to 20 hours/week (hours worked basis)
- Hourly rate: $50-70/hour depending on experience
Key Responsibilities
- Managing document lifecycle activities within the eQMS
- Supporting QA review and approval of SOPs, protocols, work instructions, and QC documentation
- Assisting with SOP authoring, revisions, and procedural improvements tied to laboratory operations
- Supporting QC and laboratory teams with compliant documentation practices
- Managing document workflows, training assignments, and controlled records
- Supporting GMP compliance, inspection readiness, and ALCOA data integrity expectations
- Working within LIMS-driven environments supporting sample management activities
What They’re Looking For
- Bachelor’s degree in a scientific or engineering discipline
- 7 years of QA / regulatory experience within CDMO, pharmaceutical or biotech environments
- Strong experience with eQMS document control systems
- Experience supporting QC laboratory operations and laboratory-facing QA activities
- Knowledge of ALCOA data integrity principles
- Experience supporting QC documentation and laboratory operations
- Experience working within LIMS environments is required
- Previous experience supporting validation documentation and regulated electronic systems strongly preferred
This is an opportunity to join a highly visible project with a growing organization at an exciting stage, with direct exposure to critical systems implementation and quality initiatives.
If you’d be interested in hearing more, please reach out directly for a confidential discussion.
Salary : $50 - $70