- Act as the Quality SME on local or global projects to which you are assigned.
- Work closely with the sponsor, key stakeholders, and project team
- Provide Quality input into the user requirements gathering and support the generation and approval of any associated change control, risk assessment and validation documentation
- Capture key decisions and provide regular updates to global Quality Management, highlighting any areas of concern and gain consensus on any discussion points requiring resolution
- Identify impacts and compliance risks and highlight to the project team
- Ensure deliverables to which you are assigned are completed in a timely manner
- Communicate updates to the wider Quality teams as required
- Facilitate the implementation of new processes or significant changes within the Quality department. In doing so:
- Work closely with Quality management (locally or globally) to define the scope of the initiative or change
- Lead the implementation exercise, track tasks, and monitor progress, providing clear visibility of key milestones and deliverables
- Facilitate the user requirements gathering and support the generation of process / data maps and the compilation and approval of any associated change control, risk assessment and validation documentation
- Work closely with department SMEs to generate / update SOPs
- Work closely with department OJT to develop educational material relevant to the changes being introduced
- Provide regular updates to local or global Quality Management, highlighting any areas of concern, gain consensus on any discussion points requiring resolution and report on project status
- Identify impacts and compliance risks and highlight to the project team
- Highlight potential inter-dependencies and identify business readiness activities
- Facilitate effectiveness checks
- HS Diploma or Equivalent
- 5+ years pharmaceutical experience with HS Diploma or equivalent
- 3+ years pharmaceutical experience with Associates Degree
- 1+ years pharmaceutical experience with bachelor’s degree
- Knowledge of Current Good Manufacturing Practices (cGMP)
- Working with Quality Systems
- Bachelor’s degree with science background
- Previous experience working under an established Quality System or within a Pharmaceutical /GxP environment
- Knowledgeable in GxP regulatory requirements
- Knowledge of Packaging/Labeling/Storing/Shipping Clinical Supplies
- Familiar with Clinical Trial Process
- Medical, Vision & Dental benefits from the 1st of the month following start date
- 20 days PTO per year, accrued monthly following start date
- 12 holidays per year
- Company paid Long and Short-term disability along with Life Insurance
- 401k company contribution
- Professional development programs/ continuous learning opportunities