🔍 QA Consultant – DS Manufacturing (Contract) | 3 Days/Week | 4–6 Months
We’re currently supporting a client in the Biotech space who is looking to bring in an experienced QA Consultant to support their team on a part‑time basis (3 days per week) over the next 4–6 months.
This role will sit within a highly collaborative QA function, reporting into senior leadership while working closely with key stakeholders across the business.
The best consultant will be someone who has extensive Biologics experience in external QA / CDMO management, and is used to working in a small virtual environment.
🔧 Key responsibilities:
- Handling deviations, change controls, and batch record review
- Supporting day‑to‑day QA activities within DS Manufacturing
- Working closely with cross‑functional teams to ensure compliance and continuity
- Providing hands‑on support to maintain operational efficiency
✅ What we’re looking for:
- Strong QA experience within Drug Substance (DS) manufacturing
- Proven experience managing deviations and change controls
- Comfortable with batch record review and operational QA support
- Someone collaborative and hands‑on, able to integrate quickly into the team
This role isn’t positioned at the most senior level — but we’re looking for someone with solid, practical experience who can add value quickly and support a busy team environment.
đź•’ Details:
- 3 days per week (with at least one day overlapping key team members)
- 4–6 month contract
- Immediate/soon start preferred
If this sounds of interest — or you know someone who might be a great fit — feel free to message me directly.