QA Specialist II
Listed on 2026-01-13
-
Healthcare
Healthcare Compliance, Data Scientist
The Fountain Group is a national staffing firm and we are currently seeking a QA Specialist - Risk Management for a prominent client of ours. This position is in Worcester, MA 01605. Details for the position are as follows:
Job Title:
QA Specialist – Risk Management (Senior QA Associate considered based on experience)
Location:
Worcester, MA
Schedule:
Hybrid
Pay Rate: $43–$46/hour
This role supports the Quality organization’s Quality Risk Management (QRM) activities within a GMP biologics manufacturing environment. The position is highly documentation-driven and compliance-focused, requiring close collaboration with cross‑functional technical teams to assess, document, monitor, and maintain risk management activities.
A candidate with a science‑based background who is comfortable working in regulated environments, managing complex documentation, and applying risk‑based decision‑making will be an excellent fit.
Key Responsibilities- Support and lead Quality Risk Management (QRM) activities across commercial biologic products and site operations.
- Develop, update, and maintain risk management documentation related to:
- Biologic drug substances
- Site and operational risk
- Cross‑contamination risk
- Facilities, utilities, and equipment risk
- Apply working knowledge of ICH Q9 (Quality Risk Management); familiarity with EU GMP Annex 1 is a strong plus.
- Collaborate with technical subject matter experts to ensure risk documentation is accurate, current, and reviewed on schedule.
- Perform periodic reviews of risk documents, manage document revisions, and identify obsolete records.
- Track and monitor open action items resulting from risk assessments and ensure timely implementation.
- Analyze data from multiple sources to identify risk trends, recurring issues, and opportunities for improvement
. - Prepare reports summarizing outputs of risk management monitoring activities.
- Exercise sound judgement to escalate risks appropriately
, including documenting rationale when escalation is not required. - Provide QA compliance support as needed, including:
- Investigations
- Audits and inspection readiness
- Continuous improvement initiatives
, preferably in biologics or sterile manufacturing
, including risk assessments and mitigation tracking
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