A career at Resilience is more than just a job - it's an opportunity to change the future.
Resilience is a technology-focused biomanufacturing company that's changing the way medicine is made. We're building a sustainable network of high-tech, end-to-end manufacturing solutions to better withstand disruptive events, serve scientific discovery, and reach those in need.
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POSITION SUMMARY:
The Deviation Specialist will play an important role in the department by writing deviations, participating in Out of Specification analysis investigation, closing batch documentation prior to release and communicating with internal stakeholders/SME and client. In addition, the Specialist will act as a point of contact between the manufacturing group, QA/client QA and regulatory agencies.
**This is a 18-Month Fixed-Term Assignment**
MAJOR RESPONSIBILITIES:
Authors deviations, Investigations, Environmental Monitoring Excursion and CAPA for Manufacturing (USP/DSP/Fill/Finish//Buffer and PST) including but not limited to investigation handling, leading corrective and preventive actions (CAPA) and tracking batch release items to meet company targets.
Participates and applies Root Cause Analysis (RCA) tools and ensures CAPAs are implemented to eliminate deviation re-occurrence
Works closely with department manager and QA to support batch release activities while ensuring investigations comply with quality system requirements.
Actively participates in regulatory, client and internal audits by compiling and providing information to department manager.
Ensures Deviations are closed within assigned timelines to meet client demand and company targets.
Participates in data gathering and analysis for Monthly and Quarterly quality matrix as well ad departmental KPI.
Ensure adherence to GDP, GMP, and safe practices at clinical and commercial scales. Implement process improvement related changes.
Ensure corrective and preventative action that have been implemented are effective via Effectiveness Checks (EC)
Provide support in ensuring batch readiness action items are completed prior to batch start Performs all other job-related duties as assigned
MINIMUM QUALIFICATIONS:
Relevant industrial experience in pharmaceutical practices.
Demonstrate ability to perform RCA investigations and lead CAPA initiatives.
Demonstrate ability to review manufacturing, engineering, and quality documentation.
Strong working knowledge GMP requirements.
PREFERRED QUALIFICATIONS:
Diploma with 3+ years or a B.Sc. degree
Experience in top-tier biopharmaceutical environment
Knowledge of regulatory agencies HC, FDA and others.
BEHAVIOURAL:
Demonstrate ability to apply the following behavioural competencies on the job:
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