Plant Quality Assurance (PQA) Snr Associate

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Location: Dublin

Type: Contract

Rate: Negotiable

Contact: mtreacy@asset.ie

Reference: MT27366

Updated: 20/10/2017 16:48:53


Plant Quality Assurance (PQA) Snr Associate

The Plant Quality Assurance (PQA) Snr Associate will typically report to a QA Manager and is a core member of the site Quality Assurance team. The PQA Snr Associate will serve as Quality point of contact for manufacturing operations.
The site is focused on continuous improvement of all work processes and practices, therefore in addition to routine Quality Assurance duties, PQA Snr Associates may be asked to carry out additional work functions to support site continuous improvement activities.
A variety of shift patterns may be required to support manufacturing operations, including but not limited to day shift, 16/5 shift, 24/5 shift and 24/7 shift. Weekend work may also be required.

Key Responsibilities:

• Perform all activities in compliance with the Clients safety standards and SOPs
• Write, review and approve Standard Operating Procedures in accordance with
the Clients Policies.
• Provide Quality support for triage and investigation of all classes of non-
conformance (NC) events
• Review and approval of NC1s and CAPAs for closure ensuring compliance with
appropriate documentation, whilst ensuring that CAPA actions address root cause
and implementation plan dates are achievable
• Participates in customer complaint investigations.
• Provides training and advice to staff in order for them to perform their
desired functions.
• Observe and provide real-time quality oversight, and support for production
unit operations, extending to formulation, vial and Syringe Fill Finish related
activities, including observation and provision of direction during media fills
and assessment of aseptic interventions.
• Perform Visual Inspection AQL inspections and provide quality oversight for the
inspection program
• Review/approve production batch records, and associated documentation in
preparation for Qualified Person disposition activities.
• Review and approve cGMP records (e.g.NC, CAPA, protocols, reports, SOP, etc.)
ensuring compliance with appropriate documentation
• Support continuous improvement and Operational Excellence initiatives
• Any other tasks/projects assigned as per manager’s request.

Basic Qualifications & Experience:

• University degree. Engineering or Science related discipline preferred.
• Relevant experience (4 yrs +) working in the pharmaceutical or biotechnology
industry or other combination of experience and educational background that may
otherwise satisfy the requirements of the role.

Preferred Qualifications & Experience:
• Excellent written and verbal communication skills
• Experience working with dynamic cross-functional teams and proven abilities in
decision making
• Strong organizational skills, including ability to follow assignments through
to completion
• Demonstrated ability in problem solving and experience in managing Root Cause
Analysis / Non Conformance /Deviation investigations
• Experience working in aseptic operations, protein formulation, vial and syringe
filling.
• Knowledge of applicable Regulatory requirements, and ability to evaluate
compliance issues
• Operational Excellence experience


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