Plant Quality Assurance Specialist
AmgenIreland - dublinUpdate time: March 30,2022
Job Description

Career Category

Quality

Job Description

Specialist Plant Quality Assurance

The Plant Quality Assurance (QA) Specialist is a senior and active role within the broader QA function. The PQA Specialist will typically report to a PQA Senior Manager and will be required to be a Subject Matter Expert in their assigned area of responsibility. PQA specialists will be required to understand and grasp a broad range of quality related competencies.

In addition to routine Quality Assurance duties, PQA Specialists may be assigned specific oversight and responsibilities for key quality systems or processes and may also serve as a primary quality partner/point of contact for functional areas within ADL, including Supply Chain, Information Systems, Manufacturing, Process Development, Validation, Engineering and Quality Control. Successful candidates will typically be educated to degree level in a Scientific or related discipline and ideally will have acquired technical skills and demonstrated competencies across a broad range of quality related disciplines. QA Specialists may be cross trained and/or assigned additional project specific duties, including continuous improvement/operational excellence initiatives.

General QA Specialist Responsibilities:

Perform all activities in compliance with Amgen safety standards and SOPs

Provide Quality direction and input at Deviation and Change Control Review Boards and assume oversight of Deviation, CAPA and Change Control records; ensuring scope of record is clear and implementation activities are robust and timely.

Write, review and approve Standard Operating Procedures in accordance with Amgen Policies.

Participate in site activities associated with QMS programs (e.g., Validation, Complaints, Change Control) and provide active input into shaping the future direction of these systems.

Review and approval of Deviations and associated 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.

Engineering support through quality review and approval of Work Orders and Job Plans

Act as Quality point of contact during batch manufacture, provide advice to ensure all activities meet internal and regulatory expectations.

Aseptic oversight during sterile formulation and filling.

Oversight during manual and automated inspection of both Syringes and Freeze dried and liquid vials.

Preparation of reports for Product Quality Reviews including batch listing to ensure that trends are acted upon and to demonstrate that products consistently meet desired critical quality attributes.

In line with business requirements, these responsibilities may expand or otherwise include additional areas of responsibility which are not described in this specification but are associated with the role. The knowledge and skills necessary to perform the duties of the PQA Specialist are typically acquired through the following combination of education, experience and knowledge.

Basic Qualifications:

University degree - Engineering or Science related discipline preferred.

Relevant experience (5+ years) 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:

Excellent written and verbal communication skills

Experience working with dynamic cross-functional teams and proven abilities in decision making and influencing

Strong organizational skills, including ability to follow assignments through to completion

Demonstrated ability in problem solving and experience in managing Root Cause Analysis / Deviation investigations

Detailed Knowledge of applicable Regulatory requirements. Experience with Regulatory inspections.

Experience working in aseptic operations, protein formulation, vial and syringe filling, Lyophilised product manufacture, Liquid and Lyophilised Product Inspection, and packaging activities.

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