QC Analyst

1w1 week ago

Pfizer

Dublin, IE · Full-time · €42,000 – €55,000

About this role

Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our flexible, innovative, and customer-oriented culture is rooted in science and risk-based compliance. Whether engaged in development, maintenance, compliance, or research analysis, your contributions have a direct impact on patient care.

You will be a member of Pfizer’s dedicated and highly effective quality control team. Responsible for activities involved in developing and maintaining quality programs, processes and procedures that ensure compliance with established standards and agency guidelines. Your contribution in quality risk management will help with commitment tracking, interpreting policies, managing site complaints and providing process analyses oversight.

You will ensure quality assurance programs and policies are maintained and modified regularly, with uniform standards worldwide and best practice sharing. Recognized as a subject matter expert with specialized knowledge in procedures, techniques, tools, materials, and equipment. Your business awareness of cross-organizational impact will elevate the quality of project deliverables.

You will adapt standard methods and procedures by applying your knowledge, prior work experience and requirements. Arrive at decisions on best fit methods for different work situations. Train others and reinforce behaviours that help achieve the goal of providing the best to patients.

Requirements

Third level Qualification in Science, Engineering or equivalent (preferred, not essential)
Strong knowledge of analytical techniques both theoretical and practical
Minimum 1-2 years' prior experience working in a GMP QC Laboratory environment
Excellent interpersonal and communication skills
Detail oriented, quick at decision making, self-motivated with good troubleshooting and problem-solving abilities
Knowledge of computer applications, including MS Office, Excel, Laboratory Information Management System, Empower and eQMS

Responsibilities

Perform analysis of quality control samples including raw materials, in-process, intermediates, stability and finished product in line with Current Good Manufacturing Practices (part of GxP)
Write up and execute Analytical Method Transfer Exercises for products being transferred to the site, ensuring compliance with site, Pfizer Quality Standards (PQS), ICH guidance and Filing requirements
Adhere to good laboratory practices and housekeeping standards
Assist in the generation and maintenance of Quality procedures and reports
Facilitate laboratory investigations and support associated product investigation
Analyse both wet chemistry and the use of analytical equipment including UV, HPLC, KF, iCE, SDS-Page, CE and compendial assays
Participate in Right First Time, Continuous Improvement and unburdening activities to facilitate Lean/Agile implementation