Use Your Power for Purpose
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 you are engaged in development, maintenance, compliance, or research analysis, your contributions have a direct impact on patient care.
Our dedication to quality and safety drives everything we do, fostering a dynamic environment where your role is crucial in advancing healthcare solutions.
What You Will Achieve
In this role, you will:
Be a member of Pfizer's dedicated and highly effective quality control team, responsible for developing and maintaining quality programs, processes and procedures that ensure compliance with established standards and agency guidelines.
Contribute to quality risk management, help with commitment tracking, interpret policies, manage site complaints, and work directly with operating entities to provide process analysis oversight.
Prepare for upcoming audits and inspections, ensuring that the quality assurance programs and policies are maintained and modified regularly.
Maintain uniform global standards and best-practice sharing to help achieve the company's mission worldwide.
Be recognized as a subject-matter expert with specialized knowledge and skills in procedures, techniques, tools, materials, and equipment.
Adapt standard methods and procedures by applying your knowledge, prior work experience, and requirements.
Make decisions on the best methods and procedures for different work situations and train others, reinforcing behaviours that help us achieve our goal of providing the best to patients.
Perform analysis of quality control samples, including raw materials, in-process, intermediates, stability, and finished products in line with Current Good Manufacturing Practice.
Write up and execute Analytical Method Transfer Exercises for products being transferred to the Grange Castle site, ensuring compliance with site, Pfizer Quality Standards (PQS), International Conference on Harmonisation 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, FTIR, KF, iCE, ICP, CE and compendial assays.
Participate and seek opportunities in the areas of Right First Time, Continuous Improvement and unburdening activities to facilitate Lean/Agile implementation.
Here Is What You Need (Minimum Requirements)
Third level qualification in science, engineering, or equivalent is preferred though not essential.
Strong knowledge of analytical techniques, both theoretical and practical.
Two years of prior experience working in a GMP QC laboratory environment.
Excellent interpersonal and communication skills.
Detail oriented, quick decision maker, self-motivated with good troubleshooting and problem-solving abilities.
Bonus Points If You Have (Preferred Requirements)
Knowledge of computer applications, including MS Office, Excel, Laboratory Information Management System Access, and Track Wise.
Work Location Assignment: On Premise
Additional Information
In order to be considered for this position in Ireland you need to be legally eligible to work in Ireland.
Please note there is no relocation support available for this position.
How To Apply
Make a difference today, all suitable candidates should apply with CV below.
We are looking forward to hearing from you
Purpose
Breakthroughs that change patients' lives...
At Pfizer we are a patient-centric company, guided by our four values: courage, joy, equity and excellence.
Our breakthrough culture lends itself to our dedication to transforming millions of lives.
Digital Transformation Strategy: One bold way we are achieving our purpose is through our company-wide digital transformation strategy.
We are leading the way in adopting new data, modelling and automated solutions to further digitize and accelerate drug discovery and development with the aim of enhancing health outcomes and the patient experience.
Equal Employment Opportunity: We believe that a diverse and inclusive workforce is crucial to building a successful business.
As an employer, Pfizer is committed to celebrating this, in all its forms – allowing us to be as diverse as the patients and communities we serve.
Together, we continue to build a culture that encourages, supports and empowers our employees.
Disability Inclusion: Our mission is unleashing the power of all our people and we are proud to be a disability inclusive employer, ensuring equal employment opportunities for all candidates.
We encourage you to put your best self forward with the knowledge and trust that we will make any reasonable adjustments to support your application and future career.
Your journey with Pfizer starts here
Job Details
Seniority level: Entry level
Employment type: Full-time
Job function: Quality Assurance
Industries: Pharmaceutical Manufacturing
Location: Dublin, County Dublin, Ireland
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