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.
Job Description: What You Will Achieve In this role, you will: Perform Microbiological testing analysis on, but not limited to, finished drug product, in process materials, stability samples and environmental monitoring.
Responsible for calibration and use of laboratory instrumentation.
Complete documentation associated with analytical results in a timely manner.
Report and document any non-conformances to the QC Manager.
Assist in the preparation and review of area documentation e.g. SOP's, Reports, Protocols.
Assist in the training of other analysts.
Ensure training compliance within assigned work area and QC.
Perform and assist in additional duties as directed by the QC Manager.
Ensure relevant assays are performed on samples in support of release test and stability test programs.
Support any validation and qualification of test methods and processes.
Facilitate laboratory investigations and support associated product investigation.
Support Laboratory inspection and audits.
Troubleshoot laboratory methods and instrument problems.
Establish and monitor trend analysis program.
Contribute to the operations of the Quality Control Laboratories.
Liaise with all customers both internal and external.
Record and review laboratory testing documentation to cGMP standard.
Implement and adhere to appropriate levels of cGMP within the laboratory.
Promote safety awareness and the established culture of IIF within the assigned work area.
Ensure that sample analysis is conducted to meet batch disposition requirements.
Here Is What You Need (Minimum Requirements) Third level Qualification in Science, Engineering or equivalent is preferred though not essential.
Exceptions may be considered where relevant skills/experience and correct attitude and behaviours exist (this may be supplemented by further education in parallel) Excellent communication and interpersonal skills This job description indicates the general nature and level of work expected of the incumbent.
It is not designed to cover or contain a comprehensive listing of all activities, duties or responsibilities required of the incumbent.
Incumbents may be asked to perform other duties as required Bonus Points If You Have (Preferred Requirements) Bachelor's Degree Experience in quality control within a biotech, pharmaceutical, or bio-pharmaceutical manufacturing environment.
Proficiency in computer applications, including MS Office, Excel, Laboratory Information Management System, Access, and Trackwise Demonstrate the GC OWNIT values Adhere to all HR Policies as appropriate Personal Development plans focusing on the 70:20:10 guidelines CI tools/- capability is a key building block for learning & development - Trained and M1 certified.
Proactive engagement with key stakeholders.
Best practices developed and shared with other teams /sites.
Best practices actively sought and copied.
Proactive & effective communication within and across shifts Work Location Assignment:On Premise 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 for 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
Quality Assurance and Control To be considered for this role you will be redirected to and must complete the application process on our careers page.
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