We're in relentless pursuit of breakthroughs that change patients' lives.
We innovate every day to make the world a healthier place.
To fully realize Pfizer's purpose – Breakthroughs that change patients' lives – we have established a clear set of expectations regarding "what" we need to achieve for patients and "how" we will go about achieving those goals.
Pfizer Global Supply proudly shoulders the responsibility of manufacturing and distributing our wide-ranging pharmaceutical products.
Pfizer offers competitive compensation and benefits programs designed to meet the diverse needs of our colleagues.
Job Title: Experienced Process Technician Job Purpose Your role will be in one of the Shift Operating Units at Grange Castle where you will be directly involved in the manufacture of one of our products, ensuring that they meet all specifications for safety, potency, and efficacy.
You will work within the guidelines of cGMP to ensure conformance with all regulatory requirements and site SOPs, while assisting in the improvement of all current processes through our Continuous Improvement Program.
This is a shift-based role (For 24/7 Operations).
12 hour shift on a 4-cycle schedule.Job Responsibilities: Responsible for execution of all tasks associated with the preparation for and production of Pfizer products in cGMP environment ensuring full attention to detail and excellent documentation skills.Assist in maintaining a safe, cGMP compliant work environment always.Responsible for completion of tasks according to SOPs and batch records (paper and electronic).Perform initial troubleshooting of issues identified during routine operations.Assist with the investigation of and operations deviations through QTS system, engaging with all relevant personnel and functions as appropriate.Assist where necessary with the training of colleagues in SOPs, process execution and equipment operation.Provide input into the creation and maintenance of area SOPs and batch records.Seek opportunities for Continuous Improvement and embrace Pfizer's 'Own It' culture to own and drive any activities associated with delivering these improvements.Use Lean Tools as part of daily operations (Standard Work, 5S, Method 1, 2 etc) to optimize efficiency and drive the culture of Continuous Improvement and Zero Defects.Education/Experience: To be successful in this role you will require:
Minimum 1 year Experience in a cGMP manufacturing, or regulated environment, preferably Aseptic processing and/ Drug Product manufacturing/ Fill Finish, Drug Substances, Chromatography/ultrafiltration/Diafiltration etc.Working knowledge of production operations with a strong focus on attention to detail and compliance to all regulatory standards.The minimum educational requirement for this position is a fully completed and passed Leaving Certificate.An ability to work independently, and as a member of a team in a dynamic, fast-paced environment that requires flexibility and initiative.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.What We Offer: Competitive Salary and Shift AllowanceAnnual Bonus and Share SchemesPension SchemeLong term Income ProtectionHealthcare for you and your familyHealth and wellbeing initiativesSports and social club (Swim Society, Women's Mentoring programme, Pfizer Pride & many more)Subsidised CanteenOnsite Gym and SaloonWork Location Assignment: Fully Onsite
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.
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