Ireland Job Openings

Pfizer

Technologist

Cork

FULL TIME

November 7, 2024

Technologist

Ringaskiddy Clinical Manufacturing Facility (RCMF)

Position Summary

The RCMF facility is a multi-product clinical API manufacturing facility enabled for batch manufacturing and continuous processing using our FAST platforms. The design is focused on combining existing capabilities from our clinical workflows with the very best advances in technology and architecture to build a truly contemporary API clinical facility which will support the needs of our new products small molecule portfolio into the future. The RCMF is part of Chemical Research and Development (CRD), within Pharmaceutical Sciences Small Molecule (PSSM), part of the Pfizer Research and Development (PRD) organisation. The RCMF will scale up new clinical products developed in our CRD laboratories at our research sites in the U.S. (Groton, Connecticut) and will tech transfer successful new products from the RCMF to our commercial manufacturing site in Ringaskiddy.

Reporting to the Operations Lead, the Technologist works in Process Teams that are aligned with new product introduction workflows utilising cutting edge continuous manufacturing technologies. Technologists are members of a dynamic, highly competent, engaged team of colleagues responsible for delivering a fully operational facility with excellent performance across the fundamentals of safety, quality, supply and cost. Technologists will develop and execute manufacturing techniques consistent with the requirements of Pfizer’s newest products, and will be committed to continuous improvement, technical up-skilling and personal development in a performance-driven environment. Technologists will be required to travel periodically to observe new processes in transferring facilities; attend, contribute to and present at on and off-site meetings as required.

The accountabilities of the Technologist position include:

Independently prioritizing and scheduling activities to support business needs and to meet requirements of the RCMF manufacturing schedule
Working shift patterns to meet business needs and the manufacturing schedule as required
Flawless RCMF manufacturing execution against safety, quality and customer service metrics for clinical campaigns conducted within the facility
Understanding and use of manufacturing control systems to execute processing steps
Assembling and disassembling of process equipment, as requiredin support of equipment changeover
Ensuring that housekeeping standards in the manufacturing facility are maintained to an audit-ready standard at all times
Adherence to all relevant quality and safety procedures
Monitoring and optimizing the quality and yield of the products including optimization of the process with regard to efficiency, quality and safety.
Observation of processes & technologies in Pharm Sci Kilo lab facility
Preparation of RCMF for new product activity from a safety, quality and operational perspective through adherence to the start-up Standard Work Plan

Real-time analysis of data (e.g. Process Analytical Technology data) and real-time decision-making in partnership with Pharm Sci colleagues

Leading and supporting investigation and resolution of process problems that may occur on plant
Collection of data, trending and generation of technical reports
Leading post-campaign reviews with Pharm Sci colleagues
Participating in cross-functional teams leading to accomplishment of RCMF goals.
Assisting with writing, review and revision of manufacturing documentation as necessary e.g. standard operating procedures, batch books etc.
Completion of personal training requirements in compliance with site procedures and using facility equipment commissioning and qualification activities as part of a comprehensive learning and development program
Providing training and support to new staff members of the RCMF team to ensure that learning objectives are met.
Co-lead technical transfer of processes from RCMF to Ringaskiddy commercial production facilities
Develop strong relationships with PGS New Products Value Stream (SEG, NPTL) to support tech transfer activities
Operational alignment with the small-scale manufacturing facilities in PGS, in particular the New Products Technology Laboratory (NPTL)
Readiness for and participation in routine safety and quality inspections
Support the technology and knowledge transfer of new products to the Ringaskiddy New Products Value Stream
Continuous improvement of the workflows associated with the RCMF operation
Permitting activities within the RCMF
Additional areas of responsibility as the business requires

SELECTION CRITERIA

Qualifications/Skills, Knowledge &Experience:

At least 3-5 years relevant experience in either API/ Biopharma manufacturing, Food Processing or Med-Tech
Have at least a level 7 or higher (NFQ framework) qualification in pharma, biopharma, chemical/process/ mechanical engineering or equivalent
API continuous manufacturing experience while not essential would be advantageous
Excellent technical, problem-solving and communication skills
Performance at a consistent level of excellence in a consistently dynamic operating environment, where the focus will be on flawless execution and demonstrate flexibility to get the job done
Comfortable as part of a highly competent and self-motivated team, and will have the ability to deal with the challenges that a facility start-up may present
Demonstrated evidence of high performance in a continuous improvement-oriented work environment. Excellent interpersonal skills, team orientation and attention to detail
Facilitation of an environment of open and team-based communication where all members of the Process Team work together to ensure that business targets are met
Strong ability to lead, challenge and positively influence in an interactive team environment
Demonstrated ability to work on own initiative and proactively respond to business needs
Problem identification and solving skills plus experience with technology transfer would be an advantage

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!

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