Process Scientist

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.
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Background:
The technical services team are seeking an experienced process scientist whose role will focus on supporting commercial manufacturing and technology transfers to the drug substance small and/or large-scale manufacturing facility.
This role will be located at the Pfizer Grange Castle site.
The drug substance facility is a multiproduct manufacturing area specialising in the manufacture of therapeutic proteins derived from mammalian cell culture for a range of clinical and commercial products.
This position will report to the drug substance technical services lead and will be an integral part of a high performing technical services team whose role will involve:
Support commercial manufacturing to meet commercial requirements including investigations, process robustness and process improvements.
Scale up of mammalian cell culture processes from bench and pilot scale to a pilot & large-scale manufacturing facility.
Perform, present and execute facility fits, mass balance generation, equipment sizing, gap assessments and mitigation of operational challenges foreseen to ensure an equivalent process is transferred to Grange Castle
Provide independent decision making for strategic input into facility and equipment design
Prepare, review & execute technology transfer protocols, supporting documentation, design of experiments and at scale process trials to deliver an efficient technology transfer
Author and review responsible sections of regulatory dossiers including health authority query responses
Partners with the management and technical team to identify best practices, technical transfer efficiencies and optimisations during technical transfer.
Develops and maintains effective working relationships with other division groups supporting technology transfer, validation and process support.
Requirements
:
Minimum of 3 - 6 years of mammalian cell culture process development/ late-stage characterisation and technical transfer / technical services experience in stainless steel and/or single use facilities
Demonstrated history and in-depth knowledge of cell culture scale up practices, technical transfer, facility fit, equipment sizing and mass balance generation for clinical/ commercial manufacture
Knowledge and experience of process validation strategies, studies and requirements
Knowledge of regulatory submissions and response of queries from health authorities
In depth knowledge of cGMP regulatory requirements related to the design and control of drug substance processes
Skills
:
High technical capability, interpret complex data, problem solving and technical learning.
Promote information sharing and excellent interpersonal skills
Capability of working in a multi-disciplinary team environment to tight timelines
Effective communication, planning and organisation skills to deliver documentation.
Background:
The technical services team are seeking an experienced process scientist whose role will focus on supporting commercial manufacturing and technology transfers to the drug substance small and/or large-scale manufacturing facility.
This role will be located at the Pfizer Grange Castle site.
The drug substance facility is a multiproduct manufacturing area specialising in the manufacture of therapeutic proteins derived from mammalian cell culture for a range of clinical and commercial products.
This position will report to the drug substance technical services lead and will be an integral part of a high performing technical services team whose role will involve:
Support commercial manufacturing to meet commercial requirements including investigations, process robustness and process improvements.
Scale up of mammalian cell culture processes from bench and pilot scale to a pilot & large-scale manufacturing facility.
Perform, present and execute facility fits, mass balance generation, equipment sizing, gap assessments and mitigation of operational challenges foreseen to ensure an equivalent process is transferred to Grange Castle
Provide independent decision making for strategic input into facility and equipment design
Prepare, review & execute technology transfer protocols, supporting documentation, design of experiments and at scale process trials to deliver an efficient technology transfer
Author and review responsible sections of regulatory dossiers including health authority query responses
Partners with the management and technical team to identify best practices, technical transfer efficiencies and optimisations during technical transfer.
Develops and maintains effective working relationships with other division groups supporting technology transfer, validation and process support.
Requirements
:
Minimum of 3 - 6 years of mammalian cell culture process development/ late-stage characterisation and technical transfer / technical services experience in stainless steel and/or single use facilities
Demonstrated history and in-depth knowledge of cell culture scale up practices, technical transfer, facility fit, equipment sizing and mass balance generation for clinical/ commercial manufacture
Knowledge and experience of process validation strategies, studies and requirements
Knowledge of regulatory submissions and response of queries from health authorities
In depth knowledge of cGMP regulatory requirements related to the design and control of drug substance processes
Skills
:
High technical capability, interpret complex data, problem solving and technical learning.
Promote information sharing and excellent interpersonal skills
Capability of working in a multi-disciplinary team environment to tight timelines
Effective communication, planning and organisation skills to deliver documentation.
Work Location Assignment:Hybrid
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
Engineering
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