Analytical Scientist

Analytical Scientists for Analytical Research & Development at the Ringaskiddy Clinical Manufacturing Facility, Cork
Why Patients Need You
Pfizer's purpose is to deliver breakthroughs that change patients' lives.
Research and Development is at the heart of fulfilling Pfizer's purpose as we work to translate advanced science and technologies into the therapies and vaccines that matter most.
In Analytical Research & Development you will apply innovative measurement science, data analytics and process development capabilities to accelerate and bring the best-in-class medicines to patients around the world.
What You Will Achieve
As a Scientist in Analytical Research and Development, you will take an active role in supporting drug development by applying a variety of analytical methodologies to support development and manufacture of clinical drug substances.
You will have working knowledge and ability to operate analytical techniques such as chromatography and spectroscopy and be involved in the application of process analytical technology for clinical manufacturing.
You will also be involved in method transfer activities in and out of the RCMF analytical lab and collaborate across various teams within Pfizer.
Responsibilities
Perform laboratory work in support of analytical testing of pharmaceutical projects with some experience in any of the following analytical methodologies: chromatography, KF, spectroscopy or mass spectrometry.
Responsibilities may include running analytical methods, testing and release of raw materials and intermediates to support pharmaceutical development efforts, documentation of experimental results.
In-process control (IPC) support for plant operations
Method Development and testing to support cleaning of production facility.
Involvement in methods transfers to and from the RCMF facility.
Development, Verification and Validation of analytical methods across a range of techniques (HPLC, UPLC, GC, UV, KF, IR, SFC, MS)
Demonstrate proficiency with a wide variety of software and information systems.
Review and verify scientific experiments and data documented in electronic laboratory notebooks.
Provide analytical support for Process Analytical Technology (PAT) in the lab and for manufacturing for batch and continuous processes across a range of techniques such as Mid-IR, UV, FBRM, Online LC.
Effectively interact with project team members for various tasks including presentation of data and critical review of data and preparation of technical reports.
The colleague must be able to interact effectively with peers and leaders as part of a multi-disciplinary team and thrive in a fast-paced environment.
Demonstrated attention to detail, strong organizational skills, the ability to multitask and meet project timelines.
Qualifications
Must-Have
BSc with 4+ years, MSc with 2+ years or a PhD with 0+ years relevant analytical experience either in a GMP lab environment, or an academic or industrial research lab.
Experience in the use of general analytical techniques e.g HPLC, GC, KF, IR and UV
Ability to meet project milestones under general supervision, plan and manage priorities for specific projects.
Experience in problem-solving skills and instrument troubleshooting.
Demonstrated oral and written communication skills, including visualization of data and drafting reports.
Experience with a wide variety of software and information systems (e.g.
electronic lab notebooks, Empower and LIMS).
Relevant analytical development and/or GMP experience
Ability to work in a team environment in GMP laboratory environment performing experiments
Ability to perform data analysis, record results in electronic lab notebooks and effectively communicate in a team environment.
Ability to adhere to safe laboratory practices
Good documentation skills with high attention to detail, strong organizational skills, team oriented, effective interpersonal and communication skills.
Nice-to-Have
Experience in analytical method transfers
Experience in a GMP laboratory
Knowledgeable in vibrational spectroscopy (NIR, IR, Raman, UV-Vis)
Process Analytics (PAT) experience including PAT installation and set-up within a manufacturing facility
NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS
Do not anticipate more than 10% travel.
Must be open to support shift work when required
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.
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.
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
Analytical Scientists for Analytical Research & Development at the Ringaskiddy Clinical Manufacturing Facility, Cork
Why Patients Need You
Pfizer's purpose is to deliver breakthroughs that change patients' lives.
Research and Development is at the heart of fulfilling Pfizer's purpose as we work to translate advanced science and technologies into the therapies and vaccines that matter most.
In Analytical Research & Development you will apply innovative measurement science, data analytics and process development capabilities to accelerate and bring the best-in-class medicines to patients around the world.
What You Will Achieve
As a Scientist in Analytical Research and Development, you will take an active role in supporting drug development by applying a variety of analytical methodologies to support development and manufacture of clinical drug substances.
You will have working knowledge and ability to operate analytical techniques such as chromatography and spectroscopy and be involved in the application of process analytical technology for clinical manufacturing.
You will also be involved in method transfer activities in and out of the RCMF analytical lab and collaborate across various teams within Pfizer.
Responsibilities
Perform laboratory work in support of analytical testing of pharmaceutical projects with some experience in any of the following analytical methodologies: chromatography, KF, spectroscopy or mass spectrometry.
Responsibilities may include running analytical methods, testing and release of raw materials and intermediates to support pharmaceutical development efforts, documentation of experimental results.
In-process control (IPC) support for plant operations
Method Development and testing to support cleaning of production facility.
Involvement in methods transfers to and from the RCMF facility.
Development, Verification and Validation of analytical methods across a range of techniques (HPLC, UPLC, GC, UV, KF, IR, SFC, MS)
Demonstrate proficiency with a wide variety of software and information systems.
Review and verify scientific experiments and data documented in electronic laboratory notebooks.
Provide analytical support for Process Analytical Technology (PAT) in the lab and for manufacturing for batch and continuous processes across a range of techniques such as Mid-IR, UV, FBRM, Online LC.
Effectively interact with project team members for various tasks including presentation of data and critical review of data and preparation of technical reports.
The colleague must be able to interact effectively with peers and leaders as part of a multi-disciplinary team and thrive in a fast-paced environment.
Demonstrated attention to detail, strong organizational skills, the ability to multitask and meet project timelines.
Qualifications
Must-Have
BSc with 4+ years, MSc with 2+ years or a PhD with 0+ years relevant analytical experience either in a GMP lab environment, or an academic or industrial research lab.
Experience in the use of general analytical techniques e.g HPLC, GC, KF, IR and UV
Ability to meet project milestones under general supervision, plan and manage priorities for specific projects.
Experience in problem-solving skills and instrument troubleshooting.
Demonstrated oral and written communication skills, including visualization of data and drafting reports.
Experience with a wide variety of software and information systems (e.g.
electronic lab notebooks, Empower and LIMS).
Relevant analytical development and/or GMP experience
Ability to work in a team environment in GMP laboratory environment performing experiments
Ability to perform data analysis, record results in electronic lab notebooks and effectively communicate in a team environment.
Ability to adhere to safe laboratory practices
Good documentation skills with high attention to detail, strong organizational skills, team oriented, effective interpersonal and communication skills.
Nice-to-Have
Experience in analytical method transfers
Experience in a GMP laboratory
Knowledgeable in vibrational spectroscopy (NIR, IR, Raman, UV-Vis)
Process Analytics (PAT) experience including PAT installation and set-up within a manufacturing facility
NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS
Do not anticipate more than 10% travel.
Must be open to support shift work when required
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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