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.
What You Will Achieve
In this role, you will:
* Serve as a key resource and potentially lead lower levels within your area of expertise.
* Manage personal time and professional development, taking accountability for results and prioritizing workflow, possibly leading and allocating work to others.
* Contribute to project and departmental tasks, providing direction and training to team members, and may be designated as a lead worker.
* Be recognized as a lead or subject matter expert, proactively identifying and resolving potential problems with basic complexity.
* Complete assignments independently, selecting the most appropriate methods, and ensuring team assignments are completed.
* Review non-standard work for sound technical judgment and may review the work of others.
* Adhere to Pfizer standards, guidelines, and values, influencing teams, and providing input on departmental standards and guidelines, while training others.
* Conduct analysis on in-process tests, intermediates, and APIs in accordance with Current Good Manufacturing Practices.
* Execute and document Analytical Method Transfer Exercises for products transitioning from the legacy facility, ensuring compliance with site standards and regulatory guidelines.
* Maintain good laboratory practices, assist in creating quality procedures and reports, facilitate laboratory investigations, and support Lean/Agile implementation through continuous improvement activities.
Here Is What You Need (Minimum Requirements)
* 2+ years of experience
* Certification in assigned area if applicable
* Relevant experience in a technical role in a pharmaceutical/healthcare laboratory
* Proven experience with analytical techniques including ICC methods such as bioassay, cell culture, PCR, mycoplasma, immunoassays or mycoplasma testing
* Previous relevant microbiological experience within a QC Good Manufacturing Practices (also cGMP) laboratory in a Pharmaceutical/Biotechnology company
* Strong knowledge of analytical techniques both theoretical and practical
* Excellent interpersonal and communication skills
* Detail-oriented, quick at decision making, self-motivated with good troubleshooting and problem-solving abilities
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
* Strong organizational skills and the ability to manage multiple priorities
* Ability to work effectively in a team environment
* Strong analytical and critical thinking skills
* Ability to adapt to changing priorities and manage time effectively
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