Use Your Power for Purpose

Every day, everything we do is driven by an unwavering commitment to delivering safe and effective products to patients. Our flexible, innovative, and customer-oriented quality culture is rooted in science and risk-based compliance. Whether you are engaged in development, maintenance, compliance, or analysis through research programs, your contribution will have a direct impact on patients. Our dedication to quality and safety ensures that we consistently meet the highest standards, making a meaningful difference in the lives of those we serve. Join us in our mission to improve patient outcomes through excellence in every aspect of our work.

What You Will Achieve

• Serve as a key resource and potentially lead lower-level team members within your area of expertise.
• Manage personal time and professional development, taking accountability for your results and prioritizing workflow.
• Contribute to project and departmental tasks, providing direction and training to team members, and may act as a lead worker.
• Be recognized as a "LEAD" or "Subject Matter Expert" in your field.
• Proactively identify and resolve basic complexity problems, considering wider implications.
• Complete assignments independently, selecting appropriate methods, and ensuring team assignments are completed.
• Review non-standard work for technical soundness and may review others' work.
• Adhere to Pfizer standards, guidelines, and values, influencing teams, and contributing to the development of departmental standards and guidelines.
• Provide input for performance assessments, ensure timely and compliant documentation, and develop processes to enhance cGMP standards.
• Maintain high standards of safety and housekeeping, participate in Continuous Improvement projects, and ensure adherence to all policies and procedures, while providing training and conducting peer reviews.

Here Is What You Need

• Bachelor's Degree in Life Sciences field
• Having obtained your last academic title related to the role up to 3 years ago
• Experience with laboratory equipment and procedures in quality control
• Knowledge of Good Manufacturing Practices (cGMP) and Good Laboratory Practices (GLP)
• Ability to write clear technical documents
• Pharmaceutical quality control and stability experience is a plus

  
#LI-PFE

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.

Flexibility  

We aim to create a trusting, flexible workplace culture which encourages employees to achieve work life harmony, attracts talent and enables everyone to be their best working self. Let’s start the conversation!  

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!

Se valorarán las candidaturas que puedan aportar certificados oficiales de discapacidad.

Las únicas localizaciones disponibles para nuevos empleados serán Madrid, y Barcelona de forma excepcional para algunas funciones específicas.

Quality Assurance and Control