Use Your Power for Purpose

As a Senior Tech Ops Engineer you will play a crucial role in improving patients lives while working at Pfizer. Your contributions will directly impact the development and delivery of innovative solutions that enhance the quality of life for patients worldwide. Join us in our mission to bring breakthroughs that change patients lives.

The Sr Tech Ops Engineer provides strategic direction and technical expertise for site Commissioning and Qualification (C&Q) activities for equipment utilities and facilities. To include execution of C&Q work for utilities facilities and global applications as well as maintenance and execution of periodic performance qualification schedule and reviews. This role serves as a Center of Excellence driving alignment with global and industry engineering standards. The engineer supports site critical programs related to C&Q while also supporting capital project execution and site-wide technical initiatives. The position plays a key role in shaping the sites technology roadmap ensuring operational excellence and fostering a self-sustaining technical work structure for the Focus Factory Manufacturing Technology teams.

What You Will Achieve

In this role you will:

• S/he acts as the SME for C&Q work for Utilities Facilities and Equipment across the site. Individual must have knowledge and application experience of technical design reviews commissioning and qualification for pharmaceutical systems.

• S/he will be expected to work routinely with cross functional groups throughout the site for process improvements and implementation. S/he must have a solid understanding and knowledge of pharma regulations and cGMP principals and demonstrated ability to apply knowledge to process improvements and changes. Person will be responsible for interfacing with auditors and presenting on site processes.

• S/he organizes coordinates and supports testing associated with the development of new process technologies and the support of new systems introductions. S/he works closely with site Quality and Engineering resources to ensure appropriate C&Q of site systems is achieved and maintained against procedures and industry guidance. S/he plans generates reviews and approves site technical reports to include validation plans/protocols design specs Risk Assessments.

• S/he will be expected to ensure site alignment to global procedures and work instructions related to C&Q work. Provide ongoing training guidance and templates to support the technical teams within the Focus Factories.

• S/he will be expected to confirm C&Q pre-requisites are met and supported by approved documentation in accordance with procedures and industry standards. Oversee and assist team members and contractor resources with their assigned projects. Support development and design of C&Q strategies studies draft and/or review project validation plans and documentation.

• S/he to provide input in technology transfer risk assessments validation deviations and/or quality deviation investigations to identify root causes and define correction and/or preventive actions (CAPA). Author and/or review risk assessment documents. Review investigations commitments procedures and batch records. Provide technical input and complete SME impact assessment to proposed change controls vetted for implementation. Participate in teams assembled to complete change control implementation for new and existing systems.

Here Is What You Need

(Minimum Requirements)

• Applicant must have a bachelors degree with at least 2 years of experience; OR a masters degree with 0 years of experience; OR an associates degree with 6 years of experience; OR a high school diploma (or equivalent) and 8 years of relevant experience

• Solid knowledge/understanding of C&Q strategies

• Understanding of various pharmaceutical equipment utility and facility systems preferably related to sterile injectable operations.

• Solid leadership organizational planning and project management skills in addition to technical knowledge is required to work with multi-disciplinary teams.

• Must be self-motivated and work with little direction

• Good interpersonal effectiveness and communication skills (written and oral) are required in order to interface across management levels and departments.

• An aptitude for understanding process technology and controls applications decision making ability and excellent oral and written communication skills are essential. Demonstrated ability to interact effectively with multiple levels of the organization. Candidate must possess flexibility to respond to changing conditions and priorities.

• Understanding of global regulations on GMP processes.

Bonus Points If You Have

(Preferred Requirements)

• Technical writing experience.

• Experience with pharmaceutical industry validation/qualification of pharmaceutical processes equipment utilities facilities and/or computer systems as related to sterile products and medical devices.

• Working knowledge of Food and Drug Administration (FDA) Regulations/Guidance and Good Manufacturing Practices (GMP).

• Ability to work both independently and in partnership with others; proven ability to use initiative and drive to achieve results.

PHYSICAL/MENTAL REQUIREMENTS

• Remains organized & positive in ambiguous and fast-paced rapidly changing environment

• Flexible and adaptable to changing priorities meeting deadlines and working well under pressure.

• Ability to process complex information and make recommendations with incomplete data set

• Ability to adjust work schedule to meet business needs overtime off shift weekends.

• Ability to travel

• Able to stand for extended hours for test runs and performance monitoring of processes will include working within special gowning for cleanroom access

• Able to climb ladders/steps

• Able to lift items of 25lbs

• Strategic thinker for issue resolution

NON-STANDARD WORK SCHEDULE TRAVEL OR ENVIRONMENT REQUIREMENTS

Pfizer operates 24/7 across most of the business units. Employee must have the ability to work extended hours holidays and/or weekends as needed. Limited travel may be required to support OEM equipment design reviews and/or Factory Acceptance Testing of new equipment. Employee will be expected to periodically work within clean room areas requiring special gowning.

Work Location Assignment:On Premise

Relocation assistance may be available based on business needs and/or eligibility.