Use Your Power for Purpose

Pfizers purpose is to deliver breakthroughs that change patients lives. At the core of fulfilling this mission is Research and Development where we translate advanced science and technologies into the therapies and vaccines that matter most. You will play a crucial role in this mission leveraging cutting-edge design and process development capabilities to accelerate and deliver best-in-class medicines to patients globally. Your work will directly impact improving patients lives while working at Pfizer ensuring drug safety and efficacy and supporting clinical trials.

What You Will Achieve

In this role you will:

• Ensure equipment is managed in accordance with governing procedures.

• Review completed equipment-related tasks in the CMMS (computerized maintenance management system).

• Launch change control records for document and/or equipment changes.

• Address equipment alarms such as for temperature excursions including moving material to alternate storage unit and assist in alarm investigations.

• Assist Equipment System Owners with purchasing equipment.

• Assist Equipment System Owners with periodic reviews of equipment and software.

• Perform equipment logbook reviews.

• Coordinate with Facilities for scheduling calibration maintenance and repairs.

• Evening weekend and/or on-call work may be required.

• May take lead role for some equipment periodic reviews.

• May take lead role for some equipment change control records.

• May assist with samples management including but not limited to physical sample/material handling shipping/receiving maintaining chain of custody and routine maintenance/cleaning of biosafety cabinets freezers and refrigerators.

• Apply the principles of good manufacturing practices (GMP) on a daily basis.

• Create and revise standard operating procedures (SOPs) and other documents as needed.

• Identify and participate in continuous improvement projects.

• Maintain training to current standards and procedures on all assigned curriculums.

• Fully comply with company health and safety procedures and practices.

• Author and own deviations as needed.

• Train other personnel.

Here Is What You Need

(Minimum Requirements)

• High School Diploma or GED with 4 years of relevant experience

• Demonstrated analytical laboratory experience in a Good Manufacturing Practices (also cGMP) regulated environment

• Ability to troubleshoot analytical methods

• Proficiency in entering computerized data

• Experience working with simple scientific equipment

Bonus Points If You Have

(Preferred Requirements)

• Demonstrated proficiency in computerized systems (Experience and use of Laboratory Information Management System)

• Strong problem-solving skills

• Excellent communication skills both written and verbal

• Ability to work effectively in a team environment

• Strong attention to detail

• Experience with advanced laboratory techniques

• Ability to adapt to changing priorities and manage multiple tasks

• Strong organizational skills

PHYSICAL/MENTAL REQUIREMENTS

N/A

Work Location Assignment:On Premise

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