Instrumentation & Controls Technician

Research & Development - Instrumentation & Controls Technician

Use Your Power for Purpose

Join Pfizer as an Associate Engineer- Instrumentation & Controls Technician, where your work will have a profound impact on improving patients' lives. Patients rely on you to deliver when it counts, by engaging in the design and optimization of manufacturing processes or by ensuring the upkeep and reliability of our production systems. Your technical expertise is crucial in ensuring our customers and patients receive the medicines they require, precisely when they need them. Collaborating with our forward-thinking engineering team, you will accelerate the distribution of medicines worldwide by envisioning possibilities and translating them into actionable solutions. Your role is essential in enhancing manufacturing production systems, aiming to boost success rates while ensuring seamless, zero-downtime operations. By melding manufacturing process expertise, operational knowledge, and equipment control with robust data systems, you will enforce a harmonious sequence of operations across diverse departments. Your dedication and sharp focus are key to propelling Pfizer toward new achievements and extending healthcare breakthroughs to patients around the world.

In this role, you will:

• Provide day-to-day support for a clinical drug product manufacturing facility utilizing automated vial filling systems and drug formulation equipment.
• Deploy and test automated systems and equipment while adhering to Good Manufacturing Practices (GMP) and executing verification protocols.
• Support process equipment during Installation, Startup, Commissioning, Qualification, and Operation throughout its lifecycle.
• Support Facility Acceptance Testing (FAT) and Site Acceptance Testing (SAT) of new equipment, including wiring diagram reviews, control panel inspections, and device testing.
• Troubleshoot electrical, mechanical, and instrumentation issues encountered during operations.
• Provide critical support for automation systems, monitoring issues and developing preventative solutions.
• Contribute to project tasks and milestones by organizing work to meet deadlines.
• Support generation of maintenance plans, safety assessments, and vendor-based maintenance/calibration activities, including LOTO plans and equipment maintenance work instructions.
• Develop Preventive Maintenance Procedures, critical spare parts lists, PM schedules, and Local Work Instructions (LWI).
• Maintain a safe work environment and safety culture in the facility.
• Document troubleshooting efforts in the Computer Maintenance Monitoring System (CMMS).
• Support manufacturing investigations as needed.
• Collaborate with Clinical Manufacturing Technology teammates, Technical Services, Operations, Quality, and other engineering departments.
• Some domestic and international travel may be required.

Here Is What You Need (Minimum Requirements)

• Applicant must have a bachelor's degree with 0+ years of experience; OR an associate's degree with 4 years of experience; OR a high school diploma (or equivalent) and 6 years of relevant experience.
• Thorough understanding of and experience working in an aseptic fill/finish environment during GMP operations.
• Working knowledge of operating high speed production systems and associated support equipment.
• Hands on knowledge of instrumentation, calibration, control panels, control valves, analytical equipment, PLCs (Programmable Logic Controllers), variable frequency drives, and SCADA (Supervisory Control and Data Acquisition)/HMI systems.
• Strong organizational skills to manage multiple projects and meet deadlines.
• Excellent oral and written communication skills for effective collaboration with diverse stakeholders (clients, management, staff, and contractors).
• Ability to blend safe work practices with technical acumen to drive innovation and efficiency.
• Experience executing verification protocols and adhering to GMP standards.

Bonus Points If You Have (Preferred Requirements):

• Engineering background within the pharmaceutical industry.
• Experience with solution formulations.
• Experience with advanced automation systems and process control.
• Familiarity with Preventive Maintenance Procedures development.
• Strong problem-solving skills and ability to make informed decisions.
• Adaptability and willingness to learn new technologies and processes.
• Strong analytical skills for data-driven decision-making.
• Ability to work independently and take initiative.
• Effective time management skills to prioritize tasks efficiently.

  
 

PHYSICAL/MENTAL REQUIREMENTS

Lifting, standing, sitting, bending are all required for the role, experience with tools and instruments used for the role, knowledge of high-speed production equipment, ability to understand and follow Standard Operating Procedures (SOPs) in a GMP environment.

NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS

Aseptic Gowning required

Off-shift work may be required to ensure production schedules are maintained

Occasional domestic and international travel may be required.

Work Location Assignment: On Premise

The annual base salary for this position ranges from $68,600.00 to $110,900.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 7.5% of the base salary. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.

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

EEO & Employment Eligibility

Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status.  Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA.  Pfizer is an E-Verify employer.  This position requires permanent work authorization in the United States.

Pfizer endeavors to make www.pfizer.com/careers accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email disabilityrecruitment@pfizer.com. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.

Engineering