Use Your Power for Purpose
At Pfizer, we believe that every role contributes to our mission of improving patients' lives. Whether you are involved in the design and development of manufacturing processes for products or supporting the upkeep of systems, engineering is crucial to ensuring customers and patients receive the medicines they need. By collaborating with our forward-thinking engineering team, you'll play a pivotal role in accelerating the delivery of medicines to the world.
What You Will Achieve
- Provide direct production support during commercial operations via expertise of process equipment and systems, manufacturing operations, and automation control (Delta V, PLC, etc).
- Additional services include review of process requirements and evaluation of equipment and systems to ensure deliverables meet or exceed process specifications and manufacturing requirements. Will provide technical guidance and systems and automation training to production colleagues. Provides controls/automation technical engineering support of cGMP clinical and / or commercial manufacturing processes and equipment working with the Manufacturing Area Leads.
- Analyzes equipment and process issues and supports related investigations.
- Advise management of non-conformance issues and opportunities for continuous improvement via data trend analysis, interpretation of data, gap analysis and implementation of corrective activities.
- Provides input on decisions for SOP's, batch records, forms or other cGMP related documents developed or revised to support continuous improvement efforts, investigation corrective actions, process descriptions, manufacturing operations, automation control (DeltaV, etc.) and regulatory audit commitments.
- Evaluates new processes for commercial / clinical production in Train 5. This includes facility fit analysis and direct input into tech transfer documentation. This may also include new capital equipment purchases and implementation of new technologies.
- Conducts all activities and makes decisions that are in accordance with Company policies & SOPs, Pfizer Values, & global regulatory guidelines (including cGMP/cGLP/cGCP), environmental guidelines, as appropriate, etc.
Here Is What You Need (Minimum Requirements)
- Applicant must have a Bachelor's degree in Chemical Engineering, Electrical Engineering / Science (or related fields), Biomedical Engineering is required with at least 2 years of experience in an FDA regulated industry OR Master's degree in Chemical Engineering, Electrical Engineering / Science (or related fields), Biomedical Engineering is required. with more than 0 years of experience in an FDA regulated industry OR an Associate's degree with 6 years of experience in an FDA regulated industry, OR High School Diploma (or Equivalent) and 8 years of relevant experience in an FDA regulated industry.
- Prior experience with Distributed Control Systems is required .
- Knowledge of scientific principles, operational and design aspects of production equipment, automation control systems, and processing requirements.
- Experience with writing software test plans, user requirements, computer systems validation, and system design documents.
- Demonstrated ability to interact effectively with colleagues at all levels of the organization to keep customers, peers, and area management up to date with progress of all projects to ensure automation activities are completed in a timely manner and on schedule.
Bonus Points If You Have (Preferred Requirements)
- Understanding of programming and proficiency in at least one language.
- Broad understanding of systems architecture and operations and related components (e.g. hardware, software, network, database, S88/S95 etc.).
- Experience in general GMP operations, single-use technology and tech transfer.
Physical / Mental requirements
- Ability to stand for extended periods of time on manufacturing floor. Ability to perform mathematical calculations and ability to perform complex data analysis.
Non-Standard work schedule, travel or environment requirements
- Adhere to safe work practices dependent on the manufacturing area (aseptic gowning).
- Ability to work off-hours shifts (2nd or 3rd shifts) on a rotating basis as applicable to support processing needs.
Other job details
- Last day to apply: Feb 18th, 2025
- Relocation Support available
- Employee Referral eligible
- Work Location Assignment: On Premise
The annual base salary for this position ranges from $80,300.00 to $133,900.00. In addition, this position is eligible for participation in Pfizer's Global Performance Plan with a bonus target of 10.0% 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.
Sunshine Act
Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care provider's name, address and the type of payments or other value received, generally for public disclosure. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.
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.
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What We Do
Our purpose ensures that patients remain at the center of all we do. We live our purpose by sourcing the best science in the world; partnering with others in the healthcare system to improve access to our medicines; using digital technologies to enhance our drug discovery and development, as well as patient outcomes; and leading the conversation to advocate for pro-innovation/pro-patient policies.
Why Work With Us
We are the inventors, the problem solvers, the big thinkers — those who surmount any hurdle to deliver breakthrough medicines to the people who are counting on them the most.
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