Manufacturing Process Engineer III

3 weeks ago


Andover, United States Pfizer Full time

Why Patients Need You

Whether you are involved in the design and development of manufacturing processes for products or supporting maintenance and reliability, engineering is vital to making sure customers and patients have the medicines they need, when they need them. Working with our innovative engineering team, you'll help bring medicines to the world even faster by imagining what's possible and taking action.

What You Will Achieve

Working with Pfizer's dynamic engineering team, you will play a critical role in developing and modifying process equipment, automation and controls to meet desired quality standards. Your production engineering skills will help in recommending and implementing improvements, modifications or additions that will help in solving problems.

As an Engineer III, your focus on this job will contribute to achieving project tasks and goals. It is your domain knowledge, commitment, collaboration and dedication that will help us achieve new milestones and patients across the globe.

How You Will Achieve It

  • Provide on the floor shift support to accommodate all manufacturing hours. This could be rotating A/B shifts or Sun-Wed and Wed-Sat support model (4 - 10 hour days weekly)

  • Provide engineering and technical support related to the operation and maintenance of process / automated equipment and systems within a biopharmaceutical manufacturing facility.

  • This may include production equipment such as bioreactors, fermenters, ultrafiltration skids, Clean - In - Place (CIP) skids, and other support equipment.

  • Tasks may include but not be limited to the support of installation, startup/commissioning, testing, and qualification of new equipment or modification of existing equipment.

  • Support the maintenance department as needed

  • Support all investigations and audits as needed

  • Provide off-shift and on call support when necessary

  • Support tech transfer and changeover for commercial and clinical processes.

  • Support reliability engineering for production and support equipment

  • Support the design and qualification of improvements, changes, or upgrades to this equipment as needed

  • Support the development of design and startup documents such as commissioning plans, User Requirement Specification (URS), Functional Requirement Specification (FRS), Configuration Specification (CS)

  • Support the development of validation and qualification documents

  • Provide the execution of commissioning and qualification activities

  • Provide equipment maintenance history review

  • Support process and component improvement projects as needed

Qualifications

Must have:

  • Applicant must have a High School Diploma (or Equivalent) and 8 years of relevant experience OR an Associate's degree with 6 years of experience OR a Bachelor's in Engineering with at least 3 years of experience OR Master's in Engineering with more than 1 year of experience.

  • The experience required for the role could be on any of the following industries: Computer Science, Chemical, Electrical, Mechanical or Pharmaceutical

  • Instrument and Controls (I&C) troubleshooting experience

  • Candidate must be able to work across functional areas such as operations, maintenance, quality and regulatory.

  • Good communication skills, verbal and written, are required.

  • Knowledge of working with computers and associated applications such as MS Word, Excel, Powerpoint are recommended.

Nice-to-Have:

  • GMP/GLP experience a Plus

  • Knowledge of database applications, Allen-Bradley PLC, GE iFix and iHistorian preferred technical writing and document review

  • Familiarity of automation network, such as Ethernet, DH+, ControlNet, etc

  • Knowledge of database applications and AutoCAD are a preferred

Other job details

  • Last day to apply: September 5th, 2024

  • Employee Referral Bonus eligible

  • Relocation support available

Work Location Assignment:On Premise

The annual base salary for this position ranges from $78,000.00 to $130,000.00. 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.

Engineering

#LI-PFE



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