Process Engineering Associate (Upstream)

Posted 20 Hours Ago
Be an Early Applicant
Washington, MI
Hybrid
65K-111K Annually
Junior
Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical
We’re in relentless pursuit of breakthroughs that change patients’ lives.
The Role
As a Process Engineering Associate, you will assist in the transition of products from research to manufacturing, ensuring the technology transfer process is smooth and efficient. Responsibilities include maintaining documentation, supporting manufacturing processes, conducting tests, and troubleshooting equipment issues to ensure consistent production performance.
Summary Generated by Built In

Why Patients Need You
Pfizer's North Creek Manufacturing Facility is clinical and commercial biologics manufacturing facility producing antibody and antibody drug conjugates for life-altering cancer treatments.
What You Will Achieve
The North Creek facility is seeking a highly motivated Process Engineering Associate (Manufacturing) that desires an opportunity to contribute to the design and development of clinical and commercial manufacturing processes of transformative cancer therapies. This role focuses on support activities involved the technology transfer from research to manufacturing and production support. Design and development may include new or revised processes.
The ideal candidate will have fundamental knowledge of the principles of upstream process engineering and/or production experience in a GMP manufacturing environment and apply these skills to achieve assigned tasks. This role also requires great teamwork and collaboration to ensure an efficient way of working and maintain high level productivity, have can-do attitude, and thrive in a high-paced environment
How You Will Achieve It

  • Play a pivotal role in transitioning products from research to manufacturing, leveraging technical skills to address challenges.
  • Assist in the transfer of processes into the North Creek facility and ensure technical responsibilities for new product introduction and resupply campaigns, such as: process modeling, material planning, manufacturing documentation, and other technical responsibilities are completed.
  • Contribute to project tasks and milestones, ensuring work is organized to meet deadlines.
  • Conduct tests and measurements throughout production stages, troubleshooting process or equipment issues.
  • Prepare and review scale-up protocols, technology transfer protocols, batch manufacturing records, and bill of materials.
  • Maintain process data to ensure consistent process performance.
  • Support deviation investigations, CAPAs, and change controls.


Qualifications
Must-Have

  • Applicant must have a bachelor's degree in Chemical or Biotech Engineering, Computer Science, or related life science engineering with 2 years of experience.
  • Fundamental knowledge of upstream operations.
  • Demonstrated knowledge and experience with Good Manufacturing Practices and Process Monitoring systems.
  • Must be capable of generating documents in Microsoft Word, Excel, PowerPoint, and Visio.
  • Strong communication skills
  • Self-motivated attitude with the ability to work with minimal direction
  • Flexibility and adaptability to changing priorities
  • Ability to meet deadlines and perform well under pressure
  • Proficiency in troubleshooting and problem-solving


Nice-to-Have

  • Prior experience in the pharmaceutical industry with GMP manufacture of recombinant antibody and high-potency antibody drug conjugate production processes
  • Knowledge of upstream equipment and operations, and engineering principles related to biotherapeutic drug substance, including disposable technologies.
  • Experience with technology transfer and scale-up processes
  • Strong attention to detail
  • Ability to navigate complex challenges and opportunities
  • Experience in a structured, process-driven environment


PHYSICAL/MENTAL REQUIREMENTS

  • Lifting, standing, gowning in cleanroom.
  • Requires good math skills, basic lab chemistry calculations, working with MS Excel.


NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS

  • May require travel from time to time.
  • Work Location Assignment: Hybrid


Other Details:

  • Last day to apply: January 15, 2025


The annual base salary for this position ranges from $64,600.00 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.
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

Top Skills

Biotech Engineering
Chemical Engineering
Computer Science

What the Team is Saying

Daniel
Anna
Esteban
The Company
HQ: New York, NY
121,990 Employees
Hybrid Workplace
Year Founded: 1848

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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