Senior Associate Scientist Chem - Analytical (R)

Posted 4 Hours Ago
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Groton, CT, USA
In-Office
69K-114K Annually
Senior level
Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical
We’re in relentless pursuit of breakthroughs that change patients’ lives.
The Role
Provide technical PAT support in GMP solid oral dose manufacturing: manage, install, calibrate, and troubleshoot NIR and FBRM instruments; monitor outputs via APC software and real-time dashboards; author SLC/SOPs and technical reports; analyze data and collaborate cross-functionally to support manufacturing campaigns and process improvement.
Summary Generated by Built In
Use Your Power for Purpose
At Pfizer, our purpose is to deliver breakthroughs that change patients' lives. As a Senior Associate Scientist, you will be at the forefront of this mission, working within our Research & Development division. Your role will be pivotal in translating advanced science and technologies into therapies and vaccines that matter most. By leveraging cutting-edge design and process development capabilities, you will help accelerate the delivery of best-in-class medicines to patients globally, ultimately improving their lives.
What You Will Achieve
As a Senior Associate Scientist - PAT Specialist, you will be a key member of the cross-functional PCMM (Pfizer Continuous Manufacturing Module) team, providing technical expertise for Process Analytical Technology (PAT) instrumentation within a clinical solid oral dose GMP manufacturing environment. You will provide analytical support to manufacturing campaigns, manage & maintain analytical instrumentation, and contribute to the development and continuous improvement of drug product manufacturing processes. Your role will blend hands-on instrument management with analytical method development, data analysis, and cross-team collaboration.
In this role, you will:
  • Manage and maintain PAT analytical instrumentation (e.g., NIR, FBRM Instruments, APC Software) for manufacturing campaigns, including preparation, installation, calibration, and performance checks.
  • Monitor instrumentation output during campaigns using advanced process control software & real-time dashboards & analytics.
  • Author and maintain system life cycle (SLC) documentation, standard operating procedures (SOPs), and technical reports.

  • Effectively interact with project team members for various tasks including presentation of data and critical review of data and preparation of technical reports.
  • Demonstrate proficiency with a wide variety of software and information systems.
  • Interact effectively with peers and leaders as part of a multi-disciplinary team and thrive in a fast-paced environment.
  • Demonstrated attention to detail, strong organizational skills, the ability to multitask and meet project timelines.

Here Is What You Need (Minimum Requirements)
  • Bachelor's Degree in Analytical Chemistry or related field, with minimum 3 years relevant experience either in a lab/manufacturing environment, or an academic or industrial research lab.
  • Ability to meet project milestones under general supervision, manage expectations for specific projects, ensure delivery of technology/transfer/submission-ready technology, data and documents.
  • Experience in problem-solving skills and instrument troubleshooting.
  • Ability to adhere to safe laboratory practices
  • Excellent oral and written communication skills with high attention to detail, strong organizational skills, team oriented, effective interpersonal and communication skills.

Bonus Points If You Have (Preferred Requirements)
  • Experience in the pharmaceutical industry.
  • Experience working in a regulated environment.
  • Experience with PAT instrumentation (NIR, FBRM), APC software, and/or data analysis in a GMP environment.

Relocation support available
Work Location Assignment: On Premise
The annual base salary for this position ranges from $68,600.00 to $114,300.00. 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.
Candidates must be authorized to be employed in the U.S. by any employer.
U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.
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.
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 [email protected] . 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.
To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers .
Research and Development

Skills Required

  • Bachelor's Degree in Analytical Chemistry or related field with minimum 3 years relevant experience
  • Ability to meet project milestones under general supervision and deliver transfer/submission-ready technology, data and documents
  • Experience in problem-solving and instrument troubleshooting
  • Ability to adhere to safe laboratory practices
  • Excellent oral and written communication skills, strong organizational skills, attention to detail, and ability to multitask
  • Demonstrated proficiency with a wide variety of software and information systems
  • Experience with PAT instrumentation (NIR, FBRM), APC software, and data analysis in a GMP environment
  • Experience in the pharmaceutical industry and/or working in a regulated environment

What the Team is Saying

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Pfizer

Pfizer Compensation & Benefits Highlights

  • Healthcare Strength Official materials describe comprehensive medical, dental, vision, and mental-health support, plus fertility/family‑building and transgender‑inclusive coverage; eligible Pfizer medications are noted as available at no cost in U.S. plans. Wellness resources such as telehealth and preventative programs are also emphasized.
  • Retirement Support Company documents highlight a 401(k) with matching contributions plus an additional Retirement Savings Contribution beyond the match. Financial planning support and company‑paid life and disability insurance further bolster long‑term security.
  • Leave & Time Off Breadth Corporate pages and job postings describe paid vacation and holidays, caregiver leave, and paid parental leave for both parents. Materials also note that details can vary by role and location.

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The Company
HQ: New York, NY
121,990 Employees
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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Pfizer Offices

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Employees engage in a combination of remote and on-site work.

Typical time on-site: 2.5 days a week
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