Sr. Associate Engineer, Clinical Manufacturing - 2nd Shift

Why Patients Need You

Pfizer's purpose is to deliver breakthroughs that change patients' lives. Research and Development is at the heart of fulfilling Pfizer's purpose as we work to translate advanced science and technologies into the therapies and vaccines that matter most. Whether you are in the discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply cutting edge design and process development capabilities to accelerate and bring the best in class medicines to patients around the world.

What You Will Achieve

As a Senior Associate Scientist, you will be at the center of our operations and you'll find that everything we do, every day, is in line with an unwavering commitment to quality. You will provide science and technology expertise in the disciplines of macromolecule purification sciences for the development and optimization of vaccine manufacturing processes. You will perform Analytical Research and Development (R&D) activities, such as method development, method validation, method transfer etc.

You will help Pfizer develop new and improved processes used in the research and development of our drugs. Your innovative mindset will help us develop economical, efficient and safe chemical manufacture of experimental and active drug materials. Your significant experience of applying knowledge of principles, concepts, and practices of the discipline will make you a critical member of the team. You are proactive in contributing to all team discussions and creating an environment of collaboration.

It is your innovative scientific temperament that will help in making Pfizer ready to achieve new milestones and help patients across the globe.

How You Will Achieve It

  • Contribute to achievement of immediate work group goals and collaborate with other team members.
  • Manage application and development of analytical methods used for the characterization and manufacturing support of therapeutic proteins and vaccines.
  • Implement effective technology development and continuous process development to ensure success on drug discovery programs.
  • Serve as the primary Technical Expert for the manufacturing methods, perform scientific laboratory studies, and make recommendations to improve manufacturing reliability, cost, safety, compliance and environmental performance.
  • Evaluate lab-scale processes and define the scaled up process for the clinical production facility.
  • Troubleshoot and/or improve established analytical test methods.
  • Represent Research and Development in cross functional project teams, where required.
  • Participate in the technical writing, review of analytical documentation & regulatory submissions and facilitate the Tech Transfer process.
  • Maintain laboratory area and equipment in clean, safe, functional order.
  • Independently plan and perform work assignments, interpret and present data.
  • Provide analytical support for product transfers, new product development and cost improvement projects.
  • Develop methods for intermediates, raw materials, in process controls, API (Active Pharmaceutical Ingredients), and Drug Products.
  • Comply with safety and regulatory requirements is expected and documented through the internal training program.



  • Bachelor's Degree
  • 3+ years of experience
  • Biopharmaceutical or pharmaceutical industry experience
  • Ability to perform complex data analysis and work in a team environment
  • Strong working knowledge of Cell Culture, Fermentation, and/or Protein Purification techniques
  • Ability to troubleshoot technical issues, plan and carry out experiments independently, and work with complex instrumentation and software
  • Excellent oral and written communication skills and ability to train and develop others
  • Strong analytical and computer skills
  • Strong mechanical aptitude
  • Energetic self-starter, hard-worker, ability to thrive in dynamic and unstructured environment with a fluid schedule and with limited oversight


  • Experience in investigative process and deviation, CAPA, and Change Control Management
  • Experience in experimental design and equipment troubleshooting
  • Direct on-the-floor GMP Manufacturing experience in a biopharmaceutical manufacturing environment
  • Experience contributing to cross-functional teams and leading technical meetings
  • Experience executing components of experimental programs in the laboratory and directly relevant experience in the biopharmaceutical industry is desirable.

  • Must be able to climb flights of stairs, and remain standing for extended periods of time.
  • Must be able to lift up to 50 lbs
  • Ability to thrive in dynamic team environment with diverse perspectives
  • Propensity for creative problem solving and courage to share and actively promote innovative ideas of self and others.


  • This is a 2nd shift position, however during training the candidate may work 1st shift hours and transition.
  • Ability to work off shift (Nights and Weekends) as needed; non-routine


Pfizer requires all U.S. new hires to be fully vaccinated for COVID-19 prior to the first date of employment. As required by applicable law, Pfizer will consider requests for Reasonable Accommodations.

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.

Research and Development