Sr. Associate Scientist

Pfizer; Bothell (WA); Presencial; USD 69.000 - 114.000; Tempo integral

Benefícios oferecidos por esta vaga

401(k) with company match

Retirement savings contribution

Paid vacation

Paid holidays

Parental leave

Medical, dental, and vision benefits

Resumo da vaga

Pfizer is seeking a Senior Associate Scientist (R2) in Upstream Process Development to design, optimize and scale recombinant protein manufacturing processes for early- and late-phase trials. You will lead bench-scale experiments, transfer technology to GMP facilities, and contribute to regulatory submissions.

The role involves documenting results, collaborating across teams, and supporting process development through scale-up and technology maturation.

Qualificações

• Bachelor’s degree with 3 years’ industrial experience or Master’s degree with 0-2 years experience in Chemical / Biochemical Engineering, Cell Biology, Biotechnology, Biomedical Engineering or a relevant field.
• Relevant research experience in a laboratory setting is required.
• Ability to grasp scientific concepts, interpret complex data, and formulate new hypothesis.
• Competency in aseptic laboratory technique and the ability to design and carry out complex experiments and interpret data.
• Demonstrated effectiveness in collaborative projects, and ability to communicate effectively with scientists and management in a highly matrixed organization.

Responsabilidades

• Design and execute experiments in appropriate scale-down models such as shake flasks and bioreactors to develop robust, high yield, scalable manufacturing processes.
• Serve as upstream technical lead; ensure accurate technology transfer to pilot and GMP manufacturing facilities; provide technical support during manufacturing campaigns as needed.
• Timely and accurately document data in electronic lab notebooks; author technical reports and contribute to regulatory submissions such as IND and BLA.
• Participate in lab and project team meetings on design of experiments and data interpretation.
• Contribute to a safe, efficient lab environment and be a collaborative team player.
• Occasionally work over the weekend to passage flasks, sample bioreactors or perform other essential tasks.

Conhecimentos

Aseptic technique

Data interpretation

Experimental design

Collaborative work

Scientific communication

Formação

Bachelor’s degree in Chemical/Biochemical Engineering or related field

Master’s degree in a relevant field

Ferramentas

ambr15

ambr250

Shake flasks

Bioreactors

Descrição da vaga

What You Will Achieve

A Senior Associate Scientist (R2) position is available in the Upstream Process Development group within the Bioprocess R&D organization. The successful applicant will join a team of scientists and engineers focused on developing and optimizing manufacturing processes for recombinant proteins and other modalities for early- and late-phase human clinical trials. In this role, the candidate will be responsible for designing and executing laboratory experiments in bench‑top bioreactors and associated scale‑down equipment with the goal of developing robust, scalable, and high productivity processes.

The work will also involve working with pilot, clinical, and commercial production facilities to ensure accurate technology transfer, successful large-scale production and associated regulatory filing activities. The candidate may also be involved in cutting edge technology development projects that seek to improve production processes and control strategies leveraging various process analytical technologies.

How You Will Achieve It

• Design and execute experiments in appropriate scale-down models such as shake flasks and bioreactors in an effort to develop robust, high yield, and scalable manufacturing processes
• Serve as upstream technical lead; ensure accurate technology transfer to pilot and GMP manufacturing facilities; provide technical support during manufacturing campaign as needed
• Timely and accurately document data in electronic lab notebooks; author technical reports and contribute to relevant sections of regulatory submissions such as IND and BLA
• Participate and contribute to discussions in lab and project team meetings on design of experiments and interpretation of data
• Contribute to safe, efficient, and harmonious lab environment; strong lab citizen and collaborative team player
• Occasionally work over the weekend to passage flasks, sample bioreactors or perform other essential tasks

Qualifications

Must Have

• Bachelor’s degree with 3 years’ industrial experience or Master’s degree with 0-2 years experience in Chemical / Biochemical Engineering, Cell Biology, Biotechnology, Biomedical Engineering or a relevant field
• Relevant research experience in a laboratory setting is required.
• Ability to grasp scientific concepts, interpret complex data, and formulate new hypothesis.
• Competency in aseptic laboratory technique and the ability to design and carry out complex experiments and interpret data.
• Demonstrated effectiveness in collaborative projects, and ability to communicate effectively with scientists and management in a highly matrixed organization.

Nice To Have

• Hands-on experience with high-throughput bioreactor platforms, including ambr15 and ambr250 systems
• Expertise in fed-batch / perfusion bioreactor operations, including process setup, control, troubleshooting, and scale-up of mammalian cell culture processes
• Proficiency in process modeling and multivariate data analysis for process characterization, and predictive process understanding
• Experience with Python programming, workflow automation, or app development to create tools that improve experimental planning, data analysis, visualization, and knowledge-sharing for process development scientists

Physical/Mental Requirements

• Lifting, sitting, standing, walking, bending, ability to perform mathematical calculations and ability to perform complex data analysis

Non-standard Work Schedule, Travel Or Environment Requirements

• May require occasional work on the weekend for essential tasks
• May need to travel occasionally to attend internal meetings or external conferences

Other Job Details

• 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 [e-mail]. 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.