Senior Scientist, BRD Portfolio Representative

Posted 2 Days Ago
Be an Early Applicant
3 Locations
Hybrid
94K-156K 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
Serve as BRD single point-of-contact on multiple Pharmaceutical Sciences Project Teams, lead BRD project teams for cell line and process development, plan resources, track portfolio metrics, implement SharePoint-based training/tools, coordinate regulatory documentation, identify process improvements, and manage multiple portfolio projects to enable timely delivery of biologics and clinical drug substance supplies.
Summary Generated by Built In
What You Will Achieve
In your role as Bioprocess Research & Development Portfolio Representative (BRD Rep) you will serve as the single point-of-contact for BRD on multiple Pharmaceutical Sciences Project Teams (PSPT) and lead the BRD project teams associated with these programs. The BRD teams, comprised of scientists from Science & Technology (S&T) lines, are responsible for cell line and process development, ensuring manufacture of regulatory toxicology and clinical Drug Substance supplies, and regulatory filings. The BRD Rep combines knowledge of BRD scientific disciplines and biologics development with project management skills to ensure project deliverables are met. You will be forecasting and planning resource requirements for your project team.
As BRD Rep you will also support the design and implementation of metric-driven systems for tracking portfolio progression, and of SharePoint-based training and tools for project teams. You will help identify needs for enhanced operational efficiency and work to establish and implement impactful work process improvements.
Leveraging matrix leadership, strategic influence, and a passion for portfolio advancement, you will connect people, science, and execution to accelerate the development of innovative therapies. Your leadership will help Pfizer deliver on its purpose-Breakthroughs that Change Patients' Lives-by advancing programs that bring meaningful impact to patients globally.
How You Will Achieve It
  • Represent BRD on Pharm Sci Project Team (PSPT), ensuring optimal coordination of activities and deliverables, and timely communication of progress, issues, and strategies.
  • Work with BRD Project Team and PSPT to develop integrated project plans to support delivery of portfolio project objectives.
  • Establish and ensure alignment of project strategy amongst all stakeholders, including BRD S&T lines, BRD leadership team, PSPT and Pre-POC Management Team.
  • Identify and communicate project risks and issues. Guide BRD project team in defining risk mitigation strategies for realized and potential issues and seek endorsement of risk mitigation strategies from appropriate stakeholders.
  • Work with the BRD Project team to facilitate decision making and problem solving for DS-related issues. As necessary, work with BRD line management and Subject Matter Experts (SMEs) to technically and strategically represent BRD in the PSPT and other management teams.
  • Work with BRD project team and PSPT to define operational planning including technology strategy, timelines, budget forecasts and FTE resources estimates.
  • Coordinate authoring and review of regulatory documentation, following internal SOPs and BRD guidelines.
  • Successfully balance workload of multiple portfolio projects.
  • Support BRD Portfolio Group initiatives for enhanced efficiency of portfolio progression through training and tools development, metric-based portfolio tracking, sharing of best practices, and other operational improvements

Qualifications (Must-Have)
  • Bachelor's degree with 8+ years of experience or Master's degree with 6+ years of experience in the area of Genetics, Molecular or Cell Biology, Biochemistry, Biological Sciences/Life Sciences, or Chemical/Biochemical Engineering with experience in development of biological therapeutics and/or vaccines within the biopharmaceutical industry.
  • Ability to prioritize and manage multiple activities and priorities simultaneously.
  • Broad technical knowledge of cell line and process development of biologics achieved through industrial experience and understanding of early phase Pharmaceutical Sciences project progression.
  • Ability to work and communicate effectively across functional lines and organizations.
  • Collaborative, team-oriented leadership and participation style, and ability to mentor less experienced team members.
  • Strong and pragmatic technical problem-solving skills.
  • Proven record of managing projects of moderate complexity and leading effective teams.
  • Demonstrated proficiency with tools used for project planning, tracking and management, including Excel, GDMS, SharePoint, etc.

Nice to Have
  • Prior experience on portfolio project teams as BRD rep or BRD line technology lead.
  • Ability to distill information from multiple sources into a cohesive project plan, and to analyze project specific experience to translate into guidance across portfolio projects.
  • Familiarity with regulatory/ICH guidelines and IND/IMPD regulatory filings.

NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS
Travel up to 10%, primarily to other Pfizer sites.
Work Location Assignment: Hybrid
The annual base salary for this position ranges from $93,600.00 to $156,000.00. In addition, this position is eligible for participation in Pfizer's Global Performance Plan with a bonus target of 12.5% of the base salary and eligibility to participate in our share based long term incentive program. 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. This role is posted in multiple locations. If you are applying for the role in an secondary job posting location where pay transparency regulations apply, your Talent Advisor will share the local pay information with you during the first interview.
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
#BI-Hybrid

Skills Required

  • Bachelor's degree with 8+ years or Master's degree with 6+ years in Genetics, Molecular/Cell Biology, Biochemistry, Biological/Life Sciences, or Chemical/Biochemical Engineering with biologics or vaccine development experience in biopharma.
  • Ability to prioritize and manage multiple activities and priorities simultaneously.
  • Broad technical knowledge of cell line and process development of biologics and understanding of early phase Pharmaceutical Sciences project progression.
  • Ability to work and communicate effectively across functional lines and organizations.
  • Collaborative, team-oriented leadership and ability to mentor less experienced team members.
  • Strong and pragmatic technical problem-solving skills.
  • Proven record of managing projects of moderate complexity and leading effective teams.
  • Demonstrated proficiency with project planning, tracking and management tools (including Excel, GDMS, SharePoint).
  • Prior experience as BRD rep or BRD line technology lead.
  • Ability to synthesize information into cohesive project plans and translate experience across portfolio projects.
  • Familiarity with regulatory/ICH guidelines and IND/IMPD regulatory filings.

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

Hybrid Workspace

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

Typical time on-site: 2.5 days a week
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