Director - Drug Product Analytics Development

Socket.dev; Groton (CT); On-site; USD 177,000 - 294,000; Full time

Benefits offered by this job

Relocation support

Bonus program (20% target)

Job summary

Pfizer in Groton, CT, seeks a senior Analytical Scientist to lead a team driving analytical development for small molecule drug products from early development through commercialization. You will shape analytical strategy, portfolio delivery, and scientific excellence while collaborating across multidisciplinary CMC teams.

The role requires leadership of diverse teams, strong communication, and a track record in regulatory filings. Location on site with travel and relocation support available.

Qualifications

• PhD in Analytical Chemistry or related field with 5+ years of pharmaceutical development experience including filing experience for novel small molecule drug products.
• 3 years of experience leading a team of scientists directly and cross-functionally
• Strong communication skills-- written, oral and presentation.

Responsibilities

• Provide leadership and coaching to Analytical Scientists, fostering technical growth and high performance.
• Define and execute analytical development strategies supporting clinical and commercial milestones.
• Lead analytical project planning, resource management, budgeting, risk assessment, and delivery of CMC analytical activities.
• Partner with Drug Product Design, Supply Chain, Quality, Regulatory, Clinical, and Commercial teams to ensure successful project execution.
• Champion innovative approaches, digital solutions, modeling, and efficient ways of working to accelerate development and improve productivity.
• Ensure robust, phase-appropriate analytical methods and regulatory-compliant deliverables.

Skills

Leadership

Communication

Project management

Regulatory understanding

External/vendor management

Education

PhD in Analytical Chemistry

Job description

POSITION SUMMARY

You will lead a team of analytical scientists supporting the development of Pfizer's small molecule drug products from early development through commercialization. You will drive analytical strategy, portfolio delivery, scientific excellence, innovation, and talent development while collaborating across multidisciplinary CMC teams.

KEY RESPONSIBILITIES

• Provide leadership and coaching to Analytical Scientists, fostering technical growth and high performance.
• Define and execute analytical development strategies supporting clinical and commercial milestones.
• Lead analytical project planning, resource management, budgeting, risk assessment, and delivery of CMC analytical activities.
• Partner with Drug Product Design, Supply Chain, Quality, Regulatory, Clinical, and Commercial teams to ensure successful project execution.
• Champion innovative approaches, digital solutions, modeling, and efficient ways of working to accelerate development and improve productivity.
• Ensure robust, phase-appropriate analytical methods and regulatory-compliant deliverables.

MINIMUM QUALIFICATIONS

• PhD in Analytical Chemistry or related field with 5+ years of pharmaceutical development experience including filing experience for novel small molecule drug products.
• 3 years of experience leading a team of scientists directly and cross-functionally
• Strong communication skills-- written, oral and presentation.

PREFERRED QUALIFICATIONS

• Experience managing multiple projects simultaneously.
• Experience implementing technical and digital concepts and innovation.
• Strong global regulatory understanding and project management skills
• Experience working with external and outsourcing partners

Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact.

PHYSICAL/MENTAL REQUIREMENTS

• Experience working in a fast-paced environment and adapting to changing priorities.
• Operating across multiple digital systems which requires significant time using a computer.

WORK LOCATION ASSIGNMENT:

On Premise

NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS

Travel is anticipated to be approximately 10% of time to visit sites and external vendors.

Relocation support available

The annual base salary for this position ranges from $176,600.00 to $294,300.00. In addition, this position is eligible for participation in Pfizer's Global Performance Plan with a bonus target of 20.0% 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.

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].

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Research and Development