Senior Scientist, Innovative Parenteral Product Development

Lake Forest, Illinois
Apr 30, 2021
May 07, 2021
Jobseeker Type
Organization Type
Full Time
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.

Role Summary:

Our Pharmaceutical Sciences function supports Pfizer's early to late stage portfolio translating new chemical entities into commercial drug products. Pharmaceutical Sciences is a fully integrated Chemistry, Manufacturing and Controls capability that encompasses state of the art active pharmaceutical ingredient synthesis and drug product design as well as cGMP manufacturing and clinical trials supply chain. Operating within PCOE, the Innovative Parenteral Product Development (IPPD) group utilizes expertise in analytical chemistry, materials science, formulation design and process development to deliver innovative new parenteral medicines.

We are seeking a strongly trained scientist to work in a team environment (under supervision of a team leader) engaged in the design, development, analyses and characterization of innovative parenteral pharmaceutical dosage forms.

You will predominantly be working in IPPD on novel drug product and technology projects. You will be responsible for experimental design, planning and execution of high-quality work, interpretation and reporting of data and communication to enable the design, development, optimization, scale-up and technology transfer of pharmaceutical dosage forms. Under the mentorship of subject matter experts, your existing knowledge and experience will be enhanced through engagement in a program of active learning and training tailored to accelerate your contribution to the diverse business of IPPD.


Leads and plans formulation/analytical assignments and activities to meet established project goals and timelines. Design and undertake high quality scientific experimentation to further the analytical development of dosage forms for novel drug candidates or product enhancement projects, which may include formulation, characterization and biopharmaceutics assessment to derive appropriate data. Role also encompasses documentation of experiments in line with IPPD and site guidelines and authoring of technical reports.

Define analytical/formulation methodology to support the manufacture of clinical supplies and commercial drug product based on development and application of advanced analytical understanding and provide scientific / technical support to colleagues in GMP manufacturing facilities where appropriate.

Contribute to the drafting of the relevant sections of the Quality modules of regulatory documentation.

Interpret scientific data to derive clear conclusions and provide direction for future work. Provide technical support to the Pharmaceutical Sciences multidisciplinary team to facilitate and influence the development of quality drug products.

Develop and maintain a contemporary in-depth understanding of the science, technology and regulation of parenteral pharmaceutical dosage forms and apply this knowledge to development of assigned drug candidates.

Communicate effectively to IPPD line managers and the wider development team and present data at departmental technical and governance meetings.

Share lessons and experience with colleagues and look for opportunities to develop novel technologies, processes and digital/computational tools to advance science of formulation and process development for dosage forms.

  • Ph.D. in Pharmaceutical Sciences, Chemistry, Pharmacy, Biomedical Engineering, Chemical Engineering, or related discipline with outstanding academic performance OR MS or BS with qualification 9+ years work experience in a relevant area practical work experience gained in an operational R&D role in pharmaceutical, drug delivery or allied industries in a relevant area (e.g. analytical development, testing and characterization of parenteral dosage forms).
  • Recognized scientific knowledge base and technical ability in requisite analytical tools (e.g. HPLC/UPLC, spectroscopic methods) to understand parenteral products.
  • The ability to use computational predictive tools, modelling software or data visualization tools.
  • Evidence of the ability to exercise sound scientific and technical judgement.
  • Good experimentalist with experience and competence in a wide range of lab technologies.
  • Effective oral and written communication.
  • Able to contribute effectively as a member of multidisciplinary teams.

Other Job Details:
  • Last Date to Apply for Job: May 6, 2021
  • Eligible for Relocation Package: no
  • Eligible for Employee Referral Bonus: yes

  • #LI-PFE

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

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