The Senior Manager Pharmaceutical Sciences applies broad pharmaceutical sciences and CMC expertise to develop and maintain commercial products that are safe effective compliant and robust across the product lifecycle. This role will provide technical leadership for an oral suspension product and a sterile injectable product including formulation/process development technology transfer external manufacturing (CDMO/CMO) oversight investigations and post-approval lifecycle management.

• Interact with external manufacturing partners and testing laboratories in support of management of development and tech transfer projects clinical supplies commercial and post-marketed products.
• Participate in the development and review of validation strategies for new products and processes including assessment of vendor change controls risk assessments annual product reports and process validation protocols and reports.
• Provide technical support for Supply Chain Quality Assurance (QA) and Regulatory Affairs Departments and Provide scientific direction and expertise to cross-functional teams.
• Be responsible for Risk Management activities including risk assessment impact analysis and Failure Modes and Effects Analysis (FMEA). Maintain working knowledge of available pharmaceutical technology in the marketplace and evaluate suitability for use with current or future development projects; as well as marketed products
• Act as the Technical Lead and project manager on multidisciplinary development teams maintaining responsibility and authority to make technical recommendations and managerial decisions that directly impact the project timeline and budget.
• Participate in the selection of technology vendors and development partners.
• Provide project updates (monthly reports data summaries) to management.
• Serve as the primary technical liaison to development laboratories and CMOs for key projects and collaborate with Shionogi Japan colleagues on technology transfer activities while overseeing drug development and manufacturing processes.
• Optimize design for manufacturing from cost reduction to line expansion capabilities.
• Review IQ/OQ/PQ activities that are related to manufacturing processes.
• Partner with manufacturing partners to identify process improvement needs and support the design and implementation of enhanced processes and practices.
• Participate in due diligence CMC reviews for new business opportunities.
• Participate in lab work in design and development of novel pharmaceutical dosage forms.

Minimum Job Requirements

• Masters Degree in Pharmaceutics Pharmaceutical Sciences Chemical Engineering Polymer Science or related discipline required; PhD preferred
• 8 years of progressive pharmaceutical development experience (or equivalent) including formulation and process development through tech transfer and commercial support.
• Demonstrated experience supporting oral liquid/suspension product and/or sterile injectable (aseptic processing/fillfinish and/or sterile filtration/terminal sterilization strategy)
• Functions independently with minimal guidance while managing multiple varied project responsibilities.
• Must offer experience in pharmaceutical analysis formulation development and manufacturing scale up/technology transfer
• Experience developing Validation Strategies for new products and processes.
• Thorough knowledge of current GMPs (Good Manufacturing Practices)
• Demonstrates expertise in ICH guidelines and regulatory authority requirements to ensure compliant pharmaceutical development testing documentation and submissions
• Thorough knowledge of functions and disciplines that contribute to the development manufacturing regulation and distribution of products intended for the pharmaceutical marketplace
• Strong oral and written communication including the ability to communicate to colleagues business partners stakeholders and upper management
• Ability to influence and coach positive behaviors within a matrixed organization as well as with the CMOs
• Strong presentation skills
• Strong analytical critical reasoning and problem-solving skills
• Must be innovative resourceful proactive and consistently effective
• Adept at the use of word processors spreadsheets and other common software
• Must be able to travel up to 40% - domestic and international
• Experience managing others in a matrix type environment is a plus

Other Requirements

• Must live a commutable distance to our US Corporate Headquarters in Florham Park NJ. Office presence required 50% per month at least 2-3 days per week.

Additional Information

The base salary range for this full-time position is $135000 - $165000. Individual pay is determined by several factors which include but are not limited to: job-related skills experience and relevant education or training. The range does not include the comprehensive benefits bonus long-term incentive applicable allowances or any additional compensation that may be associated with this role.

Shionogi Inc. is an equal opportunity employer supporting individuals with disabilities and veterans. All qualified applicants will receive equal consideration for employment opportunities based on valid job requirements without regard to race color religion sex (including pregnancy) marital status national origin age ancestry citizenship disability genetic information status as a disabled veteran a recently separated veteran Active Duty Wartime or Campaign Badge Veterans and Armed Forces Service Medal Veterans or any other characteristic protected by applicable law. It is the policy of Shionogi Inc. to undertake affirmative action for protected veterans and individuals with disabilities in compliance with all federal state and local requirements to recruit a diverse pool of protected veteran and individuals with disabilities applicants and to ensure that our employment practices are in fact non-discriminatory.

If you are qualified individual with a disability or a disabled veteran you may request a reasonable accommodation if you are unable or limited in your ability to use or access this website to apply for a vacancy as a result of your disability. You can request accommodations by calling or by sending an email to