Technical Services Senior Manager

Technical Services Senior Manager – Responsible for overseeing the development and manufacturing of pharmaceutical and nutritional dosage forms and bringing new and existing products to market within established timelines. This role develops project risk assessments, technical success criteria, target product profiles, and contingency plans; defines critical process parameters, formulates products, and manages scale‑up from lab to commercial production. The Manager authorizes technical documentation to support product launch, regulatory approval, and identifies design space through critical process parameter definition.

The position supports GMP manufacturing operations for solid and liquid dosage forms, applying Quality by Design and statistical principles to optimize scalable and transferable processes in compliance with FDA regulations.

• Oversee development and manufacturing of pharmaceutical and nutritional dosage forms.
• Develop new and marketed products within established timelines.
• Create project risk assessments, technical success criteria, target product profiles, and contingency plans.
• Define critical process parameters, lead formula development, and scale‑up of products.
• Authorize technical documentation supporting product launch and regulatory approval.
• Establish product development processes and identify design space through critical process parameters.
• Apply regulatory requirements and industry standards to product development.
• Support GMP manufacturing operations for solid and liquid dosage forms.
• Apply Quality by Design and statistical principles to optimize manufacturing processes.
• Provide telecommuting up to one day per week and accommodate up to 20 % travel.

• Master’s degree in Chemistry, Chemical Engineering, Pharmaceutical Sciences, Pharmaceutics, or a closely‑related field.
• Minimum 3 years of experience in a pharmaceutical environment scaling up products from lab‑scale to commercial production using Stage Gate.
• Proficiency in authoring technical documentation for launch and regulatory approval.
• Knowledge of GMP, FDA regulations, Quality by Design, and statistical process optimization.
• Strong analytical and process‑development skills.
• Effective communication and teamwork abilities.

Salary range: $143,000 – $165,000 per year, plus potential bonus or commission. Benefits include health care, vision, dental, retirement, paid time off, and sick leave.

Bayer Healthcare LLC is an Equal Opportunity Employer/Disabled/Veterans. Bayer Healthcare LLC is committed to providing access and reasonable accommodations in its application process for individuals with disabilities and encourages applicants with disabilities to request any needed accommodation(s) using the contact information below.