What are the responsibilities and job description for the Senior Formulation Scientist (Food Scientist - Gummies) position at Catalent Inc?
Senior Formulation Scientist (Food Scientist - Gummies)
Position Summary
Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually. Catalent Greendale site is one of Catalent's gummy technology development and manufacturing facilities in North America. The site manufactures organic and vegan-based nutraceuticals via confection to enhance wellness for all consumers. Simply put - we make healthy gummies. Within the Catalent network, we offer a broad range of integrated formulation and analytical services to solve difficult development and manufacturing challenges.
Reporting to the Director Product Development, the Senior Scientist will provide and utilize technical direction and expertise throughout the entire development process with focus on pre-formulation studies, formulation and process development, optimization studies, and informal and formal stability studies. Complex formulations and process parameters will be solved by this key position. The Senior Scientist will have an advanced knowledge of various aspects of implementing the development process of dietary supplement gummies in a regulated environment, including topics such as Quality by Design (QbD), Design of Experiment (DOE), and compliance with all regulatory guidelines. Senior Scientist will be responsible for using formulation expertise to guide and support peers through development studies.
Catalent is committed to a Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer and Catalent employee.
The Role
- Plan, coordinate, drive, and guide the development and evaluation of new products, including pre-formulation excipient compatibility studies, formulation development, process development, support process validation and scale-up manufacturing.
- Provide technical leadership and mentoring to individuals, functional area and overall organization as required.
- Ensure appropriate technical review and oversight for portfolio projects / programs as required.
- Effectively communicate on a timely basis with management, other departments within Catalent as well as customers on the coordination of development activities, results, and next posed steps of the studies.
- Operate under and maintain GMP / GLP, health and safety conditions and practices.
- Maintain and improve compliance with training, best practices, safety, and cleaning requirements. Defining development studies, authoring, and approving protocols and reports, investigations, laboratory work, providing technical expertise, and support on multiple projects in the portfolio all while maintaining a patient first culture.
- Represent functional area and projects by leading discussions at local, technical, governance, executive and customer meetings.
- Lead Catalent's strategies, initiatives, expectations, processes, and portfolio commitments.
- Other duties as assigned.
The Candidate
Why You Should Join Catalent
Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.
personal initiative. dynamic pace. meaningful work.
Visit Catalent Careers to explore career opportunities.
Catalent is an Equal Opportunity Employer, including disability and veterans.
If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.
Notice to Agency and Search Firm Representatives : Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and / or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and / or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.
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