Development Scientist II

About the role

Responsible for GMP compliance in formulation and process development. Responsible for assisting with planning and operating within a budget for the pharmaceutical area. Work directly with customers and potential customers to agree on development approaches and scope of work. Independently assist manufacturing group with batch manufacture and packaging/labeling, including set-up and cleaning. Lead efforts in solving formulation and process problems. Directly support with writing batch records, SOPs, IQ/OQ/PQ documents, development/technical reports, and CMC sections for regulatory submissions as directed. Ensure that all work is accurate, precise, properly documented and, when appropriate, performed within GMP guidelines. All other duties as assigned. The Candidate Bachelor's degree in Pharmacy, Chemistry, Biology or related field with eight or more years of experience in pharmaceutical development with focus on solids formulation required or; Master's degree in Pharmacy, Pharmaceutics, Industry Pharmacy, or related field with six or more years of experience in pharmaceutical development required or; Ph.D. in Pharmacy, Pharmaceutics, Industry Pharmacy or related field with four or more years of experience in pharmaceutical development required or; Some exposure to hazardous chemicals and other active chemical ingredients. Position requires the capacity to handle and manipulate objects using hands and arms. Requires ability to occasionally lift items in excess of 50 pounds. This position requires that a respirator be worn for your safety, and as such, employment is contingent upon being able to complete a medical evaluation with satisfactory results. The medical evaluation is conducted via an external vendor assigned by Catalent. Why You Should Work At Catalent Spearhead exciting and innovative projects Fast-paced, dynamic environment High visibility to members at all levels of the organization 152 hours of PTO + 8 paid holidays 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. Important Security Notice to U.S. Job Seekers: Catalent NEVER asks candidates to