Pharmaceutical Development Principal Scientist I

About SiteCatalent’s Kansas City facility is home to our Oral & Specialty Drug Delivery, Biologics Analytical Services and Clinical Supply Services businesses.Position SummaryWe have an opportunity for a Pharmaceutical Development Principal Scientist I to join our team. In this role, you will provide technical expertise and support for oral solid development programs. You will work closely with clients, support marketing activities, and author key technical documents. This position also involves troubleshooting, risk assessments, and contributing to strategic initiatives within the department.Shift: Monday to Friday 8am-5pmLocation: Kansas City, MO100% OnsiteThe RoleDevelop and execute laboratory work plans and schedules for self and team, using customer milestones and site performance standardsIndependently author and approve technical documents such as protocols, test methods, reports, certificates of analysis, and operating proceduresReview technical documents for accuracy, thoroughness, and regulatory complianceTrain, coach, and mentor others on technical, personal development, or business issuesSupervise technical staff, including work assignments and performance managementServe as project director on multiple projects, ensuring project outcomes and managing customer interactionsIdentify and drive department-level improvements independentlySupport development of business strategies for multiple customers across company sitesApply technical, functional, and business knowledge to design experiments and provide scientific consultationContribute to the strategic direction of the department by recommending actions based on experimental results or scientific informationPerform all other duties as assignedThe CandidateMinimum RequirementsBachelor's degree in a related life science or physical science field with 24+ years of related work experience preferred; equivalent extensive related work experience may be considered in lieu of a degreeKnowledge of high-shear granulation, fluid-bed technology, roller compaction, compression, and encapsulationKnowledge of techniques in design of experiments and statisticsAbility to maintain high-quality laboratory documentation in accordance with regulatory guidance and site standard operating proceduresAdvanced project management skills for multiple concurrent projects of moderate to high complexityExperience in most aspects of drug development and lifecycle support, with ability to develop strategies to meet regulatory milestonesBroad technical acumen with significant expertise in one or more techniques and understanding of their application in pharmaceutical servicesAbility to provide reliable interpretations of regulatory guidance and defend positions to regulatory agenciesCapable of rapid learning of unfamiliar principles or techniques with minimal trainingStrong organizational skills to manage and direct multiple activities simultaneouslyExcellent written and verbal communication skills with internal and external customersAbility to lead challenging discussions with customers and drive resolutionMay be accountable for meeting business unit revenue targetsLeadership development skills expectedProactively identifies and implements new technologies and understands their impact on offeringsRecognized as a subject matter expert with high personal credibilityExcellent motivator, skilled in team developmentLead by example according to company values and cultureWorks directly with Business Development to win new business, including conference calls and customer meetingsAbility to work effectively under pressure to meet multiple deadlinesMay publish or present externallyPhysical requirements: Stand, walk, sit, use hands to manipulate, and reach with hands and arms for up to 8 hours per day; frequent sitting, standing, walking, reading of written documents, and use of computer monitor screen; frequent travel requiredPreferred Skills & BackgroundSubstantial experience in oral solid dosage form development and manufacturing preferredDoctorate degree in a related life science or physical science field with 18+ years of related work experience preferred, or Master’s degree with 22+ years of related work experience preferredWhy You Should Join CatalentDefined career path and annual performance review and feedback processDiverse, inclusive culturePotential for career growth on an expanding team within an organization dedicated to preserving and bettering livesCompetitive paid time off plus 8 paid holidaysCommunity engagement and green initiativesMedical, dental, and vision benefits effective day one of employmentTuition reimbursementCatalent 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 View email address on click.appcast.io. 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 provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond— it is a fraudulent request. Please forward such requests to View email address on click.appcast.io for us to investigate with local authorities.California Job Seekers can find our California Job Applicant Notice HERE.SummaryLocation: Kansas City, MOType: Full time