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Pharmaceutical Development Technician I

Catalent

Pharmaceutical Development Technician I

full-timePosted: Aug 13, 2026Updated: Sep 3, 2026MO, Kansas City

Job Description

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 Technician I to join our team. In this role, you will perform setup, teardown, manufacturing, and cleaning of equipment and processes under the guidance of senior technicians. You will follow policies and procedures with a strong focus on regulatory compliance, including SOPs, cGMP, and safety standards. This position supports our mission to deliver high-quality solutions that help people live better, healthier lives.Shift: M-F 6am-2:30pmLocation: Kansas City, MO100% OnsiteThe RoleEnsure compliance with current Good Manufacturing Practices (cGMP) and maintain good housekeeping standardsFollow all Catalent safety procedures and communicate necessary adjustments to address potential safety concernsEnsure proper use of Personal Protection Equipment (PPE)Learn all equipment and testing within the core group while maintaining high quality standardsMaintain up-to-date training on equipment and site proceduresPerform daily tasks to keep working areas stocked with proper materials and suppliesConduct physical characterization testing on raw and in-process materialsSupport sampling and packaging of in-process and finished product materialMaintain active inventory of excipients and Active Pharmaceutical Ingredients (API) used for experimental processingPerform all other duties as assignedThe CandidateMinimum RequirementsHigh School Diploma or General Educational Development (GED) and 0+ years of relevant work experienceExcellent written and verbal communication skills with internal and external customers, peers, and managersWell organized with the ability to multitask and work effectively under pressure to meet deadlinesIndividual may be required to sit, stand, walk regularly and occasionally lift up to 50 poundsPreferred Skills & BackgroundOutstanding troubleshooting skillsExperience maintaining high-quality laboratory documentation in accordance with applicable regulatory guidance and site Standard Operating Procedures (SOPs)Previous experience with Good Manufacturing Practices (GMP) highly 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 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 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 spam@catalent.com for us to investigate with local authorities.California Job Seekers can find our California Job Applicant Notice HERE.

Locations

  • MO, Kansas City

Skills Required

  • Good Manufacturing Practicesintermediate

Required Qualifications

  • High School Diploma or General Educational Development (GED) and 0+ years of relevant work experience (experience)
  • Excellent written and verbal communication skills with internal and external customers, peers, and managers (experience)
  • Well organized with the ability to multitask and work effectively under pressure to meet deadlines (experience)
  • Individual may be required to sit, stand, walk regularly and occasionally lift up to 50 pounds (experience)
  • High School Diploma or General Educational Development (GED) and 0+ years of relevant work experience (experience)
  • Excellent written and verbal communication skills with internal and external customers, peers, and managers (experience)
  • Well organized with the ability to multitask and work effectively under pressure to meet deadlines (experience)
  • Individual may be required to sit, stand, walk regularly and occasionally lift up to 50 pounds (experience)

Preferred Qualifications

  • Outstanding troubleshooting skills (experience)
  • Experience maintaining high-quality laboratory documentation in accordance with applicable regulatory guidance and site Standard Operating Procedures (SOPs) (experience)
  • Previous experience with Good Manufacturing Practices (GMP) highly preferred (experience)
  • Outstanding troubleshooting skills (experience)
  • Experience maintaining high-quality laboratory documentation in accordance with applicable regulatory guidance and site Standard Operating Procedures (SOPs) (experience)
  • Previous experience with Good Manufacturing Practices (GMP) highly preferred (experience)

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