Supervisor, Manufacturing Sciences & Technology

Flagship Kansas; Kansas City (MO); On-site; USD 80,000 - 110,000; Full time

Benefits offered by this job

401(k) match

Tuition reimbursement

Paid time off

Wellness perks

Job summary

Flagship Kansas is seeking a Supervisor for Manufacturing Sciences & Technology to lead a team focused on ensuring process integrity and compliance. Located in Kansas City, this role emphasizes cross-functional collaboration across project management, operations, and quality assurance.

The ideal candidate holds a Bachelor's degree in a relevant field and has substantial experience in cGMP clinical packaging and regulatory compliance, alongside strong project management skills. Benefits include career growth opportunities and a comprehensive benefits package.

Qualifications

• Bachelor’s degree in relevant field or HS Diploma and 4+ years experience.
• Experience in project management and process development is essential.
• Knowledge of regulatory, validation and documentation requirements.

Responsibilities

• Lead the MS&T team, working cross-functionally with various departments.
• Ensure compliance with cGMP and monitor process integrity.
• Manage and document changes to production processes.

Skills

Project management experience

Knowledge of regulatory requirements

Experience with cGMP clinical packaging

Strong knowledge of Tech Transfer

Working knowledge of Microsoft Office

Ability to use TrackWise, ComplianceWire

Education

Bachelor’s degree in Biotechnology, Chemical or Pharmaceutical Engineering

HS Diploma/GED with 4+ years relevant experience

Tools

TOPS Pro

Thermoforming/cold-forming equipment

Job description

Job Description

Supervisor, Manufacturing Sciences & Technology

Position Summary

100% based on-site in Kansas City.

Work Schedule: M-F during regular business hours.

Catalent’s Kansas City (KCM) facility is a premier site for integrated drug development, manufacturing, and clinical supply services, supporting a wide range of pharmaceutical and biotech products. With cutting‑edge technologies and a collaborative work environment, it offers exciting opportunities for professionals across all functions— from science and engineering to operations and logistics.

The Kansas City Clinical Development & Supply Floor Manufacturing Sciences and Technology Supervisor will develop and lead a group, including the transfer between external clients and Manufacturing. The supervisor is responsible for leading the team of strong engineers, scientists, or qualified person to be technology transfer process owner to deliver excellent services to internal and external customers.

The Role

• Strategic client facing leader of the MS&T team on behalf of the organization.
• Works cross functionally with project managers, manufacturing, label design and control, quality assurance, quality control, supply chain, and facilities departments to effectively transfer and maintain processes in the facility.
• Participates and leads commercial manufacturing transition and support for process development.
• Enhance productivity by exploring, analyzing, facilitating, and leveraging efficiency initiatives for packaging processes through The Catalent Way.
• Ensure that changes to existing processes or the introduction of new processes are carried out and documented according to approved change control procedures and in compliance with cGMP requirements.
• Bridge the focus areas of Project Management, Operations, Quality, EHS, Supply Chain and Engineering to create common understanding and objectives and ensure robust products and flawless packaging.
• Leads the compilation of process data, including communicating project status, and delivering internal and client presentations.
• Collects and trend process data for external (Clients) and internal review to ensure process consistency.
• Provides business case for process improvement projects.
• Other duties assigned.

The Candidate

• Bachelor’s degree in Biotechnology, Chemical or Pharmaceutical Engineering, or related field, OR a HS Diploma/ GED and 4+ years of relevant experience.
• Experience with Upstream and Downstream processes of cGMP clinical packaging.
• Project management experience/skills required including method transfers, and risk assessment.
• Knowledge of regulatory, validation and documentation requirements for product development, commercial production, and site transfers.
• Experience in investigating and closing out deviations, OOS, CAPAs, and change controls.
• Experience working on late phase and commercial programs is a plus.
• Knowledge of thermoforming/cold‑forming equipment is required.
• A good working knowledge of Microsoft Office (Word, PowerPoint, Excel and Visio) and TOPS Pro (Total Optimization Packaging System) or similar software program.
• Ability to learn and use software packages (e.g. TrackWise®, ComplianceWire®).
• Demonstrated strong working knowledge of Tech Transfer (Internal and External).
• Understanding and application of Risk Assessment tools (Hazard Analysis, FMEA, etc.).

Benefits

• Career growth with a clear path and regular performance reviews.
• 401(k) match, tuition reimbursement, and wellness perks.
• Paid time off: 152 hours + 8 holidays.
• Inclusive culture with Employee Resource Groups and community initiatives.
• Discounts from 900+ merchants via Perkspot.
• A mission‑driven workplace where your work helps save lives.

Equal Opportunity Employer

Catalent is an Equal Opportunity Employer, including disability and veterans.