Senior Pharmaceutical Technician

Catalent; Kansas City (MO); On-site; USD 65,000 - 95,000; Full time

Benefits offered by this job

Competitive benefits

On-site work

Job summary

Catalent’s Kansas City facility is seeking a Senior Pharmaceutical Technician to support manufacturing operations onsite. You will set up, tear down, manufacture, and clean equipment under supervision while ensuring compliance with SOPs, cGMP, and safety standards.

The role requires attention to detail, strong organizational skills, and a commitment to quality in a fast-paced manufacturing environment. Shift is Monday–Friday, 6:00 AM–2:30 PM, with 100% onsite work in Kansas City, MO.

Qualifications

• High school diploma; equivalent years of pharmaceutical manufacturing supervisory experience may substitute for education.
• Five to seven years of experience with at least three years in a pharmaceutical or cGMP manufacturing environment.
• Technical degree or certification: three to five years of experience with at least three years in a pharmaceutical or cGMP manufacturing environment.
• Thorough knowledge of equipment processes and frameworks.
• Leadership qualities or strong potential for team management.
• Advanced operator qualification per supervisor or manager specified equipment train(s).
• Thorough knowledge of cGMP, FDA, MHRA, and DEA guidelines and their application.
• Excellent computer skills.
• Ability to manage priorities and projects effectively.
• Clear communication with all levels of management.
• Ability to work in a matrix organization.
• Maintain current knowledge of cGMP regulations and regulatory trends.
• Handle raw materials, including manipulation of drums weighing up to 150 kg and applying up to 80 lbs. of force.

Responsibilities

• Ensure cGMP compliance and maintain good housekeeping standards.
• Request work orders for processing rooms and equipment within the core group.
• Maintain 5S standards and ensure the facility is always tour ready.
• Visually inspect products to meet quality requirements.
• Communicate and execute quality system improvement ideas and maintain effectiveness of quality system components.
• Ensure operators follow all safety procedures and use proper PPE.
• Drive productivity improvements while maintaining high quality standards.
• Troubleshoot and repair equipment malfunctions; partner with scientists and manufacturing leads on batch record template issues.
• Ensure processing under GMP conditions and strict adherence to SOPs.
• Coordinate with Warehouse and Supply Chain to meet timelines and manage material movement.
• Support customer requests as needed.
• Partner with management to standardize training and develop operational training requirements.
• Collaborate with other departments for seamless communication.
• Participate in site committees such as EHS, Employee Engagement, or Quality committees.
• Perform other duties as needed.

Skills

cGMP knowledge

Leadership

Communication

Equipment operation

Safety compliance

Education

High school diploma

Technical degree or certification

Tools

Pallet jacks

Fall protection equipment

Job description

About Site

Catalent’s Kansas City facility is home to our Oral & Specialty Drug Delivery, Biologics Analytical Services and Clinical Supply Services businesses.

Position Summary

We have an opportunity for a Senior Pharmaceutical Technician to join our team. In this role, you will perform set up, tear down, manufacturing, and cleaning of equipment and processes with moderate supervision. You will ensure compliance with policies, procedures, and regulatory requirements such as SOPs, cGMP, and safety standards. This position requires attention to detail, organizational skills, and a commitment to quality and compliance in all aspects of manufacturing operations.

Shift: Monday - Friday, 6:00AM - 2:30PM

Location: Kansas City, MO

100% Onsite

The Role

• Ensure cGMP compliance and maintain good housekeeping standards.
• Request work orders for processing rooms and equipment within the core group.
• Maintain 5S standards and ensure the facility is always "tour ready."
• Visually inspect products to meet quality requirements.
• Communicate and execute quality system improvement ideas and maintain effectiveness of quality system components.
• Ensure operators follow all safety procedures and use proper Personal Protective Equipment (PPE).
• Drive productivity improvements while maintaining high quality standards.
• Troubleshoot and repair equipment malfunctions; partner with scientists and manufacturing leads on batch record template issues.
• Ensure processing under GMP conditions and strict adherence to SOPs.
• Coordinate with Warehouse and Supply Chain to meet timelines and manage material movement.
• Support customer requests as needed.
• Partner with management to standardize training and develop operational training requirements.
• Collaborate with other departments for seamless communication.
• Participate in site committees such as EHS, Employee Engagement, or Quality committees.
• Perform other duties as needed.

The Candidate

Minimum Requirements

• High school diploma required; equivalent years of pharmaceutical manufacturing supervisory experience may substitute for education.
• High school diploma: five to seven years of experience with at least three years in a pharmaceutical or cGMP manufacturing environment.
• Technical degree or certification: three to five years of experience with at least three years in a pharmaceutical or cGMP manufacturing environment.
• Thorough knowledge of equipment processes and frameworks.
• Leadership qualities or strong potential for team management.
• Advanced operator qualification per supervisor or manager specified equipment train(s); basic knowledge of all equipment within work zone.
• Thorough knowledge of cGMP, FDA, MHRA, and DEA guidelines and their application.
• Excellent computer skills.
• Ability to manage priorities and projects effectively.
• Clear communication with all levels of management.
• Ability to work in a matrix organization.
• Maintain current knowledge of cGMP regulations and regulatory trends.
• Handle raw materials, including manipulation of drums weighing up to 150 kg and applying up to 80 lbs. of force.
• Lift boxes and containers from waist to chest height; overhead lifting up to 15 lbs.
• Push and pull ingredient canisters; maneuver drums in manufacturing areas.
• Clean areas and equipment using brushes, hoses, and other tools; work in various postures including squatting, kneeling, and overhead reach.
• Transport materials using pallet jacks and other equipment; climb ladders and maneuver around equipment.
• Wear safety glasses and steel-toed shoes; use fall prevention devices and air-purifying respirators as required.
• Operate safely in a dynamic environment with changing conditions.

Preferred Skills & Background

• Thorough knowledge of solid dosage manufacturing preferred.
• A technical degree or certification is preferred.

Why You Should Join Catalent

• Defined career path with annual performance reviews and feedback.
• Diverse and inclusive culture.
• Potential for career growth within an organization dedicated to improving lives.
• Competitive paid time off plus 8 paid holidays.
• Community engagement and green initiatives.
• Medical, dental, and vision benefits effective day one of employment.
• Tuition reimbursement.

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 [e-mail]. 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.