Quality Assurance Associate — GMP & Compliance

Regulatory Jobs; Kansas City (MO); On-site; USD 55,000 - 78,000; Full time

Benefits offered by this job

Competitive PTO and 8 holidays

Medical, dental, vision benefits day 1

Tuition reimbursement

Career growth opportunities

Job summary

Catalent's Kansas City facility is seeking an Associate, Quality Assurance to support quality oversight of manufacturing processes, ensuring compliance with cGMPs, FDA and MHRA guidelines. The role focuses on maintaining product quality and safety while contributing to continuous improvement initiatives.

Shift is Monday–Friday, 6am–2:30pm, onsite in Kansas City, MO. Responsibilities include reviewing records, deviations, and batch documentation, plus participating in QA programs.

Qualifications

• Bachelor’s degree in a scientific discipline or at least one year of GMP experience.
• Ability to follow instructions and guidance from others.
• Apply quality system elements to classify and control finished products.
• Strong written and verbal communication with internal/external stakeholders.
• Lead by example in alignment with Catalent’s values and culture.

Responsibilities

• Oversee quality support functions during manufacturing of products.
• Review batch records, cleaning records, and logbooks.
• Ensure manufacturing adheres to cGMPs, FDA and MHRA guidelines and SOPs.
• Identify deviations and advise on corrective actions.
• Review and approve batch documentation for SOP and cGMP adherence.
• Participate in QA programs and facility audits.
• Assist with manufacturing floor activities and equipment approvals.
• Perform other duties as assigned.

Skills

Attention to detail

Instruction following

Problem solving

Team collaboration

Time management

Multitasking

Strong communication

Education

Bachelor’s degree in scientific discipline

Tools

Word

Excel

Outlook

PowerPoint

Job description

Catalent's Kansas City facility is seeking an Associate, Quality Assurance to support quality oversight of manufacturing processes, ensuring compliance with cGMPs, FDA and MHRA guidelines. The role focuses on maintaining product quality and safety while contributing to continuous improvement initiatives.

Shift is Monday–Friday, 6am–2:30pm, onsite in Kansas City, MO. Responsibilities include reviewing records, deviations, and batch documentation, plus participating in QA programs.