Visual Inspection Training Specialist

Kindeva Drug Delivery; Missouri; On-site; USD 65,000 - 85,000; Full time

Job summary

The Visual Inspection Trainer at Kindeva Drug Delivery designs, delivers, and continuously improves training programs for the Inspection Department in a GMP-regulated environment. You will oversee inspector qualification activities and perform operator assessments to ensure compliant, high‑quality inspection processes.

Collaborating with Quality and Operations, you will maintain training files and curricula, coach staff, and track metrics demonstrating the value of training initiatives across

Qualifications

• High School Diploma is required; Bachelor’s degree preferred.
• 3+ years in pharmaceutical manufacturing with training/teaching experience.
• Strong written and verbal communication, ability to present to groups.
• Proficiency with GMPs and quality documentation formats.
• Ability to collaborate with cross-functional teams including QA and Operations.

Responsibilities

• Develop and deliver training for Packaging and Inspection department on GMP and related topics.
• Ensure quality, compliance, safety, and production standards are met.
• Complete inspector qualification training and related procedures.
• Perform audits/quarterly assessments of production operators for compliance.
• Maintain training files, qualification records, and curricula in inspection-ready state.
• Provide coaching and hands-on guidance to operators, leads, SMEs, and investigators.
• Assist in enhancing inspector training and qualification processes for new products.
• Track metrics demonstrating the value of training programs.

Skills

Pharma manufacturing

Training

GMP knowledge

MS Office

Communication

Organization

Cross-functional collaboration

Quality documentation

Education

Bachelor's degree

Tools

Microsoft Office

Job description

Our Work Matters

At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world.

The Impact You Will Make

The Visual Inspection Trainer is responsible for the design, delivery, assessment, documentation, and continuous improvement of training programs supporting the Inspection Department within a GMP-regulated pharmaceutical manufacturing environment. This role oversees Inspector qualification activities, conducts routine operator assessments, and ensures training programs meet regulatory, quality, and operational requirements. The trainer collaborates closely with Inspection Operators, Quality, and Operations Management to ensure personnel are qualified and inspection processes remain compliant, consistent, and effective.

Responsibilities

• Accountable for developing and delivering training for the Packaging and Inspection (P&I) department on topics such as Training/Qualifications, Regulatory/Compliance, GMP, and Right First Time (e.g., Six Sigma) topics.
• Ensure that quality, compliance, safety, and production standards are met.
• Complete all Inspector qualification training and qualification per procedure.
• Perform audits/quarterly assessments of production operators to ensure compliance.
• Ensure training files, qualification records, and curricula are inspection-ready.
• Provide defect-related coaching, hands‑on demonstrations, and technical guidance to Inspection Operators, Leads, SMEs, and Investigators.
• Aid in the development of enhancements to the Inspector training and qualification process, including new products.
• Track metrics to show quality/value of executed training procedures.

Basic Qualifications

• High School Diploma
• 3+ years in pharmaceutical manufacturing, with experience in training/teaching roles.
• Strong written and verbal communication skills with the ability to present information clearly to individuals or groups.
• Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint, Outlook, and Teams).
• Strong organizational and prioritization skills with the ability to manage multiple assignments and deadlines.
• Demonstrated critical thinking, decision‑making capability, and accountability.
• Working knowledge of GMPs and training/technical documentation formats (SOPs, etc.).
• Ability to collaborate effectively with cross‑functional teams, including production colleagues and management personnel.

Preferred Qualifications

• Bachelor’s degree
• 5+ years in pharmaceutical manufacturing, OR experience in teaching/training roles.
• Familiarity with visual inspection systems, manual inspection, and/or automated inspection technologies.

California residents should review our Notice for California Employees and Applicants before applying.

Kindeva does not accept unsolicited assistance from headhunters or recruitment firms for any of our job openings. Any resumes or candidate profiles submitted to Kindeva employees—regardless of format—without a valid, signed agreement and an approved job order from an authorized signatory in Talent Acquisition will be considered the sole property of Kindeva. No fees will be paid in the event that a candidate is hired as a result of an unsolicited resume or referral.

Equal Opportunity Employer

Kindeva Drug Delivery is an Equal Opportunity/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, Protected Veteran status, sexual orientation, or any other characteristic protected by federal, state or local law.