GMP Training Lead

ZoetisAtlanta, GA
Onsite

About The Position

Zoetis is the world leader in animal health, dedicated to serving veterinarians, livestock producers, and people who raise and care for farm and companion animals in over 100 countries. We are building a new manufacturing facility in Lithia Springs, GA, to support our growing monoclonal antibody and vaccine portfolios. We are seeking a GMP Training Lead to provide flexible training support across identified functions, delivering training from startup to full operations and addressing additional training needs as they arise. This role is the primary trainer for cGMP, cGDP, contamination control, and aseptic behavior related to the aseptic manufacturing of biologic products and materials. The GMP Training Lead will design, develop, and implement curricula, and conduct training for monoclonal antibodies drug product manufacturing and biologics packaging in compliance with site procedures and global standards. This position will also identify and drive continuous process improvements related to GMP and aseptic training, and continuously improve and innovate training execution and management. The role involves conducting audits/reviews of personnel to evaluate training effectiveness and making decisions in accordance with company policies, SOPs, Core Values, and global regulatory guidelines.

Requirements

  • Bachelor’s degree in Training & Development, Instructional Design, Adult Education, Organizational Development, Learning & Development, or Engineering, Biology, Chemistry, Microbiology, Virology, Immunology.
  • Minimum of 5+ years of experience in training delivery, training coordination, curriculum development, learning and development, or related training functions, including demonstrated classroom facilitation and presentation experience.
  • Strong technical/analytical skills and possess a high degree of personal motivation.
  • Excellent interpersonal skills and ability to interact across divisional boundaries.
  • Familiar/proficient in adult learning methodologies
  • Strong technical writing skills.
  • Knowledge of FDA, APHIS, VMD, USDA regulations applicable to the Pharmaceutical/Biological industry.
  • Must be able to walk or stand for long periods of time.
  • Must be able to reach above shoulder level, bend/stoop, kneel, push/pull, and handle/grip frequently.
  • Must be able to work scheduled 40 hours with the ability to work overtime as needed.
  • Frequent lifting and carrying of 5 to 25 lbs.
  • Regular reaching, bending, stooping, and twisting
  • Repetitive motion and substantial movement of the wrists, hands, and/or fingers
  • Able to become qualified to enter clean room environments
  • Must possess or obtain authorization to work in the US for Zoetis.

Nice To Haves

  • Preferred experience in aseptic and biological product formulation (blend/fill/lyophilization), packaging, and/or testing.
  • A working knowledge of vaccine production methods and experimental design and experience in GLP or cGMP.

Responsibilities

  • Learning Management System administration (SAP SuccessFactors)
  • Facilitate New Employee Orientation (including cGMP/cGDP/cGLP), and aseptic training for initial and refresher training for site personnel, including gowning qualification and classroom process simulations.
  • Coordinates required annual training requirements with department management
  • Conducts spot checks/audits of aseptic techniques and behaviors during operations
  • Observes aseptic process simulations (media fills) for aseptic practices and best practices.
  • Network with the Global Aseptic Team to share best practices.
  • Liaison with colleagues to ensure they are trained and understand the criticality of the aseptic process work they are conducting.
  • Coordinates personnel training using available technology, including, but not limited to, virtual reality technology.
  • Integrates training sessions and training documentation into electronic training document management systems.
  • Collaborate with area Operations Team Leaders to train and lead colleagues in the performance of best practices.
  • Collaborate with QC to analyze training techniques and instructions for error prone testing
  • Collaborate with QA to analyze training techniques and instructions for incidents with patterns and trends
  • Utilize subject matter knowledge related to Aseptic Processing in the conduct of training, including GMP/Regulatory Requirements, Compliance Trends and Data Integrity, Basic Industrial Microbiology, Types of Microorganisms, Growth and Reproduction, Sources of Cleanroom Contamination, Reduction/Elimination, Measurement Systems, Site Specific Data Trends and Metrics, Facility Design / Environmental Controls, Cleaning and Disinfection, Aseptic and Controlled Area Gowning, Aseptic Training / Good Aseptic Technique, Material Transfer, Material/Personnel / Equipment Flow and Movement, Use of Isolator and Barrier Systems, Sterilization / Validation, and Bioburden Reduction.

Benefits

  • Full time Regular Colleague
© 2026 Teal Labs, Inc
Privacy PolicyTerms of Service