Associate Production Scientist - Day Shift

MerckSaint Louis, MO
Onsite

About The Position

The GMP Associate Production Scientist – Day Shift at the 3300 South Second Ave/ Cherokee site, will manufacture products according to established protocols, provide technical support to others and perform operations supporting the group and department. This role will support 24/7 manufacturing operations and work 12-hour shifts from 6:00am – 6:30pm. including a 5% shift differential. The position involves evaluating products, assisting with buffer formulation, scheduling and communication with ADC, and maintaining required training. Responsibilities include performing routine processes, cleaning equipment and areas, supporting facility functions, communicating operational status and concerns, and maintaining accurate records. The role requires interaction with other departments, independent and team-based work, participation in quality audits, and process improvement through scientific knowledge. The position also involves taking action to resolve unsafe conditions and training team members.

Requirements

  • Bachelor’s Degree in Chemistry, Biochemistry, Biology, or other science disciplines OR Associate Degree in Chemistry, Biochemistry, Biology, or other science discipline
  • 2+ years of production, GMP experience (pharmaceutical GMP operations environment, Quality, knowledge of Good Documentation Practices)

Nice To Haves

  • Familiar with laboratory instruments and production equipment
  • Knowledge of process techniques, unit operations, and safe chemical handling methods
  • Experience with Microsoft Office (Word, Outlook, Excel, etc.)
  • Mechanical and troubleshooting skills
  • Knowledge of ICH Regulatory and Quality standards
  • Knowledge of Operational Excellence

Responsibilities

  • Evaluate products according to established protocols
  • Provide technical support to others
  • Perform operations in support of the group and department
  • Safely perform operations to meet quality expectations
  • Assist with Buffer formulation
  • Schedule and communication with ADC
  • Maintain required training to perform tasks/assignments
  • Perform routine processes and unit operations
  • Clean equipment and working areas during and after operations
  • Support facility functions (e.g., maintain equipment, prepare reagents, restock supplies, waste disposal)
  • Communicate the status of operations and convey concerns to the supervisor
  • Provide complete and accurate records consistent with quality guidelines
  • Ensure all applicable logbooks are completed as required by current procedures
  • Interact with other departments as needed and perform procedures independently and as part of a team
  • Participate as needed in quality audits and customer interactions
  • Improve processes by applying scientific knowledge, experience, and principles, in compliance with change control
  • Take action to resolve unsafe conditions
  • Train team members and act as technical consultants

Benefits

  • health insurance
  • paid time off (PTO)
  • retirement contributions
  • other perquisites
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