Quality and Production Record Specialist

The Master Manufacturing Record (MMR) specialist is responsible for creating and updating Master Manufacturing Records during project implementation and internal change controls. This position will work closely with Project Management, R&D, Regulatory, and Quality to ensure design and execution of MMR’s are aligned with project deployments and site operation activities. This role is essential in ensuring the smooth operation and continuous improvement of ILS facility, which contributes significantly to organization efficiency and compliance standards.

Key Responsibilities

Create new MMRs for new customers and projects

Update Existing MMRs based on issued change controls

Submit created or updated MMRs for Operations and Quality approval

File newly created or updated MMRs within ILS documentation system

Archive existing MMRs within ILS documentation system

Engage directly with Project Management, R&D, Operations, Regulatory, and Quality departments

Create Packaging Case Labels using Zebra Software

Assist with other projects as needed.

High School Diploma (required), Associates or Bachelors (preferred)

Highly Proficient in Microsoft Excel

1-3 years Dietary supplement / Food / Pharmaceutical manufacturing operations or quality experience (preferred)

Understanding basic quality concepts of Change Control process within a GMP facility

Excellent attention to detail, organization and communication

Able to work independently with a high level of integrity.

Knowledge of Zebra Developer Label System

Benefits:

• 401(k)
• 401(k) matching
• Dental insurance
• Health insurance
• Life insurance
• Paid time off
• Vision insurance

Work Location: In person