GMP Lab Operations Coordinator

Actalent; New Jersey; On-site; USD 33,000 - 36,000; Full time

Benefits offered by this job

Medical, dental & vision

401(k) Retirement Plan

Life Insurance

Disability benefits

Job summary

Actalent is seeking personnel for contract manufacturing support in a GMP environment. The role involves preparing materials and equipment for GMP operations, supporting QA/QC activities, and ensuring documentation complies with cGMP standards.

Responsibilities include inventory management, equipment cleaning, validation readiness, and contributing to continuous improvement initiatives within a fully onsite Burlington, MA setting.

Qualifications

• GMP experience is required in a highly regulated environment.
• Ability to follow SOPs and work in a cleanroom environment.
• Experience in pharmaceutical/biotech/medical device settings is preferred.

Responsibilities

• Support manufacturing by preparing materials and equipment for GMP operations.
• Assist QA, QC, validation, and process development activities.
• Complete documentation in compliance with cGMP standards.
• Manage inventory and ensure equipment is cleaned and ready for use.
• Identify and address equipment/process/quality issues for continuous improvement.

Skills

GMP experience

SOP adherence

Cleanroom operations

Documentation

Education

HS diploma or Associate's degree

GMP experience

Job description

Actalent is seeking personnel for contract manufacturing support in a GMP environment. The role involves preparing materials and equipment for GMP operations, supporting QA/QC activities, and ensuring documentation complies with cGMP standards.

Responsibilities include inventory management, equipment cleaning, validation readiness, and contributing to continuous improvement initiatives within a fully onsite Burlington, MA setting.