Production Associate: GMP Manufacturing & Growth

Enviromedica; Austin (TX); On-site; USD 25,000 - 33,000; Full time

Benefits offered by this job

Medical, Dental, Vision benefits

401k

PTO and 8 paid holidays

Job summary

Enviromedica is seeking a Production Associate to support a variety of automated and manual manufacturing processes. You will follow a production schedule, maintain high quality, and meet deadlines in a cGMP environment.

You will perform tasks across filling, labeling, cartoning and material movements, while complying with safety standards and documenting activities. Prior manufacturing or biotech exposure is preferred.

Qualifications

• High School diploma or GED, or 4+ years production experience.
• Experience in biotech/food industry desirable.
• Experience in GMP/FDA regulated industry preferred.
• Experience in Lean Manufacturing preferred.
• Ability to perform simple math calculations.
• Must be able to lift 50 pounds from pallet to ground.

Responsibilities

• Operate a variety of production tasks to optimize operations and quality.
• Follow gowning, lab and documentation practices per GMP guidelines.
• Identify unsafe practices and report to maintain safety.
• Keep work areas, cabinets and materials organized (5S).
• Participate in line audits to ensure safety, compliance and efficiency.
• Support end-of-day data collection and maintenance of records.
• Move materials from warehouse to production line and return unused materials.
• Assist in line changeovers and setup to maximize efficiency.
• Assist in packaging, labeling and pallet loading for distribution.
• Keep production equipment clean and process rooms maintained.

Skills

Math skills

Written comms

Team player

Education

High School diploma or GED

Tools

Lean Manufacturing

GMP Manufacturing

FDA regulated industry

Job description

Enviromedica is seeking a Production Associate to support a variety of automated and manual manufacturing processes. You will follow a production schedule, maintain high quality, and meet deadlines in a cGMP environment.

You will perform tasks across filling, labeling, cartoning and material movements, while complying with safety standards and documenting activities. Prior manufacturing or biotech exposure is preferred.