Manufacturing Associate

Responsibilities

• Assemble and label pharmaceutical clinical trial treatments and supplies accurately.
• Follow all regulatory manufacturing standards, procedures, and compliance requirements.
• Support the safe and compliant preparation of clinical materials used in pharmaceutical research and production.
• Perform manual and automated filling, packaging, and labeling of pharmaceutical products.
• Count, verify, and prepare products to ensure inventory accuracy before and after production runs.
• Complete required operational training and maintain compliance with company procedures and quality standards.
• Follow GMP, safety, and manufacturing guidelines during all packaging activities.

Requirements

• A high school diploma or GED.
• Experience in pharmaceutical, biotechnology, manufacturing, or food and beverage industries preferred.
• Familiarity with packaging processes and GMP (Good Manufacturing Practice) environments is highly desired.
• Strong attention to detail and accuracy.
• Ability to read and interpret procedure manuals, training materials, batch records, and product documentation.
• Team-oriented mindset with the ability to work safely, efficiently, and collaboratively.

Qualifications

None specified.

Skills

• High school diploma or GED.
• Experience in pharmaceutical, biotechnology, manufacturing, or food and beverage industries.
• Familiarity with packaging processes and GMP (Good Manufacturing Practice) environments.
• Attention to detail and accuracy.
• Ability to read and interpret procedure manuals, training materials, batch records, and product documentation.
• Team-oriented mindset.

Benefits

None specified.

Pay

Details not specified.

Schedule

Onsite shift timings: Monday to Thursday 02:45PM to 01:30 AM (Overtime is expected frequently on Friday's from 02:00PM - 08:00PM).