Biomanufacturing Technician

AdientOne Consulting; Tennessee; On-site; USD 38,000 - 58,000; Full time

Job summary

Charles River Laboratories seeks a Biomanufacturing Technician I to support start-up and GMP production of cellular products, ensuring aseptic processing and strict adherence to regulatory guidelines.

The role requires flexibility to work night shifts, weekends, and holidays. Training lasts 6–8 weeks on the first shift, with emphasis on clean room protocols and safety in handling hazardous materials.

Qualifications

• Associate degree in a scientific field strongly preferred.
• High school diploma or equivalent required.
• Zero to 1 year of applicable experience in biotech or cell therapy.
• May consider less education and professional experience upon successful internship program completion.

Responsibilities

• Obtain and maintain qualifications necessary for aseptic activities.
• Produce, formulate, and bank cellular products (GMP, GDP, aseptic processing).
• Write GMP documents including SOPs, product specifications, equipment specs and batch records.
• Provide support in validation efforts related to the manufacturing process.
• Participate in manufacturing activities including raw material support, cell culture, and continuous improvement.
• Maintain proper clean room behavior and upkeep of clean room areas.
• Perform all other related duties as assigned.

Skills

Math (algebra)

Detail oriented

Communication skills

Professionalism

Confidentiality

Clean room experience

Biotech experience

Education

Associate degree in scientific field

High school diploma or equivalent

Job description

Note:

1 for day shift (6am-630pm) and 1 for night shift (1030am-11pm).

training is 6-8 weeks on first shift

Virtual Interview- 1 hour

Job Description

The Biomanufacturing Technician I is responsible for performing various manufacturing activities related to the start-up and GMP production of a number of novel cellular products including compliance with regulatory agencies and associated guidelines. Must be able to work night, weekends, and holidays. Must be able to meet physical requirements established in this job description.

ESSENTIAL DUTIES AND RESPONSIBILITIES

• Obtain and maintain qualifications necessary for the performance of aseptic activities.
• Responsible for the production, formulation, and banking of cellular products (including GMP, GDP, and aseptic processing).
• Write, under supervision, GMP required documents including standard operating procedures, product specifications, equipment specifications and batch production records.
• Provide support in validation efforts related to the manufacturing process.
• Participate in all aspects of manufacturing activities including raw material support, cell culture, and continuous improvement.
• Consistently practice appropriate clean room behaviors and upkeep of clean room
• areas.
• Perform all other related duties as assigned.

QUALIFICATIONS

• Associate degree in a scientific field strongly preferred.
• High school diploma or equivalent required.
• Zero to 1 year of applicable experience in biotech or cell therapy.
• May consider less education and professional experience upon successful completion of Charles River's internship program.
• Must be able to work in a clean room environment that potentially includes hazardous materials and medical equipment (including blood, tissues, and needles)
• Must have ability to perform algebraic math.
• Must be detail oriented and have excellent organizational skills.
• Must possess effective written and oral communication skills.
• Must display a high degree of professionalism and confidentiality.