Manufacturing Technician

Integrated Resources, Inc ( IRI ); Memphis (TN); On-site; USD 30,000 - 40,000; Full time

Job summary

A biomanufacturing company based in Memphis, TN is seeking a Biomanufacturing Technician I to perform manufacturing activities related to GMP production of cellular products. Responsibilities include writing GMP documentation, supporting validation efforts, and maintaining clean room standards. The ideal candidate should have a high school diploma, attention to detail, and excellent organizational skills. This position requires working nights, weekends, and holidays as needed, and offers training for new hires.

Qualifications

• Zero to 1 year of applicable experience in biotech or cell therapy.
• Ability to work in a clean room environment with hazardous materials.
• Must meet physical requirements for the role.

Responsibilities

• Perform various manufacturing activities related to GMP production.
• Write GMP required documents under supervision.
• Provide support in validation efforts related to the manufacturing process.
• Maintain appropriate clean room behaviors.

Skills

Detail oriented

Excellent organizational skills

Effective written communication

Effective oral communication

Ability to perform algebraic math

Education

High school diploma or equivalent

Associate degree in a scientific field

Job description

NOTE: Training will be provided & must be able to work at night, weekends, and holidays.

Shift

• Day Shift: 6:00am – 6:30pm rotating shift
• Night Shift: 10:30am – 11:00pm rotating shift

Training is 6-8 weeks

Schedule

• Built in OT based off the 2-2-3 set up (i.e. 48 hr week + 36 hr week = 84 hours for two-week period)

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 meet physical requirements established in this job description.
• 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.
• 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.
• 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.