Cell Therapy Training Specialist

R&D Partners; Philadelphia (Philadelphia County); On-site; USD 85,000 - 95,000; Full time

Job summary

An established industry player is seeking a Training Specialist to enhance their autologous cell therapy manufacturing program. This role requires a solid foundation in cell culture and aseptic techniques, alongside a commitment to Good Manufacturing Practices. As a subject matter expert, you will develop training materials and deliver engaging content to manufacturing technicians. Join a dynamic team where your expertise will contribute to continuous improvement and innovation in the biotechnology field. If you are passionate about training and development in a cutting-edge environment, this opportunity is perfect for you.

Benefits

Medical Insurance

Vision Insurance

401(k)

Qualifications

• Minimum 2 years of experience in biopharmaceutical GMP manufacturing.
• Technical knowledge of aseptic processing in cleanroom environments is essential.

Responsibilities

• Develop understanding of cell therapy manufacturing processes.
• Adhere to GMP and SOPs while delivering training to technicians.

Skills

Cell Culture

Aseptic Technique

Training Development

Good Manufacturing Practices (GMP)

ISO Class 5 Cleanroom Operations

Education

Bachelor's Degree in Biology

Bachelor's Degree in Biochemistry

Bachelor's Degree in Bioengineering

Job description

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This range is provided by R&D Partners. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$85,000.00/yr - $95,000.00/yr

Direct message the job poster from R&D Partners

I am hiring! | Life Sciences Recruitment | Scientific Recruiter at R&D Partners

Overview:

The Training Specialist will be a trainer for the autologous cell therapy manufacturing program. A background in cell culture, aseptic technique, aseptic gowning and qualification and ISO class 5 cleanroom operations is required.

Duties:

• Develops a basic understanding of the current cell therapy manufacturing process and the equipment utilized during processing, as this role is viewed as a subject matter expert (SME) within this specific area.
• Adheres to Good Manufacturing Practices (GMP) and Standard Operating Procedures (SOPs), including Good Documentation Practices (GDP).
• Presents and delivers content to manufacturing technicians.
• Assists with the creation, review and improvement of designated training scripts; On the Job and Instructor Led Trainings (OJTs and ILTs).
• Helps to identify training needs; assists in establishing a feedback loop to ensure continuous improvement.
• Assists with drafting SOPs, Batch Records, Deviations, CAPAs, etc. Performs revisions as needed to accurately reflect current procedures.

Qualifications:

• Minimum bachelor’s degree (B.A./B.S.) in biology, biochemistry, bioengineering, or related technical field, or equivalent industry experience
• Minimum of 2 years of experience in biopharmaceutical based GMP manufacturing operations, including experience in cell culture.
• An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
• Technical knowledge of aseptic processing in cleanroom environments is a must.
• Knowledge of and experience with in-lab skills training, including aseptic technique, cell culture processing, aseptic gowning and qualification is a must.
• Experience leading “development” initiatives such as training, coaching/mentoring, learning initiatives.

Seniority level

• Seniority level

  Associate

Employment type

• Employment type

  Full-time

Job function

• Job function

  Science

• Industries

  Biotechnology Research and Pharmaceutical Manufacturing

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Inferred from the description for this job

Medical insurance

Vision insurance

401(k)

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