Cleanroom Technician / Cleanroom Technicianess

Cleanroom Technician - Contract - Philadelphia, PA

Play a crucial role in advancing life-changing cell and gene therapies by ensuring GMP production environments remain audit-ready and contamination-free. Proclinical is seeking a Cleanroom Technician to support activities related to the disinfection and maintenance of GMP spaces and equipment. This role is vital in ensuring compliance with current Good Manufacturing Practices (cGMPs) within production facilities focused on cell and gene therapy products.

Primary Responsibilities

The successful candidate will be responsible for the following:

• Support activities and disinfection of GMP spaces, equipment, and associated areas involved in the manufacture of Master and Working Cell Banks.
• Ensure compliance with current Good Manufacturing Practices (cGMPs) within production facilities focused on Cell & Gene Therapy products.

Skills & Requirements

• High school diploma or equivalent.
• Familiarity with aseptic techniques and cleanroom protocols.
• Basic technical knowledge and understanding of GMP environments.
• Ability to follow detailed procedures and regulatory requirements.
• Strong organizational skills and attention to detail.
• Basic computer proficiency, including Microsoft applications.
• 1-2 years of relevant or equivalent experience.

Key Responsibilities

• Must be able to wear appropriate clean room attire (i.e., surgical masks) and all Personal Protective Equipment (PPE).
• Perform cleaning methods, such as wiping techniques of equipment, and wall, ceiling, and floor mopping techniques.
• Responsible for the operation, maintenance, and cleaning of equipment.
• Responsible for cleaning/sanitization solution and material preparation.
• Understands aseptic technique concepts and proper cleanroom behavior.
• Responsible for receiving and organizing gowning and cleaning materials.
• Identifies and communicates material discrepancies.
• Follows compliance and regulatory requirements and current Good Manufacturing Practices (cGMPs).
• Executes Standard Operating Procedures (SOPs).
• May participate in training activities of others on SOPs and equipment.
• Participates with technical documents such as non-conforming events and deviations.
• Suggests continuous improvement ideas.
• Assists supervision with internal pre-audit walkthroughs, cGMP housekeeping, and general organization of manufacturing spaces.

If you are interested in this exciting opportunity, please apply online using the form below. Only applications matching the job profile will be considered.

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