Manufacturing Process Associates

Responsible for manufacturing, assembly, and/or packaging of containers (medical bag) for the Biotechnology industry in a cleanroom environment. Technicians carry out production process by closely following the Standard Operating Procedures, Work Instruction Documents, and blueprints drawings as they relate to assembly, material handling, equipment operation, and finished goods packaging.

Responsibilities:

• Follow work instruction documents, standard operating procedures, and standard work practices
• Assemble product using  written instructions, blueprints and drawings
• Record correct and accurate documentation
• Perform manual assembly of tubing and connectors
• Package and labels finished product
• Perform daily housekeeping tasks as assigned
• Responsible for performing a visual inspection on in-process and finished products

Desired Qualifications:

• Strong analytical and problem-solving abilities
• Good verbal/written communication
• Ability to follow complex procedures
• Production experience in a CGMP or Lean manufacturing environment
• Ability to work in a team environment

Required Qualifications:

• Physical and Environmental Requirements:
• Ability to work in a fast-paced controlled cleanroom environment up to 8 hours a day with additional overtime as required  for production schedule adherence
• The Clean-room is a controlled environment for temperature and humidity having low ambient noise.
• Specific gowning is required including gloves, hair & beard net and face cover, safety glasses with no makeup/jewelry, and the like.
• Ability to use PPE (Personal Protective Equipment) and understand chemical hygiene
• Must have the ability to do the following activities
• Follow all safety protocols
• Stand and move about including reaching, bending, stooping, grasping
• Use hand tools and equipment including forceful gripping, grasping, pushing, and pulling
• Infrequently lift and manipulate up to 50 pounds max unassisted.