BioPharma Consulting JAD Group is seeking a skilled Manufacturing Contractor to play a vital role in our production team. You will perform routine clinical manufacturing operations with direct supervision, ensuring compliance with cGMP standards, safety, and efficiency. This role involves operating production equipment, performing cleaning processes, preparing solutions, and maintaining materials stock within manufacturing suites.

Responsibilities:

• Operate production equipment in accordance with SOPs for clinical product manufacturing.
• Execute weigh/dispense operations and solution preparation.
• Perform equipment CIP (clean-in-place), COP (clean-out-of-place), and small parts cleaning.
• Stock materials and supplies within manufacturing suites.
• Collaborate with support groups, including Facilities, QC, QA, Materials Management, and EHS, to ensure accurate and timely completion of activities.
• Execute and monitor manufacturing procedures, ensuring adherence to cGMP (current Good Manufacturing Practice) regulations throughout the production processes.
• Operate and maintain production equipment, including but not limited to mixing tanks, filling machines, and filtration systems.
• Perform routine quality checks to ensure that all products meet specified standards and specifications.
• Document all manufacturing activities accurately and in a timely manner to maintain compliance with regulatory standards.
• Participate in team meetings and training sessions to continuously improve manufacturing processes.

Skills:

• Strong understanding of manufacturing processes and cGMP guidelines.
• Experience with operating and troubleshooting manufacturing equipment.
• Excellent attention to detail and accuracy in documentation.
• Ability to work effectively in a team-oriented environment.
• Good problem-solving skills and the ability to multitask in a fast-paced environment.

Requirements

Requirements:

• Education: Biotech Certificate or a 2-year degree preferred.
• Experience: Minimum of 1+ year of industry experience preferred.
• Strong understanding of cGMP guidelines and manufacturing operations.
• Excellent attention to detail and organizational skills.
• Ability to work collaboratively with cross-functional teams.

• Standard Schedule: Wednesday to Saturday, 2:00 PM - Midnight.
• Must be able to adhere to the fixed schedule and meet weekly 40-hour requirements.