BioPharma Consulting JAD Group is actively seeking a Manufacturing Contractor I to support our clinical manufacturing operations at our Norton Manufacturing Facility. In this role, the Manufacturing Contractor I will work closely under the guidance of senior staff to ensure the production processes comply with current Good Manufacturing Practices (cGMP). Responsibilities will involve the operation of manufacturing equipment, following standard procedures, and maintaining a clean and organized workspace to facilitate an efficient production environment.

Key Responsibilities:

• Operate production equipment according to Standard Operating Procedures (SOPs) to produce clinical products.
• Handle equipment in weigh/dispense, solution preparation, cleaning-in-place (CIP), cleaning-out-of-place (COP), small parts cleaning, and materials stocking in manufacturing suites.
• Participate in the preparation of solutions and handling of raw materials for production activities.
• Ensure materials are accurately weighed, dispensed, and stocked.
• Perform routine cleaning and maintenance of production equipment, adhering to current Good Manufacturing Practices (cGMP) and environmental health and safety (EHS) standards.
• Accurately document all manufacturing activities, maintaining detailed and compliant records.
• Work closely with cross-functional teams, including Facilities, Quality Control (QC), Quality Assurance (QA), Materials Management, and Environmental Health and Safety (EHS), to ensure the seamless completion of production activities.

Requirements

Qualifications:

• Bachelor's preferred in Biology or similar or Biotech certificate and 2 Years of Pharmaceutical Industry experience or medical device
• Basic understanding of cGMP and Quality Assurance practices.
• Ability to follow detailed instructions and SOPs.
• Strong attention to detail and commitment to safety and compliance.
• Effective communication and teamwork skills.