Manufacturing Associate I - DG Growth
La Jolla, CA
Job ID: 619
Job Req code: 619
Job Type: Manufacturing
Manufacturing Associate I is responsible for completing and assisting with daily tasks associated with cell-related functions, including producing cells, intermediate product, and manufacturing final product for commercial distribution. Additionally, the Associate I will be responsible for following SOPs, performing daily tasks in a clean room/cGMP environment per the current QSRs. The Manufacturing Associate I may also be responsible for the troubleshooting of manufacturing challenges. Follows established company rules, regulations and safety precautions, and maintains quality standards.
- The Manufacturing Associate I is responsible for completing and assisting with daily tasks associated with cell-growth functions, including seeding cells, media changes, and harvest of final product for commercial distribution.
- Responsible for following SOPs, performing daily tasks in a clean room/cGMP environment per the current QSRs. May also be responsible for troubleshooting manufacturing product challenges.
- Follows established company rules, regulations and safety precautions, and maintains quality standards.
- Performs production related tasks as assigned by the Area Supervisor or Group Lead. These tasks can include, but are not limited to, Quality Event Notifications, Facilities Maintenance Requests, ordering supplies and/or equipment for Production, and collaborating with supporting teams to meet company goals.
- Assist in providing positive and constructive individual feedback and building teamwork.
- Minimum of 2 years’ prior working experience in a manufacturing environment (Biotech/Pharmaceutical Industry) with a high school diploma; 0-1 year with a Biotech Program certificate from an accredited college
- Must have hands-on-experience with commonly used production concepts, practices, and procedures such as cell culture and aseptic technique.
- General knowledge of clean room practices and familiarity with Current Good Manufacturing Practices (cGMP).
- Must be detail-oriented with an ability to set priorities, and organize daily work requirements. The Manufacturing Associate I must be able to work as a team member and independently as required.
- Ability to perform calculations using weight measurement, volume, and distance governed by Quality documents and Standard Operating Procedures.
- Experience in writing and/or revising Standard Operating Procedures (SOPs), Batch Records, and other Quality/Compliance related documents.
- Aseptic technique, clean room gowning and extensive knowledge of Good Manufacturing Practices (GMPs), with an emphasis on Biologics.
- Effectively communicate with internal and external group members by collaborating with sub-teams within manufacturing and across Organogenesis.
- Working in a clean room environment required. Must clothe in clean room gowns to perform duties.
- Effective communication and listening skills are required.
- Must work with living human cells and various chemicals.
- Must be able to push 150+ lbs. (on wheels), and lift 50lbs. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
- Due to the nature of production work, overtime and weekend work is a requirement of employment and is variable based on company needs. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
- The hours for this position are: Monday - Friday, 6:00 am - 2:30 pm with availability to work holidays.
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