Ajinomoto Bio-Pharma Services is looking for Drug Product Manufacturing Associate I in San Diego, CA.
This local job opportunity with ID 780563501 is live since 2021-04-02 20:02:16.
Together, Let’s Make A Difference.
At Ajinomoto Bio-Pharma Services, our mission is to help improve the health of humankind. As a leading, global contract development and manufacturing organization, with sites in the US, Belgium, Japan and India, we work together to empower our clients to bring drugs to market.
Every team member, from manufacturing and quality programs to development and facilities services are a critical component to this effort. At our US location, our focused expertise and capabilities makes us one of the industry’s top leaders for large molecule manufacturing and aseptic drug product fill in vials and syringes.
We believe our people are our greatest asset and we are committed to providing our employees with an environment that supports personal and professional growth. We take pride in knowing our efforts are helping countless patients for years to come.
Do you enjoy working in a dynamic, inspiring team with an amazing culture? If you do, then Ajinomoto Bio-Pharma Services is the place for you.
We are currently seeking a Drug Product Manufacturing Associate I who is responsible for executing GMP production of injectable pharmaceuticals by following all applicable SOP's. Manufacturing associates are responsible for preparing equipment and materials for GMP aseptic production and operating equipment such from glasswashers, autoclaves, depyrogenation ovens and automated filling machines.
High school diploma required. Bachelors in a science or engineering discipline preferred. Experience requirements
Minimum of zero to two (2) years of relevant experience in manufacturing, laboratory, mechanical or engineering positions.
Ability to follow instructions with direct supervision.
Detail oriented with strong written and verbal communication skills.
Demonstrated ability to follow detailed directions in a manufacturing GMP environment.
Familiarity with cGMP, manufacturing, machine operations, and data entry.
Must be familiar with Microsoft Office applications. Responsibilities
Train in one or more areas of the aseptic manufacturing injectable pharmaceuticals using GMP's in FDA regulated facility.
Train on required SOP's and execute training curriculum.
Prepare materials needed for aseptic operations.
Responsible for exhibiting professional behavior with both internal and external business associates that reflects positively on the company and is consistent with the company’s policies and practices.
Performs various routine manufacturing tasks under the guidelines of established SOP’s and cGMP regulations.
Accurately documents data and completes batch records as needed.
Reliably executes well defined SOP’s.
Collects and disposes of lab wastes according to established procedures.
Embodies Aji Bio-Pharma’s cultural values and aligns daily actions with department goals and company culture.