Manufacturing Associate

* Creates and revises Solution Records, Work Instructions, Standard Operating Procedures and other GMP documents related to the support work.
* Reviews cleaning logbook forms for accuracy.
* Execute solution records under GMP regulations and related SOPs. Document all manufacturing activities clearly and accurately, including preparation
records, testing records, and equipment use records.
* Work in collaboration with the Quality Assurance group to fulfill quality management goals and ensure the highest quality manufacturing processes.

• Prior experience following GMP rules and procedures.

• High School Diploma or equivalent and a minimum of 18 months of related bio pharmaceutical manufacturing experience in FDA regulated, controlled production environment.
  OR

• Associate's degree in a related discipline and a minimum of 1 year of related bio pharmaceutical manufacturing experience in FDA regulated, controlled production environment.
  OR
• Bachelor's degree in a scientific field and a minimum of 6 months of related biopharmaceutical manufacturing experience in FDA regulated, controlled production environment.

• Life sciences related bachelors degree

• Eager to work
• Ability to work independently and within a team environment
• Willingness to learn