US02 Lonza Biologics Inc.
Temporary Quality Assurance Lot Review Associate (Biotech)
At Lonza, we invest in great people. We encourage our employees to challenge themselves and we offer an environment that fosters creativity and success. Headquartered in Basel, Switzerland, we operate production, R&D, and business sites around the world, including Europe, North America, and Asia.
We strive to be the leading supplier using science and technology to improve the quality of life.
We work with passion, using advanced technologies, to transform life science into new possibilities for our customers.
The primary responsibility of the Temporary Quality Assurance Lot Review Specialist is the review and closeout of all production batch documentation prior to release. Documentation includes manufacturing batch records and ancillary documentation such as Lot Genealogy Reports, and QC assays used in the production of Active Pharmaceutical Ingredients (API). The Quality Lot Review Specialist I makes decisions regarding routine tasks that arise during review of records and escalates to senior members of the team for complex issues; develops a skill set appropriate to the level that includes understanding quality systems, manufacturing practices, Good Documentation Practices, as well as effective communication and listening.
** This is a contract position that will go for four to six months with the possibility of extending**
** This is a day shift Monday - Friday normal business hours role **
Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.