Job Location: Elwood, Kansas Job Type: Full Time Department:
Production Technology / Manufacturing and Production Facility:
BI Vetmedica
Our Culture
In a world where business is driven by short term financial goals, Boehringer Ingelheim is truly a company with a different philosophy. Although we are one of the largest and fastest growing pharmaceutical companies in the world, we have been able to maintain a dedication to our values. Our focus is on helping patients, serving our customers and improving the quality of life for the millions of people who rely on us. Simply put, we have remained committed to doing the right thing-for our customers, our communities, our employees and everyone we serve.
At Boehringer Ingelheim, we realize that our strength and competitive advantage lie with our people. We support our employees in a number of ways to create a healthy working environment-meaningful work, diversity, mobility, networking and work-life balance
Boehringer Ingelheim is firmly committed to ensuring a safe, healthy, productive and efficient work environment for our employees, as well as our partners and customers. As part of that commitment, Boehringer Ingelheim conducts pre-employment background checks and drug screenings.
RESPONSIBILITIES
Monitors/supervises formulation, filling, packaging and cleaning under jurisdiction to completion, ensuring cGMP’s and safety procedures are adhered to at all times.
Reviews documentation (i.e. batch records, log books, forms) for completeness and correctness.
Schedules and executes production per marketing forecast and sales.
Develops and/or revises documentation (i.e. batch records, standard operating procedures, forms) to maintain compliance with regulatory (FDA, OSHA, EPA) requirements.
Schedules/coordinates equipment and facility maintenance or repairs, including enhancement/modification to maintain compliance with regulatory (FDA, OSHA, EPA) requirements.
Trains and evaluates subordinates as required.
Requisitions purchase of operating supplies and recommends purchase of new or replacement equipment.
Executes equipment installation (EIQ), performance qualification (PQP), and system performance (SPQ) validation protocols as needed.
QUALIFICATIONS
Four year degree in relevant technical discipline or five to ten years' supervisory experience in a pharmaceutical or GMP regulated environment.
