Job Location: Saint Joseph, Missouri Job Type: Full Time Department:
Other / Other 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.
QUALIFICATIONS:
Detailed working knowledge of applicable portions of cGMP guidelines, 9CFR, and production outlines
Technical knowledge normally attained by undergraduate courses in microbiology, biology, & chemistry
Written and verbal communication skills with individuals inside and outside the company, as well as vertically and horizontally within
Ability to interpret and analyze technical data for evaluating results and solving problems
Ability to train and utilize hourly workers in a technical environment
DUTIES & RESPONSIBILITIES:
Write and review SOP's, Process Records, Quality Standards, Change Controls, Unusual Occurrences, and other reports as required. Maintain accurate and timely completion of records
Analyze product performances by maintaining and reviewing database measurements that aid in the performance of potency, sterility and stability of viral and bacterial antigens
Assists in the Transfer and Implementation of new products or product improvements through the preparation of protocols, analytical tools and controls. Also, support the Management staff in the training of Production Operators during such transfers
Assist in troubleshooting production performance issues such as but not limited to potency, stability and contamination. Evaluate trends in performance and recommend solutions. Prepare reports and assist in Unusual Occurrence Investigation for Production Management. Assist in implementation of corrective and preventative actions
Monitor Production Operator aseptic processing with regard to compliance to procedures. Evaluate improvements for implementation
Assist Management with the evaluations of processes to cut costs and stream line processes
Calculate and review product formulations and batch records
Abide by and enforce the articles of the Bargaining Unit Contract
Assist in implementing BPE initiative within the Department
