Central Services EU Operator LG4

Description:

Description\:

To perform duties in the manufacture of high quality biological products.

As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies' success. We realize that our strength and competitive advantage lie with our people. We support our employees in a number of ways to foster a healthy working environment, meaningful work, diversity and inclusion, mobility, networking and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim's high regard for our employees.

Duties & Responsibilities\:

• Prepare, review and audit for completion and accuracy all assigned records, calibration, and documentation in assigned area to ensure regulatory compliance is maintained.

• Read and follow schedules, procedures, and documents.

• Assist in training other employees in an area of responsibility as assigned.

• Assist staff in developing new procedures and methods or improving old ones.

• Use and understand computer assisted data entry, and process logic controllers (PLCs) including SAP.

• Assist lower labor grades as needed to insure the completion of daily tasks.

• Assist validation group perform department equipment validations needed

• Assign Batch Numbers to the appropriate product and Batch Record

• Prepare all assigned records, calculations, and documentation, and accurately post completed Batch Record to the appropriate Shop Packet.

• Maintain and operate laboratory equipment, such as but not limited to, pH meters, integrity testing units, Operator Interface Terminals (OIT), HMI’s, and osmometer.

• Operate and maintain all laboratory and production equipment including monitoring and properly interpreting all indicators, controls, and PLC controllers.

• Assist staff in troubleshooting equipment problems.

• Assist in the transfer of new products, new test methods, new production processes, and new technology.

• Perform filter integrity testing and prepare accurate documentation.

• Calibrate pH controllers.

• Prepare, sterilize, dispense media and solutions, disinfectants, and sanitizing solutions.

• Perform filter sterilization and heat sterilization operations.

• Sterilize Add cans, tanks, vessels, and equipment using autoclaves, ovens, clean-in-place (CIP), steam-in-place (SIP), steam docking procedures and TOC.

• Set-up filters for sterilization.

• Maintain production vessels such as but not limited to pressure hold test, inspect/change gaskets and valves.

• Perform, monitor, and assist in troubleshooting all media processes.

• Weigh out and prepare production media as needed to meet demands of production.

• Use and understand computer assisted data entry, including SAP.

• Ability to independently clean, prepare, and sterilize production equipment.

• Maintain inventory of raw materials to insure production needs are met.

• Perform scheduled preventative maintenance.

• Assist technician under supervision

• Required to perform work of a lower classification as needed.

• Other duties as assigned.

Requirements\:

• High school diploma or equivalent.

• Good verbal and written communication skills and ability to train others.

• Ability to perform calculations and conversions involving weights, volumes, and percentages.

• Ability to use basic logic to identify and solve problems

• Knowledge and skill to recognize creative ideas that add value and are able to be implemented to improve efficiency, effectiveness and reduce complexity for department

• Demonstrated understanding of systems, equipment, and processes

• Experience with Windows Operating System.

• Proficient reading, comprehension and application skills toward a diverse set complicated tasks.

Preferred Experience, Skills, and Abilities\:

• Additional Education and/or Equivalent Experience.

• Successful completion of National Career Readiness Work Keys assessment.

• Knowledge of Hazardous Waste Handling.

• Knowledge of Decontamination and Sterilization.

• Knowledge of Traffic Patterns.

• Knowledge of or evidence of working with BPE methods.

• Understanding of Basic GMP/Documentation practices.

• Demonstrated ability and understanding of Safe working habits and Material Safety Data Sheets (MSDS).

• Understanding of Basic Laboratory Practices, Measurements, Biology and Microbiology.

• Understanding of operating in an aseptic environment.

• Ability to work in a team environment.

• Demonstrated knowledge of Federal, State, and International regulations, such as cGMP, USDA, DOT, EPA, OSHA as they pertain to the employee’s work.

• Demonstrated knowledge of Corporate guidelines and Policies related to the employee’s work. Shall have an adequate knowledge of Drug and Chemical names, and be able to distinguish between similar names, physical appearance and precautions in handling.

• Must be able to proceed independently in product processing in accordance with standard methods, standard operating procedures, and Manufacturing Directions, using proper aseptic techniques.

Physical Requirements\:

• MEDIUM LEVEL 3 – Work related tasks & weights forces associated\: Lifting, push/pull in this dept. does not exceed 50 pounds of force. Lifts include hoppers weighing 25 pounds; carboys are only handled empty; the washer lifts 39 pound lids; 325 tanks using 40 pounds of force to push/pull; trucks w/new wheels taking 20-25 pounds to push/pull; pistons out of fill room are moved around 35 pounds; push/pull of autoclave doors take 25-30 pounds; push/pull of empty sub tank takes 60 pounds (2 person push taking 30 pounds each; full tanks are moved using a machine). 2 full ad cans on autoclave cart 18 pounds push/pull, 19 pounds push/pull on transfer cart

• Ability to wear a respirator as a requirement of the job, no pulmonary restrictions.

Eligibility Requirements\:

• Must be legally authorized to work in the United States without restriction.

• Must be willing to take a drug test and post-offer physical (if required).

• Must be 18 years of age or older.

Who We Are\:

At Boehringer Ingelheim we create value through innovation with one clear goal\: to improve the lives of patients. We develop breakthrough therapies and innovative healthcare solutions in areas of unmet medical need for both humans and animals. As a family owned company we focus on long term performance. We are powered by 50.000 employees globally who nurture a diverse, collaborative and inclusive culture. Learning and development for all employees is key because your growth is our growth.

Want to learn more? Visit boehringer-ingelheim.com and join us in our effort to make more health.

Boehringer Ingelheim is an equal opportunity global employer who takes pride in maintaining a diverse and inclusive culture. We embrace diversity of perspectives and strive for an inclusive environment, which benefits our employees, patients and communities. All qualified applicants will receive consideration for employment without regard to a person’s actual or perceived race, including natural hairstyles, hair texture and protective hairstyles; color; creed; religion; national origin; age; ancestry; citizenship status, marital status; gender, gender identity or expression; sexual orientation, mental, physical or intellectual disability, veteran status; pregnancy, childbirth or related medical condition; genetic information (including the refusal to submit to genetic testing) or any other class or characteristic protected by applicable law.

ACKNOWLEDGEMENT

This position description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities and qualifications required of employees assigned to the role.