Jobs for People with MS: National MS Society

The Position

As one of the leading contract manufacturers for biopharmaceuticals worldwide, the Boehringer Ingelheim Bio Business Unit drives for innovation and continuously invests in its complex, highly automated production facilities.

You enjoy working closely with Bio & Human Pharma Quality, global Quality, IT, and other Engineer &Technology Qualification Teams?

In your role you shape and standardize efficient and innovative Computer System Validation (CSV) & Qualification Standards for computerized systems across Boehringer Ingelheim Biopharmaceuticals Business Unit in accordance with pharmaceutical regulatory requirements and BI Corporate Requirements.

Tasks & responsibilities

• As Senior Global Validation Manager in HP BioP Engineering & Technology, you will bring in your skills in quality management systems and computerized systems validation to ensure lean implementation and continuous improvement of the CSV & Qualification Standards.

• Picture yourself spearheading the standardization of Equipment Qualification across diverse departments, becoming a beacon of global consistency and efficiency.

• Envision coordinating international meetings, gathering global standards, and aligning on future strategy, all while being an integral part of our dynamic team.

• You'll be the catalyst for continuous improvement, enhancing our CSV & Qualification Standards, processes, and capabilities to elevate overall quality, compliance, and efficiency.

• Dive into the creation of global templates and setting up documentation in a digital validation tool for global CSV activities, becoming a key player in our global operations.

• As the vital link between local and global Validation Managers, Quality, IT, and other Engineering & Technology Qualification Teams, you'll play a crucial role in fostering effective communication and collaboration.

Requirements

• Diploma or master’s degree (MBA, MSC, and MCA) with focus on IT, Engineering, Sciences, Pharmaceuticals, Biotechnology or equivalent

• Several years professional experience in Computerized System Validation and Equipment Qualification at global level, inclusive knowledge of GxP, CSV&C and quality regulations and in data integrity

• Strong exposure to manufacturing processes and IT program management as well as deep understanding of production- and process equipment technologies

• Project Management experience in a complex international environment

• Innovator with the ability to work in a rapidly changing environment

• Fluent in English, verbal and written

Ready to contact us?

If you have any questions about the job posting or process - please contact our HR Direct Team, Tel: +49 (0) 6132 77-3330 or via mail: hr.de@boehringer-ingelheim.com

Recruitment process:

Step 1: Online application - application deadline is July 13th

Step 2: Virtual meeting in the period from mid till end of July

Step 3: On-site interviews beginning of August

Discover our Biberach site: http://xplorebiberach.com

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.