New head of quality assurance at BGS Beta-Gamma-Service

New head of quality assurance at BGS Beta-Gamma-Service

With Sarah Haufe, BGS has a new manager for quality assurance since mid-April. The engineer and trained quality auditor comes from Biovegan GmbH, where she was most recently responsible for quality management and the areas of production and storage as a member of the management board. At BGS, Sarah Haufe is in charge of quality assurance in the business areas of radiation sterilization and radiation crosslinking.

As head of quality assurance at BGS, Sarah Haufe works closely with all business divisions and is responsible for carrying out and monitoring external and internal quality management audits. She heads the department of quality management at the different locations and is responsible for all employees from the test laboratories, quality assurance and management departments at the company’s headquarters in Wiehl, as well as the sites in Bruchsal and Saal an der Donau.

“We are pleased to have been able to recruit Sarah Haufe, an experienced leader and quality manager,” said Managing Director of BGS, Dr. Andreas Ostrowicki. “We shall continue to develop the stringent quality system at BGS together with Ms. Haufe with respect to regulatory requirements and standards as well as the needs of our customers.”

“The creative opportunities and challenges at BGS as a strongly growing company are very appealing to me. As head of quality assurance, I am looking forward to being part of this development and continuously optimising the existing business processes in direct cooperation with the management,” says Sarah Haufe.

Quality assurance and certifications at BGS

BGS has a stringent and sophisticated quality system that is being consistently enhanced. The quality management system of our company is certified pursuant to the standards ISO 9001, DIN EN ISO 13485 and EN ISO 11137. In addition, BGS is registered with the FDA and has the JAPAN PAL certificate for all three locations, which is a prerequisite for the approval of medical devices in Japan.

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