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Regulatory Affairs Specialist (m/w/d) (DE)
[13005]
Regulatory Affairs, GMP, API
Job title: Regulatory Affairs Specialist (m/w/d) Duration of employment: Unlimited Industry: Chemie Skills: Regulatory Affairs, GMP, API Ideal starting date: ab sofort Location: Neiderösterreich Tasks: ·You will work as part of a multinational team of Pharmaceutical Regulatory Affairs experts on a variety of group projects as we strive to continuously improve. ·You will also support our sales and procurement teams on a variety of regulatory topics, completing customer queries and negotiating Quality agreements ·You will work side by side with the site Qualified Person to support GMP activity at our site near Vienna Qualifications: ·University degree in life sciences ·Quality Management background, with experience working in a Pharmaceutical GMP environment ·Team player, strong communication and interpersonal skills, with ability to work across all levels, and functions ·Experience in communication with and surveillance audits by AGES ·The minimum salary for this position is € 50.000,-- (on a full-time yearly basis). Depending on your qualifications and professional experience the remuneration will be adjusted