Regulatory Compliance Officer

Κωδικός Θέσης : RCO_1118
Ημερομηνία ανάρτησης αγγελίας : 7/11/2018

Human Factor Ltd on behalf of Boehringer Ingelheim Ellas is seeking to recruit an experienced  

Regulatory Compliance Officer (ref: RCO_1118)


This is your chance to join the team of Boehringer Ingelheim Ellas which is undergoing exciting changes, as they are currently in an expansion phase - especially in their production plant in Koropi, from where they supply the global market for solid manufactured pharmaceuticals!


For this challenging and exciting role, we are looking for a person to support the Regulatory Compliance team. As RCO you will provide both Chemistry Manufacturing and Controls (CMC) support and Quality support. Routine regulatory activities include change assessment, dossier development, ensuring product and site renewals are completed on time, responding to health authority questions, and maintaining dossier compliance.


Key responsibilities:


  • Preparation of CMC documentation for submissions worldwide
  • Issuance and follow up of change control for proposed changes relative to the local manufacturing site
  • Work on product renewals and deficiency letters
  • Support business partners in regulatory topics
  • Compilation of GMP documentation packages for site accreditations


Requirements & Qualifications


  • Bachelor or Master Degree in Chemistry, Pharmacy, Chemical Engineering, Biology or other relevant fields
  • At least 2 years of working experience in Quality Organization in the pharmaceutical industry in a Manufacturing environment
  • Excellent command of Greek and English language
  • Work experience as a Quality Control Analyst will be an asset
  • Excellent organizational skills: able to keep with timelines and a sense of urgency
  • Precise working and documentation style
  • Excellent interpersonal skills
  • Excellent Team player
  • Capability to discuss and solve issues together with other business units
  • Capable of working in a fast-paced changing environment, prioritizing multiple tasks 


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 and join us in our effort to make more health.

ROPU MIDI is a Regional Operating Unit consisting of 8 mid-sized European countries; Belgium, Denmark, Finland, Greece, Nomay, Portugal, Sweden and The Netherlands. MIDI is a multicultural and diverse work environment. More than 1.800 employees are striving to work together to improve lives for patients and animals in our region.

We offer new and exciting development opportunities for ambitious people with potential for more. For more information about Boehringer Ingelheim pl visit www.




In order to comply with applicable export control laws, Boehringer Ingelheim periodically screens business relations (including job applicants) against sanctioned party lists (“SPL”). These checks may be performed by Boehringer Ingelheim or by any of its Affiliates. You acknowledge that Boehringer Ingelheim and/or its Affiliates will screen you against SPL and that for this purpose your personal data may be processed in relevant databases, including databases of third-party vendors that perform SPL screening for or on behalf of Boehringer Ingelheim or its Affiliates which may be located or accessible outside the EU. Boehringer Ingelheim is committed to ensuring an adequate level of protection of your personal data.

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