The data privacy settings of your browser prevent this site from functioning properly. Please open the site in a new tab. Alternatively, you can allow cross-sitetracking in your browser.
Open in new tab
Manager Regulatory Affairs (m/w/d) - Job Puchheim, Remote work - Karriere bei Omnivision Pharma

Manager Regulatory Affairs (m/w/d)

Manager Regulatory Affairs (m/w/d)

OmniVision GmbH is an expanding medium-sized ophthalmology company with its headquarters in Germany and locations in Austria, Italy, Spain and Switzerland. In Germany, OmniVision GmbH is one of the leading non-corporate ophthalmology companies. Our product portfolio includes pharmaceuticals, medical devices and nutritional supplements.

In the course of our strong growth, we are looking for a committed and motivated person to join our headquarters in Puchheim near Munich as soon as possible:


Manager Regulatory Affairs (m/w/d)

Your contribution:

  • Planning and submission of national change notifications and EU-variations to competent authorities
  • Planning and submission of renewal applications
  • Management of national and European variation and renewal procedures
  • Communication with European competent authorities (EU and Switzerland)
  • Answering letters of deficiency (List of Questions (LoQs))
  • Procurement and assessment of documents from international suppliers (Contract Manufacturing Organisations (CMOs))
  • Creation and revision of product information texts (SmPC, PIL, labelling) for the implementation of officially requested text amendments and/or for text adaptations to the current state of knowledge
  • Coordination of all regulatory lifecycle management activities in the OmniVision subsidiaries (Austria, Italy, Spain and Switzerland)
  • Creation of eCTD sequences for the submission of variation and renewal applications
  • Maintaining and updating the company's internal marketing authorisation database
  • Collaboration in the company's internal change control process
  • Monitoring, interpretation and implementation of new regulatory requirements

Your Profile:

  • University degree in natural sciences, preferably Pharmacy, Biology or Chemistry
  • Several years of professional and practical experience in regulatory affairs (medicinal products) within the EU
  • Experience in creating eCTD sequences
  • Ability to work in a team, service-orientation
  • Quick comprehension, analytical thinking in combination with an independent, structured and goal-oriented way of working
  • Proactive thinking and acting, assertiveness, flexibility and strong communication skills
  • Fluent in German and English with excellent oral and written communication skills
  • IT affinity: eCTD, databases, Microsoft Office suite

We offer you:

  • A permanent, long-term position in a successful, owner-managed medium-sized company in the pharmaceutical industry
  • An attractive remuneration package
  • Further training opportunities
  • Annual leave of 30 days
  • Flexible working hours including mobile working
  • A modern IT infrastructure
  • Modern offices with employee parking spaces
  • Subsidy for the company pension scheme
  • Financial support for a job bike
  • Payment of the Germany ticket
  • Subsidized company catering including free drinks
  • Company events
  • Employee discounts (gym, shopping, travel, etc.)

Does this sound interesting to you?

We look forward to receiving your application (cover letter stating your salary expectations and earliest possible starting date, CV and references) to the attention of Francisco Lopez, HR Manager.
Manager Regulatory Affairs (m/w/d) - Job Puchheim, Remote work - Karriere bei Omnivision Pharma
Submit application

OmniVision® ist ein innovatives, inhabergeführtes pharmazeutisches Familienunternehmen im Spezialgebiet der Augenheilkunde (Ophthalmologie).

Der Hauptfokus liegt in der Entwicklung und Vermarktung von ophthalmologischen Präparaten für Patienten, Augenärzte und Apotheker. Mehr