This site uses cookies. By continuing to browse the site you are agreeing to our use of cookies. Find out more here.

Close Message for pharmaceutical industry jobs
NonStop Recruitment is dedicated to putting job seekers looking for pharmaceutical industry jobs in touch with recruiters and employers.

Similar jobs you may be interested in:

Senior / Principal Regulatory Writer - MedComms - Cheshire
Regulatory Affairs Associate - Trilingual - Part time possible
Challenge yourself, RA Coordinator!
Czech Republic
Regulatory Artwork - Pharma - Contract..
Ireland (Eire)
Regulatory Affairs Manager- Pre Approval

To receive a FREE weekly email alert of all the latest pharmaceutical industry jobs added to our database enter your email address below.

Submit | Tell me more...

Sister sites:
Our sister site Our sister site
Partner sites:

At Burntsky Limited we work with a number of third parties in order to maximise the reach of the jobs posted with us including but not limited to:

JooblePartner Jooble
UK Jobs
Science Jobs

Job Details
This job has expired. Click here to view similar jobs.

Regulatory Information Manager - Training for Professionals!

Business Type: Pharmaceutical Services
Job Type: Regulatory Affairs
Job Level: Experienced (non manager)
Position: Full Time
Location: Germany
Reference: 189017 8
Closing Date: 20/06/18
Job Details:

How are you looking for a company ready to really invest in the employees?

Give a look here, maybe this is what you are looking for!

My client is a fast growing consultancy company based in Germany, who is used to work on very niche projects, thank to her long lasting relationship with many Big Pharma companies. At the moment they are looking for a new Regulatory Information Manager to strength their team in Munich.

With this company you will get the chance to step into many trainings and development programs, which will significantly enhance your technical skills, so that you will have a remarkable line on your CV. Furthermore, many experienced consultants also hold trainings for clients, so that you will get the chance to strongly boost your network in the German pharma!

Your tasks:

  • Preparation of electronic submissions in eCTD format for international registrations in EU and USA
  • Creation and validation of electronic submission for all regulatory activities (e.g. MAAs, PSUR, amendments, variations, renewals)
  • Development of eCTD strategy
  • Taking part to the validation and maintenance tasks for DocuBridge

Your requirements:

  • Relevant experience in creation and validation of submissions in eCTD format for regulatory activities
  • English on business level

Contract Type: Permanent, Full Time

Starting Datum: ASAP, but the client is willing to come toward to your needs

Location: Munich Area

Salary: Negotiable on experience basis

If you feel interested in principle, write or call me: / Dr Emma Fleury, 0049 892 109 33 63.

If you want to apply, just sent your CV IN WORD.DOC FORMAT to my email address.

Happy to recommend someone? If we manage to place your referral, you will get a small thank you gift.

Please be aware that, due to the high number of application, we could be not able to provide you with feedback, if your profile is too much distant from the one described above.

Key Words

Regulatory Operations, Information Technology, XEVMPD, IDMP, NeeS, eCTD, SOPs, WIs, electronic submission, Einreichung, Zulassung, elektronisch, Pharma, Beratung, consultancy, consultant, Berater, Home Office, Remoting, Smart Working, Training

Posted: 13/06/2018 | NPJ Ref: 216283
line graphic

Compatible with:

JobMate   Broadbean   Idibu

Site optimised for Internet Explorer 8+ / Firefox 3+
View a complete Jobs Listing

Credit cards image