MSD Senior Specialist Regulatory Affairs CMC m/w/d 

Germany, Rhineland-Palatinate 

617028481

Job Description

as soon as possible.

Main responsibilities:

• Maintenance and updating of regulatory CMC dossiers

• (Co-)development of regulatory concepts and preparation of documentation for change notifications, taking into account current regulatory quality standards

• Timely response to inquiries from countries and authorities

• Technical support of other functions in regulatory issues

• Collection and maintenance of regulatory information, taking into account the associated processes, as well as maintenance of the relevant systems and databases

Your profile:

• Master's degree in Pharmacist, Chemist, Food Chemist or Biologist

• Ideally, you have professional experience in comparable positions in the pharmaceutical industry. However, applications from university graduates are also welcome.

• Consistent, flexible, team-oriented and familiar with MS Office

• Careful and responsible way of working

• You combine organizational skills with strong communication skills in an international environment

• Very good verbal and written language (English essential, German desirable)

Our offer:

• Flexible working hours (37.5 hours/week) and an attractive company pension scheme

• Competitive salary package: 13 monthly salaries + holiday pay + target bonus

• 30 days holiday entitlement (depending on location)

• Hybrid or remote working model (depending on location)

• Internal training and promotion opportunities

• International co-operations

• Training on the job

• Contributing your own ideas to the process design

• Insights into the development of veterinary medicinal products

• Corporate benefits and free (electric) car parking

• Good company canteen and a company health management program

together inencourage our colleagues

Current Contingent Workers apply

Project Temps (Fixed Term)

Not Indicated

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