Current Job Offers

Join the team!

As part of the ROTOP Contract Development and Manufacturing Organization (CDMO) team you’ll be able to contribute to expanding our fast-growing CDMO business unit by developing and manufacturing cGMP (radio)pharmaceuticals and drug substance precursors. Discover an exciting and diverse work environment and enjoy the benefits ROTOP offers.

Permanent position/ full time

ROLE RESPONSIBILITIES

  • Structuring, implementation, and monitoring project plans
  • Managing contract development projects: cross-departmental coordination of tasks within ROTOP and communication with external partners (national + international)
  • Documenting the chemical-pharmaceutical quality of development products
  • Monitoring progress, identifying risks, and proactively implementing solutions to ensure project success

QUALIFICATIONS

  • University degree in chemistry, pharmacy or a comparable qualification
  • Knowledge in radiochemistry/Radiopharmacy preferable
  • Proficient in using IT tools (e.g., MS Office, SharePoint, project management)
  • Excellent English language skills
  • High level of commitment, dedication, and team spirit

WHAT TO EXPECT

  • A permanent position in an internationally operating company within a future-proof industry
  • Flexible working hours
  • Work from Home Options
  • Regular internal and external trainings
  • 10 paid child-sick days
  • Job bike and job ticket
  • Company events
  • and more …

Please send your application documents, including salary expectations and earliest possible start date, via email to Sven Schäfer at application@rotop-pharmaka.com.

Permanent position/ full time

ROLE RESPONSIBILITIES

  • Structuring, implementing, and tracking project plans
  • Ensuring compliance with common quality standards in the pharmaceutical industry
  • Coordinating and leading interdisciplinary teams and external resources to achieve project goals
  • Monitoring progress, identifying risks, and proactively implementing solutions to ensure project success
  • Communication with clients through calls and on-site meetings to manage expectations, provide updates, and receive feedback

QUALIFICATIONS

  • University degree in Pharmacy, Chemistry, Biology, or a related field
  • Several years of experience in project management
  • Divers project management skills
  • Business orientation and strategic thinking
  • Ability to adapt quickly and effectively to changing priorities
  • 3+ years of experience in international project management and leading a project team
  • Excellent communication skills in national and international settings

WHAT TO EXPECT

  • A permanent position in an internationally operating company within a future-proof industry
  • Flexible working hours
  • Work from Home Options
  • Regular internal and external trainings
  • 10 paid child-sick days
  • Job bike and job ticket
  • Company events
  • and more …

Please send your application documents, including salary expectations and earliest possible start date, via email to Sven Schäfer at application@rotop-pharmaka.com.

Permanent position/ full time

ROLE RESPONSIBILITIES

  • Development, implementation, and monitoring of regulatory processes/requirements in pharmaceutical development
  • Ensuring regulatory inputs and requirements for dossier preparation and submissions
  • Compliance with national and international regulations, guidelines, and laws regarding drug approval
  • Collaboration with internal project teams as well as international customers and partners
  • Establishing and evaluating current trends in Regulatory Affairs

QUALIFICATIONS

  • University degree in Pharmacy, Chemistry, Biology, or a related field
  • Several years of experience in Regulatory Affairs required
  • Regulatory experience with APIs/drug precursors and drug products, radiopharmaceuticals (preferably in nuclear medicine)
  • Knowledge of pharmaceutical regulations and understanding of approval processes in USA and EU
  • Experience with DMF/ASMF as well as regulations/requirements for clinical trial products
  • Expertise in drug approval and project management

WHAT TO EXPECT

  • A permanent position in an internationally operating company within a future-proof industry
  • Flexible working hours
  • Work from Home Options
  • Regular internal and external trainings
  • 10 paid child-sick days
  • Job bike and job ticket
  • Company events
  • and more …

Please send your application documents, including salary expectations and earliest possible start date, via email to Sven Schäfer at application@rotop-pharmaka.com.

We are also offering numerous jobs in many different fields, from product manufacturing to administration and sales on our German website.

Your Application

Apply now via PDF:
at Sven Schäfer
application@rotop-pharmaka.com