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.
Permanent position/ full time
ROLE RESPONSIBILITIES
- Supervision and training of new colleagues
- Qualification and validation of methods
- Establishment of new procedures/methods
- Creation and review of qualification and validation documents
- Independent implementation of methods
- Preparation of development reports
QUALIFICATIONS
- 5+ years of experience in quality control, with detailed method knowledge (HPLC, TLC, GC, e.g.)
- GMP documentation
- Excellent English language skills
- Cooperative management style with team player mentality
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.
