Project Manager CDMO

Career

Career

CareerLouisa Bandura2024-02-23T09:57:46+01:00

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.

Project Manager CDMO (m/f/x)

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.

Project Controller CDMO (m/f/x)

Permanent position/ full time

ROLE RESPONSIBILITIES

• Responsibility for budget planning and monitoring of CDMO projects
• Establishment of business plans and conducting target-actual analyses
• Preparation of cost estimates and project-related analyses
• International export account management
• Support in the further development of controlling processes and instruments

QUALIFICATIONS

• University degree in business administration, Finance, or a similar field
• Several years of experience in project controlling, ideally in CDMO
• Good knowledge of financial planning and analysis
• Confident handling of MS Office, especially Excel
• Fluent in both German and English, written and spoken

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.

Senior Project Manager CDMO (m/f/x)

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.

Regulatory Affairs Manager CDMO (m/f/x)

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.
More Job Offers

Your Application

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

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