Manager RAC

CARBOGEN AMCIS AG; Bubendorf; Hybrid; CHF 140,000 - 190,000; Full time

Benefits offered by this job

Flexible working time

Home office possibility

5 weeks vacation

Childcare contribution

Travel insurance

Profit-sharing bonus

13th month salary

Job summary

CARBOGEN AMCIS AG in Switzerland seeks a Manager RAC to lead Regulatory Affairs & CMC for Drug Substance projects, focusing on small molecules and ADCs. You will coordinate with global teams to prepare IND/IMPD/MAA/BLAs, ensuring compliance and timely submissions across development stages.

The role requires 5+ years in pharma regulatory affairs with CMC depth, strong communication, and project leadership skills. Hybrid work model, generous vacation, and robust benefits offered.

Qualifications

• Master or PhD in chemistry, pharmacy, or equivalent.
• 5+ years in regulatory affairs with CMC focus for small molecules.
• Experience with IND/IMPD/MAA/BLAs and regulatory submissions.
• Knowledge of cGMP and ICH guidelines; English fluent.

Responsibilities

• Authoring and reviewing registration documents for regulatory submissions.
• Lead CMC regulatory activities from preclinical to market launch.
• Coordinate with Health Authorities and customers; support change management.
• Regulatory gap analyses and project-specific regulatory strategy.
• Manage training and collaboration across departments.

Skills

Regulatory affairs

CMC development

Project management

English fluency

GMP knowledge

Education

Master's degree in Chemistry

PhD in Chemistry or Pharmacy

Tools

Docubridge

Job description

Manager RAC

We are offering a new challenge as Manager RAC (Regulatory Affairs & CMC) at our site in , Switzerland.
You will be a member of the corporate RAC and part of local Swiss regulatory affairs and CMC team dedicated to Drug Substance Business Unit. You will support customer activities focusing on Chemistry Manufacturing and Controls (CMC) for small molecules project mainly and ADCs/Bioconjugates derivatives.
In this very dynamic and hands-on role, you will work collaboratively with the other departments to coordinate the regulatory activities from clinical development up to market launch and life cycle management. You will provide regulatory support/advice internally and to external customer projects related.

Your responsibilities:

• Authoring/reviewing and maintaining registration documents (Drug Substance CMC Quality Module / sections for INDs, IMPDs, MAAs and/or BLAs) in accordance with the requirements of the authorities and customers requirements as well as international guidelines
• Assisting with the submission of post-approval change documentation
• Regulatory assessment in terms of change management (change controls, deviations)
• CMC regulatory support during the entire process and product development from the pre-clinical via the clinical phases to market launch, internally and in relation to customer projects / attending customer meetings and project team meetings
• Performing a regulatory review of the source documents in support of the CMC documentation
• Leading and/or conducting project specific CMC regulatory gap analysis as driver for CMC development (mainly small molecules drug substance)
• Managing accreditation in Japan
• Collaboration with the Health Authorities / customers: preparing briefing documents, answers to questions from authorities on submitted registration documents
• Regulatory affairs advise and hands-on support internally for improvement and customer oriented regulatory projects

Your profile:

• Master / Engineering or Ph.D degree in Chemistry, Pharmacy or equivalent scientific discipline
• understanding of regulatory affairs for Drug Substance with a strong focus on CMC development for small molecules (traditional CMC development versus accelerated development program) - You have expertise in drafting IND/IMPD/MAA regulatory files from scratch ; experience in regulations & accreditation in Japan is an added value
• knowledge of cGMP regulations
• knowledge of ICH guidelines and regulatory requirements for Small Molecules
• At least 5 years experience in the pharmaceutical industry / GMP environment: several years in a Regulatory Affairs department combined with previous CMC (R&D, Operations, Analytics) function
• Previous experience in CDMO or working in customer projects is a clear advantage
• Team oriented, pro-active / problem-solving mentality, service-oriented mindset with flexibility to handle multiple tasks, flexible working 'attitude'
• coordination and communication skills – Fluency in English required; knowledge is recommended
• sense of responsibility and reliability
• Knowledge of eCTD submission software (Docubridge) is an advantage

Your benefits:

• A dynamic working environment with high-quality infrastructure
• Flexible working time model with a 40-hour week and the possibility to work from home
• Interesting opportunities to expand your professional knowledge
• At least 5 weeks of vacation
• Contribution to childcare costs
• Travel insurance for private trips
• Privately insured in the event of an accident
• 13th month's salary, with 100% of the social deductions covered by CARBOGEN AMCIS
• If the financial year is successful, there is a profit-sharing bonus

• CARBOGEN AMCIS AG
  Hauptstrasse 171
  4416