Senior Manager Corporate Regulatory Affairs & CMC (RAC)

CARBOGEN AMCIS; Bubendorf; Vor Ort; CHF 100’000 - 140’000; Vollzeit

Zusammenfassung

CARBOGEN AMCIS is seeking a Regulatory Affairs Consultant to establish RA standards at all sites and ensure compliance in regulatory processes for new development projects. Successful candidates will contribute to a dynamic work environment, guiding teams through document submissions and regulatory strategy, requiring a Ph.D. and extensive experience in the field.

Leistungen

Flexible working hours

At least 5 weeks of vacation

13th monthly salary

Travel insurance for private travels

Private insurance in the event of an accident

Interesting professional development opportunities

Dynamic work environment

Qualifikationen

• Ph.D. Chemist or Pharmacist or equivalent scientist.
• At least 5 years experience in an RA department.
• Good to excellent English language skills.

Aufgaben

• Support regulatory compliance maintenance of regulated products.
• Guide operators in issuing and maintaining regulatory documents.
• Coordinate regulatory activities during CMC process development.

Kenntnisse

Ph.D. in Chemistry or Pharmacy

Regulatory Affairs (RAC)

GMP knowledge

e-CTD systems

Intercultural skills

Communication skills

Leadership skills

Decision-making capabilities

Ausbildung

Ph.D. Chemist or Pharmacist

Jobbeschreibung

• Supporting to elaborate, establish and apply the RA standard at all sites.
• Helping to ensure the internal standard in the regulatory compliance maintenance of the regulated products under consideration of customer requirements.
• Consult the local RAC teams in developing the CMC and regulatory strategy for new development projects with customers and internal and external development groups as required and requested by the customer and assure that the corporate RAC standard is applied.
• Guiding operators through the issuance, submission, and maintenance of all regulatory documents (DMF’s, CMC documentations for INDs, IMPDs, NDAs, MAAs, etc.).
• Providing hands-on support in the implementation and application of the corporate standard at the respective sites.
• Coordinating the regulatory activities of all CARBOGEN AMCIS RAC groups during the CMC process development for corporate projects and consulting the CARBOGEN AMCIS and customer project teams in regulatory questions and as requested and agreed with the customer.
• Chair the corporate RAC organization as part of the Corporate Quality Organization.
• Taking over process ownership of the RAC chapter in the Corporate Management Handbook, define and maintain a harmonized RAC standard.
• Maintaining the e-CTD submission software

Requirements :

• Ph.D. Chemist or Pharmacist or equivalent scientist
• Very good knowledge in RAC (drug substances and / or drug product) and CMC development
• Good GMP knowledge
• Familiar with e-CTD systems
• At least 5 years experience in an RA department (Drug Substances or Drug Products)
• At least 5 years work or management experience in an RA / GMP environment
• At least 5 years experience in dealing with authorities and customers.
• At least 5 years experience in leadership or consultancy.
• Good intercultural skills.
• Good to excellent communication style.
• Good English language skills, orally and in writing.
• Flexible working ‘attitude’ (ready to work overtime).
• Team oriented leadership skills with strong decision-making capabilities.
• Service mentality.

Your benefits :

• A dynamic work environment with high-quality infrastructure
• Interesting possibilities to develop your professional skills
• Flexible working hours for a 40-hour week
• At least 5 weeks of vacation
• Travel insurance for private travels
• Private insurance in the event of an accident
• 13th monthly salary is paid out without any social benefits deductions, in addition there is a profit sharing in a successful business year

For further information please contact the Human Resources department.