Drug Development Specialist

Drug Development Specialist
  • posted job: 2025-07-08
  • Zurich
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  • Job Country: Switzerland
  • Job Industry: Biotechnology & Life Sciences
  • Job Profile: Pharmaceutical Scientist
  • Training Duration: Not Required
  • Number of Jobs Opening: 60
  • Salary: 170000 ( 150000 Per Month)
  • Job Type: Full Time
  • Visa: Provided by company
  • Food: Provided by company
  • Accommodation: Provided by company
  • Air ticket: Provided by company
  • Medical Insurance: Provided by Company
  • Commuting to job location: Provided by company
  • Required Experience: Not Required
  • Minimum Education Level: Not Required
  • Primary Language Requirement: English
  • Level of Language: Beginner
  • Secondary Language Requirement: Not Required
  • Employee Acceptance: International
  • Work Location: Work from Home (WFH) /Remote Work
  • Hiring Need: Immediate

Job Description:

A Drug Development Specialist in Zurich oversees the lifecycle of pharmaceutical compounds from discovery through clinical trials and regulatory submission. This role includes coordinating preclinical testing, managing cross-functional development teams, and ensuring timelines and milestones are met. Specialists work with R&D, clinical, regulatory, and marketing teams to align product strategy with scientific and commercial objectives. In Zurich’s globally connected pharma ecosystem, the specialist supports IND/CTA filings, reviews technical documents, and contributes to strategic decisions. Strong knowledge of pharmacokinetics, toxicology, and regulatory pathways is vital. The role requires excellent project management, scientific communication, and stakeholder engagement skills. Experience with drug approval processes and clinical development plans is essential.

Job Requirement:

  • Demonstrated experience in laboratory research, scientific data analysis, and technical reporting.

  • Proficiency in using laboratory equipment, software tools for data interpretation, and bioinformatics platforms.

  • Familiarity with GMP, GLP, GCP, and other regulatory compliance standards applicable to clinical and laboratory environments.

  • Strong documentation and record-keeping skills in accordance with industry standards.

  • Ability to design, execute, and troubleshoot experiments and assays independently or in a team.

  • Excellent written and verbal communication skills for preparing research documentation and collaborating across departments.

  • Detail-oriented with strong analytical thinking, problem-solving, and organizational capabilities.

  • Adaptability to fast-paced, collaborative, and evolving research and clinical settings.

  • Understanding of ethical research practices and commitment to maintaining data integrity and confidentiality.

  • Previous experience with clinical trials, product development, or regulatory processes is considered an advantage.

  • Ability to work with cross-functional teams including R&D, Quality, Regulatory, and Manufacturing.

  • Good time management skills and ability to meet tight project deadlines.

  • Fluency in English is mandatory; knowledge of German or French is a plus for Swiss workplaces.

  • Willingness to undergo ongoing training and certification as required by the organization.

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