The Life Science Career Network

CTC specializes in helping companies find top talent and offers reliable HR, consulting services, and skill development programs. We support candidates in advancing their careers and provide the latest training to stay competitive.

Our client, a global leader in pharmaceuticals based in Basel, is transforming its culture and global reputation. With a focus on innovative Oncology and Ophthalmology therapies, they’re also driving a world-leading pipeline in Neuroscience and Dermatology, maintaining one of the industry’s strongest portfolios of Phase II/III studies.

We are seeking an experienced and highly motivated Scientist (Analytical Expert) for a 12-month contract position in Basel. In this role, you will perform and document laboratory experiments related to drug substances (DS) and drug products (DP) while collaborating with multifunctional project teams. 

Responsibilities

  • Plan, conduct, and document scientific experiments, including method development, validation, transfers, stability and release testing, and formulation development analytics, ensuring high-quality results and adherence to timelines.
  • Analyze and interpret experimental data, addressing issues such as SST failures, deviations, and change controls as required.
  • Ensure all data is accurately recorded in systems like LIMS and maintain compliance with good documentation (GDP) and laboratory practices (GLP).
  • Manage laboratory operations by overseeing inventory and proper use of chemicals, reagents, consumables, samples, columns, and glassware.
  • Communicate critical updates and findings to managers and project teams proactively and contribute to achieving team and organizational goals.
  • Maintain compliance with relevant guidelines, including GMP, GLP, HSE, and company policies, while meeting key quality and performance indicators.

Requirements

  • Relevant working/residency permit or Swiss/EU-Citizenship required
  • Bachelor’s or Master’s degree in Life Sciences, such as Analytical Chemistry, Organic Chemistry, Pharmacy, or Pharmaceutical Development.
  • A minimum of 3 years of experience in a GMP-compliant environment with a solid understanding of regulatory and quality expectations.
  • Strong technical expertise in analytical chemistry and method development, paired with excellent problem-solving and organizational skills.
  • Effective communication skills, including the ability to present findings and write scientific documentation.
  • Fluency in English, both written and spoken.

Would you like to learn more about CTC and the opportunity outlined? Please get in contact with us: you may either use the 'apply now' button or write an email to vanessa.gilardoni@ctcresourcing.com

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