Analytical Expert – Medical Device R&D (m/f/d)

Aequor Consulting GmbH; Basel; Vor Ort; CHF 110.000 - 150.000; Vollzeit

Benefits dieser Stelle

LinkedIn Learning access

Professional certifications support

Reka Card contribution: 20%, up to CHF

Zusammenfassung

Aequor Consulting GmbH is seeking an Analytical Expert for Medical Device R&D in Basel. The role focuses on analytical testing, method development and regulatory support across internal and external labs. Strong coordination with project teams and external partners is essential.

The position requires deep knowledge of ISO standards, Ph. Eur. and USP, plus proficiency in statistical analysis with Minitab and English communication at a professional level.

Qualifikationen

• Extensive knowledge of ISO standards, Ph. Eur. and USP and their practical application.
• Experience in analytical method development and method transfers to internal/external labs.
• Strong data analysis skills using statistical software (Minitab).
• Excellent coordination and communication with cross-functional teams and external partners.
• Fluent English (verbal and written) and ability to work across European hours.

Aufgaben

• Act as single point of contact for analytical activities in medical device testing across projects.
• Oversee and lead analytical activities, ensuring alignment with objectives and customer requirements.
• Develop project-specific analytical methods and transfer them to labs.
• Select suitable testing laboratories based on resources and strategy.
• Lead outsourced analytical work at external labs and manage partnerships.
• Coordinate activities with cross-functional teams and stakeholders.
• Contribute to regulatory documentation and project registration.
• Support regulatory inspections and present analytical work.
• Perform and oversee statistical analysis to support project decisions.

Kenntnisse

Analytical expertise

Statistical data analysis

Minitab

Coordination & communication

English language

Tools

NRV

GLIMS

1-QEM

Jobbeschreibung

Analytical Expert – Medical Device R&D (m/f/d)

Are you an experienced analytical specialist with a strong background in medical device testing, analytical method development and statistical data analysis? Do you have in-depth knowledge of international pharmaceutical standards and enjoy coordinating complex analytical activities across multidisciplinary project teams and external laboratories?

For a leading international pharmaceutical company in Basel, an experienced Analytical Expert (m/f/d) is sought to support Research & Development activities within the Medical Device area. In this role, you will take responsibility for analytical activities across assigned projects, contribute to regulatory documentation and ensure the successful development, transfer and execution of analytical testing methods in both internal and external laboratory environments.

Responsibilities

• Act as the single point of contact for all analytical activities related to medical device testing within assigned projects.
• Oversee and lead analytical activities across assigned projects, ensuring alignment with project objectives and customer requirements.
• Develop project-specific analytical methods, including the transfer of methods to internal and external laboratories.
• Select suitable testing laboratories based on resource availability, technical capabilities and the applicable insourcing or outsourcing strategy.
• Lead outsourced analytical project activities at external laboratories and contribute to the management of external partnerships across two independent projects.
• Coordinate analytical activities with cross-functional device project teams and stakeholders at drug product level.
• Contribute to the preparation and review of regulatory documentation and support project registration activities.
• Support regulatory inspections, including the presentation and explanation of analytical activities and relevant documentation.
• Perform and oversee statistical data analysis to ensure reliable analytical results and support project-related decision-making.
  

Requirements

• Extensive expertise in international ISO standards, the European Pharmacopoeia (Ph. Eur.) and the United States Pharmacopeia (USP), including their interpretation and practical application.
• Strong expertise in analytical mechanical testing methods and their practical application within the medical device area.
• Proven experience in analytical method development and method transfers to internal and external laboratories.
• In-depth knowledge of statistical data analysis and strong practical experience with statistical software, particularly Minitab.
• Excellent coordination and communication skills, with the ability to collaborate effectively with cross-functional device project teams and stakeholders at drug product level.
• Experience coordinating external laboratories and managing outsourced analytical activities is highly advantageous.
• Understanding of regulatory documentation and project registration activities within a regulated pharmaceutical or medical device environment.
• High level of motivation, resilience and ability to manage a demanding workload while consistently delivering high-quality results.
• Excellent verbal and written English communication skills.
• Experience with or access to NRV, GLIMS and 1-QEM (Novartis internal systems) is considered an advantage.
• Availability during European working hours to ensure effective coordination of work packages and project status updates.
• 5 weeks of annual vacation based on a 40-hour working week.
• Access to LinkedIn Learning with more than 5,000 online courses.
• Financial support for professional certifications and further education.
• Reka Card contribution of 20%, up to CHF 2,400 per year.