• Contract
  • Valais
  • Recruiter: Chara Boucherok

Phys-chem Lab Analytical Scientist

12 months contract with possible extension 

Fully on site in Visp

 

Our client, a global market leader in the production and process support of active pharmaceutical ingredients, both in the chemical and biotechnology sectors, is looking for a Phys-chem Lab Analytical Scientist for an initial 12 month contract (Maternity cover) with possible extension due to the high workload, based in the Valais area, Switzerland.

The Phys-chem Lab Analytical Scientist plays a critical role:

·      Support the analytical activities required for producing information and documentation suitable for clinical development up to Process Validation stage products with particular focus on  method suitability assessment/validation/verification/transfer in accordance with GMP, ICH guidelines and quality system.

·      Build up a strong scientific knowledge on physical and chemical technologies with particular focus on pharmacopeia requirements and global alignment.

 

Main Responsibilities:

·      Promote the technical innovation, scientific understanding and best practices

·      Design and perform experiments, interpretate results and review data for physical and chemical techniques to support method implementation/validation/verification/transfer.

·      Prepare validation/transfer protocols/ reports and procedures related to physical and chemical test methods. Collect and evaluate scientific data to take conclusions based on them.

·      Summarize and communicate high quality information to customers and team members

·      Provide troubleshooting and training support for analytical method and instruments

·      Collaborate in the optimization of laboratory processes and corrective measures

·    Collaborate and lead laboratory investigations, Change request and CAPA implementation

·      Serves as Subject Matter Expert for the physical and chemical techniques

·      Coordinate projects tasks correlated to Analytical science team

 

 

 

Qualifications and Experience:

·      Relevant working/residency permit or Swiss/EU-Citizenship required

·      Bachelor’s or Masters in relevant field.

·      5+ years of experience in Pharma industry /GMP/ transfer and validation.

·      Proven experience working on GMP-compliant projects, including change management and qualification activities.

·      Excellent soft skills: Flexibility, critical thinking, customer service, communication

·      LIMS, Trackwise, DMS

·      Business Fluent English, German is a plus