Phys-chem Lab Analytical Scientist (6994)

Contract

Posted 4 days ago

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