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A reputable pharmaceutical company is currently seeking a Lead Scientist for Quality Control Microbiology on a permanent basis in Switzerland. scientists work in an autonomous way with exposure to a variety of projects within the organization and opportunities for growth.
Your responsibilities:
* Manage and develop complex projects, including estimating cost, time, and resources
and coordinating globally.
* Author, review, and approve study protocols and reports, and prepare, update, or
review standard operating procedures.
* Provide design, verification, review, and approval of reports and data
* Ensure studies and activities align with best practices and quality requirements
* Manage complex projects and assess changes
* Plan and execute validation activities for microbiological methods
* Support investigations, regulatory submissions, and audits while ensuring compliance
with SOPs and documentation requirements
* Solid knowledge of sterility testing and bioburden testing.
Your profile:
*Minimum 5 years experience in microbiological and biological, chemical, or biochemical
analytics in a pharmaceutical/medicinal GMP environment
* Extensive experience in all aspects of analytical method lifecycle management,
including method development and validation
* Strong problem-solving skills and practical application of concepts into cGMP
environments
* Proficiency in microbiological testing methods and troubleshooting experience
* Experience in project management, training and coaching of colleagues, and
interacting with senior management
Lead Scientist - Quality Control Microbiology (m/f/d)
- Location Switzerland
- Salary Negotiable
- Discipline Quality
- Reference PR/418008_1679330098
Your responsibilities:
* Manage and develop complex projects, including estimating cost, time, and resources
and coordinating globally.
* Author, review, and approve study protocols and reports, and prepare, update, or
review standard operating procedures.
* Provide design, verification, review, and approval of reports and data
* Ensure studies and activities align with best practices and quality requirements
* Manage complex projects and assess changes
* Plan and execute validation activities for microbiological methods
* Support investigations, regulatory submissions, and audits while ensuring compliance
with SOPs and documentation requirements
* Solid knowledge of sterility testing and bioburden testing.
Your profile:
*Minimum 5 years experience in microbiological and biological, chemical, or biochemical
analytics in a pharmaceutical/medicinal GMP environment
* Extensive experience in all aspects of analytical method lifecycle management,
including method development and validation
* Strong problem-solving skills and practical application of concepts into cGMP
environments
* Proficiency in microbiological testing methods and troubleshooting experience
* Experience in project management, training and coaching of colleagues, and
interacting with senior management