Bioanalytical Principal Investigator LBS / GLP Study Director

Celerion Switzerland AG; Fehraltorf; On-site; CHF 110,000 - 170,000; Full time

Benefits offered by this job

Extra holidays

Sickness and accident insurance

Commuting allowance

Job summary

Celerion Switzerland AG in Fehraltorf is seeking a Bioanalytical Principal Investigator (LBS/GLP Study Director). You will own regulated studies, lead from planning to reporting, and serve as primary client contact across global drug programs.

Senior candidates will mentor staff and lead strategic client programs. The role emphasizes study leadership, regulatory compliance, and collaboration across functions within a state-of-the-art facility in Zurich cantone, with 80–100% workload and

Qualifications

• BSc / MSc in Life Sciences, Biochemistry, Biotechnology, Immunology or related field
• At least 2 years professional experience, at least 6 years for senior position
• Practical experience in relevant bioanalytical techniques (e.g. LBA, cell-based)
• Experience working in a regulated environment (GLP, GCP, GMP and/or ISO standards)
• Strong analytical and problem-solving skills
• Detail-oriented and highly organized, with the ability to manage multiple projects while maintaining a high level of quality and attention to detail
• Excellent computer and time management skills
• Highly self-motivated, reliable, and flexible, with a commitment to providing excellent service to clients.
• Strong team player with the ability to collaborate effectively across functions
• Excellent English (written and spoken), good skills are advantageous
• Previous experience as a Study Director, Principal Investigator or equivalent scientific leadership role is required for the senior position
• Knowledge of biomarker, pharmacokinetic (PK), immunogenicity (ADA) or biologics bioanalysis
• Experience working directly with pharmaceutical or biotechnology clients is advantageous

Responsibilities

• Lead scientific and operational ownership of regulated bioanalytical studies and method validations.
• Serve as the primary client contact and lead study execution from planning through reporting.
• Take on Study Director and/or Principal Investigator responsibilities for assigned studies or phases.
• Develop and approve study plans, validation protocols, reports and documentation.
• Review, evaluate and approve analytical data for regulatory compliance.
• Ensure activities comply with SOPs and client expectations.
• Coordinate laboratory activities and ensure efficient study execution.
• Train and mentor laboratory personnel and contribute to process improvements.
• Support bioanalytical data management and documentation review processes.
• For senior roles: lead complex client programs and mentor junior staff; act as SME for ligand-binding and cell-based assays; contribute to business development.

Skills

Glp/GxP knowledge

Study leadership

Client management

Laboratory coordination

English proficiency

Education

BSc/MSc Life Sciences or related

Tools

LBA techniques

Cell-based assays

Job description

This job posting was published here directly by one of our clients. The State Secretariat for Economic Affairs has no control over its content or quality.

Bioanalytical Principal Investigator LBS / GLP Study Director

Celerion Switzerland AG Vacant since : 03.11.2026 8320 Fehraltorf (ZH) 80% - 100% By agreement Permanent

(Senior) Bioanalytical Principal Investigator (100%)*

In this role, you will take scientific and operational ownership of regulated bioanalytical studies and method validations. You will serve as the primary client contact, lead study execution from planning through reporting, and play a key role in delivering high-quality data to support drug development programs worldwide.

* This is a dual-level posting. The hiring team will determine the final level and title of the role based on the skills, experience, and capabilities required for the level offered.

Main responsibilities

Study Leadership & Scientific Oversight

• Lead and oversee GLP/GxP-compliant bioanalytical studies and method validations within the Ligand Binding Services (LBS) department.
• Act as Study Director and/or Principal Investigator with full responsibility for assigned studies or study phases.
• Develop and approve study plans, validation protocols, analytical reports and associated study documentation.
• Review, evaluate and approve analytical data to ensure scientific integrity and regulatory compliance.
• Ensure all study activities are conducted in accordance with applicable SOPs, regulatory requirements and client expectations.

Client Management

• Serve as the primary scientific and operational contact for assigned clients.
• Provide regular project updates and maintain strong communication throughout the study lifecycle.
• Support client meetings, scientific discussions and audits as required.

Operational Excellence

• Coordinate laboratory activities and ensure efficient study execution.
• Train, mentor and support assigned laboratory personnel.
• Contribute to process improvements and continuous enhancement of laboratory operations and quality standards.
• Support bioanalytical data management activities and documentation review processes.

Additional Responsibilities for Senior-Level Candidates

• Lead complex or strategic client programs.
• Provide scientific mentoring and guidance to junior Principal Investigators and laboratory staff.
• Act as a subject matter expert for ligand-binding and cell-based assay technologies.
• Contribute to business development activities, client presentations and scientific initiatives.

Our requirements

• BSc / MSc in Life Sciences, Biochemistry, Biotechnology, Immunology or related field
• At least 2 years professional experience, at least 6 years for senior position
• Practical experience in relevant bioanalytical techniques (e.g. LBA, cell-based), preferably in an industry setting
• Experience working in a regulated environment (GLP, GCP, GMP and/or ISO standards)
• Strong analytical and problem-solving skills
• Detail-oriented and highly organized, with the ability to manage multiple projects while maintaining a high level of quality and attention to detail
• Excellent computer and time management skills
• Highly self-motivated, reliable, and flexible, with a commitment to providing excellent service to clients.
• Strong team player with the ability to collaborate effectively across functions
• Excellent English (written and spoken), good skills are advantageous
• Previous experience as a Study Director, Principal Investigator or equivalent scientific leadership role is required for the senior position
• Knowledge of biomarker, pharmacokinetic (PK), immunogenicity (ADA) or biologics bioanalysis
• Experience working directly with pharmaceutical or biotechnology clients is advantageous

Your chance

We provide an opportunity to assume work independently, secure long-term employment, and enjoy a competitive salary.

Your workplace will be located within our state-of-the-art equipped automated facilities in cantone Zurich as part of an international organization.

Additionally, you will experience the advantages of flexible working hours and experience the benefits of a medium-sized company with flat organizational structure within a dynamic and international team.

Our benefits: extra holidays, company-paid sickness and accident insurance, commuting allowance and access to -Checks.

Recruiting agencies: For this position, Celerion is not willing to take any unasked applications by recruiting offices. Thanks for your understanding.

• Celerion Switzerland AG
  Allmendstrasse 32
  8320 Fehraltorf

• Work location 8320 Fehraltorf (ZH)
• Workload 80% - 100%
• Employment start By agreement
• Employment duration Permanent
• By online Online form