(Senior) Bioanalytical Principal Investigator LBS / GLP Study Director (100%)

Celerion; Fehraltorf; On-site; CHF 120,000 - 180,000; Full time

Benefits offered by this job

Extra holidays

Sickness and accident insurance

Commuting allowance

Reka checks

Job summary

Celerion in Fehraltorf/Zurich seeks a (Senior) Bioanalytical Principal Investigator to lead regulated bioanalytical studies and method validations, serving as primary client contact and Study Director with full ownership of studies.

The role encompasses leadership, client management, and continuous improvement of laboratory operations, with senior-level responsibilities for strategic programs and mentoring staff. Excellent English is required; German is a plus.

Qualifications

• BSc / MSc in Life Sciences, Biochemistry, Biotechnology, Immunology or related field.
• Experience in regulated bioanalysis (GLP/GxP) and in industry setting is preferred.
• Ability to lead and mentor staff and work across functions.

Responsibilities

• Lead GLP/GxP-compliant bioanalytical studies and method validations.
• Act as Study Director/PI with responsibility for studies.
• Develop and approve study plans, validation protocols and reports.
• Provide regular updates to clients and support audits.

Skills

Analytical skills

Problem-solving

Detail-oriented

Time management

Team player

English proficiency

Education

BSc/MSc Life Sciences or related

Tools

LBA

Cell-based assays

GLP/GxP knowledge

Job description

Shape the future of bioanalysis for innovative medicines

Celerion is one of the world’s leading bioanalytical contract research organizations and has been supporting pharmaceutical and biotech drug development programs around the world for more than 40 years.

To strengthen our bioanalytical laboratory in the Ligand Binding Service Team in Fehraltorf / Zurich, we are looking for a (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 German 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-size company with flat organizational structure within a dynamic and international team.

Our benefits:

• extra holidays
• company-paid sickness and accident insurance
• commuting allowance
• access to Reka-Checks

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