Senior Bioanalytical Study Director (GLP/LBA)

Celerion Switzerland AG; Fehraltorf; On-site; CHF 110,000 - 150,000; Full time

Benefits offered by this job

Extra holidays

Company-paid sickness and accident保险

Commuting allowance

Reka-Checks

Job summary

Celerion Switzerland AG invites an experienced Senior Bioanalytical Principal Investigator to lead GLP/GxP–compliant studies and method validations in Fehraltorf/Zurich. You will serve as Study Director or Principal Investigator, manage study plans, reports and client communications, and mentor laboratory staff. Excellent English required; German is a plus.

Flexible hours in a state-of-the-art facility. The role offers responsibility for complex programs, regulatory oversight, and opportunities

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.
• Experience with regulated bioanalytical environments (GLP/GMP/GCP) and analytical techniques (LBA, cell-based).

Responsibilities

• Lead and oversee GLP/GxP-compliant bioanalytical studies and method validations.
• Serve as Study Director and/or Principal Investigator for assigned studies.
• Develop study plans, validation protocols and reports; ensure regulatory compliance.
• Act as primary client contact and manage study communications.
• Mentor laboratory staff and drive process improvements.

Skills

Analytical skills

Problem-solving

Detail-oriented

Time management

Team player

Excellent English

German language advantageous

Self-motivated

Education

BSc / MSc in Life Sciences or related field

Job description

Celerion Switzerland AG invites an experienced Senior Bioanalytical Principal Investigator to lead GLP/GxP–compliant studies and method validations in Fehraltorf/Zurich. You will serve as Study Director or Principal Investigator, manage study plans, reports and client communications, and mentor laboratory staff. Excellent English required; German is a plus.

Flexible hours in a state-of-the-art facility. The role offers responsibility for complex programs, regulatory oversight, and opportunities