QC Analytical Project Manager

Bachem Holding AG; Schweiz; Hybrid; EUR 95.000 - 127.000; Vollzeit

Benefits dieser Stelle

Dynamic working environment

Professional development opportunities

Competitive employee benefits

Zusammenfassung

Bachem Holding AG is seeking a QC Analytical Project Manager in Switzerland to coordinate analytical activities across the project lifecycle, ensuring timely delivery of customer projects with the highest quality, compliance, and operational excellence.

You will act as the QC Analytical Operations representative in cross-functional teams, manage method development, validation, specifications, and data interpretation while driving continuous improvement and regulatory compliance.

Qualifikationen

• Degree in Analytical Chemistry, Biochemistry, Pharmaceutical Sciences, or a related discipline (or equivalent industrial experience).
• Proven experience in GMP-regulated pharmaceutical project management.
• Strong understanding of analytical methods, method development, validation, and international pharmacopoeias.
• Knowledge of pharmaceutical regulatory requirements and quality systems.
• Ability to coordinate multiple stakeholders and manage cross-functional projects.
• Strong analytical thinking, problem-solving, communication and stakeholder management skills.
• Proficiency with MS Office; experience with LIMS, CDS, MasterControl and SAP is an advantage.

Aufgaben

• Act as the primary QC Analytical Operations representative within cross-functional project teams.
• Lead and coordinate analytical activities including release testing, stability studies, API characterization, method development, validation, and specification setting.
• Manage analytical transfers to internal departments, manufacturing sites, and external partners.
• Evaluate complex analytical data, provide scientific recommendations, and communicate results to customers and stakeholders.
• Define and implement analytical and quality control strategies aligned with customer needs and Bachem best practices.
• Monitor project timelines, budgets, resources, quality events, deviations, CAPAs, and change controls.
• Organize and facilitate project meetings while ensuring effective collaboration between internal and external partners.
• Drive continuous improvement initiatives and ensure GMP, regulatory, quality and safety compliance.

Kenntnisse

Stakeholder management

Project management

Analytical thinking

Communication

Problem solving

Ausbildung

Degree in Analytical Chemistry or related

Tools

LIMS

CDS

MasterControl

SAP

Jobbeschreibung

Bachem is a leading, innovation-driven company specializing in the development and manufacture of peptides and oligonucleotides for the pharmaceutical industry. To strengthen our Quality Control organization in Vionnaz (Valais, Switzerland), we are looking for a QC Analytical Project Manager (all) 100% . In this cross-functional role, you will coordinate analytical activities throughout the project lifecycle, ensuring successful delivery of customer projects while maintaining the highest standards of quality, compliance, and operational excellence.

Your Responsibilities

• Act as the primary QC Analytical Operations representative within cross-functional project teams.
• Lead and coordinate analytical activities including release testing, stability studies, API characterization, method development, validation, and specification setting.
• Manage analytical transfers to internal departments, manufacturing sites, and external partners.
• Evaluate complex analytical data, provide scientific recommendations, and communicate results to customers and stakeholders.
• Define and implement analytical and quality control strategies aligned with customer needs and Bachem best practices.
• Monitor project timelines, budgets, resources, quality events, deviations, CAPAs, and change controls.
• Organize and facilitate project meetings while ensuring effective collaboration between internal and external partners.
• Drive continuous improvement initiatives and ensure compliance with GMP, regulatory, quality, and safety requirements.

Your Profile

Degree in Analytical Chemistry, Biochemistry, Pharmaceutical Sciences, or a related scientific discipline (or equivalent industrial experience).

Proven experience in project management within a GMP-regulated pharmaceutical environment.

Strong understanding of analytical methods, method development, validation, and international pharmacopoeias.

Good knowledge of pharmaceutical regulatory requirements and quality systems.

Ability to coordinate multiple stakeholders and successfully manage cross-functional projects.

Strong analytical thinking, problem-solving, communication, and stakeholder management skills.

Excellent command of MS Office and project management tools; experience with LIMS, CDS, MasterControl, and SAP is an advantage.

Fluent in French and English; German is considered a plus.

Our offer

• A modern and dynamic working environment within a fast-growing international company.
• Challenging projects of high scientific and technical value.
• Opportunities for professional development and continuing professional development.
• A corporate culture based on collaboration, innovation and excellence.
• Attractive working conditions and competitive employee benefits.