QC Analytical Project Manager

Bachem SA; Vionnaz; Vor Ort; CHF 120.000 - 180.000; Vollzeit

Zusammenfassung

Bachem SA in Vionnaz, Switzerland, is seeking a QC Analytical Project Manager to coordinate analytical activities across the project lifecycle, ensuring delivery of customer projects with top quality and compliance.

You will lead release testing, stability studies, method development and validation, manage transfers to internal and external partners, and drive GMP adherence and continuous improvement.

Qualifikationen

• Degree in Analytical Chemistry, Biochemistry, Pharmaceutical Sciences, or related field.
• 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.

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 compliance with GMP, regulatory, quality, and safety requirements.

Kenntnisse

Cross-functional coordination

Analytical thinking

Problem-solving

Stakeholder management

Communication skills

Ausbildung

Analytical Chemistry / Biochemistry / Pharmaceutical Sciences degree

Tools

MS Office

LIMS

CDS

MasterControl

SAP

Jobbeschreibung

QC Analytical Project Manager

Bachem SA Vacant since : 02.10.2026 Number of jobs : 1 1895 Vionnaz (VS) 100% Immediately Permanent

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

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 tocustomers and stakeholders.


• Define and implement analytical and quality control strategies aligned with customer needs and Bachembest practices.


• Monitor project timelines, budgets, resources, quality events, deviations, CAPAs, and change controls.


• Organize and facilitate project meetings while ensuring effective collaboration between internal andexternal partners.


• Drive continuous improvement initiatives and ensure compliance with GMP, regulatory, quality, and safetyrequirements.

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 internationalpharmacopoeias.


• 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.

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.

Job Details

• Work location 1895 Vionnaz (VS)


• Workload 100%


• Employment start Immediately


• Employment duration Permanent

Language Skills

• English Orally : Very good knowledge Written : Very good knowledge


• French Orally : Very good knowledge Written : Very good knowledge

Application

• By online Online form