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QC Analytical Project Manager

Bachem SA · Vionnaz, Valais, Switzerland

On-siteWorkplace
TodayPosted · Oct 2
jobroomSource
$129kproject manager median
LanguageFrench · English · German

Skills in this posting

Benefits

The posting

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 a

QC 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.

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 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.

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 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.

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.

Interested ?

Would you like to drive innovation together with us?

We look forward to receiving your complete application documents via our application portal.

Learn more about the Bachem Group and get inspired by our exciting work environment at our location inVionnaz.

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