Biopharma QC: Method Transfer Lead (On‑Site)

Lonza; Oberwallis; Vor Ort; Vertraulich; Vollzeit

Benefits dieser Stelle

An agile career and dynamic working文化.

Inclusive and ethical workplace.

Competitive hourly rate.

Zusammenfassung

Lonza in Visp (Valais) seeks a senior QC/Analytical Transfer specialist to drive method transfer projects and ensure compliant release of biopharmaceutical products. The role is on site with 41 hours per week, starting as soon as possible, by Oct 1, 2026.

You will estimate effort, lead technical transfer activities, manage milestones, and coordinate changes with QC teams and contract laboratories, while documenting cGMP procedures and ensuring quality standards.

Qualifikationen

• PhD in Chemistry, Chemical Engineering, Biochemistry, Biology, or equivalent; alternatively, a Bachelor’s or Master’s degree with significant professional QC experience.
• Advanced scientific expertise in Analytical Chemistry and modern analytical instrumentation.
• Strong knowledge of regulatory frameworks, including cGMP guidelines and ISO 9001 standards.
• Practical experience with QC IT systems and software (e.g., LIMS, CDS, DMS).
• Excellent communication skills in English; minimum conversational German required
• Proven ability to navigate quality events (Deviations, Change Controls, OOS/OOT investigations).
• A collaborative, customer-focused mindset with a proactive approach to change and continuous improvement.

Aufgaben

• Estimate project effort and craft detailed project plans covering scheduling, workflow, preliminary assessments and quality assurance integration.
• Lead technical implementation and coordination during analytical method transfer activities, providing ongoing expertise and support.
• Track project milestones, monitor timelines, and escalation technical or operational bottlenecks when necessary.
• Initiate, investigate and close process-related Change Controls, Deviations and Laboratory Investigations.
• Organize and execute operational cGMP training programs within the QC department to maintain regulatory compliance.
• Act as the key liaison between operational QC teams and contract laboratories to identify and implement continuous improvements.
• Author, review, and revise cGMP documentation including SOPs, validation protocols, quality instructions and technical reports.

Kenntnisse

Analytical Chemistry

CGMP knowledge

QC IT systems

Communication skills

German knowledge

Ausbildung

PhD in Chemistry, Chemical Engineering, Biochemistry, Biology, or equivalent; or Bachelor’s/Master’s with significant QC experience

Tools

LIMS

CDS

DMS

Jobbeschreibung

Lonza in Visp (Valais) seeks a senior QC/Analytical Transfer specialist to drive method transfer projects and ensure compliant release of biopharmaceutical products. The role is on site with 41 hours per week, starting as soon as possible, by Oct 1, 2026.

You will estimate effort, lead technical transfer activities, manage milestones, and coordinate changes with QC teams and contract laboratories, while documenting cGMP procedures and ensuring quality standards.