Senior QA Ops Specialist: GMP Compliance & Quality

Lonza; Schweiz; On-site; Vertraulich; Full time

Benefits offered by this job

Competitive benefits package

GMP-compliant environment

Autonomy in an international setting

Career development opportunities

Relocation assistance where applicable

Job summary

Lonza Visp, Switzerland is seeking a QA professional within the Small Molecules team to ensure compliance with quality and regulatory requirements across the product lifecycle. You will support our production units in quality matters and contribute to GMP-compliant manufacturing of our products.

The role includes reviewing batch documents, supporting Deviations, Change Requests and CAPA actions, conducting internal audits, and collaborating with customers and regulators.

Qualifications

• Academic degree in a scientific discipline (Chemistry/ Biochemistry/ Pharmacy or similar).
• GMP knowledge and experience in chemical manufacturing are advantageous.
• Strong verbal and written communication skills in German and English.
• High sense of ownership, structured working style, and strong customer and team orientation.
• Ability to interpret regulatory requirements accurately and align them with sound business understanding.

Responsibilities

• Ensure that manufacturing is conducted in accordance with the process registered with health authorities.
• Monitor compliance with all quality agreements established with our international customers.
• Build and maintain reliable and transparent relationships with customers to consistently meet quality expectations and requirements.
• Independently review batch-related manufacturing documentation for completeness, accuracy, and GMP compliance.
• Support, assess, and approve Deviations, Change Requests, and CAPA actions.
• Contribute to quality risk assessments and prepare Quality Review Reports.
• Conduct internal audits and support customer audits as well as inspections by regulatory authorities.

Skills

German language proficiency

English language proficiency

Ownership mindset

Structured working style

Customer orientation

Team orientation

Education

Degree in a scientific discipline (Chemistry/ Biochemistry/ Pharmacy or similar)

Tools

MS Office

Documentum

LIMS

TrackWise

Job description

Lonza Visp, Switzerland is seeking a QA professional within the Small Molecules team to ensure compliance with quality and regulatory requirements across the product lifecycle. You will support our production units in quality matters and contribute to GMP-compliant manufacturing of our products.

The role includes reviewing batch documents, supporting Deviations, Change Requests and CAPA actions, conducting internal audits, and collaborating with customers and regulators.