Senior Quality Control Specialist

C028 (FCRS = CH028) Novartis Pharma AG; Basel; Vor Ort; CHF 85.000 - 159.000; Vollzeit

Benefits dieser Stelle

Hybrid working options

Parental leave (min 14 weeks)

Zusammenfassung

Novartis Pharma AG in Basel, Switzerland seeks a Senior QC Specialist in bioanalytics to support lab activities, review data, and ensure compliance with cGxP and HSE guidelines. This is a fixed-term contract of 18 months.

You will plan sampling, review analytical results for release, stability and projects, and prepare protocols/reports, trend analyses, and KPI documentation. You will lead analytical projects, support method transfers and deviations, and collaborate across functions in a GMP

Qualifikationen

• 3-5 years of relevant experience or a university degree in Pharmacy, Chemistry, or related field.
• Experience in GMP-regulated pharmaceutical environments with analytical testing.
• Ability to review data, contribute to investigations and ensure data integrity.

Aufgaben

• Plan, coordinate and support sampling activities aligned with project needs.
• Review/approve analytical results for release, stability, and projects.
• Prepare/approve protocols, reports, trend analyses and KPIs.
• Lead analytical projects, including method transfers and calibrations.
• Serve as SME for products, audits, and cross-functional governance.
• Manage deviations, CAPAs, investigations, and continuous improvement.
• Ensure compliance with cGxP, data integrity, QA, and HSE requirements.

Kenntnisse

Quality control

GxP compliance

Data integrity

Analytical testing

English communication

Ausbildung

Pharmacy degree

Chemistry degree

Tools

MS Office

Laboratory IT systems

Jobbeschreibung

Salary Range: CHF 85.400,00 - CHF 158.600,00 Band Level 4 Job Description Summary #LI-Onsite Location: Basel, Switzerland This role is based in Basel, Switzerland. Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you.

The Senior QC Specialist works in the area of bioanalytics, supporting the laboratory team with in-depth knowledge to ensure efficient performance of laboratory activities and related investigations in compliance with GxP and HSE guidelines. Performs review and approval of analytical data. Job Description We offer a fixed-term contract of 18 months.

Major Accountabilities:

• Plan, coordinate, and support sampling activities, including execution, documentation, and alignment with project and routine laboratory needs.
• Review, evaluate, and approve analytical test results for release, stability, and project-related activities in accordance with applicable procedures.
• Prepare, review, and approve analytical protocols, reports, trend analyses, KPIs/KQIs, and registration-related documentation.
• Lead or contribute to analytical project activities, including method implementation, analytical transfers, new product introduction, and routine laboratory readiness.
• Serve as Single Point of Contact or Subject Matter Expert for assigned products, pipeline activities, external initiatives, audits, inspections, and technical assessments.
• Manage deviations, OOx investigations, CAPA definition, analytical weak points, and continuous improvement actions to ensure robust laboratory performance.
• Contribute to supplier qualification, service provider management, contracts, SLAs, SOWs, QAAs, budgeting activities, and cross-functional governance meetings.
• Ensure all activities comply with cGxP, data integrity, Quality, and HSE requirements, including equipment maintenance, calibration planning, training, risk identification, and safe working practices.

Obligatory Requirements:

• Technical education with 3-5 years of relevant experience, or a university degree in Pharmacy, Chemistry, or a related scientific discipline with 0-4 years of relevant experience.
• Experience in the pharmaceutical industry, active substance manufacturing, or analytical laboratories within a GMP-regulated environment.
• Strong knowledge of Quality Control testing, sampling, laboratory equipment, GxP standards, data integrity, and quality decision-making processes.
• Experience supporting analytical release, stability testing, method transfers, deviations, CAPAs, trend analysis, and project documentation.
• Ability to collaborate effectively across functions, departments, external partners, and project teams.
• Strong communication skills, with good written and spoken English and fluency in the local language.
• Proficiency in MS Office and standard IT systems used in Quality, laboratory, and documentation activities.
• Demonstrated competencies in collaboration, result orientation, analytical problem-solving, resilience, operational excellence, continuous learning, and digital awareness.

Rewards At Novartis:

At Novartis, we’re committed to reimagining medicine together - and rewarding the people who make it happen. The rewards of being part of our team go far beyond base pay and incentives. We also offer a variety of competitive benefits in kind to help you thrive personally and professionally, such as insurance plans, retirement plans, wellbeing resources and global recognition programs. In addition, we provide flexible and hybrid working options, where possible, and a minimum of 14 weeks paid parental leave.

Expected Annual Base Salary Range for role: 85,400 - 158,600 CHF.

The salary offered is determined based on gender-neutral objectives, such as relevant skills, competencies and experience in accordance with the Novartis pay setting policy and upon joining Novartis will be reviewed periodically. In addition to your base salary, you may be eligible for a performance-based bonus depending on certain performance parameters. Further details will be provided during the application process.

Pay equity is a fundamental principle of our employment policy and reflects our commitment to create a diverse, equitable and inclusive environment that treats all employees with dignity and respect, as outlined in our Code of Ethics. Read our brochure to learn more about our global total rewards offering: https://www.novartis.com/sites/novartis_com/files/novartis-life-handbook.pdf Note: Benefits and compensation may vary by country and are subject to local legal requirements, including provisions of collective bargaining agreements where applicable. A full overview of your compensation package, including any relevant collective bargaining agreement details applicable to your role based on your employment location and Novartis employer entity, will be communicated separately to you during the application process.

Commitment to Diversity and Inclusion / EEO paragraph:

Novartis is committed to building an outstanding, inclusive work environment and diverse teams’ representative of the patients and communities we serve.

Why Novartis:

Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture

Benefits and Rewards:

Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards

Skills Desired:

• Collaboration
• Data Integrity
• Decision Making
• Leadership
• Operational Excellence

Improving the lives of people living with disease takes more than innovative science. It takes a focus on the needs of people and a community committed to meeting them. It takes a team of people like you. Working together. Learning together. Thriving together. Discover how you can join us in changing people’s lives.

In the context of China Cross-Border Data Transfer (CBDT) policy, if you need to apply for a position in China, please go to the local Recruiting System TaleNov .