Quality Assurance Operations Lead

Novartis; Zaragoza; Vor Ort; EUR 45.000 - 84.000; Vollzeit

Benefits dieser Stelle

Insurance plans

Retirement plans

Wellbeing resources

Global recognition programs

Flexible and hybrid working options

14 weeks paid parental leave

Zusammenfassung

Novartis in Spain is seeking a Quality Assurance Operations Lead to ensure safe, compliant release of sterile injectables. You will lead QA Operations on site, driving continuous improvement and a strong quality culture across the site.

The role oversees GMP-compliant manufacturing support, regulatory alignment with EMA/AEMPS, and collaboration with Production, Quality Control, and Site Management to maintain inspection readiness.

Qualifikationen

• Scientific degree in Pharmacy, Chemistry, or Biology.
• 5+ years in the pharmaceutical industry.
• Strong knowledge of QA operations and quality requirements.
• Solid understanding of cGMP regulations and regulatory standards.
• Fluent in Spanish and English, both written and spoken.

Aufgaben

• Lead compliance with GMP, AEMPS, EMA and the Novartis Quality Manual.
• Oversee QA Operations: product release, documentation, SOP approvals.
• Ensure quality oversight of manufacturing, validation, cleaning and equipment.
• Manage QA processes: OOS, deviations, CAPA, complaints, recalls.
• Support audits, inspections, and annual product quality reviews.

Kenntnisse

QA Operations

cGMP knowledge

Regulatory compliance

Aseptic manufacturing

Team leadership

Ausbildung

Pharmacy, Chemistry, or Biology degree

Jobbeschreibung

Salary Range:

€45,100.00 - €83,700.00

Band

Level 4

Job Description Summary

#LI-Onsite

Location: La Almunia de Doña Godina (Zaragoza, Spain)

This role is La Almunia de Doña Godina, Spain. Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you.

The Quality Assurance Operations Lead plays a critical role in ensuring that products are released with the highest standards of quality, compliance, and patient safety. This role oversees the release of sterile injectable products manufactured in line with the Quality System, current registrations, GMP, EMA, AEMPS, the Novartis Quality Manual, and all applicable regulatory requirements.

As a key quality leader on site, the position provides strategic oversight of manufacturing operations, ensuring that commercial activities remain fully compliant and inspection-ready. The role also leads the people, processes, and technical resources within the Quality Assurance Operations department, driving effective QA support, continuous improvement, and a strong quality culture across site operations.

Job Description

Deadline for applications: 29th October 2026.

Major Accountabilities:

• Lead the implementation and continuous improvement of compliance with applicable quality standards, including GMP, AEMPS,EMA the Novartis Quality Manual, and site quality procedures, while promoting a strong quality culture across the organization.
• Oversee QA Operations activities, including product release, documentation management, SOP approval, training, resource planning, shift organization for QPs and QA Officers, and professional development of team members.
• Ensure quality oversight of manufacturing operations, maintenance, qualification, calibration, revalidation, process validation, cleaning validation, equipment qualification, and new projects requiring QA Operations support.
• Manage and approve quality processes including OOS, OOT, OOE, deviations, change controls, CAPA, complaints, recalls, returns, investigations, and related corrective and preventive actions in accordance with cGMP and SOPs.
• Ensure timely escalation and communication of quality and cGMP issues, non-conformities, product-impacting incidents, and substantial irregularities involving products already placed on the market, including communication to relevant internal stakeholders and competent authorities when required.
• Support audits, inspections, and quality reviews by participating in authority and corporate audits, annual self-inspection planning, annual training planning, and Annual Product Quality Review preparation and review.
• Monitor, report, and drive quality performance by tracking assigned indicators, ensuring projects and responsibilities are completed on time, and supporting business continuity in collaboration with Site Management, Quality, Quality Control, and Production leaders.
• Provide QA support to commercial operations while ensuring compliance with environmental, safety, order, cleanliness, internal communication, and external communication requirements within the area of responsibility.

Obligatory Requirements:

• Scientific degree in Pharmacy, Chemistry, or Biology
• 5+ years of experience in the pharmaceutical industry, with strong knowledge of QA Operations and quality requirements.
• Strong understanding of cGMP regulations, regulatory requirements, and pharmaceutical quality standards.
• Solid knowledge of aseptic processes and aseptic manufacturing practices.
• Excellent organizational skills, attention to detail, teamwork mindset, and ability to work with urgency on assigned tasks.
• Strong communication and collaboration skills, with the ability to support smooth and safe production operations, drive productivity improvements through new technologies and processes.
• Fluent in Spanish and English, both written and spoken.

Desirable Requirements:

• Previous Experience as a certified Qualified Person is highly valued.

Rewards

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 inkindto help you thrive personally and professionally, such as insurance plans, retirement plans, wellbeingresourcesand global recognition programs. In addition, we provide flexible and hybrid working options, where possible, anda minimum of14 weekspaid parental leave.

Expected Annual Base Salary Range for role:

• Spain: EUR 45,100 – 83,700

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 diverseteams’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,supportingand 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