Global GMP Quality Auditor
- Experience
- Senior
- Employment
- Full-time
Open to MX only. Set where you work from to check your eligibility.
No BS summary
Global GMP Quality Auditor. Minimum 10 years broad pharmaceutical or medical device experience and a degree in Chemistry, Pharmacy, Biology, Engineering or related. Remote/Mexico (or Remote/Canada for Canadian role); willingness to travel ~60% globally; advanced oral and written English.
Optional languages
Band Level 4 Job Description Summary #LI-Remote Location: Remote/Mexico (or Remote/Canada for Canadian role, please see REQ-10082666) Novartis will not offer relocation support for this role. Are you passionate about safeguarding quality and driving continuous improvement across a global healthcare organization? As a Global GMP Quality Auditor at Novartis, you will play a critical role in ensuring compliance, quality, and patient safety across our global network. This is an opportunity to work with diverse manufacturing sites, development centers, contract manufacturers, laboratories, warehouses and suppliers, using your expertise to identify risks, strengthen quality systems, and influence positive change. If you thrive in a collaborative environment and are motivated by making a meaningful impact on healthcare around the world, we encourage you to apply. Job Description Key Responsibilities • Plan, lead, and execute GMP audits across global operations and external partners. • Assess compliance with regulations, quality standards, procedures, and guidance documents. • Document audit observations, prepare reports, and communicate findings to stakeholders. • Review and approve corrective and preventive action plans addressing audit findings. • Provide expert guidance and training on audit activities. • Escalate critical compliance issues and support timely mitigation activities when required. • Maintain expertise in evolving regulations, industry standards, and quality expectations. Essential Requirements •Degree in Chemistry, Pharmacy, Biology, Engineering, or another related scientific discipline; other degrees with relevant experience may be considered. •Minimum 10 years of broad experience in the pharmaceutical or medical device industry, including QA/QC management and manufacturing, development, or other relevant experience such as working at a regulatory health authority. •Expertise in at least one of the following areas: drug product (DP) manufacturing, biologics, sterile manufacturing, laboratories, microbiology, packaging, active pharmaceutical ingredients (API), excipients, medical devices, computer system validation, or quality systems. •Excellent knowledge of regulatory requirements, with experience and/or interaction with local Health Authorities and sporadically with other Health Authorities; sound and practical judgement in the interpretation and application of regulations and standards. •Strong interpersonal skills, including diplomacy, persuasion, and stakeholder management. •Willingness to travel approximately 60% globally. •Advanced oral and written English communication skills. Desirable Requirements • 3 years auditing experience • Proficiency in an additional language such as German, French, Italian, Chinese, or Spanish. Commitment to Diversity and Inclusion Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Accessibility and accommodation Novartis is committed to work with and provide reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to perform the essential functions of a position, please send an e-mail to tas.mexico@novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Skills Desired Collaboration, Data Integrity, Decision Making, Leadership, Risk Management 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. Novartis is aware of employment scams which make false use of our company name or leader’s names or recruiter’s names to defraud job seekers. Novartis does not make job offers without interview and never asks candidates for money. If you have encountered a job posting or been approached with a job offer that you suspect may be fraudulent, we strongly recommend you do not respond, send money or personal information. Novartis is not responsible for any claims, losses, damages, or expenses resulting from scams. 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 .
What you'll do
- Plan, lead, and execute GMP audits across global operations and external partners.
- Assess compliance with regulations, quality standards, procedures, and guidance documents.
- Document audit observations, prepare reports, and communicate findings to stakeholders.
- Review and approve corrective and preventive action plans addressing audit findings.
- Provide expert guidance and training on audit activities; escalate critical compliance issues and support mitigation when required.
What they require
- Degree in Chemistry, Pharmacy, Biology, Engineering, or another related scientific discipline; other degrees with relevant experience may be considered.
- Minimum 10 years of broad experience in the pharmaceutical or medical device industry, including QA/QC management and manufacturing, development, or other relevant experience such as working at a regulatory health authority.
- Expertise in at least one of the following areas: drug product (DP) manufacturing, biologics, sterile manufacturing, laboratories, microbiology, packaging, active pharmaceutical ingredients (API), excipients, medical devices, computer system validation, or quality systems.
- Excellent knowledge of regulatory requirements, with experience and/or interaction with local Health Authorities and sporadically with other Health Authorities; sound and practical judgement in the interpretation and application of regulations and standards.
- Willingness to travel approximately 60% globally.
Swiss-American multinational pharmaceutical corporation
What people say about this company
4.1/ 5
- Strong company culture and values.
- Opportunities for career growth and development.
- Supportive management and teamwork.