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Open nowPosted yesterday

QA Compliance Specialist

novartis336 open roles

Where
Targu Mures
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Your applicationOpen nowQA Compliance Specialistnovartis · Targu Mures

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The clock on this job

Early applications get read.

13.3% of postings close within 7 days. Measured by our own scanner across the market. novartis postings stay open a median of 13 days.

Share of postings closed within
  1. 2.1%1 day
  2. 4.6%3 days
  3. 13.3%7 days
  4. 21.3%14 days
  5. 35.7%30 days
  6. 59.1%60 days
This job: posted yesterday

novartis median: 13 days open

The posting

Salary Range:

lei84,560.00 - lei157,040.00

Job Description Summary

#LI-Hybrid

Location: Târgu Mureș, Romania

Relocation Support: This role is based in Târgu Mureș, Romania. Novartis is unable to offer relocation support: please only apply if accessible.

Help shape a culture where quality is built into every step. As a QA Compliance Specialist, you will play a key role in strengthening quality and compliance across our operations, partnering with colleagues to maintain robust quality systems and uphold Good Manufacturing Practice standards.

You will contribute to investigations, audits, data integrity and continuous improvement activities, helping ensure our processes consistently meet regulatory expectations. This is an opportunity to combine your quality expertise with meaningful collaboration and make a tangible impact on the reliable delivery of medicines to patients.

Job Description

We offer 1 year contract with the possibility of extension.

Key Responsibilities:

  • Maintain and continuously improve quality systems in compliance with Good Manufacturing Practice and regulatory requirements.
  • Review quality documentation to ensure accuracy, completeness, compliance, and timely approval.
  • Support investigations, deviations, corrective and preventive actions, and implementation of sustainable improvements.
  • Promote data integrity principles and ensure quality records meet established standards.
  • Support internal and external audits and contribute to inspection readiness activities.
  • Partner with cross-functional teams to identify compliance risks and strengthen quality processes.
  • Provide quality guidance and promote a proactive culture of compliance and continuous improvement.

Obligatory Requirements:

  • University degree in Pharmacy or a closely related scientific discipline.
  • At least two years of experience in the pharmaceutical industry.
  • Strong knowledge of Good Manufacturing Practice and pharmaceutical quality standards.
  • Advanced English language skills, with the ability to communicate effectively in a professional environment.
  • Solid understanding of pharmaceutical product and material quality, quality assurance, and regulatory compliance.
  • Proficiency with Microsoft Office and standard digital applications supporting quality activities.

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 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:

  • Romania: RON 84,560 – 157,040.

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

Audits Compliance, Collaboration, Communication, Data Integrity, Decision Making, Digital Fluency, Internal Auditing, Managing Ambiguity, Problem Solving, Process Quality Assurance, Quality Assurance (QA), Quality Auditing, Quality Compliance, Quality Management, Quality Management System Implementation, Regulatory Compliance, Validation Activities, Validation Management

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