Regulatory Labelling Consultant (Serbia / UK / Spain)
Updated: February 3, 2026
Location: London, United Kingdom (Remote/Hybrid – Multiple EU Locations Supported)
Job ID: 25103960-OTHLOC-3666-2DH
Employment Type: Full-Time
About the Role
Syneos Health is seeking a skilled Regulatory Labelling Consultant to support global regulatory labeling activities across multiple regions, including Serbia, the United Kingdom, and Spain. This role is critical to ensuring labeling accuracy, compliance, and lifecycle management in alignment with global regulatory standards.
The ideal candidate will bring hands-on experience in labeling quality control, document management, and regulatory compliance within a biopharmaceutical or CRO environment. The position offers the opportunity to work within a collaborative, patient-centric Clinical Development model while contributing to the timely delivery of compliant medicinal product labeling.
Key Responsibilities
Participate in labeling governance meetings and prepare clear, accurate, and timely meeting minutes.
Upload approved meeting minutes and related documentation to electronic document management systems.
Perform quality control (QC) and proofreading of regulatory labeling documents to ensure accuracy, consistency, grammar, formatting, and compliance.
Verify labeling content against source documents and regulatory requirements.
Monitor and support adherence to labeling timelines, workflows, and governance processes using label tracking systems.
Generate reports, metrics, and tracking data to support labeling compliance and operational oversight.
Develop, maintain, and update labeling department templates and controlled documents.
Collaborate effectively with cross-functional labeling stakeholders, including regulatory affairs, quality, and clinical teams.
Required Qualifications & Experience
Bachelor’s degree in Life Sciences, Pharmacy, Regulatory Affairs, or a related discipline, or equivalent relevant experience.
3–6 years of experience in regulatory labeling, labeling operations, or labeling quality control within the pharmaceutical, biotech, or CRO industry.
Proven experience in label QC, label compliance, and label tracking across the product lifecycle.
Demonstrated ability to take detailed and accurate meeting minutes and distill complex discussions into concise documentation.
Strong command of the English language with exceptional proofreading, editing, grammar, and formatting skills.
Hands-on experience with label tracking systems such as Intagras or Veeva Labeling.
Familiarity with electronic document management systems (EDMS); Veeva Vault experience is highly desirable.
Prior experience using proofreading and comparison tools such as TVT or GlobalVision is preferred.
Strong organizational skills with the ability to manage multiple tasks and timelines in a regulated environment.
Effective communication and collaboration skills when working with global, cross-functional teams.
Why Join Syneos Health?
Syneos Health is a fully integrated biopharmaceutical solutions organization committed to accelerating the delivery of innovative therapies worldwide. Over the past five years, Syneos Health has supported the majority of FDA-approved and EMA-authorized products, working across thousands of global trial sites and patients.
Employees benefit from structured career development, continuous technical and therapeutic training, supportive leadership, and a culture that values diversity, inclusion, and authenticity. Syneos Health’s Total Self culture encourages individuals to bring their whole selves to work while contributing meaningfully to patient outcomes.
Additional Information
This job description outlines the primary responsibilities of the role; additional duties may be assigned based on business needs.
Equivalent combinations of education, skills, and experience will be considered.
Syneos Health is committed to equal employment opportunity and compliance with applicable labor and equality legislation across all operating regions.
Reasonable accommodations will be provided in accordance with applicable disability and employment laws.
Job Summary
This role is ideal for a Regulatory Labelling professional with proven experience in labeling quality control, compliance, and tracking systems, seeking to contribute to global regulatory operations within a leading biopharmaceutical organization.a
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