Our client, a leading pharmaceutical company, is seeking a Reference Standard Owner to support a highly regulated GMP environment. This role manages the full lifecycle of assigned reference standards, ensuring that all qualification and requalification activities meet the highest quality standards and compliance requirements.
Our client, a leading life sciences organization, is seeking a Lab Operations Project Engineer to bridge laboratory science and process improvement. The role focuses on supporting Quality Control environments by implementing new analytical methods and ensuring compliance within regulated settings. One contributes to the smooth introduction of testing approaches while resolving technical challenges in complex laboratory environments.
Our client, a prominent pharmaceutical organization, is seeking a Laboratory Operations Project Engineer to manage compliance assessments for method validation and compendial dossiers. The role focuses on the implementation of new test methods within Quality Control operations while coordinating project activities and ensuring technical documentation standards.
Our client, a leading pharmaceutical organization, is seeking a senior professional to lead validation and planning efforts for major capital projects. This role focuses on ensuring rigorous compliance with international quality standards while managing project lifecycles, product introductions, and technical coordination between departments.
Whether you're passionate about regulatory strategy, compliance, or labeling, we offer opportunities across multiple specializations:
Regulatory Strategist – Define and drive regulatory strategy throughout the drug development lifecycle.
Regulatory Affairs Expert – Provide end-to-end regulatory support for development, submission, and post-approval activities.
Regulatory Affairs Specialist – Ensure compliance with EU and global regulations for pharmaceutical products.
Artwork & Labeling Consultant – Manage labeling processes and artwork reviews in line with regulatory guidelines.
Labeling Specialist – Oversee product information and ensure accurate, compliant labeling across markets.
CMC Regulatory Affairs Consultant – Support regulatory submissions related to Chemistry, Manufacturing & Controls (CMC).
Regulatory Project Coordinator – Coordinate timelines, submissions, and stakeholder communication in regulatory projects.
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