Analytical Research Supervisor

About the role

MS Pharma is seeking an experienced Analytical Research Supervisor to lead and coordinate analytical research and stability activities across its pharmaceutical portfolio. The role involves guiding junior staff, ensuring compliance with GLP/GMP standards, and delivering high‑quality documentation for regulatory submissions.

Key responsibilities

• Plan, organize and supervise weekly and monthly analytical research and stability programs.
• Review, approve and maintain SOPs, method development, validation/verification reports, stability protocols and laboratory records.
• Prepare and review drug substance and product specifications, justification reports and regulatory submission documents.
• Manage supplier qualification (DMF evaluation), pharmacopeia updates, stability studies, chamber monitoring and equipment maintenance.
• Lead OOS investigations, conduct root‑cause analysis and implement corrective actions.
• Supervise, train and coach team members, providing technical guidance for experiments.
• Verify stability batches, labeling, documentation and logbook entries for regulatory compliance.
• Ensure adherence to GLP, GMP, health & safety requirements and support internal/external inspections.
• Coordinate with internal departments and external stakeholders to resolve issues and drive continuous improvement.

Required profile

• Proven experience in analytical method development, validation and stability testing within the pharmaceutical industry.
• Strong knowledge of GLP, GMP and regulatory guidelines.
• Demonstrated ability to lead investigations of OOS results and implement corrective actions.
• Excellent documentation skills and experience preparing regulatory submission materials.
• Leadership experience supervising and training junior scientists.

Required skills

• Analytical method development
• Method validation and verification
• Stability testing and protocol management
• GLP and GMP compliance
• OOS investigation and root‑cause analysis
• Regulatory documentation preparation
• DMF evaluation and supplier qualification
• Pharmacopeia updates and stability chamber monitoring

What we offer

• Opportunity to work in a leading regional pharmaceutical organization.
• Continuous learning and professional development.
• Collaboration with experienced cross‑functional teams.
• Career growth within an international company.
• Culture that encourages innovation, ownership and continuous improvement.