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Senior Analytical Development Lead: GMP & Mentorship
Job Description & How to Apply Below
Key Responsibilities
Development and validation of analytical methods for drug products.
Plan and execute analytical activities aligned with project timelines. Analyze data and provide actionable insights.
Manage GMP stability studies and investigate OOS/OOT results.
Oversee daily lab activities and documentation. Ensure compliance with GMP, safety, and data integrity standards.
Support analytical equipment, CDS, and stability systems (e.g., SLIM, ELN, LIMS).
Train and mentor analysts and technicians.
Qualifications
MSc in Chemistry, Pharmaceutical Sciences, or related field
5+ years in analytical development in the pharmaceutical industry
Strong knowledge of GMP, method validation, and stability programs
Experience with chromatography systems and laboratory software (CDS, LIMS, ELN)
Strong leadership, organization, and problem-solving skills
Apply now Each role is integral to advancing OSD solutions and offers a unique chance to contribute to meaningful, industry-leading work.
Upload your Resume Drop your resume here or click to browse
Position Requirements
10+ Years
work experience
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