Manufacturing Consultant
Discover International ·
Job DescriptionSolid Dosage Manufacturing Consultant\ N6 months, full time B2B contract\ N
Key Responsibilities\ N
Lead investigations into selected GMP deviations, identifying root causes and supporting the development and implementation of effective corrective and preventive actions (CAPAs).\ N Provide subject matter expertise for CAPA and complaint management activities across ongoing improvement initiatives.\ N Draft, review, and update SOPs, work instructions, and other GMP documentation to ensure compliance and operational effectiveness.\ N Perform quality risk assessments (e.G. FMEA) and recommend appropriate mitigation strategies based on identified risks.\ N Develop and deliver GMPtraining sessions, sharing best practices and ensuring compliance with current regulatory expectations.\ N Review manufacturing records, batch documentation, and quality-related documentation for GMP compliance and accuracy.\ N Support department leadership on defined quality improvement and GMP compliance projects, acting as a technical advisor.\ N Provide specialist guidance on GMP requirements and best practices within solid oral dosage manufacturing.\ N
Required Experience\ N
Degree in Life Sciences, Pharmacy, Chemistry, Engineering, or another relevant scientific discipline (or equivalent industry experience).\ N At least five years of experience within a GMP-regulated pharmaceutical manufacturing environment.\ N Minimum three years of hands-on experience supporting solid dosage (oral solid dose) manufacturing operations.\ N Strong knowledge of EU GMP requirements, deviation investigations, CAPA processes, and quality management systems.\ N Demonstrated ability towork independently with a structured, analytical, and solution-focused approach.\ N