Position: Associate

Job type: Full-time

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DivisionQualityDepartmentQualityEmployment TypePermanentJob PurposePlan and lead the quality control operations and drive the team to confirm testing as per the GLP guidelines and regulatory requirements and achieve timely release of batches and SRB targets to meet unit OTIFAccountabilitiesI. Monitor the execution of all routine quality control operation and stability studies to ensure timely delivery and meet regulatory requirements and cGMP, GLP guidelinesII. Drive the investigation of the batch for non-conformance and ensure its closure within the timelines defined in SOPs to facilitate smooth operationsIII. Monitor completion of stability studies as per protocol/schedule to avoid delays in product launchIV. Provide technical guidance to the team w.r.t batch release and stability studies and evaluate their performance to ensure team development and improved lab efficiencyEducation QualificationB. Sc. / B. PharmRelevant Work Experience9+ years of experience in quality control function of a pharmaceutical organisationCompetencies/SkillsCommunication Skills (clarity of thought, comprehension)Likely potential for growthJob / Product / Technical Knowledge / Pharma domain knowledgePresentation & Interpersonal skills (If applicable)Managerial or People Management skillsSafety awareness (If applicable)Relevance of Previous ExperienceComprehension, Analytical & Problem solving abilitiesProductivity & Result Orientation (If applicable)AttitudeQualification fitmentSales drive (If applicable)Personality traits (Individualistic / Team player, Out spoken, Maturity level etc.)Job LocationIndoreShift Hours
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Deadline: 04-07-2024

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