Key Responsibilities: • Creating and managing specifications, schedules and testing protocols for raw materials utilized in production processes, alongside evaluating quality of material suppliers for adherence to quality and regulatory standards.• Management and evaluation of suppliers, including the upkeep of approved supplier lists, assessment based on vendor certification, and the appraisal of raw material suppliers to foster a dependable supply chain and ensure compliance with quality standards.• Validating manufacturing procedures and documenting the validation processes to ensure the consistent quality of products. This entails both maintaining validation documentation and adjusting manufacturing specifications when necessary.• Management of documentation, maintenance of quality records, and validation documentation, to ensure alignment with regulatory standards.• Management of packaging specifications, encompassing their preparation, updates, and overall maintenance to uphold regulatory compliance and ensure the integrity of products.• Ensuring adherence to regulatory standards and guidelines by tasks such as reviewing stability data, overseeing change control processes, and providing assistance during product recalls as required.• Overseeing and administering quality control measures, including activities such as validating clean-ing processes, monitoring environmental conditions, and managing pest control initiatives to ensure adherence to regulations and uphold product safety standards.• Training and fostering development among staff members by delivering instruction on quality protocols, regulatory mandates, and best practices in manufacturing. Additionally, aiding in the conduct of annual reviews of product quality when required.

Key Responsibilities: • Ensuring the quality of pharmaceutical products through the batch disposition process, which involves overseeing all aspects of manufacturing, quality control, storage, and distribution of both raw materials and finished products. • Collaborating with external partners and suppliers to establish robust Pharmaceutical Quality Systems aligned with regulations and guidelines.• Ensuring compliance during preparation and labelling of medicaments with adherence to regulatory standard, Quality Agreements, and associated procedures.• Promptly investigate and address compliance issues and performing risk assessments to prevent market supply disruptions.• Investigating customer complaints related to product quality.

Key Responsibilities: • Reviewing and approving investigations, incidents and significant investigations to maintain Good Manufacturing Practice (GMP).• Preparing and reviewing standard operating procedures (SOP) to ensure compliance and quality across various operations, including manufacturing, packaging, laboratories, warehouse, and distribution.• Participating in internal and external audits to ensure regulatory compliance and quality standards.• Working collaboratively with multidisciplinary teams to investigate and enhance manufacturing and quality-related processes.• Serving as a member of the Quality Risk Management team to mitigate quality-related risks.

Key Responsibilities:• Supporting investigation of manufacturing deviations, out-of-specification (OOS) results, and trends in stability studies.• Driving the review and approval of Corrective and Preventive Actions (CAPA) to address quality issues.• Supporting change control processes and annual product reviews of product quality.• Providing guidance and insights during investigations and action plan development to improve quality processes.• Training and fostering development among employees by delivering instruction on good manufacturing practices, regulatory requirements, and quality standards.

Key Responsibilities:• Conducting testing, analysis and research to ensure the quality and compliance of pharmaceutical products and raw materials.• Performing chemical assays for finished products and raw materials, adhering to quality control methods and standards in the pharmaceutical sector.• Developing and implementing standards for pharmaceutical products to ensure identity, purity, and strength in accordance with specified standards.• Performing validation process of pharmaceutical processes maintaining compliance of validation documentation. • Testing and analysis of drugs using various analytical techniques such as HPLC, spectrophotometry, CG, Karl Fischer, and dissolution testing.

Key Responsibilities:• Developing and validating analytical methodologies by HPLC, spectrophotometry and drug dissolution.• Writing and reviewing procedures (SOPs), validation protocols and analytical documentation.• Developing dissolution media and dissolution profile studies.• Supporting the team with Good Laboratory Practices (GLP) and laboratory routine.

Key Responsibilities:• Performing chemical analysis of finished product and stability studies by HPLC, spectrophotometry and drug dissolution techniques.• Writing and reviewing analytical documentation.• Supporting Good laboratory practices, 5S program and Kaizen.