2.0 - 6.0 years

0 Lacs

ankleshwar, gujarat

On-site

You will be responsible for providing investigation support for quality/yield failures such as OOS/OOT/Deviations/Market complaints investigations. You will be required to conduct chemistry literature search, interpret results from LCMS, GCMS, NMR, etc., and prepare Structure Elucidation and Characterization reports. Your role will also involve working on ecofriendly and cost-effective process development tasks including cost reduction and yield improvement. Additionally, you will be supporting New Vendor Qualification (NVQ) and providing plant troubleshooting support including monitoring and participating in CFT discussions. Ensuring Lab Safety compliance (SMS ratings) and maintaining laboratory GMP/RA compliance will also be part of your responsibilities. You will be expected to support HAZOPs, SHE Risk assessments, Capacity enhancement, effluent reduction, and lead a synthesis lab. Qualifications required for this role include an M.Sc in Chemistry, with a preference for a background in ADL/QC. The ideal candidate should have a minimum of 2 years of experience, with at least 12 months of experience in Zydus. If you meet these qualifications and are ready to take on these responsibilities, you can apply by sending your application to Karishma.r.kadu@zyduslife.com with the subject line ZTMP PD Lab.,

Posted 2 weeks ago

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QC Supervisor Piramal Pharma Ltd

5.0 - 9.0 years

0 Lacs

maharashtra

On-site

The role of Quality Control Manager in Critical Care Business at Bethlehem, PA involves overseeing all Quality Control functions to ensure alignment with core values and ethical practices. Your primary responsibility is to ensure that the Quality Control department meets the needs of both internal and external customers by delivering services and products on time. You will collaborate with various internal stakeholders such as API Manufacturing, Packaging, Quality Assurance, Engineering, Regulatory Affairs, EHS, Supply Chain and Logistics, as well as external stakeholders including Auditors, Customers, Regulatory Agencies, and External Suppliers. Reporting directly to the Senior Manager of Quality Control, your essential duties and responsibilities include leading a team of QC Analysts, ensuring compliance with quality systems and regulatory requirements, maintaining documentation, coordinating investigations and improvement projects, reviewing and approving test documents, managing quality processes through SAP system, overseeing batch production and testing, participating in product development support, and maintaining lab equipment. To be successful in this role, you must possess strong organizational and communication skills, critical thinking abilities, excellent customer service skills, creativity in problem-solving, energetic and motivational disposition, confidentiality maintenance, coaching skills, proficiency in computer tools, and the ability to lead a team in a fast-paced environment while managing multiple projects effectively. The ideal candidate should have a B.S. in Chemistry or a related discipline, minimum 5 years of experience in a pharmaceutical manufacturing laboratory environment, at least 3 years of supervisory experience, hands-on experience with quality systems in a GxP environment, familiarity with FDA, MHRA, and other health authority inspections, knowledge of international regulations, and audit experience. If you are looking for a challenging opportunity in Quality Control with a focus on pharmaceutical manufacturing, this role at 3950 Schelden Circle, Bethlehem, PA, 18017, US might be the perfect fit for you.,

Posted 1 month ago

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