Microbiology Manager Dadaji Lifescience Private Limited

3.0 - 7.0 years

0 Lacs

rajkot, gujarat

On-site

You will be responsible for writing and proposing revisions to Standard Operating Procedures, Analytical Methods, Lab Reports, and related Forms. You will perform reviews to support Validation, Document Control, and Change Control systems. Additionally, coordination and maintenance of the stability program for new product development and existing products will be under your purview. Tracking and reporting on Quality System Metrics relevant to testing, OOS Investigations, and training to support Quality Systems Reporting is also a key aspect of this role. Furthermore, you will provide QA Support for Audits and Inspections. To be considered for this position, you must have an M.sc in Microbiology and possess 3 to 5 years of relevant experience. This is a full-time position based in Rajkot (Padvala) with day shift schedule and weekend availability required. The work location is in person. If you are interested in this opportunity, please share your resume with us at hr@dadajilifescience.com.,

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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