11 Stps Jobs

As a Deputy Manager - Quality Assurance (QA) at Eco Paryavaran Laboratory, your role will involve supporting and strengthening the quality management processes within the Environmental Laboratory. You should possess a Bachelor's/Master's Degree in Environmental Science, Chemistry, or a related field with 5-6 years of experience. Key Responsibilities: - Assist the Quality Manager in implementing and maintaining the laboratory's Quality Management System in compliance with ISO/IEC 17025:2017. - Support NABL accreditation processes, including documentation, audits, and compliance. - Ensure laboratory safety, data integrity, and good laboratory practices (GLP). - Oversee calibration schedules fo...

As a QA/QC Manager at our company, you will be responsible for liaising between various departments such as Planning, Production, Technical Services, Marketing, and Exports. Your role will involve the following key responsibilities: - Preparation, review, and implementation of SOPs and STPs. - Checking of all QC related records like analytical reports and logbooks. - Planning and distribution of samples for analysis of Raw Materials, Intermediates, and finished products. - Designing and conducting Stability studies as per ICH Guidelines. - Developing and validating analytical testing methodology used to control raw materials, production intermediates, and final products. - Preparation and ma...

You will be working at Jubilant Pharma Limited, a global integrated pharmaceutical company that offers a wide range of products and services across different geographies. The business is organized into two segments: Specialty Pharmaceuticals and Generics & APIs. Jubilant Generics (JGL) is a wholly-owned subsidiary of Jubilant Pharma with Research & Development units in Noida and Mysore, India. JGL operates manufacturing facilities in Mysore, Karnataka, and Roorkee, Uttarakhand, focusing on APIs and Dosage manufacturing. The Mysore manufacturing site, spread over 69 acres, is USFDA approved and manufactures APIs targeting Lifestyle driven Therapeutic Areas such as CVS and CNS. The Roorkee fac...

Key Responsibilities: Analytical Method Development & Validation Develop and validate robust HPLC methods for characterization and quantification of biological products (e.g., monoclonal antibodies, recombinant proteins). Perform method optimization, robustness studies, and transfer protocols as per ICH guidelines. Routine & Stability Testing Conduct analysis of in-process, release, and stability samples using: HPLC/UPLC Capillary and Gel Electrophoresis UV spectrophotometric methods Host Cell DNA quantification (e.g., qPCR-based methods) HCP ELISA and other immunoassays Instrument Operation & Maintenance Perform routine maintenance, calibration, and troubleshooting of analytical instruments...

As a Mechanical Engineering professional at Walter P Moore, you will play a crucial role in MEP design and site coordination within the real estate/construction industry. Your responsibilities will include: - Lead MEP design and execution activities, ensuring high-quality and timely deliverables. - Coordinate with clients, vendors, consultants, and internal teams for seamless project execution. - Conduct and manage stakeholder meetings to drive alignment and progress across all phases. - Ensure compliance with relevant standards and guidelines such as EC norms, MOEF guidelines, IS codes, and NBC 2016. - Promote sustainable MEP solutions, contribute to cost estimation, and budgeting. - Review...

You will be joining the Quality Control - Analytical team at Dr. Reddys Laboratories Ltd. where your primary responsibility will be to conduct analysis of Biosimilar products including drug substance, drug products, in-process samples, and stability samples. Your role will involve ensuring accuracy in documentation, adherence to safety procedures, reporting discrepancies, and maintaining lab safety. To excel in this role, you will be required to perform various chromatography techniques like RP-HPLC, Glycan, SEC, IEX, and pep map for Biosimilar Molecules. Method validations on RP-HPLC, Glycan, SEC, IEX, and pep map will also be part of your responsibilities. Adhering to GMP practices, good d...

You will be working as the Deputy Manager - Quality Assurance (QA) at Eco Paryavaran Laboratory. Your main responsibility will be to support and enhance the quality management processes within the Environmental Laboratory. To qualify for this role, you must hold a Bachelor's or Master's Degree in Environmental Science, Chemistry, or a related field. Additionally, you should have at least 5-6 years of experience in this field. Your key duties will include assisting the Quality Manager in implementing and maintaining the laboratory's Quality Management System in accordance with ISO/IEC 17025:2017 standards. You will also be involved in supporting NABL accreditation processes, ensuring laborato...

As a quality control professional, you will be expected to strictly adhere to cGMP norms and safety rules within the factory premises. Your key responsibilities will include verifying logbooks, records, and other analytical documents on a daily basis to ensure their correctness and completeness. It will be your duty to ensure the timely preparation and revision of SOPs, STPs, and other Quality Management System (QMS) documents. You will also be responsible for the prompt completion of investigation activities related to Quality Control (QC) aspects such as Out-of-Specification (OOS), Out-of-Trend (OOT), deviations, and out-of-compliance (OOC) activities. Moreover, you will be accountable for...

You will be responsible for liaising between various departments such as Planning, Production, Technical Services, Marketing, and Exports. Your roles and responsibilities will include the preparation, review, and implementation of SOPs and STPs. You will be checking all QC related records like analytical reports and logbooks. Additionally, you will be involved in planning and distributing samples for the analysis of Raw Materials, Intermediates, and finished products. You will design and conduct Stability studies as per ICH Guidelines and develop and validate analytical testing methodology used to control raw materials, production intermediates, and final products. Your tasks will also inclu...

Oversee site operations, troubleshoot STP issues, standardize processes. Manage attendance, create daily & monthly reports. operation of STPs, ETPs and WTPs monthly meetings, submit records regularly. Standardization of operational implementation Health insurance Provident fund

Role & respons We are seeking an experienced GoAnywhere Administrator with over 5 years of expertise in managing and optimizing GoAnywhere Managed File Transfer (MFT) solutions. The ideal candidate will be responsible for ensuring the secure, reliable, and efficient transfer of data across our systems and with our partners. This role requires a deep understanding of MFT processes, security protocols, and compliance requirements. Key Responsibilities: • System Administration: Oversee the installation, configuration, and maintenance of GoAnywhere MFT systems to ensure operational efficiency and security. • Workflow Design and Automation: Develop and manage automated workflows for file transfer...