1082 Sops Jobs - Page 23

As a Finance and Accounting professional, you will be responsible for tracking invoices for timely booking, monitoring and implementing Finance SOPs and KPIs, and ensuring project-wise inventory consumption monitoring. You will review inventory physical verification and account for any deviations promptly, as well as clear vendor GRIR and advances in a timely manner. Conducting financial analysis, future projections, and monitoring budget utilization to identify deviations will be part of your role. You will also participate in financial negotiations and commercial discussions to optimize costs and support smooth site operations. Collaborating with project teams, techno-commercial department...

As the Pharmacovigilance (PV)/GCP Auditing & QMS Manager, you will be responsible for independently performing QA activities in collaboration with the Quality Head. This includes managing quality issues, events, deviations, and CAPAs. You will be involved in performing Root Cause Analyses (RCAs) or guiding staff in conducting RCAs, as well as developing CAPA plans or assisting staff in implementing CAPAs. Planning audits based on risk assessments, maintaining audit schedules, and conducting internal audits and vendor audits are also part of your role. Your responsibilities will encompass maintaining controlled documents like SOPs and templates, liaising with Project Leads/Functional Heads to...

The role of QMS Manager (Pharmacovigilance (PV)/GCP Auditing) based in Chandigarh, India requires you to perform various Quality Assurance activities either independently or in collaboration with the Quality Head. Your responsibilities include managing quality issues, events, deviations, and CAPAs, as well as conducting Root Cause Analyses (RCAs) or guiding staff in performing them. You will also be involved in developing CAPA plans and ensuring their implementation, planning audits based on risk assessment, and maintaining the audit planner in compliance with GVP and GCP requirements. Additionally, you will be responsible for preparing audit schedules, conducting internal audits and vendor ...

The Time Officer position is based in Erode with a salary ranging from 25k to 30k. The ideal candidate should possess any degree along with experience as a security officer for a minimum of 5 to 10 years. As a Time Officer, your primary responsibility will be to lead and manage the security strategy, personnel, and systems within the steel plant. This includes ensuring the safety and protection of individuals, assets, materials, and information from both internal and external threats. You will be tasked with developing and implementing security policies, standard operating procedures (SOPs), and emergency response plans specifically tailored to the steel manufacturing environment. Additional...

You will be responsible for managing the operations and maintenance of Effluent Treatment Plant (ETP) and Sewage Treatment Plant (STP) to ensure compliance with environmental norms. This includes ensuring adherence to legal and statutory requirements set by bodies such as GPCB, CPCB, DISH, and other applicable authorities. Your role will involve leading internal and external Environment, Health, and Safety (EHS) audits and ensuring timely closure of any identified non-conformities. You will be required to implement EHS programs and Standard Operating Procedures (SOPs) across the site, as well as managing hazardous waste handling, storage, and disposal in accordance with regulatory standards....

As an Assistant Manager Video Surveillance at Technomine, you will be responsible for managing our surveillance operations team consisting of over 50 personnel. Your role will involve hands-on expertise in CCTV monitoring, incident report handling, and a deep understanding of GSOC/RSOC operations while leading a high-performing team supporting international clients across multiple time zones. You will oversee 24/7 video surveillance operations, ensuring real-time monitoring, accurate reporting, and compliance with SLAs across all shifts. Managing and escalating critical incidents, preparing detailed incident reports and daily summaries, and ensuring GSOC/RSOC protocols are consistently follo...

You are a motivated and detail-oriented individual looking to kickstart your career in digital marketing operations. As a Digital Marketing Operations Intern at our dynamic marketing team in Sector 48, Gurgaon, you will have the opportunity to gain hands-on experience, collaborate with cross-functional teams, and enhance your analytical and organizational skills over a 6-month period. This internship is an excellent chance to support marketing campaigns, vendor onboarding, and interdepartmental coordination. Your key responsibilities will include executing and monitoring digital marketing campaigns across various channels such as social media, email, and paid media. You will collaborate with...

Dr. Reddys is looking for Manufacturing Scientists or senior scientists specialized in cell therapy (CAR-T) programs to join their Manufacturing facility team. As a Manufacturing Scientist, you will collaborate with Research and Product Development teams to support GMP Manufacturing operations, Technology transfer, quality assessments, and process validation of the CAR-T process for various Cell therapy programs. Your responsibilities will include designing and executing experiments to develop robust manufacturing processes for cell therapy products, leading and training a team of cell process scientists/engineers, managing T-cell culture and differentiation, documenting experimental procedu...

You will play a crucial role in maintaining and tracking inventory for IT and non-IT assets at Licious, a Bengaluru based meat and seafood company. Your responsibilities will include organizing, tagging, and updating asset records, conducting periodic audits for compliance and accuracy, and analyzing data to identify trends in asset utilization. Additionally, you will be expected to generate reports on asset performance and lifecycle, support asset procurement, maintenance, and disposal, as well as optimize and streamline asset management processes. Creating and refining Standard Operating Procedures (SOPs) for asset management and maintaining detailed records of all asset transactions will ...

You will be responsible for preparing and reviewing validation documents such as Area Qualification for new facilities, Factory Acceptance Test (FAT), Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ), Control System Qualification, commissioning, validation & re-qualification, and Revision Qualification for equipment/utilities/facilities. You will generate reports that summarize results, specifications, and acceptance criteria. Your role will also involve authoring documents in ValGenesis. In addition, you will track SOPs due for review, circulate them for comments, update comments, initiate change control, initiate ERA workflow, and follow up fo...

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...

As a Data and Process Manager joining our client's team, you will play a crucial role in data management, process optimization, and analytics. Your proficiency in Excel, Google Sheets, and data analytics tools will be essential, and experience with Zoho platforms will be preferred. Your responsibilities will include managing data workflows, ensuring data integrity, and driving process improvements to align with business objectives. In the realm of data management, you will be tasked with collecting, organizing, and maintaining accurate datasets across various platforms. It will be crucial to ensure data integrity, consistency, and security while developing dashboards, reports, and visualizat...

The job involves carrying out the complete maintenance of all instruments such as HPLC, pH meter, weighing balances, etc. It includes method development for non-pharmacopoeial and pharmacopoeial analysis of raw materials, formulations of pharmaceutical, ayurvedic, and food products. Regular analysis of raw materials, finished products, and intermediates of JP, JSRF, JIPL, and outsourced products is also part of the job description. Additionally, the analysis of stability samples of JP products, JSRF products, and outsourced products is required. The responsibilities also include maintaining spares required for the HVAC system and utility equipment, as well as carrying out validation and cali...

- Develop & implement Environmental, Health, and Safety policies, programs, & procedures to ensure compliance with local, state, and federal regulations. - Conduct regular inspections and audits to identify potential hazards & non-compliance issues. Required Candidate profile - 10+ years of experience as an EHS Manager or in a similar role. - In-depth knowledge of local, state, and federal EHS regulations and requirements.

We are seeking an experienced Clinical Research Scientist to join our clinical research team and contribute to existing and upcoming projects and trials. As a Clinical Research Associate/Scientist, you will play a crucial role in the timely execution of clinical projects by engaging with investigators, planning and setting up new studies, ensuring regulatory compliance, managing vendors, and overseeing the implementation and execution of clinical trials. Your responsibilities will include scoping upcoming projects in areas such as Oncology, Reproductive health, metabolic disorders, and neurodegenerative diseases, planning and setting up new clinical studies, conducting quality control checks...

You are an experienced and organized Retail Operations Manager with a background in the jewellery industry. Your main responsibility is to oversee day-to-day store operations in a luxury jewelry store, ensuring exceptional customer experiences. Your role requires strong leadership, multitasking abilities, and a customer-focused approach to support business goals. Your key responsibilities include overseeing inventory processes such as stock monitoring, audits, and replenishments to maintain accuracy and prevent discrepancies. You will need to develop, implement, and enforce Standard Operating Procedures (SOPs) to streamline retail operations. Additionally, you will create and manage staff sc...

The role in Pharma Solution's Quality Control department based in Lexington requires you to perform complex testing of raw materials, in-process and finished products while ensuring the calibration and maintenance of analytical instruments in compliance with cGMP standards. This night shift position directly reports to the AQC Group Lead. Your key responsibilities will include conducting routine/non-routine testing using wet chemistry and instrumental analysis methods, testing various samples such as raw materials, APIs, finished products, stability samples, and cleaning verification samples. Proficiency in HPLC/GC analysis is essential along with documenting laboratory work following GDP, c...

The ideal candidate will be responsible for creating and releasing 2D and 3D designs for engine parts and subsystems. This includes engineering releases for new or modified parts and managing Add-Del processes. You will be tasked with designing and detailing engine components and sub-assemblies using NX environment and managing part design in PLM software. Additionally, you will be involved in concept layout preparation, part level design, and detailing for new products, cost reduction, and product improvement initiatives. Furthermore, you will be responsible for developing Design Verification Plans (DVP), Design for Excellence (DFx), Design Failure Mode and Effects Analysis (DFMEA), and Sta...

As a Quality Controller, you will be responsible for ensuring the quality standards of garment production, with a focus on shirts. Your role will involve a deep understanding of garment construction, fabric properties, and quality standards in stitching, finishing, and overall appearance. You should have proficiency in quality control techniques, including knowledge of AQL standards, defect identification, root cause analysis, and corrective actions. Setting quality standards for the factory based on buyer requirements and providing guidance to departments and processes will be a key aspect of your responsibilities. It will be crucial for you to establish Standard Operating Procedures (SOPs)...

You will be responsible for creating and writing trial protocols and presenting them to the steering committee. You will identify, evaluate, and establish trial sites, as well as close them down upon completion of the trial. Training site staff on therapeutic areas, protocol requirements, proper source documentation, and case report form completion will also be a key part of your role. Your duties will include liaising with the ethics committee to ensure the rights, safety, and well-being of trial subjects. You will be in charge of ordering, tracking, and managing investigational product (IP) and trial materials. Additionally, you will oversee and document IP dispensing inventory and reconci...

As a Scientist C in the GCMSMS & LCMSMS section at our laboratory located in Gurugram, Haryana, you will be responsible for creating a conducive working environment and ensuring harmonious inter-laboratory working conditions. Your primary duties will include working in compliance with ISO17025 documentation, conducting environment monitoring of Food & chemical laboratories, maintaining log books, and standardizing titrimetric solutions. You will play a crucial role in facing technical audits conducted by regulatory bodies such as NABL, BIS, APEDA, AGMARK, FSSAI, MOEF, EIC, and CPCB, as well as customers. Your responsibilities will also involve calibration, uncertainty calculation, preparing ...

As a Drug Safety Specialist specializing in Safety Surveillance and Risk Management at Biocon Biologics, you will play a crucial role in ensuring the safety of our products by managing safety signal activities, developing risk management plans, overseeing aggregate report preparation and submission, responding to safety inquiries, and supporting clinical trial pharmacovigilance activities. You will be a key leader in monitoring safety compliance, influencing stakeholders, and serving as a subject matter expert on global safety regulations and guidelines. Your responsibilities will include supporting the signal management process, evaluating safety data, preparing Risk Management Plans, respo...

You will be the overall in charge of Plant Accounts activities, which include handling GST matters and liaising with GST authorities for ongoing assessments. You will be responsible for appearing till the level of CIT and Audit Wing Officers. You will guide the team on Ind AS and ensure proper presentation in Financials. Your role will involve reviewing Advance Tax working, assets, and Costing areas. Working on bringing budgetary controls in Plant Operations will also be a part of your responsibilities. You will coordinate with the IT team to bring controls in SAP, including Park and Post segregation for a few T-codes. Additionally, you will review monthly data on P&L, Overhead analysis, and...

Purpose of Position To carry out the Microbiological sampling and analysis of water, food and environmental samples as per the relevant national & international standards / method validations / SOPs and lab accreditation scope. The position performs in line with the Bureau Veritas Quality Assurance System, including the BV Code of Ethics, the BV Group policy, NABL, BIS, and EIC and other applicable guidelines. Major Responsibilities Perform the microbiological sampling and sample collection across the India. To carry out the microbiological analysis after getting trained. To carry out the assigned day to day tasks such as sampling and analysis as per the work plan To assist the microbiologis...

You will be joining R1, a leading provider of technology-driven solutions that assist hospitals and health systems in managing their financial systems and enhancing the patient experience. At R1, we combine the expertise of a global workforce of revenue cycle professionals with cutting-edge technology, including advanced analytics, AI, intelligent automation, and workflow orchestration. We foster a culture of bold thinking, innovation, and growth, where transparency and inclusion are key values. As part of our global community, you will collaborate with engineers, front-line associates, healthcare operators, and RCM experts to exceed expectations and serve our clients effectively. R1 India t...