611 Sops Jobs - Page 7

As a Quality Analyst Supervisor, your main responsibility will be to lead and guide the Quality Analysts team in order to ensure precise call monitoring and provide constructive feedback. You will be required to conduct regular assessments of both inbound and outbound calls, chat interactions, and email communications to evaluate the performance of agents. By identifying areas of improvement in communication, compliance, and process adherence, you will be expected to communicate actionable insights to the operations team. Developing and implementing quality frameworks, standard operating procedures (SOPs), and best practices will also be a crucial part of your role. Additionally, you will ne...

As a Smart Building Solutions Architect, your primary responsibility will be to design and architect smart building solutions tailored to meet the specific needs of our customers and site requirements. You will actively engage with end-users, consultants, and contractors throughout the pre-sales, tendering, and execution phases to ensure the successful implementation of these solutions. Your role will also involve developing detailed system designs, Bills of Quantities (BOQs), Standard Operating Procedures (SOPs), architecture diagrams, and technical documentation to support project execution. You will be expected to lead technical discussions, workshops, and presentations with key accounts ...

As a Senior Manager in the Engineering and Projects department at Sun Pharmaceutical Industries Ltd, located in Dewas SGO - Engineering Block P, your role as the Engineering Penem Head involves overseeing various engineering and maintenance activities. With over 15 years of experience and a B.E. in Electronics, you will be responsible for managing activities related to Block P (Sterile), Block F (OSD), Supporting Facilities (Micro/Stability, QC, Warehouse, and Export Warehouse), as well as the external area. Your responsibilities include maintaining and managing the expenses within the budget, reviewing and implementing preventive maintenance, facility maintenance, and calibration systems ef...

The Quality Assurance professional plays a crucial role in ensuring compliance with regulatory standards, Good Manufacturing Practices (GMP), and company policies to uphold the highest quality of pharmaceutical products. Your responsibilities will include documentation, audits, validations, and continuous enhancement of quality systems. You will be responsible for various tasks such as the issuance, archival, and retrieval of documents, providing control copies to the respective departments, and ensuring the destruction of GMP documents once the retention term has expired. Tracking all QA documents, maintaining backups of QA soft copies, and proper indexing of SOPs will also be part of your ...

The Full Stack Developer position at ClinRT Global Services in Pune requires a minimum of 2 years of experience in Angular and .NET core. ClinRT is committed to revolutionizing clinical trials through its Interactive Response Technology (IRT) platform, aimed at enhancing efficiency, accuracy, and compliance in drug development. As a trusted partner to pharmaceutical companies, researchers, and healthcare professionals, ClinRT streamlines patient interaction, randomization, drug supply management, and data management for a seamless clinical trial process. The Clinical QA Manager role involves overseeing the quality of activities related to the IRT platform used in clinical trials developed by...

You are invited to apply for the position of Quality Assurance Coordinator at Pallium India in Thiruvananthapuram. As the Quality Assurance Coordinator, you will utilize your academic knowledge to comprehend the various facets of service delivery and apply quality indicators to enhance outcomes. Your responsibilities will include managing and updating Excel sheets, conducting detailed data analysis, creating pivot tables, using advanced formulas, and designing data visualizations to identify trends and monitor service outcomes. Furthermore, you will assist in developing and implementing new Standard Operating Procedures (SOPs) to enhance service delivery. It will be your duty to ensure the e...

As a Senior Manager in R&D Quality (Pharmacovigilance Quality Assurance) at Sun Pharmaceutical Industries Ltd in Gurgaon, your primary responsibility will be to implement a well-defined Quality Assurance program in compliance with regional and global regulatory requirements, SOPs, and company policies. You will play a key role in developing and executing global Pharmacovigilance auditing programs, ensuring adherence to established Quality Systems. Your duties will include conducting audits at Sun Pharma sites associated with Pharmacovigilance activities, as well as auditing outsourced parties, affiliates, and partners involved in Pharmacovigilance operations. You will manage the Internal Aud...

You will be responsible for participating and adhering to all EHS continual improvement initiatives and line responsibilities such as emergency mock drill participation, training, permit to work, etc. It is crucial to follow all site safety requirements and demonstrate positive behavior in the safety culture transformation. You must adhere to the permit to work procedure during shop-floor activities and utilize the required Personnel Protective equipment (PPE) when performing operations. Identifying unsafe conditions or acts and promptly reporting them to the Manager/EHS team is essential, as well as reporting safety-related incidents, accidents, or illnesses to the OHC/Superiors/Manager imm...

As an Optometrist at Specsmakers, you will be an integral part of our team that is dedicated to providing stylish and high-quality eyewear at affordable prices. With over 250 retail locations across various cities, including Chennai, Bengaluru, Hyderabad, and more, Specsmakers is focused on reinventing the eyewear shopping experience to make it fun and enjoyable for our customers. Your role as an Optometrist at Specsmakers goes beyond just conducting eye check-ups; it also involves actively engaging in sales to ensure a superior customer experience. You will be responsible for performing accurate eye check-ups, offering vision correction solutions, assisting customers in choosing the right e...

Line of Service Advisory Industry/Sector GPS X-Sector Specialism Operations Management Level Senior Associate Job Description & Summary At PwC, our people in software and product innovation focus on developing cutting-edge software solutions and driving product innovation to meet the evolving needs of clients. These individuals combine technical experience with creative thinking to deliver innovative software products and solutions. In business analysis at PwC, you will focus on analysing and interpreting data to provide strategic insights and recommendations for improving business performance. Your work will involve strong analytical skills and the ability to effectively communicate finding...

Job Title - Executive Quality Assurance Department : Corporate QA Job Location - Kandivali - West, Mumbai Qualification : B Pharm / M Pharm Experience : 5 - 8 years Roles & Reponsibilities: Issuance of activity record such as calibration record sheets, log books and lab note books etc. Issuance and retrieval of SOPs applicable for AMV laboratory. Review and approval of QMS documents such as laboratory deviations, incidents, CAPA etc. Review and approval of SOPs applicable for AMV laboratory. Responsible for QA oversight on operations of AMV laboratory. On-line review of data entries (paper and electronic) as a part of a Data Reliability Review. Review and approval of Analytical method develo...

JOB DESCRIPTION: Primary Job Function: To lead and manage all regulatory affairs activities at the manufacturing site located at Mumbai and LL locations, ensuring timely regulatory submissions, compliance with regulations, and providing strategic support to institutional and international business operations. The role is critical to maintaining business continuity and regulatory compliance. Core Job Responsibilities: Regulatory Submissions and compliance Prepare and submit various applications such as additional product permission, Layout approval, facility modification approval, technical person approval, Test license, amendments in licenses, State GMP and GLP certificate applications, post...

As an Optometrist/Senior Optometrist at our client's location, you will play a crucial role in providing technical expertise through eye-checks, dispensing, and diagnosis, as well as delivering exceptional customer experiences. Your responsibilities will involve conducting eye check-ups, selling products, executing stock takes, and following standard operating procedures. Our client, India's fastest growing eyewear company, is dedicated to improving vision across the country. With a range of products including prescription eyewear, branded contact lenses, and sunglasses tailored to customers" eye powers, our client is supported by IDG Ventures, Unilazer Ventures, and TPG Capital. In this rol...

Job Description This role is responsible for achieving the collections target in the assigned area while ensuring that SOPs and legal norms are followed as per process and organizational policy Core Responsibilities: o Ensure to manage assigned portfolio to achieve expected resolution o Ensure trail/feedback needs to be update in system and report to respective stakeholders o Ensure NPA reversals and Write off recoveries should be resolve through personal visits o Ensure timely initiation and execution of legal tool: Warrants execution under Section -138/ Section -25, Timely execution Sarfaesi. o Ensure coordination with Legal team/Lawyers for timely filing of Sec 14 and obtaining DM orders ...

You should have 2-3 years of experience in a computer-related support or IT operational environment. A recognized third-level qualification in a computer-related discipline is required. Possess one or more recognized industry certifications in PC, Network, and Server support such as CompTIA A+, Server +, Network +, MCP in Windows 7/8/10. Good written and communication skills in English are essential. Experience with documentation and improving SOPs and other process documents is necessary. Customer focus and excellent timekeeping are key requirements for this role. You should have good interpersonal skills, with a focus on listening and questioning abilities. Strong problem-solving skills an...

You will be responsible for overseeing all daily store operations including sales, team management, stock handling, and billing. Your primary focus will be to drive sales targets and ensure profitability for the store. You will play a key role in training, mentoring, and managing the sales team members to deliver exceptional customer service. Handling escalations when necessary and maintaining top-notch customer service will be crucial aspects of your role. In addition, you will be required to plan and execute visual merchandising and in-store promotions to attract customers. Maintaining proper inventory levels, coordinating stock replenishment, and monitoring sales performance, customer fee...

The Quality Assurance (QA) Documentation Executive is responsible for managing and updating all quality-related documents, records, and compliance materials in alignment with industry standards and regulatory requirements. This role is crucial in supporting audits, implementing quality procedures, and promoting a compliance-driven culture. The QA Documentation Executive's primary duties include managing, reviewing, and updating QA documents, Standard Operating Procedures (SOPs), batch records, and test reports. They must ensure adherence to ISO, GMP, FDA, and other chemical industry regulations, as well as organize and maintain documentation for internal and external audits. Additionally, th...

As the QA QC Manager in the Printing Industry, you will be responsible for leading a team of 10-12 QC Executives. Your primary duties will include conducting timely and accurate quality inspections and maintaining records of incoming raw materials and semi-finished materials. You will also be in charge of checking job cards, ensuring in-process QC inspections are done as per standard frequency, and conducting final quality inspections before dispatch. Your role will involve minimizing quality complaints from clients by implementing effective quality control measures. You will be required to provide training to QC Executives and operators to enhance quality, reduce errors, and minimize wastag...

You will be working as an Operator in Nasal Spray Manufacturing, Filling & Packaging at our regulated Pharma Manufacturing Plant located in Indore. Your primary responsibility will be to perform routine operations related to nasal spray filling and packaging while ensuring compliance with cGMP, safety standards, and regulatory requirements within a sterile/cleanroom environment. Your key responsibilities will include: - Operating and assisting in activities such as sterile filtration setup, filling machine setup, bottle positioning, crimping, and sealing of nasal containers. - Conducting in-process checks for fill volume, crimp integrity, and visual inspection. - Maintaining cleanroom discip...

The Maintenance Associate position aims to support the Cinema Manager/Maintenance Engineer in overseeing Cinema Operations by executing standard operating procedures, operating and maintaining maintenance and projection equipment, ensuring electricity saving, controlling breakdowns and repair costs, and maintaining a clean and efficient working environment for all equipment. Responsibilities include operating projection equipment, sound systems, movie and KDM ingesting, Xenon lamp changing, and supporting the operations team for seamless cinema functioning. In terms of functional areas and general responsibilities, the Maintenance Associate must focus on customer satisfaction by maintaining ...

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 team member at Biocon Biologics Limited, a subsidiary of Biocon Limited, you will be part of a fully integrated global biosimilars organization dedicated to leveraging cutting-edge science and innovative tech platforms to enhance healthcare outcomes. With a strong research pipeline focusing on biosimilar molecules for diabetes, oncology, immunology, and other non-communicable diseases, we are committed to making treatment more accessible and affordable for patients worldwide. Your responsibilities will include performing line clearance for various manufacturing activities such as formulation, washing, filling, sealing, and others in designated areas. You will also be responsible for rev...

As a candidate for this role, you will be responsible for handling various Quality Management System (QMS) activities such as managing Corrective and Preventive Actions (CCF), deviations, and Out of Specification (OOS) incidents. Your duties will include preparing and reviewing Standard Operating Procedures (SOPs), Equipment Operating Procedures (EOPs), Operating Control Plans (OCPs), Batch Manufacturing Records (BMR), and other production-related documents. Additionally, you will be required to review batch reports, participate in productivity improvement initiatives, and investigate batch failures. You will also be responsible for creating and maintaining the Asset Integrity Management (AI...

You will be hired as a Scientist specializing in Strain Engineering for a client in the biotechnology sector. Your primary responsibilities will include working with various laboratory strains such as yeast, Escherichia coli, and fungi using aseptic techniques, conducting advanced molecular biology techniques like recombinant cloning and genome editing, and engineering microbial genomes to enhance phenotypes and facilitate the production of recombinant molecules. Additionally, you will be expected to perform fermentation studies for recombinant strains, design novel gene constructs, analyze metabolic fluxes, and execute experiments following established SOPs. You will be required to deliver ...

Client Details is a leading audit firm in India, offering a wide range of compliance services to businesses of all sizes. With their expertise and commitment to excellence, they help clients navigate the complex regulatory landscape and achieve their financial goals. The team of professionals is dedicated to providing personalized solutions and delivering exceptional value to clients. We are looking for a committed and detail-oriented Accounts & Compliance Executive to assist with day-to-day accounting, auditing, and regulatory compliance activities. The candidate will support bookkeeping, financial reporting, statutory filings, audits, and ensure adherence to applicable laws and standards. ...