21 Documentation Practices Jobs

You will be responsible for downstream operations related to recombinant proteins at PU 3 for Sanzyme Biologics, Karakapatla unit. This includes handling tasks such as TFF for micro and ultra filtration systems, continuous centrifuge operation, chromatography systems management with audit trailing, column packing and unpacking for high-scale BPG columns, buffer preparations, sterilization of process materials, and working in shifts as required. In addition, you should be well-versed in clean room procedures, integrity testing, documentation practices, SOPs, and hierarchy within the organization. A suitable candidate for this position should hold a B.Tech or M. Sc in Biotechnology, Biochemistry, or Microbiology, along with 2-3 years of relevant experience in downstream operations for recombinant proteins. If you meet these qualifications and are interested in this opportunity, please share your CV to the provided email address. Thank you.,

As a Procurement Manager, you will be responsible for formulating and implementing long-term procurement strategies aligned with organizational goals. You will identify, evaluate, and maintain strong relationships with key vendors and suppliers to ensure timely and cost-effective procurement of materials and services across all projects. Your role will involve driving supplier performance improvements through regular audits and performance reviews, as well as developing, monitoring, and controlling annual procurement budgets for cost optimization. Collaboration is key in this role, as you will need to coordinate closely with project, finance, and site teams to align procurement with execution timelines. Additionally, you will oversee and mentor the procurement team to ensure efficiency, compliance, and accountability. Your responsibilities will also include optimizing inventory levels and material planning to avoid shortages or excess stock while ensuring all procurement processes and contracts comply with legal and organizational standards. In this position, maintaining accurate documentation of all procurement transactions, contracts, and vendor data is crucial. You will be expected to identify and mitigate procurement-related risks such as price fluctuations and supply delays, and generate regular reports on procurement KPIs, budget usage, inventory levels, and vendor performance. Your strategic inputs for process improvements and cost-saving initiatives will be valued, and you may need to travel to vendor locations and project sites for inspections and negotiations. The ideal candidate for this role will have proficient knowledge of procurement processes in the real estate/construction industry, strong negotiation and communication skills, and the ability to multitask and coordinate with multiple teams. Proficiency in Highrise Kanixx, attention to detail, good documentation practices, and a willingness to travel as required are also desired qualities for this position.,

As a Production Executive located in Vasai (Giriraj), your primary responsibility will be to oversee and execute daily production operations of cosmetic products and personal care items. In this role, you will be required to manage shop floor activities while ensuring compliance with Good Manufacturing Practices (GMP), quality standards, safety regulations, and batch documentation protocols. Your key responsibilities will include executing production activities according to the daily production plan and Batch Manufacturing Records (BMR). You will be supervising manufacturing and filling processes for cosmetic formulations such as creams, lotions, serums, scrubs, and makeup products. It will be crucial for you to ensure GMP compliance, maintain hygiene standards, and follow standard operating procedures (SOPs) on the shop floor. In addition, you will need to coordinate with QA/QC, warehouse, and maintenance teams to facilitate smooth production flow. Maintaining accurate records for batch processing, cleaning logs, machine usage, and in-process checks will also be part of your duties. You will oversee the proper cleaning, sanitization, and changeover of equipment and production areas, as well as ensure the availability of raw materials, packaging materials, and consumables for uninterrupted production. Identifying process gaps and supporting initiatives for productivity and quality improvement will be essential. Efficient manpower planning, shift management, and adherence to company policies related to safety, quality, and housekeeping are integral aspects of this role. Your participation in audits (both internal and external) and assistance in implementing corrective actions will contribute to the overall success of the production operations. To qualify for this position, you should hold a Bachelor's degree in Pharmacy, Cosmetics Technology, or a relevant Manufacturing discipline. A minimum of 2 years of experience in cosmetics or personal care product manufacturing, specifically in creams, lotions, gels, powders, or makeup products, is required. Additionally, you must possess knowledge of cosmetic GMP, SOPs, and production processes, along with familiarity with mixers, filling lines, labeling machines, etc. Strong coordination and communication skills, the ability to manage shift operations and production staff, attention to detail, and proficiency in documentation practices are essential for this role. Basic computer skills, including proficiency in Excel and Word, will also be advantageous. If you meet the requirements and are interested in this opportunity, please send your CV for consideration. This is a full-time, permanent position with benefits including health insurance and Provident Fund. The work schedule is during the day shift, and additional bonuses may be provided based on performance. The work location is in person.,

As an employee at our organization, you will be part of a global mission to improve access to affordable healthcare and promote healthier lives for millions of people worldwide. Our company operates in nearly 60 countries and embraces a diverse workforce representing various nationalities and backgrounds. We take pride in being the world's leading manufacturer of generic medicines, with many of our products listed on the World Health Organization's Essential Medicines List. Every day, over 200 million individuals rely on our medications, driving us to constantly seek new ways to make a positive impact and welcome new team members to join us in this endeavor. Your daily responsibilities will involve analyzing samples from the Formulation department, including in-process, finished product, pre-formulation study samples, and stability samples. You will conduct analytical method development for API, in-process samples, and finished products, as well as manage methods for cleaning studies and method transfer activities. Additionally, you will be responsible for calibrating and maintaining analytical instruments, ensuring compliance with good laboratory practices, documentation standards, and quality systems. Upholding safety protocols and environmental health and safety (EHS) regulations during all operations is crucial. Any other tasks assigned by your line manager and troubleshooting analytical instruments for operational challenges will also be part of your role. To excel in this position, you should hold a PhD with at least 1 year of experience or a Master's degree in Pharmaceutical Sciences/MSc with 3 to 5 years of relevant experience. Our company is committed to equal employment opportunities for all candidates.,

ApoPharma, a member of the Apotex group of companies, is a pharmaceutical company devoted to the discovery, development and provision of new medicines to help improve the quality of life of patients with debilitating and life-threatening diseases. Investigation into the pathological role of iron in human disease, and how to use novel medicines to treat conditions created or worsened by iron, is a major research focus of ApoPharma. Job Summary A role-holder to handle/supervise the manufacturing activities and to ensure the on-time production and delivery of product with quality compliance and cost improvisation. Job Responsibilities Works in a safe manner collaborating as a team member to achieve all outcomes. Demonstrate Behaviours that exhibit our organizational Values: Collaboration, Courage, Perseverance, and Passion. Ensure personal adherence with all compliance programs including the Global Business Ethics and Compliance Program, Global Quality policies and procedures, Safety and Environment policies, and HR policies. All other relevant duties as assigned To be well disciplined & maintain the same in the production department. To maintain the safety and housekeeping practices at work place. To ensure and follow good and online documentation practices. To ensure proper labeling procedure wherever applicable as per procedure. To ensure that cleaning the area as per related SOP s are conducted and maintained as per proper cleanliness. To ensure the Calibration/Preventive maintenance of the equipment as per the schedule. To maintain and ensure cleaning and operation activities are performed as per procedure. To maintain the batch as per instruction given in batch document / procedure. To ensure material movement is conducted as per procedure. To ensure training of our self on current version of procedure prior to perform activity. To perform the activities assigned to him by the concerned section seniors or by his superiors in area. To follow the cGMP practices. To showcase the value of collobaration with own/other departments to complete the work assigned. To escalate immediately to concerned superior / manager for any deviation / non-compliance /abnormal observation. Shall always be ready to accept new challenges & multifunctional activities. Shall always stick to the time line provided or assignment given by superiors, to avoid any delays and any non-compliance. Works as a member of a team to achieve all outcomes. Performs all work in accordance with all established regulatory and compliance and safety requirements. To plan the production activities as per the weekly plan on daily basis & deliver the same to down level for its execution. To supervise the production process to produce quality formulation at optimum cost and within the time limit. To plan for various activities of the process and get it done within the specified time. Also maintain the online documentation related to production activities . To allocate the Job responsibilities for operators, housekeeping & contract labours in production area. To train the concern members on the related SOPs , newly updated SOPs , cGMP & documentation practices. To supervise the process validation & cleaning validation activities as per protocol in co-ordination with QA/QC. Create a culture which values trust and provides the opportunity for Employee development and growth in pursuit of our purpose and demonstrating our core Values Collaboration, Courage, Perseverance and Passion. All other duties as assigned. Job Requirements Education Pharmacy / M Pharmacy Knowledge, Skills and Abilities Adequate knowledge and ability in handling /supervising the manufacturing activities In depth knowledge of cGMP practices Identify and escalate equipment related issues. Experience 3 to 5 Years At ApoPharma, we are committed to fostering an inclusive, accessible work environment, where all employees feel valued, respected and supported. ApoPharma offers accommodation for applicants with disabilities as part of its recruitment process. If you are contacted to arrange for an interview or testing, please advise us if you require an accommodation. Show more Show less

ApoPharma, a member of the Apotex group of companies, is a pharmaceutical company devoted to the discovery, development and provision of new medicines to help improve the quality of life of patients with debilitating and life-threatening diseases. Investigation into the pathological role of iron in human disease, and how to use novel medicines to treat conditions created or worsened by iron, is a major research focus of ApoPharma. Job Summary A role-holder to handle/supervise the manufacturing activities and to ensure the on-time production and delivery of product with quality compliance and cost improvisation. Job Responsibilities Works in a safe manner collaborating as a team member to achieve all outcomes. Demonstrate Behaviours that exhibit our organizational Values: Collaboration, Courage, Perseverance, and Passion. Ensure personal adherence with all compliance programs including the Global Business Ethics and Compliance Program, Global Quality policies and procedures, Safety and Environment policies, and HR policies. All other relevant duties as assigned To be well disciplined & maintain the same in the production department. To maintain the safety and housekeeping practices at work place. To ensure and follow good and online documentation practices. To ensure proper labeling procedure wherever applicable as per procedure. To ensure that cleaning the area as per related SOP s are conducted and maintained as per proper cleanliness. To ensure the Calibration/Preventive maintenance of the equipment as per the schedule. To maintain and ensure cleaning and operation activities are performed as per procedure. To maintain the batch as per instruction given in batch document / procedure. To ensure material movement is conducted as per procedure. To ensure training of our self on current version of procedure prior to perform activity. To perform the activities assigned to him by the concerned section seniors or by his superiors in area. To follow the cGMP practices. To showcase the value of collobaration with own/other departments to complete the work assigned. To escalate immediately to concerned superior / manager for any deviation / non-compliance /abnormal observation. Shall always be ready to accept new challenges & multifunctional activities. Shall always stick to the time line provided or assignment given by superiors, to avoid any delays and any non-compliance. Works as a member of a team to achieve all outcomes. Performs all work in accordance with all established regulatory and compliance and safety requirements. To plan the production activities as per the weekly plan on daily basis & deliver the same to down level for its execution. To supervise the production process to produce quality formulation at optimum cost and within the time limit. To plan for various activities of the process and get it done within the specified time. Also maintain the online documentation related to production activities . To allocate the Job responsibilities for operators, housekeeping & contract labours in production area. To train the concern members on the related SOPs , newly updated SOPs , cGMP & documentation practices. To supervise the process validation & cleaning validation activities as per protocol in co-ordination with QA/QC. Create a culture which values trust and provides the opportunity for Employee development and growth in pursuit of our purpose and demonstrating our core Values Collaboration, Courage, Perseverance and Passion. All other duties as assigned. Job Requirements Education Pharmacy / M Pharmacy Knowledge, Skills and Abilities Adequate knowledge and ability in handling /supervising the manufacturing activities In depth knowledge of cGMP practices Identify and escalate equipment related issues. Experience 3 to 5 Years At ApoPharma, we are committed to fostering an inclusive, accessible work environment, where all employees feel valued, respected and supported. ApoPharma offers accommodation for applicants with disabilities as part of its recruitment process. If you are contacted to arrange for an interview or testing, please advise us if you require an accommodation. Show more Show less

As a Sr. Executive / Asst Manager (Shift Incharge) in the Production Fermentation (Upstream) department at Natural Biogenex Pvt. Ltd., you will play a crucial role in overseeing and leading shift-wise operations effectively. With 6 to 10 years of experience and a background in M.Sc. / B.Tech. / B.Sc. in Biotechnology, Microbiology, or Industrial Microbiology, you will be responsible for ensuring the smooth functioning of fermentation processes in compliance with SOPs and production schedules. Your key responsibilities will include supervising and monitoring shift activities, ensuring operational efficiency, timely escalation of issues, maintaining documentation as per GMP standards, managing shift planning and manpower allocation, promoting a culture of safety-first practices, and assisting in data analysis for process improvement. Your strong technical knowledge of fermentation processes, effective team leadership skills, and sound decision-making abilities will be essential in driving optimal plant efficiency and adherence to regulatory standards. At Natural Biogenex Pvt. Ltd., you will have the opportunity to work in a modern biotech production environment, with structured career growth plans, exposure to advanced fermentation technologies, and a professional and inclusive work culture. Joining our team will allow you to be a part of a leading API manufacturing company with cutting-edge technology, global regulatory standards, and opportunities for professional development and competitive compensation.,

The ideal candidate for this position will have a mission to make good health more affordable and accessible, helping millions around the world enjoy healthier lives. Working with the leading manufacturer of generic medicines, you will be a part of a team that produces products listed on the World Health Organizations Essential Medicines List. With at least 200 million people worldwide taking our medicines daily, we are continuously striving to make a positive impact and are looking for individuals to join us in this mission. Your responsibilities will include conducting Microbiological testing on various products, such as in-process, finished products, pre-formulation study samples, and stability samples. You will review analytical results, develop and validate Microbial methods, and manage laboratory resources efficiently. In addition, you will be responsible for calibration and maintenance of analytical instruments, ensuring compliance with regulatory requirements, and maintaining safe practices in the work environment. To be successful in this role, you should have an M.Sc. in Microbiology or Biotechnology, with at least 6 to 10 years of experience in a pharmaceutical company. You should possess FDA approval in Microbiology, be familiar with regulated markets (US/EU/Canada), and have a strong understanding of Microbiology, Microbial analysis, and method validation. Proficiency in basic computer skills (MS Excel, Word) is required. If you are a dedicated Microbiologist with a passion for making a difference in the healthcare industry, we encourage you to apply for this position and be a part of our team dedicated to improving global health outcomes.,

Job Description Summary Responsible for test creation, testing a large module or a large component and designing a feature, set of features, or whole feature area independently, Contributing to the immediate team and to other teams across business; Leading software quality engineering discussions and mentoring of other junior quality engineers. Job Description Roles and Responsibilities In This Role, You Will Apply principles of SDLC and methodologies like Lean/Agile/XP, CI, Software and Product Security, Scalability, Documentation Practices, refactoring and Testing Techniques. Integrate project testing with continuous-integration process. Lead and manage team members to diagnose bugs and formulate solutions. Provide expertise in the quality engineering, test planning and testing methodology for a software project and keeps abreast of evolving QA industry processes and standards. Develop and execute maintainable automation tests for acceptance, functional, and regression test cases. Master the basics of underlying transmission and distribution software applications domain. Education Qualification For Roles Outside USA Bachelor&aposs Degree in Computer Science or STEM Majors (Science, Technology, Engineering and Math) with advanced experience. For roles in USA: Bachelor&aposs Degree in Computer Science or STEM Majors (Science, Technology, Engineering and Math) with minimum years of experience6years Desired Characteristics Technical Expertise Bachelors Degree in Computer Science or in equivalent. A minimum of 10 to 12 years of Software Testing experience with Web or SaaS Platform based products, Postgress databases. Experience on building Test Automation Frameworks specifically in Java, Javascript / Type Script, Selenium. Experience testing web services (SOAP/REST) Experience testing hosted or SaaS-based solutions. Familiar with relational database design and good working knowledge of SQL for querying, updating, and deleting data. Strong proficiency with functional, regression, performance and stability testing techniques. Experience working in a cross-functional development team with the ability to influence quality of products in that environment. Demonstrates the initiative to explore alternate technology and approaches to solving problems. Skilled in breaking down problems, documenting problem statements and estimating efforts. Strong oral and written communication skills. Effective team building and problem-solving abilities. Business Acumen Understands the technology landscape, up to date on current technology trends and new technology, brings new ideas to the team. Displays understanding of the project&aposs value proposition for the customer. Shows commitment to deliver the best value proposition for the targeted customer. Learns organization vision statement and decision-making framework. Able to understand how team and personal goals/objectives contribute to the organization vision Leadership Voices opinions and presents clear rationale. Uses data or factual evidence to influence. Learns organization vision statement and decision-making framework. Able to understand how team and personal goals/objectives contribute to the organization vision. Seeks to understand problems thoroughly before implementing solutions. Gide the team with questions to clarify requirements when ambiguities are present. Identifies opportunities for innovation and offers new ideas. Takes the initiative to experiment with new software frameworks Adapts to new environments and changing requirements. Pivots quickly as needed. When coached, responds to need & seeks info from other sources. Note Note To comply with US immigration and other legal requirements, it is necessary to specify the minimum number of years' experience required for any role based within the USA. For roles outside of the USA, to ensure compliance with applicable legislation, the JDs should focus on the substantive level of experience required for the role and a minimum number of years should NOT be used. This Job Description is intended to provide a high level guide to the role. However, it is not intended to amend or otherwise restrict/expand the duties required from each individual employee as set out in their respective employment contract and/or as otherwise agreed between an employee and their manager. Additional Information Relocation Assistance Provided: Yes Show more Show less

Would being part of a digital transformation excite you Are you passionate about infrastructure security Join our digital transformation team. We operate at the heart of the digital transformation of our business. Our team is responsible for the cybersecurity, architecture, and data protection for our global organization. We advise on the design and validation of all systems, infrastructure, technologies, and data protection. Partner the best. As a Staff Infrastructure Architect, you will support the design and execution of our infrastructure security roadmap. Collaborating with global teams and customers, you will help architect solutions that enable our business to grow in an agile and secure manner. You will be responsible for supporting and improving our tools/process for continuous deployment management, supporting solution Infra Architect to deploy the application and infra to customer private/public cloud, debugging the Docker images/containers, Kubernetes clusters issues, building monitoring tools around Kubernetes/AKS clusters, and developing process tools to track the customer releases and create update plans. You will also be responsible for developing processes to ensure the patching/updates take place without affecting the operation SLA, meeting availability SLA working with Infra and application team responsible for 24x7, profiling deployment process and identifying bottlenecks, demonstrating expertise in writing scripts to automate tasks, implementing Continuous Integration/Deployment build principles, providing expertise in the quality engineering, test planning, and testing methodology for developed code/images/containers, and helping businesses develop an overall strategy for deploying code. To be successful in this role, you will need a Bachelor's education in Computer Science, IT, or Engineering, at least 4+ years of production experience providing hands-on technical expertise to design, deploy, secure, and optimize Cloud services, hands-on experience with containerization technologies (Docker, Kubernetes) is a must (minimum 2 years), experience with creating, maintaining, and deploying automated build tools for a minimum of 2 years, in-depth knowledge of Clustering, Load Balancing, High Availability, and Disaster Recovery, Auto Scaling, Infrastructure-as-a-code (IaaC) using Terraform/CloudFormation, good knowledge of Application & Infrastructure Monitoring Tools like Prometheus, Grafana, Kibana, New Relic, Nagios, hands-on experience of CI/CD tools like Jenkins, understanding of standard networking concepts such as DNS, DHCP, subnets, Server Load Balancing, Firewalls, knowledge of Web-based application development, strong knowledge of Unix/Linux and/or Windows operating systems, experience with common scripting languages (Bash, Perl, Python, Ruby), and the ability to assess code, build it, and run applications locally on his/her own. Additionally, you should have experience with creating and maintaining automated build tools, facilitating and coaching software engineering team sessions on requirements estimation and alternative approaches to team sizing and estimation, publishing guidance and documentation to promote adoption of design, proposing design solutions based on research and synthesis, creating general design principles that capture the vision and critical concerns for a program, and demonstrating mastery of the intricacies of interactions and dynamics in Agile teams. We recognize that everyone is different and that the way in which people want to work and deliver at their best is different for everyone too. In this role, we can offer flexible working patterns, including working remotely from home or any other work location and flexibility in your work schedule to help fit in around life. Talk to us about your desired flexible working options when you apply. Our people are at the heart of what we do at Baker Hughes. We know we are better when all of our people are developed, engaged, and able to bring their whole authentic selves to work. We invest in the health and well-being of our workforce, train and reward talent, and develop leaders at all levels to bring out the best in each other. About Us: We are an energy technology company that provides solutions to energy and industrial customers worldwide. Built on a century of experience and conducting business in over 120 countries, our innovative technologies and services are taking energy forward making it safer, cleaner, and more efficient for people and the planet. Join Us: Are you seeking an opportunity to make a real difference in a company that values innovation and progress Join us and become part of a team of people who will challenge and inspire you! Let's come together and take energy forward.,

As an R&D Intern at Teva Pharmaceuticals, you will be part of a team dedicated to making good health more affordable and accessible to help millions around the world enjoy healthier lives. With a presence in nearly 60 countries and a diverse mix of nationalities and backgrounds, you will work with the world's leading manufacturer of generic medicines and contribute to producing essential medicines listed by the World Health Organization. Every day, at least 200 million people worldwide benefit from our products, but we are constantly looking for new ways to make a difference and seeking new talents to join us in this mission. Your primary responsibilities will include analyzing samples received from the FRD department, which encompass in-process, finished products, pre-formulation study samples, and stability samples. You will also be tasked with developing analytical methods for APIs, in-process samples, and finished products, including methods for cleaning studies. Additionally, you will handle analytical method transfer activities, calibration, and maintenance of analytical instruments, ensuring adherence to good laboratory and documentation practices and existing quality systems. Safety protocols and EHS systems on-site will be strictly followed, and troubleshooting of analytical instruments for daily operational challenges will be part of your routine tasks. To qualify for this role, you should hold a Master's degree in pharmaceutical sciences, MSc, or M. Pharm with 0 to 1 year of relevant experience. Experience in regulated markets such as the US, EU, or Canada is preferred, along with expertise in routine analysis, chemistry, analytical method development, and instrumental methods of analysis. If you are passionate about contributing to the pharmaceutical industry's advancement, ensuring product quality, and promoting health worldwide, we invite you to apply now and be a part of our team at Teva Pharmaceuticals.,

You will be joining Qualcomm India Private Limited as a Sub-System Hardware Architect specializing in ASIC design for AI within the Engineering Group > Hardware Engineering. Your primary responsibility will be to define and lead the hardware architecture for ASIC components within the Turing subsystem, ensuring they meet performance, reliability, power, and scalability requirements. You should have proven experience in designing ASIC sub-system hardware components for AI applications, strong knowledge of ASIC design tools and methodologies, and excellent problem-solving skills. Your role will involve collaborating with cross-functional teams to define hardware requirements, developing and implementing ASIC hardware architecture strategies for AI, conducting power assessment, and writing detailed hardware specifications. To qualify for this role, you should have a Bachelor's or Master's degree in Electrical Engineering, Computer Engineering, or a related field, along with 8 to 12 years of experience in ASIC design and architecture. Additionally, you should possess expertise in micro-architecture, RTL coding, clock controller design, low power designs, and have excellent communication skills. You will be expected to provide technical guidance and mentorship to junior engineers, stay updated with the latest advancements in ASIC technology and AI applications, and ensure compliance with company policies and procedures. Qualcomm is an equal opportunity employer and is committed to providing accommodations for individuals with disabilities during the application/hiring process. If you require accommodations, you can contact Qualcomm at disability-accommodations@qualcomm.com. Please note that this email address is specifically for disability accommodations and not for updates on applications or resume inquiries.,

As a Manager in the Finance Department at HAPPY GROUP, you will play a crucial role in overseeing the Approved Project Finance (APF) processes, managing customer bookings and documentation, and ensuring smooth loan processing and disbursement. Your responsibilities will involve coordinating with banks and financial institutions, maintaining project documentation, overseeing unit availability and booking processes, and managing booking and CRM software functionality. Your role will also entail facilitating customer home loan applications, coordinating with legal and accounts teams for agreement and invoicing processes, ensuring compliance with RERA norms, and maintaining consistent communication with banking partners. Additionally, you will handle escalations, provide training and support to staff for efficient software usage, and ensure timely issuance of allotment letters. To excel in this position, you should possess an MBA in Finance from a recognized institution, along with 2-5 years of relevant experience in project finance, booking operations, or real estate finance. Proficiency in booking software/CRM tools, Microsoft Office (especially Excel), and excellent communication, coordination, and team leadership abilities are essential. Strong stakeholder management skills, organizational skills, and the ability to handle high-pressure situations with a customer-centric approach are also key attributes for success in this role. If you have experience in the real estate sector or housing finance domain, familiarity with RERA compliance and documentation practices, and a strategic mindset along with operational excellence, you are encouraged to apply for this exciting opportunity. This is a full-time, permanent position with benefits such as health insurance, provident fund, and bonuses based on performance. The work location is in person at Jaipur/Ajmer. Join us at HAPPY GROUP and be part of a dynamic team that values precision, proactive management, and seamless coordination in financial and customer processes.,

The Software Engineer plays a crucial role in demonstrating leadership by effectively communicating business goals and processes within a specific area or business segment. As a Software Engineer, you will leverage your experience and expertise to address challenges, establish objectives for yourself and your team, and drive both short-term and long-term business objectives. You will be responsible for various tasks, including representing high-quality design and development practices as a valuable member of the Digital Mining Software team. Your role will involve developing multi-threaded C++ applications on an embedded Linux operating system, as well as working on Embedded JAVA, Qt, and QML projects. Additionally, you will contribute to the creation of high-performing, scalable, and innovative web applications from end to end. Collaboration is essential in this role, as you will work closely with system engineers, frontend developers, and software developers to implement solutions that align with shared platforms and solutions. By applying principles of Software Development Life Cycle (SDLC) and methodologies like Lean/Agile/XP, Continuous Integration (CI), Software and Product Security, Scalability, Documentation Practices, refactoring, and Testing Techniques, you will ensure the success of the projects you work on. Key responsibilities also include writing code that meets standards and fulfills the required functionality using the designated technology for each project. You will be involved in building features such as web services and Queries on existing tables. Furthermore, understanding performance parameters, evaluating application performance, working on core data structures, design patterns, and algorithms, and implementing them in C++ 14 or higher are integral parts of your role. Participation in design and code reviews is another crucial aspect of the Software Engineer position. By actively engaging in these reviews, you contribute to maintaining the quality and integrity of the software development process. Qualifications and Requirements: - Bachelor's degree in information systems, Information Technology, Computer Science, or Computer/Electronic Engineering. - Experience in software development and hands-on coding across various high-level programming languages and embedded platform and processors. Desired Characteristics: - Master's degree in information systems, Information Technology, Computer Science, or Computer/Electronic Engineering. - Over 5 years of experience in software development and hands-on coding in multiple high-level programming languages and embedded platform and processors. - Proven track record of delivering successful high-quality embedded software products in C/C++ under embedded real-time operating systems like Linux or QNX. - Experience with developing and optimizing Linux device drivers for embedded applications. - Proficiency in communication protocols such as RS232/485, CAN Bus, TCP/IP, Bluetooth, WIFI, GPS, GPS tracking, packet radio telemetry, mining methods, and vehicle types. - Familiarity with web applications, front-end technologies, Microsoft Technologies, TDD, BDD, DevOps, CI/CD, data structures, algorithms, and software engineering principles. - Strong oral and written communication skills, as well as exceptional interpersonal and leadership abilities.,

As a Junior HR Executive at Softtrix in Mohali, Punjab, you will play a crucial role in supporting the day-to-day HR operations. With a preference for candidates with a certification in HR or related field and 6 months of experience, this full-time on-site position is perfect for individuals passionate about Human Resources, especially those from Humanities or History backgrounds aiming to gain practical experience in an IT-driven environment. Your responsibilities will include assisting with employee documentation, data entry, record maintenance, coordinating interviews and onboarding sessions, planning employee engagement activities, wellness programs, and internal events. Additionally, you will be involved in IT and technical recruitment, sourcing candidates, screening resumes, and maintaining employee records while contributing to a positive work culture through various HR-related communications. To excel in this role, you should possess strong verbal and written communication skills, a good understanding of IT recruitment processes, basic knowledge of HR operations, and documentation practices. Maintaining confidentiality, being highly organized, and having the ability to multitask are essential. A proactive mindset, willingness to learn, and grow in the HR domain are also key competencies required. Joining Softtrix offers you a great opportunity to kickstart your HR career, providing exposure to comprehensive HR functions, technical hiring, and employee engagement. You will have the chance to learn from experienced HR professionals in a collaborative environment with a 5-day workweek. In addition to a comprehensive learning experience, you will have access to benefits such as health insurance and Provident Fund. The work schedule is during day shift, Monday to Friday with morning shifts. As part of the application process, please specify your salary expectation as a Fresher and confirm if you are an immediate joiner. If you have at least 1 year of experience in iRecruitment and are looking for an in-person work location, we encourage you to apply and be part of our dynamic HR team at Softtrix.,

You will join our dynamic team at Exeliq Tech Solutions Pvt Ltd. as a Procurement Executive. Your primary responsibility will be to optimize the procurement process, focusing on material procurement, vendor identification and management, vendor negotiation, and overall procurement efficiency. Successful vendor negotiations, meticulous documentation practices, and a strategic approach to procurement are essential qualities we are looking for in the ideal candidate. As a Procurement Executive, you will work closely with internal stakeholders to identify and procure required materials, components, and supplies from reliable vendors. You will actively search for potential vendors, evaluate them based on quality, pricing, delivery times, and reliability, and maintain a comprehensive vendor database. Coordinating with vendors and internal teams, you will ensure timely and accurate dispatch of materials, monitor shipment status, and maintain proper documentation for material receipt and delivery. Maintaining accurate records of procurement activities, preparing regular reports highlighting procurement performance, cost savings, and areas for improvement, and continuously evaluating and improving procurement processes will be part of your responsibilities. Staying updated with industry trends, best practices, and emerging technologies in procurement and supply chain management is crucial for success in this role. To qualify for this position, you should have a Diploma in Electronics or a relevant Graduate degree, along with a minimum of 1 year of work experience in procurement, purchasing, or supply chain management. Excellent communication and negotiation skills, strong analytical and problem-solving abilities, proficiency in Microsoft Office suite, knowledge of procurement software and tools, attention to detail, organizational skills, ability to work under pressure, and meet deadlines are additional requirements for this role. If you are ready to take on the challenge and contribute to our procurement process optimization efforts, we encourage you to submit your application. Please note that the interview and selection process will include a face-to-face interview, and candidates available for immediate joining will be preferred.,

As a part of ACG Associated Capsules Pvt. Ltd., your primary responsibilities will involve strategic planning activities. You will be responsible for ensuring the preparation of Feed Tank (FT) according to production requirements in a shift. It is crucial to maintain Good Manufacturing Practices (GMP), gowning, and safety protocols. You will oversee the shift handover/takeover on the shop floor and be accountable for any issues from the previous shift. Your duties will include compliance with the daily dipping schedule for FT preparation, color changes, and ZMICs for specific batch requirements. It is essential to ensure shade compliance on Mac bath to prevent productivity loss due to color shade variation. You will review and ensure 100% compliance with documentation practices for daily records, including various verifications and monitoring tasks. Furthermore, you will be responsible for executing Mac Bath Calibration, recipe verification for new shades, viscosity verification, and optimizing gelatin and water consumption. Compliance with safety guidelines, Environmental Management Systems, c-GMP, and other applicable norms is paramount. Internally, you will prepare various reports, monitor Multiskilling initiatives, and provide effective training to operators. People development is a key aspect, and you will ensure proper manning, shift handling, and activities. Achieving first-time-right feed tank preparation and optimizing gel consumption are critical Key Result Areas. Your interactions will involve internal interfaces such as Gel room, Stores, Quality, Engineering, and external interfaces including Customers, Auditors, and Visitors. Proficiency in GDP, GMP, MS Excel, AVSU, and knowledge of additives, colors, and manufacturing processes are essential competencies for this role. Your personal attributes as a Persona-Partner, Persona-Integrator, and Persona-Builder will contribute to your success in this position. The demonstration of values such as Caring, Collaborative, and Progressive during discussions will be evaluated. In summary, the Solution Preparation role at ACG Associated Capsules Pvt. Ltd. encompasses various strategic planning activities, documentation compliance, safety adherence, people development, and efficient production processes to achieve organizational goals effectively.,

The Credit Executive holds a crucial position in the credit evaluation and underwriting process for EV asset financing, specifically L3 e-rickshaws and lithium-ion batteries. Your responsibilities will include conducting comprehensive credit checks, evaluating risk profiles, verifying customer documentation, analyzing financial and non-financial data, and ensuring that all loans adhere to company policies and regulatory standards. This role is dedicated to serving individual drivers and fleet operators in urban and semi-urban markets. Your key responsibilities will involve: Credit Evaluation and CIBIL Checks: - Perform thorough credit assessments of loan applicants by scrutinizing their CIBIL score/report and other credit bureau data like Experian and CRIF. - Identify warning signs such as recent multiple loan applications, delinquency, or high EMI-to-income ratios. Document Verification and KYC: - Examine customer KYC documents such as Aadhaar, PAN, voter ID, and address proof. - Validate income proof, business ownership or employment details, and documents for informal or semi-formal income sources. - Review and confirm guarantor details and documents where necessary. Loan Approval and Compliance: - Ensure all credit decisions align with internal credit policies, product parameters, and risk tolerance. - Make recommendations for approval or rejection based on a comprehensive risk assessment. - Escalate borderline or high-risk cases to senior credit approvers or risk committees. Requirements: - Bachelor's degree in Finance, Commerce, Business Administration, or a related field. - Minimum of 3 years of experience in credit underwriting or loan processing, preferably in vehicle, EV, or asset financing. - Proficient knowledge in CIBIL and credit bureau reports, informal income assessment, and retail underwriting standards. - Familiarity with field verification, KYC norms, and documentation practices. - Detail-oriented with exceptional analytical and risk assessment skills. - Willingness to travel if required. Preferred Qualifications: - Experience in NBFCs or fintechs financing 2W/3W vehicles, EVs, or related sectors. - Understanding of low-income customer segments and Tier 2/3 lending environments. - Multilingual capabilities, particularly in regional or local dialects. - Exposure to underwriting non-prime or financially underserved customers.,

You should have a minimum of 3-12 years of experience for the position in Lucknow. Your responsibilities will include a strong understanding of Mobility 4G/5G/6G technologies and their application in software development. Proficiency in programming languages such as Java, C++, and Python will be required. Additionally, you should be familiar with Linux operating systems and their application in development environments. Your role will involve solid experience in troubleshooting and resolving software issues. It is essential to have good knowledge of CMMI standards and documentation practices.,

You are a highly motivated Compliance Software Implementation Specialist with experience in healthcare regulatory standards. Your main responsibility will be to lead the implementation of compliance platforms at Ambulatory Surgery Centers (ASCs). This will include gathering requirements, configuring the software, providing end-user training, and ensuring ongoing system support. Your role will involve close coordination with clinical, IT, and administrative teams. You will be leading and managing the implementation of compliance software at ASCs, ensuring that the software meets regulatory, accreditation, and facility-specific needs. Additionally, you will be responsible for training ASC staff on system use, workflows, and compliance documentation. It is crucial to ensure adherence to regulatory standards such as CMS, AAAHC, and Joint Commission. Your role will also involve providing ongoing support, troubleshooting, and optimization of the platform, as well as coordinating with internal IT teams, ASC administrators, and super users. Documenting workflows, changes, and implementation outcomes will also be part of your responsibilities. To excel in this role, you should have experience with healthcare or compliance software, such as incident reporting, infection control, or credentialing. Familiarity with ASC regulations including CMS, AAAHC, and Joint Commission is essential. Strong project management skills and effective stakeholder communication are required. You should also be able to train both clinical and non-technical staff, demonstrate a basic technical aptitude in software configuration and system integration, and possess excellent verbal and written communication skills. Attention to detail in regulatory and documentation practices is a key attribute. The ideal candidate for this position would hold a Bachelor's degree in Nursing, Life Sciences, Healthcare Administration, Engineering, or a related field. Additional certifications in healthcare compliance or project management would be advantageous.,

The Quality Control (QC) Reviewer plays a crucial role in ensuring the accuracy, completeness, and compliance of laboratory and clinical data with regulatory guidelines, company policies, and industry standards. Your responsibilities include reviewing raw data, study documentation, and analytical reports to ensure adherence to protocols and regulatory requirements. By identifying discrepancies and errors, you will provide recommendations for corrective actions to maintain data integrity. Collaboration with laboratory analysts, study coordinators, and quality assurance teams is essential to resolve issues related to data accuracy and compliance. As a QC Reviewer, you will document your findings meticulously, preparing detailed reports for management and regulatory bodies. Additionally, you will participate in audits and inspections to uphold quality standards. To excel in this role, you should hold a Bachelors/Masters degree in Life Sciences, Pharmacy, Chemistry, or a related field. With 2-6 years of experience in Quality Control/Quality Assurance within the pharmaceutical or biotech industry, you are expected to have a strong understanding of GLP, GCP, FDA, EMA, and ICH guidelines. Proficiency in reviewing analytical data, clinical study reports, and laboratory documentation, along with excellent attention to detail and problem-solving skills, are essential. Effective communication and interpersonal skills are necessary to collaborate with cross-functional teams. Moreover, staying updated with regulatory changes and industry best practices will contribute to enhancing the organization's quality standards. Experience with bioanalytical, clinical, or preclinical study reviews, knowledge of electronic data capture (EDC), and the ability to handle multiple projects with tight deadlines are preferred skills for this role. Proficiency in Microsoft Office and Laboratory Information Management Systems (LIMS) would be advantageous.,