7 Validation Process Jobs

You will be joining Godrej Agrovet Limited (GAVL), a diversified agri-business company dedicated to enhancing the productivity of Indian farmers through innovative products and services. GAVL holds leading market positions in various sectors such as Animal Feed, Crop Protection, Oil Palm, Dairy, Poultry, and Processed Foods. With a pan India presence, GAVL annually sells over a million tons of high-quality animal feed and cutting-edge nutrition products. The company has actively developed large Oil Palm Plantations to bridge the demand-supply gap of edible oil in India. Additionally, in the crop protection segment, GAVL meets the niche requirements of farmers through innovative agrochemical offerings. Through its subsidiary Astec Life Sciences Limited, GAVL is a bulk manufacturer of fungicides & herbicides. The company also operates in Dairy, Poultry, and Processed Foods through its subsidiaries Creamline Dairy Products Limited and Godrej Tyson Foods Limited. Furthermore, GAVL has a joint venture with the ACI group of Bangladesh for the animal feed business in Bangladesh. As a Manager-Production at the Mahad location, your role will involve production planning, organizing, staffing, and directing plant operations. You will be responsible for executing monthly production targets, implementing new products, ensuring compliance, and contributing to long-range production strategies. Your expertise in validation processes, troubleshooting, and continuous improvement of technology, product quality, safety, and environment will be crucial. You will drive productivity improvement and cost reduction through innovative ideas, manage a team of professionals, and ensure high performance. Coordinating, establishing, implementing, and maintaining an Integrated Management System comprising all standard requirements will be part of your responsibilities. You should be well-versed in audit standards and compliance, legal requirements, risk assessments, and HSE training. The ideal candidate for this role should have a BE Chemical educational qualification with 12-15 years of experience. A diverse and inclusive mindset is valued at Godrej, with a strong emphasis on non-discrimination and embracing diversity. If you are passionate about contributing to the growth of Indian agriculture and possess the required skills and qualifications, we encourage you to apply for this position at Godrej Agrovet Limited.,

You will be responsible for overseeing all aspects of quality management and ensuring the highest level of compliance across projects. This includes driving the validation process, supporting the authoring, reviewing, and approving of CSV deliverables, coordinating with project managers to align project outputs with quality standards, and managing change control processes for tool updates and deployments. Additionally, you will evaluate data and QM processes for improvements, support audits and inspections for compliance, oversee root cause analysis and corrective actions, and provide training on quality standards and procedures. Minimum Requirements: - Minimum of 10 years experience in Quality Management, preferably in Pharma or regulated industries. - Proven experience in managing GxP/non GxP projects from requirement definition to retirement. - Working experience in all lifecycle stages of IT systems, including System retirement. - Ability to drive innovative validation strategies and knowledge of IT systems in the Pharma industry. - Exceptional leadership and interpersonal skills with attention to detail. - Bachelor's degree in IT, Pharmacy, or related field. Novartis is committed to diversity and inclusion in the workplace, creating an outstanding work environment that reflects the patients and communities served. The company also provides accessibility and accommodation for individuals with disabilities, aiming to support reasonable accommodations during the recruitment process. If you are interested in staying connected with Novartis for future career opportunities, you can join the Novartis Network. Additionally, you can learn more about the benefits and rewards offered by Novartis in the Novartis Life Handbook.,

The culture at our organization is defined by the people who contribute to it. We foster a culture of passion for technology solutions that have a tangible impact on businesses. Additionally, we prioritize the pursuit of individual passions by our team members. Collaborating with us offers you the opportunity to gain a deep understanding of various industries and cutting-edge technologies. This knowledge enables us to develop forward-thinking and impactful solutions. Moreover, being a part of MarvyLogic can facilitate personal growth, leading you towards a more enriching and fulfilling life. To be considered for this role, you should possess the following qualifications: - A minimum of 10 years of experience in FPGA Design and Debug, preferably working with Xilinx Ultrascale+ and Virtex7 - Proficiency in utilizing tools such as Xilinx Vivado/Coregen/Synplify and developing/maintaining Timing/IO constraints (UCF) - Experience with managing multiple high-speed clock domains and integrating third-party IP onto Xilinx transceivers - Familiarity with working on FMC daughter-cards, High-Speed Cables/Connectors, etc. - Extensive debugging experience using Xilinx ILA, Protocol Analyzers, Oscilloscope, Logic Analyzers, etc. - Proficiency in PERL/TCL scripting and database management between FPGA and ASIC RTL - Knowledge of front-end RTL tools such as RTL Simulation, Synthesis, DFT, Timing - Ability to modify/adapt RTL designs for FPGA implementation and optimize designs to achieve FPGA area/performance goals - Collaboration with DV and Firmware/Software teams throughout the validation process, including post-silicon bring-up Your responsibilities in this role will include: - Effectively collaborating and communicating with multi-site teams - Reviewing FPGA netlist releases (block/chip) and overseeing ASIC product life cycle stages, including requirements, design, implementation, testing, and post-silicon validation If you meet the specified qualifications and are ready to take on these responsibilities, we welcome you to apply for this challenging and rewarding opportunity.,

The prototype engineer role involves creating prototypes of new products to test their design and functionality before full production. You will work closely with the engineering team to develop and test new product designs, as well as participate in research and development activities to generate new engineering ideas or enhance existing designs. Evaluating new technology and materials for potential applications in current or new products will also be part of your responsibilities. In this role, you will be accountable for metal integration in vehicle components, as well as modifying metal parts in stretcher designs. Testing prototypes to measure performance against design specifications, overseeing manufacturing processes for quality and safety, and coordinating with other departments for efficient and cost-effective production are key tasks you will undertake. Desired qualifications for this position include proficiency in workshop operations, experience with power tools and measuring instruments, and the ability to use various machining tools like cutting, grinding, finishing, and welding. You should have a deep understanding of prototyping, testing, homologation, and validation processes, along with the capability to interpret 2D, 3D, and line sketch drawings to visualize the final product output. Key competencies for this role include being result-oriented and goal-driven, possessing strong interpersonal skills, being self-motivated with a problem-solving attitude, and demonstrating the highest level of integrity in teamwork, confidentiality, ethics, and performance. A sense of ownership and pride in your work, as well as understanding its impact on the company's success, are essential attributes for success in this position.,

Method development and validation processes. Ability to plan, coordinate, and execute projects from initiation to completion, Commitment to maintaining Good Laboratory Practices (GLP) Maintenance and preventive maintenance of instruments. Required Candidate profile supervising, mentoring, and guiding both junior and senior research associates. Prep HPLC as part of the overall industry experience. Proven hands-on experience with HPLC and LC-MS techniques.

Method development and validation processes. Ability to plan, coordinate, and execute projects from initiation to completion, Commitment to maintaining Good Laboratory Practices (GLP) Maintenance and preventive maintenance of instruments. Required Candidate profile supervising, mentoring, and guiding both junior and senior research associates. Prep HPLC as part of the overall industry experience. Proven hands-on experience with HPLC and LC-MS techniques.

Method development and validation processes. Ability to plan, coordinate, and execute projects from initiation to completion, Commitment to maintaining Good Laboratory Practices (GLP) Maintenance and preventive maintenance of instruments. Required Candidate profile supervising, mentoring, and guiding both junior and senior research associates. Prep HPLC as part of the overall industry experience. Proven hands-on experience with HPLC and LC-MS techniques.