6 Environmental Practices Jobs

You will be responsible for strictly adhering to cGMP, Safety, and Environmental Practices while working in the manufacturing plant. Your duties will include filling Batch Manufacturing records, cleaning equipment, following Good Manufacturing practices, maintaining Good Housekeeping, wearing proper personnel protective equipment, and planning for Raw Material availability for daily production as per the production plan. Additionally, you will be required to maintain documents like Issue and dispensing register, carry out processes as per Batch Manufacturing Record (BMR) without any deviation, and ensure adherence to data integrity in online documentation. Hazardous operations should be handled safely, and resources like Utility, Men, and Machine should be effectively utilized. To qualify for this role, you should hold a B.E/B.Tech degree in a relevant field such as Chemical or Chemistry. The ability to work collaboratively in a team-oriented environment and strong communication skills, both verbal and written, are essential. Piramal Group, with three decades of existence, follows a growth strategy of both organic and inorganic methods. The group is committed to inclusive growth while upholding ethical and values-driven practices. Equal employment opportunity is a fundamental principle where employment decisions are based on merit, qualifications, skills, and achievements, ensuring equal opportunities for all applicants and employees. Piramal Pharma Solutions (PPS) is a Contract Development and Manufacturing Organization (CDMO) providing end-to-end solutions across the drug life cycle. Your role will be in API Production at Piramal Enterprises Limited in Chennai, Tamil Nadu. The company offers a wide range of services, including drug discovery solutions, process & pharmaceutical development services, clinical trial supplies, commercial supply of APIs, and finished dosage forms. Specialized services like the development and manufacture of highly potent APIs, antibody-drug conjugations, sterile fill/finish, peptide products & services, and potent solid oral drug products are also available. Services for biologics such as vaccines, gene therapies, and monoclonal antibodies are offered through investment in Yapan Bio Private Limited. With a proven track record, PPS is a trusted partner for innovators and generic companies worldwide. This is a full-time position requiring a Master's Degree, and the job identification number is 8465.,

As a Manufacturing Team Manager, your primary responsibility will be to assess and manage the Manufacturing Team in order to maximize service to customers. You will provide direction and leadership by focusing on sound operating principles, coaching employees to develop critical skills, clearly communicating strategy and vision, and helping teams translate those business strategies into their daily work. It will be important to share and communicate critical, best practice manufacturing processes and performance standards, while monitoring and analyzing key performance indicators to ensure control and compliance. You will actively lead service improvements throughout managing responsibility, driving improved productivity, efficiencies, safety, and lower costs within the scope of the collective bargaining agreement. It will also be your duty to lead production standards to ensure they are maintained and administer and enforce policies and procedures for SP3. Additionally, developing and maintaining a strong positive working relationship with all internal departments locally and internationally will be crucial. To qualify for this role, you should have 5-7 years of demonstrated experience in manufacturing management within a specialized industry. A strong work ethic, self-motivation, independence, and the ability to make decisions are essential qualities for this position. You should possess excellent organization and time management skills, exceptional presentation skills, and a high energy level with excellent verbal and written communication skills. Ideally, you will have 3-5 years of experience in a high-technology chemical or coating process manufacturing environment. Knowledge of thin film coatings and/or CVD/PVD processes is desirable, and previous work in a cleanroom environment is a plus. A working understanding of safety, health, and environmental practices, as well as knowledge of software programs and computers, is also required. A high level of quality awareness is essential for success in this role. In return, we offer a market competitive salary, benefit eligibility, and vesting that start on your 1st day with us (including medical, vision, dental, STD, LTD, 401k), as well as opportunities for career development through training both locally and abroad, and tuition reimbursement.,

As a Simulation Engineer at Valeo, you will play a crucial role in validating the thermal behavior of products through simulation. Your primary mission will involve applying thermal simulation methods, managing the thermal simulation plan of products, and validating designs while proposing solutions to enhance them in line with thermal specifications and integration constraints. You will be responsible for not only validating the proposed solutions but also correlating calculations with measurements. In addition, you will ensure cross-metier collaboration with mechanical, electronic, and laboratory teams. Your role will also involve supporting methodology development and application of simulation tools, participating in the definition of design rules, and contributing to the improvement of methodologies. Your responsibilities will extend to capitalizing on the simulation method improvements, reporting procedures, validating test methods, storing reports in TMT, and participating in QRQC resolution. You will also provide support for P1 developments, including LEDs systems, and actively engage in networking within your metier at the Product Group and Business Group levels. Moreover, you will be expected to adhere to Valeo's procedures and Environmental, Safety, and Security good practices, be aware of potential risks associated with your activities, and take necessary action plans. If you are involved in people management, you will be responsible for managing a team and ensuring effective leadership. To excel in this role, you should hold an Engineer or Master of Science degree with thermal and mass transfer competence, possibly a Ph.D., and possess 3-5 years of experience in the Thermal/Mass transfer phase change domain. Proficiency in areas such as mass transfer, experimental validation of simulations, and the use of tools like FLUENT, CATIA, and ANSYS will be essential. Your key competences should include technical skills, problem-solving abilities, automotive expertise, project management skills, and a commitment to Valeo values. Additionally, you should be proficient in English and French, hold a vehicle license for night drive tests, and be open to occasional trips lasting from 1 to 5 days within France or other countries. Join Valeo, one of the largest global innovative companies, where you will work alongside more than 20,000 engineers in Research & Development. Embrace a multi-cultural environment that values diversity and international collaboration, with over 100,000 colleagues across 31 countries, offering ample opportunities for career growth. Valeo is deeply committed to minimizing its environmental impact and has been recognized as the top company in the automotive sector for sustainable development by Corporate Knights. For more information on Valeo, visit https://www.valeo.com.,

You will be responsible for strictly following cGMP, Safety and Environmental Practices, as well as ensuring Good Manufacturing practices during operation. This includes filling Batch Manufacturing records and equipment cleaning records, maintaining proper personnel protective equipment usage, and ensuring good housekeeping in the respective plant area and its equipment. You will need to plan and ensure raw material availability for daily production as per the production plan, maintain documents like Issue and dispensing register, and carry out processes as per Batch Manufacturing Records (BMR) without any deviation. It is essential to adhere to data integrity in online documentation and handle hazardous operations in a safe manner. Additionally, you will be expected to effectively utilize resources such as utility, men, and machines. Piramal Pharma Solutions (PPS) is a Contract Development and Manufacturing Organization (CDMO) that offers end-to-end development and manufacturing solutions across the drug life cycle. PPS serves customers globally through a network of facilities in North America, Europe, and Asia. The services provided include drug discovery solutions, process and pharmaceutical development services, clinical trial supplies, commercial supply of APIs, and finished dosage forms. Specialized services such as the development and manufacture of highly potent APIs, antibody-drug conjugations, sterile fill/finish, peptide products and services, and potent solid oral drug products are also offered. PPS caters to the development and manufacturing of biologics such as vaccines, gene therapies, and monoclonal antibodies. With experience across varied technologies, PPS has established itself as a trusted service provider and a preferred partner for innovators and generic companies worldwide.,

You will be responsible for strictly following cGMP, Safety, and Environmental Practices in the manufacturing facility. This includes filling out Batch Manufacturing records and equipment cleaning records. It is crucial to adhere to Good Manufacturing practices during all operations and ensure Good Housekeeping in the plant area and its equipment. You must use the proper personnel protective equipment as required for each task. Planning and ensuring the availability of Raw Materials for daily production as per the production plan is essential. Keeping track of documents such as Issue and dispensing register is part of the responsibilities. Carrying out the manufacturing process according to the Batch Manufacturing Record without any deviation is a key aspect of the role. Ensuring adherence to data integrity in online documentation is of utmost importance. Handling hazardous operations in a safe manner is critical for the safety of yourself and others. Effective utilization of resources such as Utility, Manpower, and Machinery is required to meet production targets. It is essential to be detail-oriented, safety-conscious, and proactive in ensuring the smooth and compliant operation of the manufacturing processes.,

You will be responsible for strictly following cGMP, Safety, and Environmental Practices in the manufacturing facility. Your duties will include filling Batch Manufacturing records and equipment cleaning records, as well as following Good Manufacturing practices during operations. It will be important to ensure Good Housekeeping in the plant area and equipment, and to use proper personal protective equipment as required. You will be in charge of planning and ensuring the availability of raw materials for daily production according to the production plan. Additionally, you will need to maintain documents such as Issue and dispensing register, and carry out processes as per Batch Manufacturing Record without any deviation. It will be crucial to adhere to data integrity in online documentation and handle hazardous operations safely. Part of your role will involve effectively utilizing resources such as utilities, personnel, and machinery to support efficient production processes.,