5 Fda Requirements Jobs

As a Quality Control professional at Piramal Pharma Solution in Pithampur, your primary responsibility will be to conduct testing on various samples including in-process material, bulk drug substance, finished drug product, and stability samples. You will be instrumental in ensuring the quality and compliance standards are met within a cGMP laboratory environment. In this role, you will report to the QC lab Supervisor, working collaboratively to uphold the standards set by cGMP and FDA regulations. The ideal candidate will have 2 to 6 years of relevant experience in a cGMP laboratory setting and possess a strong understanding of cGMP and FDA requirements. Join our team at Piramal Pharma Solution and contribute your expertise to maintaining high-quality standards in pharmaceutical manufacturing.,

Wondering what's within Beckman Coulter Diagnostics Take a closer look. At first glance, you'll see that for more than 80 years we've been dedicated to advancing and optimizing the laboratory to move science and healthcare forward. Join a team where you can be heard, be supported, and always be yourself. We're building a culture that celebrates backgrounds, experiences, and perspectives of all our associates. Look again and you'll see we are invested in you, providing the opportunity to build a meaningful career, be creative, and try new things with the support you need to be successful. Beckman Coulter Diagnostics is proud to work alongside a community of six fellow Diagnostics Companies at Danaher. Together, we're working at the pace of change to improve patient lives with diagnostic tools that address the world's biggest health challenges. The Staff Technical Operations Scientist for Beckman Coulter Diagnostics is responsible for ensuring the successful establishment of Beckman Coulter products being manufactured in India by an OEM partner. The role will i nclude aspects of Quality Assurance, Design Transfer, Test Method Transfer and the setup and validation of equipment and manufacturing processes. This position is part of the located in and will be located at the OEM manufacturing site. At Beckman Coulter, our mission is to Relentlessly Reimagine Healthcare, One Diagnosis at a Time. You will be a part of the and report to the Senior Staff Technical Transfer Scientist who isresponsible for If you thrive in a multifunctional, fast paced & supporting role and want to work in a Technical Operations Team and be involved in product realization, read on. In this role, you will have the opportunity to: . . . . . . . . The essential requirements for the role include: Bachelor's degree with 9+ years experience OR Master's degree with 7+ years experience. Proven problem investigation and problem solving skills are essential. Demonstrated ability to effectively prioritize and lead a team to deliver on commitments and meet the needs of the business. Prior experience managing strategic Supply chain projects. A good working understanding of cGMP and ISO/FDA requirements. At Beckman Coulter Diagnostics we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, remote working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. This position is eligible for a remote work arrangement in which you can work remotely from your home. Additional information about this remote work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Beckman Coulter Diagnostics can provide. Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit .

The Quality Control department at Piramal Pharma Solution in Pithampur is seeking a dedicated individual to join their team as a QC Analyst. In this role, you will be responsible for performing testing on in-process samples, raw materials, finished drug products, and stability study samples to support production, packing release, and regulatory filings. You will report directly to the QC lab Supervisor. The ideal candidate should have 3 to 6 years of experience in a cGMP laboratory setting and be familiar with cGMP and FDA requirements. This position offers an exciting opportunity to contribute to the quality control processes in the pharmaceutical industry and work in a dynamic environment. If you are passionate about maintaining high standards of quality and ensuring compliance with regulatory guidelines, then this role may be the perfect fit for you. Join our team at Piramal Pharma Solution and be a part of our commitment to excellence in pharmaceutical manufacturing.,

You will be responsible for performing testing on in-process material, bulk drug substance, finished drug product, and stability samples in a cGMP laboratory setting. Your role will involve ensuring compliance with cGMP and FDA requirements. The position reports to the QC lab Supervisor. The ideal candidate should have 2 to 6 years of experience in a cGMP laboratory environment and be familiar with cGMP and FDA requirements.,

As a Quality Control Analyst at Piramal Pharma Limited in Pithampur, your primary responsibility will be to perform testing on in-process samples, raw materials, finished drug products, and stabilities to support production and regulatory filings. You will be reporting to the QC Lab Supervisor. To excel in this role, you should have 0-1 years of experience in a cGMP laboratory setting. It is essential that you are familiar with cGMP and FDA requirements to ensure the quality and compliance of the testing processes. Your attention to detail, analytical skills, and understanding of regulatory standards will be crucial in contributing to the quality control operations of the company. Join our team at Piramal Pharma Limited and be a part of our commitment to delivering high-quality pharmaceutical products that meet regulatory standards.,