7 Fda Requirements Jobs

As a Quality Control member at Piramal Pharma Solutions in Pithampur, your role involves 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 to the QC lab Supervisor. Key Responsibilities: - Perform testing on in-process samples, raw materials, finished drug products, and stability study samples - Support production, packing release, and regulatory filings Qualifications Required: - 3 - 6 years of experience in a cGMP laboratory setting - Familiarity with cGMP and FDA requirements Kindly note that no additional details about the company were provided in the...

**Job Description:** As a Process Engineer, your role involves reviewing the process flow according to customer requirements and developing process flows for pharmaceutical formulations. You will work closely with the project manager to conduct capacity and cycle time analysis, define equipment sizing, and create technical specifications (TS) and data sheets for production, packaging, and process equipment. Your responsibilities will also include floating inquiries to vendors, resolving technical queries, and following up with vendors for offers. Additionally, you will organize meetings with vendors, create a make/vendor list of production machinery within the project budget, and participate...

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 Solu...

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...

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....

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 t...