Website Hetero Biopharma
Hetero Biopharma is steadily establishing itself as a path breaking devlopers in the field of biosimilars. Biosimilars are becoming increasingly important in providing affordable access to life-saving treatments for patients with chronic conditions. With a strong focus on research and development, and a commitment to maintaining the highest standards in manufacturing, Hetero Biopharma is well-positioned to continue making a significant impact in the industry.
Having 36 state-of-the-art manufacturing facilities located globally is also a testament to Hetero’s commitment to providing quality care to patients around the world. Having received approval from numerous regulatory authorities is also a positive indication of Hetero’s commitment to following strict guidelines and ensuring that their products are safe and effective.
Department, Experience & Qualification :
This job posting is for a position in the Formulation department at Hetero Biopharma, with a requirement for a candidate with 3-5 years of experience in the field. The ideal candidate should hold a Master’s degree in Science, Technology, Biotechnology, Biochemistry or a Master’s or Bachelor’s degree in Pharmacy.
The role in the Formulation department likely involves developing and manufacturing pharmaceutical products, ensuring that they meet the required standards and specifications. The candidate will be expected to have knowledge of various formulation techniques and processes, as well as experience with quality control and regulatory requirements.
The candidate should have a strong understanding of biopharmaceuticals, as well as a passion for contributing to the development of new treatments for patients with chronic conditions. If you have the required experience and qualifications, this could be an exciting opportunity to join a dynamic and innovative company, and make a meaningful impact in the healthcare industry.
Job Profile :
This job posting is for a position at Hetero Biopharma with a focus on Lyophilization in the Formulation department. The ideal candidate should have knowledge and experience in handling R&D scale Lyophilizers, as well as experience with formulation development trials, product compatibility trials, and filter validation studies. The candidate should also be familiar with Lyophilization cycle development, and be able to monitor all relevant parameters during the process.
In addition to technical expertise, the candidate should have basic knowledge of Quality Management System (QMS) activities, including change control, deviation, CAPA, and investigation. The candidate should be comfortable with data entry in Batch Manufacturing Records (BMR) and log books, and have good communication skills, both verbal and written.
If you meet the requirements outlined in the job profile and are interested in the opportunity, you can submit your CV to chakradhar.b@Hetero.com for consideration.
Candidates interested in the position should make sure to submit their CV by February 25th, 2023 to be considered for the role.
For more articles, Kindly Click here.
For pharmaceutical jobs, follow us on LinkedIn
For more jobs, kindly visit our job section.
To apply for this job please visit Hetero.com.
