Hetero Biopharma is hiring for process maintenance (mechanical)

About company:

Bringing together diverse strengths to achieve a common goal, from bench to bedside.

R&D Capabilities: With state-of-the-art R&D facilities and skilled scientists, biosimilars can achieve the highest levels of QSE (quality, safety, and efficacy) processes, and they can be developed quickly using Hetero’s platform technology.

Manufacturing: Manufacturing facilities for biologics deploy the latest technology, including single-use and state-of-the-art equipment from reputed companies, providing enough capacity to manufacture and cater to large markets, with ample scope for expansion. Additionally, they are built and operated according to cGMP standards.

Regulatory Affairs & Clinical Expertise: Capable of providing CTD and e-CTD forms of dossiers as per ICH and other major international formats. The Clinical Development and Medical Affairs [CDMA] team complies with global regulatory requirements and supports clinical evaluation from phase I to IV and pharmacovigilance programs.

Project Management: From planning to execution, our exclusive project team possesses hands-on experience in successfully transferring different technology models across various geographies.

Global Business Operations: As a result of our in-depth knowledge of biosimilar commercial pathways, we can overcome entry barriers to the early commercialization of biosimilars. Our flexible business model reflects our passion for introducing complex biosimilars to emerging markets through strategic partnerships.

Department:

Process Maintenance-mechanical

Qualification:

Diploma/B.Tech

Experience:

5-8 yrs

Send resumes to this email: praveen.ko@hetero.com

1. Responsible for trouble shooting and maintenance of equipment’s like: vial washing, Tunnel, vial filling, vial sealing, autoclave, Lyophilizer and PFS filling equipment’s.

2. Responsible for execution of preventive maintenance & facility maintenance works as per Schedule

3. Responsible for attending and rectifying breakdowns.

4. Follow the procedure as per GMP

5. Breakdown percentage should be maintained as closer to ZERO.

6. Responsible for advance planning of all type’s maintenance works and necessary intimation to the reporting authority.

7. Responsible to maintain the required inventory level for all equipment spares.

8. Responsible for energy conservation activities.

9. Maintenance works will be carried out as per regulatory, statutory requirements.

10. Responsible for execution of Qualification/Validations

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