Neuland Laboratories Limited – Walk-In Interviews for Production on 16th to 20th Aug’ 2022


 Neuland Laboratories Limited was established in 1984 and today is a publicly listed company headquartered in Hyderabad, India. Neuland is a leading manufacturer of active pharmaceutical ingredients (APIs) and an end-to-end solution provider for the pharmaceutical industrys chemistry needs. We provide solutions across the full range of the pharmaceutical industry’s chemistry requirements, from the synthesis of library compounds to supplying NCEs and advanced intermediates at various stages in the clinical life-cycle, as well as commercial launch. Our strength is our expertise in manufacturing of APIs and advanced intermediates from our US FDA approved facilities. Our core competency lies in the application of strong process chemistry to manufacturing in a regulatory compliant environment, which is supported by a strong, well-qualified team of more than 1000 employees.

Roles and Responsibilities:

1. Reports to Designee/HOD.

2. Guides the operating personnel to carry out the production activities effectively as per the standard operating procedures.

3. Responsible for maintaining all documents related to production.

4. Indenting and receiving of raw materials, / packing materials from stores as per requirement and same shall be checked while receiving the raw materials / packing materials.

5. Responsible for good housekeeping and keeping the production area in an orderly manner.

6. Pack the intermediates / APIs as per customer requirements and transfer through prescribed formats.

7. Reporting of all deviations to AM/Dy. Manager/Manager.

8. To raise the engineering requisitions related to production equipment breakdowns and preventive maintenance and coordinates with maintenance personnel to complete the jobs effectively.

9. Responsible for conducting operations towards achieving 100% DDP, as per the given production plan.

10. Responsible for conducting operations towards ensuring 100% compliance to the norms of cGMP, ISO-14001, and OHSAS-18001.

11. Responsible for identifying the needs of Training of all the personnel working under him to ensure the adequate awareness in all of them towards the above requirements.

12. Responsible for checking the completed BMSs for their appropriateness before submitting to QA.

13. Review of all the filled production batch manufacturing sheets and related records ensuring that all the data is correct or not

14. Make sure that production facilities are always maintained clean and hygienic conditions.

Share your CVs to RohiniB@neulandlabs.com

Walk-In Date: 16th August – 20th August , 2022

Time: 10.30 AM – 4.00 PM

Venue: Neuland Laboratories Limited Unit-1, Survey No: 474, 347, 490/2: Veerabhadraswamy Temple Road,, Jinnaram,, Bonthapally Village, Telangana 502313



Source link

Published by Pharma Jobs
Tell us something about yourself.
Get Connected!
Come and join Pharma Community. Expand your network in Pharma!

Comments

No comments yet