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.
Walk-In Interviews @ Neuland Laboratories Limited
- Qualification: B.Sc
- Experience: 03-05+years
- Salary: 3.25-5 Lacs P.A.
- Job Location: Hyderabad( Bonthapally )
- Openings: 05
- Department: Quality Assurance
- Role: Chemist / Officer
WALK-IN INTERVIEW DETAILS:
- Date: 30 July – 1st August, 2024
- Time: 11.00 AM – 3.00 PM
- Venue: Neuland – U1, Survey No: 474, 347, 490/2, Veerabhadraswamy Temple Road,, Jinnaram,, Bonthapally Village, Telangana 502313
Job description
Roles & Responsibilities: (QMS Activities):
- Reporting to Asst. Manager QA / Head of Quality Assurance and assists him in Quality Assurance activities.
- Responsible for day to day Quality assurance activities, functions and programs designed by Asst. Manager/Manager Quality Assurance.
- Responsible for Quality Management System (QMS) Activities .
- Responsible for document control and issuance.
- Responsible for carry out periodic quality assurance checks of facilities, systems, procedures and records of different departments to maintain quality of the products at all stages of manufacturing and testing.
- Review of the completed Batch manufacturing sheets, Chromatographic Errors and analytical raw data.
- Supporting for Change Control, Deviations, Out of Specifications, Out of Trend results and CAPA management.
- Supporting for customer audits and Compliance of audit observations.
- Preparation and review of Annual Product Quality Review.
- Preparation and review of Validation and Qualification documents.
- Any other responsibilities delegated by the reporting authority.
Roles & Responsibilities: (IPQA Activities):
1. Responsible for day-to-day activities of Quality assurance, functions and programs are designed by Designee/Head QA.
2. Responsible to carry out periodic quality assurance checks of facilities, systems, procedures, and records of different departments to maintain quality of the products of all stages manufacturing and testing.
3. Plant round and verify all the documents during the manufacturing process. Line clearance of all type -II equipments and area cleanings and online monitoring.
(Cleaning validation, product change over, campaign cleaning).
4. Review and approval of executed batch manufacturing sheets and packing records and equipment cleaning records.
5. Responsible for reviewing quality systems and related documents, like OOS and Deviations.
6. Issuance of documents like SOPs, BMS, Formats, registers, Specifications and Method of Analysis.
7. Review of specifications, method of analysis for raw materials, packing materials, intermediates, and APIs.
8. Responsible for preparation of Annual product quality review (APQR).
9. Responsible for monitoring of CMS projects.
10. Any other responsibilities delegated by the reporting authority.
Exp : 03 to 05 years of Exp in Quality Assurance.
Experience from IPQA & QMS background are highly preferrable.
Candidate from API Background are only considered.
Immediate joiner’s are Highly Appreciated.
Share your Resume : [email protected]
Please carry your 03 months Pay slip & Updated CV along with you
