Linux Lifesciences Private Limited, a whole subsidiary of Linux Laboratories Pvt. Ltd., one-source partner to navigate the oral solid manufacturing journey. LLS located in Puducherry, our single-campus facility provide customers with an end-to-end solution under a WHO-cGMP registration. We offer a leading edge in manufacturing general and cephalosporin oral solids, including dry syrup formulations with precision quality and making healthcare, affordable and accessible.Linux Lifesciences Private Limited, with best-in-class equipments, strong compliance record and experienced team make us the ideal partner for your novel oral solid formulations.Our strong drug development capabilities combined with our dossier-centric approach devoted to helping customers to manufacture dosage forms from initial concept to global commercialization.
Vacancy details:
- Department:Senior Executive / Assistant Manager QA-LLS Formulation UNIT
- Experience: 7 – 12 years
- Qualification: B.Pharma in Pharmacy
- Salary:₹ 4.75-6 Lacs P.A.
Job Description : Greeting from Linux Life sciences private limited !!!!
Important Details :
- Location: Puducherry,Puducherry
- Post of date:29/03/2024
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face to face
- Interview Rounds of Interview: HR
Walkin Interview Details:
Job description
Job description
- Preparation of BMR & BPR
- Preparation of master formula record ( MFR )
- Implementation of new SOP in a site.
- Artwork checking as per the current guidelines.
- Preparation , Issue , retrieve and review the BMR & BPR
- Implementation of the IPQA activities and report duty to the Head QA
- Issue of log sheet & formats and retrieval of the same.
- Issue and receive the log sheet for Environmental monitoring, Balance calibration, Preventive maintenance and other related formats to various departments as per the predetermined schedule
- Preparation of Process validation and cleaning validation protocol accordingly conducting sampling for Process Validation ( PV ) & Cleaning Validation ( CV ) . Preparation , consolidation of validation reports.
- Monitor the compliance of SOP
- APQR preparation.
- Able to provide QMS training to the subordinates.
- Maintaining cGMP documents in the plant
- Ensure the Internal & External Calibration
- In process checks during manufacturing and packing activities
- Co ordinate with Internal & External ,Regulatory Audits
- Co ordination with change control & Deviations
- Implementing the Requirement of Quality Management System ( QMS)
- Ensure the equipments in Production and Utilities confirmed with Preventive Maintenance as per the schedule. And etc,..
Preferred candidate profile B, Pharmacy with relevant Experience in Pharmaceuticals Formulation Company
Perks and benefits
As per industry standard
ABAC
