Sun Pharmaceutical Industries Ltd. (Sun Pharma) is the fourth largest specialty generic pharmaceutical company in the world with global revenues of US$ 5.4 billion. Supported by 43 manufacturing facilities, we provide high-quality, affordable medicines, trusted by healthcare professionals and patients, to more than 100 countries across the globe.
- Vacancy details:
- Department: MS&T Injectables
- Qualification: B.Pharma, M.Pharma
- Experienced: 1Â –Â 6Â years
- Salary:₹Not Disclosed
Job Description: Greeting from Sun Pharmaceutical Industries Ltd. .!!!!!
- Important Details :
- Location:Halol
- Post of date :18/07/2024
- 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:
Date: 21st July
Time:9.30 AM – 1.00 PM
Venue: VENUE OF INTERVIEW ; SUN PHARMACEUTICALS INDUSTRIES LIMITED NEAR AKSHAR CHOWK, SUN PHARMA ROAD, TANDALJA, BARODA -390012
Job description
SUN PHARMACEUTICALS INDUSTRIES LIMITED
WALKIN INTERVIEW IN MS&T INJECTABLES AT BARODA
BRIEF JOB DESCRIPTION:
Execution of technology transfer to Sun/CMO Site transfer, Scale up, Exhibit, Process validation batches plan with effective planning and utilization of men, materials and machineries.
Documentation work like new production introduction form, Scale-up reports, review of Sun/CMO BMR, sampling plan, PV protocol, URS preparation, and Dashboard preparation.
To ensure that product is produced and stored according to the appropriate documentation in order to obtain the desired quality.
Responsible for Review & comments of MF, FMEA, RA & protocol (Sampling plan, Process validation protocol) and compliance.
Handling & Support of Trouble shooting batches for data comparison and route cause
Investigation at Sun/CMO.
Investigation for product trouble shooting
To ensure that the Packing operations or activities are carried out on timely.
To monitor & prior checkup of equipment planned for usage in Scale up, Exhibit, Process
validation batches i.e. Equipment preparation, vial washing & dehydrogenation, CIP/SIP
System, PLCs, instruments etc.
Responsible for Supervise and perform skid trials for better product development and process improvements and also minimizing manufacturing related constraints in future.
To prepare the Scale up report, get evaluated and signed by authorized person prior going
to Exhibit batches & their submitted to QA.
Responsible to help the officers and operators to standardize production activities to
achieve better efficiency and quality.
To review validation protocol, SOP and other cGMP Documents.
Close coordination with all the supporting departments i.e. Production, NPQC, QA, QE
(Engineering) and warehouse for smooth running of Scale up, Exhibit, Process validation
batches.
To ensure the compliance of various in-process control instructions provided in MF, FMEA,
RA, BMR, and MBMR.
Candidates who are unable to attend interview may sent their CVs on HR.Tandalja@sunpharma.com
Disclaimer – Sun Pharma does not seek payment of any kind from a prospective candidates for employment with company or authorize any agency or any individual to collect or charge payment for recruitment. Please be cautious while dealing with any recruitment agency or anyone asking you to pay money representing himself to be part of Sun Pharma.
