Sun Pharma is the world’s fourth largest specialty generic pharmaceutical company and No. 1 in India. We provide high-quality, affordable medicines trusted by customers and patients in over 100 countries. Sun Pharma’s global presence is supported by more than 40 manufacturing facilities spread across 5 continents, R&D centres across the globe and a multi-cultural workforce comprising over 50 nationalities.Â
- Vacancy details:
- Department:Analytical Development
- Qualification: MS/M.Sc(Science), M.PharmaÂ
- Experience:2Â –Â 5Â years
Greetings from Sun Pharmaceutical Industries Ltd. …!!!!
Important Details :
- Location:Vadodara
- Post of date:17/09/2024
- 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:
Walk-In Date:Sunday, 22nd September’ 2024
Time:10:00 am to 3:00 pm
Venue: Sun Pharmaceutical Ind Ltd., Sun Pharma Road, Tandalja, Vadodara 390012
Job description
Walk in Drive Baroda
Department: Analytical Development
Garde: Executive/ Senior Executive
Experience range 2 to 5 years (in R&D Analytical Development)
Job Description-Â Analytical Non Oral
Experience in pharmaceutical industries with ADD department with bench work and documentation.
- Knowledge of method optimization & validation of analytical methods Using instrument like HPLC, GC, UC Autotitrator.
- Basic computer knowledge like word, Excel, power point.
- Knowledge of GMP and Pharmaceutical Guideline.
Job Description-Â Analytical Oral
Analysis and reporting of Analytical method validation, method verification and method transfer.
Calibration of instruments
Preparation of method transfer / co-validation intimation/ protocol/ report/ /waiver/certificate generated in laboratory.
Make availability of document package (Specification, STP and pre-validation reports and related follow-up as and when required.
Make availability of Procurement of logistics for method validation / method transfer or batch analysis
Timely query response with the help of section head and R & D Quality.
Oral / written communication with internal / external persons at the time of protocol & report etc. preparation.
Document submission for the product registration.
Training and development activities.
Maintain cleanliness and housekeeping of the working area.
Any other responsibilities assigned by Department head/Designee from time to time orally or in writing.
Preparation of Protocols/ Reports / Documents generated in Laboratory
Preparation of SOP
Online data, log books review on shop floor
Training and development to new analyst for analysis
- Daily monitoring of laboratory activities for the compliance against GMP
- Follow and maintaining GMP during analytical activities
Disclaimer – Sun Pharma does not seek payment of any kind from 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 him/her self to be part of Sun Pharma.
