Saturday, 6 June 2020

Sun Pharmaceutical Recruitment 2020 | Careers | Job For Freshers, QA, QC, Production, MR

Sun Pharmaceutical Recruitment 2020 | Career | Job Openings For Freshers
Welcome to the pharma job portal. here we are providing Sun Pharma Recruitment details. read all the details carefully before apply to any post.

Sun Pharmaceutical Recruitment 2020 | Careers





SUN PHARMA - Golden Opportunity for Freshers || Interviews for B.Pharm / B.Sc / M.Sc / B.E (Electronics, Electrical, Instrumentation) / ITI / Diploma Freshers - Apprenticeship on 15th - 20th June' 2020



Golden opportunity for Freshers
to start a career with the world's top-rated Pharmaceutical Company under the National Apprenticeship scheme in Dewas Location...


Interview Dates: From 15-Jun-2020
to 20-Jun-2020 Daily @ 02:00 pm
Call for Interview details
07272-496774
07272-496131
08878879188
Or share your resume on
manishkumar.kushwaha@sunpharma.com
Qualification & Stipend per Month Details-
ITI (Electrician, Fitter, Machinist, Turner, AOCP)
Stipend - Rs. 9459 + Rs.700 (Attendance Bonus)
Diploma (Electronics, Instrumentation, Electrical, Pharmacy)
Stipend - Rs. 10000/-
B.Sc. (Chemistry Subject Must)
Stipend - Rs. 10000/-
M.Sc. (Chemistry) / M.Sc. (Microbiology)
Stipend - Rs. 12500/-
B.Pharmacy
Stipend - Rs. 12500/-
B.E. (Electronics, Electrical, Instrumentation)
Stipend - Rs. 12500/-
Note:
* Entry strictly prohibited without Mask due to COVID-19.
* Vacancies are only for 2017 / 2018 / 2019 / 2020 Batch Passed-Out Candidates
* Documents- Fresher's Resume, 10th, 12th, Final Semester Marksheet, PAN Card, Adhar Card, Passport Photograph + Ballpen
* Interview-Based Selections only
* No Commission Charges


Regards,
Manish / Chandan
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Sun Pharma – Job Opening for OFFICER / SR. OFFICER – QUALITY CONTROL
Vacancy Details:- 

Post:- OFFICER / SR. OFFICER – QUALITY CONTROL
Req. Experienced:- 3 – 7 Yr
Qualification:- B.Sc – Chemistry, MS/M.Sc(Science)
Total Opening:- 5
Job Location:- Dadra and Nagar Haveli

Job Description
Expertise in handling of Deviations, OOS (Out of Specification), OOT (Out of Trend), CAPA (Corrective Actions and Preventive Actions) Management, Audit trail review of Instruments.
Document Management for QC & QA.
Check the Practices against GLP.
Internal Audits of QC Department as well as cross-functional departments.
To Monitor and ensure appropriateness of analytic activities during analysis.
Lab Compliance (Lab Instrument’s audit trail review, procedural compliance verification, Lab round, and verification of online QC Activities.
Approval of Method and Specification in LIMS
                             Apply online

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Sun Pharma – Job Opening for EXE / SR EXE – R&D ( FORMULATION DEVL – INJECTABLE )
Vacancy details:

Post Name: EXE / SR EXE – R&D

Qualification: M.Pharm.

Experienced:3 – 6 yrs

Location: Vadodra

Job Description
M.Pharm. (Pharmaceutics) with about 3 – 6 yrs experience in R&D product development with injectable product development that includes liquid, lyophilized and complex injectables.
1. To conduct Literature search and Patent search for assigned project.
2. To procure raw materials (API / excipients), packaging materials and innovator samples in consultation with packaging/purchase department.
3. To fill form 29 for the grant of manufacturing license for the purpose of Examination, Testing and Analysis.
4. To perform pre-formulation and formulation development trials with QbD approach and therefore to develop a robust formulation.
5. To manufacture batches for stability studies and write experiments in Laboratory Notebook.
6. To prepare Technology Transfer documents like MF, Development Study Report, Risk Assessment and FMEA.
7. To review analytical reports and prepare compilation sheet and discuss results with superior.
8. To co-ordinate with cross-functional departments like ADD, RA, QA, Plant for project/product related activity.
9. To prepare SOP’s related to systems and laboratory equipment’s
10. To be familiar with regulatory guidelines.
11. To execute scale up/ exhibit batches in support with superior.
12. Comply with the systems and SOP’s while execution of experiments.
13. To prepare stability protocol and load the stability batches
14. Review the stability batches data and report preparation.
15. Preparation of specification proposal with justifications
16. Address the regulatory queries

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