M/s. RAKS Pharma was conceptualized to become a significant API player so as to manufacture & supply APIs & Drugs Intermediate to Regulated & Non-Regulated Market from its present manufacturing site inDahej (Gujarat) India. Raks is an interesting blend of consistency in maintaining both quality standard and growth in terms of addition of new products to its existing list of API’s and intermediates. To realize this goal it has a team of experienced, dedicated and highly motivated professionals in all fields of the business..
- Vacancy details:
- Department: Officer To Executive – QC/Officer To Executive – Production
- Experience: 2 to 8 YearsÂ
- Qualification: B. Pharm,Msc,Mpharm,B.Tech/B.E. in Chemical
- Salary:₹2.5-7.5 Lacs P.A.
Job Description: Greeting from M/s. RAKS Pharma !!!
Important Details :
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Work Location: Bharuch, Dahej, Ankleshwar
- Post of date 03/12/2024
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face to face
- Interview Rounds of Interview: HR
Time and Venue
8th December , 9.00 AM – 6.00 PM
Hotel Lords Plaza, GIDC, Old National Highway No. 8, Near Ankleshwar Railway Station, Ankleshwar –393 002  (View on map)
Contact – HR Department Â
HPLC Analyst, Operation of HPLC, Troubleshooting, Analysis of all In-process, Intermediates, RM, PM, Finish Product, Stability samples and other analytical samples of lab. Operation of GC, IR, UV, KF, Auto titrator, SOR and Wet Lab analysis.
Preferred candidate profile
Minimum 2 to 7 Years of experience required
Perks and benefits
Best in the Industry
Role & responsibilities
- Responsible for all process operation / activities during the shift as per CGMP.
- To maintain BMR/BPR/BCR etc. for record the batches.
- To co-ordinate with engineering department for the shift break down jobs.
- To monitor the utility operation in the plant and report any abnormality to concern department.
- To handle manpower during the shift as per process operations.
- To work in safe work environment and ensure the sub ordinate are working in safe condition.
- To check before charging of batch, visual verification of cleanliness status of process equipment.
- To maintain good housekeeping in respective area.
- To co-ordinate for the raw material from warehouse for issuing the raw materials.
- To co-ordinate to QC dept. for In- process and Intermediate testing.
- To fill the entire document legible.
- To record and maintain all the documents online as per CGMP.
- To monitor and record temperature, Humidity and differential pressure in clean area (Level-I, Level-II & III).
- To check and record daily weighing balance calibration and verification.
- To review all filled documents after completion of activity and submitted to quality assurance department.
Preferred candidate profile
Education : B.E or B.Tech Chemical Engineering with 1 to 5 Year Experience
Perks and benefits
Best in the Industry
