Malladi was founded in the year 1980 by Mr. Malladi Lakshmi Narayana Sastry and a group of scientists and technologists.Within a short span of time, it grew up to become the leader in manufacturing Ephedrine and Pseudoephedrine salts.Malladi has evolved as a knowledge driven company while testing the limits of its research capabilities. Its reliable customer base and cost effective manufacturing capabilities has grown into a successful player in the market.
- Vacancy details:
- Department:Quality Control Officer
- Experience:2 – 6 years
- Qualification: B.Sc in Bio-Chemistry, Chemistry, B.Pharma in Any Specialization, B.Tech/B.E. in Chemical PG: MS/M.Sc(Science) in Chemistry
Greetings From Malladi Drugs & Pharmaceuticals Ltd … !!
- Important Details :
- Location:Ranipet
- Post of date:29/07/2024
- 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: 29 July – 7th August
Time: 10.00 AM – 4.30 PM
Venue: Malladi Drugs & Pharmaceuticals Ltd., Unit-3 No.7B & 7C, SIPCOT Industrial Complex, Ranipet – 632 403
Job description
Role & responsibilities
- Ensuring the cleanliness and housekeeping activities in the laboratory.
- Ensuring the laboratory safety.
- Sampling of Raw material, Finished products, Packing material, Intermediates, Stability sample, Elemental analysis sample and XRD sample.
- Calibration of analytical instruments like Analytical balance, pH meter, Polorimeter, Conductivity, FTIR, UV, Metrohm Autotitrator, Melting point apparatus, Malvern Particle size 3000, Alpine sieve jet analyzer, EMS and Bulk density apparatus.
- Analysis of Finished products test like solubility, identification by IR/UV, Optical rotation, Assay by Manual/Autotitrator, TLC, Particle size, Bulk density, LOD and Sulphated Ash.
- Daily Temperature & Humidity monitoring wet lab.
- Daily Temperature & Humidity monitoring for Refrigerator.
- Analysis of Vendor samples as part of vendor qualification.
- Other unit sample analysis.(M1 & M5)
- Preparation and standardization of laboratory volumetric solutions.
- Preparations of laboratory reagents
Preferred candidate profile
- Analytical Chemistry
- Documentation skills
- GMP, cGMP/ GLP Skills
- Interpersonal skills
- 5S skills( Sort, Straighten, Shine, Standardize& Sustain)
- Vacancy details:
- Department: Documentation Executive/AM – Production(API)
- Experience:3 – 7 years
- Qualification: B.Sc, B.Pharma, B.Tech/B.E., MS/M.Sc(Science) in Chemistry
Job description
Role & responsibilities
- To monitoring all the operations done as per SOP and cGMP
- To verify the batch production records, log book and other records are filled properly
- To involve improvement activities
- To train the production personnel for new SOPs before effective dates
- To co-ordinate with other departments
- To prepare and execute validations as per protocols
- To prepare validation reports
- To prepare Batch production records, Master instructions and SOPs
- To prepare monthly reports.
Preferred candidate profile
Documentation skills
- cGMP operations
- Supervisory skills
- Production Scheduling
- Knowledge in MS word, MS Excel and Power point
