Hetero walk-in Drive 1st to 8th May 2023 Bpharm,Mpharm Freshers & experience

SWARNALATHA B

Apr 28

Hetero Drugs Walk In Interview 2023. Hetero Drugs Notification full details below.Interested and eligible candidates can attend interview on scheduled time and venue.Hetero is an Indian pharmaceutical company and the world's largest producer of anti-retroviral drugs. It is also among the world's leading producers of key Active Pharmaceutical Ingredients with presence in 145+ countries and backed by 30 years of experience in the pharma sector.

Vacancy details:

Department: QUALITY ENGINEER
Qualification: B.Pharma in Pharmacy/M.Pharma in Pharmacy
Experienced: 0-3 yrs
Salary: ₹ 2-4 Lacs P.A.

Job Description: Greetings from HETERO LABS LIMITED.. !

Important Details :

Location:Baddi
Post of date:28/04/2023
Selection Process: The selection will be on the basis of Interview.
Mode of Interview: Face To face Interview
Interview Rounds of Interview: HR

Walk-in Interview Details

30th April - 8th May, 9.30 AM - 1.00 PM

Hetero labs Limited, Unit III(Formulation division) Factory: Kalyanpur (Vil), Chekkan Road, Tehsil Baddi, Solan(Dist) H.P, India - 173205

Contact - M Harishwar Goud (9182806108)

Description of the Quality Control in Pharmaceutical Industry

The Quality control in Pharmaceutical Industry is responsible for the following activities:

Sampling & analysis of Raw materials, IPQC Samples, Packaging Materials and Finished Products.
Documentation related to sample handling and analysis.
Preparation & review of Specifications and test procedures for Raw materials, In- process samples,
Finished
Products and Packaging materials.
Preparation & review of QC SOPs.
Investigation of QC failures
Calibrations of the instruments and equipment in the QC laboratory.
Stability testing.
Ensuring GLP in laboratory
Incoming, In-Process & Final Inspection of products.
Internal Calibration of equipments.
Management of laboratory equipments.
Management of samples.
Management of inspection and calibration records.
Review and approve the Specification and Standard testing procedures.
Review and approve the Calibration record.
Review and approve the working standard qualification record.
Analysis of raw materials/packaging materials/In Process & Finished Products as per the Specification and standard test procedure. View and approve the volumetric solution preparation and standardization record
Analytical Raw Data and Report of Raw material, in-process, semi-finished and finished product.
Specification/STP/GTP/TDS of Raw Material /Packaging materials /In Process & Finished Products.