UMEDICA is one of the leading manufacturer of pharmaceutical formulations & export house in India, offering a broad spectrum of chronic and acute therapies. UMEDICA Laboratories Pvt Ltd. was founded in 1982 by late Mr. Umed Doshi, a dynamic entrepreneur whose vision is being spurred further by the able leadership of his son, Mr. Manish Doshi – a true technocrat and an aggressive marketeer.
- Vacancy details:
- Department: Officer To Executive For Quality Control
- Qualification: B.Sc , MS/M.Sc(Science)
- Experienced: 2 – 7 years
- Salary:₹Not Disclosed
Job Description: Greeting from Umedica Labs .!!!!!
- Important Details :
- Location:Vapi
- Post of date :05/08/2024
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face to face
- Interview Rounds of Interview: HR
Walk-In Interview
Date : 11th August 2024 (Sunday)
Timing : 9.00 AM to 2.00 PM
Venue : Umedica Laboratories Pvt, Ltd.
Plot No 221, II Phase GIDC Nr Morarji Circle, Vapi 396195.
1. Quality Control
Position: Officer ,Sr.Officer & Executive.
Qualification: MSc Analytical Chemistry , Organic Chemistry and Msc Micro
Experience: 2 to 10 years
No. of Vacant Position: 20
Analyst:
Candidates having educational qualification of BSc/MSc with specialization in Chemistry. Organic chemistry/Analytical chemcistry with experience of 2 to 7 years in Quality control departments. Working exposure in HPLC, GC, UV Vis spectrophotometer, FTIR, Melting point, Dissolution Apparatus etc with regulatory exposure of USFDA/MHRA/EU/Brazil ANVISA/TGA/WHO audit.
- To analysis and documentation of Finished products and Stability samples as per good documentation practices,
- Knowledge of Good laboratory practices as per regulatory requirements,
- Knowledge of Operation and calibration of Analytical balance, PH meter, HPLC, GC, LCMS and other QC instruments,
- Knowledge of Investigation of Laboratory Incident, Out of Specification results and OOT related to analytical results obtained in Quality Control Department.
- Handling and operational knowledge of Chromeleon 7.2.
Reviewer-QC:
Candidates having educational qualification of BSc/MSc with specialization in Chemistry. Organic chemistry/Analytical chemistry with experience of 7 to 10 years in Quality control departments. Working exposure in HPLC, GC, UV Vis spectrophotometer, FTIR, Melting point, Dissolution Apparatus etc with regulatory exposure of USFDA/MHRA/EU/Brazil ANVISA/TGA/WHO audit.
1. Knowledge of Investigation of Laboratory Incident, Out of Specification results and OOT related to analytical results obtained in Quality Control Department
2. Preparation of SOPs , STPs, Stability protocols/report and Standard.
3. Responsible for the Calibration and qualification of laboratory instruments.
4. Preparation of Method Transfer / Method Validation / Verification, Innovator and Multimedia Dissolution Samples Analytical Protocol and Reports.
5. Proficient in handling of HPLC, UV spectrophotometer, GC.
6. Knowledge of Sampling & Analysis of Raw Materials, Finished goods and Stability.
7. Capable to supervising analytical work and documentation as per 21 CFR Part 11 compliance requirements.
8. Handling and operational knowledge of Chromeleon 7.2 and SAP.
Kindly carry below listed documents during interview.
1. Latest Passport size photo
2. Latest updated resume
3. Xerox copy of Qualification Certificates
4. Salary Slip / Appointment letter copy of current company / CTC Proof
