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. Since its inception, UMEDICA has established itself as a company delivering products meeting international quality standards. UMEDICA is a Government recognized Export House, with global business in over 85 countries viz US, EU, Canada, Australia, Middle East, Central & South American countries, Africa, Asian & CIS countries.
UMEDICA Laboratories Walk-In Interview
- Department:QC/ OSD Packing
- Qualification: B.Sc / M.Sc / B.Pharm / M.Pharm / ITI / Diploma
- Positions : Officer To Executive
- Experience : 02 to 07 Yrs.
- Job Location: Vapi
- Openings: 30
Time and Venue
2nd June , 9.00 AM – 2.00 PM
Venue : Umedica Laboratories Pvt, Ltd. Plot No 221, II Phase GIDC Nr Morarji Circle, Vapi 396195.
Contact – Nikhil Patil
Job description
1. Tablet Packing Department:
- Should have sound knowledge in SOPs, BPR, Line Clearance, Daily formats &records, Manpower Handling GDP, GMP.
Position: Officer to Sr. Officer
Qualification: B.Pharma / M.Pharma
No. of Vacant Position: 20
Experience: 2 to 5 years
- (To Operate Blister Pack Machine ELMACH 3015 PDA machine/ IC 150C / WKH100 Cartonator machine/ Track and Trace machine with Temper Evident., CVC Line)
Position: Technical Associates (Operator)
Qualification: ITI / Diploma
Experience: 2 to 5 years
No. of Vacant Position: 20
2. Quality Control
Position: Officer , Executive , Sr Executive
Qualification: MSc Analytical Chemistry , Organic Chemistry and Msc Micro
Experience: 2 to 12 years
No. of Vacant Position: 25
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 12 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
