Friday, 7 December 2018

USV PHARMA LIMITED, Walk-In Interview on 09th December for production and R&D Department ,Nerul, Navi Mumbai, Maharashtra

Department: Analytical Research Laboratory (Position Code: ARL1)

Location: Govandi (Mumbai)
Position: Research Analyst / Sr. Research Analyst (Multiple Vacancies)
Experience : 2+ years
Qualification : M.Sc (Chemistry)
Job profile:
Method development/ Method optimization
Method Validation/ Verification/ Comparison
Routine Analysis
cGMP related documentation
Other details: 
Candidates should have exposure of regulatory audits like USFDA, MHRA etc.
Interested applicants may send their resumes to deepti.joshi@usv.in
Department: Drug Delivery and Research Laboratory (Position Code: DDRL1 )
Location: Govandi (Mumbai)
Position: Research Pharmacist
Experience : 2+ years
Qualification : M. Pharm
Position Code: DDRL
Job profile:
Formulation development of modified / immediate release dosage forms for Regulated Markets.
Technology transfer to manufacturing location.
Documentation-review of PDR, QOS, Batch documents like BMR, Process validation protocol, Cleaning validation protocol, etc.
Other details: 
Candidates should have exposure of regulatory audits like USFDA, MHRA etc. Exposure to the QBD methodology and experience in Solid orals or Parenterals will be highly preferred. 
Interested applicants may send their resumes to reena.bhole@usv.in
Department: Biologics Research Laboratory – Quality Assurance (Position Code: BRL1)
Location:MIDC Industrial Area, Shiravane, Nerul, Navi Mumbai, Maharashtra 400706 
Position: Officer / Executive / Sr. Executive
Experience : 2+ years
Qualification : Graduate or Post Graduate in Biotechnology / Biochemistry / Microbiology / Chemistry / Pharmacy.
Job profile:
Knowledge of validating processes like fermentation, purification using chromatography techniques etc.
Well versed with line clearances, issuance & retrievals of documents.
IPQA monitoring of the processes and reporting deviations and non-compliance’s
Reviewing of batch records, clean utilities and coordinating for internal audits.
Cleaning validations, CIP and SIP validations etc.
Experience in failure investigations, in-process data reviews and qualifications of process equipments
Other details: 
Candidates should have experience of GMP.
Interested applicants may send their resumes to kajal.bhanushali@usv.in

AUROBINDO PHARMA LTD - WALK-IN Interviews on 9th December, 2018 @ Hyderabad


Thursday, 6 December 2018

Zydus - Walk-In Interview for QC / QA / Manufacturing / Packing / Warehouse / Engineering / Technician / Operators on 16th December 2018


Encube Ethicals Pvt. Ltd - Walk-In Interview for Analytical Experienced Professionals on 7th December 2018


Alembic Pharma Ltd - Walk-In Interviews on 8th December 2018 for QC / QA / Microbiology

Alembic Pharmaceuticals is looking for competent personnel to be an integral part of our Quality team for our new Formulation plant based at Karakhadi / Panelav in Vadodara, Gujarat.
Below are the details.
Venue:
Alembic Pharmaceuticals Ltd,
Corporate Office
3rd Floor, HRM Division,
Admin Building,
Opp. Bhailal Amin General Hospital,
Gorwa Road, Vadodara
Date & Day: 8th December 2018, Saturday
Time: 9:00 AM to 12:00 Noon
Experience: 2 to 6 years
Qualification: B.Pharm / M.Sc / M.Pharm
Job Openings:
Executive: Quality Control (IP/FP & Stability)
Responsibilities:
- Analysis of in-process, finished & stability samples of formulation-oral solids/injectable products.
- Preparation of stability protocols & handling of stability chambers.
- Exposure on analysis of process validation, hold time study and cleaning verification samples analysis
- Handling of QC instruments like HPLC, UV, KF, etc.
- Analysis of Reconstitution/Diluent Compatibility/In-use/Water loss studies
Executive: Quality Assurance (Analytical QA & Validation)
Responsibilities:
- Review of method validation/verification/transfer protocol and reports.
- Review of Specification, Analysis Report, Standard test procedure, Record of Analysis, General Test Procedure and Logbooks.
- Review of Water Reports, Raw Material, Packaging Material, In-Process, Finished Product and Stability analytical data.
- Review of analytical data in SAP.
- Review of analytical data in LIMS.
- Verification of electronic data generated at laboratory during testing.
- Laboratory instrument audit trail review.
- Handling of laboratory investigation.
- Review of SOP and Instruments Operating and calibration.
- Review and Verification of qualification/validation package for equipment / instrument.
- Verification of computer system validation data.
- Review of Calibration data.
- Review and impact evaluation of deviation and change control.
Executive: Microbiology
Responsibilities:
- Environmental Monitoring of Microbiology Laboratory and Manufacturing area.
- To carryout water sampling activities
- Preparation of trends for Environmental Monitoring and Water Quality Monitoring.
- To participate in Media Fill Activity.
- To participate in HVAC qualification of Microbiology Laboratory as well as manufacturing area.
- Qualification of Microbiology laboratory equipments as per the approved protocols as per requirement.
Preparation of Environment Monitoring and Water sampling related SOPs, Protocols and IOCPs.
To follow the Good Laboratory and Good Documentation Practices.
Coordinating with the Environment Monitoring team members and cross functional teams for better productivity.
- To prepare the trends as per the applicable frequency for Environmental Monitoring.
- Responsible for disposal and decontamination of used/expired media & Microbial Culture as per the defined procedures.
- Interested professionals matching the requirement may join us for Personal Interviews on 8th December '18 @ 9:00 AM.
Regards,
Alembic HR team

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