Explore
New Horizons with Amneal
Company:
Amneal Pharmaceuticals
Walk-In Date: 8th October, 2016 (Saturday)
Walk-In Date: 8th October, 2016 (Saturday)
We
are looking for competent, dynamic and motivated candidates for suitable
positions for Injectable & OSD (oral solid dosage) unit for our Ahmedabad
SEZ Matoda Plant.
Venue:
Amneal
Pharmaceuticals Pvt. Ltd,
5th
Floor,
Venus
Atlantis Corporate Park,
Behind
Shell Petrol Pump,
Near
Prahladnagar Garden,
Ahmedabad
Please
find the details of openings for our various departments:
OSD Unit:
-Analytical
Research & Development (ARD/ADL- OSD)
-Manufacturing (OSD Tablet /Capsules)
-Manufacturing (OSD Tablet /Capsules)
Injectable unit:
-Quality
Assurance (Injectable/Parenteral IPQA & QMS only)
Please
find the detail job specification for all the above mentioned vacancies:
Officer/Sr.
Officer/Executive/Sr. Executive: Analytical Research & Development (ARD/ADL
OSD):
Qualification: M.Sc. (Analytical Chemistry)/ B.Pharm/M.Pharm
Experience: 02 to 08 years
Desired Profile
-Openings are for various groups in ARD like Exploratory, Method development ,Raw Material Analysis, Routine & in process sample analysis, Stability group, Release group, Validation and Regulatory documentation group.
-Candidates working in QC Stability can also apply for ARD/ADL OSD.
Qualification: M.Sc. (Analytical Chemistry)/ B.Pharm/M.Pharm
Experience: 02 to 08 years
Desired Profile
-Openings are for various groups in ARD like Exploratory, Method development ,Raw Material Analysis, Routine & in process sample analysis, Stability group, Release group, Validation and Regulatory documentation group.
-Candidates working in QC Stability can also apply for ARD/ADL OSD.
Manufacturing
(OSD Tablet /Capsules)
Officer/Sr.
Officer/Executive/Sr. Executive/Operators:
Qualification: B.Pharm/M.Pharm/ITI/Diploma
Experience: 02 to 08 years
Desired profile:
-Candidates should have experience of solid orals granulation, compression, coating and TTS/Sorting, Packing, documentation and should be well versed with cGMP norms of all regulatory.
Qualification: B.Pharm/M.Pharm/ITI/Diploma
Experience: 02 to 08 years
Desired profile:
-Candidates should have experience of solid orals granulation, compression, coating and TTS/Sorting, Packing, documentation and should be well versed with cGMP norms of all regulatory.
Quality
Assurance- Injectable:
IPQA-Injectable:
Qualification:
B. Pharma / M. Pharma
Experience : 02-08 Yrs
Desired Profile :
-Responsible for review of BMR / BPR
-Give Line clearance at shop floor
-Monitoring of different sample collections
-Responsible for reserve sample management, annual review etc
-Responsible for tracking stability sample collection as per protocol.
Experience : 02-08 Yrs
Desired Profile :
-Responsible for review of BMR / BPR
-Give Line clearance at shop floor
-Monitoring of different sample collections
-Responsible for reserve sample management, annual review etc
-Responsible for tracking stability sample collection as per protocol.
Quality
Assurance- QMS INJECTABLE:
Qualification:
B. Pharma / M. Pharma
Experience: 02-08 Yrs
Desired Profile:
-Person should be from parenteral background and should have experience of handling deviations, change controls, market complaint, CAPA, OOS, OOT, Quality risk management (QRM).
-Investigation of deviations, failures and market complaints etc and derive CAPA. Review and impact analysis of Change controls. Review of CAPA, Quality risk managements (for new equipments, new products etc).
-To perform the self-inspection (internal audit) of each department and review of compliance report.
-To prepare the trend of deviation, change controls, self-inspections, CAPA.
Handling of contract service providers. Periodic review and assessment of service provider and agreement.
-Monitoring of documents and follow ups to concern department/persons to ensure timely closing of documents.
-To maintain and prepare of quality index, monthly & half year quality review reports.
-The candidate with good communication and inter personal skills, computer knowledge and exposure to cGMP Knowledge and understanding of regulatory requirement is essential.
Experience: 02-08 Yrs
Desired Profile:
-Person should be from parenteral background and should have experience of handling deviations, change controls, market complaint, CAPA, OOS, OOT, Quality risk management (QRM).
-Investigation of deviations, failures and market complaints etc and derive CAPA. Review and impact analysis of Change controls. Review of CAPA, Quality risk managements (for new equipments, new products etc).
-To perform the self-inspection (internal audit) of each department and review of compliance report.
-To prepare the trend of deviation, change controls, self-inspections, CAPA.
Handling of contract service providers. Periodic review and assessment of service provider and agreement.
-Monitoring of documents and follow ups to concern department/persons to ensure timely closing of documents.
-To maintain and prepare of quality index, monthly & half year quality review reports.
-The candidate with good communication and inter personal skills, computer knowledge and exposure to cGMP Knowledge and understanding of regulatory requirement is essential.
-Candidates
meeting above requirements may walk in for an interview between 9 am to 2 pm on
8th October, 2016.
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