Biodata |
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| Name of the Candidate | : | [Private] |
| Name of the Post Applied | : | Quality Assurance Officer |
| Job related skills / software | : | Sampling Of Intermediate & Finished Products As Per Sop, Online Documentation, In Process Parameter Checking & Monitoring Of Fabrication, Filling, Compression And Packaging Operations. |
| Category | : | Medical |
| Sub Category | : | Quality Assurance Executive |
| Years of Experience | : | 6 years |
| State | : | West Bengal |
| Gender | : | Male |
| Salary Expected per Month(Rs) | : | Negotiable |
| Highest Qualification attained | : | B.Pharm. : Bachelor of Pharmacy |
| Major / Specialization | : | Pharmacy |
| Email Id | : | [Private] |
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| Are you looking for job now? | : | No |
| Can the recruiter contact you? | : | No |
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Objective :
Professional skills :
Being a pharmacy graduate, experienced in manufacturing of tablets, capsules and dry syrups shall be looking forward to join a company that offers good learning exposures and rewarding career opportunities.
Good at diagnosing problems
Quick decision making & implementation
Aggressive & result oriented outlook
Good inter personal skills & leadership qualities
Computer literacy
Education :
2007 B.Pharmacy with 73.33% marks from Gupta college of Technological Sciences, under West Bengal University of Technology
Experience :
September 2007till date : Ranbaxy Laboratories Ltd. as Sr.QA Officer.
Gross Annual Renumeration3.24lacs per annum
Current Job Profile :
Working as a Senior QA officer in USFDA approved facility & undergoing following job activities.
Handling of change control/deviation tracking follow up and closure
Cleaning validation sampling.
Calibration of laboratory instruments in IPQA laboratory.
Certification of BPRs at all respective stages & identifying deviations if any, for compliance.
Monitoring of formulated products against stipulated conditions mentioned in Batch production record
Sampling of intermediate & finished products as per SOP, online documentation , in pro
cess parameter checking & monitoring of fabrication, filling, compression and packaging operations.
Line clearances and coding approval.
Collection of control and stability sample.
Tracking of stability samples for submission of annual addition , change control/deviation , commitment batches and DRA requirements.
Tracking of validation batches on shop floor & their sampling as per protocol.
Ensuring online documentation of ongoing production activities as per cGMP guidelines.
Face audits by USFDA, ANVISA Brazil, UKMHRA, WHO.
SOP’s review and other document preparation as per international auditory requirement
Professional Exposure :
Key Areas :
Assist research & development time to time in launching various products for regulatory markets
Attended time to time various training programs conducted by the company pertaining with cGMP guidelines & standard operating procedures.
All time readiness for External Audits and surprise internal audits.
Compliance of cGMP training for all plant personnel as per calendar
To boost morale in all the plant personnel
Personal Profile :
Marital status Unmarried
Languages known English, Hindi, Bengali.
Project :
A major project on Noble Drug Delivery System in B.Pharmacy VIII semester.
Interested Areas :
QA, VALIDATION
Date :
Place :
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