AMIT SHARMA's Profile
AMIT SHARMA | |
Head of Department (QA, GxP), World leading Pharmaceutical's organisation | |
 | World leading Pharmaceutical's organisation  |
Professional summary
To apply the concept hitherto learnt, continue with my learning process and climb thecorporate ladder in the field of latest Analytical technology by dint of multi skilled task, hard work, sincerity, dedication and pursue a career of challenge and responsibility in Quality assurance/continuous improvement.
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Current Experience:
Head of Department (QA, GxP), World leading Pharmaceutical's organisation
Current Experience: Grade Deputy General Manager, Alkem Laboratories Limited
Previous: Grade Deputy General Manager, Alkem Laboratories Limited
Grade Deputy General Manager, Alkem Laboratories Limited
Grade Deputy General Manager, Alkem Laboratories Limited
Grade Deputy General Manager, Alkem Laboratories Limited
1. Ranbaxy Laboratories Limited
Designation Deputy General Manager, Period Employed
Designation Deputy General Manager, Period Employed
Designation Deputy General Manager, Period Employed
DEPUTY GENERAL MANAGER, HEALTH BIOTECH LTD.
Designation Deputy General Manager, Period Employed
Designation Deputy General Manager, Period Employed
Designation Sr. Manager, Period Employed
Designation Sr. Manager, Period Employed
Designation Sr. Manager, Period Employed
Designation Sr. Manager, Period Employed
Designation Sr. Manager, Period Employed
Designation Sr. Executive, Period Worked
Designation Sr. Executive, Period Worked
Designation Sr. Executive, Period Worked
Designation Sr. Executive, Period Worked
Designation Sr. Executive, Period Worked
Designation Production Associate, Period Worked
Designation Production Associate, Period Worked
Designation Production Associate, Period Worked
Designation Production Associate, Period Worked
Designation Production Associate, Period Worked
Period Worked
Period Worked
Period Worked
Period Worked
Period Worked
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Gurukula Kangri Vishwavidyala, Hardwar, (Uttranchal)
Gurukula Kangri Vishwavidyala, Hardwar, (Uttranchal)
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16.5 Years
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Quality Assurance (Continuous Improvement), Business Excellence, Contract manufacturing, Third party ...
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2 recommendations
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Contribution score:(137 points)
- Contacts: 19 connections, 20 following, 20 followers
AMIT SHARMA's Experience
| Current : |
Head of Department (QA, GxP), World leading Pharmaceutical's organisation |
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| Pharmaceuticals | ||
| India, Chandigarh | ||
Working from 2009 | ||
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Brief summary :
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| Current : |
Grade Deputy General Manager, Alkem Laboratories Limited |
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Working from 2009 | ||
Brief summary :
1) Alkem Laboratories Limited, Period Employed from July09 to till date. Designation/Grade Deputy General Manager (Quality Assurance/Quality Control, ANDAs, Stability, Technology Transfer-M8 Area of Operation Gangtok (Sikkim) / Baddi / Daman / Taloja (Mumbai) Nature of business Global player in the field of Manufacturing of Non sterile Tablet, Capsule, Sterile Injectables (Dry Powder) with a turn over of 2500 cr. through own leading brand. No.7 ranking in Pharmaceutical formulations. Job responsibilities: Presently Heading Stability section, ANDAs of own regulated products and regulated audit. Leading and Liasoning with statutory bodies like WHO, US-FDA, UK-MHRA, TGA, MCC, Oman, Yemen, Weight and measures, ISO (safety) certifying bodies. Leading and Monitoring independently Packaging Lab for Primary and Secondary packaging materials and their development in accordance with customer requirement. Handling a Team of 40-45 QA/QC Executives/officers, 06 Plant QA/QC Managers, 10 RDI along with a team of 12-14 Associates for GxP, cGMP, international compliance Implementation of on-line inspection system, procedures and maintaining all stipulated systems. Conducting of internal quality audits in the organization to fulfill contract manufacturing requirement. Conducting of external audits at the vendor site, vendor rating and their approvals for cost reduction projects. Implementation of calibration procedures, SOPs, working instructions of all Operational machines as well as QA/QC Lab. Equipments as per regulated market guidelines. Leading a team of 20 Officers and Executives in IPQA/QC/ANDA department. Conducting training classes at all levels. Review of Batch production record and monitoring yield reconciliation. Implementation of Cross functional investigations. Complaint handling and their redressal, product stability studies and product recall system. Implementation of validation and stability studies, also execute Validation Master plan and checking their execution. Implementation of Change/Deviation control procedure by listing out deviations and to implement proper corrective action. Preparation of Raw and Packaging material specifications, test procedure and operational procedures including Master formula. Implementation of market feed back system regarding product quality and stability. Implementation of regularity approvals in Personnel Hygiene System, ISO 9001 (QMS), ISO 14000 (EMS), and WHO-GMP under Schedule M, H, T (in accordance with Drug and Cosmetics Act). Implementation of product release system as per cGLP, cGMP, cGDP. New Research and development activities Technology transfer, Scale Up Batch, Validation and Commercial related to ADL. Commissioning, Validation and verification qualification as per IQ, OQ of all Laboratory equipments and plant machineries. Process and product Validation of Injectables, Tablet, capsules and Liquid syrups. Preparation of Site Master File, Master Batch Records, Updation of BMR, BPR, MBR and GMP files. Review, Release and Approval of Art works of Unit cartons, Labels, Stiffeners, Wrapper, Shipper, Aluminum Foils, Glass vials, Ampoules, HDPE bottle and caps etc. Co-ordination with R and D for Validation, Exhibit batches of our own new product. To set up the In process Quality checks at every level of Process and Audit system. Build up Quality team and consciousness among the business process and each individuals mind. Leading Total Quality Assurance and establishment of Quality control tools. Coordinate for the all Quality activities of QA at HO like planning, IPQA, packaging, Handling of Market complaints, Product Recalls, and their change control to avoid future occurrence. Establishment of Quality Assurance facility and procurement of regulated inspection for new facility. Research, Development and Implementation though Training. (Previous) 2. Health Biotech Limited, | ||
| Previous : |
Grade Deputy General Manager, Alkem Laboratories Limited |
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Worked from 2009 to 2012 | ||
Brief summary :
1) Alkem Laboratories Limited, Period Employed from July09 to till date. Designation/Grade Deputy General Manager (Quality Assurance/Quality Control, ANDAs, Stability, Technology Transfer-M8 Area of Operation Gangtok (Sikkim) / Baddi / Daman / Taloja (Mumbai) Nature of business Global player in the field of Manufacturing of Non sterile Tablet, Capsule, Sterile Injectables (Dry Powder) with a turn over of 2500 cr. through own leading brand. No.7 ranking in Pharmaceutical formulations. Job responsibilities: Presently Heading Stability section, ANDAs of own regulated products and regulated audit. Leading and Liasoning with statutory bodies like WHO, US-FDA, UK-MHRA, TGA, MCC, Oman, Yemen, Weight and measures, ISO (safety) certifying bodies. Leading and Monitoring independently Packaging Lab for Primary and Secondary packaging materials and their development in accordance with customer requirement. Handling a Team of 40-45 QA/QC Executives/officers, 06 Plant QA/QC Managers, 10 RDI along with a team of 12-14 Associates for GxP, cGMP, international compliance Implementation of on-line inspection system, procedures and maintaining all stipulated systems. Conducting of internal quality audits in the organization to fulfill contract manufacturing requirement. Conducting of external audits at the vendor site, vendor rating and their approvals for cost reduction projects. Implementation of calibration procedures, SOPs, working instructions of all Operational machines as well as QA/QC Lab. Equipments as per regulated market guidelines. Leading a team of 20 Officers and Executives in IPQA/QC/ANDA department. Conducting training classes at all levels. Review of Batch production record and monitoring yield reconciliation. Implementation of Cross functional investigations. Complaint handling and their redressal, product stability studies and product recall system. Implementation of validation and stability studies, also execute Validation Master plan and checking their execution. Implementation of Change/Deviation control procedure by listing out deviations and to implement proper corrective action. Preparation of Raw and Packaging material specifications, test procedure and operational procedures including Master formula. Implementation of market feed back system regarding product quality and stability. Implementation of regularity approvals in Personnel Hygiene System, ISO 9001 (QMS), ISO 14000 (EMS), and WHO-GMP under Schedule M, H, T (in accordance with Drug and Cosmetics Act). Implementation of product release system as per cGLP, cGMP, cGDP. New Research and development activities Technology transfer, Scale Up Batch, Validation and Commercial related to ADL. Commissioning, Validation and verification qualification as per IQ, OQ of all Laboratory equipments and plant machineries. Process and product Validation of Injectables, Tablet, capsules and Liquid syrups. Preparation of Site Master File, Master Batch Records, Updation of BMR, BPR, MBR and GMP files. Review, Release and Approval of Art works of Unit cartons, Labels, Stiffeners, Wrapper, Shipper, Aluminum Foils, Glass vials, Ampoules, HDPE bottle and caps etc. Co-ordination with R and D for Validation, Exhibit batches of our own new product. To set up the In process Quality checks at every level of Process and Audit system. Build up Quality team and consciousness among the business process and each individuals mind. Leading Total Quality Assurance and establishment of Quality control tools. Coordinate for the all Quality activities of QA at HO like planning, IPQA, packaging, Handling of Market complaints, Product Recalls, and their change control to avoid future occurrence. Establishment of Quality Assurance facility and procurement of regulated inspection for new facility. Research, Development and Implementation though Training. (Previous) 2. Health Biotech Limited, | ||
| Previous : |
Grade Deputy General Manager, Alkem Laboratories Limited |
|
Worked from 2009 to 2012 | ||
Brief summary :
1) Alkem Laboratories Limited, Period Employed from July09 to till date. Designation/Grade Deputy General Manager (Quality Assurance/Quality Control, ANDAs, Stability, Technology Transfer-M8 Area of Operation Gangtok (Sikkim) / Baddi / Daman / Taloja (Mumbai) Nature of business Global player in the field of Manufacturing of Non sterile Tablet, Capsule, Sterile Injectables (Dry Powder) with a turn over of 2500 cr. through own leading brand. No.7 ranking in Pharmaceutical formulations. Job responsibilities: Presently Heading Stability section, ANDAs of own regulated products and regulated audit. Leading and Liasoning with statutory bodies like WHO, US-FDA, UK-MHRA, TGA, MCC, Oman, Yemen, Weight and measures, ISO (safety) certifying bodies. Leading and Monitoring independently Packaging Lab for Primary and Secondary packaging materials and their development in accordance with customer requirement. Handling a Team of 40-45 QA/QC Executives/officers, 06 Plant QA/QC Managers, 10 RDI along with a team of 12-14 Associates for GxP, cGMP, international compliance Implementation of on-line inspection system, procedures and maintaining all stipulated systems. Conducting of internal quality audits in the organization to fulfill contract manufacturing requirement. Conducting of external audits at the vendor site, vendor rating and their approvals for cost reduction projects. Implementation of calibration procedures, SOPs, working instructions of all Operational machines as well as QA/QC Lab. Equipments as per regulated market guidelines. Leading a team of 20 Officers and Executives in IPQA/QC/ANDA department. Conducting training classes at all levels. Review of Batch production record and monitoring yield reconciliation. Implementation of Cross functional investigations. Complaint handling and their redressal, product stability studies and product recall system. Implementation of validation and stability studies, also execute Validation Master plan and checking their execution. Implementation of Change/Deviation control procedure by listing out deviations and to implement proper corrective action. Preparation of Raw and Packaging material specifications, test procedure and operational procedures including Master formula. Implementation of market feed back system regarding product quality and stability. Implementation of regularity approvals in Personnel Hygiene System, ISO 9001 (QMS), ISO 14000 (EMS), and WHO-GMP under Schedule M, H, T (in accordance with Drug and Cosmetics Act). Implementation of product release system as per cGLP, cGMP, cGDP. New Research and development activities Technology transfer, Scale Up Batch, Validation and Commercial related to ADL. Commissioning, Validation and verification qualification as per IQ, OQ of all Laboratory equipments and plant machineries. Process and product Validation of Injectables, Tablet, capsules and Liquid syrups. Preparation of Site Master File, Master Batch Records, Updation of BMR, BPR, MBR and GMP files. Review, Release and Approval of Art works of Unit cartons, Labels, Stiffeners, Wrapper, Shipper, Aluminum Foils, Glass vials, Ampoules, HDPE bottle and caps etc. Co-ordination with R and D for Validation, Exhibit batches of our own new product. To set up the In process Quality checks at every level of Process and Audit system. Build up Quality team and consciousness among the business process and each individuals mind. Leading Total Quality Assurance and establishment of Quality control tools. Coordinate for the all Quality activities of QA at HO like planning, IPQA, packaging, Handling of Market complaints, Product Recalls, and their change control to avoid future occurrence. Establishment of Quality Assurance facility and procurement of regulated inspection for new facility. Research, Development and Implementation though Training. (Previous) 2. Health Biotech Limited, | ||
| Previous : |
Grade Deputy General Manager, Alkem Laboratories Limited |
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Worked from 2009 to 2011 | ||
Brief summary :
1) Alkem Laboratories Limited, Period Employed from July09 to till date. Designation/Grade Deputy General Manager (Quality Assurance/Quality Control, ANDAs, Stability, Technology Transfer-M8 Area of Operation Gangtok (Sikkim) / Johannesburg, South Africa) Nature of business Global player in the field of Manufacturing of Non sterile Tablet, Capsule, Sterile Injectables (Dry Powder) with a turn over of 2500 cr. through own leading brand. No.7 ranking in Pharmaceutical formulations. Job responsibilities: Presently Heading Stability section, ANDAs of own regulated products and regulated audit. Leading and Liasoning with statutory bodies like WHO, US-FDA, UK-MHRA, TGA, MCC, Oman, Yemen, Weight and measures, ISO (safety) certifying bodies. Leading and Monitoring independently Packaging Lab for Primary and Secondary packaging materials and their development in accordance with customer requirement. Handling a Team of 40-45 QA/QC Executives/officers, 06 Plant QA/QC Managers, 10 RDI along with a team of 12-14 Associates for GxP, cGMP, international compliance Implementation of on-line inspection system, procedures and maintaining all stipulated systems. Conducting of internal quality audits in the organization to fulfill contract manufacturing requirement. Conducting of external audits at the vendor site, vendor rating and their approvals for cost reduction projects. Implementation of calibration procedures, SOPs, working instructions of all Operational machines as well as QA/QC Lab. Equipments as per regulated market guidelines. Leading a team of 20 Officers and Executives in IPQA/QC/ANDA department. Conducting training classes at all levels. Review of Batch production record and monitoring yield reconciliation. Implementation of Cross functional investigations. Complaint handling and their redressal, product stability studies and product recall system. Implementation of validation and stability studies, also execute Validation Master plan and checking their execution. Implementation of Change/Deviation control procedure by listing out deviations and to implement proper corrective action. Preparation of Raw and Packaging material specifications, test procedure and operational procedures including Master formula. Implementation of market feed back system regarding product quality and stability. Implementation of regularity approvals in Personnel Hygiene System, ISO 9001 (QMS), ISO 14000 (EMS), and WHO-GMP under Schedule M, H, T (in accordance with Drug and Cosmetics Act). Implementation of product release system as per cGLP, cGMP, cGDP. New Research and development activities Technology transfer, Scale Up Batch, Validation and Commercial related to ADL. Commissioning, Validation and verification qualification as per IQ, OQ of all Laboratory equipments and plant machineries. Process and product Validation of Injectables, Tablet, capsules and Liquid syrups. Preparation of Site Master File, Master Batch Records, Updation of BMR, BPR, MBR and GMP files. Review, Release and Approval of Art works of Unit cartons, Labels, Stiffeners, Wrapper, Shipper, Aluminum Foils, Glass vials, Ampoules, HDPE bottle and caps etc. Co-ordination with R and D for Validation, Exhibit batches of our own new product. To set up the In process Quality checks at every level of Process and Audit system. Build up Quality team and consciousness among the business process and each individuals mind. Leading Total Quality Assurance and establishment of Quality control tools. Coordinate for the all Quality activities of QA at HO like planning, IPQA, packaging, Handling of Market complaints, Product Recalls, and their change control to avoid future occurrence. Establishment of Quality Assurance facility and procurement of regulated inspection for new facility. Research, Development and Implementation though Training. (Previous) 2. Health Biotech Limited, | ||
| Previous : |
Grade Deputy General Manager, Alkem Laboratories Limited |
|
Worked from 2009 to 2011 | ||
Brief summary :
1) Alkem Laboratories Limited, Period Employed from July09 to till date. Designation/Grade Deputy General Manager (Quality Assurance/Quality Control, ANDAs, Stability, Technology Transfer-M8 Area of Operation Gangtok (Sikkim) / Mumbai / Johannesburg (South Africa) Nature of business Global player in the field of Manufacturing of Non sterile Tablet, Capsule, Sterile Injectables (Dry Powder) with a turn over of 2500 cr. through own leading brand. No.7 ranking in Pharmaceutical formulations. Job responsibilities: Presently Heading Stability section, ANDAs of own regulated products and regulated audit. Leading and Liasoning with statutory bodies like WHO-GMP, US-FDA, UK-MHRA, TGA, MCC, Japan, ANVISA Oman, Yemen, Weight and measures, ISO (safety) certifying bodies. Leading and Monitoring independently Packaging Lab for Primary and Secondary packaging materials and their development in accordance with customer requirement. Leading a Team of 40-45 QA/QC Executives/officers, 06 Plant QA/QC Managers, 10 RDI along with a team of 12-14 Associates for GxP, cGMP, international quality compliance for contract manufacturing. Implementation of on-line inspection system, procedures and maintaining all stipulated systems. Conducting of internal quality audits in the organization to fulfill contract manufacturing requirement. Conducting of external audits at the vendor site, vendor rating and their approvals for cost reduction projects. Implementation of calibration procedures, SOPs, working instructions of all Operational machines as well as QA/QC Lab. Equipments as per regulated market guidelines. Conducting training classes at all levels. Review of Batch production record and monitoring yield reconciliation. Implementation of Cross functional investigations. Complaint handling and their redressal, product stability studies and product recall system. Implementation of validation and stability studies, also execute Validation Master plan and checking their execution. Implementation of Change/Deviation control procedure by listing out deviations and to implement proper corrective action. Preparation of Raw and Packaging material specifications, test procedure and operational procedures including Master formula. Implementation of market feed back system regarding product quality and stability. Implementation of regularity approvals in Personnel Hygiene System, ISO 9001 (QMS), ISO 14000 (EMS), and WHO-GMP under Schedule M, H, T (in accordance with Drug and Cosmetics Act). Implementation of product release system as per cGLP, cGMP, cGDP. New Research and development activities Technology transfer, Scale Up Batch, Validation and Commercial related to ADL. Commissioning, Validation and verification qualification as per IQ, OQ of all Laboratory equipments and plant machineries. Process and product Validation of Injectables, Tablet, capsules and Liquid syrups. Preparation of Site Master File, Master Batch Records, Updation of BMR, BPR, MBR and GMP files. Review, Release and Approval of Art works of Unit cartons, Labels, Stiffeners, Wrapper, Shipper, Aluminum Foils, Glass vials, Ampoules, HDPE bottle and caps etc. Co-ordination with R and D for Validation, Exhibit batches of our own new product. To set up the In process Quality checks at every level of Process and Audit system. Build up Quality team and consciousness among the business process and each individuals mind. Leading Total Quality Assurance and establishment of Quality control tools. Coordinate for the all Quality activities of QA at HO like planning, IPQA, packaging, Handling of Market complaints, Product Recalls, and their change control to avoid future occurrence. Establishment of Quality Assurance facility and procurement of regulated inspection for new facility. Research, Development and Implementation though Training. (Previous) 2. Health Biotech Limited, | ||
| Previous : |
1. Ranbaxy Laboratories Limited |
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Worked from 2002 to 2011 | ||
Brief summary :
n Sterile Formulation (100% Regulated Export - Pharmaceutical) Duration : July 2002 - Till date (continued)1. Ranbaxy Laboratories Limited, Period Employed from June 02 till date. Designation Sr. Manager (Quality Assurance) Area of Operation Paonta Sahib (Himachal Pradesh) Nature of business Multicrore formulation MNC set on a high growth path specializing in Non sterile Formulation tablet, Soft hard gelatin capsules with Modern sophisticated 100% Export plant, Regulated by US-FDA, UK-MHRA, SA-MCC, Aust. - TGA, JAPAN, Brazil-ANVISA, Uganda - NDA, Canada - TPP, Europe-EMEA and WHO- GMP regulatory and non regulated markets. Job Responsibilities: 1) Presently working on technology transfer for contract manufacturing of products at various vendors. 2) Monitoring independently laboratory of Primary, Secondary packaging materials and their development. 3) Implementation of on-line inspection system and procedures. 4) Conducting of internal quality audits in the organization to fulfill contract manufacturing requirement. 5) Conducting of external audits at the vendor site, vendor rating and their approvals for cost reduction projects. 6) Implementation of calibration procedures, SOPs, working instructions of all Operational machines as well as QA/QC. Lab. Equipments as per regulated market guidelines. 7) Conducting training classes at all levels. 8) Issuing and monitoring Batch production record including yield reconciliation. 9) Implementation of Cleaning system and Cross contamination controls. 10) Implementation of Cross functional investigations. 11) Complaint handling and their redressal, product stability studies and product recall system. 12) Implementation of validation stability study activities and Validation Master plan checking their execution. 13) Implementation of Change/Deviation control procedure by listing out deviations and to implement proper corrective action. 14) Preparation of Raw Packaging material specifications, test procedure and operational procedures including Master formula. 15) Implementation of market feed back system regarding product quality and stability. 16) Implementation of regularity approvals in Personnel Hygiene System, OHSAS-18001, ISO 9001 (QMS), ISO 14000 (EMS), USFDA, TGA, MHRA, MCC, ANVISA, WHO-GMP and non regulated. 17) Implementation of product release system, Implementation as per cGLP, cGMP, 18) New Research and development activities related to PDL. 19) Commissioning, Validation verification qualification as per IQ, DQ, OQ, VQ of all Laboratory Equipments plant machineries. 20) Process Validation - LVP, SVP, Anticancer drugs, Tablet, Capsules Injectables (Dry powder). 21) Preparation of Site Master File, Master Batch Records, Updation of BMR, BPR, MBR and GMP files. 22) Release of Batch, Handling of Market complaints, Product Recalls, Designing Approval of Art works of Unit cartons, Labels, Literatures, Shipper, Blister Foils, Aluminum Foils, HDPE, Glass bottles, etc. 23) Co-ordination with PDL (Local ARD) for Validation, Exhibit batches of new product. 24) To set up the Quality, Process and Audit system. 25) Build up Quality team and consciousness among the business process and each individuals mind. 26) Leading Total Quality Assurance and establishment of Quality control tools. 27) Coordinate for the all Quality activities at different locations of planning, production, procurement, packaging complaint control. 28) Establishment of Quality Assurance facility and procurement of inspection for new infrastructure. (Previous) 2. SABOO-BERLAC Limited (a joint venture technical collaboration with Berlac AG, Switzerland) Period Worked from July 00 to June 02 Designation Sr. Executive (QA, QC, Production, ISO certifications). Nature of Business Designer finishes, Speciality Paints, Lacquers, Thinners for industrial purpose. Area of Operation Industrial Area, Chandigarh (Punjab) 3. ICI PAINTS Limited (Indian collaboration with Imperial Chemical Industries, London) Period Worked from Dec.97 to June00 Designation Production Associate (Chemical Product development). Nature of Business Automotive, Refinish, Decorative, Motor Industrial paints and Thinners Area of Operation Industrial Area, Mohali (Punjab) 4. HONEY-BEE NATURAL PRODUCTS Limited (100% Export oriented unit of Dabur Group) Period Worked from Oct.95 to Oct.97 Designation Production cum Approved Agmark Chemist. Nature of Business Export of Bulk Honey processing, honey based Food and ayurvedic products. Area of Operation Lalru, Distt: Patiala (Punjab) Salary Drawing CTC 9.50 Lac. PA Expected Monthly Salary : 25 - 35 % growth in present CTC or as per ur company policy/grade Availability : One month advance notice or Basic salary after receiving offer letter. | ||
| Previous : |
Designation Deputy General Manager, Period Employed |
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Worked from 2008 to 2009 | ||
Brief summary :
Period Employed from Sept. 08 to June `09. Designation Deputy General Manager (Quality Assurance/Control) Area of Operation Baddi (Himachal Pradesh) Nature of business Global player in the field of Contract Mfg. of Sterile Injectables (Dry and Liquid), SVP and LVP Liquid syrup, Anticancer and Personal care products with a turn over of 120 crore through own leading brand and B2B Business of various MNC like Cipla, Nicholas, Sherya Lifescience, Elder, Claris, German Remedies, Panacea Biotech, Blue cross, Piramal, Cadila , Cipla, Alkem etc. 3. Ranbaxy Laboratories Limited, (100% Export oriented unit) | ||
| Previous : |
Designation Deputy General Manager, Period Employed |
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Worked from 2008 to 2009 | ||
Brief summary :
Period Employed from Sept. 08 to June `09. Designation Deputy General Manager (Quality Assurance/Control) Area of Operation Baddi (Himachal Pradesh) Nature of business Global player in the field of Contract Mfg. of Sterile Injectables (Dry and Liquid), SVP and LVP Liquid syrup, Anticancer and Personal care products with a turn over of 120 crore through own leading brand and B2B Business of various MNC like Cipla, Nicholas, Sherya Lifescience, Elder, Claris, German Remedies, Panacea Biotech, Blue cross, Piramal, Cadila , Cipla, Alkem etc. 3. Ranbaxy Laboratories Limited, (100% Export oriented unit) | ||
| Previous : |
Designation Deputy General Manager, Period Employed |
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Worked from 2008 to 2009 | ||
Brief summary :
Period Employed from Sept. 08 to June `09. Designation Deputy General Manager (Quality Assurance/Control) Area of Operation Baddi (Himachal Pradesh) Nature of business Global player in the field of Contract Mfg. of Sterile Injectables (Dry and Liquid), Liquid syrup, Anticancer and Personal care products with a turn over of 120 crore through own leading brand and B2B Business of various MNC like Cipla, Nicholas, Sherya Lifescience, Elder, Claris, German Remedies, Panacea Biotech, Blue cross, Piramal, Cadila , Cipla, Alkem etc. 3. Ranbaxy Laboratories Limited, (100% Export oriented unit) | ||
| Previous : |
DEPUTY GENERAL MANAGER, HEALTH BIOTECH LTD. |
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| Pharmaceuticals | ||
Worked from 2008 to 2009 | ||
| Previous : |
Designation Deputy General Manager, Period Employed |
|
Worked from 2008 to 2009 | ||
Brief summary :
Period Employed from Sept. 08 to June `09. Designation Deputy General Manager (Quality Assurance/Control) Area of Operation Baddi (Himachal Pradesh) Nature of business Global player in the field of Contract Mfg. of Sterile Injectables (Dry and Liquid), SVP and LVP Liquid syrup, Anticancer and Personal care products with a turn over of 120 crore through own leading brand and B2B Business of various MNC like Cipla, Nicholas, Sherya Lifescience, Elder, Claris, German Remedies, Panacea Biotech, Blue cross, Piramal, Cadila , Cipla, Alkem etc. 3. Ranbaxy Laboratories Limited, (100% Export oriented unit) | ||
| Previous : |
Designation Deputy General Manager, Period Employed |
|
Worked from 2008 to 2009 | ||
Brief summary :
Period Employed from Sept. 08 to June `09. Designation Deputy General Manager (Quality Assurance/Control) Area of Operation Baddi (Himachal Pradesh) Nature of business Global player in the field of Contract Mfg. of Sterile Injectables (Dry and Liquid), Liquid syrup, Anticancer and Personal care products with a turn over of 120 crore through own leading brand and B2B Business of various MNC like Cipla, Nicholas, Sherya Lifescience, Elder, Claris, German Remedies, Panacea Biotech, Blue cross, Piramal, Cadila , Cipla, Alkem etc. 3. Ranbaxy Laboratories Limited, (100% Export oriented unit) | ||
| Previous : |
Designation Sr. Manager, Period Employed |
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Worked from 2002 to 2008 | ||
Brief summary :
Period Employed from June 02 to September `08. Designation Sr. Manager (Quality Assurance)-M03 Nature of business Multicrore formulation MNC set on a high growth path specializing in Non sterile Formulation tablet, Soft and hard gelatin capsules withModern and sophisticated 100% Export plant, Regulated by US-FDA, UK-MHRA, SA-MCC, Aust. - TGA, JAPAN, Brazil-ANVISA, Uganda - NDA, Canada - TPP, Europe-EMEA, EU-GMP and WHO- GMP (Geneva) regulatory and non regulated markets. Area of Operation Poanta Sahib, (Himachal Pradesh)/Dewas (MP) 4. SABOO-BERLAC Limited (a joint venture and technical collaboration with Berlac AG, Switzerland) | ||
| Previous : |
Designation Sr. Manager, Period Employed |
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Worked from 2002 to 2008 | ||
Brief summary :
Period Employed from June 02 to September `08. Designation Sr. Manager (Quality Assurance)-M03 Nature of business Multicrore formulation MNC set on a high growth path specializing in Non sterile Formulation tablet, Soft and hard gelatin capsules withModern and sophisticated 100% Export plant, Regulated by US-FDA, UK-MHRA, SA-MCC, Aust. - TGA, JAPAN, Brazil-ANVISA, Uganda - NDA, Canada - TPP, Europe-EMEA, EU-GMP and WHO- GMP (Geneva) regulatory and non regulated markets. Area of Operation Poanta Sahib, (Himachal Pradesh)/Dewas (MP) 4. SABOO-BERLAC Limited (a joint venture and technical collaboration with Berlac AG, Switzerland) | ||
| Previous : |
Designation Sr. Manager, Period Employed |
|
Worked from 2002 to 2008 | ||
Brief summary :
Period Employed from June 02 to September `08. Designation Sr. Manager (Quality Assurance)-M03 Nature of business Multicrore formulation MNC set on a high growth path specializing in Non sterile Formulation tablet, Soft and hard gelatin capsules withModern and sophisticated 100% Export plant, Regulated by US-FDA, UK-MHRA, SA-MCC, Aust. - TGA, JAPAN, Brazil-ANVISA, Uganda - NDA, Canada - TPP, Europe-EMEA, EU-GMP and WHO- GMP regulatory and non regulated markets. Area of Operation Poanta Sahib, (Himachal Pradesh)/Dewas (MP) 4. SABOO-BERLAC Limited (a joint venture and technical collaboration with Berlac AG, Switzerland) | ||
| Previous : |
Designation Sr. Manager, Period Employed |
|
Worked from 2002 to 2008 | ||
Brief summary :
Period Employed from June 02 to September `08. Designation Sr. Manager (Quality Assurance)-M03 Nature of business Multicrore formulation MNC set on a high growth path specializing in Non sterile Formulation tablet, Soft and hard gelatin capsules withModern and sophisticated 100% Export plant, Regulated by US-FDA, UK-MHRA, SA-MCC, Aust. - TGA, JAPAN, Brazil-ANVISA, Uganda - NDA, Canada - TPP, Europe-EMEA, EU-GMP and WHO- GMP (Geneva) regulatory and non regulated markets. Area of Operation Poanta Sahib, (Himachal Pradesh)/Dewas (MP) 4. SABOO-BERLAC Limited (a joint venture and technical collaboration with Berlac AG, Switzerland) | ||
| Previous : |
Designation Sr. Manager, Period Employed |
|
Worked from 2002 to 2008 | ||
Brief summary :
Period Employed from June 02 to September `08. Designation Sr. Manager (Quality Assurance)-M03 Nature of business Multicrore formulation MNC set on a high growth path specializing in Non sterile Formulation tablet, Soft and hard gelatin capsules withModern and sophisticated 100% Export plant, Regulated by US-FDA, UK-MHRA, SA-MCC, Aust. - TGA, JAPAN, Brazil-ANVISA, Uganda - NDA, Canada - TPP, Europe-EMEA, EU-GMP and WHO- GMP regulatory and non regulated markets. Area of Operation Poanta Sahib, (Himachal Pradesh)/Dewas (MP) 4. SABOO-BERLAC Limited (a joint venture and technical collaboration with Berlac AG, Switzerland) | ||
| Previous : |
Designation Sr. Executive, Period Worked |
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Worked from 2000 to 2002 | ||
Brief summary :
Period Worked from July 00 to June 02 Designation Sr. Executive (QA, QC, Production, ISO certifications). Nature of Business Designer finishes, Specialty Paints, Lacquers, Thinners for industrial purpose. Area of Operation Industrial Area, Chandigarh (Punjab) 5. ICI PAINTS Limited (Indian collaboration with Imperial Chemical Industries, London) | ||
| Previous : |
Designation Sr. Executive, Period Worked |
|
Worked from 2000 to 2002 | ||
Brief summary :
Period Worked from July 00 to June 02 Designation Sr. Executive (QA, QC, Production, ISO certifications). Nature of Business Designer finishes, Specialty Paints, Lacquers, Thinners for industrial purpose. Area of Operation Industrial Area, Chandigarh (Punjab) 5. ICI PAINTS Limited (Indian collaboration with Imperial Chemical Industries, London) | ||
| Previous : |
Designation Sr. Executive, Period Worked |
|
Worked from 2000 to 2002 | ||
Brief summary :
Period Worked from July 00 to June 02 Designation Sr. Executive (QA, QC, Production, ISO certifications). Nature of Business Designer finishes, Specialty Paints, Lacquers, Thinners for industrial purpose. Area of Operation Industrial Area, Chandigarh (Punjab) 5. ICI PAINTS Limited (Indian collaboration with Imperial Chemical Industries, London) | ||
| Previous : |
Designation Sr. Executive, Period Worked |
|
Worked from 2000 to 2002 | ||
Brief summary :
Period Worked from July 00 to June 02 Designation Sr. Executive (QA, QC, Production, ISO certifications). Nature of Business Designer finishes, Specialty Paints, Lacquers, Thinners for industrial purpose. Area of Operation Industrial Area, Chandigarh (Punjab) 5. ICI PAINTS Limited (Indian collaboration with Imperial Chemical Industries, London) | ||
| Previous : |
Designation Sr. Executive, Period Worked |
|
Worked from 2000 to 2002 | ||
Brief summary :
Period Worked from July 00 to June 02 Designation Sr. Executive (QA, QC, Production, ISO certifications). Nature of Business Designer finishes, Specialty Paints, Lacquers, Thinners for industrial purpose. Area of Operation Industrial Area, Chandigarh (Punjab) 5. ICI PAINTS Limited (Indian collaboration with Imperial Chemical Industries, London) | ||
| Previous : |
Designation Production Associate, Period Worked |
|
Worked from 1997 to 2000 | ||
Brief summary :
Period Worked from Dec.97 to June00 Designation Production Associate (Chemical and Product development). Nature of Business Automotive, Refinish, Decorative, Motor and Industrial paints and Thinners Area of Operation Industrial Area, Mohali (Punjab) 6. HONEY-BEE NATURAL PRODUCTS Limited (100% Export oriented unit of Dabur Group) | ||
| Previous : |
Designation Production Associate, Period Worked |
|
Worked from 1997 to 2000 | ||
Brief summary :
Period Worked from Dec.97 to June00 Designation Production Associate (Chemical and Product development). Nature of Business Automotive, Refinish, Decorative, Motor and Industrial paints and Thinners Area of Operation Industrial Area, Mohali (Punjab) 6. HONEY-BEE NATURAL PRODUCTS Limited (100% Export oriented unit of Dabur Group) | ||
| Previous : |
Designation Production Associate, Period Worked |
|
Worked from 1997 to 2000 | ||
Brief summary :
Period Worked from Dec.97 to June00 Designation Production Associate (Chemical and Product development). Nature of Business Automotive, Refinish, Decorative, Motor and Industrial paints and Thinners Area of Operation Industrial Area, Mohali (Punjab) 6. HONEY-BEE NATURAL PRODUCTS Limited (100% Export oriented unit of Dabur Group) | ||
| Previous : |
Designation Production Associate, Period Worked |
|
Worked from 1997 to 2000 | ||
Brief summary :
Period Worked from Dec.97 to June00 Designation Production Associate (Chemical and Product development). Nature of Business Automotive, Refinish, Decorative, Motor and Industrial paints and Thinners Area of Operation Industrial Area, Mohali (Punjab) 6. HONEY-BEE NATURAL PRODUCTS Limited (100% Export oriented unit of Dabur Group) | ||
| Previous : |
Designation Production Associate, Period Worked |
|
Worked from 1997 to 2000 | ||
Brief summary :
Period Worked from Dec.97 to June00 Designation Production Associate (Chemical and Product development). Nature of Business Automotive, Refinish, Decorative, Motor and Industrial paints and Thinners Area of Operation Industrial Area, Mohali (Punjab) 6. HONEY-BEE NATURAL PRODUCTS Limited (100% Export oriented unit of Dabur Group) | ||
| Previous : |
Period Worked |
|
Worked from 1995 to 1997 | ||
Brief summary :
Period Worked from Oct.95 to Oct.97 Designation Production cum Approved Agmark Chemist. Nature of Business Export of Bulk Honey processing, honey based Food and ayurvedic products. Area of Operation Lalru, Distt: Patiala (Punjab) Salary Drawing Break up can be provided at the time of final interaction as per your current industry norms and my professional experience.Expected Monthly Salary: 25 - 30% growth in present package plus family relocation allowance and work permit for international assignments as per standard company policy/grade. Availability : 30-90 days. (Negotiable) advance notice / deduction of salary after receiving confirmed appointment letter. | ||
| Previous : |
Period Worked |
|
Worked from 1995 to 1997 | ||
Brief summary :
Period Worked from Oct.95 to Oct.97 Designation Production cum Approved Agmark Chemist. Nature of Business Export of Bulk Honey processing, honey based Food and ayurvedic products. Area of Operation Lalru, Distt: Patiala (Punjab) Salary Drawing NET CTC 14.50 Lac. PA (Variable) + 2.5 Lac PA (Fixed) - Next revision in Jan. 2012 (expected present growth 22% = 21 lac pa). Break up can be provided at the time of final interaction as per your current industry norms and my professional experience.Expected Monthly Salary: 25 - 30% growth in present package plus family relocation allowance and work permit for international assignments as per standard company policy/grade. Availability : 30-90 days. (Negotiable) advance notice / deduction of salary after receiving confirmed appointment letter. | ||
| Previous : |
Period Worked |
|
Worked from 1995 to 1997 | ||
Brief summary :
Period Worked from Oct.95 to Oct.97 Designation Production cum Approved Agmark Chemist. Nature of Business Export of Bulk Honey processing, honey based Food and ayurvedic products. Area of Operation Lalru, Distt: Patiala (Punjab) Salary Drawing Break up can be provided at the time of finalization of interaction as per your current norms and experience.Expected Monthly Salary : 15 - 25 % growth in present package and family relocation allowance and work permit as per standard company policy/grade. Availability : 30-90 days. (negotiable) advance notice / deduction of salary after receiving confirmed appointment letter. | ||
| Previous : |
Period Worked |
|
Worked from 1995 to 1997 | ||
Brief summary :
Period Worked from Oct.95 to Oct.97 Designation Production cum Approved Agmark Chemist. Nature of Business Export of Bulk Honey processing, honey based Food and ayurvedic products. Area of Operation Lalru, Distt: Patiala (Punjab) Salary Drawing NET CTC 14.50 Lac. PA (Variable) + 2.5 Lac PA (Fixed) - Next revision in Jan. 2012 (expected present growth 22% = 21 lac pa). Break up can be provided at the time of final interaction as per your current industry norms and my professional experience.Expected Monthly Salary: 25 - 30% growth in present package plus family relocation allowance and work permit for international assignments as per standard company policy/grade. Availability : 30-90 days. (Negotiable) advance notice / deduction of salary after receiving confirmed appointment letter. | ||
| Previous : |
Period Worked |
|
Worked from 1995 to 1997 | ||
Brief summary :
Period Worked from Oct.95 to Oct.97 Designation Production cum Approved Agmark Chemist. Nature of Business Export of Bulk Honey processing, honey based Food and ayurvedic products. Area of Operation Lalru, Distt: Patiala (Punjab) Salary Drawing Details and break up of salary can be discussed at the time of finalization of interaction and candidature.Expected Monthly Salary : 35 - 55 % growth in present package and family relocation allowance and work permit as per standard company policy/grade. Availability : 30-90 days advance notice / deduction of salary after receiving confirmed appointment letter. | ||
AMIT SHARMA's Education
Gurukula Kangri Vishwavidyala, Hardwar, (Uttranchal) |
|
| M.Sc | |
| India | |
| From 1993 to 1995 | |
Gurukula Kangri Vishwavidyala, Hardwar, (Uttranchal) |
|
| B.Sc | |
| India | |
| From 1990 to 1993 | |
| Recommendation |
AMIT SHARMA IS A HIGHLY SKILLED PROFESSIONAL WITH A STRONG INTER-PERSONAL SKILLS.HIS DEVOTION TO HIS WORK IS EXTRAORDINARY AND IS ALWAYS KEEN TO BRING OUT INNOVATIVE IDEAS.
Amit has great work ethics with a definitive inclination towards success, I would wish him luck in all his future endeavors.
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