This is Uday Sankar, Hr ,POLARIS SOFTWARE LAB LIMITED.
We have come across your profile in one of the job sites and are impressed with the areas of expertise and technologies you possess.
We are currently in the process of hiring an excellent resource with hands on expertise on
Skills : C++ with Unix
Experience : With 3 - 6Yrs,
Position Type : Developer cum Production Support engineer
And other related technologies.
Work Location : Hyderabad
Please Apply: Who can join with in 1 week to 15 days Time
An initial look at your profile is promising and makes a good fit for our requirement.
Contact Person : Uday Sankar ,HR , uday.sankar@polaris.co.in
Note:
1. If, Your Candidature has not been processed by us from last 3 months and If you are interested in exploring this opportunity with us.
2. we request you to send your updated Profile’s to: uday.sankar@polaris.co.in
3. Please Send Your Updated Profiles with in 2 days.
Sunday, September 13, 2009
Friday, September 4, 2009
Sr Manager - Regulatory Affairs - GRA CMC (Thane)
Organization: Reputed MNC
Work Location India - Mumbai
Functional Area Regulatory Affairs
Job Description Leads the GRA CMC group based in India, acts as the senior point of contact for all RA CMC related activities in Thane / Indian labs
• Senior member of GRA CMC organization in India accountable to manage the CMC deliverables according to strategy / decision / plan set by Management /Head GRA CMC
• Interacts closely with the Global RA CMC organization for all projects or products developed or supported at Thane labs and reports progress and issues proactively.
• Operates closely with local site management in Thane for OTC R&D.
• Manages all regulatory CMC activities for allocated projects or products: e.g., but not limited to, Venous subcategory (new files, renewals, variations).
• Member of Category Global Regulatory Team for assigned projects/products.
• Collaborates strongly with Category Liaisons to handle shared activities and accountabilities with Sandoz India for GI US products containing PPI.
• Ensures high quality interactions with HAs for CMC aspects and supports local /regional regulatory organizations for advisory meetings with agencies or any other technical contacts to defend submission strategy or challenge file evaluation outcomes for allocated projects /products.
• Accountable to deliver high quality registration / accreditation documents according to plans for assigned local and global projects and products.
• Establishes RA CMC strategy and executes global/regional technical regulatory activities in collaboration with the Regional RA Liaisons (North America, Europe, SGM) as appropriate to support Category objectives.
• Provides RA CMC advice and training for the Thane Pharmaceutical and Analytical Development teams and to the Thane technical documentation cell associates with respect to regulatory CMC topics and deliverables.
• Supports Due Diligence activities as required for assigned projects and delivers inputs for ER, DR and Scope changes in Ideal process, in terms of technical information, RA CMC requirements and evaluation of resources needs.
• Acts as Member of the GEMA CMC platform team, supports full implementation and use of GEMA CMC cabinet and interacts with Global Reg Ops for e-submission activities.
• Implements RA CMC initiatives, contribute to special assigned activities and projects and rep-resents GRA in cross functional teams (e.g. RSEC, QA.. ).
The experience in a multinational company with relevant personal involvement in EU and USA CMC regulatory affairs activities (registration files, variations, knowledge of international guidelines, document management system) is a must.
Minimum requirements Minimum Qualification
Minimum MPharm, Preferred PhD
Minimum requirement of atleast 10-12 years of relevant experience
Post your resume to gangotrinath@gmail.com (or) ravi.namana@gmail.com
Work Location India - Mumbai
Functional Area Regulatory Affairs
Job Description Leads the GRA CMC group based in India, acts as the senior point of contact for all RA CMC related activities in Thane / Indian labs
• Senior member of GRA CMC organization in India accountable to manage the CMC deliverables according to strategy / decision / plan set by Management /Head GRA CMC
• Interacts closely with the Global RA CMC organization for all projects or products developed or supported at Thane labs and reports progress and issues proactively.
• Operates closely with local site management in Thane for OTC R&D.
• Manages all regulatory CMC activities for allocated projects or products: e.g., but not limited to, Venous subcategory (new files, renewals, variations).
• Member of Category Global Regulatory Team for assigned projects/products.
• Collaborates strongly with Category Liaisons to handle shared activities and accountabilities with Sandoz India for GI US products containing PPI.
• Ensures high quality interactions with HAs for CMC aspects and supports local /regional regulatory organizations for advisory meetings with agencies or any other technical contacts to defend submission strategy or challenge file evaluation outcomes for allocated projects /products.
• Accountable to deliver high quality registration / accreditation documents according to plans for assigned local and global projects and products.
• Establishes RA CMC strategy and executes global/regional technical regulatory activities in collaboration with the Regional RA Liaisons (North America, Europe, SGM) as appropriate to support Category objectives.
• Provides RA CMC advice and training for the Thane Pharmaceutical and Analytical Development teams and to the Thane technical documentation cell associates with respect to regulatory CMC topics and deliverables.
• Supports Due Diligence activities as required for assigned projects and delivers inputs for ER, DR and Scope changes in Ideal process, in terms of technical information, RA CMC requirements and evaluation of resources needs.
• Acts as Member of the GEMA CMC platform team, supports full implementation and use of GEMA CMC cabinet and interacts with Global Reg Ops for e-submission activities.
• Implements RA CMC initiatives, contribute to special assigned activities and projects and rep-resents GRA in cross functional teams (e.g. RSEC, QA.. ).
The experience in a multinational company with relevant personal involvement in EU and USA CMC regulatory affairs activities (registration files, variations, knowledge of international guidelines, document management system) is a must.
Minimum requirements Minimum Qualification
Minimum MPharm, Preferred PhD
Minimum requirement of atleast 10-12 years of relevant experience
Post your resume to gangotrinath@gmail.com (or) ravi.namana@gmail.com
Metro Medical Manager - Delhi
Work Location India - North Region
Functional Area Sales
Industry: Pharma
Job Description
• Achievement of Sell out objectives
• Drive entire range of consumer and prescription driven brands
• Effectively lead and coach Metro Medical team
• Preparing Optimal Customer List (Medical) based on business potential on the basis of agreed matrix
• Lead RCPA and retail execution for entire range of brands at these outlets
• Effective planning and execution of Medical strategies by Metro Medical team
Minimum requirements Qualification : Bachelor from any stream, Management Degree from Tier 1 or Tier 2, B - School desirable and basic computer knowledge.
Experience: Atleast 3 - 4 years of team Management Experience in a reputed Mid to Large size pharma company.
Recruiter Amit Sanas (sanasam1)
Functional Area Sales
Industry: Pharma
Job Description
• Achievement of Sell out objectives
• Drive entire range of consumer and prescription driven brands
• Effectively lead and coach Metro Medical team
• Preparing Optimal Customer List (Medical) based on business potential on the basis of agreed matrix
• Lead RCPA and retail execution for entire range of brands at these outlets
• Effective planning and execution of Medical strategies by Metro Medical team
Minimum requirements Qualification : Bachelor from any stream, Management Degree from Tier 1 or Tier 2, B - School desirable and basic computer knowledge.
Experience: Atleast 3 - 4 years of team Management Experience in a reputed Mid to Large size pharma company.
Recruiter Amit Sanas (sanasam1)
Metro Medical Manager - Delhi
Work Location India - North Region
Functional Area Sales
Industry: Pharma
Job Description
• Achievement of Sell out objectives
• Drive entire range of consumer and prescription driven brands
• Effectively lead and coach Metro Medical team
• Preparing Optimal Customer List (Medical) based on business potential on the basis of agreed matrix
• Lead RCPA and retail execution for entire range of brands at these outlets
• Effective planning and execution of Medical strategies by Metro Medical team
Minimum requirements Qualification : Bachelor from any stream, Management Degree from Tier 1 or Tier 2, B - School desirable and basic computer knowledge.
Experience: Atleast 3 - 4 years of team Management Experience in a reputed Mid to Large size pharma company.
Recruiter Amit Sanas (sanasam1)
Functional Area Sales
Industry: Pharma
Job Description
• Achievement of Sell out objectives
• Drive entire range of consumer and prescription driven brands
• Effectively lead and coach Metro Medical team
• Preparing Optimal Customer List (Medical) based on business potential on the basis of agreed matrix
• Lead RCPA and retail execution for entire range of brands at these outlets
• Effective planning and execution of Medical strategies by Metro Medical team
Minimum requirements Qualification : Bachelor from any stream, Management Degree from Tier 1 or Tier 2, B - School desirable and basic computer knowledge.
Experience: Atleast 3 - 4 years of team Management Experience in a reputed Mid to Large size pharma company.
Recruiter Amit Sanas (sanasam1)
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