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  • Support the U.S. BD team on all necessary initiatives, in particular, to create thoughtful and targeted collateral for meetings with prospective clients Conduct research to comprehensively analyze and understand different teams/groups at each prospect to create a tailored message instead of a generic deck Compile and maintain a central repository for all such research above Assist with other BD ...

  • Looking Consultant for Kelly Scientific Resources minimum 2 +yrs of experience in pharma & healthcare recruitment

  • Formulate strategies and marketing plans for products;managing existing product portfolio & new product launches. Competition mapping Identifying the target areas of competition presence & formulating strategies for market penetration through innovative products by making our customer competitive across the supply chain. Establishing tie-ups with financially strong and reliable channel partners ...

  • Job Title-CustomerCare Executive Key Responsibilities:- 1. Handling incoming calls from customers/Patients 2. Respond to them in a soft and empathetic voice 3. Identify and assess customer needs to achieve satisfaction 4. Provide accurate, valid and complete information by using the right methods/tools (as per the defined FAQ’s) 5. Handle complaints, provide appropriate solutions and alternatives within the ...

  • Candidate should have good: Personality Traits Flexible, go getter attitude Hardworking, sincere and with positive attitude Leadership Professional Skills Good communication skills

  • Exposure in FMCG Sector with big Brand Names Exposure in General Trade & Channel Sales Trade Marketing Initiative Brand Building Managing Trade Marketing Calendar to manage objectives Designing Cost Structure Promotions Developing Business Strategy Should have at least 3 years experience with top brand companies in Personal and Home Care products Work experience in North India is must

  • 1. Candidate should be of M.Pharma/Ph.D from a reputed university. 2. Candidate should have a minimum of 10-15yrs experience in the development of softgels for US and other regulated markets. 3. should be able to design around patents, with good understanding on patents candidate with PIV

  • 1. Candidate should be of M.Pharma/Ph.D from a reputed university. 2. Candidate should have a minimum of 10-15yrs experience in the development of softgels for US and other regulated markets. 3. should be able to design around patents, with good understanding on patents candidate with PIV

  • 1. Coordinate with QA/Mfg etc. at plant and Corporate RA at Manesar. 2. Signatory for documentation generated at plant as RA responsible person. 3. Review of all mfg/ quality documents from regulatory/ adequacy perspective. 4. Provide inputs for changes planned at the plant, based on regulatory guidelines. 5. Share regulatory submission/ approval information with plant. 6 Support post-approval changes ...

  • 1. Performing chemical analysis (wet) of Raw material, In process, intermediate and finished product as per need. 2. Performing Instrumental analysis of Raw material, In process, intermediate and finished product. 3. Perform analysis using advance instrumental techniques i.e.NMR, XRD, LCMS, GC-HS-MS, UPLC, DSC, TGA, preparative HPLC etc. 4 . To develop suitable analytical method as per product requirement. 5 ...

  • 1. Preparation & Up gradation of Standard Operation Procedures formats and designed new documents as per global quality standards. 2. Compilation of data for API Drug Master Files for US and European markets. 3. Preparation of Daily and Monthly GMP reports & annual budget for up gradation as per cGMP & regulatory requirement and planning accordingly. 4. Maintaining cGMP in manufacturing area and training of ...

  • 1. Performing chemical analysis (wet) of Raw material, In process, intermediate and finished product as per need. 2. Performing Instrumental analysis of Raw material, In process, intermediate and finished product. 3. Perform analysis using advance instrumental techniques i.e.NMR, XRD, LCMS, GC-HS-MS, UPLC, DSC, TGA, preparative HPLC etc. 4 . To develop suitable analytical method as per product requirement. 5 ...

  • 1. QA :- API Plant Exp :- 5 to 10 Years Qualification :- B.Sc or M.Sc Place of Posting :- Sotonala, Behror, Rajasthan. No of Open Position :- 10 2. QC :- API Plant Exp :- 5 to 10 Years Qualification :- B.Sc or M.Sc Place of Posting :- Sotonala, Behror, Rajasthan. No of Open Position :- 10 3. Production :- API Plant Exp :- 5 to 10 Years Qualification :- B.Sc, M.Sc, B.Tech Place of Posting :- Sotonala, Behror, Rajasthan. No of Open Position :- 10

  • 1. Preparation & Up gradation of Standard Operation Procedures formats and designed new documents as per global quality standards. 2. Compilation of data for API Drug Master Files for US and European markets. 3. Preparation of Daily and Monthly GMP reports & annual budget for up gradation as per cGMP & regulatory requirement and planning accordingly. 4. Maintaining cGMP in manufacturing area and training of ...

  • 1. Performing chemical analysis (wet) of Raw material, In process, intermediate and finished product as per need. 2. Performing Instrumental analysis of Raw material, In process, intermediate and finished product. 3. Perform analysis using advance instrumental techniques i.e.NMR, XRD, LCMS, GC-HS-MS, UPLC, DSC, TGA, preparative HPLC etc. 4 . To develop suitable analytical method as per product requirement. 5 ...

  • 1. Preparation & Up gradation of Standard Operation Procedures formats and designed new documents as per global quality standards. 2. Compilation of data for API Drug Master Files for US and European markets. 3. Preparation of Daily and Monthly GMP reports & annual budget for up gradation as per cGMP & regulatory requirement and planning accordingly. 4. Maintaining cGMP in manufacturing area and training of ...

  • - Responsible for implementation and compliance of quality management system (QMS) in pharmaceuticals. - Responsible for scale-up and process validation of new and existing pharmaceutical drug substances and verification of technology transfer (TT) documents. - Preparation of protocol and reports for Process Validation. - Responsible for interaction with R&D and marketing for improvement of quality of the ...

  • 1. Molecular Biology and clone development. 2. Cell line development, bioreactor process development, culture media optimisation. 3. Protein Purification, chromatography process development, micro/ultra/nano-filtration, formulation. 4. Analytical Techniques for Protein Characterisation, HPLC, electrophoresis, ELISA, bioassay ...

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