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  • Thorough knowledge of QMS/ ISO 13485 / Regulatory affairs Thorough knowledge of QMS/ ISO 13485 a regulatory subject matter expert through cross functional collaboration with R&D and relevant stakeholders to ensure regulatory compliance healthcare ind

  • Thorough knowledge of QMS/ ISO 13485 / Regulatory affairs Thorough knowledge of QMS/ ISO 13485 a regulatory subject matter expert through cross functional collaboration with R&D and relevant stakeholders to ensure regulatory compliance healthcare ind

  • Roles and Responsibilities: We do have immediate job openings for Regulatory Affairs at Chennai location. Key Responsibilities: 1) Looking for around 2-6 years of experience. 2) Looking for person who has strong experience in Regulatory affairs especially in Europe and US market. 3) Should have

  • Roles and Responsibilities: We do have immediate job openings for Regulatory Affairs at Chennai location. Key Responsibilities: 1) Looking for around 2-6 years of experience. 2) Looking for person who has strong experience in Regulatory affairs especially in Europe and US market. 3) Should have

  • Organization Name : Top Pharma Dept : Regulatory Affairs Years of experience : 4- 9 Years Work Location : Bangalore Source Location : India US Market and Europe Markets We are looking from Top Global Pharma And CRO's Candidates must have experience in below mentioned points. Dossier Management

  • to the systems or tools ensuring Regulatory Compliance o Support global/local team members with data management workload when necessary to provide flexible support for the portfolio. o Adhere to compliance standards o Act as Regulatory Data SME in regions supported o Produce country/regional reports Technical Skill Requirements o Computer literacy in MS Word/Outlook/Excel/Adobe Acrobat. o Proven ...

  • to the systems or tools ensuring Regulatory Compliance o Support global/local team members with data management workload when necessary to provide flexible support for the portfolio. o Adhere to compliance standards o Act as Regulatory Data SME in regions supported o Produce country/regional reports Technical Skill Requirements o Computer literacy in MS Word/Outlook/Excel/Adobe Acrobat. o Proven ...

  • to the systems or tools ensuring Regulatory Compliance o Support global/local team members with data management workload when necessary to provide flexible support for the portfolio. o Adhere to compliance standards o Act as Regulatory Data SME in regions supported o Produce country/regional reports Technical Skill Requirements o Computer literacy in MS Word/Outlook/Excel/Adobe Acrobat. o Proven ...

  • The Senior Specialist/Associate Manager I may take on the accountabilities for a number of different roles within a Global Regulatory Execution Team (GRET): Regulatory Project Management, Global Labelling Management and Dossier Management. The Senior Specialist/Associate Manager I/II is expected to be able to work flexibly

  • to the systems or tools ensuring Regulatory Compliance o Support global/local team members with data management workload when necessary to provide flexible support for the portfolio. o Adhere to compliance standards o Act as Regulatory Data SME in regions supported o Produce country/regional reports

  • New Submissions - Submission of dossiers to Global Health Authorities (esp. US, EU, CANADA & ANZ). Experience in Parenteral Dosage forms is preferable. Life-Cycle Management - Submission of post-approval changes (Supplements/Variations) to Global Health Authorities (esp. US, EU, CANADA & ANZ) and renewal applications. Biosimilars - Submission of registration dossiers & post-approval changes to Global Health Authorities ...

  • At present we have an urgent opening for Regulatory Affairs in highly reputed formulation manufacturing company.* Candidate should have experience 1 to 2 years in formulation industries.* Experiance in Dossier

  • At present we have an urgent opening for Regulatory Affairs in highly reputed formulation manufacturing company.* Candidate should have experience 1 to 2 years in formulation industries.* Experiance in Dossier

  • At present we have an urgent opening for Regulatory Affairs in highly reputed formulation manufacturing company.* Candidate should have experience 1 to 2 years in formulation industries.* Experiance in Dossier

  • At present we have an urgent opening for Regulatory Affairs in highly reputed formulation manufacturing company.* Candidate should have experience 1 to 2 years in formulation industries.* Experiance in Dossier

  • At present we have an urgent opening for Regulatory Affairs in highly reputed formulation manufacturing company.* Candidate should have experience 1 to 2 years in formulation industries.* Experiance in Dossier

  • of different roles within a Global Regulatory Execution Team (GRET): Regulatory Project Management, Global Labelling Management and Dossier Management. The Senior Specialist/Associate Manager I/II is expected to be able to work flexibly to deliver these varied accountabilities as assigned to them by their line

  • for a number of different roles within a Global Regulatory Execution Team (GRET): Regulatory Project Management, Global Labelling Management and Dossier Management. The Senior Specialist/Associate Manager I/II is expected to be able to work flexibly to deliver these varied accountabilities as assigned to them

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