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  • 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 ...

  • policies and procedures to ensure that regulatory compliance is maintained or enhanced. Provide regulatory guidance to departments or development project teams regarding design, development, evaluation or marketing of products. Communicate regulatory information to multiple departments and ensure Qualification: Bachelor Degree in a scientific discipline. Experience: 10 - 15 years experience in Regulatory ...

  • 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

  • issues related to Medical Devices and work closely with divisions to develop and implement strategies to address the impact from regulatory perspective * Work with other divisional regulatory leads to ensure compliance and standardization across divisions * Completes other regulatory activities

  • issues related to Medical Devices and work closely with divisions to develop and implement strategies to address the impact from regulatory perspective * Work with other divisional regulatory leads to ensure compliance and standardization across divisions * Completes other regulatory activities

  • Qualification: B.Pharm / MPharm. Exp: 10-12 years. Should have hands on experience for end to end ANDA preparations & submissions. Sound knowledge of current regulatory expectations wrt GDUFA II. Sound knowledge of ICH / FDA Guidance documents ...

  • Qualification: B.Pharm / MPharm. Exp: 10-12 years. Should have hands on experience for end to end ANDA preparations & submissions. Sound knowledge of current regulatory expectations wrt GDUFA II. Sound knowledge of ICH / FDA Guidance documents ...

  • Qualification: B.Pharm / MPharm. Exp: 10-12 years. Should have hands on experience for end to end ANDA preparations & submissions. Sound knowledge of current regulatory expectations wrt GDUFA II. Sound knowledge of ICH / FDA Guidance documents ...

  • Qualification: B.Pharm / MPharm. Exp: 10-12 years. Should have hands on experience for end to end ANDA preparations & submissions. Sound knowledge of current regulatory expectations wrt GDUFA II. Sound knowledge of ICH / FDA Guidance documents ...

  • Qualification: B.Pharm / MPharm. Exp: 10-12 years. Should have hands on experience for end to end ANDA preparations & submissions. Sound knowledge of current regulatory expectations wrt GDUFA II. Sound knowledge of ICH / FDA Guidance documents ...

  • To get Dossier Done Up-to ,Tentative date for submissions, Completing Post Submission Activities till Obtain MA Issued and Renewed, Streamline the registration status and Planning for new submissions, Providing Technical Support to the Marketing/B

  • To get Dossier Done Up-to ,Tentative date for submissions, Completing Post Submission Activities till Obtain MA Issued and Renewed, Streamline the registration status and Planning for new submissions, Providing Technical Support to the Marketing/B

  • To get Dossier Done Up-to ,Tentative date for submissions, Completing Post Submission Activities till Obtain MA Issued and Renewed, Streamline the registration status and Planning for new submissions, Providing Technical Support to the Marketing/B

  • To get Dossier Done Up-to ,Tentative date for submissions, Completing Post Submission Activities till Obtain MA Issued and Renewed, Streamline the registration status and Planning for new submissions, Providing Technical Support to the Marketing/B

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