Regulatory Manager-Pharma

Job Description: Job responsibilities:Preparation, Compilation and review of registration dossier of tablet /capsule/injection in CTD,ACTD as well as country specific format for countriesPreparation, Compilation and review of registration dossier of capsule/syrup/balm in a Herbalproducts for country specific format in countries of African Region,...

Opening: 1 Nos.- Job ID: 60909- Employment Type: Full Time- Reference: - Work Experience: 4.0 Year(s) To 5.0 Year(s)- CTC Salary: 3.00 LPA TO 4.00 LPA- Function: Pharma / Biotech / Healthcare / Medical / R&D- Industry: Pharma/Biotech/Clinical Research- Qualification: B.Pharma - Pharmacy; M.Pharma - Pharmacy- Location: - Vadodara/baroda Posted On: 24th May,...

**Qualification**: B.Pharma - Pharmacy or M.Pharma - Pharmacy **Experience**: 2.0 Year **To** 4.0 Year **( Must have experience in Pharma Formulations)** 1. Preparing dossiers as per country specific guidelines 2. Countries knowledge - Africa, South East Asia They must have excellent organizational, analytical, project management, and communication...

Job Description: Job responsibilities are to Assist Regulatory manager: Preparation, Compilation and review of registration dossier of tablet /capsule/injection in CTD, ACTD as well as country specific format for countries Preparation, Compilation and review of registration dossier of capsule/syrup/balm in a Herbal products for country...

Job Description: Job responsibilities are to Assist Regulatory manager: Preparation, Compilation and review of registration dossier of tablet /capsule/injection in CTD, ACTD as well as country specific format for countries Preparation, Compilation and review of registration dossier of capsule/syrup/balm in a Herbal products for country...

Qualification: M. Pharma Minimum Experience: 10-15 years Role: Manager – Regulatory & Business Continuity Industry Preference: Pharma Job Description: Preparation of registration strategy for various health authorities like Russia, Belarus, Kazakhstan, Ukraine, Azerbaijan Review of documents related to product registration...

Qualification: M. Pharma Minimum Experience: 10-15 years Role: Manager – Regulatory & Business Continuity Industry Preference: Pharma Job Description: Preparation of registration strategy for various health authorities like Russia, Belarus, Kazakhstan, Ukraine, Azerbaijan Review of documents related to product registration and...

Job Description: Job Description: Experience in handling regulatory affairs for ROW market mainly Central and Latin American, African & Asian countries for Pharma Formulations. ? Preparation, Compilation & Review of Registration documents that include Administrative & Technical. ? Reviewing the technical documents provided by QA, QC,...

Job responsibilities are to Assist Regulatory manager: - Preparation, Compilation and review of registration dossier of tablet /capsule/injection in CTD, - ACTD as well as country specific format for countries - Preparation, Compilation and review of registration dossier of capsule/syrup/balm in a Herbal - products for country specific format in countries...

Opening: 1 Nos Job ID:Employment Type:Full Time- Reference:Work Experience: 4.0 Year(s)To 5.0 Year(s)- CTC Salary: 3.00 LPA TO 4.00 LPA- Function: Pharma / Biotech / Healthcare / Medical / R&D- Industry: Pharma/Biotech/Clinical Research- Qualification: B.Pharma - Pharmacy; M.Pharma - Pharmacy- Location: Vadodara/barodaPosted On: 24th May, 2023Duties and...

**Description**: - They must have excellent organizational, analytical, project management, and communication skills. - They work frequently with other employees and team members to coordinate complex activities, often with competing priorities. - Most regulatory affairs positions are full time. - Regulatory Responsibility means a duty or responsibility,...

Job Role : Responsibilities : Ensure assessment of Regulatory inspection citations identified at Sunpharma sites to derive the global action Ensure assessment of 483s, warning letter issued to other organization by USFDA to derive the global action Ensure assessment of internal learning (such as Quality alert) to derive the global action Preparation of...

**Post**: RA Executive **Experience**: 5+ Years Experience in Regulatory Affairs in Pharma Industry (Formulation) **Location**: Vadodara - Experience in handling regulatory affairs for ROW market mainly Central and Latin American, African & Asian countries for Pharma Formulations. - Preparation, Compilation & Review of Registration documents that include...

Opening: 3 Nos.- Job ID: 64869- Employment Type: Full Time- Reference: - Work Experience: 2.0 Year(s) To 3.0 Year(s)- CTC Salary: 2.40 LPA TO 3.00 LPA- Function: Pharma / Biotech / Healthcare / Medical / R&D- Industry: Pharma/Biotech/Clinical Research- Location: - Vadodara/baroda Posted On: 25th Jul, 2023 **Job responsivities are to assist Regulatory...

Job Role :Responsibilities :Ensure assessment of Regulatory inspection citations identified at Sunpharma sites to derive the global actionEnsure assessment of 483s, warning letter issued to other organization by USFDA to derive the global actionEnsure assessment of internal learning (such as Quality alert) to derive the global actionPreparation of Global...

Job Role :Responsibilities :Ensure assessment of Regulatory inspection citations identified at Sunpharma sites to derive the global actionEnsure assessment of 483s, warning letter issued to other organization by USFDA to derive the global actionEnsure assessment of internal learning (such as Quality alert) to derive the global actionPreparation of Global...

Job Role :Responsibilities :Ensure assessment of Regulatory inspection citations identified at Sunpharma sites to derive the global actionEnsure assessment of 483s, warning letter issued to other organization by USFDA to derive the global actionEnsure assessment of internal learning (such as Quality alert) to derive the global actionPreparation of Global...

Position: Senior Manager Job Title: Job Grade: Function: Corporate Quality Compliance Sub-function: Global Actions Management Manager's Job Title: Skip Level Manager's Title: Function Head Title: Sr. General Manager Location: Vadodara No. of Direct Reports (if any) 3 Areas of Responsibility Ensure assessment of...

Job Role : Responsibilities : Ensure assessment of Regulatory inspection citations identified at Sunpharma sites to derive the global action Ensure assessment of 483s, warning letter issued to other organization by USFDA to derive the global action Ensure assessment of internal learning (such as Quality alert) to derive the global action Preparation of...

Job Role :Responsibilities :Ensure assessment of Regulatory inspection citations identified at Sunpharma sites to derive the global actionEnsure assessment of 483s, warning letter issued to other organization by USFDA to derive the global actionEnsure assessment of internal learning (such as Quality alert) to derive the global actionPreparation of Global...