Dr.Reddys Laboratories Ltd Hiring for Pharmacovigilance (PV) Specialist

Dr.Reddys Laboratories Ltd Walk-in Interview.Dr.Reddys Laboratories Ltd Notification full details below.Interested and eligible candidates can attend Interview on scheduled time and venue.

Important Details :

• Selection Process: The selection will be on the basis of Interview.
• Mode of Interview: Face to face
• Interview Rounds of Interview: HR
• Job Location: Hyderabad

Vacancy details:

• Department: Pharmacovigilance (PV) Specialist – ROW Market
• Qualification: Bachelor’s degree in pharmacy, Master’s degree is preferred.
• Minimum work experience: Minimum 8 years of experience in pharmacovigilance out of which at least 3 years in core pharmaceutical company.

Job Description : Greeting from Dr.Reddys Laboratories Ltd..!!!!

Purpose:

We are seeking a dedicated and detail-oriented PV Specialist to join our team. The associate will work under the guidance of respective Head of Pharmacovigilance of the assigned region and shall be responsible for managing various pharmacovigilance tasks. The ideal candidate will have excellent communication and organizational skills, as well as a strong understanding of regulatory requirements in ROW countries.

Responsibilities:

Assist in updating both local and core PSMFs

Collaborate with partners to create and update SDEAs with the latest consumer healthcare information under the supervision of the Head of Pharmacovigilance of ROW region.

Ensure compliance with SDEA requirements, such as reconciliation of PV activities in ROW region.

Keep activity tracking spreadsheets up-to-date to ensure all tasks are consistently monitored and recorded.

Manage the Eudravigilance database and perform signal detection activities as required.

Manage RMP queries and CMDh risk notifications.

Update RMPs post-authorization and track related variations with RA.

Ensure compliance for aggregate reports, including PSUSAs, for regulatory intelligence and tracking tasks to be addressed in the next PSUR, as well as establishing a close monitoring list.

Manage deviations and CAPAs: Identify and report any deviations in procedures and participate in CAPA development, assuming responsibility for CAPA completion when assigned.

Provide support during audit and inspection preparation, actively participate during audits, address any observations, and assist in CAPA closure

Able to manage any assigned task of Pharmacovigilance on ad-hoc basis.

Relationship Management

Working with other regional teams and central cross functional teams across the Globe.

Interactions with vendor’s/service providers for PV activities.

Process Improvement / Standardization

Participate in process improvement initiatives under supervision of Head of Pharmacovigilance of respective region.

Qualifications

Desired Skills & Competencies

Bachelor’s degree in pharmacy, Master’s degree is preferred.

Minimum 8 years of experience in pharmacovigilance out of which at least 3 years in core pharmaceutical company.

Strong understanding of regulatory requirements and guidelines of respective countries

Excellent communication and organizational skills

Proficiency in Microsoft Office, including Excel, PowerPoint

Ability to work independently and as part of a team.

Detail-oriented and able to manage multiple tasks simultaneously.

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