Pv Professional

3-4 years

Not Disclosed

Bangalore

10 Sept. 19, 2024

Job Description

Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Who We Are

At Teva Pharmaceuticals, we’re dedicated to making good health more affordable and accessible, helping millions worldwide lead healthier lives. Our mission connects our diverse team across nearly 60 countries, uniting individuals from various nationalities and backgrounds. As a leading manufacturer of generic medicines and a proud contributor to the World Health Organization’s Essential Medicines List, our products are taken by at least 200 million people daily. We’re continually seeking innovative ways to make a difference and welcome new team members to join us in this important mission.

How You’ll Spend Your Day

Conduct comprehensive literature reviews and develop effective search strategies for specific products using databases like Embase, Medline, Pubmed, and Ovid.
Evaluate the impact of regulatory changes on existing processes and contribute to process simplification.
Utilize knowledge of the Teva portfolio to support pharmacovigilance efforts, including case processing, training, quality assurance, audits, and inspections.
Serve as a consultant or single point of contact (SPOC) for various case-related activities, maintaining an up-to-date knowledge repository of regulatory changes.
Communicate effectively with internal and external stakeholders to ensure transparency in processes.
Analyze quality data for trends to support process stabilization and ensure regulatory compliance by meeting key performance indicators.
Operate independently and take initiative to make informed decisions in a dynamic regulatory environment.
Assist with team transitions, certification processes, and conduct workshops and training sessions to address error trends and process improvements.
Provide analytical support during audits and inspections, mentoring new hires in case processing and tracking their progress.

Your Experience and Qualifications

A degree in life sciences, pharmacy, healthcare, or a related field (B. Pharmacy, M. Pharmacy, Pharm D, BDS).
3-4 years of experience in pharmacovigilance, particularly in the literature review process for Individual Case Safety Reports (ICSR).
Solid knowledge of pharmacovigilance concepts, regulations, and procedures.
Proficiency in Microsoft Office applications.
Adaptability to shifting team priorities.
Excellent communication skills—written, verbal, and non-verbal—and strong interpersonal skills.
Good analytical and problem-solving abilities.

Teva’s Commitment to Equal Employment Opportunity

Teva Pharmaceuticals is committed to providing equal employment opportunities to all individuals. Our global policy ensures that hiring practices are free from discrimination based on age, race, religion, gender, disability, sexual orientation, and other protected statuses. We strive to create a diverse and inclusive workplace for everyone. If you require accommodations during the recruitment process, please let us know, and we will treat your information confidentially to ensure an accessible candidate experience.

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Pv Professional

Job Description

Who We Are

How You’ll Spend Your Day

Your Experience and Qualifications

Teva’s Commitment to Equal Employment Opportunity

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