Teva Pharmaceuticals Posted September 30, 2026

Mgr Pharmacovigilance

Bangalore, India Type not listed
Notify me about similar jobs

Teva Pharmaceuticals is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

We Are Teva

We’re Teva, a leading innovative biopharmaceutical company, enabled by a world-class generics business. Whether it’s innovating in the fields of neuroscience and immunology or delivering high-quality medicine worldwide, we’re dedicated to addressing patients’ needs now and in the future. Here, you will be part of a high-performing, inclusive culture that values fresh thinking and collaboration. You'll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together.

Our Team, Your Impact

This section is where we attract the attention of potential candidates and sell the role. How has the role come about? What makes it appealing? What are the key responsibilities? How is the role better with Teva than with another company? Wherever possible, we should bring through the essence of our EVP pillars, i.e., we care, we’re in it together, and we make work fulfilling.

How You’ll Spend Your Day

Perform medical review and clarification of Trial related (AE's) & Post marketing Adverse Events (ADR's) including narrative content, queries, coding for events and lab reports, expectedness, seriousness, causality, labelling and medical assessment comments as applicable.

Serve as a global safety physician and as an internal (within Teva) & external (to vendors) consultant to pharmacovigilance case processing groups. To have active interactions and provide inputs with other functions for topics related to labelling, causality, seriousness, MedDRA coding and other medical concepts etc.

Maintain awareness of medical-safety-regulatory industry developments to participate in trainings, workshops, product transitions, audit preparations, supporting UAT activities and knowledge transfer transition initiatives.

Support audits and inspections for case processing & medical review aspects

Create and update Standard Operating Procedures and Working Instructions to ensure optimal operational management of ICSR and related activities

Maintain regular communication with the external vendor regarding medical review workflow, process updates and maintain a necessary oversight to address any gaps/risks.

Perform routine quality check to measure the medical review quality for vendor and in-house team

Attend and conduct internal meetings with various stake holders and vendors on various queries/ clarification related to medical assessment concepts for better awareness amongst case processing groups.

Provide support to EU Qualified Persons for Pharmacovigilance (QPPV) teams as applicable. Signal detections following preparation of Risk Management Programs, PSUR/DSUR surveillance activities, participate in Business Continuity Plans (BCP) as required.

Manage paid time off, appropriate backups for the team to ensure smooth operations with minimal disruption.

Your Skills and Experience

Medical Degree (MBBS with 5.5 years degree which includes internship of 1 year). Board approved/certified equivalent or 2 years post-graduation with valid medical license.

Clinical medical experience of about 1-2 years and PV experience of about 3-4 years as medical safety reviewer is recommended so as to fulfil the job role technical requirements on medical judgements.

Project Management experience is an advantage.

Fluent in English.

Also Good to Have

Adaptability & Flexibility: The ability to respond positively to change and new ways of working; be prepared to rise to the challenge of dealing with the unfamiliar and cope with the new or unexpected. Effectively address work-related problems, pressures and stresses in a professional and positive way. Ability to adapt, adjust and change to new situations and shift strategies to meet different types of challenges. Can effectively cope with change; can decide and act without having the total picture; can comfortably handle risk and uncertainty.

Cross-functional Communication The ability to communicate ideas, strategies and concerns to cross-functional stakeholders; Understanding of appropriate audience for discussions, and ability to identify appropriate stakeholder for specified messages; Ability to facilitate meetings and drive discussion around a specified agenda; Ability to articulate a business case.

Time-management (Prioritization): Ability to handle multiple tasks/projects simultaneously. Determination to stay focused on results and deadlines until the task or project is completed; Spends his/her time and the time of others on what’s important.

Proactivity: To challenge and lead the organization and self to achieve results and excellence. Enjoys working hard; is action oriented and full of energy for the things he/she sees as challenging; not fearful of acting with a minimum of planning; seizes more opportunities than others.

Critical & Analytical Thinking: Having a process of breaking down complex information into components to analyze, interpret, evaluate and construct reasoned arguments in order to solve a problem or reach a conclusion. Breaks down raw information and undefined problems into specific, workable components that in-turn clearly identifies the issues at hand. Makes logical conclusions, anticipates obstacles, and considers different approaches to the decision-making process.

Results and Performance-Driven: Assumes personal ownership and accountability for business results and solutions; consistently delivers results that meet or exceed expectations; makes the customer central to all thinking; keeps the focus on driving customer value.

Excellent Communication Skills, both written and Oral: Communication style should be diplomatic and direct, but not confrontational. He or she must be able to summarize information in an articulate, clear, tangible, manner both in written form and orally.

Salary Range

How We’ll Take Care of You

At Teva, better health starts from within, and that includes you. From day one, you’ll be supported with benefits designed to help you thrive in and out of work. This includes generous annual leave, reward plans, flexible working schedules (dependent on role), access to tailored health support, and meaningful ways to give back to the community.  When it comes to your career, you’ll be encouraged to explore, evolve, and shape your path. Twist, our one-stop shop for career development platform, gives you access to a wide range of possibilities, from learning programs and short-term projects to opportunities for internal growth. Here, you’ll be part of a culture that empowers you to reach your goals and prioritize your wellbeing every step of the way.

Already Working @Teva?

Make sure to apply through our internal career site on Twist, your one-stop shop for career development

Teva’s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.

Job details

Seniority
Not listed
Function
Pharmacovigilance
Therapeutic area
Not listed
Location
Bangalore, India
Employment type
Not listed

How this role compares

Computed from every other active Pharmacovigilance role in our database, not just this employer's listings.

We currently track 159 comparable Pharmacovigilance roles across 53 biopharma companies.

159Comparable roles tracked
149Currently active
53Companies hiring similar roles
31Countries represented

Salary context

38 of 159 peers report a salary range (USD, annualized)

Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.

This roleSubject Not listed on this posting
Lowest disclosed · Drug Safety Associate II · Exelixis Inc $104,500/yr – $148,000/yr
Peer group range $126,250 – $380,650 (median $264,000)

Where these roles are based

Top locations among the 159 comparable roles

United States63
China15
India8
France8
United Kingdom8
Japan7

+ 25 more countries

Seniority mix

116 of 159 peers have a known seniority level

Director34
Senior27
Manager23
Associate9
Associate Director8
Intern/Fellow/Postdoc7
Senior Director5
Executive/VP2
Principal1

Therapeutic area mix

27 of 159 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology12
Neuroscience6
Immunology5
Ophthalmology1
Rare Disease1
Vaccines & Infectious Disease1
Respiratory1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

40%similar
Amgen Technology Pvt Ltd. Hyderabad, India Manager
Same function Same country
40%similar
Amgen Technology Pvt Ltd. Hyderabad, India Senior
Same function Same country
40%similar
Amgen Technology Pvt Ltd. Hyderabad, India Manager
Same function Same country
40%similar
Amgen Technology Pvt Ltd. Hyderabad, India Senior
Same function Same country
40%similar
AstraZeneca Bangalore, India Manager
Same function Same country
40%similar
AstraZeneca Bangalore, India Director
Same function Same country

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

Or follow a whole field: get every new Pharmacovigilance job in India, and choose locations and companies.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

40%
Senior Manager - Regulatory Data Management
Amgen Technology Pvt Ltd. · Hyderabad, India · Manager
Function Therapeutic area Seniority Country
40%
Sr Assoc Pharmacovigilance Operations
Amgen Technology Pvt Ltd. · Hyderabad, India · Senior
Function Therapeutic area Seniority Country
40%
Medical Director, Patient Safety Physician
AstraZeneca · Bangalore, India · Director
Function Therapeutic area Seniority Country
25%
Director, Patient Safety (MD)
Gilead Sciences, Inc. · Foster City, United States · Director
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.