Manager, Third Party Strategy and Oversight

Hyderabad, India Full time
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Bristol-Myers Squibb Business Services India Private Limited 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

At Bristol Myers Squibb, our employees often ask, “Who are you working for?”, a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it.

Position Summary

The Manager, Third Party Strategy and Oversight (TPSO) supports the operational execution of third‑party oversight activities within Patient Safety (PS). This role is responsible for monitoring performance, maintaining oversight metrics, supporting compliance activities, and contributing to continuous improvement of outsourced pharmacovigilance (PV) activities.

The role works closely with TPSO leadership and cross‑functional stakeholders to ensure third parties operate in compliance with global PV regulations, GVP requirements, BMS quality standards, and contractual obligations. The role is primarily execution‑focused, providing data, analysis, documentation, and recommendations to support effective governance and decision‑making.

Duties/Responsibilities

Third‑Party Oversight & Monitoring

Perform day‑to‑day management and oversight activities for assigned third‑party vendors, distributors, or business partners performing PV‑related activities.

Collect, track, and maintain third‑party performance data, KPIs, and quality metrics in accordance with established oversight processes.

Review metrics and reports for completeness, accuracy, and trends; flag potential risks or compliance concerns for escalation and proactively recommend mitigation and improvement/corrective actions to PS teams.

Support investigation and documentation of compliance issues, including deviations, root cause analysis inputs, and CAPA tracking.

Compliance, Quality & Inspection Readiness

Support audit and inspection readiness activities related to third‑party oversight, including document preparation, evidence collection, and response tracking.

Assist in the review of safety agreements (e.g., PVAs, SOWs) to ensure oversight requirements are addressed and understood.

Maintain accurate and inspection‑ready records supporting third‑party oversight activities.

Stakeholder Collaboration & Communication

Work collaboratively with BMS stakeholders to resolve third‑party issues in a timely manner.

Prepare oversight inputs, summaries, and data for governance forums and management reviews.

Communicate clearly and professionally with internal stakeholders and external partners within defined role scope.

Support projects that build strategic third-party oversight capabilities, processes and standards to ensure delivery of PS objectives.

Contribute to the development of standard operating procedures and training relating to core responsibilities as needed.

Culture & Ways of Working

Demonstrate a strong quality mindset and promote a culture of quality and compliance, accountability, transparency, and continuous improvement.

Contribute positively to a collaborative and inclusive team environment.

Support broader SQM initiatives and book of work, as assigned.

This role reports to: Head of Third-Party Oversight and Strategy

Qualifications

Knowledge, Skills and Abilities

Bachelor’s degree in Life Sciences, Pharmacy, Nursing, Public Health, or a related discipline.

4–7 years of experience in Pharmacovigilance, Safety Operations, Quality, or a related pharmaceutical function.

Experience supporting vendor or third‑party oversight activities in a regulated environment.

Working knowledge of global PV regulations, GxP principles, and quality system expectations.

Experience working with performance metrics, KPIs, compliance tracking, or quality indicators; ability to interpret complex data and translate it into actionable insights.

Strong attention to detail, organisational skills, project management and ability to manage multiple tasks effectively.

Ability to analyse data, identify issues or trends, and escalate appropriately.

Good written and verbal communication skills, with the ability to collaborate in a matrixed environment.

Demonstrates integrity, sound judgement, and commitment to quality and compliance.

We hire for skills and capabilities, not just credentials – if this role excites you, but doesn’t perfectly match your resume, we encourage you to apply anyway.

How We Work

Where you work matters – because collaboration, innovation and patient impact happen in many settings. Our roles are structured across four work models: site-essential, site-by-design, field-based and remote-by-design. The model assigned to this role is based on its core responsibilities. Learn more at https://careers.bms.com/ways-of-working.

Supporting People with Disabilities

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to  adastaffingsupport@bms.com . Visit  careers.bms.com/eeo-accessibility  to access our complete Equal Employment Opportunity statement.

Candidate Rights

BMS will consider qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

For roles based in Los Angeles County only:  If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information:  https://careers.bms.com/california-residents/

Data Protection

We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at  https://careers.bms.com/fraud-protection .

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

If this posting is missing required information required by local law or incorrect, contact BMS at  TAEnablement@bms.com with the Job Title and Requisition number. Do not send application-related inquiries to this email. To check your application status, please login to your Candidate Home Account.

R1605755 : Manager, Third Party Strategy and Oversight

Job details

Seniority
Manager
Function
Pharmacovigilance
Therapeutic area
Not listed
Location
Hyderabad, India
Employment type
Full time

How this role compares

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

We currently track 41 comparable Manager Pharmacovigilance roles across 22 biopharma companies.

41Comparable roles tracked
37Currently active
22Companies hiring similar roles
15Countries represented

Salary context

7 of 41 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Lowest disclosed · Manager, Pharmacovigilance Case Processing (Boston, MA, US) · Servier $131,000/yr – $150,000/yr
Peer group range $140,500 – $205,000 (median $186,375)

Where these roles are based

Top locations among the 41 comparable roles

United States14
India5
Poland4
France3
Japan3
China2

+ 9 more countries

Seniority mix

41 of 41 peers have a known seniority level

Manager29
Associate Director9
Associate3

Therapeutic area mix

0 of 41 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

No peers with a known therapeutic area yet.

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.

60%similar
Amgen Technology Pvt Ltd. Hyderabad, India Manager
Same function Same seniority Same country
60%similar
Amgen Technology Pvt Ltd. Hyderabad, India Manager
Same function Same seniority Same country
60%similar
Amgen Technology Pvt Ltd. Hyderabad, India Manager
Same function Same seniority Same country
60%similar
Amgen Technology Pvt Ltd. Hyderabad, India Manager
Same function Same seniority Same country
60%similar
Bristol-Myers Squibb Business Services India Private Limited Hyderabad, India Manager
Same function Same seniority Same country
45%similar
Mylan AB Solna, Sweden Manager
Same function Same seniority

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.

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.

60%
Pharmacovigilance Operations Senior Manager
Amgen Technology Pvt Ltd. · Hyderabad, India · Manager
Function Therapeutic area Seniority Country
60%
Senior Manager GRAAS Operations
Amgen Technology Pvt Ltd. · Hyderabad, India · Manager
Function Therapeutic area Seniority Country
45%
Senior Manager, Patient Safety Scientist
BMS Services Sp. z o.o. · Warsaw, Poland · Manager
Function Therapeutic area Seniority Country
45%
Drug Safety Specialist/Non-Line Manager or Staff/Patient Safety and Pharmacovigilance (Shinagawa, Japan, Tokyo)
Boehringer Ingelheim · Shinagawa, Japan · Manager
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.