Lead PV Scientist

Posted 01 Apr 2024

Bangalore, Karnataka - India

Req Id 273172


Work Your Magic with us!

Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.

United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.


Lead PV Scientist

The purpose of this role is to collaborate with the GPS safety strategy leads to provide integrated medical safety strategies for assigned investigational and core (high-risk) marketed products. This includes input into safety aspects of clinical development, risk management, and benefit-risk management for the assigned products.


Key Responsibilities:


  • Collaborate with GPS safety strategy leads to develop integrated medical safety strategies for assigned products.
  • Provide input into safety aspects of clinical development, risk management, and benefit-risk management for assigned products.
  • Author safety reports and ensure the submission of safety data in compliance with relevant regulations.


Required Professional Experience:


  • MD: Clinical experience and pharmaceutical industry experience or similar (e.g. Health Authority); PhD/advanced science degree: Pharmaceutical industry experience or similar (e.g. Health Authority).
  • Advanced experience in Pharmacovigilance in both clinical development and post-marketing areas, including submission experience.
  • Experience working in cross-functional, global teams across different regions.


Required Technical Skills:


  • Advanced understanding of the end-to-end drug lifecycle and the drug development process.
  • In-depth knowledge and demonstrated ability in the application of relevant regulations.
  • Proficiency in interpreting individual cases, aggregate safety data, and applying statistical principles to safety data.
  • Understanding of current approaches to benefit-risk and signal management.
  •  Demonstrated ability to author safety reports.


Required Personal Skills:


  • Strong team player with excellent networking skills.
  • Solution and results-oriented.
  • Ability to work in an intense, fast-paced, multinational environment, and to cope with resistance and solve problems.
  • Demonstrated ability to work under pressure and achieve strict timeline targets, and to lead through complex situations.
  • Embraces change and adapts to changing environments.
  • Ability to take on responsibilities to further develop oneself.
  • Excellent verbal and written communication skills in English.


What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!
Apply now and become a part of our diverse team!

US Equal Employment Opportunities

The Company is an Equal Employment Opportunity employer. No employee or applicant for employment will be discriminated against on the basis of race, color, religion, age, sex, sexual orientation, national origin, ancestry, disability, military or veteran status, genetic information, gender identity, transgender status, marital status, or any other classification protected by applicable federal, state, or local law.  This policy of Equal Employment Opportunity applies to all policies and programs relating to recruitment and hiring, promotion, compensation, benefits, discipline, termination, and all other terms and conditions of employment. Any applicant or employee who believes they have been discriminated against by the Company or anyone acting on behalf of the Company must report any concerns to their Human Resources Business Partner, Legal, or Compliance immediately. The Company will not retaliate against any individual because they made a good faith report of discrimination.

We are committed to an equitable hiring process for candidates from a diverse range of backgrounds. As part of this commitment, applicants with disabilities may be entitled to reasonable accommodations. Please contact USLeavesandAccommodations@milliporesigma.com, if a reasonable accommodation is needed or if you otherwise need assistance to participate in the hiring process.

North America Disclosure

If you are a resident of California, Colorado, New York, or Washington, you are eligible to receive additional information about the compensation and benefits, which we will provide upon request. You may contact 855 444 5678 from 8:00am to 5:30pm ET Monday through Friday, for assistance.

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