Sr Specialist Aggregate Safety Process

Posted 3 Days Ago
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Mumbai, Maharashtra
Junior
Healthtech • Pharmaceutical
The Role
The Sr Specialist is responsible for quality review and compliance monitoring of aggregate safety reports, ensuring they adhere to regulatory requirements. This role entails calculating patient exposure, tracking metrics, collaborating with stakeholders to address quality issues, and maintaining procedural documents relevant to compliance. The specialist participates in inspection readiness activities and contributes to process improvements.
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Job Description

The Position

The Aggregate Safety Process, Sr Specialist maintains and performs the necessary processes to ensure high quality and compliant reporting of aggregate safety reports in accordance with PV regulations.

Responsibilities:

  • Perform quality review and compliance monitoring of aggregate safety reports to Health Authorities and Business Partners adhering to regulatory requirements.

  • Measure quality effectiveness by tracking appropriate metrics and evaluating key performance indicators.

  • Responsible for extracting, calculating and overall QC of patient exposure for aggregate reports.

  • monitors the quality of aggregate safety reports and compliant reporting to ensure internal and regulatory compliance.

  • Partner with internal and external stakeholders to identify, prioritize and monitor quality and compliance issues and develop solutions to minimize risk and ensure the overall quality of aggregate safety reports.

  • Extract, calculate and quality review of patient exposure data.

  • Implement emerging regulations to ensure global alignment of quality and compliance activities and processes.

  • Assess the impact of internal procedural changes to quality and compliance monitoring activities and update of these activities to remain relevant.

  • Participate in various important pharmacovigilance processes, IT and quality initiatives.

  • Maintain procedural documents relevant to quality review and compliance

  • Participate in inspection readiness activities and preparation as needed.

  • Assist in the review of responses to regulatory agency questions with regards to quality and compliance monitoring activities.

  • Develop and maintain tools to streamline the monitoring of quality and compliance, introducing automation where possible

  • Provide training and support to new team members

  • Management of Aggregate Report operations of mailbox

  • Contribute to continuous improvement efforts in the process

Required Education, Experience, and Skills:

  • Bachelor's degree or master's degree in a life science/health care/pharmaceutical related field

  • Knowledge of PV principles, systems, and requirements in addition to PV regulations

  • Strong analytical skills and quality focus

  • Problem solving, conflict resolution and critical thinking skills

  • Ability to function with a high degree of autonomy, quickly adapt to changes in business priorities and effectively manage competing priorities.

  • Proficient in basic Office 365 suite applications

  • Strong English written and verbal communication skills

  • Ability to organize and multi-task with attention to detail

  • Strong working knowledge of Microsoft Office and IT tools used for assigned process

  • Analytical skills to manage process data, metrics and KPIs

  • Ability to collaborate well with others and develop effective relationships, motivate and influence in a cross-functional environment

Secondary Job Description

Who We Are:

Organon delivers ingenious health solutions that enable people to live their best lives. We are a $6.5 billion global healthcare company focused on making a world of difference for women, their families and the communities they care for. We have an important portfolio and are growing it by investing in the unmet needs of Women’s Health, expanding access to leading biosimilars and touching lives with a diverse and trusted portfolio of health solutions. Our Vision is clear: A better and healthier every day for every woman.

As an equal opportunity employer, we welcome applications from candidates with a diverse background. We are committed to creating an inclusive environment for all our applicants. 

Search Firm Representatives Please Read Carefully 
Organon LLC, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. 

Annualized Salary Range

Annualized Salary Range (Global)

Annualized Salary Range (Canada)

Please Note: Pay ranges are specific to local market and therefore vary from country to country.

Employee Status:

Regular

Relocation:

No relocation

VISA Sponsorship:

Travel Requirements: Organon employees must be able to satisfy all applicable travel and credentialing requirements, including associated vaccination prerequisites

Flexible Work Arrangements:

Shift:

Valid Driving License:

Hazardous Material(s):

Number of Openings:

1

The Company
HQ: Jersey City, NJ
6,952 Employees
On-site Workplace

What We Do

Organon is a global healthcare company with a portfolio of therapies and products in women’s health, biosimilars, and established medicines across a wide array of conditions and diseases. Our mission is to deliver impactful medicines and solutions for a healthier every day.

This site is intended for residents of the United States and its territories.

You are reminded to protect yourself against recruiting fraud from individuals, organizations or other entities claiming to represent Organon. All official Organon recruitment emails will come from accounts formatted as [email protected] or [email protected], and Organon will never conduct interviews by chat or email, or make job offers through social media or online forums. All candidates for roles at Organon will first meet with a recruiter and interview team, via Teams or in person. Organon will never ask you to make financial transactions on its behalf or ask you to receive or ship packages or goods.

For more information on adverse event reporting, visit http://bit.ly/AEReporting.

To read our community guidelines, visit http://bit.ly/OrganonCommunityGuidelines.

Follow us on Twitter at Organon (@OrganonLLC).
Follow us on Instagram at Organon (@OrganonLLC).

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