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Operational scientist

High Wycombe
Kenvue
Scientist
€30,000 a year
Posted: 31 October
Offer description

Operational Scientist

Location: High Wycombe (hybrid working)

Duration: Until June 2026

Hours: 40 hours per week

Imagine your next project where you will be working in the position of an Operations Scientist and be responsible for supporting the operational management of case receipt, case processing, and safety reporting functions and collaborating with staff in Global Safety Operations, and across various functions within Kenvue to facilitate compliant, timely, and efficient end-to-end case management.


Roles and Responsibilities

* Supports functional oversight of vendor staff involved in case receipt, case processing, and safety reporting. In addition to liaising with vendor partner(s) and resolving potential issues.
* Expertise in operational activities including case processing; providing subject matter expertise in pharmacovigilance (PV) and global/local AE regulatory reporting requirements.
* Identifies and implements process efficiencies and continuous quality improvements to support business objective of cost‑efficient sustainable and scalable end‑to‑end case management solutions.
* Supports development of standard operating procedures, work instructions and training to support case management activities; ensuring vendors are adequately trained.
* Supports internal audits and external inspections and develops corrective and preventative actions to address non‑conformances.
* Participates in cross‑functional governance teams to ensure alignment of priorities among key business partners.


Qualifications

* A minimum of bachelor’s degree in life sciences or health‑care field with 3 years of experience in Pharmacovigilance OR Advanced degree (e.g., MS, MPH, PharmD, or PhD) with 2 years of experience in Pharmacovigilance or related activities; industry activities preferred.


Knowledge, Skills and Abilities

* Demonstrated experience working in a matrix environment and cross‑functional teams.
* Practical knowledge of global and local regulatory pharmacovigilance requirements.
* Understanding of medical terminology and ability to summarize medical information.
* Working knowledge of safety databases to identify system enhancements and efficiencies including MedDRA and product dictionaries and version updates.
* Proficient in Microsoft office applications.


Benefits

This role offers a very competitive hourly rate. This contract will run until June 2026.


Application process

* This role falls Inside IR35.
* PAYE or Umbrella options only.
* Please apply with a WORD CV.
* If your application is successful, you will be sent some pre‑screen questions; please ensure to complete these before your screening call.


Diversity, Equity & Inclusion

Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment based on business needs, job requirements, and individual qualifications, without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, protected veteran status, or any other legally protected characteristic, and will not be discriminated against on the basis of disability.

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