Life Sciences Job at Kyowa Kirin International | Apply Now
Looking for a promising life sciences job in the pharmaceutical industry? Kyowa Kirin International plc is hiring a Specialist, GPV Performance Excellence – Monitoring Team (18-month FTC) in Marlow, England, United Kingdom. This exciting pharmacovigilance job offers professionals the opportunity to work in regulatory intelligence, vendor governance, and pharmacovigilance operations within a globally recognized pharmaceutical company. If you are searching for a job in UK within life sciences and drug safety, this opportunity could be the perfect fit for your career growth.
- Job Position: Specialist, GPV Performance Excellence – Monitoring Team (18-month FTC)
- Company: Kyowa Kirin International plc
- Location: Marlow
- Industry: Pharmaceutical / Pharmacovigilance
- Employment Type: 18-month Fixed Term Contract
- Department: GPV Performance Excellence
About the Company
Life sciences job opportunities at Kyowa Kirin International plc provide professionals with the chance to work in an innovative and patient-focused pharmaceutical environment. Kyowa Kirin International plc is dedicated to improving patient outcomes through groundbreaking medicines and compassionate healthcare solutions. The company operates with a strong culture based on Teamwork, Commitment to Life, Innovation, and Integrity. Their mission, “Leaping Forward to Make People Smile,” reflects their dedication to patients, healthcare professionals, and employees worldwide.
Life Sciences Job Description
Life sciences job seekers interested in regulatory intelligence and drug safety will find this pharmacovigilance role highly valuable. Kyowa Kirin is seeking a Specialist, GPV Performance Excellence to join the GPV Performance Excellence Monitoring team.
The role focuses on ensuring pharmacovigilance regulatory intelligence is identified, assessed, actioned, and tracked according to global regulatory requirements. The selected candidate will collaborate with subject matter experts and cross-functional stakeholders to support regulatory intelligence activities, monitor implementation changes, maintain GPV vendor governance activities, and support metrics-related tasks. This pharmacovigilance job also involves documentation management, vendor oversight, and supporting updates to Pharmacovigilance System Master Files (PSMFs).
Qualifications
Life sciences job applicants applying for this pharmacovigilance role should meet the following qualifications and skills requirements:
- Bachelor’s degree in a life sciences discipline (minimum requirement)
- Good knowledge of global pharmaceutical and pharmacovigilance regulations such as ICH and GVP
- 1–2 years of experience in pharmacovigilance, regulatory affairs, or quality assurance within the pharmaceutical or biotechnology industry
- Strong proficiency in Microsoft Office tools including Word, PowerPoint, Excel, SharePoint, and Teams
- Highly organised with the ability to manage multiple priorities and deadlines
- Excellent written, verbal, and interpersonal communication skills
- Strong attention to detail with analytical and problem-solving abilities
- Ability to work independently and adapt quickly in a fast-paced environment
Key Responsibilities
Life sciences job responsibilities for this role include managing multiple pharmacovigilance and regulatory intelligence activities efficiently.
- Continuously monitor, gather, and analyse global pharmacovigilance regulatory intelligence from public and subscription-based sources
- Perform initial assessments and coordinate reviews with relevant SMEs
- Collate impact assessments and communicate outcomes to stakeholders
- Facilitate impact analysis meetings and track implementation actions to completion
- Maintain regulatory intelligence trackers, action logs, and timelines
- Ensure timely submission of deliverables to the Global Regulatory Intelligence Organization (GRIO)
- Prepare metrics, dashboards, and presentations to visualize progress and challenges
- Support preparation of regulatory intelligence meeting materials and presentations
- Ensure documentation such as audit trails, training records, and presentations are appropriately stored in Veeva and/or SharePoint
- Support vendor oversight activities and maintain GPV vendor lists
- Support updates to PSMF(s)
- Assist with management of shared GPV mailboxes
Why Apply for this Life Sciences Job?
Life sciences job opportunities at Kyowa Kirin offer professionals the chance to contribute to meaningful healthcare innovations while working in a collaborative and inclusive environment. Employees benefit from:
- Exposure to global pharmacovigilance operations
- Opportunities to work with international stakeholders
- Experience in regulatory intelligence and compliance
- A supportive and values-driven company culture
- Career growth within the pharmaceutical industry
