At a Glance
- Tasks: Lead pharmacovigilance audits and support regulatory inspections to enhance healthcare quality.
- Company: Join Johnson & Johnson, a leader in healthcare innovation and inclusivity.
- Benefits: Competitive salary, diverse work environment, and opportunities for professional growth.
- Other info: Dynamic global team with opportunities for travel and career advancement.
- Why this job: Make a real impact on health by developing smarter treatments and solutions.
- Qualifications: Bachelor’s degree in natural/biological sciences and strong teamwork skills required.
The predicted salary is between 60750 - 74250 £ per year.
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.
About Innovative Medicine: Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Position Overview: Johnson & Johnson IM is currently recruiting for a Pharmacovigilance QA Auditor Specialist. As a Pharmacovigilance QA EMEA Auditor Specialist, you will be part of a dynamic global team working to enhance quality across the Company through pharmacovigilance audit and business partner collaboration.
Key Responsibilities:
- Leads the planning, conduct and reporting of Pharmacovigilance routine audits.
- Supports non-routine Pharmacovigilance audits of activities, data, internal facilities and processes in GxP areas.
- Participates in projects or serves on teams, as assigned by supervisor.
- Supports regulatory inspections in various supporting roles.
- May assist in the preparation of training material if requested.
- Provides consultation to business partners on routine tasks with occasional supervision.
- Cooperates with business partners when contacted for compliance inquiries and seeks advice on non-routine and more complex issues to ensure a departmental unified position.
Qualifications:
- Bachelor’s or equivalent University degree required; Focused degree in natural/biological sciences or equivalent.
- Strong verbal and written communication skills, including presentation skills.
- Strong teamwork and analytical skills.
- Ability to work effectively as part of a collaborative team.
- Fluency in English.
Preferred:
- Minimum of 2 years’ experience in a GVP-regulated environment is preferred, with demonstrated exposure to Pharmacovigilance activities.
Other: This position requires 10%-30% domestic and international travel.
Required Skills: Agile Internal Audit, Analytical Reasoning, Audit and Compliance Trends, Audit Reporting, Business Behavior, Compliance Management, Compliance Policies, Compliance Risk, Critical Thinking, Detail-Oriented, Problem Solving, Quality Control (QC), Quality Standards, Regulatory Environment.
Location: High Wycombe, Buckinghamshire, United Kingdom
Type: Full time
Pharmacovigilance QA EMEA Auditor in Milton Keynes employer: Johnson & Johnson
Johnson & Johnson in High Wycombe is an exceptional employer, offering a dynamic work culture that fosters innovation and collaboration. Employees benefit from comprehensive growth opportunities, competitive compensation, and a commitment to compliance excellence, making it a rewarding environment for those passionate about quality systems and regulatory standards.
