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  • 4 days ago

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We are hiring a creative Regulatory Affairs Manager to join our incredible team at Abbott Laboratories in Kilkenny, Co. Kilkenny.
Growing your career as a Full Time Regulatory Affairs Manager is an incredible opportunity to develop productive skills.
If you are strong in cooperation, people management and have the right personality for the job, then apply for the position of Regulatory Affairs Manager at Abbott Laboratories today!

Regulatory Affairs Manager page is loaded Regulatory Affairs Manager
Apply locations Ireland - Kilkenny time type Full time posted on Posted 4 Days Ago job requisition id 31055056 JOB DESCRIPTION:

Have you ever wanted to make a difference?

At Abbott, you will play a crucial role to help people live more fully at all stages of their lives. Abbott is a global healthcare leader and our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritional products and... branded generic medicines. Our 113,000 colleagues have a daily impact on the life of people in more than 160 countries.

Abbott Ireland

In Ireland, Abbott employs over 5,000 people across nine sites. We currently have six manufacturing facilities located in Clonmel, Cootehill, Donegal, Longford and Sligo and a third-party manufacturing management operation in Sligo. Abbott also has commercial, support operations and shared services in Dublin and Galway. We have been making a difference in the lives of Irish people since 1946.

Diabetes Care Kilkenny

Abbott Diabetes Care is opening a new site, in Kilkenny, that will be at the forefront of Diabetes care with the latest technology, to manufacture FreeStyle blood glucose test strips and FreeStyle Sensors for use in diabetes management. Among Abbott Diabetes Care leading brands are the FreeStyle Precision, FreeStyle Lite and FreeStyle Libre systems.

This is how you can make a difference at Abbott:

In this role you will be in charge of managing teams within the Regulatory Affairs Sub-Function.

Focus is on policy and strategy implementation and control rather than development and you will typically handle short-term operational/tactical responsibilities.

It will be a very big plus if you can bring experience in developing projects or sites from square one.

As the Manager of the Regulatory Affairs Sub-Function, you will be responsible to:
• Oversee the strategy implementation and operations for directing development of product registration submission, progress reports, supplements, amendments, or periodic experience reports.
• Interact with regulatory agency to expedite approval of pending registration.
• Serve as regulatory liaison throughout product lifecycle.
• P articipate in some of the following: product plan development and implementation, regulatory strategy, risk management, chemistry manufacturing control (CMC).
• Ensure timely approval of new drugs, biologics or medical devices and continued approval of marketed products.
• Serve as regulatory representative to marketing, research teams and regulatory agencies.
• Advise development and/or marketing teams on manufacturing changes, line extensions, technical labeling, appropriate regulations and interpretations.

For this position it will be necessary to bring:
• Manufacturing operations and manufacturing change experience.
• People management experience.
• Experience resolving any issues regarding nonconformance.
• Strong attention to detail.
• Solid communication skills and ability to communicate at all levels.
• Experience with EU and US regulatory bodies.
• Strong organisational skills.

You should also have:
• Ability to adapt to change.
• Capacity to keep external communication to governing bodies clear and concise, avoiding any confusion with regulatory bodies.
• Experience reviewing manufacturing changes.
• Optimization of regulatory acceptance changes.
• Supporting manufacturing operations.
• Dealing with Ad Hoc Issues.
• Capability to work with tight deadlines.

QUALIFICATIONS AND EXPERIENCE
• Minimum Level 8 Degree in Engineering or Science or related discipline.
• Minimum of 5 years of experience in a similar position and experience with EU Regulatory bodies in regards to applications and submissions or equivalent international experience.

Abbott is an equal opportunities employer.

Connect with us at or on LinkedIn at on Facebook at and on Twitter @AbbottNews.

The salary for this role is between:
N/A JOB FAMILY:
Regulatory Operations DIVISION:
ADC Diabetes Care LOCATION:
Ireland > Kilkenny : Kilkenny Business and Technology Park ADDITIONAL LOCATIONS:
WORK SHIFT:
Ie - Shftpre0 (Ireland) TRAVEL:
Yes, 20 % of the Time MEDICAL SURVEILLANCE:
Yes SIGNIFICANT WORK ACTIVITIES:
Not Applicable About Us
Abbott is about the power of health. For more than 125 years, Abbott has been helping people reach their potential — because better health allows people and communities to achieve more. With a diverse, global network serving customers in more than 160 countries, we create new solutions — across the spectrum of health, around the world, for all stages of life. Whether it’s next-generation diagnostics, life-changing devices, science-based nutrition, or novel reformulations, we are advancing some of the most innovative and revolutionary technologies in healthcare, helping people live their best lives through better health.

The people of Abbott come to work each day with relentless energy, enthusiasm and a promise to enhance the health and well-being of millions of people. They push the boundaries to help manage and treat some of life’s greatest health challenges.

We invite you to explore opportunities at Abbott , to see if your talents and career aspirations may fit with our openings. An equal opportunity employer, Abbott welcomes and encourages diversity in our workforce.

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Benefits of working as a Regulatory Affairs Manager in Kilkenny, Co. Kilkenny:

● Learning opportunities
● Opportunities to grow
● Competitive salary

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