A career at our company is an ongoing journey of discovery: our around 52,000 people are shaping how the world lives, works and plays through next generation advancements in healthcare, life science and performance materials. For more than 350 years and across the world we have passionately pursued our curiosity to find novel and vibrant ways of enhancing the lives of others.
An exciting opportunity has arisen for a Regulatory Expert for APIs based in Arklow, Ireland.
The Regulatory Expert will support regulatory submissions of active pharmaceutical ingredients (APIs) and excipients. This role will ensure that relevant changes to product registrations and listings are properly notified to the relevant authorities and maintained. In-depth knowledge about requirements for filing, registration, and notification of pharmaceutical starting materials, excipients and APIs is required. In addition,knowledge of import and export requirements related to Good Distribution Practices for APIs is also desired.
This role will be part of a global regulatory team where you will interact closely with the quality and operational units at the site. You will collaborate with internal experts within the business areas and across the business organisation to gather data and support efforts. In addition, you will support the manufacturing sites and distribution activities to comply with regulatory requirements and good regulatory practices. Participation as the Regulatory Representative in the product development process to develop and execute regulatory strategies, assessments and plans is key, and interaction with external customers will be required.
Key responsibilities include:
- Technical writing of DMF documents in the dedicated document management system
- Support regulatory requirements on import and export of APIs
- Prepare and review documents for submission to Regulatory Agencies in compliance with requirements, to ensure their timely written submissions
- Support the regulatory tracking databases for planning, scheduling, submissions, and action dates, and overall project management
- Create policies and operating procedures to strengthen regulatory compliance
- Support the issuance of Letters of Authorization (LoA)
- Support provision of responses to Customer Regulatory Queries
- Drive and Support provision of responses to Customer Regulatory issues
Who you are:
- Bachelor or Master level of education in Pharmacy or Life Sciences with a strong emphasis in Chemistry or Biology
- Several years (ideally 3 – 5) of relevant industry experience and/or regulatory affairs related to APIs, pharmaceutical excipients and process materials
- Knowledgeable of US FDA and EU drug regulations, specifically for submissions in CTD format. Knowledge of regulatory landscape of other important regions, e.g., in Asia.
- Expertise in QC and QA for pharmaceutical starting materials and requirements of pharmacopeias
- Experience in submissions in CTD format. Experience in e-submission tools is welcome
- Knowledge of regulations relevant to pharmaceutical starting materials, quality requirements and preferably processing of APIs and excipients in general. You should be well-versed in regulatory trends for pharmaceutical raw and starting materials.
- Proficient in MS Office Software (Word, Excel, PowerPoint, Project) and ERP Systems such as Oracle or SAP. Demonstrate good communication & project management skills. Work successfully within a multidisciplinary international team.
What we offer: With us, there are always opportunities to break new ground. We empower you to fulfil your ambitions, and our diverse businesses offer various career moves to seek new horizons. We trust you with responsibility early on and support you to draw your own career map that is responsive to your aspirations and priorities in life. Join us and bring your curiosity to life!
Curious? Apply and find more information at https://jobs.vibrantm.com