Are you a hardworking and proactive Regulatory Affairs Specialist looking to take the next step up to a Senior Regulatory Affairs Specialist role?
As the Senior Regulatory Affairs Specialist you will be responsible for determining and supporting the regulatory activities which lead to, and maintain regulatory compliance and approval the companies products globally
Key responsibilities -Coordination and management of regulatory and product registration activities -Preparatio ...
I am looking for a Regulatory Affairs Specialist (Quality Assurance Analyst) to join my client Regulatory Affairs division. This is an amazing opportunity to grow with an industry leader and grow career within medical devices.
Regulatory Affairs Specialist will report to the Director of Regulatory Affairs division. RA Specialist will use technical and regulatory knowledge to perform regulatory affairs activities supporting following activities: product registrations, import/export support, product development, safety and environmental regulation, manufacturing (GMP), and regulatory data collection and management.
RA, GMP, FDA, technical writing, dossiers, medical devices
Se quello che cerchi Ă¨ una posizione a tempo indeterminato nell'ambito di Medical Devices, dove puoi crescere e fare la differenza, questa Ă¨ un'opportunitĂ per te. Sto cercando un Regulatory Affairs Specialist (Quality Assurance Analyst) che farĂ parte della divisione Regulatory Affairs. Questa Ă¨ una straordinaria opportunitĂ che ti permetterĂ di crescere all'interno di un'azienda leader nel settore.
Regulatory Affairs Specialist - Scientific Consultant in Part 2/CMC in Veterinary Pharmaceuticals.
Permanent. North East England
A global consultancy based in North East England are looking for new members for their team due to expansion. This is a permanent position working within the regulatory affairs team in both human health and animal health.
My client a global medical device company is seeking a Regulatory Affairs Specialist to join their Regulatory Affairs team in Cork.
Working as part of the orthapeadic Regulatory Affairs team your responsibilities will include:
- Provide necessary information to fulfil international regulatory requests and product registrations. - Investigate complaints for medical reporting and filing to the appropriate competent authorities when required. ...
My Client a Cork based start up generic company are seeking a Regulatory Affairs Specialist to join there team for a 4 month contract. A â‚¬35000-â‚¬45000 salary is on offer.
Under general direction of the Quality Assurance, Laboratory & Regulatory Manager, you will be primary responsible for regulatory affairs in launching finished product and compliance with cGMPâ€™s in addition support release of finished product, supplier management and investigation of product issues. ...
Our client are a leading medical device company based in Bavaria, Germany. This role provides a great opportunity for a young professional looking to develop their career within an interesting and innovative product line. Our client produce class III medical devices on a global scale in a niche therapy area. Gain invaluable experience and develop your career with this fantastic opportunity! Ensure you apply today to find out more!
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