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101 AmerisourceBergen Jobs
Specialist-SPM-Regulatory Affairs
AmerisourceBergen
posted 3+ weeks ago
Job Role Insights
Flexible timing
Key skills for the job
Job Description
Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health, come join our innovative company and help us improve the lives of people and animals everywhere. Apply today!
Job Details
- Develop and maintain strong client relationships and actively explore opportunities for increased service support to Line Manager.
- Participation in regulatory processes to gain and maintain marketing authorizations for human and veterinary medicinal products (applications, renewals, variations) including medical devices, cosmetics, food supplements and herbal products.
- Preparation, review and compilation of documents within the framework of regulatory affairs projects.
- Communication with clients and Health Authorities.
- Support with scientific advice procedures and representation of clients with health authorities.
- Responsible for the planning and execution of client projects in accordance with KPIs. Coordination of project teams with colleagues and qualified external partners.
- General guidance (consultancy) of colleagues and clients regarding Regulatory Strategy and Procedure Management.
- Regulatory intelligence - develop and maintain personal regulatory knowledge, apply to client projects and actively share with colleagues.
- Present seminars and lectures for colleagues, clients and professional audiences. Active contribution and distribution of department relevant expertise.
- Support with VDC strategy implementation and optimization.
- Comply with, maintain and contribute to optimizing internal processes.
- Support with VDC led commercial, marketing and business development activities including proposal input.
- Support respective lead in delivery to budget with accurate and timely reporting and provide project insights to address invoicing queries.
- In agreement with Head of VDC REG providing on-site regulatory support to clients.
- The employee agrees to take over other reasonable tasks that are corresponding with their abilities upon agreement with their Line Manager/Practice Area Lead/Head of VDC REG.
.
- Qualification: B.Pharm/M.Pharm
- Experience: 2 -5 years
- Regulatory Affairs experience in a pharma company, preferably including experience in cosmetics, food supplements and/or herbal products
- Experience in EU submission process
- Knowledge of EU regulatory affairs disciplines
- Knowledge of labelling regulations and guidance
- Excellent verbal and written communication skills
- Attention to detail and accuracy
Benefit offerings outside the US may vary by country and will be aligned to local market practice. The eligibility and effective date may differ for some benefits and for team members covered under collective bargaining agreements.
Cencora is committed to providing equal employment opportunity without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, age, disability, veteran status or membership in any other class protected by federal, state or local law.
Cencora is committed to providing reasonable accommodations to individuals with disabilities during the employment process which are consistent with legal requirements. If you wish to request an accommodation while seeking employment, please call 888.692.2272 or email hrsc@cencora.com . We will make accommodation determinations on a request-by-request basis. Messages and emails regarding anything other than accommodations requests will not be returned
Employment Type: Full Time, Permanent
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Flexible timing
Monday to Friday
No travel
Day Shift
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