Regulatory Affairs Specialist, Human Pharma
Boehringer Ingelheim
**The Position**
**Regulatory Affairs** **Specialist** **, Human Pharma**
+ To achieve timely & successful product registrations in accordance with corporate & local strategies.
+ To collect any information on new Regulations and Guidelines, and to share it in local RA team.
+ To ensure compliance with Company regulatory policies, regulations & procedures.
**Duties & Responsibilities**
**1. Regulatory Planning and Submission**
+ Manage all the regulatory tasks & projects, including attaining, maintaining product licenses and operation licenses for assigned portfolio on behalf of BoehringerIngelheim as required by local regulations.
+ Compile registration applications for assigned portfolio and ensure timely approval.
+ Monitor progress of submissions & coordinate timely responses to all questions from the health authorities.
+ Be Compliant with Corporate policies, regulations & procedures, in particular implementation of current Company Core Data Sheet (CCDS), Change Review Committee (CRC) and local change control procedures
**2. Regulatory Intelligence and Interaction**
+ Responsible to collect new or updated local regulations via various potential sources and keep the local RA team and ROPU informed
+ Communicate with Regulatory Authorities and local industry groups on regulatory issues
**3. Cross-functional collaboration and support**
+ Provide regulatory consultation &collaborate with local business stakeholders
+ Provide feedback to the implementation of global initiatives when required
**4. Quality and Compliance**
+ Timely submission of CCDS, CRC, Renewals, PSUR and other local variations in compliance with internal KPIs
+ Ensures that regulatory database is up to date to reflect the current registration status or regulatory requirements
+ Support local inspection readiness
+ Archiving of local regulatory submission documents
**Requirements**
**Minimum Education** **/** **Degree Requirements** **:** Bachelor’s degree in Pharmacy preferred
**Skills required:**
+ Good knowledge of National Drug Regulations and Procedures
+ Good communication skills for internal & external interactions
+ Proactive and assertive attitude
+ English proficiency
+ Good computer literacy skills, comfortable working with databases
**Experience:** Minimum 3 years of experience working in the pharmaceutical, medical device or healthcare industry with strong performance record in the previous position.
**READY TO CONTACT US?**
Please contact our Recruiting Team: Ms. Phuong Vo: phuong.vo@boehringer-ingelheim.com
All qualified applicants will receive consideration for employment without regard to a person’s actual or perceived race, including natural hairstyles, hair texture and protective hairstyles; color; creed; religion; national origin; age; ancestry; citizenship status, marital status; gender, gender identity or expression; sexual orientation, mental, physical or intellectual disability, veteran status; pregnancy, childbirth or related medical condition; genetic information (including the refusal to submit to genetic testing) or any other class or characteristic protected by applicable law.
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