Sector: Pharmaceutical Manufacturing Industry

Multinational Pharmaceutical Manufacturing client has an excellent opportunity for a Regulatory Compliance – Project Manager 1 year contract with the potential of becoming permanent.

Purpose: Enhance the Pharmaceutical Regulatory Portfolio and coordinate Technology Transfer in the manufacturing facility.

Qualifications Required:
Pharmacist Degree and SAPC Registration

Your Pharmaceutical Expertise Required, but not limited too:
2 years experience in a similar role with Pharmaceutical Manufacturer
Co-ordinate technical agreements and responsible for the Technology Transfer
Experience in Regulatory Affairs and Compiling registrations of dossiers for submissions
Liaise with Regulatory bodies internal and external
Product problem solving, product research and development
Authorisation of registration applications on all products in relevant countries
Ensure Regulatory Affairs department applies the latest Procedures and Guidelines
Optimize the regulatory portfolio in all sectors and cooperate with all departments and stakeholders

Email applications with reference PM – PE – MK to: (email address) To enquire, please call 0860 100 MVG(684)

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