A Global Multinational Company headquartered in Italy, is seeking a target oriented, self-motivated individual who would be interested in working as Analytical Senior Scientist.
Key Responsibilities:
• Development and Validation of Drug Substance (DS) & Drug Product (DP) analytical method;
• Transfer the analytical methods to R&D QC;
• Identify the Critical Quality Attributes for both Drug Substance and Drug Product (including interaction with device and CCS), for the appropriate definition of critical specifications and related scientific justification;
• Ensure that DS/DP characterization is conducted in accordance to Company SOPs and protocols and with cGMP/ICH where applicable;
• Ensure that all laboratory documentation is completed according to company standards including all relevant investigations;
• Ensure a continuous innovation of the analytical technologies, in order to keep a high level and excellence of scientific know-how.
• Develop scientific networking, interacting with advanced CROs/academia.
With a Ph.D. in Analytical Techniques and at least six years of relevant pharmaceutical & analytical development experience in a well-structured company, the ideal candidate has got an international experience, strong knowledge of modern analytical techniques and development of different pharmaceutical forms, good understanding of analytical method development & validation requirements of pharmaceutical industry, a good knowledge of chromatographic sciences and spectroscopic technologies e.g. UV, IR, MS, NMR, XRD.
Strong knowledge of characterization techniques in physical and aerodynamic properties, chemical and solid state stability. The right candidate is a scientific problem solver who works well independently and in a team environment and with the determination and ability to foster organisational and cultural (i.e. scientific and innovation) change. Strong knowledge about Drug Substance/Excipients compatibility studies and good understanding of cGMP, ICH and FDA requirements.
Additional experience in pharmaceutical dosage forms for pulmonary delivery [i.e. Pressurized Metered Dose Inhalers (pMDI’s), dry powder inhalers (DPI), liquid-nebulizers (UDV)] could be relevant.
Fluent in English, good communication skills are required.
The Client offers a permanent position, competitive salary and generous social benefits, the opportunity for development and advancement within a constantly growing company and an innovative and stimulating atmosphere of a multicultural environment, plus a relocation package.
If you are interested in this new, exclusive career opportunity, please email your application to sergio.carito@secpharma.com or call Sergio Carito on +44 207 255 6665.
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