MEDREICH LIMITED – Urgent Openings for AR&D / Regulatory Affairs / Packaging Development Departments
We are at Medreich R&D looking for Analytical Research & Development Scientists with 1-5 years of experience in solid oral (Tablet/Capsules).
Key Skills: HPLC, GC analysis, IC analysis, Dissolution testing, Multimedia dissolutions, Excipients compatibility, Development support analysis, Method development, Method validations, Stability analysis, Method optimisation, Method transfer, Method verification, API qualification, Working standard generation, Preparation of Method development report, Validation protocols and reports, Method transfer protocols and reports.
Job Location: Bommasandra, Bangalore.
Interested candidates can share their profile to firstname.lastname@example.org / email@example.com
We are looking for Regulatory specialists with 1-4 years. Preparation, review and compilation of CTD dossier for Europe, Canada, Australia and Emerging market countries..
Position is based at Bangalore and interested candidates may share the profiles to firstname.lastname@example.org
We are looking for Packaging Development professionals with prior experience of 4-8 years in the pharmaceutical industry. The role includes designing and development of packaging materials for new product launches as per regulatory/customer/production requirements. This position will identify, lead support cost-saving initiatives in packaging.
Candidate must be IIP graduate and the position is based at Bengaluru.
Interested candidates can share their profiles to email@example.com
Mr. Shiv Kumar is the Author and founder of pharmaceutical guidance, he is a pharmaceutical Professional from India having more than 14 years of rich experience in pharmaceutical field.
During his career, he work in quality assurance department with multinational company’s i.e Zydus Cadila Ltd, Unichem Laboratories Ltd, Indoco remedies Ltd, Panacea Biotec Ltd, Nectar life Science Ltd. During his experience, he face may regulatory Audit i.e. USFDA, MHRA, ANVISA, MCC, TGA, EU –GMP, WHO –Geneva, ISO 9001-2008 and many ROW Regularities Audit i.e.Uganda,Kenya, Tanzania, Zimbabwe. He is currently leading a regulatory pharmaceutical company as a head Quality. You can join him by Email, Facebook, Google+, Twitter and YouTube