Hyderabad

Coordination with stakeholders in SIM (Supplier Information Management) approval process for Quality deliverables.

Applicants for the above positions should have a Master's degree (MTech, MSc, or IMSc) with aggregate marks greater than 70% or a 7.5 CGPA from a reputed university.

Preferably PharmD with Experience in Coordinating and conducting clinical trials. Conducting and coordinating clinical trials in the department of Medical Oncology.

LOOKING FOR OPERATORS AND SUPERVISORS WHO ARE HANDLING RMG,FBD,COMEL,SHIFTER,MILLER 

M.Pharm. or M.S (Pharm) (Medicinal Chemistry or Process Chemistry) GPAT Qualified. Development of Peripherally Restricted RAGE Inhibitors as Safe Therapeutics for Diabetic Peripheral Neuropathy.

Masters/ Integrated Masters Degree in Natural or Pharmaceutical Sciences OR bachelors degree in Engineering or Technology or Medicine from a recognized University or equivalent.

Senior Medical device documentation Associate. Good understanding of the medical imaging devices compliance from a global and regional perspective, registration procedures, preparation of answers to questions from health authorities. PAREXEL

Exposure to handle analytical equipments like GC, HPLC. KF, Potentiometer, IR & UV. Knowledge on ICH guidelines, analytical validations & Regulatory Knowledge.

M.Pharm / MSc in Chemistry / Biochemistry / Pharmaceutical sciences / a relevant branch of Engineering or Life Sciences, or evidence of exceptional ability, preferable with experience in formulation research and development.