5+

Daily routine analysis Wet lab and Instrument, Manage data records for the lab activities, Manage documentation of lab experiments, Co-ordinate with R&D for daily analysis.

M.Pharm, B.Pharm, D.Pharm, Diploma. Encube Ethicals is a pharmaceutical company dedicated to only topical formulations serving patients and leading pharmaceutical brands around the world with high - quality, affordable topical products with the help of 3 state-of-the-art facilities.

D.Pharm, B.Pharm, M.Pharm. Blister - Cartonator, Uhlmann, BQS, IMA PG Bottle - CVC, Pharmapack, Countec, Labeling

Personnel handling this profile will be responsible for performing reactions as per the requirement of the project. They are also responsible for documenting the observations in relevant note books. They are to follow instructions from the supervisor and work in a group (or individually) to accomplish the tasks in a timely and efficient manner. 

Ensure process is in place to maintain the PV QD Training Matrix, training curriculum updated. Ensure global traceability and monitoring of investigations of all identified quality gaps, quality risks and ensure that Corrective and preventive Action Plans are implemented in timely manner.

The Quality Manager responsible for handling technical complaints is tasked with investigating and managing technical complaints raised by clinical investigator sites regarding Investigational Medicinal Products and Medical Devices. Support data integrity incidents, manage escalations, and contribute to global DI networks and initiatives.

Work with the Team to achieve and exceed targets within the frame given by the Group Leader and Team Leader of Process Innovation. Keep self updated on the state of the art in synthetic chemistry development and techniques, while putting specific focus on innovative process research

Plan, implement and evaluate experiments for establishing of composition, manufacturing procedures and packaging via support of def. evaluation experiments taking product stability, bioequivalence and possible production site into consideration.

2 TO 8 YEARS YEARS OF EXPERIENCE IN COMPRESSION, GRANULATION AND PACKING. EXPERIENCE IN RECEIPT & DISPENSING ACTIVITY, INWARD & OUTWARD ACTIVITY