...<span>recording of activity in logbooks, Batch manufacturing record & Responsible for completing documentation as required in the manufacturing of </span><b>product </b><span>and the cleaning of facilities and equipment, following cGMP's and...
...<span>Experience
1. Knowledge of Contract Manufacturing Operations (</span><b>CMO)</b><span> process for the Pharmaceuticals.
2. Knowledge of current regulatory requirements such as Schedule M, Eu GMP, USFDA, ICH etc.
3. Rich experienc...
MAIN PURPOSE OF ROLE
Summarize the main purpose of the role.
Individual contributor that works under limited supervision.
Applies subject matter knowledge.
Requires capacity to understand specific needs or requirements to apply skills/kno...
Followings Will Be The Responsibilities Of The Position Holder
Compliance cGMP norms in warehouse as well as dispensing area.
Compliance warehouse respective area SOP in daily routine work.
Compliance EHS norms in warehouse as well as di...
Experience Required: B.Pharm / M. Sc. with 6-10 years of experience in Micro QC. Approved chemist licensed candidate shall be preferred. Well versed with CAPA, GMP Documentation, should have exposure to regulatory audits such as MHRA, USFDA etc...
