Rameshwar Verma Email & Phone Number

Indore, Madhya Pradesh, India

• Maintain the area as per cGMP norms.• Preparation of URS for new equipments.• Handling a wide range of packing activities.• Trouble shooting of serialization system at line level. • Responsible for DSCSA compliance audit readiness.• Identifying areas of improvement and recommending process modifications.• Managing packing operations to ensure timely accomplishment of targets.• Hands on experience in process validation and qualification of equipements… Show more • Maintain the area as per cGMP norms.• Preparation of URS for new equipments.• Handling a wide range of packing activities.• Trouble shooting of serialization system at line level. • Responsible for DSCSA compliance audit readiness.• Identifying areas of improvement and recommending process modifications.• Managing packing operations to ensure timely accomplishment of targets.• Hands on experience in process validation and qualification of equipements. • Coordinating with cross functions team for smooth & uninterrupted running of all packing activities.• Coordinating monthly & weekly packing plans for bottle packing lines in view with maximum capacity utilization.• Good Knowledge about 21 CFR part 11 complient systems such as Caliber E-log, Reetrak Client, Reetrak Communicator, RfXcel, Clarisoft etc.).• Overseeing quality assurance & control, document issuance and submission; handling deviation and Change Control, SOP Revision, maintaining safety standards at work place.• Setting direction, energizing, mentoring, coaching, motivating, guiding and supporting teams. Show less

Ahmedabad, Gujarat, India

Ahmadabad, Gujarat, India

QMS/Alert management/Serialization/Reetrak/Rfxcel/Clarisoft/Zebra designer Systems and EU FMD Regulation. Fully knowledgeable in Packaging Activities.

Ahmedabad, Gujarat, India

Serialization/Reetrak/Rfxcel/Clarisoft/Zebra designer Systems and EU FMD Regulation. Fully knowledgeable in Packaging Activities.

Ranipool, East Sikkim

• Maintaining all the records as per cGMP standard.• Responsible to handle equipments as per . SOPs• Responsible for documentations of BPRs and general.• Cleaning records as per procedures.• Minimization of the probabilities of line clearance failures by providing training to the concerned about the critical points to be checked during line clearance, so as to avoid product mix-up at any stage.• Responsible for daily usage log, equipment usage log calibration log.• A… Show more • Maintaining all the records as per cGMP standard.• Responsible to handle equipments as per . SOPs• Responsible for documentations of BPRs and general.• Cleaning records as per procedures.• Minimization of the probabilities of line clearance failures by providing training to the concerned about the critical points to be checked during line clearance, so as to avoid product mix-up at any stage.• Responsible for daily usage log, equipment usage log calibration log.• A sense of urgency. • Supervision of online packing. • To evaluate potential ability of man power handling. • Knowledge of regulatory bodies like USFDA, MHRA , TGA etc Show less

Bachelor'S Degree, Pharmacy, Pharmaceutical Sciences, And Administration, A

Activities and Societies: Debate Team, Seminars Bachelor of Pharmacy

High School, Biology, General