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Senior Executive, Manufacturing Process Operations at Amneal India

Ahmedabad, gujarat, India -

Full Time

Start Date

Immediate

Expiry Date

07 Sep, 26

Salary

0.0

Posted On

09 Jun, 26

Experience

10 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Manufacturing, Processing, Packaging, Documentation, Training, Equipment Coordination, Safety Compliance, Material Management, Batch Records Review, SOP Implementation, cGMP Compliance, Process Study, Cleaning Procedures, Operational Management, Drug Product Handling, Stability Batches

Industry

Pharmaceutical Manufacturing

Description

* Supervision of manufacturing, processing, packaging and holding of drug product as per define and approved procedures for stability batches and commercial batches. * Maintaining the area and equipment in orderly manner as per cGMP requirements in a good state of repair and sanitized condition. * To perform online documentation with respect to departmental procedures as per good documentation. * To impart training of operation and cleaning related SOP to all subordinates and operators. * Co-ordination for IQ / OQ for any new equipments / system. * To perform PQ for any new equipments / system. * To follow all concern departmental SOPs for day to day operation and cleaning. * To handle and manage material movement as per defined procedure and approved Batch Manufacturing Record / Batch Packing Record. * Review, execution and implementation of Batch Manufacturing Records, Batch Packaging Records, Process Study Protocols, Process Study Reports and all relevant Documents. * To follow all safety rules and departmental general instructions. * To perform work other than defined in the Job responsibility are to be done, as per the requirement of HOD, by following HODs instruction and guidance.

Responsibilities

The Senior Executive will supervise the manufacturing, processing, packaging, and holding of drug products according to approved procedures. They will also maintain equipment and areas in compliance with cGMP requirements and manage documentation and training for subordinates.