Senior Manager-1 Job Vacancy in Sun Pharmaceutical Industries, Inc. Halol, Gujarat – Updated today

Are you looking for a New Job or Looking for better opportunities?
We got a New Job Opening for

Full Details :
Company Name : Sun Pharmaceutical Industries, Inc.
Location : Halol, Gujarat
Position :

Job Description : Title: Senior Manager-1
Date: Feb 24, 2022
Location: Halol 1 – Plant
Company: Sun Pharmaceutical Industries Ltd
Qualification required
Full time Graduate in Pharmacy (B. Pharm) / Post graduate in Pharmacy (M. Pharm)

Experience required
10 to 12 years in Manufacturing in Pharma Industries.

Job Location
Halol

Industry preferred
Preferably from Pharma OSD Manufacturing Business

Reporting to
Block Head / Production Head

Preferable proficiency
Proficiency in English Communication, Good Presentation

Employment Type
Full Time

Job Responsibility
Manufacturing and packing operations of tablet formulation.
Daily planning and machine loading, ensuring plan V/s Actual & Quality output.
Ensure Investigations, CAPA, Batch records preparation completion schedule is prepared, tracked and execution of schedule as per plan.
Responsible for cGMP document like: Batch Manufacturing records, in process and finished products test requisitions etc.
Responsible for QMS activity – Incidents, Investigations and its related activities. In track wise system finalization, approval and timely closing of Investigation reports and its documentation of the tablet and hard shell department
Responsible for completion of CAPA and related activity in Track wise system.
Protocol / SOP / BMR preparation for the New Machines, New Product. Revision of protocol / SOP / BMR whenever required and execution of Protocol / SOP / BMR.
Responsible for calibration qualification and validation activity of respective equipment for products.
Make daily reports to production manager / superiors on day to day activities concerning the department.
Coordination with other departments like Admin, Warehouse, QC, QA, QE, MIS and engineering for related activities.
Maintaining the GMP documents like equipment logbooks, records of physical monitoring and housekeeping records.
To assist establishing a system in accordance with Good Manufacturing practice guidelines and responsible for follow established / new procedures, maintaining and updating existing procedures in the department.
Responsible to co-maintain, coordinate for validation and GMP in all departments along with the Quality Assurance officer and to coordinate with Quality Control department in matters relating to Product Quality.
Training the subordinates and manpower to meet the organizational goals and achieve GMP compliance.
Optimization of resources namely man, material and machine in respective department.
Help the officers / subordinates into standardize production activities to achieve better efficiency and product quality.
Destruction note preparation, approval and execution.
Should have fluency in English and presentable.

This post is listed Under  Technology
Disclaimer : Hugeshout works to publish latest job info only and is no where responsible for any errors. Users must Research on their own before joining any company