Ananta Medicare Limited Walk-in Interview 2022/Ananta Medicare Limited Notification full details below.Interested and eligible candidates can Send Resume.Ananta Medicare» aims to protect and preserve the most important human values – good health and quality of life.Group of companies Ananta Medicare» specializes in manufacturing and marketing of high-quality generic medicines as well as food supplements and cosmetic products with natural components.

• Vacancy details:
• Post Name: QA Executive/QC Executive (OSD)/Production Executive (Cephalosporin Unit)
• Qualification: M.Pharma in Pharmacy
• Experienced:5 to 8 years
• Openings:06
• Salary:₹ 4,00,000 – 5,50,000 P.A.

Job Description: Greeting from Ananta Medicare Limited !!!

• Important Details :
• Location: Ganganagar
• Post of date:29/12/2022
• Selection Process: The selection will be on the basis of Interview.

QA Executive(OSD)

Please mail your resumes at hrplant@anantamedicare.in

Assist in quality control stability testing, prepare and maintain stability records and summaries.

Involve in training and transfer of methods to and from quality control department.

Modify and validate analytical procedures to meet QCs needs.

Support design and development of experimental protocols, SOP’s, etc., consistent with cGMP/GLP.

Participate in special projects and department meetings via input, feedback and execution of assigned tasks.

Execute special projects on analytical and instrument problem solving.

Perform water testing for all types of water.

Adapt, maintain and operate analytical instrumentation.

Involve in procedure review and propose modifications and updates.

Ensure work environment is clean and safe complying with safety and pharmaceutical regulation.

Report monthly on supplies for QC orders involving devices and reagents.

Contribute to industrial, R&D qualification and validation activities and support routine maintenance.

Conduct various analytical testing procedures as per manufacturing/QC SOPs.

Prepare and test samples from all phases including production process (Raw Materials Analyst), during production itself (In Process Analyst), at the end of manufacture (Finished Product testing) or other handling process, with the goal of determining if the substance meets the standards or requirements of the project.

Ensure that experiments are completed according to established Standard Operating Practices (SOPs), and also Good Laboratory Practices (GLP)as per regulations (EU GMP).

Prepare technical documents that report the results of their lab work.

Responsible for minor equipment troubleshooting, calibration and repair.

Establish specifications for conducting assays and writing standard operating procedures.

QC Executive (OSD)

Please email your resume to hrplant@anantamedicare.in

Roles & Resonsibilities

• To provide administration support to QC Manager and provide necessary information to QC team members when required.
• Update and maintain Company Online Quality Management System for Procedures, policy and standard forms, as and when are required.
• To keep track on record in internal audits for project sites and head office.
• Assist QC manager to prepare reports for top management.
• Write technical reports such as quality alerts, construction excellence award write ups, minutes for meeting, etc.
• Maintain QC department library, manage and record QC tools and equipment.
• Adherence to safety practices in the work place.

Qualifications and Education Requirements

• Education: Minimum M. Pharm.
• Experience: At least 5 years of experience in Pharma industry.

Production Executive

• Provides overall direction for the technical and administrative operations in the warehouse, dispensing, processing and packaging.
• Prepares production schedules in co-operation with the Marketing Manager or Director.
• Responsible for reviewing all Batch Processing Record and Batch Packaging Record and ensures that the production is executed in accordance with the batch processing procedures and batch packaging procedures.
• Development and validation of critical processes.
• Ensures availability of Master Formula Record for each product
• Analyses market complaints and identify causes, suggest remedies.
• To provide guidance and support for Registration of Medicines for Export.
• Discusses production failure with Quality Control Head and determines causes of the failures and the solution.
• Responsible for ensuring that all equipment are correctly validated and utilized.
• Assists in conducting GMP inspections.
• Responsible for maintaining high level employee morale competence, development and training and conducting annual appraisal on all subordinates.
• Prepares production annual budget
• Improves the production cost.
• Any other responsibility assigned from time to time.
• Compliance of all rules, regulations and notifications etc. as may be applicable from time to time in respect of production and such other regulatory requirements as may be applicable pertaining to anyone or more functions falling within the ambit of the department.
• To circulate MIS report in respect of the aforesaid functions to such persons and with such periodicity as may be decided by the Management.