Manager - Production Pharma - Ankleshwar, Gujarat

Job Title: · Executive – Production · Educational Qualification and Experience · Diploma holder from a reputed university with 6-8 years of experience in pharma primary and secondary packing sections. · Key Responsibilities · Implement monthly production schedule maintaining qu ...

Job Title: Executive · – · Production, Pharma · Educational Qualification And Experience · Diploma Pharmacy/Diploma Mechanical, Instrumentation, Electrical Engineer from a reputed university, · having 6 to 8 years · in the pharmaceutical Primary and secondary packing section, and ...

Implementing monthly production schedules with consistent quality and adhering to regulatory guidelines. · ...

D. Pharm from a reputed university with experience in pharmaceutical production and manufacturing. · ...

Manager, Production - Pharmaceuticals · Graduate / Post Graduate in Pharmacy with 12 to 15 years of experience in Pharmaceutical Production · Strong leadership · Production Techniques/Troubleshooting · Communication & Time management & team management skills. · Reporting · Inter- ...

Sr. Executive – Production Pharma with 6 to 10 years of experience in pharmaceutical Primary and secondary packing section. · ...

Assistant Manager-Production Pharma · ∗ Educational Qualification: · ∗ M.pharm / B.Pharma from a reputed University( Note : It must be reputed) · ∗ Experience: · ∗ 8 - 10 Years In Pharmaceutical Primary And Secondary Packing Section. · . Exposure To Manufacturing Granualtion Co ...

This is a job for Sr. Executive- Production Pharma. The ideal candidate will have M. Pharm / B. Pharm from reputed university with 6 to 10 years of experience in primary and secondary packing section of pharmaceutical industry. · ...

Assistant Manager for Production in Pharma responsible for implementing monthly production schedules, ensuring quality and adhering to regulatory guidelines. · ...

We are looking for a Production Officer to join our team in Dahej,Vapi. · To ensure production activities. · To verify the cleaning of the process equipment's · To implement all GMP requirements. · ...

Ensures Products meet established standards by developing and implementing quality control procedures. · ...

The Sales and Marketing Manager will be responsible for leading B2B sales, key account management, and business development for pharma intermediates and specialty organic molecules. · ...

Production Operator responsible for manufacturing pharma and agrochemical intermediates. · Operates reactors. · Monitors batches. · ...

The incumbent will assure individual compliance with all concerned regulatory requirements, GxP's and applicable department programs. · Assess and ensure compliance to QC regulatory requirements and track quality metrics. · Effectively manage the site Quality Control activities i ...

We are hiring a Production Chemist for our pharmaceutical manufacturing unit. · Operate and monitor reactors , granulators , dryers , and related equipmentMaintain batch records , logbooks , and production documentationEnsure adherence to GMP , safety , and quality standards Coor ...

Ensure quality compliance in agro pharma/pesticide intermediates by monitoring processes inspections documentation GMP/ISO adherence testing audits and regulatory standards for agrochemical products. · ...

The ideal candidate will be responsible for building out our sales and marketing strategy, sales forecasting reports, and sales pipeline. You will then monitor our sales performance with the goal of expanding our company's market share. Your collaborative nature will help you suc ...

We have multiple openings in the Quality Control function for candidates with experience in the API/formulation pharma industry.Required candidate profile: analysis of samples as per approved specification and recording of analytical data. · ...

Perform analysis of raw materials in-process and finished products using HPLC. Operate and maintain HPLC instruments as per SOPs. · ...

The QA officer will have 2+ years of experience in the QA role. They will be responsible for verifying documents as per cGMP and GLP norms during plant rounds. · ...