2.0 - 5.0 years

5 - 6 Lacs

hyderabad, bengaluru

Work from Office

Role & responsibilities : Perform fogging and VHP generator operations for bio-decontamination services. Handle validation and installation of decontamination equipment, generators, and foggers. Execute cleanroom validation processes specific to fogging and VHP systems. Conduct and document GDP qualification activities - IQ, OQ, PQ Troubleshoot and resolve breakdown activities for fogging/VHP systems. Carry out Preventive Maintenance (PM) and calibration of fogging and VHP generators. Ensure compliance with pharma production requirements and cleanroom practices. Maintain accurate documentation in line with GDP/GMP standards. Travel to client sites across multiple locations as required. Candidate Requirements: Proven experience in fogging and VHP generators (operation and validation). Hands-on experience in equipment installation, qualification, and maintenance. Strong knowledge of cleanroom practices and contamination control in pharmaceutical facilities. Familiar with IQ, OQ, PQ validation protocols and regulatory compliance . Ability to handle technical troubleshooting and corrective maintenance. Experience in preventive maintenance and calibration activities. Good communication, documentation, and problem-solving skills. Willingness to travel extensively for project execution.

Posted 7 hours ago

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CQV Lead/ Engineer (OSD/Injectables Process Equipment Qualification Hyde Engineering + Consulting

4.0 - 10.0 years

0 Lacs

hyderabad, telangana

On-site

You will be responsible for performing commissioning and qualification of Pharmaceutical equipment, specifically systems for Oral Solid Dosage, Injectables, and Fill/Finish. This includes a variety of equipments such as RMG, CoMil, Tablet press, Coating Machine, blister packing machine, Vial Filling Line, PFS Line, Isolators (Negative & Positive), RABs (Open and Closed), GL Reactors, Dryer, Nutsche Filters, Centrifuges, Lyophilizers, etc. Your responsibilities will include developing CQMP, VMP, FRA, cGMP review sheet, interdependencies, System boundary, URS, SCA/SLIA, CLIA, DQR, SRA/QRA, SAT protocol, commissioning protocol, IQ protocol, OQ protocol, PQ protocol, process validation, and cleaning validation protocol. You will execute Commissioning, qualification, and validation activities for Pharma Process Equipments for API, Fill/Finish, and OSD. Additionally, you will review, analyze, and interpret system performance data, handle deviations/discrepancies, conduct investigations, CAPA, and ensure promotion of cGMP and regulatory compliance in assigned projects. Furthermore, you will exercise good judgment in selecting methods and techniques for obtaining solutions, maintain GDP, ALCOA practices, and have hands-on experience with Pharma Process Equipments. Drafting equipment operation SOPs will also be a part of your role. Qualifications & Other Requirements: - BS/MS in Engineering (Chemical, Pharma). - 4-10 years of experience in validation, quality systems, operations, engineering, or a combination thereof. - Experience in multiple GMP validation disciplines with advanced technical knowledge. - Knowledge of Validation Lifecycle approach, international regulatory requirements, and standards. - Experience with Documentum or Maximo is a plus. - Strong verbal and written communication skills, excellent organizational and time utilization skills. - Ability to work independently and within project teams. - Industry experience related to cGMP drug manufacturing, validation, and chemical process design. - Strong computer knowledge including Microsoft Office products.,

Posted 1 month ago

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RBDS Technician Nalco Water

5.0 - 10.0 years

6 - 9 Lacs

Hyderabad, Pune, Mumbai (All Areas)

Work from Office

Key Responsibilities: Troubleshoot and resolve issues in technical systems and pharmaceutical equipment Operate and maintain systems in clean room environments Monitor and manage air ventilator systems to ensure compliance with safety and quality standards Handle and maintain edge wax systems used in pharmaceutical processes Collaborate with cross-functional teams to support project execution Travel to project sites as required (3 to 6 days per assignment) Key Skills Required: Strong troubleshooting and problem-solving abilities Experience with pharmaceutical equipment and clean room protocols Knowledge of air ventilator and edge wax systems Ability to work independently and manage time effectively Excellent communication and documentation skills

Posted 1 month ago

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RBDS Technician Nalco Water

1.0 - 5.0 years

3 - 8 Lacs

Hyderabad, Pune, Mumbai (All Areas)

Work from Office

Key Responsibilities: Troubleshoot and resolve issues in technical systems and pharmaceutical equipment Operate and maintain systems in clean room environments Monitor and manage air ventilator systems to ensure compliance with safety and quality standards Handle and maintain edge wax systems used in pharmaceutical processes Collaborate with cross-functional teams to support project execution Attend pre-site customer meetings, conduct site surveys, plan and explain the process to customers Travel to project sites as required (3 to 6 days per assignment) Key Skills Required: Strong troubleshooting and problem-solving abilities Experience with pharmaceutical equipment and clean room protocols Knowledge of air ventilator and edge wax systems Ability to work independently and manage time effectively Excellent communication and documentation skills

Posted 1 month ago

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Sales Marketing Manager South India, Exp in Pharmaceutical Equipment International Recruiters

8.0 - 13.0 years

20 - 35 Lacs

Hyderabad

Work from Office

Driving revenue growth, expanding market presence, building a strong sales team, targets, ensuring high customer satisfaction. Exp in Containment Solution Technologies (CST), Powder Handling Technologies (PHT), Particle Size Technologies (PST). Required Candidate profile Must handle sales Hyderabad and South India . The candidate should hv exp in selling Isolators and pharmaceutical process equipment, including granulation, coating, and liquid manufacturing systems.

Posted 2 months ago

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