5.0 - 9.0 years

0 Lacs

karnataka

On-site

As a Contracts Manager at Wernick Modular Hire, your role will involve supervising subcontractors and the workforce on-site, liaising with clients, issuing orders to subcontractors, and providing essential information for valuations. You will collaborate with the Production Manager and Logistics Manager, conduct site surveys, and prepare site progress reports. It will be crucial for you to be present on-site during critical contract phases, ensure projects run within allocated costs, and comply with Quality and Environmental Procedures. Additionally, you will prepare key documents such as Construction Phase Method Statements, Risk Assessments, and Construction Phase Plans, as well as compile...

Posted 1 month ago

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Operator II - Packaging 2nd Shift Piramal Pharma Ltd

0.0 - 4.0 years

0 Lacs

maharashtra

On-site

As a Pharmaceutical Operator at Pharma Solution in Sellersville, your primary responsibility will be to perform entry level operations such as equipment and facility cleaning, scale verifications, and general housekeeping as assigned by the Supervisor or Group Leader. You will have the opportunity to advance by disassembling and reassembling departmental equipment in accordance with cGMPs and SOPs. The equipment may include low and high shear mixers, mills, fluid bed dryers, packaging fillers, and manufacturing tanks. Additionally, you will rotate to other Manufacturing or Packaging departments based on business needs. Please note that this is a safety sensitive position and it is a 2nd shif...

Posted 1 month ago

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Senior Executive - DQA Piramal Pharma Ltd

5.0 - 9.0 years

0 Lacs

telangana

On-site

Role Overview: You will be responsible for overseeing and supporting the overall activities during the product development life cycle from a quality perspective in R&D (API and intermediates). Your role will involve understanding the site needs for system establishment and sustainability, authoring/reviewing/approving SOPs/work directions, and ensuring effective implementation of quality systems in R&D activities as per GLP and regulatory requirements. Additionally, you will be required to review and approve various reports, conduct periodic audits of the R&D laboratory, ensure effective maintenance of records, and perform cGMP audits of R&D facilities and operations. Training the R&D team f...

Posted 2 months ago

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