Supervisor (IR &ADMIN)

2 weeks ago

Vizag, Andhra Pradesh, India Larsen & Toubro Full time

1. As a Supervisor (IR & ADMIN), Candidate should look after and manage the day-to-day activities involving administrative services at site.

2. Candidate should manage the available resources (Labour and Vehicles) effectively and should estimate the requirements beforehand and then plan as per the schedule provided to him from the Site.

3. Candidate should Coordinate with the Site team on regular basis and arrange the required vehicles as and when required.

4. Candidate should have the basic knowledge of MS Office package (MS EXCEL, MS WORD, MS POWERPLANT) for standardizing the quality of document management.

5. Candidate should manage gatepass and other permits required for all the staff and labours working on the site.

6. Candidate should possess Inter-Personal skills, sound knowledge on the subject matter, Leadership qualities for managing the team.

  • Accounts and Admin Incharge

    2 weeks ago

    Vizag, Andhra Pradesh, India Larsen & Toubro Limited Full time

    Ability to understand and prepare all financial reports like Ledgers, Balance sheet, Cost statement, etc.,Abundant knowledge on Taxation system (GST).Must have the awareness regarding SCM functions like Inventory management, procurement, etc.,Knowledge on Government statutory norms (PF, ESI, F&F etc.,) and acts (Companies Act, Factories Act, labour laws,...

  • Graduate Apprentice

    2 weeks ago

    Vizag, Andhra Pradesh, India Pfizer Full time

    1. Responsible for ensuring operating state of cGMP compliance in solution/emulsion preparation, vial/ampoule washing, depyrogenation, filling and capping operations.Maintain regulatory compliance in accordance with cGMP practices.Ensure manufacturing policies and procedures conform to Pfizer standards.Knowledge and hands on experience in reviewing eBR and...

  • Associate - Quality Assurance

    2 weeks ago

    Vizag, Andhra Pradesh, India Pfizer Full time

    B. Pharma / M. Pharma / M.Sc.2-4 years' experience in Manufacturing Quality Assurance / Quality Assurance/ Production of a pharmaceuticals manufacturing facility.Responsible for ensuring operating state of cGMP compliance in solution/emulsion preparation, vial/ampoule washing, depyrogenation, filling and capping operations.Maintain regulatory compliance in...