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QHSE Manager

  • Location

    North West London

  • Sector:

    FMCG Food Manufacturing, Pharmaceutical & Chemical

  • Job type:

    Permanent

  • Salary:

    £55000 - £60000 per annum, Benefits: benefits

  • Contact:

    Helen Darnell

  • Contact email:

    helend@scantec.co.uk

  • Contact phone:

    +44 (0)151 666 8967

  • Job ref:

    082661/NWL-HD

  • Published:

    13 days ago

  • Duration:

    n/a

  • Expiry date:

    2019-07-02

  • Start date:

    ASAP

A leading FMCG Manufacturer is currently seeking a QHSE Manager to take responsibility for ensuring the department meets all its objectives.

The successful Quality, Health, Safety and Environmental Manager will be responsible for developing the site QMS to ensure the manufacture of safe, legal and good quality products. The remit of the role covers site Health & Safety, Environmental and Quality.

The successful QHSE Manager will have a basic understanding of chemistry, analytical methods and knowledge of NPD Process and flavor development. You will understand the principles of GMP, have a good knowledge of Lab, Production and Warehouse and be familiar with legal / regulatory affairs from a Quality and Health & Safety perspective.

Responsibilities of the QHSE Manager:
Management of ISO 9001 / 2015 standard, ISO 14001 and ISO 45000
Ensure the company complies with all legal and moral responsibilities with regards to Quality, Health & Safety and Environmental management.
Conduct regular internal audits / inspections on site at agreed frequency as part of the QHSE strategy.
Deal with customer complaints and be the key point of contact for customer quality matters.
Set and track customer complaint service standards.
Manage and utilise quality tools including SPC charts, cause and effect diagrams, flow charts, FMEA, 5 Why / Fishbone, 8D, Root cause analysis.
Determine, negotiate and agree in‐house quality procedures, standards and / or specifications.
Assess NPD / NPI projects and agree deliverables ensuring that these are met.
Ensure that all major changes are approved via the change management process.
Ensure all major changes are validated.
Approve the design of all new equipment and facilities, ensuring that they are compliant with GMP / ISO standards.
Ensure all SOP’s are approved, available and in date.
Audit all suppliers at regular intervals, ensuring they maintain a high‐quality standard.
Ensuring that manufacturing processes comply with standards of both GMP and ISO requirements.

Application via CV

Scantec Personnel Limited is acting as an employment business and an employment agency. For contract or interim roles (and unless otherwise stated), all pay rates stated are on a Limited Company basis.

Due to the high volume of applications Scantec receives it is not always possible to acknowledge every application. Shortlisted applicants will be contacted within 28 days. If you don’t hear from us within 28 days your application has not been shortlisted at this time, to be considered for future vacancies please register with us on our website.