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Maintenance & Facilities Lead

SRG

Stockport

On-site

GBP 40,000 - 70,000

Full time

2 days ago
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Job summary

An established industry player is seeking a Technical Engineer to join their engineering team at a state-of-the-art pharmaceutical facility. This role offers the chance to provide vital technical expertise in maintaining HVAC and utility systems while ensuring compliance with regulatory standards. As part of a dynamic and fast-growing company, you will lead initiatives to improve operations and drive strategy on site. If you have a strong background in engineering within a GMP environment and are passionate about making a difference, this opportunity is perfect for you.

Qualifications

  • Qualified engineer with experience in clean utility systems.
  • Strong technical background in HVAC and GMP regulated environments.

Responsibilities

  • Lead compliance activities and support new equipment installation.
  • Establish maintenance strategies for site utilities and equipment.

Skills

HVAC Systems
Technical Engineering
GMP Compliance
Troubleshooting
Process Equipment Maintenance

Education

Engineering Degree

Tools

Calibration Equipment
Validation Tools

Job description

Job Description

Are you a Technical Engineer who has specialised in HVAC and other site utilities?

Or are you working in FMCG, food or chemical industry looking for a route into the pharmaceutical industry?

An opportunity has arisen for an Engineering & Facilities Lead to join a team in Manchester – on a permanent basis.

About the organisation:

You will be joining a dynamic and fast-growing pharmaceutical company specialising in the development of solid dose products. This is an exciting opportunity to become part of the engineering team at a pivotal time, as the organisation establishes operations in a brand-new, state-of-the-art facility.

About the Job:

You will provide technical expertise to the facility, ensuring HVAC, valves, water systems and other process equipment are maintained. You will be responsible for identifying gaps, implementing improvement and driving strategy on site.

  1. You will lead and support activities to maintain compliance of the facility.
  2. You will support installation and validation of new equipment.
  3. You will establish the maintenance and calibration strategy for site utilities, equipment and instruments.
  4. You will lead first response to any breakdowns and troubleshooting activities.
  5. You will contribute to the creation and review of Plans, Work Instructions, and Standard Operating Procedures (SOPs).

About you:

You will be a qualified engineer, with a strong background and experience with clean utility systems within a GMP regulated manufacturing environment. Strong technical engineering experience with purified water, water for injection, clean steam, compressed gases, and HVAC systems.

  1. Project experience within system upgrades, compliance initiatives, and operational improvements.
  2. Strong understanding of GMP, FDA, and EU regulatory requirements.
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