General Operator I

Construction, Property and Engineering; Swindon; On-site; GBP 40,000 - 60,000; Full time

Job summary

A leading construction firm in Swindon is seeking a General Operator I for a 3-month contract. The role involves supporting pharmaceutical production operations by maintaining cleanroom standards and handling materials. Candidates should have secondary education and prior experience in a manufacturing environment. Shift work is required with competitive pay of £13.28/hour. Overtime is also available.

Benefits

Overtime available

Qualifications

• Experience in a manufacturing, operations, production, lab setting or related field.
• Preferred: Experience in a cGMP environment.

Responsibilities

• Complete all activities to acquire and maintain a Bronze License Badge.
• Follow area SOPs for correct gowning and cleaning.
• Assist with materials handling procedures.
• Ensure stocks for operation are maintained.
• Perform cleaning and maintenance according to SOPs.

Skills

Attention to detail

Ability to follow instructions

Education

Secondary Education, Advanced Certificate, or equivalent

Job description

Overview

Job Title: General Operator I

Work Location: Swindon - onsite

Contract Duration: 3 months - full time

Shift & shift pattern: Shift: different shifts every week - early and late shift/ early: 7:00-15:00/ late: 15:00-23:00

Overtime: available

Pay rate: £13.28/hour

The main function of a General Operator is to support pharmaceutical production operations by maintaining cleanroom standards, handling materials, performing equipment tasks, and completing accurate documentation in compliance with cGMP and regulatory procedures. Within your role as a General Operator you'll do meaningful work, and work closely with a team that values performance, quality and innovation.

Responsibilities

• Complete all activities to acquire and maintain a Bronze License Badge.
• Follow area SOPs for correct gowning and cleaning of non-aseptic and aseptic filling lines area.
• Preparing cleaning bucket and perform cleaning regime as per the SOPs.
• Assist with the materials handling procedures to help transfer materials into the classified area
• Ensure that stocks required for operation of the production area are maintained and in expiry date.
• Cleaning and maintenance of area/equipment to SOPs, cGMP and pharmaceutical industry regulatory standards.
• Perform Part Washer and Autoclave loading.
• Perform duties associated with line end run off, packaging, labelling and in process weight checks.
• To ensure any instances of non-conformance are communicated to the area leader, Manager or Quality Assurance representatives to ensure that they are investigated and rectified.
• Once fully bronze qualified, conduct environmental monitoring in Grade C / D classified areas in accordance with procedures.
• Complete all documentation in adherence with Data Integrity principles, SOPs and training.

Education

Education: Secondary Education, Advanced Certificate, or equivalent.

Experience

• Experience in a manufacturing, operations, production, lab setting or related field
• Preferred: Experience in a cGMP environment

Knowledge, Skills, Abilities

• Ability to follow verbal and written instructions and production schedules.
• Ability to remain focused and have attention to detail.

Equality and Compliance

Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.

Candidates must be eligible to live and work in the UK.

For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.