Manufacturing Operator / Assembling/ Assembler
Posted on Jun 15, 2026 by CV-Library
Renfrew, Renfrewshire, United Kingdom
Manufacturing
Immediate Start
£13.2 - £13.2 Hourly
Temporary
Job Description: Manufacturing Operator I
Role Overview
Location:(UK - Paisley)
Position Type: (6 Months)
Work Schedule: 8-12 hour shifts (depending on rota), Monday to Friday with additional overtime as required by production schedules.
Position Summary
The primary function of the Manufacturing Operator I is to execute the day-to-day production process in a highly controlled, fast-paced cleanroom environment. You will closely follow Standard Operating Procedures (SOPs), Work Instruction Documents, and technical drawings to manage medical device assembly, materials handling, and packaging of finished goods. All duties are performed in strict accordance with Good Manufacturing Practices (GMP) and safety regulations.
Key Responsibilities
Manual Assembly: Manually assemble specialized medical-grade tubing, connectors, and fluid bags according to precise customer requirements and blueprints.
Technical Compliance: Read and interpret manufacturing drawings, using tools like tape measures to ensure product accuracy.
Quality & Inspection: Perform rigorous visual checks on both in-process and completed products; escalate defects immediately to maintain a high-quality output.
Documentation: Accurately complete and record operational paperwork in absolute compliance with strict GMP standards.
Process Improvement: Actively participate in team-based Lean Practical Process Improvement (PPI) initiatives to drive safety, efficiency, and quality.
Physical & Environmental Requirements
Cleanroom Protocol: Comfortable working inside a controlled cleanroom environment with low ambient noise.
Strict Gowning: Required to wear comprehensive cleanroom garments daily (including gloves, hair/beard nets, face covers, and safety glasses). No makeup or jewelry is permitted on the production floor.
Physical Stamina: Ability to stand, reach, bend, stoop, and move about for extended periods (8-12 hours per shift).
Manual Dexterity: Strong hand-eye coordination with the ability to perform repetitive hand tool operations requiring forceful gripping, pushing, and pulling.
Lifting: Capabilities to infrequently lift and manipulate components weighing up to 50 lbs max unassisted.
Candidate Requirements
Required Skills & Experience:
Experience working in a similar fast-paced processing, assembly, or manufacturing industry.
Proven ability to interpret and carefully follow written Standard Operating Procedures (SOPs).
Strong manual dexterity and hand coordination for repetitive task execution.
Good verbal and written communication skills with basic computer literacy.
Solid basic mathematical skills.
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
Role Overview
Location:(UK - Paisley)
Position Type: (6 Months)
Work Schedule: 8-12 hour shifts (depending on rota), Monday to Friday with additional overtime as required by production schedules.
Position Summary
The primary function of the Manufacturing Operator I is to execute the day-to-day production process in a highly controlled, fast-paced cleanroom environment. You will closely follow Standard Operating Procedures (SOPs), Work Instruction Documents, and technical drawings to manage medical device assembly, materials handling, and packaging of finished goods. All duties are performed in strict accordance with Good Manufacturing Practices (GMP) and safety regulations.
Key Responsibilities
Manual Assembly: Manually assemble specialized medical-grade tubing, connectors, and fluid bags according to precise customer requirements and blueprints.
Technical Compliance: Read and interpret manufacturing drawings, using tools like tape measures to ensure product accuracy.
Quality & Inspection: Perform rigorous visual checks on both in-process and completed products; escalate defects immediately to maintain a high-quality output.
Documentation: Accurately complete and record operational paperwork in absolute compliance with strict GMP standards.
Process Improvement: Actively participate in team-based Lean Practical Process Improvement (PPI) initiatives to drive safety, efficiency, and quality.
Physical & Environmental Requirements
Cleanroom Protocol: Comfortable working inside a controlled cleanroom environment with low ambient noise.
Strict Gowning: Required to wear comprehensive cleanroom garments daily (including gloves, hair/beard nets, face covers, and safety glasses). No makeup or jewelry is permitted on the production floor.
Physical Stamina: Ability to stand, reach, bend, stoop, and move about for extended periods (8-12 hours per shift).
Manual Dexterity: Strong hand-eye coordination with the ability to perform repetitive hand tool operations requiring forceful gripping, pushing, and pulling.
Lifting: Capabilities to infrequently lift and manipulate components weighing up to 50 lbs max unassisted.
Candidate Requirements
Required Skills & Experience:
Experience working in a similar fast-paced processing, assembly, or manufacturing industry.
Proven ability to interpret and carefully follow written Standard Operating Procedures (SOPs).
Strong manual dexterity and hand coordination for repetitive task execution.
Good verbal and written communication skills with basic computer literacy.
Solid basic mathematical skills.
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
Reference: 225247706
https://jobs.careeraddict.com/post/113409409
Manufacturing Operator / Assembling/ Assembler
Posted on Jun 15, 2026 by CV-Library
Renfrew, Renfrewshire, United Kingdom
Manufacturing
Immediate Start
£13.2 - £13.2 Hourly
Temporary
Job Description: Manufacturing Operator I
Role Overview
Location:(UK - Paisley)
Position Type: (6 Months)
Work Schedule: 8-12 hour shifts (depending on rota), Monday to Friday with additional overtime as required by production schedules.
Position Summary
The primary function of the Manufacturing Operator I is to execute the day-to-day production process in a highly controlled, fast-paced cleanroom environment. You will closely follow Standard Operating Procedures (SOPs), Work Instruction Documents, and technical drawings to manage medical device assembly, materials handling, and packaging of finished goods. All duties are performed in strict accordance with Good Manufacturing Practices (GMP) and safety regulations.
Key Responsibilities
Manual Assembly: Manually assemble specialized medical-grade tubing, connectors, and fluid bags according to precise customer requirements and blueprints.
Technical Compliance: Read and interpret manufacturing drawings, using tools like tape measures to ensure product accuracy.
Quality & Inspection: Perform rigorous visual checks on both in-process and completed products; escalate defects immediately to maintain a high-quality output.
Documentation: Accurately complete and record operational paperwork in absolute compliance with strict GMP standards.
Process Improvement: Actively participate in team-based Lean Practical Process Improvement (PPI) initiatives to drive safety, efficiency, and quality.
Physical & Environmental Requirements
Cleanroom Protocol: Comfortable working inside a controlled cleanroom environment with low ambient noise.
Strict Gowning: Required to wear comprehensive cleanroom garments daily (including gloves, hair/beard nets, face covers, and safety glasses). No makeup or jewelry is permitted on the production floor.
Physical Stamina: Ability to stand, reach, bend, stoop, and move about for extended periods (8-12 hours per shift).
Manual Dexterity: Strong hand-eye coordination with the ability to perform repetitive hand tool operations requiring forceful gripping, pushing, and pulling.
Lifting: Capabilities to infrequently lift and manipulate components weighing up to 50 lbs max unassisted.
Candidate Requirements
Required Skills & Experience:
Experience working in a similar fast-paced processing, assembly, or manufacturing industry.
Proven ability to interpret and carefully follow written Standard Operating Procedures (SOPs).
Strong manual dexterity and hand coordination for repetitive task execution.
Good verbal and written communication skills with basic computer literacy.
Solid basic mathematical skills.
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
Role Overview
Location:(UK - Paisley)
Position Type: (6 Months)
Work Schedule: 8-12 hour shifts (depending on rota), Monday to Friday with additional overtime as required by production schedules.
Position Summary
The primary function of the Manufacturing Operator I is to execute the day-to-day production process in a highly controlled, fast-paced cleanroom environment. You will closely follow Standard Operating Procedures (SOPs), Work Instruction Documents, and technical drawings to manage medical device assembly, materials handling, and packaging of finished goods. All duties are performed in strict accordance with Good Manufacturing Practices (GMP) and safety regulations.
Key Responsibilities
Manual Assembly: Manually assemble specialized medical-grade tubing, connectors, and fluid bags according to precise customer requirements and blueprints.
Technical Compliance: Read and interpret manufacturing drawings, using tools like tape measures to ensure product accuracy.
Quality & Inspection: Perform rigorous visual checks on both in-process and completed products; escalate defects immediately to maintain a high-quality output.
Documentation: Accurately complete and record operational paperwork in absolute compliance with strict GMP standards.
Process Improvement: Actively participate in team-based Lean Practical Process Improvement (PPI) initiatives to drive safety, efficiency, and quality.
Physical & Environmental Requirements
Cleanroom Protocol: Comfortable working inside a controlled cleanroom environment with low ambient noise.
Strict Gowning: Required to wear comprehensive cleanroom garments daily (including gloves, hair/beard nets, face covers, and safety glasses). No makeup or jewelry is permitted on the production floor.
Physical Stamina: Ability to stand, reach, bend, stoop, and move about for extended periods (8-12 hours per shift).
Manual Dexterity: Strong hand-eye coordination with the ability to perform repetitive hand tool operations requiring forceful gripping, pushing, and pulling.
Lifting: Capabilities to infrequently lift and manipulate components weighing up to 50 lbs max unassisted.
Candidate Requirements
Required Skills & Experience:
Experience working in a similar fast-paced processing, assembly, or manufacturing industry.
Proven ability to interpret and carefully follow written Standard Operating Procedures (SOPs).
Strong manual dexterity and hand coordination for repetitive task execution.
Good verbal and written communication skills with basic computer literacy.
Solid basic mathematical skills.
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
Reference: 225247706
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