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41 results

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Vehicle Technician

Standard job
Recruiter
James Haugh (Dumfries) Limited
Salary
Competitive
Location
Dumfries and Galloway
Job term
Permanent
Job hours
Full time

Vehicle Technician required.

We are looking for an experienced qualified Vehicle Technician to join our existing Aftersales team. For the right candidate we can offer a secure, progressive, exciting and rewarding career. Previous Vauxhall experience is not essential. MOT qualifications would be a distinct advantage for this position.

Both Vacancies will receive an attractive salary, 30 days holiday, full training, company pension and preferential car purchase scheme.

This is a key position within our business and to apply, in the first instance, please write to:
Mr Simon Haugh,
James Haugh (Dumfries) Limited,
2 St. Marys Street, Dumfries,
DG1 1HD

or email Mr Haugh.

Contact
Simon Haugh
Posted
Reference
224107355-01a

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Production Supervisor

Standard job
Recruiter
Cytori Therapeutics
Salary
Competitive
Location
Aberdeenshire
Job term
Permanent
Job hours
Full time

Cytori Therapeutics is opening a small medical device manufacturing facility in Deeside.

We are seeking a Production Supervisor (hands-on-position)
Department: Operations
Reports To: Sr. Director of Operations
Location: Deeside, UK

ABOUT US
Cytori Therapeutics, Inc. is dedicated to developing and delivering innovative cell-based therapies to improve the quality and length of life. We are a global, public company engaged in the development and commercialization of stem and regenerative cell therapies for the treatment of cardiovascular disease, reconstructive surgery and many other serious, chronic, and life threatening conditions.

SUMMARY
Manages the operation of manual and computerized equipment located in the production areas. Supervises the activity of production personnel. Oversees the repair and modification of production equipment. Develops and implements production procedures. Coordinates production activities with Operations, Development and Quality staff. Is responsible for hiring, performance appraisals, performance coaching, and pay reviews of production employees. This is a hands-on supervisor role and requires documentation skills. This individual will serve as the most senior on-site leader for the UK manufacturing facility.

ESSENTIAL DUTIES AND RESPONSIBILITIES include the following.
Supervise production team, including: setting goals and objectives; providing opportunities for future growth and advancement; training and supervising Production employees
Act as liaison between departments, including coordination of on-side manufacturing and US department needs and requirements.
Create production travelers
Control and update calibration of equipment.
Write work instructions, LHRs, planned deviations, NCMRs, change orders, protocols and maintenance schedules related to the production process.
Ensure the production areas are in compliance (ISO and internal audits)
Programming, set up, and troubleshooting of all production related equipment
Production flow analysis
Schedule and execute production builds
Ensure safe working practices in accordance with governing safety authorities and company requirements
Ensure production areas are presentable
Ordering of parts and facility related items
Be able to give input on jig design
Must be able and available to travel to the US approximately four (4) times per year.
Other duties as assigned.

SUPERVISORY RESPONSIBILITIES
Supervises production team. Promotes a team environment within the department. Providing assistance and support for the staff members. Cooperates and assists all departments in resolving issues related to manufacturing and the UK site. Communicates directly with the Sr. Director of Operations on all employee issues.

KNOWLEDGE, SKILLS, AND ABILITIES
Knowledge of Medical GMP, Six Sigma, Lean Manufacturing principles, Kaizen, ISO standards preferred
MRP experience a plus
Ability to adapt rapidly to changes in priorities
Working knowledge to control, operate, and calibrate: measuring gauges, torque tools, electric multi meters. Ability to create a positive and productive working environment
Possess excellent organizational skills
Strong writing and verbal communication skills
Strong attention to detail
Proactive; ability to independently triage and prioritize efforts with minimum supervision as well as to communicate critical information to key stakeholders
Responsible and dedicated person, self-motivated and team-oriented, performs well under pressure
Excellent ability to resolve differences of opinion or conflicting information

EDUCATION and/or EXPERIENCE
Familiarity with new plant start-up strongly preferred
Experience in technology transfer from product development to manufacturing required
Experience in working with non-UK based headquarters strongly preferred
Five years related manufacturing experience and /or training, or an equivalent combination of education and experience in the medical device field.
Secondary degree required, Bachelor’s a plus
Experience working in ESD ( Electric Static Discharge) environment

SYSTEMS TECHNOLOGY SKILLS
Knowledge in utilization of Microsoft Word, Excel, Outlook, and Internet applications. Knowledge of MAS 200 and SolidWorks an advantage.

WORK ENVIRONMENT Employee has to work in an ESD (Electro Static Discharge) environment. AC and DC Power above 60V are present at the workstation. Employee will be provided with sufficient lighting, heat and cooling. Employee is required to handle sharp instruments.

TO APPLY
For more information and to apply please visit our website

Contact
Cytori Therapeutics
Posted
Reference
224107981-01

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Senior Quality Assurance Specialist

Standard job
Recruiter
Cytori Therapeutics
Salary
Competitive
Location
Aberdeenshire
Job term
Permanent
Job hours
Full time

Cytori Therapeutics is opening a small medical device manufacturing facility in Deeside.

We are seeking a Sr. Quality Assurance Specialist
Department: Quality Assurance
Reports To: Director, Quailty
Location: Deeside, UK

ABOUT US
Cytori Therapeutics, Inc. is dedicated to developing and delivering innovative cell-based therapies to improve the quality and length of life. We are a global, public company engaged in the development and commercialization of stem and regenerative cell therapies for the treatment of cardiovascular disease, reconstructive surgery and many other serious, chronic, and life threatening conditions.

SUMMARY
Provides the required support to maintain the Quality System in accordance with ISO 13485, ISO 9001 and Cytori Quality System at the Cytori UK Facility. Responsible for incoming and in process inspections, calibrations system, environmental monitoring, quality records, training system and finished product release. Provides input and follow-up on NCMRs, CAPAs, investigations, validations, customer complaints, audits, audit reports, distribution activities; and provide administrative support within the Quality Assurance Department.

ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. other duties may be assigned
Maintains the processes for control, calibration, maintenance of inspection, measuring, and test equipment.
Provides quality assurance monitoring for the facility and facility monitoring devices.
Collects and maintains quality system and medical device product records.
Monitors, maintains, and operates the Quality Systems Training program.
Reviews and processes controlled documents.
Updates/Maintains Quality Databases.
Closes & Reviews open LHRs and Service records.
Manages the training process including printing and assemble of the training binders.
Performs QA Review of History Records and then Product Release.
Assists in audits and publish Audit Reports (Internal and External).
Maintains the CAPAs, Complaints, & Audits Systems for the facility.
Performs QC function for incoming and in-process inspection of product.
Assists QA management with special projects.

KNOWLEDGE, SKILLS, & ABILITIES
Excellent working understanding of ISO 13485/9001 ability to apply knowledge to medical device manufacturing and test facility.
Excellent attention to detail and follow-up skills.
Knowledge of Preventative Maintenance (PM), Nonconforming Material Reporting (NCMR), Corrective and Preventative Action (CAPA), Calibration, Inspection/Test, Process Controls and Auditing in a medical device manufacturing environment.
Knowledge of Electronic / Manufacturing Resource Planning (ERP / MRP) Systems is a plus.

EDUCATION and/or EXPERIENCE
Previous experience in Medical Device Field (ISO 13485) required.
Bachelor’s Degree, or, Foundation Degree with minimum 4 years work experience in Quality Assurance and/or Quality Control.
Certified Quality Auditor, Certified Quality Manager or Certified Quality Engineer a plus.

SYSTEMS TECHNOLOGY SKILLS
Knowledge in utilization of Microsoft Word, Excel, Outlook and Internet applications.

PHYSICAL DEMANDS
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

While performing the duties of this job, the employee is regularly required to talk or hear. The employee frequently is required to stand, walk, bend, and sit. Specific vision abilities required by this job include close vision, distance vision, and ability to adjust focus. The employee must have the manual dexterity and manual ability to effectively use computer terminals.

TO APPLY
For more information and to apply please visit our website

Contact
Cytori Therapeutics
Posted
Reference
224107981-01b

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Device Assembly Technician

Standard job
Recruiter
Cytori Therapeutics
Salary
Competitive
Location
Aberdeenshire
Job term
Permanent
Job hours
Full time

Cytori Therapeutics is opening a small medical device manufacturing facility in Deeside.

We are seeking a Device Assembly Technician
Department: Product Development
Reports To: Production Supervisor
Location: Deeside, UK

ABOUT US
Cytori Therapeutics, Inc. is dedicated to developing and delivering innovative cell-based therapies to improve the quality and length of life. We are a global, public company engaged in the development and commercialization of stem and regenerative cell therapies for the treatment of cardiovascular disease, reconstructive surgery and many other serious, chronic, and life threatening conditions.

SUMMARY
Constructs and wires subassemblies into finished systems for medical devices.

ESSENTIAL DUTIES AND RESPONSIBILITIES include the following.
Reads Blueprints
Following assembly instructions
Complete and initiate work-travelers (LHR’s)
Route cables
Crimp connectors onto cable assemblies
Understand cable gages
Troubleshoots problems and performs / initiates the repair
Follows ESD procedures
Keeps the assembly area presentable
Performs High Pot testing
Follows Safety guidelines
Other duties may be assigned

KNOWLEDGE, SKILLS, & ABILITIES
Ability to perform basic mathematical computations
Ability to apply concepts such as fractions, percentages, ratios and proportions to practical situations
Ability to use digital and analog measuring instruments
Ability to use small hand tools
Knowledge of Medical GMP, Six Sigma, Lean Manufacturing principles, Kaizen, ISO standards a plus
MRP experience a plus
Ability to adapt rapidly to changes in priorities
Working knowledge to control, operate, and calibrate: measuring gauges, instruments, Strong attention to detail
Responsible and dedicated person, self-motivated and team-oriented

EDUCATION and/or EXPERIENCE
4 years related experience and /or training, or an equivalent combination of education and experience.
Secondary school degree required.
Experience working in ESD ( Electric Static Discharge) environment

SYSTEMS TECHNOLOGY SKILLS
Knowledge in utilization of Microsoft Word, Excel, Outlook and Internet applications.

PHYSICAL DEMANDS
While performing the duties of this job, the employee is regularly required to talk or hear. The employee frequently is required to stand, walk, bend, and sit. Ability to lift objects up to 40 lbs, could be required. Specific vision abilities required by this job include close vision, distance vision, and ability to adjust focus. The employee must have the manual dexterity and manual ability to effectively use computer terminals.

WORK ENVIRONMENT
Employee has to work in an ESD (Electro Static Discharge) environment. AC and DC Power above 60V are present at the workstation. Employee will be provided with sufficient lighting, heat and cooling. Employee is required to handle sharp instruments.

TO APPLY
For more information and to apply please visit our website

Contact
Cytori Therapeutics
Posted
Reference
224107981-01a

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Graduate Mechanical Design Engineer - Glasgow

Basic job
Recruiter
RE & M (Recruiting Engineers & Managers) Ltd
Salary
Competitive + Benefits
Location
Glasgow
Job term
Permanent
Job hours
Full time

Our client is a dynamic, growing company developing a range of novel technologies at their Glasgow facility. Due to rising demand and an expanding product range, they are now looking to recruit an additional Mechanical Design Engineer to play a key role in the development of this world-class technology company.

We need enthusiastic people who have shown that they can hit the ground running and work to a high standard in a fast moving environment.
You will be required to have excellent hands-on-skills as well as theoretical knowledge. This position would suit a recent graduate or someone who has gained some work experience after graduating.

Requirements:
Graduate (with minimum 2.1 degree) ideally with a qualification in a relevant area.
Experience of working with 3D CAD software. Ideally SolidWorks.
Attention to detail and passionate about your work.

Lots moire vacancies at [contact details removed]

Contact
Neil Jarvis
Posted
Reference
NJ76055/

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Sales and Service Advisor

Basic job
Recruiter
Morgan Turner
Salary
From £15,000 to £15,000 per year
Location
Edinburgh
Job term
Permanent
Job hours
Full time

Our client a national manufacturing company are looking to recruit a highly organised Sales and Service Advisor to assist in the day to day running of the Store and helping to achieve Sales / Margin targets by serving customers in a professional manner.

Administrative Responsibilities:

To process the daily cash paperwork and prepare banking including petty cash and maintain accurate filing systems.
To ensure cash/cheques banked on a daily basis.
To monitor stock movements and deliveries. To raise invoices/credit notes accurately.
To ensure payment for goods is received accurately and/or credit approval obtained.
To report any discrepancies (monetary or otherwise) to the Store Manager immediately.
To perform any general admin duties as required.
Counter responsibilities:

To actively sell (face to face and over the telephone) and promote equipment ensuring correct procedures are followed.
To serve customers politely and efficiently either at the counter, off site, on the telephone, providing professional and timely advice products and accessories.
To advise and take orders for product fitting updating the diary accordingly. To liaise with the workshop team as required.
Ensure all stock orders received are shelved at the earliest opportunity and are presented safely, tidily and in an attractive manner. Displays should be updated and maintained regularly to maximise customer interest.
Liaise with the Store Workshop to ensure they are kept supplied with a steady workload. To perform Workshop duties as and when required.
To assist with stock takes as required.
To keep work area tidy and operate within the Health and Safety policy of the Company.
To be trained and drive a Fork Lift Truck as required.
To hold a full, current driving licence.
To perform any other duties deemed reasonable on request.
The hours are 8.30am-5.30pm Monday to Friday, with Saturday mornings on a rota basis

Contact
Sarah Hughes
Posted
Reference
140408-001-RP

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Plant Operator

Standard job
Recruiter
Iain Watt Haulage
Salary
Competitive
Location
Ayrshire
Job term
Permanent
Job hours
Full time

Animal Feed Blending Plant Operator required.

Experience in this type of work would be an advantage. Applicants should hold a current HGV Licence as possibility of additional work available.
Must be competent in using Machinery & Loadall.

Applicants should send their C.V. by Email.

Contact
Iain Watt Haulage
Posted
Reference
224095998-01

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Quality Development Technologist (Process Improvement) BLUQ11106

Basic job
Recruiter
Blue Octopus Recruitment Ltd
Salary
Up to £750,000 per year + Salary £28,000 - £30,000 dependent on skills / experience
Location
Livingston
Job term
Permanent
Job hours
Full time

Our client is a leading worldwide supplier of stamping foils used to enhance the appearance of products and packaging in all types of consumer goods sectors. Their foils are sold and supplied through an extensive network of owned and third party distributors in Europe, the Americas, Africa, Asia and Australasia.

As a Quality Development Technologist, you will become part of the Technical Department and will carry out project work and other activities to reduce customer complaints.
Leading product and process improvement initiatives generated from customer feedback, you will review individual customer complaints and investigate root cause; reporting your findings to customers and identifying collective potential improvement projects to reduce customer complaints.

Prioritising and co-ordinate projects and bringing them to a successful conclusion in a timely manner, you must issue monthly reports communicating the complaints overview and projects’ status and maintain accurate systems data reflecting the changes in the business needs.

To be successful in this role, candidates must have experience of leading improvement initiatives in a manufacturing environment and of implementing process controls. With strong leadership and communication skills, you will be a logical problem solver with the ability to collect and manipulate data (inc. Excel skills) and present recommendations and implement changes.

You should have the ability to prioritise and adapt workloads, carrying out investigatory work and audits to manage customer requirements whilst maintaining strong project management and analytical skills to meet deadlines and achieve departmental and business goals.

Knowledge of foils / stamping processes, the Q-Pulse quality system and any technical / scientific / laboratory experience would be beneficial but is not essential.

This is a Blue Octopus Recruitment Ltd vacancy who are operating as an employment agency. Once you have clicked to apply for this vacancy, we will then send you more information on the role including a copy of the application form via email.

Contact
Blue Octopus Team
Posted
Reference
BLUQ11106

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Mechanic

Standard job
Recruiter
Carrylift Materials Handling ltd
Salary
Competitive
Location
Scotland
Job term
Permanent
Job hours
Full time

Due to work load, we currently require a Full Time Served Mechanic who will work on Diesel, gas and electric fork lift trucks, training will be given prior to any field
work, the work would be carried out in the central region of Scotland.

A current driving licence is essential with a company vehicle supplied.

Apply in Writing to:
William McCluskie,
Carrylift Materials Handling,
6 Rosehall Road,
Bellshill Industrial estate,
Lanarkshire
ML4 3NR.

Contact
William McCluskie
Posted
Reference
224087940-01

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Blinds & Window shutter Installer

Standard job
Recruiter
The Appeal Group Ltd
Salary
From £35,000 to £45,000 per year + Computer,Phone
Location
Airdrie
Job term
Self Employed
Job hours
Full time

Conservatory Roof Blinds ,Window Blinds and Wooden Window Shutter Installer based in the Edinburgh or Glasgow area. An opportunity to join a national supplier of blinds and shutters for throughout the home. Survey and install quality products with 97% customer satisfaction.

Self Employed, own transport essential.

Experience advantageous full training given.

Please call or email us now for application form

Contact
Bruce Johnson
Posted
Reference
Scotland BAJ

Applied

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