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We are currently looking for a QA Officer on a 12 month maternity cover to join a leading clinical and commercial manufacturer of biologics and pharmaceuticals based in the Midlands. As the QA Officer you will be responsible for assisting in the maintenance of the Quality System to help ensure that processes and products comply with appropriate Regulatory requirements.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the QA Officer will be varied however the key duties and responsibilities are as following:
1. Creation and revision of operational GMP documentation within Quality Assurance
2. Administration, coordination and review of GMP…
£17500 - £20000/annum
Rullion Resource are recruiting an experienced Quality Control Technician for an established manufacturer based in Knowsley, Merseyside. The position is permanent working a 3 shift rotation of 7-3, 3-11,11-7. Our client is a leader in their industry and part of a Global Group.
Duties will include:
-Testing raw materials, intermediates and finished goods
-Labelling samples accurately
-Checking finished goods prior to dispatch
-Developing and maintaining a good working knowledge of test methods & schedules
- Maintain timely…
Location:- Sudbury, Suffolk
Description:- Quality inspector/Manager
A quality inspector/manager is required for a busy, expanding company manufacturing components for the communication, Scientific & Aerospace sectors amongst others.
You would be required to inspect component using manual equipment and CMM with PCDMIS software, to produce FAIR’s and inspection reports as required. Maintain our ISO 9001-2008 system.
A good knowledge of AS9100 would be an advantage as the company is intending to introduce this system.
This is an ideal opportunity for the right person…
Salary £45,000 - £55,000 pa depending on skills
Hitchin, Hertfordshire Commutable from Milton Keynes, Luton and Stevenage
Our client is a leading developer and manufacturer of natural products and extracts to the Healthcare, Cosmetic and Food & Drinks industries. With over one hundred and sixty years of experience they have stayed true to a love of nature and their roots in botanicals but have adapted to harness the latest in scientific techniques and to meet the changing needs of markets and customers.
They currently have an exciting opportunity available for a Quality…
Reporting to the Head of Quality the main function of this role is to execute business system improvements utilising statistical thinking and methodologies to identify opportunities, plan improvements, expedite those Plan's and then follow up to ensure business results have been statistically improved and sustained, especially with regard to meeting customer expectations.
We are looking for a motivated QA Engineer to help us ensure that our products meet the high standards of Quality, Ease of Use, and Reliability that our customers expect.
Working within a dedicated product team, and alongside other members of the QA Department, you will be involved in designing quality into our new products from the beginning of the development process. You will help to devise QA approaches that facilitate early risk reduction, as well as planning and executing functional, non-functional, and user acceptance tests. Additionally, you will have your own areas of technical responsibility within the QA Department…
This is a fantastic opportunity to join an established dynamic company providing bespoke machining and fabrication solutions for manufacturing industries.
You will be the company interface for Supplier Quality Management to ensure the quality requirements are fully understood and achieved by the supply chain.
Duties and responsibilities:-
• Conduct Supplier Audits (Process and QMS).
• Conduct source inspection (paperwork and dimensional).
• Manage all aspects of supplier non-conformance (Root cause analysis and corrective action).
• Conduct and/or approve First Article Inspection Reports (to AS9102).
• Manage supplier KPIs…
£40000 - £50000/annum
The main purpose of this newly created role is to develop and maintain a robust Quality Management system in this highly regulated rapidly growing industry.
Duties to include:
Lead Quality related projects aiming to define, establish and improve good manufacturing, distribution and sales practices as part of the Quality Management System of the organisation.
Manage departmental budget based on product range, forecast and organisation objectives…
We're hiring a Test Analyst (QA Tester) to to join our team and help with the continuing expansion of the UK's fastest growing job board.
You will be working closely with the Development and Design teams, as well…
Title: Quality Engineer
Location: Cheshire, North West
A leading manufacturer of high performance Scientific equipment is currently looking to recruit an experienced Product focused Quality Engineer to join their team based in Cheshire.
As you will work within product related quality control across the organisation and with suppliers to ensure continual improvement of processes and products, thus helping reduce defects, problems, etc. You will drive improvements within the organisation and within the supply chain by implementation of relevant and timely actions…
A fantastic opportunity to join a highly successful instrument vendor!
Are you an experienced quality professional with experience of ISO13485? Do you have good communication skills and a practical approach to problem solving? Then this could be the role for you!
You will work within the Quality Control supply chain to ensure continuous improvement of processes and products. As a key member of the Quality Team you will use your communication skills to manage suppliers in order reduce the number of product non-conformances. This role will also involve reviewing and updating current QA processes and documentation, helping the company…
Design Quality Engineer - £24,000 to £30,000 - County Armagh (Relocation Package Available)
A Design Quality Engineer is required for a large and well established pharmaceutical organisation based in County Armagh. This is a good opportunity for a Design Quality Engineer to support the company's design control activities.
The core function of the Design Quality Engineer will be to ensure designs comply with medical device standards and to help assist design and reviews design. Other duties will involve assisting supplier audits with the quality team and maintaining documents for the design team.
In order to be considered for the role of…
Have you experience in QA within a Pharmaceutical environment?
Have you knowledge of FDA and MHRA requirements?
Do you conduct internal audits?
*Flagship site of a well-known Pharmaceuticals manufacturing company, committed to continuous improvement
*Part of a worldwide group
*Large site with excellent career prospects
*Committed to FDA regulation standards
*Preferably Degree qualified
*Positive, can-do attitude
*Worked on the quality assurance of a regulated manufacturing site
*Able to provide a quick response to internal customers
*Familiar with documentation control, CAPA etc.
*cGMP knowledge and experience…
We are looking for an experienced Quality Assurance professional to join a well established private sector company in the heart of Anglesey. This is a great opportunity to co-ordinate the functions relevant to implementing and maintaining the quality and food safety standards of the company and assist senior management in achieving its quality objectives.
In the Quality Assurance job based in Anglesey, North Wales you will;
* interpret relevant legislation and regulations and implement and/or maintain policies, procedures and processes to
meet all necessary requirements
* have clear knowledge and understanding of the company's HACCP…
Senior Controls Engineer
The Senior Control Engineer is a key engineering role supporting the newly created Advanced Technology function. The role will provide technical expertise, leadership and product development experience to a wide range of current and future emissions and environmental technology projects, some of which represent a significant diversification for the company.
* Support the scoping of projects for active aftertreatment control and new products.
* Define requirements for control system software and hardware.
* Lead the development of control system software and hardware…
Reporting to the Quality Control Supervisor the purpose of this post is to carry out the sampling and testing of components and raw materials within the business. This post is laboratory based and requires strict adherence to Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP) and Health and Safety Regulations.
Record keeping is required into laboratory books, master documentation and onto computer databases; accuracy and attention to detail are therefore paramount to this role at all times.
Duties & Responsibilities:
Following training, the key duties of the post are as follows:
• Carry out sampling…
Job Title – QA Manager
Salary – negotiable + benefits
Location – Egham, Surrey (TW20 9NF)
Job Profile -
Our client specialises in the development and manufacture of premium quality, scientifically validated products that assist in maintaining optimal health and wellbeing. Such as vitamins, supplements and skincare.
In this role you will be responsible for managing the day-to-day quality and compliance activities for our clients business, and related manufacturing sites. You will oversee and ensure compliance of products to specification, as well as GMP or other relevant regulatory / industry requirements. The role will…
QC MANAGER - SURREY - £55,00k - £60,000k
A leading healthcare manufacturing organisation are looking for a permanent QC Manager at their Plant in Surrey.
Reporting to the Quality Director, the core function of the role will be to lead the management of day to day laboratory testing activities associated with the Microbiology and Chemistry Quality Control departments. You will develop and implement strategies to ensure that Quality Control work in the laboratories complies with the appropriate Regulatory and Safety standards specifically those relating to cGMP.
In order to be considered candidates will need to have strong managerial…
Position: QA Officer
A leading international clinical and commercial manufacture of biologics and pharmaceuticals are looking to recruit a QA Officer for a 12 month period to cover maternity leave. You'll report to the QA Systems leader and will assist in the maintenance of the Quality System ensuring processes and products comply with regulations.
*Creation and revision of operational GMP Documentation within Quality Assurance
*Administration, coordination and review of GMP Manufacturing documentation
*Maintenance of the Supplier Assurance programme
*Coordinating and performing…
Fantastic opportunity to join a world-leading scientific organisation!
Do you have experience working to GMP regulations in a pharmaceutical organisation? Have you worked with biological samples including human tissue? Are you seeking a highly rewarding position in Quality Control? Then this could be the role for you!
Working as part of a friendly team your duties will involve QC checking of incoming deliveries and materials prepared for despatch. The materials will include biological samples including cells and tissues as well as clinical trials kits. You will also have some responsibility for updating SOPs, cross-training fellow team…
QC Analyst - Pharmaceutical
My client operates in the pharmaceutical industry and is now looking for a QC Analyst to come on board.
The main responsibilities are to carry out analysis of finished products, raw materials, intermediates and stability samples. All analysis must be carried out in accordance with approved methods, ensuring Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
This opportunity is a 6 month contract.
* To undertake physical and chemical analysis of incoming raw materials, in-process bulk materials and finished to the approved specification.
* Assist in the analysis of batches of…
Tenni at CK Science is currently recruiting for a QC Analyst to join a privately owned pharmaceutical company which manufactures and distributes pharmaceutical and healthcare products to the UK market. They offer a wide range of products and services which include specials, generic drugs, branded medicines, parallel trade and over the counter (OTC) medicines. With over 1000 employees and still growing they believe that investing in their people has been the key to their success.
This role will operate on a rotating shift basis from 9am - 7pm on one of the following days:
- Monday - Friday
- Tuesday - Saturday
- Wednesday - Sunday
QA Officer- Biopharmaceuticals –Staffordshire – 12 Months
This is an excellent opportunity to join an international biologics manufacturer on a 12 month temporary basis as a QA Officer. The QA officer will assist in the maintenance of their Quality System to help ensure that processes and products comply with appropriate regulatory requirements.
The responsibilities of QA Officer will be:
- Create/revise of operational GMP documentation within QA
- Administration, coordination and review of GMP manufacturing documentation
- Maintenance of supplier assurance and compliance
- Coordinating and supporting internal and supplier audits…
QA Officer - Pharmaceuticals
Our North West based pharmaceutical client are actively looking for a QA Officer
The successful candidate will be performing documentation review, production line audits and providing process support. Monitoring process performance and supporting review processes to demonstrate product Quality and compliance to cGMP.
Duties will include but not be limited to:
To carry out the assessment of all batch related data to ensure that all the required steps for documentation review are carried out in a timely manner to meet customer service requirements. Focusing on:-
- Batch file review
QC TEAM LEADER - CHESHIRE - c£30,000 - £35,000
A long established healthcare manufacturing organisation are now recruiting for a QC Team Leader to work in the Quality Control Laboratory.
The core function of the QC Team Leader role is day to day responsibility for sample testing, workload planning, managing of staff (approx. 8-10 Analysts) and efficient use of resource / technical "trouble shooting" of equipment & analytical methods, initial Laboratory OOS Investigations & CAPA actions.
In addition to this you will be responsible for;
> Stability testing
> Analytical method development & validation
> Routine duties - laboratory…
Graeme Pallas at CK Engineers is recruiting for a Process Validation Engineer to join a leading medical device organisation at their state of the art facility in Inverness on a contract basis for 8-10 months.
As a Process Validation Engineer you will be responsible for leading validation projects (IQ, OQ, PQ) across the site in line with company regulations and ISO13485.
Further responsibilities will include:
- Managing quality systems across site in relation to product, manufacturing, process & systems across site in line with ISO 13485:2003; 21 CFR Part 820, ISO 14971 and ISO 15197.
- Supporting planning of quality objectives to meet…
LONG TERM CONTRACT (UP TO 2 YEARS)
£30.00 - 35.00 P/HR
We currently have a fantastic opportunity for a contract NPI/APQP Engineer with strong knowledge and experience of the NPI Process Cycle from concept to delivery.
Assess manufacturing process capability and define process/validation plans
Assess and manage quality risks in design, manufacturing and supply chain processes
APQP (Advanced Product Quality Process)/PPAP (Production Part Approval Process)
Produce project reports ensuring all line managers are regularly updated
PFMEA (Process Failure Mode Effect Analysis)
Review and apply best…
Fantastic opportunity for a junior engineer to join an international leader in scientific instrumentation!
Do you hold a qualification in an Engineering discipline such as Mechanical or Electrical Engineering? Do you have hands-on experience of XYZ systems or pneumatic systems? Are you interested in fulfilling an integral role in the design and development of scientific instrumentation? Then this could be the role for you!
Working within a busy team environment you will be responsible for the testing, calibration and inspection of instruments and components to ensure the highest build quality is maintained. You will work with pneumatic…
Technical Officer - Pharmaceutical
My client operates in the pharmaceutical industry and is now looking for a Technical Officer to come on board.
You will be responsible to provide technical support activities to all departments in order to promote the technical, regulatory and commercial interest of the business, including co-ordinating the implementation of manufacturing site transfer projects; this may result from process changes, line extensions or new product introductions.
This is an 18 month contract position.
* Assist in providing technical support to all departments, and to assist in dealing with queries and problems…
Our client is a leading developer of systems and equipment for global precision manufacturing industries including Aerospace, Automotive, Biomedical.
We are currently seeking a Software Engineer to work on new application software development.
The role will primarily involve being responsible for the implementation of high quality user interfaces and custom user controls. This is a unique opportunity to join a growing team where your inputs will be influential to the design and readily recognised.
Duties and responsibilities of the role will include:
• Focusing on managing the daily demands of iterative, incremental, UI development…
Location: West Midlands, Birmingham, Leamington, Bromsgrove, Warwick, Solihull, Walsall, Stafford, Telford, Coventry, Dudley, Cannock, Redditch, Stourbridge, Kidderminster, Wolverhampton, West Bromwich, Tamworth, Worcester, Nuneaton, Burton on Trent, Derby, Rugby, Leicester, Nationwide
Salary: £35,000 - £40,000 + 25 days holiday + Company Pension + Life assurance
My client specialises in the supply of high-technology instruments and displays to the automotive and motorcycle markets.
Maintain and improve current processes and equipment.
Carry out machine and process capability studies.…
Our client is a global medical communications agency established. With over 25 years of experience, their clients are some of the leading companies within pharma and they are currently looking to hire a Medical Editor in either of their UK offices (Oxford and Macclesfield).
In this role, you will be responsible for ensuring that all materials are clear, concise, and accurate, in terms of both language and scientific content to ensure the production of high-quality end products. The core of their business is publication planning, but their editors are also involved in content for scientific meetings, marketing materials, and training…