Amazon LogisticsCardiff
Become an Amazon delivery partner/entrepreneur in logistics and write your own success story!.Are you customer-oriented, have good leadership skills and interested in setting up and developing a business? .Then the Amazon Delivery Service Partner (DSP) programme could be just the thing for you....
Cardiff, 6 mi from Caerphilly
failure analysis based on customer warranty returned product, ensuring robust countermeasures will be put in place
Leading introduction of basic quality tools into production lines (first offs, controlled rework, etc)
Planning and performing manufacturing...
Ystrad Mynach, 5 mi from Caerphilly
ISO standards.
Experience in conducting audits, root cause analysis, and implementing corrective and preventive actions (trained auditor preferable).
Experience with quality management systems and tools.
Experience dealing with customers and suppliers...
ea ChangeCardiff, 6 mi from Caerphilly
Role: Business Analyst (Retail Banking) Rate: £500 - £550/day (via umbrella) Duration: 6 months (long-term extensions beyond initial contract) Location: Cardiff (Hybrid Working) Multiple Business Analysts are required to join a leading Retail...
Hays Accountancy and FinanceCardiff
Working with a large independent Accountancy Practice based in Cardiff.This firm has an excellent local reputation and prides themselves on the flexibility it gives to staff.This will be a mixed role covering Personal Tax Returns, P11d's, Corporate Tax Returns and Partnership returns.You will cover ...
qed legalCardiff, 6 mi from Caerphilly
Quality AuditorCardiff BasedWe're working with a highly ranked top 100 full-service law firm offering specialist legal and financial advice. They're now looking to expand their quality and risk department. You will join a close-knit team performing...
Qed LegalCardiff, 6 mi from Caerphilly
Quality Auditor Cardiff Based We're working with a highly ranked top 100 full-service law firm offering specialist legal and financial advice.
They're now looking to expand their quality and risk department. You will join a close-knit team...
Vibe RecruitCaerphilly
analysis, monitoring quality control data to identify trends, deviations, and potential issues, and implement corrective actions as needed.
Collaborate with laboratory staff to develop and implement training programs on quality assurance protocols...
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Biocompatibility Engineer
Caerphilly | Permanent | www.cv-library.co.uk |
We are looking to recruit for a Bio-compatibility Engineer, you will be a part of the R&D team that is responsible for implementing technical strategies, evaluating and developing products, and providing a superior level of technical support.
Duties:
The main responsibilities involve the biological safety risk assessment, by chemical analysis and characterisation, of medical devices in development.
You develop protocols, reports, and regulatory summaries in collaboration with cross-functional teams, laboratories and suppliers.
Management of external test laboratories and ensure compliance with global regulatory requirements and standards related to biological safety.
You are also entrusted with defining testing strategies for materials, design and process that satisfy cost and technical requirements as well as analysing bio-compatibility testing (
Review and approves external chemical analysis reports
Keep GOP and associated templates updates
Skills
Bachelor's degree or higher in Biochemistry, Chemistry, Chemical Engineering, (Bio)Medical Engineering or Physics.
In-depth knowledge of quality assurance techniques, practices, ISO and Regulatory (FDA) compliance.
In-depth knowledge of medical device regulations and standards
Knowledge of analyticaly/physical/organic chemistry and ability to translate this knowledge into a consistent work programme to analyse the properties of devices and materials.
Ability to work with a Team in accordance with company objectives.
Ability to define problems, collect and analyse data, establish facts, and draw valid conclusions.
Ability to verbally communicate ideas and issues effectively to other team members and management.
Actively network with the internal and external scientific, technical, and regulatory community to maintain state of the art knowledge.
Partner with Quality to support the development, maintenance and adherence to quality systems and continuous process improvement.
Partner with product development and regulatory functions to ensure new and sustaining products meet all necessary requirements.
Benefits
o 38.5 hours per week (Mon-Thurs 8.30am-5.00pm, Fri 8.30am-3.30pm)
o 4 days per month WFH
o 25 days holiday (plus bank holidays)
o Pension - salary sacrifice (3% ER / 5% EE)
o Annual company performance bonus
o Annual pay review
o Benefits - Health cash plan, income protection, life assurance (2 x salary), holiday trading, monthly benefit fund to use or put in pension pot
Duties:
The main responsibilities involve the biological safety risk assessment, by chemical analysis and characterisation, of medical devices in development.
You develop protocols, reports, and regulatory summaries in collaboration with cross-functional teams, laboratories and suppliers.
Management of external test laboratories and ensure compliance with global regulatory requirements and standards related to biological safety.
You are also entrusted with defining testing strategies for materials, design and process that satisfy cost and technical requirements as well as analysing bio-compatibility testing (
Review and approves external chemical analysis reports
Keep GOP and associated templates updates
Skills
Bachelor's degree or higher in Biochemistry, Chemistry, Chemical Engineering, (Bio)Medical Engineering or Physics.
In-depth knowledge of quality assurance techniques, practices, ISO and Regulatory (FDA) compliance.
In-depth knowledge of medical device regulations and standards
Knowledge of analyticaly/physical/organic chemistry and ability to translate this knowledge into a consistent work programme to analyse the properties of devices and materials.
Ability to work with a Team in accordance with company objectives.
Ability to define problems, collect and analyse data, establish facts, and draw valid conclusions.
Ability to verbally communicate ideas and issues effectively to other team members and management.
Actively network with the internal and external scientific, technical, and regulatory community to maintain state of the art knowledge.
Partner with Quality to support the development, maintenance and adherence to quality systems and continuous process improvement.
Partner with product development and regulatory functions to ensure new and sustaining products meet all necessary requirements.
Benefits
o 38.5 hours per week (Mon-Thurs 8.30am-5.00pm, Fri 8.30am-3.30pm)
o 4 days per month WFH
o 25 days holiday (plus bank holidays)
o Pension - salary sacrifice (3% ER / 5% EE)
o Annual company performance bonus
o Annual pay review
o Benefits - Health cash plan, income protection, life assurance (2 x salary), holiday trading, monthly benefit fund to use or put in pension pot
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