Total 8 Manager level Quality Assurance / Control job vacancies in Bedfordshire, MK43 0LA

National Highways have an excellent opportunity for a Construction Assurance Manger to join our team in the East region. The Construction Assurance Manager will play a key role in the delivery of National Highways Capital Investment Schemes by representing the companies interests on civil engineering construction and maintenance sites. Reporting directly to the Construction Manager, you will actively ensure construction schemes are delivered in line with time, cost, quality and safety standards, and customer experience is not adversely impacted. This well-established team pride itself on its culture and this role will give you a varied, challenging workday, every day.

Please note additional and/or unsociable working hours including night working may be required for which there will be paid overtime and/or a nightwork uplift. 

This role will require travel across the East region and can be based from either Bedford, Cambridge or Ipswich.

You will also be required to drive as part of your role and you will need to have no more than 3 points to be considered for this position and during employment.
 
What you'll be leading on

• Assuring the completion of planned works to agreed standards and escalate any concerns to the Construction Manager, in line with agreed governance requirements.
• Ensuring that all works are constructed in line with: CDM regulations, HSE Legislation, Chapter 8 requirements, Design Manual for Roads and Bridges (DMRB) and Manual of Contract Documents for Highways Works (MCHW).
• Ensuring Project Managers receive regular and timely feedback on scheme construction progress, risks, early warnings, design related issues, and act as the initial point of escalation for any on-site issues that need to be resolved.
• Acting as liaison between all key supply chain partners and co-ordinate the delivery programme, ensuring buildability reviews are carried out on all projects.
• Maintaining good liaison with Project Managers and Commercial & Procurement colleagues, providing relevant and timely information on Early Warnings and Compensation Events

To be successful

• Proven highways/structures maintenance/construction experience; experience of working on high speed Trunk Road/Motorway Networks is desirable
• Knowledge of site-based processes, relevant legislation, practices and polices for health & safety, environmental and quality management, including good understanding of the DMRB, MCHW, Chapter 8 of the Traffic Signs Manual and CDM Regulations.
• Institution of Occupational Safety and Health (IOSH) or Site Management Safety Training Scheme (SMSTS) preferred.
• Excellent communication and interpersonal skills including stakeholder management, with a strong customer focus and managing geographically dispersed teams.
• Experienced in using the NEC 4 ECC form of contract. 

A bit about us

Making sure our customers have safe and reliable journeys is at the heart of everything we do in Operations. We keep the roads open for business and play a key role in making sure the network we manage is fit for purpose today and for the future. We achieve this through the delivery our capital programme, supporting customers on the road with our Traffic Officer Service and managing incidents effectively.

Proud member of the Disability Confident employer scheme

Job Advert

Are you ready to lead a key transformation within the pharmaceutical industry?

We are looking for a driven and knowledgeable Quality Projects and Implementation Manager to join our team on a 12 Month FTC.



Benefits

We have an onsite gym in Bedford, offer discounted PureGym membership, 33days of annual leave including bank holidays as well as
the option to buy more, as well as access to a rewards platform, free flu vaccine, a workplace pension, access to simply health
and other perks. You’ll also have access to My Rewards our benefits platform offering a variety of high street discounts, cashback
and savings.



Purpose of the role

This role will focus on optimising our quality processes and systems, ensuring we meet the ever-evolving demands of the
pharmaceutical industry while maintaining full compliance. Reporting to the Quality Director, you'll work closely with
cross-functional teams to drive operational efficiency and continuous improvement.



Key Responsibilities

* Lead the continued rollout of the Electronic Quality Management System (EQMS), with a focus on modules such as Non-Conformance,
CAPA, Change Control, and Continuous Improvement.
* Oversee client integration processes, ensuring compliance with change control and risk assessments.
* Host and support client audits, providing timely responses to audit reports and maintaining Quality Technical Agreements.
* Collaborate with the Commercial Team to support new business inquiries, ensuring client requirements are fully integrated into
our Quality Management System.
* Build and maintain strong relationships with external client quality teams, delivering clear communication and exceeding client
expectations.

Technical and Behavioural Skills

* Proven ability to work independently and within a team, delivering high performance in a fast-paced, deadline-driven
environment.
* Excellent communication and presentation skills, with confidence in engaging with diverse audiences.
* Strong problem-solving abilities, organisational skills, and proficiency in managing multiple priorities.
* In-depth knowledge of Good Distribution Practices (GDP), Good Manufacturing Practices (GMP), and pharmaceutical compliance
standards.
* Experience in pharmaceutical product transportation, storage, and distribution.

Desirable Qualifications:

* RP Gold Standard Training.
* Qualified Lead Auditor certification.
* Experience as a Registered Responsible Person (RP) in the pharmaceutical industry.

This is an exciting opportunity to play a key role in shaping the future of our business, as we continuously improve and maintain
the highest standards of quality and compliance. If you have the expertise and drive to make a real impact, we’d love to hear from
you!

Job Title: Quality Manager - Medical Devices

Location: Bedfordshire

Are you an energetic Quality Manager with a knack for inspiring teams and driving excellence? If you're passionate about coaching and empowering others, we want you!

Join a global leader in consumer products with a strong presence in the medical device industry. Known for innovation and quality, this company offers a stunning, collaborative work environment where your growth is a priority.

Lead and motivate a talented team of five quality professionals as you oversee and enhance a newly implemented Quality Management System (QMS), ensuring top-tier compliance and continuous improvement. This is your chance to make a real impact!

Key Responsibilities:

• Lead, mentor, and motivate a team of five quality professionals with varying levels of experience. Foster a culture of continuous improvement, trust, and collaboration.
• Take ownership of the newly implemented Quality Management System (QMS), ensuring it meets regulatory requirements and aligns with company standards. Drive continuous improvements to enhance its effectiveness and efficiency.
• Ensure compliance with all relevant medical device regulations, including ISO 13485, FDA 21 CFR Part 820, and other applicable standards. Lead internal and external audits as required.
• Provide ongoing coaching, training, and development opportunities for the quality team. Create individualised development plans to help team members grow in their careers and enhance their skill sets.
• Collaborate closely with other departments, including R&D, manufacturing, and regulatory affairs, to ensure quality is integrated into all aspects of product development and production.
• Identify areas for process improvement within the QMS and across the organisation. Implement best practices to enhance product quality, reduce risk, and increase efficiency.

Qualifications:

• Minimum of 5 years of experience in quality management within the medical device industry.
• Strong knowledge of QMS implementation and management, including ISO 13485 and FDA regulations.
• Proven experience in leading and managing a team, with a passion for coaching and

I am looking for an experienced Operational Quality Manager to join our rapidly expanding Aseptics team producing cancer drugs.

About the Role:

As an integral part of our state-of-the-art aseptic manufacturing facility, you'll lead and inspire a high-performing quality team, ensuring unwavering adherence to GMP and GDP standards. You'll be instrumental in driving continuous improvement, managing regulatory compliance, and contributing to our mission of delivering life-saving medications to patients.

Key Responsibilities:

• Build and lead a world-class quality team
• Drive quality initiatives and monitor KPIs
• Ensure regulatory compliance and manage audits
• Foster a culture of quality excellence

Your Profile:

• Proven experience in a similar role within the pharmaceutical industry
• Strong leadership and people management skills
• In-depth knowledge of GMP and GDP regulations
• A scientific degree and ideally, a registered pharmacist
• A passion for quality and patient safety

The Offer

• Competitive salary and benefits package
• Opportunities for professional growth and development
• Be part of a company making a real difference
• A supportive and collaborative work environment
• Exciting company perks including flexible shifts, free food and drink, and social events

Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

Are you working in medical device quality and feel that it is time for a change? How do you feel about flexible working, stylish workspaces, great benefits and exciting products? Tempting enough to read on?

As the Quality Manager (Systems) you will have overall accountability for the Quality Management System.

Along with the flexible working, attractive benefits and great workplace, you as the Quality Manager, will be working for a world leader in research and have the opportunity to be part of a company that produces some fantastic diagnostic products .

Ideally we would like you to possess IVDR experience, worked to ISO 13485, US FDA 21 CFR 820 standards and having a Lead Auditor qualification would be desirable.

If you have a mixture of the skills required then please do get in contact and we can discuss further.

Advinia Healthcare are looking for a Quality Manager (preferably Registered Nurse qualified) based in the Northamptonshire area to cover our Care Homes in the Midlands and South.

This role will cover the following areas:


Midlands
London
Norfolk
Lincolnshire


Main Duties & Responsbilities:


Comply with Quality Assurance Framework that ensures that standards of Good Clinical Governance, safety netting and best practice are met.
Perform audits, process information and recommend appropriate actions, highlight the best practice. Audits will include all aspects of patient care such as results, post-operative care, onward referrals, etc.
Perform quality consultations audits at regular interval and report all findings and outcomes.
Peform quality audits in accordance to annual schedule
Promote continous improvment in the quality and safety of patient services
Promote monthly analysis and reporting of quality assurance
Promote an organisation culture that recongises issues of quality, risk and patient safety and adheres to policies and protocols. Champion and raise awareness at all levels.


Candidate Requirements:


Previous strong Home Management experience
Experience working in turnaround, quality improvement, and working at a regional level
Extensive knowlege of residential/nursing home setting
RGN qualified (preferable)
Ability to critically analyse data and solve problems as well as the ability to neogtiate and influence others


For your commitment and hard work, we will offer you:

- Competitive pay rate
- Flexible pay - Wagestream
- Free DBS
- Professional training and ongoing career development

If this role sounds as though it would be of interest then please apply today!

PRI6

Are you working in medical device quality and feel that it is time for a change? How do you feel about flexible working, stylish workspaces, great benefits and exciting products? Tempting enough to read on?

As the Quality Manager (Innovations) you will have experience of design and development within medical devices and are able to maintain design controls and software as a medical device.

Along with the flexible working, attractive benefits and great workplace, you as the Quality Manager, will be working for a world leader in research and have the opportunity to be part of a company that produces some fantastic diagnostic products .

Ideally we would like you to possess IVDR experience and have worked to ISO 13485 standards, so if you have a mixture of the skills required then please do get in contact and we can discuss further.

Advinia Healthcare are looking for a Quality Manager to cover our Care Homes in the South.

Main Duties & Responsbilities:


Comply with Quality Assurance Framework that ensures that standards of Good Clinical Governance, safety netting and best practice are met.
Perform audits, process information and recommend appropriate actions, highlight the best practice. Audits will include all aspects of patient care such as results, post-operative care, onward referrals, etc.
Perform quality consultations audits at regular interval and report all findings and outcomes.
Peform quality audits in accordance to annual schedule
Promote continous improvment in the quality and safety of patient services
Promote monthly analysis and reporting of quality assurance
Promote an organisation culture that recongises issues of quality, risk and patient safety and adheres to policies and protocols. Champion and raise awareness at all levels.


Candidate Requirements:


Previous strong Home Management experience
Extensive knowlege of residential/nursing home setting
Ability to critically analyse data and solve problems as well as the ability to neogtiate and influence others


For your commitment and hard work, we will offer you:

- Competitive pay rate
- Flexible pay - Wagestream
- Free DBS
- Professional training and ongoing career development

If this role sounds as though it would be of interest then please apply today!

PRI2