940 Quality Director jobs in the United Kingdom

Quality Director - Childrens Residential Services

A Wilderness Way Ltd

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Job Description

Quality care starts with one child - and one leader who makes it happen.
Lead with purpose. Drive excellence. Transform lives.

Are you a passionate leader in children's social care with a relentless focus on quality? Do you want to shape the future of residential services that change lives every day?

We're looking for an outstanding Quality Director to spearhead excellence across our portfolio of .

ZIPC1_UKTJ

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Pharmaceutical Quality Assurance Director

B4 6NF Birmingham, West Midlands £90000 Annually WhatJobs

Posted 3 days ago

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full-time
Our client, a leading pharmaceutical company, is actively seeking a highly experienced and dynamic Pharmaceutical Quality Assurance Director. This critical role, based at our client's state-of-the-art facility, will be responsible for overseeing and implementing the company's comprehensive quality assurance strategy. You will lead a dedicated QA team, ensuring strict adherence to regulatory requirements, cGMP guidelines, and internal quality standards across all pharmaceutical manufacturing and development processes. Your responsibilities will include developing and maintaining the Quality Management System (QMS), conducting internal and external audits, managing deviations and CAPAs, and overseeing validation activities. This position requires a deep understanding of pharmaceutical quality principles, regulatory affairs, and risk management. You will play a pivotal role in ensuring product quality, patient safety, and compliance with global regulatory bodies such as the MHRA, FDA, and EMA. The ideal candidate will possess a strong track record of leadership within the pharmaceutical industry, with a minimum of 10 years of progressive experience in quality assurance or quality control. A Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related life sciences field is essential. Excellent leadership, communication, strategic thinking, and decision-making skills are paramount. You will be expected to collaborate effectively with cross-functional teams, including R&D, manufacturing, regulatory affairs, and supply chain. This is an exceptional opportunity to join a highly reputable organisation and shape the future of pharmaceutical quality. The successful candidate will be instrumental in upholding the highest standards of quality and integrity.
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Quality Assurance Quality Control Engineer

Thirsk, Yorkshire and the Humber Employment Solutions

Posted 7 days ago

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Ready to elevate your career with a top-tier steel fabrication leader?


We're expanding our team in Thirsk and looking for a skilled QA/QC Engineer to help drive excellence across major industries like Petrochemical, Pharmaceutical, and Nuclear. Join us on our exciting journey of growth and innovation, where you'll benefit from robust career development opportunities, clear progression paths , and the chance to shape the future of engineering excellence.


Who this job suits:

This role is ideal for an experienced Quality Engineer with a meticulous eye for detail, analytical skills, and prior exposure to large, complex, multi-disciplined projects in regulated environments. Your knowledge of Welding, ISO 3834 & EN 1090 will be high advantageous.


Key Responsibilities:

  • Liaise with internal and external stakeholders to ensure project inspections and technical requirements are met.
  • Ensure compliance to ISO 3834, EN 1090, ISO 9001.
  • Collate and analyse data, support audits, and liaise with clients.
  • Utilize extensive hands-on experience in Quality Management Systems and Principles.
  • Interpret and accept contract NDT reports on behalf of the business.


Skills and Experience:

  • CSWIP 3.1 certified
  • Auditor certified
  • PCN Level 2 certified
  • Time-served apprenticeship, HNC, HND or equivalent
  • Knowledge of ISO 3834 (welding inspection) and/or EN 1090 advantageous
  • Experience with LTQRs advantageous


Location : Thirsk

Contract: 12 month FTC - Fixed Term Contract

Salary: circa £40k - £45k (dependent on experience)

Hours: 37.5 hours per week. 07.45 – 16:45 Monday - Thursday, 7.30 - 12:00 Friday.

Benefits: Pension, Medical Cover, 25 days + BH, Cycle to Work, Save as you earn scheme, Counselling & Support, further Benefit schemes.


APPLY NOW!

Contact Jacob Golding for further details – –

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Director of Quality Assurance

Sheffield, Yorkshire and the Humber IC Resources

Posted 4 days ago

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We are seeking an accomplished Director of Quality Assurance to lead the Quality function within a rapidly growing, high-technology company in the semiconductor industry. This strategic position will oversee the company’s Quality Management System (QMS), supplier and subcontractor performance, product reliability, and customer quality support — ensuring world-class standards are achieved and maintained across all operations.


Key Responsibilities

  • Provide strategic direction and leadership for all Quality Assurance activities across manufacturing, supplier management, and customer support.
  • Oversee and continuously improve the company’s Quality Management System, ensuring compliance with ISO 9001 and relevant industry standards (JEDEC, AEC).
  • Drive product reliability initiatives and implement robust quality processes across design, development, and production.
  • Manage supplier and subcontractor performance, establishing strong partnerships and accountability for quality and delivery.
  • Lead internal and external audits, and act as the primary contact for customer quality escalations and certifications.
  • Chair Health & Safety meetings, conduct inspections, and ensure all regulatory and safety policies are effectively implemented.
  • Use data-driven insights to identify root causes, implement corrective actions, and enhance process capability.
  • Promote a culture of quality, safety, and continuous improvement across all levels of the organisation.


About You

  • Proven track record in senior Quality leadership within the semiconductor or electronics manufacturing sectors.
  • Deep knowledge of JEDEC, AEC, and ISO 9001 quality standards and regulatory frameworks.
  • Strong background in supplier quality management, product reliability, and customer quality support.
  • Experienced in driving data-driven decision-making and leading cross-functional quality initiatives.
  • Lean Six Sigma (Green or Black Belt) certification strongly preferred.
  • Excellent leadership, communication, and stakeholder management skills, with the ability to influence at executive level.


Apply now for more information!

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Director, Quality & Regulatory

London, London Medtronic

Posted 10 days ago

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At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You'll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.
**A Day in the Life**
Medtronic is hiring a Quality System Director. The person is Management and supervisory professionals with one or more employees who are focused on tactical, operational and some strategic activities within a specified area. Levels within the management career stream typically have six or more direct reports. The majority of time is spent overseeing their area of responsibility, managing performance, developing talent, engagement and inclusion, communicating business and operational developments, planning, prioritizing and / or directing the responsibilities of direct reports. Goal achievement is typically accomplished through performance of direct and / or indirect reports. A key responsibility of roles in this career stream is managing people. which includes accountability for mentoring, developing and coaching staff on meeting/exceeding performance expectations and defined objectives, providing leadership to staff ensuring the prioritization of strategic and department level initiatives to include defining performance goals and targets, conducting performance reviews, and staff 1:1s to guide performance management and employee development efforts and manage toward departmental goals.
This position is an exciting opportunity to work with Medtronic's Diabetes business. Medtronic has announced its intention to separate the Diabetes division to promote future growth and innovation within the business and reallocate investments and resources across Medtronic, subject to applicable information and consultation requirements. This separation provides our team with a bold opportunity to unleash our potential, enabling us to operate with greater speed and agility. As a separate entity, we anticipate leveraging increased investments to drive meaningful innovation and enhance our impact on patient care.
**Responsibilities may include the following and other duties may be assigned:**
-Provides oversight for the development and maintenance of quality programs, systems, processes and procedures that ensure compliance with policies and that the performance and quality of services conform to established internal and external standards and guidelines.
-Provides expertise and guidance in interpreting policies, regulatory and/or governmental regulations, and internal regulations to assure compliance.
-Works directly with operating entities to provide process analyses oversight on a continuing basis to enforce requirements and meet regulations.
-Leads audit and inspection preparation, resolution of audit and inspection findings and liaises with auditing groups and inspectors through all stages of the audits.
-Prepares reports and/or necessary documentation (ex Corrective and Preventative Actions) and provides to applicable stakeholders, both internal and external.
-Co-ordinates legal requests in support of government investigations or litigations.
-Ensures the quality assurance programs and policies are maintained and modified regularly.
-Facilitates uniform standards worldwide and enables best practice sharing, thereby fostering the achievement of company's mission globally.
**Required Knowledge and Experience:**
-Autonomy: Manages department (s) or small unit that includes multiple teams led by managers and / or supervisors. Provides motivational leadership for the area managed. Provides thought and technical leadership. Performs work without appreciable direction.
-Organizational Impact: Leads the development of the strategy for own department or business area, ensuring links to the company's aims and objectives. Management authority to make large business decisions and some strategic decisions. Decisions impact the financial performance, employees, or public image of the operational unit and/or company. Typically has budget or P&L accountability for a department, broad functional area or geography.
-Innovation and Complexity: Drives innovation across the business area, encouraging best practice and knowledge sharing. Significantly improves, changes or adapts own department or business area's processes, systems, products or services. Problems and issues faced are complex, difficult and undefined, and require detailed information gathering, analysis and investigation to understand the problem.
-Communication and Influence: Develops long term strategic relationships and alliances with key internal and external stakeholders. Communicates and conducts briefings with senior or executive leadership regarding ongoing operations and strategic initiatives. Influences across functions and businesses to negotiate and gain cooperation on operational issues and internal divergent objectives.
-Leadership and Talent Management Directs and leads a department, broad functional area or geography, including one or more teams led by managers and / or supervisors. Determines supervisory relationships and creates workforce and staffing plans to accomplish business results. Authorizes hiring, firing, Job Description promotion and reward within own area.
-Requires broad management and leadership knowledge to lead multiple job areas, and detailed functional and operational expertise. Typically has mastery level knowledge and skills within a specific technical or professional discipline with broad understanding of other areas within the job function.
**Physical Job Requirements**
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position. 
**Benefits & Compensation**
**Medtronic offers a competitive Salary and flexible Benefits Package**
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.
This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).
This position is eligible for an annual long-term incentive plan.
**About Medtronic**
We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.
Our Mission - to alleviate pain, restore health, and extend life - unites a global team of 95,000+ passionate people.
We are engineers at heart- putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.
Learn more about our business, mission, and our commitment to diversity here ( lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.
Our Mission - to alleviate pain, restore health, and extend life - unites a global team of 95,000+ passionate people.
We are engineers at heart- putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.
**We change lives** . Each team member, each day, helps to improve and redefine how the world treats the most pressing health conditions, from heart disease to diabetes. Our industry leadership comes from the passion and ingenuity of our people. That's who we are. Working alongside one another, we use science, medicine, and a profound understanding of the human body to build extraordinary technologies that can transform lives.
**We build extraordinary solutions as one team** . With one Medtronic Mindset defining how we work. Speed and decisiveness run through our DNA. Diverse perspectives inspire our bold answers to any challenge that comes our way. And we deliver results the right way, breakthrough after patient breakthrough.
**This life-changing career is yours to engineer** . By bringing your ambitious ideas, unique perspective and contributions, you will.
+ **Build** a better future, amplifying your impact on the causes that matter to you and the world
+ **Grow** a career reflective of your passion and abilities
+ **Connect** to a dynamic and inclusive culture that welcomes the challenge of life-long learning
These commitments set our team apart from the rest:
**Experiences that put people first** . Respect for people is the hallmark of our humanity. It fuels our team to positively impact even a single life. And it means we put our people first at Medtronic as well, creating a culture of belonging and always pushing to get you the career-building resources you need.
**Life-transforming technologies** . No matter your role, you contribute to technologies that transform lives. What we build empowers patients to live life on their terms.
**Better outcomes for our world** . Here, it's about more than the bottom line. Our Mission to improve human welfare drives us. We advance healthcare, society, and equity with every design, inside and outside our walls.
**Insight-driven care** . Fresh viewpoints. Cutting-edge AI, data, and automation. You're shaping the future of healthcare technology and defining the next generation of breakthroughs in care
It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.
For sales reps and other patient facing field employees, going into a healthcare setting is considered an essential function of the job and we expect our employees to comply with all credentialing requirements at the hospitals or clinics they support.
This employer participates in the federal E-Verify program to confirm the identity and employment authorization of all newly hired employees. For further information about the E-Verify program, please click here ( .
For updates on job applications, please go to the candidate login page and sign in to check your application status.
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Quality Control and Assurance Specialist

OX1 2JD Oxford, South East £45000 Annually WhatJobs

Posted 11 days ago

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full-time
Our client, a leading organisation committed to maintaining the highest standards of cleanliness and hygiene across various sectors, is seeking a meticulous and proactive Quality Control and Assurance Specialist to join their fully remote team. This role is vital in ensuring that all services and products meet rigorous quality benchmarks and regulatory requirements. The Quality Control and Assurance Specialist will be responsible for developing, implementing, and monitoring quality management systems, conducting audits, analysing performance data, and identifying areas for improvement. Key duties include creating and updating quality control protocols, performing remote inspections and assessments of service delivery, investigating and resolving quality-related issues, and preparing comprehensive reports for senior management. You will collaborate closely with operational teams to promote a culture of quality and continuous improvement. The ideal candidate will have a proven track record in quality assurance or quality control, ideally within the facilities management, cleaning, or hospitality industries. A Bachelor's degree in a relevant field or equivalent professional experience is required. Strong knowledge of quality management frameworks (e.g., ISO 9001) and experience with quality auditing are essential. Excellent analytical, problem-solving, and communication skills are paramount for effective reporting and stakeholder engagement. We are looking for a detail-oriented individual with a passion for upholding standards and driving operational excellence within a remote working setup. This is an excellent opportunity to contribute significantly to an organisation that values quality and customer satisfaction, and to advance your career in quality assurance in a flexible, home-based role. Join our client and help ensure exceptional quality across all operations.
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Quality Control Analyst

Dewsbury, Yorkshire and the Humber Network Scientific Recruitment

Posted 1 day ago

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Are you looking for some further experience in Pharmaceutical QC? Do you have prior experience with GC & HPLC in a cGMP environment?


A Global Pharmaceutical Manufacturer are seeking a QC Analyst to join the team at their site in Kirklees. This is a 6 month FTC and would be ideal if you are immediately available and looking to add to your existing experience in Pharmaceutical QC.


Role Overview


  • Full Time , 6 month Fixed term Contract. Day Shifts. £27,000pa.
  • Analysis of Raw Materials and Finished Products to SOPs.
  • Utilise analytical equipment , predominantly HPLC & GC.
  • Interpretation and checking of Analytical Data.
  • Monitoring, Calibration and occasional basic troubleshooting/maintenance of instruments and analytical equipment.
  • Preparation of all relevant documentation in line with applicable standards.


Requirements


  • Prior working experience in a cGMP environment using HPLC and GC is essential.
  • Degree or equivalent in relevant scientific discipline (or equivalent working experience) is essential.
  • Ability to work independently in time pressured environment.
  • Excellent communication skills and attention to detail.


In return


This 6 month FTC is an excellent opportunity to add some additional experience to your CV, working alongside industry leaders in a well renowned pharmaceutical organisation.


For more information, please contact Louis Williams


If this QC Analyst job is not quite right for you, but you’re interested in similar opportunities, please take a look at our other Jobs in the Pharmaceutical Sector. Network Scientific is a multi-award-winning recruitment agency dedicated to connecting top talent with opportunities across the scientific and technical sectors. We specialise in temporary, permanent, and contract placements, and pride ourselves on being an ethical and knowledgeable consultancy with a strong focus on candidate care.

Please note that all applicants for this role should be able to prove that they are legally entitled to work in the country specified. Network Scientific Recruitment, part of Network Scientific Ltd. is an Employment Business/Agency.

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Quality Control Inspector

Deeside, Wales Employment Solutions

Posted 1 day ago

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A Quality Inspector (Weld & NDT) role is pivotal in upholding quality standards and compliance within manufacturing environments. Responsible for inspections and documentation review, this position fosters a culture of operational satisfaction and adherence to project requirements.


Who this job would suit:

Ideal for CSWIP 3.1 & PCN Level 2 certified QA/QC professionals with meticulous attention to detail and excellent communication skills. Suitable for those experienced in welding procedures and quality assurance protocols, who thrive in collaborative environments.


Key Responsibilities:

  • Complete inspections to ensure material at goods inwards meet the required standards.
  • Liaise with sub-contractors and treatment works to carry out inspections of sites.
  • Visit suppliers and produce relevant inspection reports.
  • Utilise your Welding inspection and NDT knowledge to ensure work is completed to a safe and high standard in compliance with company and ISO standards are followed.

Requirements:

  • CSWIP 3.1 certified is essential.
  • PCN Level 2 in MPI & DPI essential
  • Experience within Nuclear, MOD or Heavy Fabrication is highly advantageous.


Permanent

Pay rate: £24.11 per hour (47k basic) + Overtime at premium rates + Bonus! (OTE circa £55k+)

Location: Deeside

Working Hours: 37.5 hrs (Mon-Thurs), (Fri)


Contact Details:

For inquiries or to apply, please contact Jacob on or

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Analyst, Quality Control

Oxford, South East Moderna

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The Role:

Joining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology, with a diverse pipeline of development programs across various diseases.

As an employee, you'll be part of a continually growing organization, working alongside exceptional colleagues and strategic partners worldwide, contributing to global health initiatives.

Moderna's commitment to advancing the technological frontier of mRNA medicines ensures a challenging and rewarding career experience, with the potential to make a significant impact on patients' lives worldwide.

Moderna's mission is to establish a leading-edge research, development, and manufacturing facility at Harwell, as part of a long-term commitment to onshore mRNA vaccine production for respiratory diseases. This initiative will create a multitude of highly skilled jobs and foster collaboration with academic, NHS and government partners across the UK. We're looking for global experts eager to join us in this endeavour, contributing to a future where access to life-saving vaccines is a reality for all.

This position, reporting to the Associate Director, Quality Control, is an essential part of the Harwell QC team focused on GMP-compliant stability and analytical chemistry testing. As a key contributor, you will support critical release and stability testing operations and play a major role in the management of global stability programs. You will operate and maintain a suite of sophisticated instrumentation, manage cGMP documentation, and support the timely delivery of results across the QC chemistry function. The role offers direct involvement with cutting-edge analytical techniques, stability data management, and regulatory compliance frameworks — as well as exposure to Generative AI tools and digital platforms enhancing Moderna's QC infrastructure.

Here's What You'll Do :

Your key responsibilities will be:

  • Execute routine analytical chemistry and stability testing using HPLC, UPLC, GC, UV, Karl Fischer, particle size analysis (DLS), and other analytical techniques.
  • Support testing across raw materials, components, in-process and drug substance samples.
  • Complete all cGMP documentation for analytical work in full compliance with applicable guidelines.
  • Perform LIMS (LabVantage) data entry and complete electronic assay forms for traceability and review.
  • Carry out HPLC (AEX) and NaOH plate-reader assays in support of manufacturing stat testing.
  • Provide general laboratory support: reagent preparation, inventory management, equipment maintenance, and housekeeping.
  • Ensure safe laboratory operations, actively contributing to EHS compliance.
  • Participate in procurement and stock management of lab consumables and supplies.

Your responsibilities will also include:

  • Conduct stability program operations: set down, pull, labeling, verification, inventory updates, and disposal.
  • Author, review, and revise stability protocols, SOPs, and technical reports.
  • Maintain and trend stability data, performing statistical analyses and ensuring real-time visibility of study progress.
  • Interface with external labs for sample shipment and testing data coordination, and update internal databases and binders accordingly.
  • Support regulatory submissions by contributing to stability sections and ensuring alignment with FDA, EU, and ICH guidelines.
  • Assist with troubleshooting analytical methods and instrumentation as required.
  • Support training and mentorship of junior staff as needed.
  • Contribute to quality systems documentation including investigations, deviations, CAPAs, and change controls.
  • Promote a positive, inclusive, and collaborative culture in line with Moderna's values.
  • Ensure strict adherence to GDP, data integrity, and internal SOPs across all executed tasks.
  • Complete all required training and qualifications in accordance with assigned learning plans.

The key Moderna Mindsets you'll need to succeed in the role:

  • We obsess over learning. We don't have to be the smartest—we have to learn the fastest.

    In this highly technical and regulated environment, your ability to absorb evolving regulatory guidance, apply new analytical tools, and quickly learn from experimental data will be critical to your effectiveness.
  • We digitize everywhere possible using the power of code to maximize our impact on patients.

    With increasing use of Generative AI tools and digital systems like LIMS at the core of Moderna's QC infrastructure, your comfort with digital platforms and data-driven execution will allow you to unlock greater speed, accuracy, and compliance.

Here's What You'll Need :

  • Education: BA/BSc in Chemistry or Biology (preferred) or other relevant scientific discipline
  • Experience: At least 5-7 years in Quality Control Laboratory of a Pharmaceutical Company
  • Demonstrated aptitude or ability to learn in order to gain a strong understanding of GxP regulations (specify GMP, GLP, GCP, GVP or other applicable standards)
  • This position is site-based, requiring you to be at Moderna's site full-time. This position is not eligible for remote work.
  • As part of Moderna's commitment to workplace safety, this role may require an enhanced pre-employment check.

At Moderna, we believe that when you feel your best, you can do your best work. That's why our global benefits and well-being resources are designed to support you—at work, at home, and everywhere in between.

  • Quality healthcare and insurance benefits
  • Lifestyle Spending Accounts to create your own pathway to well-being
  • Free premium access to fitness, nutrition, and mindfulness classes
  • Family planning and adoption benefits
  • Generous paid time off, including vacation, bank holidays, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown
  • Savings and investments
  • Location-specific perks and extras

The benefits offered may vary depending on the nature of your employment with Moderna and the country where you work.

About Moderna

Since our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines are created and delivered, and a world-class team. We believe in giving our people a platform to change medicine and an opportunity to change the world.

By living our mission, values, and mindsets every day, our people are the driving force behind our scientific progress and our culture. Together, we are creating a culture of belonging and building an organization that cares deeply for our patients, our employees, the environment, and our communities.

We are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S.

As we build our company, we have always believed an in-person culture is critical to our success. Moderna champions the significant benefits of in-office collaboration by embracing a 70/30 work model. This 70% in-office structure helps to foster a culture rich in innovation, teamwork, and direct mentorship. Join us in shaping a world where every interaction is an opportunity to learn, contribute, and make a meaningful impact.

If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit to learn more about our current opportunities.

Moderna is a smoke-free, alcohol-free, and drug-free work environment.

Moderna is a place where everyone can grow. If you meet the Basic Qualifications for the role and you would be excited to contribute to our mission every day, please apply

Moderna is committed to equal opportunity in employment and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status, or any other personal characteristic protected under applicable law. We consider qualified applicants regardless of criminal histories, consistent with legal requirements.

We're focused on attracting, retaining, developing, and advancing our employees. By cultivating a workplace that values diverse experiences, backgrounds, and ideas, we create an environment where every employee can contribute their best.

Moderna is committed to offering reasonable accommodation or adjustments to qualified job applicants with disabilities. Any applicant requiring an accommodation or adjustment in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should contact the Accommodations and Adjustments team at .

LI-DS2
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