37 Quality Director jobs in London

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 ( .
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Quality Control Assistant

Are you an established Quality or Technical Auditor seeking your next step up in your career?

Worked within a similar role in a fast paced manufacturing environment?

Want to join a company that is on an upwards journey of growth?

Major Recruitment are seeking a Quality Control Assistant to join our client’s manufacturing site near Brent, London

As a Quality Control Assistant you will support the technical and process function to launch safe, legal and high-quality product.  Working closely with the Technical and Process Function managing and keeping up to date technical paperwork.

Key Responsibilities Quality Control Assistant:

• Draw up and maintain product factory paperwork (including recipes, calculation of batching).
• Coordinated internal approval of all factory paperwork (including technical and process sign off).
• Responsible to maintain factory trackers (e.g. debrining, ph/salt).
• Surveillance routine testing: support the management of the routine testing schedule (covering microbiological and nutritional testing, etc), updating internal trackers.
• Manage internal training of new processes and quality system paperwork for Factory Personnel for any new products.
• Responsible to maintain the following folders up to date: artworks folders, factory floor paperwork folders.
• Responsible to create spiderweb graph for any new olives.
• Responsible to keep up to date Demarco database.
• QUOR system SME deputy.

• Assist with Customer visits.

What’s in for you?

• Salary up to £32,000 per annum
• Monday - Friday
• Pension Fund 
• Career progression

Skills required to be a Quality Control Assistant.

• Experience working in a food manufacturing environment (preferrable).
• Excellent computer skills (Microsoft Office).
• Excellent attention to detail and organisation skills.
• Confident communicator with the ability to work across departments.
• Excellent level of literacy.
• Passionate about delivery high-quality products.
• A proactive, can-do attitude.

Qualifications

• HACCP Level 2 Training & Auditing would be desirable

If you are interested, please click apply now and one of our recruitment specialists will be in touch.

Major Recruitment are an employment agency working on behalf of our client. Should you be seeking a new permanent position, temporary assignment, or contract you will find our staff professional and courteous and our interview process straight forward.

INDSS

**Do you want your voice heard and your actions to count?**
Discover your opportunity with Mitsubishi UFJ Financial Group (MUFG), one of the world's leading financial groups. Across the globe, we're 120,000 colleagues, striving to make a difference for every client, organization, and community we serve. We stand for our values, building long-term relationships, serving society, and fostering shared and sustainable growth for a better world.
With a vision to be the world's most trusted financial group, it's part of our culture to put people first, listen to new and diverse ideas and collaborate toward greater innovation, speed and agility. This means investing in talent, technologies, and tools that empower you to own your career.
Join MUFG, where being inspired is expected and making a meaningful impact is rewarded.
Mitsubishi UFJ Financial Group, Inc. (MUFG) is one of the world's leading financial groups. Headquartered in Tokyo and with over 360 years of history, MUFG has a global network with around 3,000 offices in more than 50 markets. The Group has over 180,000 employees, and offers services including commercial banking, trust banking, securities, credit cards, consumer finance, asset management, and leasing.
As one of the top financial groups globally with a vision to be the world's most trusted, we want to attract, nurture and retain the most talented individuals in the market. The size and range of MUFG's global business creates opportunities for our employees to stretch themselves and reap the rewards, whilst our common values, to behave with integrity and responsibility, and to build a culture which is fair, transparent, and honest, underpin everything that we do. We aim to be the financial partner of choice for our clients, whatever their requirements, building long-term relationships, serving society, and fostering shared and sustainable growth for a better world.
Please visit our website for more information - mufgemea.com.
The Client On-Boarding team is part of the Client Management Services, which is situated within the Corporate and Investment Banking Division of MUFG Bank. However, this function acts as a centralized 1st line support team, providing support to Investment Banking and Corporate Banking in EMEA, Capital Markets and MUFG Securities both in London and in Amsterdam.
**MAIN PURPOSE OF THE ROLE**
This individual will be responsible for conducting Quality Control (QC) assessments across new on-boarding, Periodic Reviews and Event Driven Reviews - including KYC and Regulatory Classifications. The Client On-Boarding Team covers a highly varied portfolio of Circa. 6,000 entities - ranging from simple listed customers, to much more complex structures, entities and product offerings, as such it will be key for this individual to fully understand all customers and to assist the lead to design effective Quality Control program - identifying and escalating risks appropriately.
This function is critical during both on-boarding and other reviews to ensure that the KYC process effectively mitigates the risks of Money Laundering, Bribery and Corruption, reputational and any other associate risks. With this in mind, the successful individual needs to have good experience within KYC, and a demonstrable strong knowledge of the AML/KYC environment.
Key stakeholders in this role are; Operational KYC counterparts, QA Counterparts, Financial Crime (2nd line of Defence), Front Office RM/Trader/Account Officers and Audit. Working closely with stakeholders to both standardize and clarify requirements and proactively identify future issues with procedures/process. Driving forward and influencing change is therefore essential in this role.
This function will also assist the lead in the development and roll out of a suite of training (related to requirements / roles and responsibilities) for new and existing individuals within the team and for those within the various front office functions, where required. Working closely with individuals to improve the understanding of both the process and the underlying rationale for requirements.
**KEY RESPONSIBILITIES**
In this role, you will be responsible for KYC across MUFG's banking arm and securities business under a dual-hat arrangement. Under this arrangement, you will act and make decisions on behalf of both the bank and the securities business, subject to the same remit and level of authority and irrespective of the entity which employs you.
+ Ensure that thorough and effective Customer Due Diligence is completed, by conducting Quality Control Assessments on entities/structures across all business lines (predominantly the complex structure/entities/product offerings) - including New Business, Periodic Reviews and Event Driven Reviews. Raising issues and ensuring appropriate actions are undertaken before KYC approval.
+ Identifying thematic issues within the On-Boarding process, highlighting to management and recommending appropriate actions.
+ Liaising with Quality Assurance on any issues identified within the QA process, to consider impact and where needed make relevant changes to the QC process. In addition, where remedial action is required - liaising and notifying the operational leads accordingly.
+ Liaising with Financial Crime KYC team on any issues identified within the 2nd line checks / testing, to consider impact and where needed make relevant changes to the QC process. In addition, where remedial action is required - liaising and notifying the operational leads accordingly.
+ Supporting the lead to understand, challenge and implement any changes to procedures.
+ Assist in the development of a suite of Training for New & Existing Team members on all KYC/On-Boarding procedural related aspects.
+ Deliver training, where required, to front office representatives on KYC/On-Boarding procedural related aspects.
+ Deliver and support lean processes, to deliver effective and efficient KYC process.
+ Training and Development of more junior members of the team
+ Act as a Subject Matter Expert in relation to all AML On-Boarding aspects, assisting on ad-hoc queries where required.
+ Support the QC Lead, producing relevant reports to key counterparties, identifying and resolving Anti Money Laundering issues, and providing support/guidance to more junior members of the team.
+ Keep abreast of developments in current trends and progress on money laundering, bribery and corruption and it prevention.
**WORK EXPERIENCE**
Essential:
+ At least 3 years' experience in Anti Money Laundering, fraud and bribery or Financial Crime roles (ESSENTIAL)
+ Experience with Investment Banking & the On-Boarding of Corporate entities (Inc. Private Companies and SPVs) (ESSENTIAL)
+ Experience of managing a KYC team or function. (BENEFICIAL)
**SKILLS AND EXPERIENCE**
**Functional / Technical Competencies:**
+ Awareness of UK & European Anti-Money Laundering regulations (ESSENTIAL)
+ Knowledge of various corporate structures (ESSENTIAL)
+ Able to communicate effectively to key stakeholders at all levels. (ESSENTIAL)
+ Attention to detail is essential (ESSENTIAL)
+ Ability to effectively utilize Microsoft Office (particularly word & excel). (ESSENTIAL)
**Education / Qualifications:**
+ Degree Level or relevant industry experience (ESSENTIAL)
+ Relevant qualifications in Anti Money Laundering, fraud and bribery or Financial Crime roles. (BENEFICIAL)
**PERSONAL REQUIREMENTS**
+ Excellent communication skills
+ Results driven, with a strong sense of accountability
+ A proactive, motivated approach.
+ The ability to operate with urgency and prioritise work accordingly
+ Strong decision making skills, the ability to demonstrate sound judgement
+ A structured and logical approach to work
+ Strong problem solving skills
+ A creative and innovative approach to work
+ Excellent interpersonal skills
+ The ability to manage large workloads and tight deadlines
+ Excellent attention to detail and accuracy
+ A calm approach, with the ability to perform well in a pressurised environment
+ Strong numerical skills
+ Excellent Microsoft Office skills
+ A confident approach, with the ability to provide clear direction to more junior members of the team
+ A strategic approach, with the ability to lead and motivate more junior members of the team
We are open to considering flexible working requests in line with organisational requirements.
MUFG is committed to embracing diversity and building an inclusive culture where all employees are valued, respected and their opinions count. We support the principles of equality, diversity and inclusion in recruitment and employment, and oppose all forms of discrimination on the grounds of age, sex, gender, sexual orientation, disability, pregnancy and maternity, race, gender reassignment, religion or belief and marriage or civil partnership.
We make our recruitment decisions in a non-discriminatory manner in accordance with our commitment to identifying the right skills for the right role and our obligations under the law.
At MUFG, our colleagues are our greatest assets. Our Culture Principles provide a roadmap for how each of our colleagues must think and act to become more client-obsessed, inclusive and innovative. They reflect who we are, who we want to be and what we expect from one another. We are excited to see you take the next step in exploring a career with us and encourage you to spend more time reviewing them!
**Our Culture Principles**
+ Client Centric
+ People Focused
+ Listen Up. Speak Up.
+ Innovate & Simplify
+ Own & Execute

Our client, a leading manufacturer renowned for its commitment to excellence, is seeking a highly skilled Senior Quality Control Engineer to enhance their production processes. This role, based in **London, England, UK**, offers the flexibility of being fully remote, allowing you to apply your expertise from anywhere within the UK. You will be instrumental in developing, implementing, and overseeing rigorous quality control systems and procedures across all manufacturing stages. Your primary objective will be to ensure that all products meet stringent quality standards, customer specifications, and regulatory requirements, thereby safeguarding the company's reputation for superior product quality.

Key responsibilities include:

• Developing and implementing comprehensive quality management systems (QMS) and standard operating procedures (SOPs).
• Designing and conducting quality control tests, inspections, and process audits.
• Analysing quality data, identifying trends, and implementing corrective and preventive actions (CAPA).
• Collaborating with production, engineering, and R&D teams to resolve quality issues and improve product reliability.
• Ensuring compliance with relevant industry standards and regulatory requirements (e.g., ISO 9001).
• Leading and mentoring junior quality control personnel.
• Developing and delivering quality training programs for manufacturing staff.
• Managing the supplier quality assurance process, including supplier audits and performance monitoring.
• Staying abreast of new quality control technologies and methodologies.
• Preparing detailed quality reports for management review.

The ideal candidate will possess a Bachelor's degree in Engineering, Manufacturing Technology, or a related field, with a minimum of 6 years of experience in quality control or quality assurance within a manufacturing environment. A strong understanding of statistical process control (SPC), Six Sigma methodologies, and quality management systems (QMS) is essential. Experience with various testing and measurement equipment is required. Excellent analytical, problem-solving, and communication skills are paramount. The ability to work independently, manage multiple projects, and effectively collaborate with cross-functional teams in a remote setting is crucial. This is an exceptional opportunity to drive quality excellence and contribute significantly to the success of a prestigious manufacturing firm from a remote location.

Our client, a leading pharmaceutical company, is seeking a meticulous and driven Pharmaceutical Quality Control Analyst to join their dedicated team. This role is critical to ensuring the highest standards of quality and compliance in the manufacturing of pharmaceutical products. You will be responsible for performing a wide range of laboratory tests and analyses on raw materials, in-process samples, and finished products. This includes operating and maintaining analytical instruments, documenting test results accurately, and ensuring all activities comply with Good Manufacturing Practices (GMP) and regulatory guidelines.

The ideal candidate will hold a degree in Pharmacy, Chemistry, Biology, or a related scientific field, coupled with proven experience in a pharmaceutical QC laboratory setting. Strong knowledge of analytical techniques such as HPLC, GC, UV-Vis spectroscopy, and dissolution testing is essential. You must possess excellent attention to detail, strong problem-solving skills, and the ability to work independently as well as collaboratively within a team. This role requires adherence to strict protocols and meticulous record-keeping.

Key responsibilities include developing and validating analytical methods, investigating out-of-specification (OOS) results, and contributing to the continuous improvement of quality control processes. You will also be involved in preparing QC reports, participating in internal and external audits, and staying up-to-date with evolving regulatory requirements. This is a hands-on laboratory position based in London, England, UK , where you will play a vital role in safeguarding product quality and patient safety. Your contributions will be instrumental in maintaining our client's reputation for excellence in the pharmaceutical industry.

**Quality Control Editor with German**
**Location** - London (22 Bishopsgate, City of London, London EC2N 4A)
**Work Model** - Hybrid.
We are seeking in the Quality Control Editor with 1-3 years' experience in the Maps POI editing. The ideal candidate will possess expertise in QA/QC and technological knowhow of online Maps.
**Job Expectations:**
- Basic understanding end user operational and online maps and their uses for navigation, information and other nuances
- L2 Editor will be working on multiple short to long term pilots within online maps space and should be able to adapt to new projects, workspaces and technical specifications
- Comfortable dealing with rapidly evolving work environment
- Strict adherence to policies with understanding of work productivity and efficiency
- Willing to work in a shift-based hybrid work schedule
**Skills Required:**
- Graduate/Postgraduate in any discipline
- POI editing experience 1-3 years
- QC experience 1-3 years
- Work closely with leads/SMEs/editors to communicate quality metrics
- Strong analytical skills and attention to details
- Ability to identify errors/defects and qualitatively analyze and validate all attributes of L1 tickets sampled size and ensure that editors have adhered to defined specifications and policies.
- Ensure accuracy of all curated info pertaining to the POIs by referencing various data sources like websites, imagery etc.
- Good written and verbal communication skills
- Gather data through web search
- Comfortable being held to metrics to measure performance
- Meet with peers and trainers for ad-hoc sessions policy related
- Knowledge of working on MS Excel / Quip Spreadsheets would be a plus
- Fluency in German language is required
#LI-AD1
Cognizant is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law.

Our client, a prominent pharmaceutical company located in the heart of London, England, UK , is seeking a meticulous and experienced Senior Pharmaceutical Quality Control Analyst to uphold the highest standards of product quality and safety. This role is integral to ensuring that all manufactured pharmaceutical products meet stringent regulatory requirements and internal specifications before they reach the market. The successful candidate will be responsible for performing a wide range of analytical tests on raw materials, in-process samples, and finished products using sophisticated laboratory equipment.

Key duties involve operating and maintaining analytical instruments such as HPLC, GC, UV-Vis spectrophotometers, and dissolution apparatus. You will meticulously document all experimental procedures, results, and observations in accordance with Good Laboratory Practice (GLP) and Good Manufacturing Practice (GMP) guidelines. The Senior Pharmaceutical Quality Control Analyst will also be involved in method validation, troubleshooting analytical issues, and contributing to the continuous improvement of laboratory processes. This role requires a deep understanding of pharmacopoeial standards (e.g., USP, EP, BP) and regulatory guidelines from bodies such as the MHRA and FDA. You will collaborate closely with research and development, production, and regulatory affairs teams to resolve quality-related issues and support product lifecycle management. The ability to interpret complex data, generate comprehensive reports, and communicate findings clearly and concisely is paramount. This position offers an excellent opportunity to advance your career within a highly respected organisation known for its commitment to innovation and quality in the pharmaceutical industry. A strong emphasis is placed on accuracy, attention to detail, and a rigorous approach to scientific investigation.

Qualifications:

• BSc or MSc in Chemistry, Pharmaceutical Science, Biochemistry, or a related scientific discipline.
• Minimum of 4 years of hands-on experience in pharmaceutical quality control or a similar analytical laboratory environment.
• Proficiency in analytical techniques such as HPLC, GC, FT-IR, UV-Vis, and dissolution testing.
• In-depth knowledge of GLP, GMP, and relevant pharmacopoeial standards (USP, EP, BP).
• Experience with method validation and troubleshooting analytical instruments.
• Strong data analysis and report writing skills.
• Excellent attention to detail and a commitment to accuracy.
• Ability to work effectively both independently and as part of a laboratory team.
• Familiarity with regulatory submission processes is a plus.
• Good understanding of aseptic techniques and environmental monitoring.

This role requires a proactive and diligent individual dedicated to ensuring the highest quality of pharmaceutical products.

Junior Quality Control Admin Assistant
Location: Basildon, Essex
Reports To: Quality Control Manager
Hours: Monday Friday, 09:00 17: hours per week)
Salary: £23,015 per annum

Our Mission

We are recruiting on behalf of a well-established UK-based importer and distributor of everyday value products. With over 50 years of trading history, the company is committed to sourcing and supplying products that meet market demands in terms of price and quality, while delivering them with speed, efficiency, and accuracy.

About the Role

RGH-Global is seeking a Junior Quality Control Admin Assistant to support a busy Quality Control department. The successful candidate will be detail-oriented, organised, and motivated, with strong communication and IT skills. This is a fantastic opportunity for someone looking to grow within a supportive team environment.

Understanding the Quality Control Department

The Quality Control department plays a vital role in ensuring product and process integrity. It focuses on five key areas:

• Identification of risks
• Prevention through controls
• Monitoring and Detection of issues
• Resolution of compliance matters
• Advisory support to the business

Key Responsibilities

• Updating Excel spreadsheets
• Maintaining records in the TIMS system
• Digital scanning of documents
• Accurate data inputting
• Communicating effectively with team members
• Supporting a collaborative team environment
• Demonstrating strong attention to detail

A leading manufacturing firm based in **London, England, UK** is seeking an experienced Senior Quality Control Inspector with a specialization in aerospace components. This critical role ensures that all manufactured products meet the highest standards of quality, precision, and safety, adhering strictly to aerospace industry regulations and specifications. The Senior Quality Control Inspector will be responsible for conducting detailed inspections of raw materials, in-process components, and finished products using a variety of precision measuring instruments and testing equipment. This includes visual inspections, dimensional checks, and functional testing. You will meticulously document inspection results, identify non-conforming products, initiate corrective actions, and collaborate with production teams to resolve quality issues promptly. A thorough understanding of quality management systems (e.g., AS9100), blueprints, and technical specifications is essential. The ideal candidate will have a keen eye for detail, a strong understanding of manufacturing processes, and excellent problem-solving skills. You will also be involved in process audits and continuous improvement initiatives to enhance overall product quality. This role requires excellent communication and interpersonal skills to liaise effectively with production staff, engineers, and management. A minimum of 5 years of experience in quality control within the aerospace manufacturing sector, with a proven ability to interpret complex technical drawings and standards, is required. Relevant certifications (e.g., CQI) are advantageous. This is an outstanding opportunity for a dedicated quality professional to join a reputable company and play a vital role in maintaining the integrity and excellence of aerospace components produced in London.