219 Quality Administrator jobs in the United Kingdom

The role

The Intake Audit Administrator plays a vital role in ensuring that Debenham's Group products meet defined  quality standards set by Product Technology/ Product Safety & Compliance to ensure that products held out for sale are safe, fit for purpose and legally compliant in the markets in which we retail.

This role involves supporting the intake audit team with various administrative tasks and coordination efforts and, when required, conducting inspections and audits.

Your team

Responsible Sourcing and Product Operations is reimagining how the Group works globally. We cover Sustainability, Sourcing, Ethical Trade, Product Quality and Operational Efficiency. We turn challenges into opportunities so we can be as commercially and operationally effective as possible while still being ethical and sustainable! In some companies, what we do gets split into many smaller teams. Not us. Together we align all areas and achieve our goals, constantly pushing for better.

What you'll be doing

• Maintain accurate and organised records of quality control activities, post shipment inspection reports, pre-shipment inspection reports and compliance documentation to ensure easy access and retrieval.

• Input and manage data related to quality inspections, tests, and audits in databases, assisting in the analysis of quality trends and metrics.
• Prepare regular quality control reports and metrics for management, highlighting key quality indicators, trends, and areas for improvement.
• Assist in ensuring that products adhere to industry regulations, standards and safety guidelines by reviewing documentation and supporting compliance efforts.
• Coordinate logistics and provide administrative support for quality control activities such as merchandise inspections and audits managing schedules, preparing presentations  ensuring smooth execution and timely completion.
• Identify opportunities to streamline administrative workflows and enhance efficiency within the quality control process.
• When required be prepared to conduct post shipment inspections, and targeted audits generated by returns analysis and customer complaints, of materials, components, and finished products to ensure they meet established quality standards, to verify product quality

Working with us

To succeed here, you have to love working at pace. It’s relentless, but we love it. Change is a certainty – you need to adapt and be agile. We want you to challenge the status quo, innovate and be open to trying new things. We’re always pushing boundaries. We empower our people, giving them freedom and autonomy to learn and grow in their roles. We’re passionate, agile, creative and one team.

About you

• Proven experience in an administrative role, preferably in a quality control or manufacturing environment.
• Strong organisational skills and attention to detail.
• Proficiency in data entry, database management, and basic data analysis.
• Excellent communication skills, both written and verbal.
• Ability to multitask and manage priorities in a fast-paced environment.
• Familiarity with quality control concepts and terminology
• Proficiency in using Microsoft Office Suite (Word, Excel, PowerPoint, Outlook).
• Problem-solving mindset with a proactive and collaborative approach.
• Knowledge of industry regulations and standards related to product quality and safety is a plus.

Why join us

We’ve set our sights on dominating the global e-commerce fashion market, and because we’re 13 brands (and counting), there are plenty of opportunities to grow your career. Our mission is to create a workplace where everyone is respected, their individual differences are valued, and they can be themselves at work without exception.

• You’ll get the opportunity to take part in our various share schemes
• Core hours enable you to flex your working times around your needs on an ad hoc basis
• Benefits that support your health and wellbeing
• There’s up to 40% discount off our all of our brands
• Our social calendar? Next level
• With HQs in Manchester and London and offices across the globe (some are dog friendly!), we offer a buzzing atmosphere and the Debenham's family culture wherever you work

#LI-HG1

We'll inspire and empower you to deliver your best work so you can evolve, grow and succeed – today and into tomorrow. We offer an exciting range of opportunities to develop your career within a supportive and diverse team who always strive to do the right thing for our people, clients and communities.

People are our greatest asset, and we offer a competitive package to retain and attract the best talent.

In addition to the benefits you'd expect, UK employees also receive free single medical cover and digital GP service, family-friendly benefits such as enhanced parental leave pay and free membership of employee assistance and parental programs, plus reimbursement towards relevant professional development and memberships. We also give back to our communities through our Collectively program which incorporates matched-funding, paid volunteering time and charitable donations.

Work-life balance and flexibility is a key focus area for us. We're happy to discuss hybrid, part-time and flexible working hours, patterns and locations to suit you and our business.

About the Opportunity

We are Quality Administrator to join our team to help support a large portfolio of projects. They will be responsible for supporting Quality and Handover functions ensuring Quality documentation and Lifetime Records (LTR`s) are managed in compliance with processes, policies, and procedures. They will be required to offer knowledge and skills to generate and promote best working practices. As this is an entry level role it will ideally suit someone who is looking for a career within Quality.

Roles and responsibilities:

• The role will be working closely with the Quality and Handover teams.
• Uploading of schedules and reports onto the Business Management System and administer Non conformance Reports, Performance Improvement Notices, Client Feedback and Audit Reports.
• Assist with the compilation of Lifetime Quality Records throughout the project delivery phase.
• Photocopying and working closely with the Document Controller to ensure documentation is issued on time to the client and has an auditable trail.
• Ensure that suppliers and project team understand the AWE Handover Process and are aware of AWE's handover expectations.
• Assess Handover performance of external suppliers.
• Input and manage project Quality and Handover trackers using Excel.
• Engage with suppliers regarding LTR requirements.

Qualifications:

• Positive attitude, adaptable and resilient to change.
• Have excellent organisational skills.
• Self-motivated.
• Attention to detail.
• Have a methodical approach.
• Proficient in MS Office tools.
• Confident in ability to learn computer-based data bases.
• Security Clearance or be happy to obtain Security Clearance.
• Experience using MS Office Tools is essential.

Our Culture

Our values stand on a foundation of safety, integrity, inclusion and diversity. We put people at the heart of our business, and we genuinely believe that we all succeed by supporting one another through our culture of caring. We value positive mental health and a sense of belonging for all employees.

We aim to embed inclusion and diversity in everything we do. We know that if we are inclusive, we're more connected, and if we are diverse, we're more creative. We accept people for who they are, regardless of age, disability, gender identity, gender expression, marital status, mental health, race, faith or belief, sexual orientation, socioeconomic background, and whether you're pregnant or on family leave. This is reflected in our wide range of Global Employee Networks centered on inclusion and diversity.

We are committed to offering a career within one company and recognise the exceptional talent we have in our people. As our business evolves, we want to inspire and empower you to develop your career so you too can evolve, grow and succeed – today and into tomorrow.

Work-life balance and flexibility are key focus areas. We're happy to discuss hybrid, part-time and flexible working hours, patterns and locations to suit you and our business.

We're invested in you and your success, and we value the transferable skills you can bring to a new role. We want to support you in expanding and diversifying your experience so you can develop your career and help deliver the boldest solutions in a changing world.

As a Disability Confident employer, we will interview all disabled applicants who meet the minimum criteria for a vacancy. We welcome applications from candidates who are seeking flexible working and from those who may not meet all the listed requirements for a role. If you require further support or reasonable adjustments with regards to the recruitment process (for example, you require the application form in a different format), please contact

We partner with VERCIDA to help us attract and retain diverse talent. For greater online accessibility, please visit to view and access our roles. As a Disability Confident employer, we will interview all disabled applicants who meet the minimum criteria for a vacancy. We welcome applications from candidates who are seeking flexible working and from those who may not meet all the listed requirements for a role.

If you require further support or reasonable adjustments with regards to the recruitment process (for example, you require the application form in a different format).

Amentum is proud to be an Equal Opportunity Employer. Our hiring practices provide equal opportunity for employment without regard to race, sex, sexual orientation, pregnancy (including pregnancy, childbirth, breastfeeding, or medical conditions related to pregnancy, childbirth, or breastfeeding), age, ancestry, United States military or veteran status, color, religion, creed, marital or domestic partner status, medical condition, genetic information, national origin, citizenship status, low-income status, or mental or physical disability so long as the essential functions of the job can be performed with or without reasonable accommodation, or any other protected category under federal, state, or local law. Learn more about your rights under Federal laws and supplemental language at Labor Laws Posters.

Location - Adlington Business Park, Macclesfield (SK10 4NL)

The Quality Administrator will play a pivotal role in maintaining and improving the quality management system (QMS) at Uniphar Medtech. This position will involve extensive management of quality documentation, ensuring compliance with industry standards, and supporting continuous improvement initiatives. The ideal candidate will have a keen eye for detail, strong organizational skills, and a solid understanding of quality assurance processes.

Candidates will be required to travel between different Medtech sites across the UK (Manchester and Northampton), so ideally you should have a valid driver's license and access to a car.

Specific duties and responsibilities

• Maintain and update quality management system documentation, including policies, procedures, work instructions, forms, and records.
• Create, revise, and archive quality documents ensuring they meet regulatory and organizational standards.
• Coordinate the review and approval process for quality documents, ensuring timely completion and dissemination.
• Ensure that all documentation is up to date and accurately reflects current practices and regulatory requirements.
• Prepare and organize documentation for internal and external quality audits, ensuring readiness and compliance.
• Conducts Internal audits – ISO 9001:2015 standard and internal procedures.
• Track Audit findings and follow up on action items, ensuring timely resolution and documentation of corrective actions.
• Manages document control processes, including version control, approvals and distribution.
• Document non-conformance reports (NCRs) and corrective action requests (CARs), ensuring accuracy and completeness
• Supporting the QMS Manager with external audits – Supplier, Customer and Competent authority

Qualifications & Experience

• Minimum of 1 years’ experience in a similar role
• Internal Quality auditor experience within the medical device manufacturing, distribution or other regulated environment would be advantageous 
• ISO 9001:2015 Auditors Course

Skills

• Knowledge of the Q-Pulse program is preferred but not required.
• Be well organised, with strong time management skills
• Excellent communication and listening skills
• Ability to obtain, analyse and present information
• Computer literate, including Outlook, Excel, Work and Power point
• Strong analytical and problem-solving abilities
• Ability to work independently and as part of a team.

Our core values, titled our Medtech Mindset, guides our culture and work environment:

• We Go Forward Together: We operate as a unified team, leveraging diverse specialties to make swift, collaborative decisions and embrace progress over perfection.
• We Take Our Business Seriously: We prioritise compliance and risk management to ensure the best outcomes for our patients and partners, supported by our innovative portfolio and commitment to sustainability.
• We Deliver Exceptional Results: We focus on quality, customer satisfaction, and commercial success to achieve outstanding results for our patients, customers, and business.

Uniphar Medtech is an equal opportunities employer

Uniphar Medtech comprises 10 businesses across 21 markets and is the medical device arm of the Uniphar Group.

Uniphar Medtech represents global leading medical device manufacturers across a multitude of specialities. We train, we educate, and we support our customers through dedicated clinical specialists across Sales & Technical Service, Clinical IT, Clinical Applications, Training and Education and Customer Service.

We are more than a distributor; we are a total solutions provider. Each of our businesses compete under their individual brand identity and respective specialities. Uniphar Medtech is the umbrella structure for all 10 brands and in addition incorporates our centralised support functions across Quality and Compliance, Logistics, Warehousing, Operational Excellence, Marketing, HR, Finance & IT. Business website:

Uniphar Medtech is a Division of the Uniphar Group.

Job Title: Quality Control Administrator

Location: Knighton

Pay Rate: £13.76 per hour (weekly pay)

Hours: Monday to Friday, 8:00am 4:00pm or 9:00am 5:00pm

Contract Type: Temporary 6 months (with potential for further opportunities within the company)

?

About the Role

We are seeking a highly organised and proactive Quality Control Administrator to join our team, supporting one of our prestigious clien.

ZIPC1_UKTJ

About this Role

Are you ready to dive into the fast paced world of Fleet Quality? At Dawsongroup truck and trailer, were the trusted partner to businesses across the UK, providing high quality HGV asset solutions that keep the supply chain moving. This role is all about keeping things organised and running like clockwork, ensuring that repair invoices are accurate and customer ready.

• Review and proc.

ZIPC1_UKTJ

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.

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

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 .

Join Our Dynamic Onsite Technical Team at IPL Inchture

We are thrilled to announce an exciting opportunity for a Quality Control Inspector to become a vital part of our onsite Technical Team at our Potato site in Inchture. If you are passionate about Quality and are eager to contribute to a dynamic team, this role is perfect for you

Position Details:

• Schedule: Monday - Friday, 7:30am - 4:00pm

• Location: IPL, Inchture - Site Based Role

• Contract Type: Permanent

Key Responsibilities:

• Effectively and efficiently manage the quality of stock from arrival at the site to despatch

• Make decisions on the most effective and efficient use of the product

• Provide the Senior Product Manager with accurate and timely information to communicate to the grower

• Investigate all rejections for their product

• Ensure all reports are completed, scrutinised and progressed on a daily basis

• Interaction with the Packhouse to maintain ASDA Specification and Compliance

• Complete internal audits

What are we looking for?

• Educated to GCSE Level A, B or C (or equivalent) in English and Maths

• Basic knowledge of Microsoft Office programmes such as Word and Excel

• Experience of working in a food manufacturing environment

• Basic knowledge of BRC Auditing

• Basic Food Hygiene Certificate

• Working Knowledge of the PR2 data system

• Assertive (Willing and able to challenge the norm)

• Self-disciplined, Systematic and Precise

What's in it for you?

At IPL, Forza, and Kober , we're dynamic businesses, dedicated to fostering the development of our colleagues and creating an exceptional work environment. We believe in the power of teamwork and collaboration to drive our success. To continue our growth, we're seeking individuals who embody our values, culture, and commitment.

In return, we offer opportunities for professional development, a competitive salary, and a comprehensive benefits package, including:

15% Asda In-store Discount

Paid Annual Leave Allowance – varies depending on shift pattern

Enhanced pension scheme

Life Assurance - All our colleagues benefit from life assurance of 4 x their annual base salary

- Free, direct access to health and wellbeing support service, including unlimited video consultations with a UK-based GP 24/7, physiotherapy, and mental health support

Grocery Aid - We've partnered with Grocery Aid to provide our colleagues and their families with a wide range of emotional, practical, and financial support services

Electric Vehicle Scheme*

Asda Mobile Discount - 30% off a wide range of Asda Mobile bundles and add-ons for our colleagues and one of their family members

Discounted health assessments - We have exclusively negotiated rates on Self-Pay BUPA Health Assessments for you and members of your household

Asda Pet Insurance discount – Up to 10% Discount

Mortgage Advice Bureau (MAB) - MAB can provide fee-free*, no-obligation mortgage and protection advice

Exclusive Exchange Rates via Asda Money - our colleagues can get a better exchange rate for their travel money when buying currency through Asda Travel Money (TravelEx)

Ride-to-work scheme - We work with Evans to provide our colleagues with great savings across their range of bikes, clothing, and equipment

Care Concierge - The Care Experts. Talk to us - we're listening - Legal & General's Care Concierge resource

Plus, lots more Depending on job band, other fantastic benefits are also available including private healthcare, car allowances, and long-term incentive schemes.

Like what you've read? Then do your research, update your CV, and once you're ready, hit the apply button. Don't delay, apply today

Our purpose here at IPL, Forza & Kober is simple, we are one team who creates exceptional value for our customers and our mission is to support Asda on their journey to becoming #2 in the marketplace.

Through our people we live and breathe our values and we play to our strengths, but we also support each other's development. We are a community of passionate individuals who possess a wide variety of skills and expertise, who work collectively to form a high performing team and a company to be proud of.

We are committed to a fully inclusive business that is representative of our customers, locations and the communities we serve. We recognise the value in diversity and welcome applications from all candidates regardless of sex, age, race, religion, gender or sexual identity and socio-economic background. We are committed to making IPL, Forza and Kober a place where everyone can enjoy a successful career and have systems in place to support all our colleagues. We are seeking applications from candidates who share our values, culture and celebrate diversity in all its forms.

Our culture is our people and our people are our culture