Bertelsmann Logo

Bertelsmann

Quality Officer

Posted 6 Days Ago
Be an Early Applicant
Hybrid
Midland, England
Entry level
Hybrid
Midland, England
Entry level
Supports the Quality Management System through QA administration, audit readiness, change control, deviations, CAPA, supplier management, KPI reporting, investigations, and complaint handling. Provides compliance guidance to operational teams under GDP, ISO 9001, and ISO 13485 requirements. Assists with client onboarding, validation, SAP testing, documentation reviews, temperature data management, internal audits, regulatory inspections, and maintaining accurate quality records.
The summary above was generated by AI
Company Description

Arvato is an innovative and leading global 3PL service provider in supply chain management and e-commerce. With 20,000 team members at over 100 locations, we focus on the Consumer Products, Tech, Healthcare, Automotive and Publisher industries.

You will work in an environment built on collaboration, respect, commitment and curiosity, where you can grow, contribute your ideas, and make an impact. Be part of the team that delivers logistics excellence and shapes supply chains globally. Working at Arvato means: Together, we’re on it.

Job Description

Salary: Up to £42,000.00 depending upon experience.

Location: East Midlands Gateway with Travel to Kings Norton in Birmingham

Hours: 40 hours per week, Monday to Friday 8.30-17.00 (flex on start/ finish available)

You’ll assist the Quality department in supporting the Quality Management System (QMS) by providing efficiencies in administration and promoting continual compliance to regulatory and client requirements with the internal departments, and suppliers.

 Your Tasks

  • Provide QA support to internal departments to ensure activities are undertaken in compliance with GDP and Arvato procedures,
  • Provide quality assurance support/ advice to operational departments in support of compliance to process.
  • Initiate and maintain change control, deviation and Corrective and Preventative Action (CAPA) records ensuring effectiveness of activities proposed.
  • Provide administrative support to QA scheduling of suppliers, internal audits, and annual reviews
  • Collate data to be used in reports, investigations, key performance indicators (KPIs), and other quality metrics.
  • Participate in the self-inspection audit programme when required by supporting the QA management team.
  • Support Client audits and regulatory inspections by prepping documents and ensuring audit readiness by scheduling internal team prep.
  • Support the Supplier Management process, including verifications, audit actions, and surveys.
  • Aid as necessary, the Quality Management System in line with GDP, ISO 9001, and 13485.
  • Liaise with internal and external stakeholders relating to QMS activities or non-compliance actions linked to co-ordinator tasks and build relationships and trust.
  • Support client onboarding ensuring compliance with QMS activities including validation, SAP testing, and process walk-throughs.
  • Support the ongoing compliance with the Arvato Global Quality system, and report KPIs into the Global QA team.
  • Support product quality, process safety and complaint investigations.
  • Complete QA review on inbound packs, return documentation, and temperature data management, ensuring documentation is completed to ALCOA principles and archived according to client requirements.

 

Qualifications

The ideal candidate will be organised, methodical, and can prioritise a busy workload and be able to liaise with stakeholders and customers of all levels.

  • We are also looking for experience in:
  • Quality administration; managing a busy mailbox, control of documents, scheduling, annual supplier/client audits, and information
  • supporting QMS activities; Investigations, complaint management, gathering change control evidence, audit readiness, compiling KPIs, track completion to SLA
  • and/or knowledge of Good Distribution Practice (GDP), ISO 9001, and ISO 13485 and systems such as SAP, electronic QMS, and temperature monitoring portals
  • and competent with Office applications (Word, Excel, Visio, Projects etc)
  •  Previous quality assurance experience in Healthcare, medical devices/pharmaceuticals would be an advantage, but not essential.

Additional Information

• 25 days annual leave plus 8 bank holidays with the option to purchase up to an additional 5 days

• Pension contribution

• A life assurance policy that pays out 4 x Salary

• Employee Assistance Programme that provides you with confidential support, information, and advice to help you

• Employee Discount Scheme through Benefit Hub

• Free Parking

 

 

Disclosure requirements pertaining to the collection of your personal data:

Responsible for processing the information provided in your application is the company specified in the job advertisement, with its registered office as indicated. The company processes your data for the purpose of establishing an employment relationship on the basis of Art. 6 (1) b GDPR / Section 26 (1) sentence 1 BDSG.

The retention period for your data is determined by the statutory time limits applicable in the respective country, beginning upon completion of the recruitment process. You can find these here.

You can contact the company’s Data Protection Officer at the above-mentioned postal address. 

Further information on data protection and your rights can be found here.
 

Recruiting-Platform powered by SmartRecruiters.

Similar Jobs

3 Days Ago
In-Office
Entry level
Entry level
Healthtech • Professional Services • Biotech • Pharmaceutical
Support the site Quality Management System across GMP, GLP, and GCP environments. Responsibilities include conducting internal audits, reviewing and approving quality documents and agreements, supporting supplier qualification and Veeva eQMS activities, managing quality events, assisting with customer audits and regulatory inspections, tracking corrective actions, and delivering GxP training.
Top Skills: GCPGlpGmpGxpVeeva Eqms
20 Days Ago
In-Office
London, Greater London, England, GBR
Senior level
Senior level
Biotech
Conducts independent GCP audits of clinical investigator sites and vendors across the UK and EU, authors audit documentation, develops CAPA plans, resolves findings, monitors compliance, and supports Quality and Compliance activities. Requires expertise in GCP, CRO operations, clinical trials, pharmaceutical development, FDA regulations, 21 CFR Part 11, and GxP requirements. The role is home-based in the UK with travel of up to 30%.
Top Skills: 21 Cfr Part 11Fda RegulationsGood Clinical Practice (Gcp)GxpMS Office
3 Days Ago
In-Office
Entry level
Entry level
Edtech • Social Impact
Conduct internal audits, quality reviews and compliance checks across operational and corporate functions. Analyse service performance, feedback and quality data to identify risks and improvement opportunities. Produce audit reports, action plans and management information, support risk mitigation, maintain quality records, and promote continuous improvement through guidance, training and stakeholder collaboration.
Top Skills: Data Analysis ToolsMS OfficeQuality Management Systems

What you need to know about the London Tech Scene

London isn't just a hub for established businesses; it's also a nursery for innovation. Boasting one of the most recognized fintech ecosystems in Europe, attracting billions in investments each year, London's success has made it a go-to destination for startups looking to make their mark. Top U.K. companies like Hoptin, Moneybox and Marshmallow have already made the city their base — yet fintech is just the beginning. From healthtech to renewable energy to cybersecurity and beyond, the city's startups are breaking new ground across a range of industries.

Sign up now Access later

Create Free Account

Please log in or sign up to report this job.

Create Free Account