Quality Assurance Associate (M/F/D)

Posted Yesterday
Be an Early Applicant
GBR
Mid level
Biotech
The Role
The Quality Assurance Specialist will ensure product conformity, maintain traceability in the supply chain, conduct internal audits, manage supplier quality, assist with customer audits, and monitor quality performance. This role requires close collaboration with the QA team to continuously improve processes and documentation within a regulated environment.
Summary Generated by Built In

The Opportunity:

Avantor is seeking a detail-oriented Quality Assurance Associate to join our team at the Hichrom site in Theale, Reading. In this role, you will provide essential quality support to ensure product conformity and maintain full traceability within our supply chain.

Hichrom is our production site in Reading manufacturing and testing a wide range of ultra-high performance and high-performance liquid chromatography (UHPLC & HPLC) columns and accessories.

Working hours will be:

Monday – Friday from 9 AM – 5 PM (with some flexibility)

The team

Under the supervision of the Quality Manager (UK Manufacturing), the QA Associate will support the Senior QA Specialist with maintaining the Quality Management (QM) systems, evaluating their application in the laboratory, and reviewing non-conformances arising from production.

What we’re looking for

  • Language: Fluent verbal and written communication in English is essential
  • Education: Bachelor’s degree in a scientific field, such as Environmental Science, Microbiology, or Chemistry. 
  • Experience: Minimum 3 years of experience in a Quality Assurance role
  • Understanding/experience of a quality management system desirable
  • SAP knowledge is desirable, but full training will be given
  • Experience within a GMP environment and/or a cleanroom environment is desirable.
  • High levels of attention to detail essential
  • Self-motivated, demonstrating initiative and results orientated.
  • Strives for continual improvement, demonstrates innovation and organizational agility
  • Excellent communication skills, both verbal and written
  • Ability to prioritize workload and multi-task
  • Strong numerical skills with an understanding of volumetric weights/analysis
  • Positive, energetic, professional, and passionate with a “can do” attitude
  • Knowledge of the Irradiation process would be advantageous


How you will thrive and create an impact

  • Undertake Internal Audits of the Quality processes. This may include travel to other sites to support the UK Quality team as required.
  • Management of suppliers, including initial supplier approvals, sending and scoring supplier quality questionnaires, participating in supplier audits, and sending/managing supplier complaints (SCARS).
  • Assisting and participating with customer and certification audits. This includes pre- and post-audits.
  • Management of Change, including the generation and review of change requests.
  • Monitor and report performance, gather data, and produce statistical reports on quality-related KPI’s.
  • Goods-in inspection of raw materials and hardware components at the point of receipt.
  • Final Release of Goods from QC.
  • Investigation and QA Review of Complaints, Non-Conformities, Corrective and Preventive Actions (CAPA’s), and other quality documentation within the electronic Quality Management System (EtQ Reliance).
  • Ensure continuous improvements are undertaken, including the review and update of local work instructions in association with the Production Manager.
  • Administration of training system and records.
  • Assist and participate in any quality-related training.
  • Assist in any other duties as reasonably requested by the Quality Manager and Senior QA Specialist.

Are you a passionate QA Associate hungry for amazing opportunities? Don’t miss out—apply now and join our dynamic team!

#LI-Onsite

Disclaimer:

The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position. Avantor is proud to be an equal opportunity employer.

Why Avantor?

Dare to go further in your career. Join our global team of 14,000+ associates whose passion for discovery and determination to overcome challenges relentlessly advances life-changing science.
 
The work we do changes people's lives for the better. It brings new patient treatments and therapies to market, giving a cancer survivor the chance to walk his daughter down the aisle. It enables medical devices that help a little boy hear his mom's voice for the first time. Outcomes such as these create unlimited opportunities for you to contribute your talents, learn new skills and grow your career at Avantor.
 
We are committed to helping you on this journey through our diverse, equitable and inclusive culture which includes learning experiences to support your career growth and success. At Avantor, dare to go further and see how the impact of your contributions set science in motion to create a better world. Apply today!

EEO Statement:

We are an Equal Employment/Affirmative Action employer and VEVRAA Federal Contractor. We do not discriminate in hiring on the basis of sex, gender identity, sexual orientation, race, color, religious creed, national origin, physical or mental disability, protected Veteran status, or any other characteristic protected by federal, state/province, or local law.

If you need a reasonable accommodation for any part of the employment process, please contact us by email at [email protected] and let us know the nature of your request and your contact information. Requests for accommodation will be considered on a case-by-case basis. Please note that only inquiries concerning a request for reasonable accommodation will be responded to from this email address.

Privacy Policy:

We will use the personal information that you have submitted to us in order to consider your application for the relevant role.
 

Your privacy is important to us. Please click here for our Privacy Policy which explains the purposes for which we will use your personal information and the ways in which we will handle and retain your information. It also explains the rights you have in relation to your information, and how to contact us with any queries or requests.

3rd Party Non-Solicitation Policy:

By submitting candidates without having been formally assigned on and contracted for a specific job requisition by Avantor, or by failing to comply with the Avantor recruitment process, you forfeit any fee on the submitted candidates, regardless of your usual terms and conditions. Avantor works with a preferred supplier list and will take the initiative to engage with recruitment agencies based on its needs and will not be accepting any form of solicitation.

The Company
HQ: Radnor Township, PA
9,968 Employees
On-site Workplace
Year Founded: 1904

What We Do

Avantor®, a Fortune 500 company, is a leading global provider of mission-critical products and services to customers in the biopharma, healthcare, education & government, and advanced technologies & applied materials industries.

Our portfolio is used in virtually every stage of the most important research, development and production activities in the industries we serve.

Our global footprint enables us to serve more than 225,000 customer locations and gives us extensive access to research laboratories and scientists in more than 180 countries. We set science in motion to create a better world.

More than 13,500 strong, our associates are passionate about our mission to set science in motion to create a better world. We share enthusiasm for innovation, excellence, and achievement. Whether we are collaborating with our customers to advance science or solve multifaceted problems, we help them reach their goals more efficiently and effectively.

Visit our website to learn more about Avantor.


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