QbD Group

Quality Management Specialist

QbD Group  •  Rubí, ES (Onsite)  •  2 months ago
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Job Description

QbD Group's team offers knowledge & tailored (software) solutions in development, clinical, regulatory & compliance, production and distribution for companies active in Pharma, ATMP and Medical Devices/IVD. We are looking for our next QbD’er in Quality management

What do we expect from you as a Quality Management Specialist?

  • You keep your knowledge within your expertise up to date with the latest guidelines, methodologies, and trends.
  • You provide advice and support on Quality Management Systems, corrective/preventive actions (CAPA), change control, processes, and complaints.
  • QA batch record review, support materials release and support batch release process.
  • Collaborate with internal and external stakeholders to improve quality.
  • You will work within a QA team in an innovative environment

Who are we looking for?

  • You have a scientific Bachelor or Master’s degree in pharmacy, bioengineering, biomedical sciences, or applied sciences.
  • You have a minimum of 3 years’ experience in QA in a GMP environment, preferably in a commercial GMP manufacturing setting.
  • A keen eye for detail and product quality is your main concern. You think and act in a structured way, are flexible and stress resistant.

A true QbD’er can be recognized by the following qualities:

  • Resilient Your strong and positive attitude helps you overcome any challenge
  • Hungry for knowledge: You are always open to learning
  • No non-sense mentality: you can be straightforward in a respectful way
  • Innovative You are constantly looking for new and better solutions
  • (Not too) serious your job is serious, but you don’t take yourself too serious.

What’s in it for you?

  • QbD Group offers you an attractive and competitive salary package, that will be tailored to individual needs, considering legal requirements and local laws and regulations.
  • Join us to build a sustainable career, where job security is ensured, and lasting, meaningful connections are formed.
  • As we’re a knowledge-based company, you’re guaranteed to embark on a continuous journey of learning and development.
  • Be part of our global success story. As an award-winning company we value everyone’s contribution and celebrate achievements together

Our promise to you:

  • As an ambitious and pioneering company, we want to offer you the best possible environment to thrive within the life sciences.
  • Moreover, we aim to create a joyful community where you dare to be and can be yourself. Because the best way to grow is by growing together as unique individuals.
  • In short … We stand for? JPEG Joy in Partnership, going for the Extra mile to Get things done!

Interested? Send us your CV and motivation letter and who knows, we might welcome you soon in our QbD family!

QbD Group

About QbD Group

The QbD Group supports life science companies worldwide throughout the entire product lifecycle – from idea to patient. We are a global company with over 700 high-qualified employees.

Our experienced team serves the wider life science industry, with a strong focus on ATMPs, medical devices, IVDs, and digital health, thanks to the specific expertise we have built in these areas. The services we offer fall under the following divisions:

• Regulatory Affairs: We help our clients in their journey throughout the entire drug and medical device regulatory lifecycle.

• Clinical: We are an expert clinical solutions provider specialized in medical devices and biotech, offering global CRO services and consultancy.

• Qualification and Validation: We guarantee that products meet quality demands and comply with regulation through the qualification and validation of your processes, equipment, and software.

• Quality Assurance: We offer the full range of QA services necessary to get your product to market in a safe and compliant way, including auditing from certified auditors, setting up your QMS, and all QP (Qualified Person) activities.

• Quality Control: Our QC division consists of a GMP laboratory that offers analytical services for testing pharmaceutical raw materials, excipients, and release testing of finished products.

• Software solutions: Cloud-based and pre-validated Quality Management Software built for the life sciences, as well as eIFU services which enable IVD and MD manufacturers to digitalize paper Instructions For Use (IFU).

• Go to market: We help you launch your product to market by providing marketing and communication services, business development support and sales strategy.

Industry
Consulting & Advisory
Company Size
501-1,000 employees
Headquarters
Antwerp, BE
Year Founded
Unknown
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