Quality Assurance Associate

Há 5 dias


Lisboa, Lisboa, Portugal Hovione Tempo inteiro

About Hovione

Hovione is an independent, family-owned international group of companies. Our innovative technological and productive capabilities have positioned us as a leading Contract Development and Manufacturing Company dedicated to helping pharmaceutical customers bring new and off-patent drugs to market.

We pride ourselves on our diverse team of over 1,950 members from 36 different nationalities located across Asia, Europe, and North America. Our global presence includes four production sites.

We are committed to excellence in everything we do, striving to innovate and improve continuously for our clients, partners, and most importantly, patients. This mindset is reflected in our company motto, 'In it for life.'

Job Description

We are seeking a Quality Assurance Associate with a strong background in the pharmaceutical industry to join our team. As a key member of our quality assurance department, you will be responsible for ensuring compliance with current Good Manufacturing Practices (cGMP) and maintaining the highest standards of quality throughout the product lifecycle.

Main Responsibilities

  • Guarantee cGMP compliance in all activities and systems related to project execution.
  • Implement policies, procedures, and methods to evaluate and continuously improve the quality of products and operations.
  • Provide global supplier qualification services in support of new product introduction and existing products.
  • Collaborate with suppliers and procurement to ensure the quality of their products, materials, components, and/or operations.
  • Rigorously manage all quality activities for assigned projects and/or products in accordance with applicable regulations.

Requirements

To succeed in this role, you should possess:

  • A university or equivalent qualification in chemistry, chemical engineering, pharmaceutical sciences, or a similar scientific field.
  • Experience working in a QA GMP environment within the pharmaceutical industry is desirable.
  • Knowledge of GMP practices and regulatory affairs is essential.
  • Fluency in English and proficiency in MS Office are required.
  • Excellent documentation skills and attention to detail are necessary.

Salary and Benefits

The estimated salary range for this position is $70,000-$90,000 per annum, depending on experience. We offer a comprehensive benefits package, including health insurance, retirement savings, and paid time off.

Culture and Values

We value diversity and inclusion at Hovione. We strive to create a work environment where everyone feels supported, respected, and has the opportunity to achieve their full potential.



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