Vor 8 Tagen veröffentlicht

Internship Documentation Control 80-100% (m/f/d)

Internship Documentation Control 80-100% (m/f/d)

Internship Documentation Control 80-100% (m/f/d)

Internship Documentation Control 80-100% (m/f/d)

Lonza AG

Pharma, Medizintechnik

Visp

  • Art der Anstellung: Studierende
  • Vor Ort

Internship Documentation Control 80-100% (m/f/d)

Über diesen Job

Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.

We have built this position for the CQV Biologics team. To support our qualification and re-qualification work in all areas of Biologics. A good level of training in GMP, cGMP, GDP and H&S as well as a general overview of pharmaceutical drug manufacturing can be provided here.

Be part of this great opportunity and join our team by applying for this internship role.

Duration: 6-12 months.

Key responsibilities:

  • General office duties including Document / Binder organizer with Project
  • Coordinate with relevant departments to chase signatures for review and approval sign-offs
  • Assisting with PQ (Performance Qualification) material from Black storage area to clean areas (Precise clean down is required for all material, training to be provided), Ross Shell storage and availability for new project - 92 Max load studies TCU
  • Scan completed PQ documents and attachments into the Document Management System (DMS) for workflow approval
  • Assisting with preparation of documents for availability to Vendors and collaborating closely with vendor for document completion and GDocP corrections.

Key requirements:

  • Bachelor’s degree in Biotechnology, Chemistry, Engineering, or a related field, or equivalent experience will be considered
  • Proficiency in Word and Excel, with strong computer, printer, and scanner skills
  • Experience in Good Manufacturing Practices (GMP) is a plus
  • Ability to work independently after training, with excellent communication skills
  • Awareness of Health and Safety protocols or equivalent experience
  • Demonstrated passion and eagerness to learn
  • Excellent personal presentation and time management skills
  • Fluency in English is required; German proficiency is a bonus

Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.

People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.

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Unternehmens-Details

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Lonza AG

Pharma, Medizintechnik

Schweiz

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