MSAT Packaging Expert

at  Lonza

Verviers, Wallonie, Belgium -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate26 Nov, 2024Not Specified29 Aug, 2024N/APackaging,Project Planning,Closure,Biotechnology,Chemistry,English,Biology,Communication Skills,RootNoNo
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Description:

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.
For our site in Verviers, Belgium we are currently looking for a MSAT Packaging Expert (m/f/d). In this role, you will act as Subject Matter Expert in the fields of packaging, closure integrity, shipping validation, manufacturing technologies, manufacturing environment, analytical testing and product know-how. You will lead shipping validation projects, closure integrity validation projects as well as performing product quality impact assessment when introducing new primary packaging. Become part of this exciting opportunity and apply now!

Key responsibilities:

  • Lead closure and shipping validation projects
  • Execute validation tasks if needed and ensure validation documentation is clear, scientifically based and in compliance with European GMP, ISO13485 expectations, 21CFR820
  • Ensure closure and shipping processes are maintained in a validate state of control
  • Lead product impact assessment when new primary packaging is introduced

• Lead technical investigations and support experiments • Provide support to other MSAT projects.

  • Provide exhaustive planning and accurate budget evaluation for projects

Key requirements:

  • Master degree in Biotechnology, Chemistry, Biology or related field
  • Proven scientific knowledge and experience in packaging & closure integrity in pharmaceutical/biotechnology domain
  • Good understanding of cGMP and validation principles
  • Strong knowledge of Microsoft Office software’s (Excel, PowerPoint, Word)
  • Strong analytical and problem solving skills
  • Proven ability to perform investigations and use root cause analysis tools
  • Strong organizational skill and ability to build accurate project planning and budget
  • Excellent communication skills in English and French

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

Responsibilities:

  • Lead closure and shipping validation projects
  • Execute validation tasks if needed and ensure validation documentation is clear, scientifically based and in compliance with European GMP, ISO13485 expectations, 21CFR820
  • Ensure closure and shipping processes are maintained in a validate state of control
  • Lead product impact assessment when new primary packaging is introduce


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Information Technology/IT

IT Software - Other

Software Engineering

Graduate

Biology, Chemistry

Proficient

1

Verviers, Belgium