Junior Packaging Validation Engineer (GMP)
Location: NetherlandsSIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!
THE COMPANY
Our client is a professional Biotechnology and Pharmaceutical organization, based in Noord-Brabant Netherlands.
You will be working in a dynamic environment of a growing pharmaceutical company.
ROLE DESCRIPTION
As a Junior Packaging Validation Engineer you will be working in the process development department. Your main responsibilities will be designing, qualify, verify and implement secondary packaging components used for site operations and transportation packaging.
RESPONSIBILITIES
- Writing documents according to the Good Documentation Practices is a significant part of this role.
- Create technical reports such as User Requirements, Assessments, Protocols, Reports, Verification Documentation.
- Create and revise packaging component specifications if required.
- Provide accurate information for Bill of Material (BOM), Master Packaging Configuration (MPC) and Transport packaging configuration (TPC) to be used on
site.
- Coordinate or participate in multi-disciplinary projects related to packaging component changes or new packaging designs
- Develop test material; coordinate test materials and inventory as required by studies.
- Creation of Qualification and Verification Plans
- Coordinate testing to be performed for packaging related studies impacting the site.
- Assist and contribute to Site Acceptance Test (SAT) and may assist in establishing Equipment validation Documentation.
REQUIREMENTS
- Master’s degree with minimum 1 - 2 year experience working in a Package Development and/or Validation/Engineering environment
- Experience in a Pharmaceutical / GMP environment
- Good understanding of current Good Manufacturing / Documentation Practices
- Fluency in English, both in oral and written communication
- Good (technical) written and verbal communication skills
- Ability to work in multi-functional teams and adapt to rapidly changing environment
- Defines project timeframes and priorities based on project objectives and ongoing assignments
- Recognizes and escalates problems in a timely manner
- Occasionally work outside office hours
- Comprehensive understanding of materials used in packaging
- Familiarity with validation processes and protocols
- Understanding of equipment used in the packaging industry
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Rowin van der Zwaan.
