Job opening - Lifecycle Management specialist Consultant in Zaventem | Randstad

summary

zaventem, vlaams-brabant
permanent
full-time

job category
sales

job details

Lifecycle Management Specialist Consultant

Are you a detail-oriented professional with a passion for pharmaceutical excellence? Join the J&J Innovative Medicine MSAT Large Molecule Drug Product team and play a pivotal role in ensuring the quality and compliance of primary packaging materials. This is your chance to manage critical lifecycles w ...

ithin a world-class manufacturing environment, driving innovation and stability in primary container systems.

The Role

As a Lifecycle Management Specialist, you will act as a key technical anchor for the Primary Container team. Your primary mission is to oversee and execute Change Controls triggered by supplier notifications, ensuring that every material in the portfolio meets the highest quality standards. You will bridge the gap between technical specifications and operational excellence, ensuring seamless processability for our drug products.

Should you have any questions about this position, please feel free to get in touch with Peggy Vancoillie. She can be reached at +32 2 472 92 14 or peggy.vancoillie@randstad.be. We look forward to hearing from you.

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Lifecycle Management Specialist Consultant

Are you a detail-oriented professional with a passion for pharmaceutical excellence? Join the J&J Innovative Medicine MSAT Large Molecule Drug Product team and play a pivotal role in ensuring the quality and compliance of primary packaging materials. This is your chance to manage critical lifecycles within a world-class manufacturing environment, driving innovation and stability in primary container systems.

The Role

As a Lifecycle Management Specialist, you will act as a key technical anchor for the Primary Container team. Your primary mission is to oversee and execute Change Controls triggered by supplier notifications, ensuring that every material in the portfolio meets the highest quality standards. You will bridge the gap between technical specifications and operational excellence, ensuring seamless processability for our drug products.

Should you have any questions about this position, please feel free to get in touch with Peggy Vancoillie. She can be reached at +32 2 472 92 14 or peggy.vancoillie@randstad.be. We look forward to hearing from you.

key responsibilities
- Change Control Leadership: Lead and manage all change controls associated with supplier notifications for primary packaging materials, including the preparation of all required deliverables.
- Technical Specification Review: Critically evaluate supplier specifications to ensure total alignment with own quality standards.
- Reporting & Analysis: Author comprehensive comparability reports to assess the processability of primary packaging materials.
- Activity Coordination: Oversee all functional and technical testing activities related to Change Control processes.
skills
- Productengineering
- Product Planning
- Product Management
- Productinformatie Management
- Product Lifecycle Management
- Product Lifecycle
- Product Strategieën
- Lifecycle Management
- Productadvies
qualifications
- Experience: Generally requires 4–6 years of relevant work experience.
- Background: Proven experience in Pharmaceutical operations or manufacturing environments.
- Subject Matter Expertise: Deep knowledge of primary packaging materials and parenteral production processes.
- Soft Skills: Strong analytical and project management skills with a meticulous eye for detail.
- Communication: Fluent in English.
- Technical Proficiency: Skilled in SAP, Comet software, Minitab, Excel, and PowerPoint.
education
- Bachelors or equivalent

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