Process Packaging Specialist

TailorMinds

Noord-Brabant

On-site

EUR 45,000 - 65,000

Full time

14 days+

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Job summary

A leading Project Management firm is seeking an Associate to work in Boxmeer, North Brabant. This full-time role involves acquiring technological knowledge, managing various studies, and writing protocols in a highly regulated pharmaceutical environment. The ideal candidate will hold a relevant degree and possess project management skills along with technical expertise in packaging. This position offers an opportunity to contribute significantly to innovative projects within the industry.

Qualifications

  • Experience with CQV (writing protocols and execution).
  • Technical expertise in packaging materials (blistering, case packing, palletising).

Responsibilities

  • Acquiring and retaining technological knowledge related to products and processes.
  • Coordinating, executing and reporting on studies for investigations and analyses.
  • Writing validation and engineering protocols and reports.
  • Setting up and maintaining quality management systems (QMS) and change control.

Skills

Project management skills
Technical expertise in packaging equipment
Experience with technology transfer
Experience in a pharmaceutical environment

Education

MSc or BSc degree in a relevant area

Tools

SAP

Job description

Overview

Our client is a leading Project Management and Engineering company serving the pharmaceuticals industry around the world. Their reputation is based on forming successful partnerships with clients, providing them with innovative designs and cost effective solutions in the context of sound judgement, strong management and technical excellence.

Responsibilities
  • Acquiring and retaining technological knowledge related to products, processes, equipment and suppliers
  • Setting up, coordinating, executing and reporting studies for investigations, root cause analyses, tech transfers, CAPEX projects, validations, changes or improvements
  • Lead or participate in project teams
  • Write validation and engineering protocols and reports, (project) plans, risk analyses, changes, URS, VMP and qualification protocols and reports
  • Setting up, maintaining and working with systems such as the quality management systems (QMS), SHE systems, change control and SAP
  • Ensuring conditions are in place that enable colleagues and team to comply with the relevant laws, regulations and company rules regarding GMP and SHE
The Ideal Candidate
  • MSc or BSc degree in a relevant area or experience
  • Experience in a pharmaceutical environment
  • Technical expertise in packaging equipment and packaging materials (Blistering – second packaging – case packing – palletising)
  • Project management skills and/or certified in this field
  • Experience with technology transfer
  • Experience with CQV (writing protocols and execution)
Seniority Level

Associate

Employment Type

Full-time

Job Function

Project Management, Engineering, and Manufacturing

Industries

Pharmaceutical Manufacturing

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Location: Boxmeer, North Brabant, Netherlands

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