Senior Sterilization Validation Engineer (mfd)

Antwerp - Belgium

Monthly Salary: Not Disclosed

Posted on: Yesterday

Vacancies: 1 Vacancy

Job Summary

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow and profoundly impact health for more at .

As guided by Our Credo Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson we respect the diversity and dignity of our employees and recognize their merit.

Job Function:

Supply Chain Engineering

Job Sub Function:

Process Engineering

Job Category:

Scientific/Technology

All Job Posting Locations:

Beerse Antwerp Belgium

Job Description:

Senior Sterilization Validation Engineer (m/f/d)

Johnson & Johnson Innovative Medicine is recruiting for a Senior Sterilization Validation Engineer within Manufacturing Science And Technology (MSAT) located in Beerse Belgium.

A MSAT Sterilization Validation Engineer is a member of the MSAT Life-Cycle Management Validation team. This team has a passion for sterility processes and works together with operations and quality to deliver safe and quality products to our patients. Within this team process improvements and innovation are an important focus. By working in a pharmaceutical environment you can have direct impact on the lives of our patients!

Key Responsibilities

Subject Matter Expert (SME) for sterilization validations processes (such as thermal dry heat gamma irradiation VHP decontamination APS) and sterilization/aseptic manufacturing systems such as autoclaves SIP systems isolators.
Manage and execute Validation Master Plan (VMP) and coordinate the Validation Master Planning.
Continuously focussing on safety quality GMP and operational discipline while ensuring contemporary validation standards are followed.
Participate in system and process improvements and optimization processes.

Qualifications:Education

Masters Degree in Engineering or Science or equivalent.
Other relevant fields of study are accepted and will be considered.

Experience and Skills

Minimum 3 to 5 years of relevant experience in a pharma/life sciences environment.
Expertise on pharmaceutical manufacturing processes & products and/or equipment & facility engineering (if applicable) especially for the involved technology platform.
Experience in at least one of the following functions: clinical supply chain commercial supply chain or in a support role for sterilization validation engineering.

Required

Strong interest in working in a pharmaceutical environment with a focus on sterilization validation processes
Team player with a can-do mentality
Ability to be a key team member in business-critical projects
Ability to work independently and manage complex issues and changes in a problem-solving manner
Ability to connect globally within J&J with SME of other sites
Ability to act as a spokesperson during audits

Preferred

Expertise in aseptic manufacturing
Knowledge of international regulations guidelines and industry practices related to sterilization validation
Knowledge and interest in statistics and multi variate analysis
Proficiency in Dutch as interaction with our operators in the supply chain is required. Fluent in written and spoken English
Certification or training as an FPX project manager

Required Skills:

Preferred Skills:

Agile Decision Making Coaching Corrective and Preventive Action (CAPA) Critical Thinking Emerging Technologies Issue Escalation Lean Supply Chain Management Problem Solving Process Control Process Engineering Product Costing Product Improvements Science Technology Engineering and Math (STEM) Application Situational Awareness Technical Research Technologically Savvy Validation Testing Vendor Selection

Required Experience:

Senior IC