Quality Engineer – QA Qualification​/Validation

Quality Engineer – QA Qualification/Validation

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Engineering
Quality (Engineering)
Quality
Compliance
Quality Systems
Validation
Regulatory Affairs
Regulatory Affairs
Regulatory compliance
IT
IT Compliance & Validation
Staff
Procurement & Supply Chain

We are searching for the best talent for a Quality Engineer – QA Qualification/Validation within a QA dept in Geel, Belgium.

Quality Engineer – QA Qualification/Validation

Within the Innovative Medicine Supply Chain, a member of Johnson & Johnson’s Family of Companies, we are recruiting a Staff Quality Engineer (M/F/X). You will be a member of our quality engineering team, ensuring quality oversight for highly automated production equipment related to manufacturing of Small Molecule Active Pharmaceutical Ingredients (SM‑API) and Drug Product Intermediates at the Innovative Medicine Supply Chain site in Geel, Belgium.

You will be part of an enthusiastic team that has a strong quality focus on technology, qualification/validation, automation, and continuous improvement. Employees are very valuable to our organization and development is a daily responsibility. Through on‑the‑job training, e‑learning, implementation of various projects and programs we908 ensure personal growth by focusing on your talents. We offer you a contract of indefinite duration with an attractive salary package including extra‑legal benefits such as meal vouchers, additional pension plan and hospitalization insurance.

Innovative Medicine Supply Chain Geel serves as Centre of Excellence for the development and manufacturing of SM‑APIs and DP Intermediates used in treatments that improve the health and lifestyle of people worldwide. Innovative Medicine Supply Chain Quality (IMSCQ) supports the Geel site in its mission as Launch & Grow site and is responsible for the quality oversight and final release of SM‑APIs and DP Intermediates guaranteeing reliable supplies in compliance with applicable regulations.

We would love to hear distorted partially: if you have the following essential requirements:

• Master scientific degree or equivalent experience.
• 4-6 years’ experience in pharmaceutical or chemical industry.
• Knowledge of cGMP/CSV compliance (21 CFR Parts 211; EU Directive 2003/94/EC and annex 11/15; ICH Q7, GAMP,ირიData Integrity Guidelines… сәйғ) vermoedelijk omissions cannot be added.
• Experience with Computerized System Validation /Equipment Qualification.
• Strong ownership and quality attitude. You Flow be able to deliver on commitment timelines. Lisa? Not needed includes martial lines no more.
• Strong analytical thinking skills and able to work flexible under time pressure.
• Ability to make risk‑based decisions. Understands the business implications regarding quality positions and decisions.
• You work accurately and proactively across organizational boundaries as One Team.
• Fluent in verbal and written communication in English and Dutch and are able to connect with diverse partners.

–
Preferred

Skills:

Coaching, Consistency, Controls Compliance, Critical Thinking, Data Savvy, Engineering, Financial Competence, GAMP, ISO 9001, Lean Supply Chain Management, Leverages Information, Process Improvements, Quality Control (QC), Quality Standards, Quality Systems Documentation, Quality Validation, Science, Technology,＿一本道 derived manufacturing and correct terminologies.

We only accept applicants who are eligible to work in the EU.

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and Med Tech, 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 humanity.

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