Sr. QA Associate (80-100)

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.

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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 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 humanity. Learn 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.

Senior QA Associate (80100%) permanent

Responsibilities

• QA responsibility for multiple products
• Independent management of projects (e.g. establishment and reorganization of specific areas process improvements introduction of new techniques) including within international teams
• Handling tracking and ensuring timely closure of non-conformances
• Advising other departments such as Production Planning and Engineering in a GMP environment and supporting the implementation of improvements
• Ensuring GMP-compliant processes and documentation
• Reviewing batch documentation of manufacturing processes and releasing batches for further processing and final release
• Reviewing and approving quality-relevant master data for materials
• Supporting Production on quality-related issues including regular walkthroughs/plant rounds
• Supporting inspections and audits; acting as subject-matter expert (SME) for selected areas

Profile

• Ideally a degree in a scientific or technical field
• More than 5 years professional experience in Quality Assurance or pharmaceutical manufacturing required
• Experience in aseptic manufacturing / hygiene / microbiology is a definite plus
• Comprehensive knowledge of relevant regulations
• Excellent German and English communication skills (written and spoken)
• Confident user of MS Office
• Solution-oriented independent and a team player

You can expect a varied and exciting position in a highly technological production environment with attractive conditions.

If you are self-motivated and enjoy working precisely and reliably we look forward to receiving your online application via our career portal.

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