Summary
Assures that non-conformance investigations, laboratory investigations and quality systems are in compliance with the good manufacturing practices and good laboratory practices as established in the code of local government regulations and company procedures.
Description
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 https://www.jnj.com
Job Function:
QualityJob Sub Function:
Customer/Commercial QualityJob Category:
ProfessionalAll Job Posting Locations:
FR018 Issy les Moulineaux_Stalingrad, GB017 Pinewood, IE012 Liffey Valley, PL001 Szyszkowa, PL003 ACT Warsaw, PolandJob Description:
Johnson & Johnson Vision is recruiting for a Quality Engineer to support distribution and commercialization of medical devices across EMEA.
At Johnson & Johnson Vision, we are driven by a powerful purpose—to change the trajectory of eye health worldwide. We deliver innovative solutions that enable eye care professionals to create better outcomes for their patients throughout their lives from sight correction, including world leading surgical technologies and contact lenses; to dry eye diagnosis, treatment and management; and the restoration of vision for cataract patients. Serving more than 52 million patients a day across 103 countries, we are committed to helping people see better, connect better and live better.
In this role, you will be responsible for supporting quality engineering processes for Johnson & Johnson Vision products in the EMEA Supply Chain. You will drive key Quality Engineering initiatives related to sustaining and improving performance as a member of the EMEA Commercial Quality team.
Key Responsibilities:
You'll be responsible for development of quality systems based on business, regulatory and customer requirements. You'll also provide training and consultation to various parts of the business and resolve procedural breakdowns.
The role will include working with multiple QMS (Quality Management Systems) and require candidates to demonstrate leadership skills.
More generally, the candidate:
Leads and participates in quality systems and engineering improvement initiatives, with specific focus on supply chain performance and commercial initiatives.
Utilizes industry and process excellence standards in daily quality operations, including good distribution practices (GDP) and international organization for standardization (ISO).
Addresses or escalates product and process complaints. Evaluates contract manufacturer performance metrics and supports management reviews.
Identifies root causes of quality issues and develops corrective actions and recommendations.
Implements comprehensive measurement systems to monitor effectiveness of quality and reliability systems to identify, correct and prevent defects, demonstrating continuous improvement.
Qualifications
Education:
Bachelor degree in Science or Engineering related field preferred
Experience and Skills:
Required:
Excellent interpersonal skills, able to influence peers and leaders in cross-functional environments
Self-starter, able to work effectively, and with agility, under limited supervision
Proficient with Office applications and Adobe artwork files
Medical device experience, preferably in a Quality role (2-5yrs)
Preferred:
Experience in delivering successful projects (as part of core team, management would be a bonus but not required)
Other:
Excellent verbal and written English proficiency required. Additional languages helpful.
Travel percentage – 10% travel domestically and internationally.
