Technical/IT Lead - Quality Assurance
Date de publication :
20 septembre 2024Taux d'activité :
100%Type de contrat :
Durée indéterminée- Lieu de travail :Massachusetts
Johnson & Johnson MedTech is recruiting for a Technical / IT Lead - Quality Assurance, to be located in Bridgewater, Massachusetts.
A pre-identified candidate for consideration has been identified. However, all applications will be considered.
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/.
For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world. Our diverse workforce and culture of belonging accelerate innovation to solve the world’s most pressing healthcare challenges. We know that the success of our business – and our ability to deliver meaningful solutions – depends on how well we understand and meet the diverse needs of the communities we serve. Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued, and our people can reach their potential. At Johnson & Johnson, we all belong.
Established and productive individual contributor, who works under moderate supervision. Helps implement projects, programs, tools and processes in support of the organization's overall Quality system. Applies practical knowledge of the In-Process Quality field to administer best of class policies, procedures, and plans for the area.
Participation in complex quality investigations and/or internal audits to assess conformance to specifications, company procedures and overall compliance to regulations is required. Assist in Non-Conformance and CAPA investigations as necessary.
This candidate must possess the ability to work in a fast-paced team environment. Individual will need strong customer service skills, demonstrated ability to work independently and with flexibility to meet changing business needs
Key Responsibilities:
This is not meant as an all-inclusive list but top-level list of duties that this person generally completes. It is also understood that an associate may receive special projects outside of this list.
- Provide support and robust guidance for Quality Systems, including document management and metrics reporting.
- Ensure compliance with the Quality Systems procedures and policies.
- Review wide variety of documents for compliance to procedures, including SOPs, Work Instructions, Technical Documents, Logbooks, Forms.
- Drive alignment and efficiencies between global and local processes.
- Provide quality input on quality systems related issues and represent department in meetings.
- Coordinate and conduct Quality Systems Review meetings.
- Support internal and external audits, inspections, pre-inspection readiness, certifications, tracking, and trending activities.
- Work closely with management and various team members to propose and complete improvements activities.
- Develop / maintain digital tools to support department efficiencies and compliance.
- Ability to respond swiftly to departmental and interdepartmental requests.
- Perform tasks in a manner consistent with the safety policies, quality systems, and cGMP requirements.