Quality Assurance specialist
at Johnson Johnson
Helsingborg, Skåne län, Sweden -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 16 Sep, 2024 | Not Specified | 19 Jun, 2024 | 2 year(s) or above | English,Management Skills,Analytical Skills,Interpersonal Skills | No | No |
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Description:
WHO WE ARE
At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands — including OTC brands such as NICORETTE®, RHINOCORT®,IPREN®, LIVOSTIN®, IMODIUM®, PEPCID® and consumer health brands like NEUTROGENA®, LISTERINE®, NATUSAN®, PIZ BUIN® and o.b. ®. Our employees share a digital-first mindset, an approach to innovation grounded in deep human insights, and a commitment to continually earning a place for our products in consumers’ hearts and homes.
The Kenvue site in Helsingborg, Sweden is the home of the strong and growing brand NICORETTE®, a global market leader in smoking cessation. In 2021 our production facility was recognized as a Lighthouse by World Economic Forum, marking us as a beacon in The Fourth Industrial Revolution.
The Helsingborg site is one of the largest employers in the city of Helsingborg, and the business is divided in two separate departments: Operations, where we house our manufacturing activities and R & D, our global development center for excellence working in three therapeutic areas for selfcare treatments: Smoking Cessation, Digestive Health and Cough & Cold.
Responsibilities:
The Quality Assurance Specialist is responsible for maintaining accurate and timely quality records, coordinating change control documentation, proposing and assisting in corrective action plans, conducting investigations and preparing reports, assessing and recommending improvements to quality systems, product release and facilitating audits and inspections. You will also provide quality support for technology transfer and improvement of existing manufacturing processes.
Key Responsibilities
- Develop and implement quality assurance policies and procedures.
- Release products to market
- Conduct regular audits to ensure compliance with established quality standards
- Prepare for and facilitate audits and inspections
- Collaborate with cross-functional teams to identify areas for improvement and implement corrective actions
- Provide training and support to team members to ensure adherence to quality standards
- Stay up-to-date with industry trends and best practices to continuously improve quality assurance processes
- Lead and manage quality related projects to ensure timely completion and compliance with quality standards
- Provide coaching and training to employees on quality assurance practices and procedures
- Conduct investigations, collect data, analyze trends and prepare reports for assigned quality processes
- Ensure compliance with good manufacturing practices as established in the code of local government regulations and company procedures
- Review and approve pending investigation reports for quality assurance
- Assess current quality systems and recommend improvements in order to enhance quality and reduce cycle time
- Monitor trends, identify issues, recommend and implement appropriate actions
- Assure adherence to compliance requirements and policies outlined for marketing companies, external manufacturers, packaging and labeling, product testing, returned goods, product complaints, and recalls
Qualifications
REQUIREMENT SUMMARY
Min:2.0Max:7.0 year(s)
Pharmaceuticals
Production / Maintenance / Quality
Software Testing, Clinical Pharmacy
Graduate
Relevant Field
Proficient
1
Helsingborg, Sweden