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Requistion ID : 77500

Dentsply Sirona is the world’s largest manufacturer of professional dental products and technologies, with a 130-year history of innovation and service to the dental industry and patients worldwide. Dentsply Sirona develops, manufactures, and markets a comprehensive solutions offering including dental and oral health products as well as other consumable medical devices under a strong portfolio of world class brands. Dentsply Sirona’s products provide innovative, high-quality and effective solutions to advance patient care and deliver better and safer dentistry. Dentsply Sirona’s global headquarters is located in Charlotte, North Carolina, USA. The company’s shares are listed in the United States on NASDAQ under the symbol XRAY.

Bringing out the best in people

As advanced as dentistry is today, we are dedicated to making it even better. Our people have a passion for innovation and are committed to applying it to improve dental care. We live and breathe high performance, working as one global team, bringing out the best in each other for the benefit of dental patients, and the professionals who serve them. If you want to grow and develop as a part of a team that is shaping an industry, then we’re looking for the best to join us.

QA Training Manager – Mölndal, Sweden

Making people smile is more than an expression at Dentsply Sirona. It’s a promise we’ve lived by for more than a century!

We are driven by our passion for innovation and are committed to pushing ourselves forward. Now we are looking for a Training Manager to join our team in Mölndal. You will be part of a dedicated team and operate in an international environment towards both local and global stakeholders.

Are you ready to join the trailblazing team that’s shaping the dental industry around the world?

In this role you will design, develop, implement, and facilitate our GxP trainings to ensure compliance with applicable regulations within Medical Device Industry. You will play an important role securing appropriate documentation, qualified trainers, and approved training content.

Responsibilities:

• Support and lead Training and Training Program initiatives in Quality and Regulatory.

• Develop and implement role-based Training Matrices.

• Serve as technical resource or subject matter expert for the acquisition and use of learning technology.

• Design, plan and deliver training courses associated with specific Quality and Productivity initiatives, as well as other soft skills training.

• Liaise with HR for troubleshooting/enhancements of the electronic Learning Management System (LMS).

• Work with Groups/Locations to identify and maintain employee curricula.

• Lead Training-related communities of practice.

• Lead and approve Training program-related Nonconformity/CAPA.

• Manage day to day tasks and assignment of responsibilities.

• Develop and manage Training program goals and initiatives.

Qualifications:

• Bachelor's degree (B. A.) from four-year college or university.

• Minimum of four years of experience with preference in a medical device/pharmaceutical environment.

• Experience needed in Instructional Design, Needs Analysis, Curriculum Development and Project Management.

• Experience working with electronic Learning Management Systems and tools.

• Proven ability to manage complex projects, including several sites around the globe.

• Ability to identify training needs for users at Groups/Locations.

• Ability to communicate effectively with individuals at all levels of ability and understanding.

• Excellent computer skills (MS Office Suite).

• Excellent customer service skills.

• Successful track record of developing and delivering comprehensive professional development programs.

If this is something for you, don´t hesitate to apply. Note that we will evaluate applications continuously.

We look forward hearing from you!