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Labeler

Company:
SGS CONSULTINGS
Location:
Plymouth, Minnesota, 55442, United States
Posted:
February 13, 2018
Description:

Hi

This is Vaibhav from the recruiting team of SGS. Currently we are sourcing for a Labeler one of our Fortune 500 clients’ I am enclosing a synopsis of the opportunity for your perusal as well as some background information about our organization. I would like to discuss this opportunity with you in more detail. Please reply back to this e-mail with the best contact # and time to reach you or feel free to call me at my direct # 609-436-9208 or

Job Title: Labeler

Location: Plymouth, MN, 55442

Duration: 12 months

Shift: 1st 8:30 AM – 5:00 PM

JOB DESCRIPTION:

We are seeking a high caliber Labeling Specialist. This position is responsible for the development of product labeling for all medical device divisions, serving multiple US and international operations facilities and ensuring compliance to world-wide regulations.

KEY RESPONSIBILITIES:

• Responsible for developing and maintaining label content for new and existing medical device products.

• Designs product labels, packaging artwork and other related materials according to branding guidelines.

• Works with external customers to manage labeling developed for or at external suppliers.

• Collaborates with cross functional teams (including Engineering, Marketing, Clinical, Design Assurance, Legal, and Regulatory) to ensure compliance to world -wide regulations, company policies & operating procedures.

• Coordinates production implementation by managing changes within the Quality Management System

• Collects & maintains Unique Device Identification (UDI) information within GUDID database.

• Advises functional teams on labeling and UDI impacts regarding manufacturing changes, technology upgrades or new regulations.

• Maintains positive and cooperative communication with all levels of employees, internal & external customers.

• Partners with IT to support Operations by troubleshooting production issues. Supports technology upgrades by executing software or hardware validation.

QUALIFICATIONS:

• BA or BS degree (degree in a technical discipline highly preferred).

• A minimum of 1 to 4 years’ technical experience in a medical device industry and/or in a broader enterprise/cross-division business unit model preferred.

• Ability to work in a highly matrixed and geographically diverse business environment.

• Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization.

• Ability to identify and solve problems and work independently with little oversight.

• Knowledge of FDA & EU regulations, GMP, GS1 and ISO standards.

• Experience working with design software such as, CAD, Adobe Illustrator/Photoshop.

• Familiarity with enterprise PDM & ERP systems

• Advanced skills with Excel, Access, or database management software.