Sede: Heredia | Publicado 25 Abril

Designer I

Responsible for modeling/designing components for new and existing medical device products (e.g.assemblies/equipment/fixtures/programmers/leads/stents) into detail drawings and documentation using CAD and other tools.

Sede: Coyol | Publicado 18 Abril

Technician II, Laboratory

Participation in Problem-Solving sessions and understanding of Root Cause Analysis tools and methodologies (Ishikawa, 6M’s, 5 Why’s). Perform testing associated with respective QA Laboratories (proficient use of QA laboratory equipment) and correctly record data, write and review reports, and communicate results precisely, promptly and in a timely manner. Lead product failure analysis (i.e. significant support on CAPA activities) and involve required assistance if required. Initiate and assist in the investigation and disposition of nonconforming materials, designs and/or systems (when applicable). Create, maintain and update data files, databases, spreadsheets and forms, such as the maintenance of the lab´s record file in order to ensure proper record flow, track and monitor department activities. Assist in developing and qualifying test methods, data sheets, test fixtures, testing equipment, processes and train peers on these areas. (CIS) Conduct complaint investigations as per requirements.

Sede: Heredia | Publicado 18 Abril

Packaging R&D Engineer I

Area of works involves packaging design and processes with interaction between R&D, regulatory, document control, purchasing and outside vendors. Develops a proficient understanding of the FDA regulations, ISO standards and BSC policies and procedures. •Supports project work by performing any of the following supports Package Engineering cost savings and improvements projects; writes packaging validation protocols and reports; performs package testing; updates and maintains assigned packaging component, manufacturing and quality specifications; develops and communicates project timetables; other activities of limited scope requiring knowledge of principles and techniques commonly employed in the specific area of assignments. •Demonstrates an understanding of the goals, objectives and strategies of a team/ group, specifically in instances of working with assemblers, production supervisors and engineers in troubleshooting problems on the production floor and in performing MRR investigations. •Interface with internal customers including, QA, QAE, Purchasing, Production, Manufacturing Engineering and other members to resolve packaging issues. Assists in root cause analysis. •Trains assemblers, quality control and technicians, as necessary, on processes, equipment and documentation.

Sede: Heredia | Publicado 09 Abril

Supplier Engineer I

A Supplier Engineer tackles challenges concerning business continuity of our suppliers. We also look for opportunities that could result in cost reduction and increase savings for BSC and our suppliers. This in turn will result in an overall quality of our products that our customers will receive. As an Supplier Engineer we lead several projects with different departments within the company. This results in great planning and leadership skills, which are critical in our daily basis.

Sede: Heredia | Publicado 09 Abril

Supplier Quality Engineer I

Area of works involves packaging design and processes with interaction between R&D, regulatory, document control, purchasing and outside vendors. Manage non-conformance, Develops a proficient understanding of the FDA regulations, ISO standards and BSC policies and procedures. Develop Inspection plans to EUMDR components, develops an understanding of how own function is to conform to those standards and how own project work impacts the business.

Sede: Heredia | Publicado 05 Abril

Health Care Provider Analyst I

Analysts will be responsible for the processing of Health Care Providers Expense Reports and Set up of Health Care Providers Identification numbers.

Sede: Heredia | Publicado 27 Marzo

Engineer II, Design Compliance

The Design Assurance Engineer is a quality engineer that directly supports medical device product development from concept through commercialization. You will support product sustainment activities assessing product performance for trends including signal escalation. This position will help lead, communicate, and coordinate complaint reduction and post marketing projects and initiatives. Guarantee compliance with Quality System Regulations, Corporate Quality Manual and corporate and local standard operating procedures.

Sede: Heredia | Publicado 22 Marzo

Meetings & Events Specialist

Work with clients to understand their meeting and provide consultative website, mobile app and survey build services that exceed expectations.

Sede: Heredia | Publicado 22 Marzo

Full Stack Software Developer

Designs, develops, enhances, documents, and supports the customization of internally developed or off the shelf (OTS) software applications to meet business needs.