Operations Associate II - S20-006

at  Confluent Medical Technologies

Costa, West Virginia, USA -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate29 May, 2024Not Specified01 Mar, 20242 year(s) or aboveGood communication skillsNoNo
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Description:

Job Description:
Confluent Medical Technologies is dedicated to working collaboratively with our customers, taking their projects from rapid prototype into high volume production. Our unparalleled technical expertise, proven experience and partnership with our clients has allowed us to perfect the process necessary to deliver world-class medical devices through innovative material science, engineering, and manufacturing. Our primary capabilities include: Nitinol components, balloon expandable stents and balloon catheters, delivery systems, biomedical textiles, access kits, and guidewires. We take pride in our position as the leader in the medical technology space and are driven by a passion to create products that our clients have envisioned for their customers.
We are looking for a XXXXX to join our team. As a uniquely qualified candidate, you will be responsible for production planning and inventory control for multiple products while prioritizing operations to ensure maximum performance and minimum delay. This individual will take a lead role in continuous improvement, product flow and capacity improvement to improve the overall efficiency of manufacturing while service level targets.
SUMMARY: Under direct supervision, performs and documents production functions relating to fabrication, modification and assembly of components or finish medical devices.
ESSENTIAL DUTIES AND RESPONSABILITIES include the following. Other duties may be assigned. Performs and documents operations in the production process. Sets up, adjust and operates laboratory/manufacturing equipment. Performs process/product tests and audits for conformity to quality and/or regulatory requirements. Performs self-inspections of own work. Follows standard operating procedures for all tasks. Maintains clean and orderly work area. Has completed all appropriate safety and environmental hazard training .Responsible for ensuring personal and company compliance with local and company regulations, policies and procedures for Health, Safety and Environmental compliance.
EDUCATION and/or EXPERIENCE: Elementary school degree. 2-3 years of related experience. Basic personal computer skills.
OTHER SKILLS and ABILITIES: Ability to read and understand technical documentation associated with specific discipline. Must be able to successfully complete company/department training courses in manufacturing techniques. Ability to learn regulatory (GMP) requirements. Ability to read and comprehend simple instructions. Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals. Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals.
COMMENTS: This job description is an outline of the major recurring responsibilities of the job. It is not intended to be all-inclusive of the work to be performed. Other related job objectives, special assignments and less significant responsibilities will typically be performed by the incumbent(s)

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Responsibilities:

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REQUIREMENT SUMMARY

Min:2.0Max:3.0 year(s)

Pharmaceuticals

Production / Maintenance / Quality

Clinical Pharmacy

Graduate

Proficient

1

Costa, WV, USA