Job Details

ID #52932892
Estado Minnesota
Ciudad Osseo
Full-time
Salario USD TBD TBD
Fuente Randstad US
Showed 2024-11-21
Fecha 2024-11-22
Fecha tope 2025-01-21
Categoría Etcétera
Crear un currículum vítae
Aplica ya

Quality technician ii

Minnesota, Osseo, 55369 Osseo USA
Aplica ya

quality technician ii.

osseo , minnesota

posted today

job detailssummary

$20 - $25.52 per hour

contract

associate degree

category life, physical, and social science occupations

reference49457

job detailsjob summary:As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you!location: Maple Grove, Minnesotajob type: Contractsalary: $20.00 - 25.52 per hourwork hours: 9 to 5education: Associateresponsibilities:This individual will work within a high-performance cross-functional team performing routine medical device particulate testing ensuring delivery of the highest quality result to the customer. We are seeking a highly motivated individual who thrives in a fast-paced environment, with excellent good documentation practices, and exceptional attention to details.

Performs routine testing assignments requiring basic interpretation of established procedures.

Gather and record data, analyze results and verify & report test results.

Assignments require broad judgment in troubleshooting.

Create and maintain data files and forms.

Communicate with a wide variety of company personnel in and outside of the plant.

Identify areas of improvement and participate in continuous improvement projects.

Use documentation systems to research information and generate Change Requests.

Assist in developing and qualify data sheets, equipment/fixtures, visual standards, and test methods.

Initiate, investigate, and assist in generation and completion of NCEPs.

Assist engineers in failure analysis and CAPA activities.

Assist with product failure analysis.

Communicate testing results to teams.

Support process and product qualification activities.

Perform "special" quality initiatives with guidance.

In all actions, demonstrates a primary commitment to patient safety and product quality by maintaining compliance to the company Quality Policy and all other documented quality processes and procedures.

Employ basic analytical lab skills such as reading a meniscus, pipetting, using a balance, using a stir plate. etc.

qualifications:Required:

1 year with AA degree or an equivalent combination of education/work experience

Prior experience in a lab environment including analytical laboratory skills (weighing, pipetting, scientific method, etc.).

Knowledge of Microsoft Office (Word, Excel, Outlook) required.

Must be physically able to lift up to 35 lbs.

Must be able to stand for 8 hours.

Preferred:

DV test protocol training and execution experience

Strong problem-solving skills.

Quick learner; willing to learn the current test processes and procedures in a regulated environment.

Able to multitask between projects in different stages of development.

Demonstrated experience analyzing and fulfilling documentation requirements.

Ability to communicate detailed information to the project teams.

Ability to work in a team environment interacting with engineers and technicians.

Prior experience in test documentation through lab notebooks or reports.

Experience in medical device industry preferably testing medical devices.

Operate and maintain test equipment.

skills: MS-WORD, CAPA, MS-EXCELEqual Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact [email protected] offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility).This posting is open for thirty (30) days.

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