Quality Control Spec I Jobs in Iowa

Experience in creating clear and concise documents (PowerPoint, memos, etc.) for educational purposes and statewide distribution.

At least 2 years of related experience in a hospital, regional or central cancer registry.

Bachelor’s degree in a health-related field, or substitute with four additional years of related experience.

Must maintain CTR credentials by attending either in-person or virtual educational meetings or other methods as prescribed by the NCRA.

Excellent knowledge of medical terminology, medical procedures, anatomy and physiology, and the cancer disease process.

Strong communication skills. Must have the ability to communicate accurately, concisely, and clearly.

1-2 years related experience preferred

Knowledge of accounting (construction) principles and controls

Excellent written and verbal communication skills both internally and externally

Ability to evaluate, recommend, plan, and manage projects

Preferred experience in construction job cost accounting

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Applies knowledge or quickly learn cGXPs, relevant SOP curriculum, routine project procedures, project management, and other training as appropriate.

Direct or indirect industry knowledge.

1 year experience preferred in medical device quality, sterility assurance or sterilization operations.

Serves as project lead with projects of intermediate scope and cross-functional teams.

Developing and validating sterilization processes for new and existing products

Qualifying, maintaining, and troubleshooting sterilization of products and associated equipment

Ensures that corrective measures meet acceptable reliability standards and that documentation is compliant with requirements.

0 years of experience required

Responsibilities may include the following and other duties may be assigned.

Develops, modifies, applies and maintains quality standards and protocol for processing materials into partially finished or finished materials product.

Collaborates with engineering and manufacturing functions to ensure quality standards are in place.

Devises and implements methods and procedures for inspecting, testing and evaluating the precision and accuracy of products and production equipment.

Every employee is responsible for performing his/her job safely and for calling to management’s attention unsafe conditions, practices, or equipment.

0-3 years of experience (medical device experience preferred)

Document development work including writing specifications for manufacturing or scientific test results.

Solve routine design and engineering tasks with some assistance. Able to solve problems with periodic monitoring.

Assist in the preparation and participation in technical reviews and responsible for organizing data and preparing appropriate documentation for assigned projects.

Repetitive work with a personal computer.

Experience with the following disciplines: manufacturing/process engineering, CAPA, risk management, or supplier quality

Participates in team decision-making and displays team problem-solving/communication skills

Knowledge of analytical techniques, problem solving, and statistical analysis (Excel, Minitab)

Experience managing multiple projects across various organizational disciplines

Strong written and verbal communication skills

Apply sound, systematic problem-solving methodologies in identifying, prioritizing, communicating, and resolving quality issues

Minimum of one (1) year of experience in a clinical or industrial/pharmaceutical laboratory

Knowledgeable in GMP & laboratory techniques

Strong communication skills (verbal & written)

Ability to attain clean room gowning certification

Accuracy & Scientific Soundness of Lab Data

Maintain testing proficiency for methods