Job description

Product Quality / Surveillance Specialist

Our client is a global life sciences leader in the dental and spine markets that develops, manufactures, and delivers products and solutions designed to treat a wide range of restoration procedures for spine pathologies and support dental tooth replacement.

Job Summary:

This position effectively supports a defined process and adheres to all corporate and site-specific procedures as applicable. This individual executes to the process with a focus on a defined step of the process. This position is responsible for decision making of the defined steps of a process. Provides guidance and feedback to other team members pursuant to the defined procedures. Responsible for follow up with division personnel, site team, and international team members to ensure effectiveness and responsiveness related to process. Responsible for communication of data related to the process to site and division leadership.

Principal Duties and Responsibilities:

· Adheres to all corporate and site-specific procedures.

· Identifies and investigates solutions to procedure and process related issues. Revises the procedure or process as needed to increase efficiency and compliance.

· Documents and maintains records in accordance with corporate and site-specific procedures.

· Creates, maintains, and monitors appropriate metrics to measure key performance indicators of the unit.

· Evaluates, assesses, and executes the assigned steps within in the process.

· Provides direction to internal and external personnel on issues related to the defined steps/process.

· Assists Management in special projects as required.

· Other duties may be assigned

Expected Areas of Competence (i.e., knowledge, skills, and abilities)

· Good organizational and time management skills.

· Good written, oral, and presentation communication skills.

· Knowledge of EtQ, JD Edwards, Internet, Microsoft Office applications and the ability to learn other software quickly as required.

· Detail-oriented.

· Ability to consistently meet high standards of input accuracy, produce quality documents, compile data, and perform simple analyses with accuracy.

· Good decision-making skills and proven ability in balancing priorities among the many ongoing tasks, and being responsive to critical situations, as this position has a high volume of work, regulatory mandated time limits, and often changing priorities.

· Action-orientated: Ability to take initiative to correct problems or make changes for improvement without waiting for direction.

· Proven ability to work in a team setting. Willing to share the load and participate in projects outside of normal job scope. Ability to work closely with others to assure functional commitments is met.

· Proven ability to provide training to Team Members as needed.

· Ability to work with all individuals in a congenial and cooperative manner.

Education/Experience Requirements

· Bachelor of Science degree in biology, health sciences, engineering, or nursing preferred or Bachelor’s degree in another discipline with relevant experience.

· Co-op or Intern experience in medical devices, preferred.

This role is restricted to U.S. persons (i.e., U.S. citizens, permanent residents, and other protected individuals under the Immigration and Naturalization Act, 8 U.S.C. 1324b(a)(3)) due to access to export-controlled technology. Our client will require proof of status prior to employment.

We thank all candidates for their application, however only those that qualify will be contacted.

ROC1

Job Types: Full-time, Contract

Salary: Up to $22.00 per hour

Benefits:

• 401(k)
• Dental insurance
• Health insurance
• Life insurance
• Paid time off
• Vision insurance

Schedule:

• 8 hour shift
• Day shift
• Monday to Friday

Work setting:

• In-person

Ability to commute/relocate:

• Palm Beach Gardens, FL: Reliably commute or planning to relocate before starting work (Required)

Education:

• Bachelor's (Preferred)

Experience:

• Microsoft Word and Excel: 2 years (Preferred)
• medical device or pharma documentation review/control: 2 years (Preferred)
• JD Edwards: 2 years (Preferred)
• Production Quality Assurance: 2 years (Preferred)

Work Location: In person

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