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Quality Assurance Compliance Manager

Integra LifeSciences

This is a Contract position in Irving, TX posted August 23, 2021.

SUMMARY DESCRIPTION Manage and provide oversight on Quality Compliance for projects and daily operations which may include leading project teams focused on key initiatives including quality process improvements, process changes, and other site quality support projects.

Responsible for assessing, developing and maintaining plant quality audit, change, and training requirements in compliance.

Oversee generation and review of documents, processes.

This position will also focus on key initiatives in addition to base business priorities related to Compliance.

They will perform all duties in accordance to the requirements of overall corporate policies, FDA regulations, ISO 9001, ISO 13485, the medical device directive, and the other applicable regulatory agencies.

Responsible for ensuring site processes maintain compliance with Global and Regional policies and procedures, US and Global QSRs Ensure cross-functional partners understand quality system requirements and how they impact product quality and regulatory compliance.

Works with Senior Management to achieve alignment of Quality Goals and functions and ensure proper resourcing.

Identifies the minimum baseline training requirements for all personnel at the plant.

Ensures change control program is effective and efficient.

Ensures Internal Auditing maintains compliance to identify site items requiring remediation.

Engage in team development.

Participates in FDA inspections, ISO certifications, surveillance audits, and customer audits.

Identify and implement opportunities for continuous improvement, including document revisions in order to maintain accurate SOPs.

Provide compliance support to various departments as needed, e.g.

engineering, product development, etc.) May serve as an alternate to the Director, Quality Operations for review and approval of compliance documentation including NCs, Change Controls, risk and validation documentation etc.

Assist in training new associates according to the Quality System Regulations and company SOPs as applicable.

May also perform other related duties, responsibilities, and special projects as assigned.


degree in life science or engineering and minimum 8 years in progressive experience in Medical Device or Pharma.

At least 2 years medical device or pharma managerial experience directly managing people or leadership experience leading project teams and/or programs.

Extensive knowledge of appropriate global medical device regulations, requirements, and standards such as 21 CFR Parts 803, 806, 820, ISO 13485, ISO 14971 and Medical Device Directive, EUMDR.

Demonstrated ability to build an engaged and cohesive team, maintain a positive working environment and integrate quality objectives across multiple functions Excellent written and verbal communication skills.

Must be able to effectively present at staff and department meetings.

Strong organizational skills, self-directed, strong problem solving and interpersonal skills.

Must be able to work independently with minimal supervision required.

Expert MS office user a plus.

ASQ-CQT desirable.

Ability to define problems, collect data, establish facts and draw valid conclusions Ability to work effectively in a cross functional environment Attention to detail, strong time management are essential

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