Manufacturing STEM OPT Jobs in Delaware

INTRODUCTION

Designs, implements and maintains quality assurance protocols and methods for processing materials into partially finished or finished products. Responsible for planning, implementing and managing compliance of manufacturing and production processes with internal and external safety, quality and regulatory standards requirements for worldwide distribution. Designs methods and procedures for inspecting, testing and evaluating the precision and accuracy of production processes, production equipment and finished products. Performs analysis of reports and production data to identify trends and recommend updates or changes to quality standards and procedures when necessary. May ensure compliance to in-house and/or external specifications and standards (i.e. GLP, GMP, ISO, Six Sigma).

Works on problems of moderate scope where analysis of situations or data requires a review of a variety of factors. Exercises judgment within defined procedures and practices to determine appropriate action. Builds productive internal/external working relationships.

Essential Duties and Responsibilities:

The incumbent may be asked to perform other function-related activities in addition to the below-mentioned responsibilities as reasonably required by business needs.

• Write & Execute TMV's and Simple Change Orders (Simple Procedure updates, no validations required, clarifications, etc)
• Support Moderate to Complex Project Change Orders (validations, risk analysis updates, creation or major changes of SOP's/documents, etc)
• Write & Execute PQ's; Lead/Own CAPA's; Support HRA's/HHE's
• Model all quality values and coaches others on BSH quality system requirements and standards to elevate team's ability to produce high-quality products and implement best practices that emphasize defect prevention, reduction in variation and waste and provide for continuous improvement.
• Provide quality engineering support to Operations, Engineering and R&D in the design and manufacture of medical devices to ensure robust product builds and the production of high-quality products and manufacturing practices.
• Responsible for ensuring that the products produced meet applicable regulatory and quality standards and customer expectations.
• Develops and implements procedures, inspection procedures and test methods in compliance with QMS, Medical Device Quality System Regulation and Medical Device Directive requirements. Provides training as required.
• Acts with urgency to Identify and provide timely resolution to quality issues. Perform risk assessments and update risk management documentation as required.
• Perform customer complaint investigations, root cause investigations, root cause analysis, problem solving and corrective actions.
• Reviews technical publications, articles and abstracts to stay abreast of technical developments in the industry.
• Investigates and processes Quality System Investigations (QSI) and Non-Conforming Events (NCE).
• Prepares reports assessing the suitability and effectiveness of assigned areas of the quality system.
• Active participation in processes and meetings such as MRB, NCE, CAPA and SCAR process.
• Review and approve routine to moderately complex ECO’s product related change orders, engineering studies, sustaining engineering products, specifications, drawings, manufacturing procedures, design process verification and validation documentation.
• Active participant in facility and supplier audits and Notified Body and FDA inspections.

QUALIFICATIONS

Education

• Preferred Minimum Technical/Advanced Degree: Technical Bachelor’s Degree

Experience

• Preferred Minimum Technical/Advanced Degree: 1-2 Years with Technical Bachelor’s Degree, 0-2 Years with Master’s Degree
• Experience in an FDA regulated industry is beneficial.

Skills

• Excellent computer skills including ability to use word processing, spreadsheet programs and databases
• Excellent ability to read, analyze and interpret professional journals, technical procedures and government regulations.
• Excellent technical writing skills with ability to write quality assurance reports and details procedures
• Good presentation skills
• Good interpersonal skills to interact with all levels of the company, sometimes in an adversary role
• Knowledge of GMP and GDP Principles
• Working knowledge of medical device Quality System Regulations (21CFR820), ISO 13485 and MDD requirements is beneficial.
• Knowledge of microbiology, molecular biology, biochemistry, chemistry and/or related disciplines is beneficial.
• Understanding of nucleic acid amplification and detection technologies is beneficial.
• Understanding of Scientific Method and statistical analysis is beneficial.
• Knowledge of Oracle and Agile is beneficial.
• Certified Quality Engineer is beneficial.

Why join Hologic?

We are committed to making Hologic the destination for top talent. For you to succeed, we want to enable you with the tools and knowledge required and so we provide comprehensive training when you join as well as continued development and training throughout your career.

The annualized base salary range for this role is $78,000 - $100,000 and is bonus eligible. Final compensation packages will ultimately depend on factors including relevant experience, skillset, knowledge, education, business needs and market demand.

Agency and Third-Party Recruiter Notice

Agencies that submit a resume to Hologic must have a current executed Hologic Agency Agreement executed by a member of the Human Resource Department. In addition, Agencies may only submit candidates to positions for which they have been invited to do so by a Hologic Recruiter. All resumes must be sent to the Hologic Recruiter under these terms or they will not be considered.

Hologic, Inc. is proud to be an Equal Opportunity Employer inclusive of disability and veterans.