Job Description
Job Description
Job Posting : Project Manager
Location : Des Plaines, IL (onsite only)
Pay Rate : $50-$55 / hour
Duration : 1 Year with possible extension
Type : W2 Contract (Must be authorized to work in the US; no sponsorships available)
Overview : We are seeking a highly motivated Project Manager to join our client in Des Plaines, IL. This onsite role requires expertise in the pharmaceutical or medical device industries and a strong understanding of Design Control principles. The hiring manager is looking for a candidate who can start as soon as possible to contribute effectively to ongoing projects.
Responsibilities
- Design Control Management : Oversee the implementation of design control processes throughout the product development lifecycle, ensuring compliance with FDA regulations and ISO standards.
- Cross-Functional Collaboration : Work closely with R&D, quality assurance, regulatory affairs, and manufacturing teams to ensure alignment on project objectives and deliverables.
- New Product Development : Support the development of new products by utilizing industry best practices and methodologies, from concept through to commercialization.
- Documentation and Reporting : Maintain accurate project documentation, including design history files, risk management files, and validation protocols, and ensure timely reporting of project status to stakeholders.
- Creative Problem Solving : Apply innovative thinking to overcome challenges and streamline processes while maintaining compliance with internal and external requirements.
- Training and Mentorship : Provide guidance and training to team members on design control practices and project management methodologies, fostering a culture of continuous improvement.
- Project Management : Utilize project management tools to track progress, manage timelines, and ensure that project milestones are met efficiently.
Qualifications
Education : Bachelor’s Degree in business, engineering, science, information systems, or a closely related field is preferred.Experience : Minimum of 5 years of related work experience in the pharmaceutical or medical device industry, with a demonstrated track record of successful project management.Desirable : Master’s Degree (MBA or MS) is a plus but not essential.Certification : Project Management certification (e.g., PMP, CAPM) is preferred.Skills :Strong knowledge of new product development methodologies, including Design Thinking, Stage-Gate processes, and Agile methodologies.
Excellent problem-solving skills, with the ability to creatively achieve objectives while ensuring compliance with regulatory standards.Exceptional communication and collaboration skills to effectively liaise with cross-functional teams and stakeholders.Proven ability to manage multiple projects simultaneously, demonstrating strong organizational skills and attention to detail.Proficiency in project management software and tools (e.g., MS Project, JIRA, Trello) is advantageous.