Project Scheduler Position Available In McDowell, North Carolina

Job Description We are seeking a Project Scheduler to support the expansion of our medical device manufacturing facility. This role will work closely with Validation Engineers to develop and maintain project schedules, ensuring timely execution of validation activities, regulatory compliance, and seamless integration of new systems within the expanded site.

Key Responsibilities:

• Collaborate with Engineering personnel to align project schedules with validation protocols and regulatory requirements.
• Develop and maintain detailed timelines for site expansion activities, including equipment installation, commissioning, and qualification.
• Track progress, identify potential delays, and implement corrective actions to keep the expansion on schedule.
• Ensure compliance with FDA, ISO, and GMP regulations throughout the validation process.
• Coordinate with cross-functional teams (engineering, quality assurance, operations) to ensure smooth execution of expansion plans.
• Utilize Microsoft Project to create, update, and analyze project schedules.
• Experience with Smartsheet is preferred for enhanced project tracking and collaboration.
• Prepare reports and presentations on project milestones, risks, and resource allocation.
• Support risk management efforts by identifying scheduling conflicts and proposing solutions.

We are a company committed to creating inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity employer that believes everyone matters. Qualified candidates will receive consideration for employment opportunities without regard to race, religion, sex, age, marital status, national origin, sexual orientation, citizenship status, disability, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com . The EEOC “Know Your Rights” Poster is available here (https://www.eeoc.gov/sites/default/files/2023-06/22-088_EEOC_KnowYourRights6.12ScreenRdr.pdf) . To learn more about how we collect, keep, and process your private information, please review

Insight Global’s Workforce Privacy Policy:

https://insightglobal.com/workforce-privacy-policy/ . Skills and Requirements

• Bachelors degree in Engineering, Project Management, Business Administration, or a related field.
• 2+ years of experience in project scheduling
• Proficiency in Microsoft Project
• Strong understanding of validation processes, regulatory requirements, and quality standards.
• Excellent communication and organizational skills.
• Ability to work in a fast-paced, deadline-driven environment.
• Experience with Lean Manufacturing, Six Sigma, or Agile methodologies
• Master’s Degree or PMP Certification
• Experience in medical device manufacturing or a regulated industry
• Smartsheet null We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day.

We are an equal employment opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment without regard to race, color, ethnicity, religion,sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military oruniformed service member status, or any other status or characteristic protected by applicable laws, regulations, andordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to HR@insightglobal.com.