Manager R&D

Medline; Northfield Township, Northern (IL, KY); On-site; USD 134,000 - 201,000; Full time

Benefits offered by this job

Health insurance

Life and disability insurance

401(k) contributions

Paid time off

Job summary

Medline is seeking a Manager of R&D to lead a team of Compliance Project Managers responsible for planning, executing, and monitoring enterprise quality and regulatory compliance initiatives in Northfield, IL. You will coordinate complex programs including post-market management, audit readiness, and manufacturing improvements.

You will provide leadership, governance, and project management expertise to ensure timely delivery of high-priority compliance objectives, while mentoring staff and

Qualifications

• Bachelor’s degree in Chemistry, Biology or related science field.
• At least 4 years of experience in a medical device or pharmaceutical related field.
• Experience in indirect management of team members, including development, training and assignment of work.
• Experience assessing and initiating actions independently.
• Experience coordinating and prioritizing multiple projects with varying deadlines.

Responsibilities

• Lead, mentor and develop a team of project managers to ensure deadlines and goals are met.
• Collaborate with divisional personnel, quality, regulatory, legal, and manufacturers to establish timelines and resources.
• Monitor progress of compliance initiatives and identify risks that could impact timelines or commitments.
• Lead escalation and issue resolution with senior leadership and sponsors.
• Facilitate alignment across total compliance initiatives to ensure holistic integration of corrective actions.

Skills

Leadership

Project Management

Cross-functional

Mentoring

Stakeholder management

Risk management

Regulatory understanding

Education

Bachelor’s degree in Chemistry, Biology or related science field

Job description

## Manager R&DApplyremote type: Hybridlocations: Northfield, Illinoistime type: Full timeposted on: Posted Todayjob requisition id: R2616081**Job Summary**Lead a team of Compliance Project Managers responsible for planning, executing, and monitoring enterprise quality and regulatory compliance initiatives. This role serves as the central coordination point for complex stainability programs, including product file updates, quality management processes, post market management, audit readiness, manufacturing enhancements and other strategic compliance projects. The Manager provides leadership, governance, and project management expertise to ensure successful execution of high-priority business and compliance objectives.**Job Description****MAJOR RESPONSIBILITIES:*** Lead, mentor and develop a team of project managers to ensure that deadlines and project goals are met.* Contribute to resource planning based on evolving organizational needs.* Collaborate with divisional personnel, quality, regulatory, legal, and manufacturers to develop timelines, identify necessary resources, and establish clear lines of communication to ensure successful execution.* Monitor progress of compliance initiatives and proactively identify risks that could impact timelines, deliverables, or regulatory commitments.* Lead escalation and issue resolution processes with senior leadership and project sponsors.* Facilitate alignment across total compliance initiatives to ensure holistic integration of corrective actions and communication**Management responsibilities include:*** Day-to-day operations of a group of employees.* May have limited budgetary responsibility and usually contributes to budgetary impact.* Interpret and execute policies for departments/projects and develops.* Recommend and implement new policies or modifications to existing policies. Provide general guidelines and parameters for staff functioning.* Hiring staff, recommending pay increases, performing performance reviews, training and development of staff, estimating personnel needs, assigning work, meeting completion dates, interpreting and ensuring consistent application of organizational policies.**Education:*** Bachelor’s degree in Chemistry, Biology or related science field.**Work Experience:*** At least 4 years of experience in a medical device or pharmaceutical related field.* Experience in the indirect management of team members, including assisting in the development, training and assignment of work/projects to other members of a team.* Experience assessing and initiating actions independently.* Experience taking charge of a situation, team or project.* Experience processing all relevant details, understanding and prioritizing their importance and drawing clear and concise conclusions.* Experience using time management skills such as prioritizing/organizing and tracking details and meeting deadlines of multiple projects with varying completion dates.**PREFERRED JOB REQUIREMENTS:*** PMP Certification* Experience supporting post market activities* At least 5 years of R&D experience in the healthcare industry.* Experience supervising and leading cross-functional teams.* Experience controlling and coordinating concurrent projects, competing priorities and critical deadlines.Medline Industries, LP, and its subsidiaries, offer a competitive total rewards package, continuing education & training, and tremendous potential with a growing worldwide organization.The anticipated salary range for this position:$134,000.00 - $201,000.00 AnnualThe actual salary will vary based on applicant’s location, education, experience, skills, and abilities. This role is bonus and/or incentive eligible. Medline will not pay less than the applicable minimum wage or salary threshold.Our benefit package includes health insurance, life and disability, 401(k) contributions, paid time off, etc., for employees working 30 or more hours per week on average. For roles where employees work less than 30 hours per week, benefits include 401(k) contributions, paid time off, as well as access to the Employee Assistance Program, Employee Resource Groups and the Employee Service Corp. For a more comprehensive list of our benefits please click here.We’re dedicated to creating a Medline where everyone feels they belong and can grow their career. We strive to do this by seeking diversity in all forms, acting inclusively, and ensuring that people have tools and resources to perform at their best. Explore our Belonging page here.Medline Industries, LP is an equal opportunity employer. Medline evaluates qualified individuals without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, age, disability, neurodivergence, protected veteran status, marital or family status, caregiver responsibilities, genetic information, or any other characteristic protected by applicable federal, state, or local laws.