Manager Regulatory Affairs

Medline Industries; Eagan (MN); Hybrid; USD 116,000 - 174,000; Full time

Benefits offered by this job

Health insurance

401(k) contributions

Paid time off

Life and disability

Job summary

Medline Industries is hiring a Manager Regulatory Affairs in Eagan, MN with a hybrid work model. The role oversees regulatory affairs for Medline product lines, guiding teams to develop and execute strategies for domestic and international approvals of medical devices.

The position requires a Bachelor's degree in Regulatory Affairs or related field and 4+ years of regulatory experience. SAP experience and 510(k)/CE filing know-how are preferred. Up to 15% travel may be required.

Qualifications

• Bachelor’s degree in Regulatory Affairs, Life Sciences or Engineering.
• At least 4 years of regulatory affairs experience for medical devices.
• Ability to lead regulatory filings and develop strategies for domestic and international approvals.

Responsibilities

• Guide regulatory decision-making based on medical device requirements.
• Lead regulatory filings with internal and external groups.
• Develop and implement regulatory processes for pre- and post-market activities.
• Communicate regulatory requirements to stakeholders and regulators.
• Monitor regulatory changes and adjust strategies accordingly.

Skills

Regulatory affairs

Regulatory strategy

Project management

Communication

SAP

510(k) preparation

FDA regulations

Microsoft Word

Microsoft Excel

Education

Bachelor's degree in Regulatory Affairs/Life Sciences/Engineering

Tools

SAP

Microsoft Word

Microsoft Excel

Job description

Job SummaryMedline Industries has an immediate opening for a Manager Regulatory Affairs at our Eagan, MI location. This role will work a hybrid work model. Oversee regulatory affairs for Medline product divisions.
Responsible for leading the Regulatory Affairs team to develop regulatory strategies for domestic and international approvals of medical devices. Provide leadership and develop Regulatory Affairs professionals.Job DescriptionMAJOR RESPONSIBILITIES:Guide regulatory and licensing decision-making processes based on relevant regulatory requirements of medical devices.Complete and maintain regulatory filings by leading internal groups, collaborating with external groups, providing direction to obtain supporting technical information, and implementing focused solutions for identified changes and challenges.Oversee the communication of regulatory requirements to internal or external customers. Lead communication with critical regulators to respond to non-conformances, deficiencies, and questions.Develop and implement processes and procedures to maintain regulatory compliance related to medical device pre and post market activities involving regulatory, R&D, quality and medical affairs.Monitor changes in the regulatory and legislative environment.Recommend regulatory pathways, strategies, solutions, and future actions for specific and diverse scenarios, accounting for business objectives and factors relevant to other departments/functional areasReview and provide direction to ensure supporting evidence meets appropriate regulatory requirements. Assess records against multiple requirements sources, including regulations, guidance documents, and standards utilized in various applicable markets that have been identified as applicable.Management responsibilities include:-Typically oversees professional employees/teams OR typically manages non-professional employees through Supervisors in manufacturing, distribution or office environments-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.MINIMUM JOB REQUIREMENTS:Education:Bachelor’s Degree in Regulatory Affairs, Life Sciences (e.g. biology, chemistry) or Engineering.Certification / Licensure:NoneWork Experience:At least 4 years of experience working in regulatory affairs for medical devices.Knowledge / Skills / Abilities:Ability to manage multiple projects and work in a fast paced, changing environment.Advance skills in Word and Excel.Strong understanding of medical device regulations for pre-market approvals/clearances for medical device. Understanding of post- market regulatory requirements of medical device.Skill and ability to diagnose, isolate, and resolve complex issues and recommend and implement strategies to resolve problems.Requires the ability to present and communicate with various audiences (e.g. senior management and non-technical audiences).Position requires up to 15% travelPREFERRED JOB REQUIREMENTS:Education:NoneCertification / Licensure:RAC Certification.Work Experience:Experience working with SAP.Knowledge / Skills / Abilities:Experience writing 510(k)s and CE technical files.Experience directly managing people including hiring, developing, motivating, and directing people as they work.Experience applying knowledge of EPA VOC, Prop 65, FIFRA, OSHA HAZCOM, CPSC, DOT, FDA, and/or VAWD.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:$116,000.00 - $174,000.00 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.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.