Welcome to Abbott - a global healthcare company committed to improving lives through innovative technology and cutting-edge research. We are currently seeking a highly motivated and detail-oriented MLR Operations Specialist to join our team. As an MLR Operations Specialist, you will play a crucial role in ensuring the timely and accurate review of promotional materials in compliance with regulatory guidelines. This is an exciting opportunity to be a part of a dynamic team that is dedicated to making a positive impact on the healthcare industry. We are looking for someone with a strong background in MLR operations and a passion for driving operational excellence. If you are a self-starter with excellent communication skills, attention to detail, and a strong understanding of regulatory requirements, we encourage you to apply for this role and help us make a difference in patients' lives.
- Review and approve promotional materials in accordance with regulatory guidelines and company policies.
- Collaborate with cross-functional teams including marketing, legal, and regulatory to ensure timely and accurate review of materials.
- Maintain expertise in MLR processes and procedures and communicate changes and updates to relevant stakeholders.
- Identify and escalate potential compliance issues to the appropriate parties.
- Develop and maintain a thorough understanding of regulatory requirements and industry best practices.
- Provide guidance and training to team members on MLR processes and procedures.
- Manage and maintain the MLR database and track progress of promotional materials through the review process.
- Conduct quality checks on promotional materials to ensure accuracy and compliance.
- Coordinate and facilitate MLR meetings to review and discuss materials.
- Develop and implement process improvements to enhance efficiency and effectiveness of MLR operations.
- Generate reports and analyze data to identify trends and areas for improvement.
- Maintain confidentiality of sensitive information and adhere to data protection regulations.
- Communicate proactively with team members and stakeholders to ensure clear understanding of expectations and timelines.
- Stay updated on industry trends and changes in regulatory requirements to ensure compliance.
- Represent the company in a professional and ethical manner at all times.
Bachelor's Degree In Business Administration, Finance, Or A Related Field.
Minimum Of 3-5 Years Of Experience In Medical Device Or Pharmaceutical Industry, Preferably In A Regulatory Or Quality Role.
Knowledge Of Fda Regulations And Guidelines For Medical Devices And Drug Products.
Strong Attention To Detail And Ability To Work With Complex Data And Information.
Excellent Communication And Problem-Solving Skills, With The Ability To Work Independently And In A Team Environment.
Quality Assurance
Process Improvement
Communication Skills
Project Management
Data Analysis
Time Management
Technical Writing
Risk assessment
Regulatory compliance
FDA regulations
Documentation management
SOP Development
Communication
Conflict Resolution
Emotional Intelligence
Leadership
Time management
creativity
Attention to detail
Teamwork
Adaptability
Problem-Solving
According to JobzMall, the average salary range for a MLR Operations Specialist in Alameda, CA, USA is between $60,000 and $80,000 per year. The exact salary may vary depending on factors such as experience, qualifications, and the specific company or organization hiring for the position.
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From removing the regular pain of finger sticks as people manage their diabetes to connecting patients to doctors with real-time information monitoring their hearts, from easing chronic pain and movement disorders to testing half the world’s blood donations to ensure a healthy supply, our purpose is to make the world a better place by bringing life-changing health technologies to the people who need them. That’s our commitment to helping you live your best life.

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