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Drug Safety & Product Complaint Associate

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world.

The purpose of the Drug Safety & Product Complaint Associate is to assist the local legal contact for Pharmacovigilance and the Lead Medical Shared Services to ensure legal duties are executed within the required timelines.

In addition, you will serve as a point of contact for Drug Complaints, compile complaints from Belgium and Luxembourg, coordinate follow-up and entry into complaints database and report issues as appropriate at affiliate level.

You will also support regulatory affairs activities including packaging development activities.

Job Responsibilities

1.Drug Safety

Responsible for optimizing the value of Lilly products through the promotion of patient safety, ensure training within the affiliate.

Handle, for Belgium and Luxembourg, Adverse Events Receipt and Data Collection, Case Management Quality Review, and submission of reports to Agency (Belgium/Luxembourg).

Coordinate the local implementation of risk minimization activities when these activities are included in Risk Management Plan.

Ensure Reporting within Belgian affiliate/Hub level.

2.  Product Complaint

Serve as point of contact for receipt and collection of product complaints.

Ensure the follow up of the complaint by identifying, retrieving, acknowledging the complaints information, collect follow-up, enter the complaint in global complaint database, coordinate and prepare the letters to customers. 

Keep local complaint database updated and ensure internal communication to responsible pharmacist/Complaint Coordinator.

3.  Medical Need Program (MNP)

Participate to the redaction of MNP submissions together with Medical Lead and other functions within the affiliate, communicate with the requesting HCP, and liaise with other department to ensure optimal delivery.

Calendar the periodic reports for Unmet Need division of FAMPH.

Ensure yearly evaluation of the ongoing programs.

4.  Labelling activities

Ensure and coordinate development, implementation and maintenance of printed packaging components for Lilly marketed products according to the legal requirements.

Create full and abbreviated (when applicable) versions of the approved labels, transmit them to relevant parties.

Support regulatory activities in connection with the regulatory regional team.

Qualification Requirements

Master degree (in health sciences is an advantage)

Good understanding of legal/deontological environment in drug safety and regulatory affairs

Demonstrated skills

Strong interpersonal skills, communication, teamwork, project management and pro-activity

Ability to execute tasks in parallel and prioritize broad deliverables

Proficiency in computer skills and database entry

Compliance with all procedural requirements

Demonstrated success in multi-tasking projects

Being customer-oriented service minded and pragmatic

Ability to work effectively and share information within a team environment

Fluent in Dutch and/or French, and English

What we offer

An exciting culture, based on respect for people, striving for excellence and high integrity

A work environment based on collaboration and team spirit

An occasion to be part of a continuous innovating company

The possibility to invest in your personal development

Have a high level of autonomy in your daily activities

A pharma competitive salary & benefit package

Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.

#WeAreLilly

Average salary estimate

$70000 / YEARLY (est.)
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$60000K
$80000K

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What You Should Know About Drug Safety & Product Complaint Associate, Lilly

Are you ready to make a difference? Join Lilly as a Drug Safety & Product Complaint Associate in the vibrant heart of Brussels, Belgium! At Lilly, we unite caring with discovery to create a better world for those in need. We are a global healthcare leader, dedicated to improving health outcomes and making life-changing medicines accessible. As a Drug Safety & Product Complaint Associate, your role will be pivotal in ensuring the safety and efficacy of our products. You’ll work closely with our Pharmacovigilance team and manage the local legal duties while being the go-to person for drug complaints in Belgium and Luxembourg. Your responsibilities will include compiling and entering complaints into our database, managing case quality reviews, and ensuring compliance with regulatory requirements. You'll also engage with healthcare professionals regarding unmet medical needs and coordinate critical labeling activities for our products to ensure they meet legal standards. To thrive in this role, a Master’s degree in health sciences or a related field is preferred, along with a solid understanding of the legal aspects of drug safety. Strong interpersonal skills, exceptional project management abilities, and proficiency in both Dutch/French and English are crucial. At Lilly, we foster a culture of respect, excellence, and autonomy where your input truly matters. You will not only be part of an innovative environment but also have numerous opportunities for personal development. If you’re passionate about making life better for people around the world, consider applying to join our dedicated team at Lilly!

Frequently Asked Questions (FAQs) for Drug Safety & Product Complaint Associate Role at Lilly
What are the main responsibilities of a Drug Safety & Product Complaint Associate at Lilly?

As a Drug Safety & Product Complaint Associate at Lilly, your primary responsibilities will include managing adverse event data collection, ensuring the quality review of case management, and coordinating product complaints. You'll also support labeling activities and engage with healthcare professionals regarding unmet medical needs, ensuring compliance with local regulations effectively.

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What qualifications are required to become a Drug Safety & Product Complaint Associate at Lilly?

To qualify for the Drug Safety & Product Complaint Associate position at Lilly, candidates typically need a Master's degree in Health Sciences or a related field. Additionally, a good understanding of the legal environment surrounding drug safety and regulatory affairs is necessary, along with strong communication skills and proficiency in Dutch/French and English.

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How does Lilly support employees in the Drug Safety & Product Complaint Associate role?

Lilly is committed to fostering a positive work environment for its employees. As a Drug Safety & Product Complaint Associate, you will benefit from a collaborative culture, autonomy in your daily activities, and access to personal development opportunities. This support aligns with Lilly's mission to provide the best care possible and enhance the professional growth of its team members.

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What skills are essential for success as a Drug Safety & Product Complaint Associate at Lilly?

Successful Drug Safety & Product Complaint Associates at Lilly must exhibit strong interpersonal and communication skills, effective project management abilities, and a proactive approach to tasks. Multitasking and prioritizing broad deliverables while maintaining compliance with procedural requirements will be key to thriving in this role.

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What is the work culture like at Lilly for a Drug Safety & Product Complaint Associate?

At Lilly, the work culture emphasizes respect for people, excellence, teamwork, and high integrity. Employees in the Drug Safety & Product Complaint Associate role will find a supportive and inclusive workplace where their contributions are valued and innovative thoughts are encouraged.

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Common Interview Questions for Drug Safety & Product Complaint Associate
Can you explain the drug safety process and how you would ensure compliance?

In the interview, emphasize your understanding of pharmacovigilance, rating adverse events, and following regulatory guidelines. Discuss your experience in documenting and reporting safety events to ensure adherence to compliance standards and demonstrate your expertise in managing drug safety.

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What strategies do you use to handle multiple tasks in a fast-paced environment?

Highlight your organizational skills and prioritize tasks based on deadlines and importance. You can share examples of how you've effectively managed multiple projects in previous roles, showcasing your ability to stay focused and maintain quality.

Join Rise to see the full answer
How do you approach customer complaints related to drug safety?

Explain your process for receiving and documenting complaints, emphasizing the importance of communication. Mention techniques you’ve used to follow-up with customers, ensuring they feel heard and reassured while you manage the investigation process.

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Describe your experience with regulatory submissions.

In your response, discuss specific experiences you’ve had with compiling and preparing documentation for regulatory agencies. Emphasize the importance of attention to detail and accuracy in these submissions and your ability to work within tight timelines.

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What is your understanding of risk management in drug safety?

Show that you have a solid grasp of risk management concepts, including risk analysis, mitigation strategies, and implementation in compliance with regulations. You can reflect on your experience with risk minimization activities and how it contributes to patient safety.

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How would you facilitate communication within a team when handling drug complaints?

Talk about the importance of open communication and ensuring everyone is on the same page. Share strategies for using internal tools or regular meetings to ensure that all team members are informed throughout the complaint handling process.

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Can you provide an example of a challenging situation you've resolved related to drug safety?

Use the STAR method to outline a specific challenge you faced, the actions you took, and the outcome. Discuss the steps you undertook to evaluate the situation critically and communicate effectively with stakeholders involved.

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Why are you interested in working for Lilly as a Drug Safety & Product Complaint Associate?

Express your admiration for Lilly’s commitment to improving lives through healthcare innovation. Explain how your skills align with the company’s values and objectives, showcasing your passion for contributing to a healthcare leader.

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How do you ensure accuracy in data entry for safety reports and complaints?

Discuss your meticulous approach to data entry, emphasizing practices such as double-checking information, using checklists, and maintaining organized records. Highlight any technology or software you’ve utilized to ensure data integrity.

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What steps would you take if you discovered a potential safety issue with a Lilly product?

Outline the protocol you would follow, including reporting the issue internally, collaborating with the necessary departments, and ensuring that the situation is handled with urgency and diligence, keeping patient safety as a priority.

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DATE POSTED
March 29, 2025

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