What are the responsibilities and job description for the Associate Director - QA PR&D Quality System and Compliance position at BioSpace?
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.
Position Overview
The PR&D Quality System Associate Director provides critical leadership, oversight, and cross functional influence and integration to ensure that the processes and systems supporting the PR&D Quality System (QS) are well managed. The PR&D Quality System Associate Director partners cross functionally with the business to implement key quality projects, uphold quality standards and compliance to applicable regulations, and drive continuous improvement efforts within PR&D. The PR&D Quality System Associate Director is responsible for the overall leadership and management of the PR&D Quality System (QS), including the business processes supporting PR&D QS documents.
Responsibilities
Leadership and People Development
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 is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.
Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ Allies), Veterans Leadership Network (VLN), Women’s Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Learn more about all of our groups.
Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is
$118,500 - $173,800
Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly’s compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.
#WeAreLilly
Position Overview
The PR&D Quality System Associate Director provides critical leadership, oversight, and cross functional influence and integration to ensure that the processes and systems supporting the PR&D Quality System (QS) are well managed. The PR&D Quality System Associate Director partners cross functionally with the business to implement key quality projects, uphold quality standards and compliance to applicable regulations, and drive continuous improvement efforts within PR&D. The PR&D Quality System Associate Director is responsible for the overall leadership and management of the PR&D Quality System (QS), including the business processes supporting PR&D QS documents.
Responsibilities
Leadership and People Development
- Supervise a team that manages the PR&D QS documents through applicable preparation, review, approval, and maintenance processes necessary to meet business and compliance needs for PR&D.
- Elevate the team’s performance by setting clear goals and objectives and providing real time feedback, coaching/mentoring, career development, and succession management to staff.
- Ensure that staff is highly trained in the activities they execute in support of the PR&D QS including knowledge of the applicable cGXP expectations and requirements.
- Ensure the right organizational structure is in place for accomplishing goals, developing talent, and staffing to meet future needs by understanding and anticipating required future skills.
- Ensure the continuing integrity of the PR&D QS through effective management and execution of the document management processes and systems.
- Work with PR&D QA Leadership to continually re-evaluate the strategy and state of compliance of for PR&D QS. Proactively provide solutions to drive continuous improvement.
- Identify and measure quality metrics that are relevant and drive improvement.
- Lead/participate on teams and projects focused on efforts to improve systems and processes.
- Participate as a member of the PR&D Quality Lead Team(s) to ensure engagement with customer groups.
- Ensure PR&D QS is compliant with global quality standards and procedures and external regulations.
- Actively network internally and externally to expand knowledge of applicable technology, regulations, and best practices that ultimately drive continuous quality improvements throughout PR&D and drive a quality mindset.
- Support internal audits and external regulatory inspections.
- Bachelor’s degree in a scientific or medical related field or equivalent work experience.
- 7 years of QMS experience within the pharmaceutical industry.
- Experience in Quality, the business and supervision.
- Strong working knowledge of cGMP requirements and GCP regulations.
- Strong leadership and teamwork skills.
- Able to work and accomplish results through people.
- Solid judgement and initiative.
- Strong influence skills.
- Strong and effective written and verbal communication skills in cross functional settings and across different levels of the organization.
- Demonstrated change agent.
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 is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.
Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ Allies), Veterans Leadership Network (VLN), Women’s Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Learn more about all of our groups.
Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is
$118,500 - $173,800
Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly’s compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.
#WeAreLilly
Salary : $118,500 - $173,800
