Demo

Deviation Mentor - Parenteral Manufacturing

Eli Lilly and Company
Indianapolis, IN Full Time
POSTED ON 3/17/2025
AVAILABLE BEFORE 4/8/2025

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.

Actual compensation will depend on a candidate’s education, experience, skills, and geographic location.  The anticipated wage for this position is

111,000 - $191,400

Organization Overview :

The Deviation Mentor is a member of the IPM Quality organization that educates, mentors and guides deviation investigations and analytical investigators.  The Deviation Mentor is also responsible for the training program associated to deviation system and may leads deviation review boards, participates in deviation assessment review pre-approval and post-approval. The Deviation mentor leads the site metrics related to deviation system. He / she can also lead complex investigations.  They participate in regulatory inspections and collaborate in the site inspection readiness program and assist and advice the lead investigators, functional leaders and Site Quality Leader and Quality Directors in issue investigation matters.

Responsibilities :

  • Provide advice and guidance to lead investigators in deviation investigation and analytical investigations (assessment, quality impact evaluation, root cause analysis method), investigation write-up (technical writing), support data, CAPA establishment and effectiveness.
  • Coach the deviation review board : review of deviations prior to deviation approval. Provide advice and assist deviation reviewers and approvers on issue investigation matters.
  • Owns the elaboration and reviews of deviation trend reports.
  • Facilitates the implementation of DRB Playbook at the plants and site level and connect plant / site metrics, trending and procedures with its implementation.
  • Establishes linkages with network and global teams and participate in relevant forums, such as global deviation CoP, ensuring the communication and implementation of best practices within the site.
  • Lead the review of the quality of deviation investigations (post-approval).
  • Design and elaborate site deviation metrics.  Participate in the review of plant deviation trend analysis.
  • Integrate global initiatives and / or projects related to the deviation management program into the site quality standards and processes.
  • Design and deliver deviations related to deviation management training programs.
  • Escalate concerns / issues and develop mitigation plans.
  • Trained as a lead investigator, deviation assessor and approver. Can act as a technical reviewer for deviation investigations and analytical investigations. Can approve deviation investigations, either as technical or quality approver, including minor and moderate deviations.
  • Can Lead complex investigations.
  • Ensures procedures, tools, and templates are in place (as applicable) for consistency and sustainability.
  • Participates on plat / site CAPA effectiveness program evaluation.
  • Ensures trends are timely identified and investigated to prevent recurrence.
  • Coach individuals on inspection interactions.
  • Collaborates in regulatory inspections, assisting in the preparation of key quality and compliance topics for audit and inspection readiness.
  • Responsible for maintaining a safe work environment, working safely and accountable for supporting all HSE Corporate and Site Goals.

Basic Requirements :

  • BSc or MSc in a scientific or technical degree (chemistry, biology, microbiology, engineering or equivalent scientific / technical degree).
  • 5 years of experience in deviation management and analytical investigation experience in pharmaceutical industry, parenteral manufacturing experience preferred.
  • Additional Skills / Preferences :

  • Experience in TS / MS, Engineering, QC and / or QA is preferred with expertise on parenteral products manufacturing.
  • Excellent technical writing skills.
  • Strong Influencing skills and interpersonal and teamwork skills.
  • Strong self-management and organizational skills.
  • Demonstrated successful cross-functional teamwork.
  • Critical thinking skills.
  • Good knowledge of cGMP, external Regulations and Quality Systems requirements.
  • Excellent communication skills.
  • Additional Information :

  • This is an onsite role based in Indianapolis, Indiana.
  • Travel (domestic and international) may be required (less than 10%).
  • 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 an EEO / Affirmative Action Employer and 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.

    Our employee resource groups (ERGs) offer strong support networks for their members and help our company develop talented individuals for future leadership roles. Our current groups include : Africa, Middle East, Central Asia Network, African American Network, Chinese Culture Network, Early Career Professionals, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinos at Lilly, PRIDE (LGBTQ Allies), Veterans Leadership Network, Women’s Network, Working and Living with Disabilities. Learn more about all of our groups.

    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 : $111,000 - $191,400

    If your compensation planning software is too rigid to deploy winning incentive strategies, it’s time to find an adaptable solution. Compensation Planning
    Enhance your organization's compensation strategy with salary data sets that HR and team managers can use to pay your staff right. Surveys & Data Sets

    What is the career path for a Deviation Mentor - Parenteral Manufacturing?

    Sign up to receive alerts about other jobs on the Deviation Mentor - Parenteral Manufacturing career path by checking the boxes next to the positions that interest you.
    Income Estimation: 
    $76,615 - $106,090
    Income Estimation: 
    $115,491 - $158,336
    Income Estimation: 
    $102,413 - $133,130
    Income Estimation: 
    $109,705 - $144,044
    Income Estimation: 
    $119,541 - $162,386
    Income Estimation: 
    $128,922 - $170,025
    Income Estimation: 
    $202,324 - $278,779
    Income Estimation: 
    $62,165 - $80,351
    Income Estimation: 
    $79,991 - $102,697
    Income Estimation: 
    $79,991 - $102,697
    Income Estimation: 
    $102,492 - $128,675
    Income Estimation: 
    $102,492 - $128,675
    Income Estimation: 
    $114,147 - $153,954
    View Core, Job Family, and Industry Job Skills and Competency Data for more than 15,000 Job Titles Skills Library

    Job openings at Eli Lilly and Company

    Eli Lilly and Company
    Hired Organization Address Indianapolis, IN Full Time
    At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare lea...
    Eli Lilly and Company
    Hired Organization Address Providence, RI Full Time
    At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare lea...
    Eli Lilly and Company
    Hired Organization Address Salt Lake, UT Full Time
    At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare lea...
    Eli Lilly and Company
    Hired Organization Address Indianapolis, IN Full Time
    At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare lea...

    Not the job you're looking for? Here are some other Deviation Mentor - Parenteral Manufacturing jobs in the Indianapolis, IN area that may be a better fit.

    Manufacturing Deviation Investigator

    i-Pharm GxP, Lebanon, IN

    AI Assistant is available now!

    Feel free to start your new journey!