What are the responsibilities and job description for the Scientist - Visual Inspection (TS/MS, IPM) position at Lilly?
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 Brand Description:
Provide technical support to achieve the reliable and compliant manufacture of parenteral drug product to predetermined global quality standards via a detailed set of manufacturing instructions and procedures.
Key Objectives / Deliverables:
- Responsible for maintaining a safe work environment, leading safety initiatives, and working safely and accountable for supporting all HSE Corporate and Site Goals.
- Understand the scientific principles required for manufacturing parenteral drug products, including the interaction of the chemistry, equipment, aseptic processes, and container closure systems.
- Ensure that an accurate instruction set (tickets & procedures) and PFD describe the process as performed and the control strategy for the discrete manufacturing steps.
- Develop, monitor, and appropriately react to established statistically based metrics in real - time to assess process variability and capability.
- Understand, justify, and document the state of validation (process and cleaning, sterility assurance, etc.) with data that evaluate the capability of the manufacturing process to meet its stated purpose.
- Prepare, review, approve, and provide technical support for preparation of relevant technical documents, as required, such as: change controls, regulatory submissions, deviation investigations, validation protocols and summary reports, processing records, procedures, PFDs, VMPs, APRs, QPPAs, etc. Participate in development and implementation of process improvements, including capital expansions and technical projects. Work within or lead cross - functional teams in positive fashion to implement TS/MS objectives and deliver on business plan and quality objectives.
- Support and / or lead technical projects (experimental, modeling and / or production data analysis) to improve process control, yield, purity, and / or productivity.
Basic Requirements:
- Bachelors in scientific disciplines of Biochemistry, Chemistry, Microbiology, Pharmacy, Engineering or other related field.
- Minimum 1 year of experience directly supporting pharmaceutical manufacturing or quality, with experience in aseptic manufacturing preferred.
Additional Preferences:
- Experience in Visual Inspection of injectable products preferred.
- Technical / Scientific knowledge
- Good written and oral communications
- Clear understanding of cGMPs
- Teamwork and interpersonal skills
- Computer skills.
- Decision making
- Multi - tasking
- Ability to influence groups and communication skills
- Problem solving
- Teamwork and interpersonal
- Good written and oral communications
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
$64,500 - $143,000Full-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.
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Salary : $64,500 - $143,000