3 Manufacturing jobs in Mallow
Sr. Scientist Technical Services/Manufacturing Science API-EM

Kinsale, Munster
Lilly
Posted 2 days ago
Job Viewed
Job Description
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. **Organization Overview:** Join the energetic and growing Active Pharmaceutical Ingredient - External Manufacturing Organization (API-EM) that delivers a diverse portfolio of medicines essential to our patients around the world. The API-EM TS/MS (Technical Services / Manufacturing Science) Sr. Scientist will provide technical and scientific expertise within a dynamic external manufacturing environment. The Sr. Scientist is responsible for providing technical support to achieve the reliable and compliant manufacture of API drug substance at external contract manufacturing groups to predetermined global quality standards. This person interacts daily with a wide variety of people, primarily external partners team members and site management. The candidate will be responsible for process monitoring, response to issues, and improvements where necessary. A strong understanding of manufacturing principles and Lilly systems is required to ensure those same standards are applied to the external contract manufacturers. This is a Large Molecule (mAb and ADC) position. The position requires knowledge of cGMPs, applicable global regulatory manufacturing guidance, and the corporate/industry standards. The position requires working cross-functionally within the site and other functions to deliver on technical objectives. **Responsibilities:** + Provide technical oversight for monoclonal antibody and antibody drug conjugate manufacturing processes. + Leads resolution of technical issues including those related to control strategy and manufacturing. + Employ excellent communication skills to manage internal and external relationships. + Build and maintain relationships with development and central technical organizations. + Ensure proper characterization of processes and products and ensure effective documentation of the process description, measures, acceptable ranges, and specifications (and the justification of these measures, acceptable ranges, and specifications). + Ensure that processes are compliant, capable, in control, and maintained in a validated or qualified state. + Understand, justify and document the state of validation with data that evaluate the capability of the manufacturing process to meet its stated purpose. + Influence and implement the network technical agenda and drive continuous improvement. + Maintaining mAb and ADC processes in a state of compliance with US and global regulations + Understanding the scientific principles required for manufacturing intermediates and drug substances, including the interaction of chemistry and equipment. + Operate with 'Team Lilly' in mind - including coaching and mentoring of peers and other scientists. **Basic Requirements:** + Bachelors in scientific disciplines of Biotech, Chemistry, Biochemistry, Biology, Pharmacy, or Engineering (Biotech/Biochemistry strongly preferred) + 3+ years of demonstrated hands on working experience and proficiency with pharmaceutical manufacturing and working knowledge of regulatory expectations. **Additional Preferences:** + Strong understanding of regulatory requirements and their application in a manufacturing environment + Proficient in data management practices across manufacturing operations + Demonstrates adaptability, a collaborative mindset, and a positive attitude toward change + Proven ability to effectively communicate and influence across diverse technical and business teams + Skilled in managing and delivering complex, cross-functional initiatives + Demonstrated project management expertise with a track record of coordinating and executing multifaceted projects **Additional Information:** + Some travel (<25%) is required + Some off-shift work (night/weekend) may be required to support 24/7 operations. 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 ( ) 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 - $167,200 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
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0
Sr. Director - Technical Services & Manufacturing Sciences (TSMS) - Tech Transfer

Kinsale, Munster
Lilly
Posted 2 days ago
Job Viewed
Job Description
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.
**Organization Overview:**
At Lilly, we serve an extraordinary purpose. We make a difference for people around the globe by discovering, developing and delivering medicines that help them live longer, healthier, more active lives. Not only do we deliver breakthrough medications, but you also can count on us to develop creative solutions to support communities through philanthropy and volunteerism
**Position Summary:**
The Senior Director of TSMS - Tech Transfer is a strategic leadership role within the central TSMS organization, responsible for leading global technical teams in the successful transfer of drug substance and dry oral products (including SDD) processes across internal and external manufacturing sites. This role ensures consistent execution of Lilly's commercialization strategy, drives technical excellence, and fosters collaboration across development, manufacturing, and regulatory functions.
**Key Responsibilities:**
**Tech Transfer Leadership**
+ Lead organization of TSMS technical experts on global tech transfer teams supporting both the initial commercialization of pipeline products and node to node transfers of commercial products across the drug substance and dry products portfolio.
+ Responsible for the development of standardized business processes and Playbooks to support global tech transfers across multiple platforms and multiple sites (including simultaneous transfers to dual sourcing sites).
+ Ensure alignment of Playbooks with Single Process Map deliverables and ensure buy-in from BR&D/SMDD and Analytical (AQCL) on generation of standardized business processes.
+ Ensure the team is appropriately structured to own and continuously improve Tech Transfer Playbooks and associated training programs.
+ Ensure consistency in technical deliverables and documentation across transfers.
**Strategic & Portfolio Management**
+ Partner with CMC PMs and development teams to guide tech transfer execution using Lilly's Single Process Map.
+ Co-own commercialization playbooks with Commercialization and Molecule Stewards.
+ Ensure adequate staffing and capability of tech transfer teams.
+ Provide escalation and troubleshooting support for complex tech transfer challenges.
**Organizational Leadership**
+ Represent TSMS at governance bodies and technical network meetings.
+ Build relationships and influence across manufacturing sites and central functions.
+ Lead performance management, talent development, and succession planning.
+ Mentor and coach project managers and technical leaders in commercialization and tech transfer.
**Qualifications:**
**Education**
+ Minimum: B.S. in Chemistry, Pharmacy, Engineering, or related scientific discipline.
+ Preferred: Master's or Ph.D. in Pharmaceutical Sciences, Biochemistry, Chemical Engineering, or Microbiology.
**Experience**
+ 15+ years in pharmaceutical manufacturing or technical services within a cGMP environment.
+ 5+ years of experience in drug substance or dry product tech transfer and commercialization.
+ Proven leadership in cross-functional teams and successful molecule transfers.
+ Deep technical knowledge of parenteral products and control strategies.
**Skills & Competencies**
+ Strong project management and strategic planning skills.
+ Excellent communication and stakeholder engagement.
+ Ability to influence across sites and central functions.
+ Experience mentoring and developing technical talent.
**Additional Information:**
Some domestic and international travel may be required.
This role is part of the TSMS leadership team and contributes to long-term business planning and organizational capability 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 ( ) 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
$151,500 - $244,200
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
**Organization Overview:**
At Lilly, we serve an extraordinary purpose. We make a difference for people around the globe by discovering, developing and delivering medicines that help them live longer, healthier, more active lives. Not only do we deliver breakthrough medications, but you also can count on us to develop creative solutions to support communities through philanthropy and volunteerism
**Position Summary:**
The Senior Director of TSMS - Tech Transfer is a strategic leadership role within the central TSMS organization, responsible for leading global technical teams in the successful transfer of drug substance and dry oral products (including SDD) processes across internal and external manufacturing sites. This role ensures consistent execution of Lilly's commercialization strategy, drives technical excellence, and fosters collaboration across development, manufacturing, and regulatory functions.
**Key Responsibilities:**
**Tech Transfer Leadership**
+ Lead organization of TSMS technical experts on global tech transfer teams supporting both the initial commercialization of pipeline products and node to node transfers of commercial products across the drug substance and dry products portfolio.
+ Responsible for the development of standardized business processes and Playbooks to support global tech transfers across multiple platforms and multiple sites (including simultaneous transfers to dual sourcing sites).
+ Ensure alignment of Playbooks with Single Process Map deliverables and ensure buy-in from BR&D/SMDD and Analytical (AQCL) on generation of standardized business processes.
+ Ensure the team is appropriately structured to own and continuously improve Tech Transfer Playbooks and associated training programs.
+ Ensure consistency in technical deliverables and documentation across transfers.
**Strategic & Portfolio Management**
+ Partner with CMC PMs and development teams to guide tech transfer execution using Lilly's Single Process Map.
+ Co-own commercialization playbooks with Commercialization and Molecule Stewards.
+ Ensure adequate staffing and capability of tech transfer teams.
+ Provide escalation and troubleshooting support for complex tech transfer challenges.
**Organizational Leadership**
+ Represent TSMS at governance bodies and technical network meetings.
+ Build relationships and influence across manufacturing sites and central functions.
+ Lead performance management, talent development, and succession planning.
+ Mentor and coach project managers and technical leaders in commercialization and tech transfer.
**Qualifications:**
**Education**
+ Minimum: B.S. in Chemistry, Pharmacy, Engineering, or related scientific discipline.
+ Preferred: Master's or Ph.D. in Pharmaceutical Sciences, Biochemistry, Chemical Engineering, or Microbiology.
**Experience**
+ 15+ years in pharmaceutical manufacturing or technical services within a cGMP environment.
+ 5+ years of experience in drug substance or dry product tech transfer and commercialization.
+ Proven leadership in cross-functional teams and successful molecule transfers.
+ Deep technical knowledge of parenteral products and control strategies.
**Skills & Competencies**
+ Strong project management and strategic planning skills.
+ Excellent communication and stakeholder engagement.
+ Ability to influence across sites and central functions.
+ Experience mentoring and developing technical talent.
**Additional Information:**
Some domestic and international travel may be required.
This role is part of the TSMS leadership team and contributes to long-term business planning and organizational capability 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 ( ) 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
$151,500 - $244,200
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
This advertiser has chosen not to accept applicants from your region.
1
Senior Director - Technical Services & Manufacturing Sciences (TSMS) - Technical Agenda

Kinsale, Munster
Lilly
Posted 2 days ago
Job Viewed
Job Description
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 Summary**
The Senior Director of TSMS - Technical Agenda is a strategic leadership role within the central TSMS organization, responsible for shaping and delivering the technical agenda across the Drug Substance and Dry Product portfolio. This role will drive a focused effort on delivering critical technical agenda projects and initiatives at a product basis through a team of Associate Directors responsible for laboratories and Pilot Plants across the platforms of biologics and synthetic products. The Senior Director will lead technical experts, drive innovation and technical excellence, and ensure alignment with Lilly's commercialization strategy, manufacturing productivity agenda and evolving API/Dry Network needs.
**Key Responsibilities**
**Strategic Leadership & Technical Direction**
+ Drive generation of technical agenda for products/processes with PR&D minimally on a biannual basis (Strategic Plan and Business Plan) through purposeful workshops to ensure active hopper of projects and initiatives.
+ From collaborative workshops, define the technical agenda for drug substance and dry products, including Spray Dry Dispersion/DP intermediates, and other innovation platforms.
+ Using prioritization tools, present and gain alignment on the technical agenda priority project through the ADN -LT, utilizing the Commercialization Lead Team as the decision forum.
+ Lead strategic planning for development and execution of tertiary loop/technical agenda projects and significant and impactful process optimization projects.
+ Use internal lab and Pilot Plant resources to deliver initial proof of concept (PoC) studies to support direction of tech agenda. Maximize internal resourcing, and where necessary use external capability/capacity to achieve full development package (process definition and data) to point of readiness for technology transfer to commercial sites. Where necessary, de-risk tech transfer and PV of the optimized process, by orchestrating Pilot scale batches.
+ Drive the completion of technology transfer package for implementation of the tech agenda at the manufacturing sites.
**Organizational Leadership**
+ Lead a global team of Associate Directors (responsible for scientists/specialists/ operators) and technical experts supporting execution of technical agenda across drug substance, dry product and drug product intermediates.
+ Build and maintain strong technical relationships at a Senior Director level with BR&D, SMDD, and manufacturing sites.
+ Work closely with Molecule Stewards, Product Leads in developing and delivering technical agenda across products.
+ Serve as the initial point of escalation for technical issues across the lab/Pilot Plant programs.
+ Drive performance management, talent development, and succession planning.
+ Foster a culture of innovation, collaboration, and continuous improvement.
+ Represent TSMS at governance bodies and technical network meetings.
**Change Management & Transformation**
+ Support organizational redesign efforts to align with Lilly's centralization strategy.
+ In consultation with TSMS AVP - Synthesis/TIDES, and AVP - Biologics, and in collaboration with Fellows team, support the setting up of appropriate teams responsible for Tech Agenda development and and execution.
+ Lead integration of impacted teams into the central TSMS structure.
+ Communicate effectively during transitions, ensuring clarity and support for affected employees.
**Qualifications**
**Education**
Minimum: BSc in a science, engineering, or technical field.
Preferred: MSc or Ph.D. in Pharmaceutical Sciences, Biochemistry, Chemistry, Chemical Engineering, or Microbiology.
**Experience**
+ 10+ years in pharmaceutical manufacturing or technical services within a cGMP environment.
+ Proven leadership in managing technical teams and delivering strategic initiatives.
+ Experience in drug substance development, dry product formulation and regulatory support.
**Skills & Competencies**
+ Strong strategic thinking and decision-making capabilities.
+ Excellent communication and stakeholder management skills.
+ Deep technical expertise in drug substance manufacturing and commercialization.
+ Ability to lead through change and build high-performing teams.
**Additional Information**
This role may require occasional travel to Lilly sites, external partners, or industry conferences.
The position is part of the TSMS leadership team and contributes to long-term business planning and organizational capability 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 ( ) 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
$151,500 - $222,200
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 Summary**
The Senior Director of TSMS - Technical Agenda is a strategic leadership role within the central TSMS organization, responsible for shaping and delivering the technical agenda across the Drug Substance and Dry Product portfolio. This role will drive a focused effort on delivering critical technical agenda projects and initiatives at a product basis through a team of Associate Directors responsible for laboratories and Pilot Plants across the platforms of biologics and synthetic products. The Senior Director will lead technical experts, drive innovation and technical excellence, and ensure alignment with Lilly's commercialization strategy, manufacturing productivity agenda and evolving API/Dry Network needs.
**Key Responsibilities**
**Strategic Leadership & Technical Direction**
+ Drive generation of technical agenda for products/processes with PR&D minimally on a biannual basis (Strategic Plan and Business Plan) through purposeful workshops to ensure active hopper of projects and initiatives.
+ From collaborative workshops, define the technical agenda for drug substance and dry products, including Spray Dry Dispersion/DP intermediates, and other innovation platforms.
+ Using prioritization tools, present and gain alignment on the technical agenda priority project through the ADN -LT, utilizing the Commercialization Lead Team as the decision forum.
+ Lead strategic planning for development and execution of tertiary loop/technical agenda projects and significant and impactful process optimization projects.
+ Use internal lab and Pilot Plant resources to deliver initial proof of concept (PoC) studies to support direction of tech agenda. Maximize internal resourcing, and where necessary use external capability/capacity to achieve full development package (process definition and data) to point of readiness for technology transfer to commercial sites. Where necessary, de-risk tech transfer and PV of the optimized process, by orchestrating Pilot scale batches.
+ Drive the completion of technology transfer package for implementation of the tech agenda at the manufacturing sites.
**Organizational Leadership**
+ Lead a global team of Associate Directors (responsible for scientists/specialists/ operators) and technical experts supporting execution of technical agenda across drug substance, dry product and drug product intermediates.
+ Build and maintain strong technical relationships at a Senior Director level with BR&D, SMDD, and manufacturing sites.
+ Work closely with Molecule Stewards, Product Leads in developing and delivering technical agenda across products.
+ Serve as the initial point of escalation for technical issues across the lab/Pilot Plant programs.
+ Drive performance management, talent development, and succession planning.
+ Foster a culture of innovation, collaboration, and continuous improvement.
+ Represent TSMS at governance bodies and technical network meetings.
**Change Management & Transformation**
+ Support organizational redesign efforts to align with Lilly's centralization strategy.
+ In consultation with TSMS AVP - Synthesis/TIDES, and AVP - Biologics, and in collaboration with Fellows team, support the setting up of appropriate teams responsible for Tech Agenda development and and execution.
+ Lead integration of impacted teams into the central TSMS structure.
+ Communicate effectively during transitions, ensuring clarity and support for affected employees.
**Qualifications**
**Education**
Minimum: BSc in a science, engineering, or technical field.
Preferred: MSc or Ph.D. in Pharmaceutical Sciences, Biochemistry, Chemistry, Chemical Engineering, or Microbiology.
**Experience**
+ 10+ years in pharmaceutical manufacturing or technical services within a cGMP environment.
+ Proven leadership in managing technical teams and delivering strategic initiatives.
+ Experience in drug substance development, dry product formulation and regulatory support.
**Skills & Competencies**
+ Strong strategic thinking and decision-making capabilities.
+ Excellent communication and stakeholder management skills.
+ Deep technical expertise in drug substance manufacturing and commercialization.
+ Ability to lead through change and build high-performing teams.
**Additional Information**
This role may require occasional travel to Lilly sites, external partners, or industry conferences.
The position is part of the TSMS leadership team and contributes to long-term business planning and organizational capability 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 ( ) 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
$151,500 - $222,200
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
This advertiser has chosen not to accept applicants from your region.
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