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Printed Packaging Development Technical Lead
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Printed Packaging Development Technical Lead
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BioSpace
Organization Overview 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 Printed Packaging Development Team assures patients worldwide of safe and efficacious drug product labeling, through development of artwork to support product submissions, and production packaging on time and according to regulatory and technical requirements. The PPD Technical Lead is responsible for providing technical guidance for members of the PPD team, working with the Graphic Agencies for project support, daily support, and artwork project management for packaging – Indianapolis Device Assembly and Packaging (IDAP), Concord, Lilly Research Triangle Park (RTP) and Drug Product External Manufacturing (DPEM). The PPD Technical Lead works as a team member supporting multiple labeling functions to achieve timelines while providing BLUE project oversight and guidance.
Responsibilities
Responsible for maintaining a safe work environment, working safely, and accountable for supporting all HSE Corporate and Site Goals.
Provide technical expertise and coaching to PPD team members, packaging engineering, supply chain, regulatory, marketing and quality personnel to increase printed packaging development knowledge and to drive improved outcomes.
Work with cross‑functional teams to identify both local and global process improvement projects and drive solutions and implementation at the site.
Lead weekly priority meetings with PPD team members and external Graphic Agencies to ensure the highest quality of artwork electronic files, and ensure materials are delivered on time and according to specifications.
Represent PPD department on product launch teams, product planning teams, supply chain / customer service, third parties, regulatory, and global manufacturing teams to influence outcomes of complex regulatory, business, or technical issues.
Responsible for the management of BLUE projects, change controls and specifications following established cGMP processes and applicable procedures.
Coordinate communications with regulatory, quality, marketing, graphics, printer, and packaging to compile critical data (i.e., Regulatory Truth Copy, Branding / Country Specific Requirements and Technical Specifications), make key technical assessments and provide guidance ensuring printed materials are produced in compliance with cGMP.
Effectively utilize project management skills and available resources to prioritize and schedule work, ensuring all due dates and commitments are met.
Communicate status of artwork creation / revision with management, project teams, print vendors, graphics and PPD team members.
Education Requirements
Bachelor’s Degree in STEM field.
Basic Requirements
Strong technical skills related to packaging and / or printing.
Demonstrated relevant experience in a GMP facility.
Solid project management, organization, and scheduling skills.
Prior experience in pharmaceutical operations, packaging, cGMP quality control, printing, regulatory, or marketing.
Demonstrated strong interpersonal skills and the ability to work as a team, or independently.
Demonstrated ability to learn quickly, multi‑task, and utilize new skills.
Computer skills (MS Word, MS Excel, Adobe Acrobat, etc.).
Additional Skills/Preferences
Strong oral and written communication.
Ability to work with constant changes, time pressure, interruptions, and distractions.
Knowledge and application of operation systems: BLUE, SAP, Veeva, and TrackWise.
Additional Information
Position is first shift Monday through Friday, but off‑hours shift work may be required.
Occasional overtime may be required, planned and unplanned, including weekends.
Some travel may be required.
Training and qualification required and provided in the form of computer‑based training, standard operating procedure reviews and on‑the‑job training.
EEO Statement 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.
Salary and Benefits Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is $127,500 - $187,000. Full‑time equivalent employees will also 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.
Other Details Seniority Level: Mid‑Senior level
Employment Type: Full‑time
Job Function: Design, Art/Creative, and Information Technology
Industry: Internet News
#J-18808-Ljbffr
Printed Packaging Development Technical Lead
role at
BioSpace
Organization Overview 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 Printed Packaging Development Team assures patients worldwide of safe and efficacious drug product labeling, through development of artwork to support product submissions, and production packaging on time and according to regulatory and technical requirements. The PPD Technical Lead is responsible for providing technical guidance for members of the PPD team, working with the Graphic Agencies for project support, daily support, and artwork project management for packaging – Indianapolis Device Assembly and Packaging (IDAP), Concord, Lilly Research Triangle Park (RTP) and Drug Product External Manufacturing (DPEM). The PPD Technical Lead works as a team member supporting multiple labeling functions to achieve timelines while providing BLUE project oversight and guidance.
Responsibilities
Responsible for maintaining a safe work environment, working safely, and accountable for supporting all HSE Corporate and Site Goals.
Provide technical expertise and coaching to PPD team members, packaging engineering, supply chain, regulatory, marketing and quality personnel to increase printed packaging development knowledge and to drive improved outcomes.
Work with cross‑functional teams to identify both local and global process improvement projects and drive solutions and implementation at the site.
Lead weekly priority meetings with PPD team members and external Graphic Agencies to ensure the highest quality of artwork electronic files, and ensure materials are delivered on time and according to specifications.
Represent PPD department on product launch teams, product planning teams, supply chain / customer service, third parties, regulatory, and global manufacturing teams to influence outcomes of complex regulatory, business, or technical issues.
Responsible for the management of BLUE projects, change controls and specifications following established cGMP processes and applicable procedures.
Coordinate communications with regulatory, quality, marketing, graphics, printer, and packaging to compile critical data (i.e., Regulatory Truth Copy, Branding / Country Specific Requirements and Technical Specifications), make key technical assessments and provide guidance ensuring printed materials are produced in compliance with cGMP.
Effectively utilize project management skills and available resources to prioritize and schedule work, ensuring all due dates and commitments are met.
Communicate status of artwork creation / revision with management, project teams, print vendors, graphics and PPD team members.
Education Requirements
Bachelor’s Degree in STEM field.
Basic Requirements
Strong technical skills related to packaging and / or printing.
Demonstrated relevant experience in a GMP facility.
Solid project management, organization, and scheduling skills.
Prior experience in pharmaceutical operations, packaging, cGMP quality control, printing, regulatory, or marketing.
Demonstrated strong interpersonal skills and the ability to work as a team, or independently.
Demonstrated ability to learn quickly, multi‑task, and utilize new skills.
Computer skills (MS Word, MS Excel, Adobe Acrobat, etc.).
Additional Skills/Preferences
Strong oral and written communication.
Ability to work with constant changes, time pressure, interruptions, and distractions.
Knowledge and application of operation systems: BLUE, SAP, Veeva, and TrackWise.
Additional Information
Position is first shift Monday through Friday, but off‑hours shift work may be required.
Occasional overtime may be required, planned and unplanned, including weekends.
Some travel may be required.
Training and qualification required and provided in the form of computer‑based training, standard operating procedure reviews and on‑the‑job training.
EEO Statement 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.
Salary and Benefits Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is $127,500 - $187,000. Full‑time equivalent employees will also 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.
Other Details Seniority Level: Mid‑Senior level
Employment Type: Full‑time
Job Function: Design, Art/Creative, and Information Technology
Industry: Internet News
#J-18808-Ljbffr