Quality Assurance Process Team Device and Packaging - Associate at Lilly

Concord, North Carolina, United States -

Full Time

Start Date

Immediate

Expiry Date

07 Mar, 26

Salary

162800.0

Posted On

07 Dec, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Quality Assurance, Leadership, Teamwork, Deviation Management, Change Control, Procedure Updates, Commissioning, Qualification Activities, Technical Writing, Computer Systems Validation, Manufacturing Execution Systems, Regulatory Knowledge, Communication Skills, Mentoring, Continuous Improvement, Quality Metrics

Industry

Pharmaceutical Manufacturing

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 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. Responsibilities: The Quality Assurance Process team member is responsible for demonstrating leadership, teamwork, and quality knowledge on a day to day basis. They are responsible to lead, mentor, and coach operations and support personnel on quality matters. They will provide support on deviations, change controls, procedure updates, commissioning, and qualification activities. This role will have a regular presence in the operational areas to monitor and confirm execution according to quality standards. This role will participate on the local process team for one of following manufacturing areas: Device Assembly Packaging Project Focus for DAP Responsibilities include: Active presence in operational areas Provide quality oversight for the verification and qualification of the manufacturing equipment, buildings, including review of test cases, test execution, discrepancy resolution, etc. Provides guidance for leveling, resolving, reviewing and approving deviations and change controls Demonstrate a comprehensive understanding of the process and its associated equipment, facilities, computer systems and operations Lead and establish annual quality floor time plan Support resolution of batch documentation such as alarm response, exceptions, etc Support asset qualification monitoring reviews and reports May be required to respond to operational issues outside of core business hours / days. Attend and provide update on quality at daily process team meeting Support the site organization in building technical capability, in Quality, the project team, and area process teams, including mentoring and training of new Quality staff Resolve or escalate any compliance issues to Quality Management Identify and implement continuous improvements Measure, maintain, and achieve quality metrics Serve as positive role models for their Process Team peers and for the organization in general Basic Requirements: Bachelors or equivalent degree in a scientific field 4+ years’ experience in Quality pharmaceutical manufacturing required Previous experience with C&Q / Verification and Validation oversight including automation and computer systems validation Use process knowledge and control strategy to make quality decisions Demonstrated knowledge and use of US, EU, Japan and other regulations in the area of pharmaceutical manufacturing Demonstrated ability to communicate with cross-functional teams including good oral and written communication skills Ability to work independently as a Quality SME with minimal supervision Proficiency with computer systems including SAP, Trackwise, MES etc. Responsible for maintaining a safe work environment, Ability to work 8 hour shifts onsite (not eligible for remote work) Ability to work overtime as required Qualified candidates must be legally authorized to be employed in the United States. Lilly does not anticipate providing sponsorship for employment visa status (e.g., H-1B or TN status) for employment positions on the B or S paths or at levels M1-M2 or P1-P4. Additional Skills/Preferences: ASQ Certified CSQA experience Previous experience with device assembly or packaging, Previous experience with Manufacturing Execution Systems. Previous use of KNEAT – or other electronic validation software Previous technical writing experience 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 $63,000 - $162,800 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 At Lilly we strive to ensure our employees are part of a team that cares about them and our shared purpose of making life better for those around the world. How do we do this? We continue to look for ways to include, innovate, accelerate and deliver while maintaining integrity, excellence and respect for people. We hope that you seek to join us on our journey as we create medicine and deliver improved outcomes for patients across the globe! #WeAreLilly

Responsibilities

The Quality Assurance Process team member is responsible for leading and mentoring personnel on quality matters while providing oversight for manufacturing equipment and processes. They will also participate in daily process team meetings and support compliance and continuous improvement initiatives.