Quality Assurance Process Team Device and Packaging – Associate Position Available In Merrimack, New Hampshire

Quality Assurance Process Team Device and Packaging Associate locations
US, Concord NC
time type
Full time
posted on
Posted 21 Days Ago
job requisition id
R81758
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 lifechanging 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 lifechanging 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 crossfunctional 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., H1B or TN status) for employment positions on the B or S paths or at levels M1M2 or P1P4.

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 (careers.lilly/us/en/workplaceaccommodation) 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
Fulltime 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 companysponsored 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 wellbeing 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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About Us
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