Technician - Sterility Assurance TSMS (Day Shift)
Location: Durham
Posted on: June 23, 2025
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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. The Technician - Sterility
Assurance TSMS (Day Shift) role provides continuous support of the
parenteral operations to enhance and improve assurance of sterile
product manufacture. This role works closely with Operations and
Environmental Monitoring personnel during all aseptic production
activities and is responsible for addressing any sterility or
product quality related questions during manufacturing. The
Technician will work closely with cross-functional teams to address
all unplanned events within the classified areas that may require
remediation or aseptic interventions to be executed. You will be
expected to continue to develop a high level of expertise in
aseptic processing within TS/MS whilst supporting the RTP
Parenteral Facility. As designated by management, additional
support for qualification/validation activities or other routine
responsibilities within the TS/MS group could be assigned. Key
Objectives / Deliverables: The objective of the role is actively
coaching, auditing, and communicating within the Aseptic Processing
areas for the majority of shift. Must be an extension of Sterility
Assurance within the classified areas to monitor and reinforce best
aseptic practices. Ability to identify and report on events related
to the maintenance of aseptic conditions within clean rooms with a
focus on Sterility Assurance during manufacturing operations.
Promptly communicates with Operations regarding aseptic techniques
and behaviors of personnel. Gather, organize & analyze data to
develop solutions & alternative methods of proceeding compliantly.
Conduct periodic internal reviews or audits to ensure that
procedures are followed. Lead and organize remediation activities
from day-to-day unplanned events or shutdown activities. Lead,
coach and mentor personnel on aseptic techniques and practices
during manufacturing activities and when executing smoke studies or
other qualification activities. Correcting and communicating proper
aseptic technique when needed and communicating with supervisors as
needed on corrected behaviors. Be a point of contact for aseptic
operations and bioburden control Provide technical support for
non-routine investigations (e.g., deviations, complaints),
including the execution of required studies. Execute or assist in
qualification/validation activities to support the bioburden
control of the facility or equipment Support other routine
responsibilities with the TS/MS group, as assigned by management.
Ensure a safe working environment through compliance with safety
rules and improve safety culture by actively participating in
safety-related activities. Minimum Requirements: High school
diploma or GED Minimum 2 years of pharmaceutical experience
supporting cGMP manufacturing Experience with parenteral drug
product manufacturing Additional Preferences: Experience in aseptic
processing, environmental monitoring, microbiology, equipment
qualification and validation Ability to analyze data and solve
problems Demonstrated strong written and verbal communication
skills Previous experience with deviation and change management
systems, including Trackwise Previous experience with Kneat Strong
interpersonal and teamwork skills Strong self-management and
ability to work independently Oral and written communication skills
that demonstrate an ability to effectively communicate with all
levels of the organization Ability to effectively prioritize and
conduct a variety of tasks and requests Other Information: The
position is 12 hr. shifts on a 2-2-3 rotation. Must be flexible in
providing support to accommodate other inputs (production
schedules, shutdowns, etc.). Occasional extended hour and / or
off-hour work may be required. 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 $17.30 - $39.06
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
Keywords: , Greenville , Technician - Sterility Assurance TSMS (Day Shift), Manufacturing , Durham, North Carolina