QC - Environmental Monitoring Technician (Day Shift)

Eli Lilly and Company; Concord (NC); Vor Ort; USD 26.000 - 50.000; Vollzeit

Benefits dieser Stelle

401(k)

Pension

Vacation benefits

Medical, dental, vision

Flexible benefits

Life insurance

Time off and leave

Well-being benefits

Zusammenfassung

Eli Lilly and Company in Concord, NC is seeking a QC Environmental Monitoring Technician to support Parenteral Operations by performing environmental monitoring in classified manufacturing areas and utility sampling within Parenteral Operations and QC Laboratory buildings.

The role emphasizes training and mentoring of technicians, adherence to cGMP, and participation in continuous improvement projects as the site scales up its state-of-the-art manufacturing capabilities in a 12‑hour shift

Qualifikationen

• 3+ years of Environmental Monitoring in a GMP pharmaceutical facility.
• Experience with viable surface, air, water sampling and analysis.
• Experience with Laboratory IT systems (LIMS, LES, MODA).

Aufgaben

• Perform environmental monitoring in classified manufacturing areas.
• Conduct utility sampling and analysis in Parenteral Operations and QC Lab.
• Assist with training and mentoring QC Environmental Monitoring Technicians.
• Help author SOPs and work instructions.
• Support safety and cGMP compliance.

Kenntnisse

Environmental monitoring

GMP experience

Laboratory IT systems (LIMS, LES, MODA

Ausbildung

High School Diploma or equivalent

Associate Degree preferred

Tools

LIMS

LES

MODA

Jobbeschreibung

At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, selfless work—but it’s work worth doing. If you’re driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us.

Organization Overview:

Lilly is designing and building a new state of the art Parenteral, Device, and Packaging Assembly Facility in Concord, North Carolina. This is an exciting opportunity to help build a state-of-the-art facility and Quality System from the ground up. The Quality Control Laboratory assures patients worldwide receive safe and efficacious drug and drug/device combination products through effective execution of product testing.

Position Description:

The QC Environmental Monitoring Technician will provide support for Parenteral Operations by performing environmental monitoring of the classified manufacturing areas and by performing utility sampling and analysis within the Parenteral Operations and QC Laboratory buildings. The QC Environmental Monitoring Technician will assist the QC Environmental Monitoring management with training QC Environmental Monitoring Technicians and providing support in the manufacturing areas during routine environmental monitoring and utility sampling.

Key Objectives/Deliverables:

• Adhere to and promote compliance with all cGMP procedures, Quality Systems, and Good Documentation Practices.
• Provide support for Parenteral Operations activities by performing environmental monitoring of classified manufacturing areas.
• Provide support for manufacturing and laboratory activities by performing utility sampling and analysis within the Parenteral Operations and QC Laboratory buildings.
• Assist with technical training and mentoring of QC Environmental Monitoring Technicians through formal process/program.
• Participate in department/company continuous improvement projects and initiatives.
• Assist with authoring Standard Operating Procedures and Work Instruction documentation.
• Adhere to and promote compliance of all safety standards.

Minimum Requirements:

• Education
• High School Diploma or equivalent, Associate Degree is preferred.
• Experience
• 3+ years of demonstrated relevant experience in performing Environmental Monitoring in a GMP Pharmaceutical Manufacturing facility, preferably associated with aseptic production.
• Demonstrated ability in performing environmental monitoring techniques including, but not limited to viable surface monitoring, viable and non‑viable air monitoring, compressed air monitoring, and water (potable, purified water, water for injection, clean steam) collection and analysis.
• Previous experience with Laboratory IT systems such as LIMs, LES, and MODA.

Additional Preferences:

• Experience with cGMP requirements and regulatory compliance associated with a cGMP Manufacturing facility.
• Strong interpersonal skills and ability to train/mentor QC Environmental Monitoring Technicians.
• Strong oral and written communication skills for communicating to colleagues, management, and other departments.
• Ability to work in a lab environment including wearing appropriate PPE and other safety related equipment or considerations.
• Ability to gown into facility dedicated cleanroom attire, as required to perform job responsibilities.

Other Information:

• The role will be phased from a project support role to a routine support role as the development facility and processes progress.
• Tasks may require repetitive motion and standing or walking for long periods of time.
• Tasks may require lifting of up to 30 pounds and may require the ability to pass, push, and pull to execute specific aspects of the job role.
• Ability to work 12-hour shifts.Ability to have a flexible schedule as the position may require training or working on day/night shift for a short duration prior to transitioning to designated day/night shift.
• Travel will be required during the project phase for training and implementation of the Environmental Monitoring Program for the Concord site.

The job specification is intended to provide a general overview of the job requirements at the time it was prepared. The job requirements of any position may change over time and may include additional responsibilities not specifically described in the job specification.

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 (AMECA), Black Employees at Lilly (BE@Lilly), Chinese Culture Network (CCN), EnAble, Evolve, Lilly Indian Network (LIN), Organization of Latinx at Lilly (OLA), Pride (LGBTQ+ Allies), Veterans Leadership Network (VLN) and Women’s Initiative for Leading at Lilly (WILL).

Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is

$18.75 - $35.96

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,

• eligible 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
• 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.

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