Lead Technician – QA Parenteral (Nights)

BioSpace; Durham (NC); On-site; Full time

Job summary

A leading company in the healthcare sector is seeking a Lead Technician – QA Parenteral for their Raleigh-Durham facility. This position involves overseeing QA operations, ensuring compliance with GMP standards, and providing daily support for production functions. Ideal candidates will have a background in pharmaceutical manufacturing and strong communication skills, looking to make a significant impact on patient safety.

Benefits

Comprehensive benefit program

401(k) and pension eligibility

Flexible benefits (e.g., healthcare spending accounts)

Employee assistance program

Qualifications

• Demonstrated relevant pharmaceutical experience in aseptic manufacturing.
• Experience in Production QA, QC is desirable.
• Experience with TrackWise Deviation and Change Management processes.

Responsibilities

• Responsible for maintaining a safe work environment and compliance with quality systems.
• Monitor GMP programs and documentation.
• Provide QA support to reconcile issues in multiple systems.

Skills

Strong attention to detail

Strong oral and written communication

Interpersonal skills

Education

High school diploma or equivalent

Associates degree in a science, engineering or pharmaceutical related field

Tools

TrackWise

SAP

PMX

Veeva

GMARS

Job description

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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 Quality Assurance Floor Support Team assures patients worldwide of safe and efficacious drug products, through effective quality oversight of Indianapolis Parenteral Operations activities.

The QA Floor Lead Tech is responsible for providing daily support and oversight to GMP operations in Raleigh-Durham North Carolina. The QA Floor Support Lead Tech works as a team member supporting multiple production functions (formulation, filling, and visual inspection), from operations to maintenance, to achieve site goals while providing Quality oversight and guidance.

Key Objectives/Deliverables

• Responsible for maintaining a safe work environment, working safely and accountable for supporting all HSE Corporate and Site Goals
• Provides daily presence in operational areas to:
• monitor GMP programs and quality systems and ensure adherence and understanding of good documentation practices and compliance with applicable procedures for both Operations and Support personnel.
• monitors for, retrieves, and completes review of all paperwork in need of quality review in each area supported and coordinates delivery to the associated area when complete.
• Supports visual inspection AQL inspection.
• Review and approve GMP documentation in support of daily operations such as:
• Cycle Summary Reports for equipment
• Electronic batch record initiation
• Daily documentation of quality on the floor oversight
• Maintenance action plans
• Return to Service and Release of equipment, product, and area HOLDs
• Work Order assessments and issue resolution
• Other documents as required
• Provide guidance and assistance in identifying potential product quality impact and assessing if Observations are required
• Performs observational requirements for Aseptic Process Simulation 14-Day Reads and supporting observation during formulation and fill related aseptic activities.

• Provide QA systems support to reconcile issues in multiple systems such as:
• SAP (inventory management)
• PMX (electronic batch record)
• TrackWise (compliance
• Veeva (controlled document repository)
• GMARS (calibration and maintenance system)
• And other systems as required
• Work within team to ensure all manufacturing areas receive QA support needed to maintain daily operations
• Reviews GMP documents (e.g., Procedures, Protocols, and Production Record Instructions)
  
  

Requirements (Education, Experience, Training)

• High school diploma or equivalent
• Demonstrated relevant pharmaceutical experience in aseptic manufacturing
• Associates degree in a science, engineering, computer, or pharmaceutical related field of study, preferred
• Strong oral and written communication and interpersonal skills
• Strong attention to detail
• Experience in Production QA, QC is desirable
• Experience in Visual Inspection is desirable
• Experience with TrackWise Deviation and Change Management processes
  
  
  

Additional Information

• This position will support a 24/7 operation, working a rotating twelve (12) hour night shift schedule. During the project and onboarding phase, role will work eight (8) hours Monday-Friday day shift, then transition to the rotating twelve (12) hour night shift stated above upon approval from Supervision/Management.
• 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 this employment position.
• Completion of Post Offer Exam or Completion of Work Simulation if applicable
• Maintain qualifications and certifications for access to all supported areas required of the position.
• Mandatory overtime may be required, planned and unplanned.
  
  
  

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

$28.12 - $46.88

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

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