Label Project Coordinator II
West Point, Pennsylvania
Contract
$36.5/hr - $36.5/hr
Label Project Coordinator II
Job Summary:
The Label Project Coordinator II is responsible for identifying future tasks and engaging with relevant stakeholders. This role requires a deeper understanding of supply chain impacts. The Label Project Coordinator II will be responsible for reading, comprehending, and translating clinical trial protocols/packaging specifications into clinical label generation software. The Label Project Coordinator II will design clinical supplies trial labels for primary, secondary, and auxiliary packaging applications within the label systems. The Label Project Coordinator II will interpret randomization schemes, input into label software system, and utilize system to verify correct labels are produced according to cGMPs.
Key Responsibilities:
- Identify future tasks and engage with stakeholders for next steps.
- Collaborate with team members to ensure operational success.
- Maintain accurate documentation related to technical activities.
- Ensures all clinical supplies and associated documentation are processed according to GMPs/GDP's and appropriate safety requirements to meet exacting standards defined by the FDA and EU or other international regulatory agencies.
- May be responsible for any or all the following:
- Coordination of translation requests.
- Generation of clinical label content.
- Liaise with country-level Clinical Operations personnel or Regulatory Affairs to address questions, revise translations, update regulatory requirements, etc.
- Maintain label translations library.
- Interpret clinical study design and Clinical Supply Strategy (CSS).
- Design and verify label models.
- Coordinate MLBL manufacturing at vendors.
- Perform visual inspection and accountability for label proofs and clinical labels.
- Provide detailed analysis of issues and collaborate for creative problem solving.
- Liaise with Clinical Supply Project Managers, Quality, Pharmaceutical Sciences, or other stakeholders.
- May represent Clinical Packaging on internal or cross-functional teams. Will undertake and lead specific projects within the group on as needed basis.
- Participate as necessary in complaint and deviation investigations with a focus on true root cause, and creation of appropriate Corrective and Preventative actions (CAPA's). Drive CAPA's to closure.
- Train Label Project Coordinator Level I team members and remain proficient in appropriate systems and software.
- Responsible for the physical facility and good housekeeping practices within their area.
Qualifications: - Bachelor's degree preferred; candidates with relevant experience may be considered.
- 3+ years of experience in a related field; candidates without a degree should have 6+ years of relevant experience.
- Working knowledge of Packaging Operations and related work centers.
- Knowledge of general computer skills (i.e., MS Word, Excel, PowerPoint).
- Strong organizational and detail-oriented skills.
- Problem-solving and troubleshooting abilities.
- Interpersonal skills, including verbal and written communication.
- Understanding supply chain impacts and operational efficiency.
As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability.
As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan.
Click here for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.
