Data Coordinator

Data Coordinator


Job ID: 9670381

West Chester, OH, US

Office

High School or equivalent

Full Time, Temp to Hire

Entry Level

On-site

Biotechnology/Pharmaceuticals

First Shift (Day)

West Chester, OH, US

Entry Level

Full Time, Temp to Hire

Biotechnology/Pharmaceuticals

On-site

Office

High School or equivalent

First Shift (Day)

Job details

Data Coordinator
Location: West Chester, OH
Shift: 1st Shift, 8:30 AM – 5:00 PM (Monday – Friday)
Hourly Rate: $24 per hour
Type: Temp to Hire


Position Overview:
The Data Coordinator will execute tasks related to controlled document management within the Quality department, ensuring proper documentation practices and compliance with company and regulatory standards.

Essential Job Functions:

  • Perform data entry tasks and maintain accurate records.

  • Prepare and document activities, actions, and results.

  • Complete required training and ensure adherence to documentation practices.

  • Gather, organize, and communicate operational information effectively.

  • Write, review, and revise Standard Operating Procedures (SOPs) for area equipment, systems, and processes.

  • Collaborate with site functions to ensure documentation is compliant with organizational and local requirements.

  • Work within cross-functional teams to achieve shared goals.

  • Strong organizational skills and attention to detail.

  • Communicate any issues related to the document management system to management.

  • Attend team meetings to provide updates on progress and initiatives.

  • Able to multitask, work independently, and stay focused on tasks for extended periods.

Other Duties:

  • Uphold and communicate organizational and departmental policies and procedures.

  • Communicate priorities and progress to the team regularly.

Minimum Requirements:

  • High school diploma or equivalent.

  • At least 2 years of experience in data and documentation management in a regulated or cGMP environment.

  • Proficient in Microsoft Word.

Preferred Qualifications:

  • 2 years of experience in manufacturing within a regulated or cGMP environment.

Interested? Send resume to Dans465@kellyservices.com to be considered, or use this link to schedule directly on my calendar https://calendly.com/dans465

9670381

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