QC Associate I

Astrix; Wilmington (OH); On-site; Full time

Job summary

A leading company in the pharmaceutical sector is seeking a QC Associate I to join their team in Wilmington, OH. This entry-level position offers a competitive hourly wage and the chance to make a meaningful impact in quality control processes. The role involves sampling, inspection, and documentation, with opportunities for career growth and development in a supportive environment.

Qualifications

• Minimum of 1 year’s experience in a pharmaceutical or regulated industry preferred.
• Experience with LIMS and documentation processes is beneficial.
• Entry-level position with opportunities for growth.

Responsibilities

• Follow procedures for sampling and inspection.
• Log samples into LIMS and verify labeling.
• Identify non-conforming materials and assist in investigations.

Skills

Attention to Detail

Problem Solving

Documentation Review

Education

Associate's degree or equivalent experience

Bachelor’s degree in a scientific discipline

Tools

LIMS

SAP

Veeva

Microsoft Office

Maximo

Job description

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Our client, focusing on therapies for widespread, chronic diseases such as central nervous system disorders, addiction, diabetes, and autoimmune disorders, is looking for a QC Associate to join their team. This role offers opportunities for career growth and making a meaningful impact.

Schedule: Monday-Friday, 1st shift

Pay: $25/hr

Type: 12-18 month contract (possibility of extension/conversion)

Qualifications:

• Associate's degree or equivalent experience required; bachelor’s degree in a scientific discipline preferred
• A minimum of 1 year’s experience in a pharmaceutical or regulated industry preferred
• Log samples into LIMS, verify labeling

Responsibilities:

• Follow procedures for sampling and inspection
• Review documentation and assign dates
• Coordinate sampling of incoming materials
• Log samples into LIMS, verify labeling
• Operate equipment and conduct inspections
• Identify non-conforming materials
• Plan and execute periodic retain inspections
• Author/review SOPs and train colleagues
• Assist in investigating non-conformances
• Use LIMS, SAP, Veeva, Microsoft Office, Maximo

This job description provides a comprehensive list of desired skills, but not all are required. We encourage candidates with some of these skills to apply. We look forward to learning more about you!

Additional Details:

• Seniority level: Entry level
• Employment type: Full-time
• Job function: Research, Analyst, and Information Technology
• Industries: IT Services and IT Consulting

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