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Company

Original Job Post

KCAS Bio · 6 days ago

Quality Specialist II

Olathe, KS

Contract

Onsite

Mid Level

3+ years exp

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BiotechnologyPharmaceutical

Growth Opportunities

Hiring Manager

Erin Page

Insider Connection @KCAS Bio

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Responsibilities

Perform quality review and approval of documents, data, protocols, and/or reports.

Conduct quality audits and/or inspections, and distribute audit reports in a timely manner.

Review laboratory deviations and investigations.

Maintain accurate quality assurance files, records, and databases, and perform analysis and trending.

Provide training assistance in routine quality and compliance topics.

Assist with the development/writing of quality SOPs, documents, and/or reports as needed.

Offer consultation on quality and compliance topics and contribute to quality improvement initiatives.

Qualification

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Quality AssuranceLaboratory Processes

Required

BS in chemistry, biology, or related scientific field.

Experience with GLP, GCLP or GCP required

Minimum 3 years of Quality Assurance experience.

Exposure to and basic awareness of laboratory processes.

Benefits

Company sponsored events like food trucks, family days, and spirit days

Access to KCAS University for career growth

Connect with like-minded employees for wellness, inclusion, and community outreach

Participation in the stock ownership program

Access to the latest technology

Paid time off to volunteer

Company

KCAS Bio

With its presence in three locations across North America and Europe, KCAS Bio leading contract research organization (CRO) employing top scientific talent which provides comprehensive bioanalytical services to the global biopharmaceutical industry from early discovery support through product registration and beyond.

Founded in 1979

Shawnee, Kansas, USA

201-500 employees