Contract Opportunities: North America
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0000103594-Quality Control Analyst I
City:
State: MN
Min Salary: $0.00
Max Salary: $0.00
Job Description:
Job description:
OBJECTIVES:
• Perform supportive activities for general lab readiness, laboratory equipment qualification and method transfers.
• Conduct critical biological test methods including samples generated for in-process, drug substance and stability.
• Use a variety of laboratory instrumentation and computer systems to collect and record data (such as LIMS).
• Follow SOPs to perform methods requiring precise analytical skills and understanding of biology and chemistry principles.
ACCOUNTABILITIES:
• Demonstrate a functional understanding of a laboratory setting and Standard Operating Procedures (SOPs).
• Complete all testing, including special project / protocol testing in a timely and appropriate manner.
• Maintain data integrity and ensure compliance with company SOPs, specifications and cGMP regulations.
• Exercise judgment within defined Quality Control procedures and practices to determine appropriate action.
• Initiate low severity level deviations, CAPAs and change controls within the electronic Quality Management System.
• Occasionally participate in functional efforts involving teams to solve problems of moderate scope where analysis of situations or data requires a review of identifiable factors.
• Author minor revisions to existing SOPs.
• Receives general instructions on routine work and detailed instructions on new assignments.
• May be required to work overtime or be assigned to a different shift as needed.
• May perform equipment maintenance and calibrations as required.
• May perform other duties as assigned.

Minimum requirements:
EDUCATION, EXPERIENCE, KNOWLEDGE AND SKILLS:
• Bachelor’s or Master’s Degree in any Life Sciences with relevant laboratory coursework and 0-3 years of relevant experience.
• Previous experience in a regulated environment desirable.
• Ability to handle multiple tasks concurrently, and in a timely fashion.
• Must have basic understanding of laboratory instrumentation.
• Must be able to communicate effectively with supervisors and peers.
• Must be able to read, write and converse in English.
• Must be computer literate. Able to navigate, conduct searches, and complete online forms on Personal Computer for the purposes of training, performance management, and self service applications.
• Good interpersonal skills and be able to work effectively and efficiently in a team environment.
• Knowledge of cGMP manufacturing preferred.
• Knowledge of basic chemical and biological safety procedures.
• Must display eagerness to learn and continuously improve.
• Must have the following personal attributes: integrity and trust, work ethic, sound judgment, intellectual honesty, pragmatism, courage and conviction.
• In general, the position requires a combination of sedentary work and standing for extended periods of time in the Quality Control labs.


Please send resume to jobs@inventivhealth.com
For further details or to apply for this job, please contact: jobs@inventivhealth.com
Syneos Health, Inc. is an Equal Opportunity Employer, M/F/Disabled/Vets that values the strength that diversity brings to the workplace.