Associate QC Laboratory Analyst (Bio)

Purpose:

The primary function is to support the Quality Control Laboratories with independent effective and timely testing services and able to ensure that tasks are performed according to requirements with review/verification of results and problem solving for issues identified.

Major Responsibilities:

• Responsible for the timely completion and data verification of all testing of raw material intermediates in-process control samples and final product
• Maintain up-to-date complete and precise records of all tests performed
• Ensure that all test equipment is used and maintained properly in GMP environment
• Acts as an SME for simple to complex instruments and techniques where needed
• Lead and perform any method transfer or method validation protocols or equipment qualifications and support the transfer of new products
• Understands implements and maintains cGMP and 6S concept
• Able to present clearly and lead confidently during audits and site leadership inquiries
• Write/revises procedures as necessary and make recommendations for process improvement
• Effectively perform a multitude of laboratory techniques for which they are trained on with minimal error
• Trains new analysts and technicians on all instruments/techniques as well as routinely reviewing that all Bio lab personnel are adhering to proper GMP standards
• Responsible for assisting the lab supervisor in following up with corrective actions
• Responsible for ownership of laboratory investigation - Able to lead the whole laboratory investigation and work alongside with QA for success closure of investigation
• Participate in tier meeting for manufacturing updates on incoming raw materials/in-process samples and final product
• Understands and maintains a safe work environment for themselves and others in accordance with procedural requirements by driving all EHS standards procedures and policies

Qualifications :

• Bachelor of Science majoring in Biology Chemistry Biochemistry or related scientific degree
• At least 1-3 years of experience in a pharmaceutical manufacturing environment
• Strong GMP background and proficient with using laboratory equipment
• Highly motivated independent and able to work under pressure
• Possess good interpersonal and communication skills
• Strong analytical problem solving and writing skills
• Team motivator able to motivate and be role model for less experienced peers
• Total commitment to quality and maintaining a high standard of work at all times

Additional Information :

AbbVie is an equal opportunity employer and is committed to operating with integrity driving innovation transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. 

US & Puerto Rico only - to learn more visit  & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:

Work :

No

Employment Type :

Full-time