Senior Laboratory Analyst I (Bio)
Senior Laboratory Analyst I (Bio)
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Job Description
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 API 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 API
- 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 5 years of experience in a QC Lab
- 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:
No
Employment Type :
Full-time
Employment Type
Full-time
