QC Lab Analyst

• Maintain and comply with Laboratory Documentation and Computerized Systems Data Integrity requirements.
• Understand Regulations and business processes required to maintain Laboratory Data Integrity.
• Be responsible for housekeeping duties in the lab.
• Be responsible for the timely completion of chemical testing of raw material.
• Ensure that all test equipment is used and maintained correctly.
• Be responsible for raising change requests and data verification as assigned.
• Ensure all in-process sampling and testing are completed in a timely manner.
• Maintain up-to-date, complete, and precise records of all tests performed.
• Adhere to cGMP and GLP requirements.
• Assist in the resolution of quality problems as required.
• Develop and change in-house laboratory procedures as appropriate.
• Aid in training of new analyst.
• Support the transfer of new products.
• Adhere to and support all EHS & E standards, procedures and policies.

Qualifications

• 3rd level qualification in a relevant Science discipline required.
• A minimum of 6 months of experience in HPLC or GC.
• Experience operating to cGMP standards utilizing laboratory equipment.
• Previous experience in a pharmaceutical manufacturing environment is desirable but not essential

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 https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html