Energy Jobline ZR
Auditor, Audit and Compliance in North Chicago
Energy Jobline ZR, North Chicago, Illinois, us, 60086
Energy Jobline is the largest and fastest growing global Energy Job Board and Energy Hub. We have an audience reach of over 7 million energy professionals, 400,000+ monthly advertised global energy and engineering jobs, and work with the leading energy companies worldwide.
We focus on the Oil & Gas, Renewables, Engineering, Power, and Nuclear markets as well as emerging technologies in EV, Battery, and Fusion. We are committed to ensuring that we offer the most exciting career opportunities from around the world for our jobseekers.
Purpose The function of Audit and Compliance Auditor is to perform comprehensive audits for compliance with U.S. and foreign regulation requirements, providing constructive evaluation of quality‑related systems for AbbVie plants, affiliates, quality service areas and/or suppliers that provide materials, services, and products to AbbVie. The audit ensures activities are performed and documented in accordance with AbbVie policies and procedures and applicable quality and regulatory requirements intended to assure the quality, effectiveness, and safety of our products.
Responsibilities
75% travel
Assesses compliance of systems, facilities, and procedures per applicable regulations, ensuring compliance with regulatory requirements and AbbVie specifications.
Provides feedback in the form of audit observations and reviews corrective actions to determine if commitments have been properly implemented, proven effective, and maintained at the supplier or internal AbbVie site. For internal sites, formulates recommendations for corrective actions.
Participates in strategic initiatives to improve compliance with regulatory requirements and standards.
Collaborates with R&D QA to coordinate and conduct joint audits.
Communicates and coordinates supplier audit activities with internal stakeholders such as procurement, SQA, EQA, manufacturing sites and commercial affiliates as well as external stakeholders.
Ensures audits are conducted according to the annual audit schedule.
Ensures no product launch delays or business interruptions due to supplier audit delays, thereby assuring supply to AbbVie patients.
Qualifications
Bachelor’s Degree preferably in a technical or scientific area (Chemistry, Pharmacy, Biology, Microbiology, or Engineering) or equivalent industry experience (at least 4 years) with sufficient exposure to pharmaceutical, medical device, biologics and combination products, cosmetics, eye care or aesthetics related industries. ASQ certification desired.
6+ years of total relevant experience, including 4+ years in Quality Assurance with some project management experience in the pharmaceutical, medical device, biotechnology or related industry and 2+ years in compliance/auditing.
Must have a technical background, including an understanding of the quality assurance audit process and knowledge of worldwide requirements related to GMP regulations for quality systems and compliance.
Must understand a variety of quality/operational systems that support facility, product design, development, production, distribution, installation, support, and service and understand the principles of quality management.
Excellent oral and written communication skills. Must exhibit strong interpersonal skills, tact, open‑mindedness, maturity, tenacity, self‑reliance, organizational/administrative skills, and sound judgment.
Must be able to effectively communicate and influence others outside of the company as well as internal stakeholders across functional and technical areas.
Additional Information
The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
This job is eligible to participate in our short‑term incentive programs.
This job is eligible to participate in our long‑term incentive programs.
Equal Opportunity 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
If you are interested in applying for this job please press the Apply Button and follow the application process.
#J-18808-Ljbffr
We focus on the Oil & Gas, Renewables, Engineering, Power, and Nuclear markets as well as emerging technologies in EV, Battery, and Fusion. We are committed to ensuring that we offer the most exciting career opportunities from around the world for our jobseekers.
Purpose The function of Audit and Compliance Auditor is to perform comprehensive audits for compliance with U.S. and foreign regulation requirements, providing constructive evaluation of quality‑related systems for AbbVie plants, affiliates, quality service areas and/or suppliers that provide materials, services, and products to AbbVie. The audit ensures activities are performed and documented in accordance with AbbVie policies and procedures and applicable quality and regulatory requirements intended to assure the quality, effectiveness, and safety of our products.
Responsibilities
75% travel
Assesses compliance of systems, facilities, and procedures per applicable regulations, ensuring compliance with regulatory requirements and AbbVie specifications.
Provides feedback in the form of audit observations and reviews corrective actions to determine if commitments have been properly implemented, proven effective, and maintained at the supplier or internal AbbVie site. For internal sites, formulates recommendations for corrective actions.
Participates in strategic initiatives to improve compliance with regulatory requirements and standards.
Collaborates with R&D QA to coordinate and conduct joint audits.
Communicates and coordinates supplier audit activities with internal stakeholders such as procurement, SQA, EQA, manufacturing sites and commercial affiliates as well as external stakeholders.
Ensures audits are conducted according to the annual audit schedule.
Ensures no product launch delays or business interruptions due to supplier audit delays, thereby assuring supply to AbbVie patients.
Qualifications
Bachelor’s Degree preferably in a technical or scientific area (Chemistry, Pharmacy, Biology, Microbiology, or Engineering) or equivalent industry experience (at least 4 years) with sufficient exposure to pharmaceutical, medical device, biologics and combination products, cosmetics, eye care or aesthetics related industries. ASQ certification desired.
6+ years of total relevant experience, including 4+ years in Quality Assurance with some project management experience in the pharmaceutical, medical device, biotechnology or related industry and 2+ years in compliance/auditing.
Must have a technical background, including an understanding of the quality assurance audit process and knowledge of worldwide requirements related to GMP regulations for quality systems and compliance.
Must understand a variety of quality/operational systems that support facility, product design, development, production, distribution, installation, support, and service and understand the principles of quality management.
Excellent oral and written communication skills. Must exhibit strong interpersonal skills, tact, open‑mindedness, maturity, tenacity, self‑reliance, organizational/administrative skills, and sound judgment.
Must be able to effectively communicate and influence others outside of the company as well as internal stakeholders across functional and technical areas.
Additional Information
The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
This job is eligible to participate in our short‑term incentive programs.
This job is eligible to participate in our long‑term incentive programs.
Equal Opportunity 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
If you are interested in applying for this job please press the Apply Button and follow the application process.
#J-18808-Ljbffr