Compliance Specialist
@ AbbVieCompliance Specialist
About the job
AbbVie is a global biopharmaceutical company focused on innovative medicines. This role involves developing data platforms, ensuring data quality, security, and collaborating across teams to deliver insights and optimize data processes.
Requirements
- 5 years working with SQL & NoSQL databases
- Experience with data quality & analytics
- Designing ETL systems & performance testing
- Managing stakeholder & business requirements
- Cloud tech & AWS services, incl
Qualifications
- BS in engineering or related field
- Experience in large data environments
- Knowledge of data frameworks like Data Vault
- Strong report & dashboard creation skills
- Ability to manage projects & teams
Full job description
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.
Responsible for assisting with the internal audit system that will assure that all production and support functions at the manufacturing facility operate in compliance with all applicable regulations and standards.
Responsibilities
- Assists with planning and conducting internal compliance audits of all operations within the facility.
- Provides support with company and regulatory agency (i.e. DEA, FDA) inspections.
- Follow up on audits to assure that action plans are developed and completed in a timely fashion.
- Assist with management review and associated metrics for the plant
- Provides support in the metrics collection and analysis for compliance-related corrective and preventive actions (CAPA’s).
- Responsible for supplier qualifications including new suppliers, changes and re-qualifications.
- Bachelor’s Degree, preferably in Science or Engineering, or equivalent related work experience is required.
- 3+ years of Biopharmaceutical experience
- Quality Assurance/Regulatory Affairs/Compliance is preferred
- Knowledge of regulations and standards for pharmaceuticals (e.g. CFR, MCA, DEA).
- Must have some knowledge of plant and company level procedures.
- Ability to evaluate quality, production and support areas for compliance to GMPs. BOPs, etc.
- Ability to identify and investigate problems and help to resolve them.
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
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 ofthis 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.
Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of anybonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's soleand absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.
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
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