Location: Omaha, NE
Embark on a pivotal journey as a Manager of Quality Assurance at a leading pharmaceutical manufacturing firm nestled in the heart of Omaha, NE. This role stands at the forefront of ensuring the highest standards of quality and compliance within a dynamic and innovative environment. Your leadership will guide the Operational Quality Assurance team to excel, making a significant impact on product integrity and patient safety.
Why You Should Apply
Opportunity to lead a critical function within a highly respected pharmaceutical manufacturing entity.
Engage in meaningful work that directly contributes to the health and wellbeing of communities.
Highly competitive compensation package, including salary and bonus.
Comprehensive family-friendly benefits: 100% company-paid premiums for medical, dental, and vision; 401k with company match; paid time off.
Professional growth supported by a range of training and development programs.
What You'll Be Doing
Manage and oversee Operational Quality Assurance to ensure compliance with Quality Policies and Standards.
Lead the QA team in writing, reviewing, and approving critical documentation.
Responsible for product release, conducting investigations, and supporting QC testing.
Identify and implement quality-related processes and projects.
About You
Bachelor's degree in a scientific discipline, preferred.
Minimum of five years of experience in FDA and cGMP environments within the pharmaceutical industry.
Advanced understanding of manufacturing in cGMP environments and stringent documentation practices.
Exceptional organizational, time management, and communication skills.
How To Apply
We'd love to see your resume, but we don't need it to have a conversation. Send us an email to ******** and tell me why you're interested. Or, feel free to email your resume. Please include Job#18492.
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