Associate Scientist II

tsu.edu; Houston (TX); On-site; USD 59,000 - 111,000; Full time

Job summary

AbbVie is seeking an Associate Scientist II to independently generate precise, reliable, and reproducible data in late-stage and commercial GMP manufacturing settings at AbbVie. The role emphasizes technical leadership, data interpretation, and collaboration with cross-functional teams to drive process improvements.

The candidate should have a Bachelor's or Master’s degree with relevant experience and be prepared to contribute to validation, process verification, and technical transfers across

Qualifications

• Bachelor's Degree or Master's Degree; typically 3+ years' experience for Bachelor's or equivalent education.
• Theoretical and practical knowledge to carry out job function.

Responsibilities

• Serve as downstream technical lead for late-stage and commercial GMP manufacturing processes.
• Author validation protocols/reports and technical assessments to support process performance qualification and continuous process verification.
• Collect and organize process data to perform process monitoring and statistical data analysis.
• Communicate and present work.
• Collaborate with cross-functional teams to resolve technical challenges.
• Provide on-the-floor support of GMP manufacturing operations to support investigations and identify areas for process improvements.
• Perform root cause analyses, author impact assessments, and propose corrective and preventive actions in response to nonconformities/deviations.
• Manage relationships with contract manufacturing clients.
• Support technical transfers and scale-up of GMP manufacturing processes.
• Perform laboratory-scale studies to support investigations or process improvements as needed.

Education

Bachelor's Degree or Master's Degree

Job description

Associate Scientist II AbbVie Full-time R00149312 Compensation: 58656-110500 USD / year

About AbbVie

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 including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.

Purpose

Independently generate precise, reliable and reproducible data in a timely manner. Demonstrate experimental precision and strong data interpretation skills and should possess understanding of core discipline.

Responsibilities

• Serve as the downstream technical lead for late-stage and commercial GMP manufacturing processes
• Author validation protocols/reports and technical assessments to support process performance qualification and continuous process verification
• Collect and organize process data to perform process monitoring and statistical data analysis
• Communicate and present work
• Collaborate with cross-functional teams to resolve technical challenges
• Provide on-the-floor support of GMP manufacturing operations to support investigations and identify areas for process improvements
• Perform root cause analyses, author impact assessments, and propose corrective and preventive actions in response to nonconformities/deviations
• Manage relationships with contract manufacturing clients
• Support technical transfers and scale-up of GMP manufacturing processes
• Perform laboratory-scale studies to support investigations or process improvements as needed

Qualifications

Bachelor's Degree, or equivalent education, with typically 3 or more years' experience or Master's Degree or equivalent education (no additional experience). Theoretical and practical knowledge to carry out job function.

Additional Information

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 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 long-term incentive programs.