This job posting isn't available in all website languages

​AbbVie has acquired Allergan, and we’ve moved sites!

As one company, we have brought together over 30 brands and leadership positions, expanding and diversifying our product portfolio. Join us in making a remarkable impact on people’s lives around the world. Visit careers.abbvie.com to explore our career opportunities. If you are a current AbbVie or legacy Allergan employee, please visit your intranet site to apply internally.

To apply internally on the Allergan intranet site please go to https://allergan.sharepoint.com/sites/GEP. Select the “AbbVie Jobs” tile under the Tools section.

To apply internally on the AbbVie intranet site please go to myabbvie.abbvienet.com. Next, hover over resources and then select Human Resources. After that, you will select “Global Job Board.” You are now viewing jobs on our internal site.

Senior Manager, Product Release

184688 Requisition #
Thanks for your interest in the Senior Manager, Product Release position. Unfortunately this position has been closed but you can search our 45 open jobs by clicking here.
The following listed requirements need to be met at a minimum level to be considered for the job:
  • Bachelor’s degree in the Sciences or related field. Technical degree preferred.
  • Supervisory experience preferred.
  • Ten (10) years’ experience in a Quality Operations role.
  • Six (6) years’ experience in Quality:  relevant areas include Documentation, Batch Review, Product Release, and/or Quality Laboratories and Systems.
  • Proficient in Microsoft Office (Word/Excel) and functional user experience with SAP preferred.
  • Four (4) years in the medical device or pharmaceutical industry.
  • Experience working in a GMP regulated environment preferred.
  • Experience working in an Aseptic Production environment preferred.
  • Excellent verbal and written communication skills. 
  • Detail-oriented and self-motivated.
  • Excellent organization skills.
  • Ability to manage multiple tasks. 
  • Will interact with all functional departments within the company including hourly, professional and management personnel.
  • Must have GMP experience in an FDA related environment, inclusive of 21 CFR Part 11 compliance criteria.
  • Working knowledge of Quality Assurance systems and cGMPs, ISO13485, CMDRs, and EMEA regulations.

My Profile

Create and manage profiles for future opportunities.

Go to Profile