[Remote] Supervisor II, Quality Assurance (OSD) (3rd shift)

Note: The job is a remote job and is open to candidates in USA. AbbVie is dedicated to discovering and delivering innovative medicines and solutions that address serious health issues. The Quality Assurance Supervisor II will oversee the Quality Assurance team, ensuring compliance with regulations and maintaining product quality while supporting manufacturing operations.


Responsibilities

  • Leads a team in the Quality function and is responsible for hiring, setting performance expectations, driving team engagement, providing continuous and on-time performance feedback, developing staff, assisting team in problem-solving, and handling of employee matters. Ensures that the department has the appropriate talent and level of performance to meet business objectives. Monitors administration of training, identifies training needs, and development of team
  • Provide Quality support on the manufacturing shop floor
  • Responsible for supporting Operations efforts in meeting established production schedule
  • Partner with Operations employees to document exception documents, including re-inspection and resolve other outstanding plant quality/compliance issues
  • Propose changes update, author, and implement departmental procedures consistent with objectives of simplification and process efficiencies/improvements which ensure ongoing compliance
  • Investigate QC hold, quarantine and reject for materials not meeting standards, ensure the initiation of exception documentation and oversee the implementation of any corrective action
  • Responsible for the review and approval of Procedures and Change Requests
  • Assist/serve/provide feedback on continuous improvement initiatives/teams
  • Reviews and releases batch records
  • May serve as a backup when the Quality Manager is unavailable. Performs other tasks/projects as assigned

Skills

  • Bachelor's degree in sciences or engineering required
  • 2+ years of experience supervising a team and at least 2 years of experience in a manufacturing production environment
  • Experience in regulated pharmaceutical industry
  • Thorough knowledge of Quality Assurance operations with multiple years of experience in safety, application of FDA and GMP regulations
  • Effective problem-solving, decision-making, teamwork, influence, negotiation, and conflict resolution skills required
  • Ability to work cross-functionally and coordinate work both within the department and with other departments
  • Ability to identify, communicate, and follow through to completion and assist in the development of necessary corrective action plans to resolve problems with supervision
  • Demonstrated strong leadership skills and ability to foster an inclusive environment
  • The candidate must have availability to work on a 3rd shift (Monday to Friday, 9:00 p.m. - 6:00 a.m.; and alternate weekends)
  • Direct manufacturing and regulatory interface experience is preferred

Benefits

  • Paid time off (vacation, holidays, sick)
  • Medical/dental/vision insurance
  • 401(k) to eligible employees
  • This job is eligible to participate in our short-term incentive programs

Company Overview

  • At Allergan Aesthetics, an AbbVie company, we develop, manufacture, and market a portfolio of leading aesthetics brands and products. It was founded in undefined, and is headquartered in Irvine, California, USA, with a workforce of 1001-5000 employees. Its website is https://www.allerganaesthetics.com.

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