AbbVie

Manufacturing Technician II

Employer
AbbVie
Location
Dublin, CA, United States
Posted
Feb 20, 2021
Ref
205954
Required Education
High School or equivalent
Position Type
Full time
About AbbVie
AbbVie's mission is to discover and deliver innovative medicines 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, eye care, virology, women's health and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on Twitter , Facebook , Instagram , YouTube and LinkedIn .

Manufacturing Technician II

Summary:

Perform production line duties required to meet production goals while complying with quality standards and safety requirements. This manufacturing leader will primarily be responsible for interpreting and relaying information as the Subject Matter Expert (SME) for their assigned team of up to 10 assemblers, assist Production Supervisor/Manager with daily scheduling of tasks for line operators, working with Planning/Procurement to ensure inventory correlates with product demand and forecasting, product in-line inspection and transactions, troubleshooting, and performing assembly as needed to ensure team meets daily production targets. In addition, this individual will work closely with the Supervisor/Manager as the "Point of Contact" for production floor status. This individual will lead daily team Tier meetings. This individual must be able to hold others accountable. This role is measured by team outputs.

Essential Duties and Responsibilities include the following (other duties may be assigned.):
  • In support of the Production Supervisor, responsible for production by communicating job expectations; monitoring, and appraising job results; initiating, coordinating, and enforcing systems, policies, and procedures.
  • Maintains workflow by monitoring steps of the process and completes production plan by establishing priorities; monitoring progress; revising schedules; resolving problems; reporting results of the processing flow on shift production summaries.
  • Maintains quality service by establishing and enforcing organization standards.
  • Provides manufacturing information by analyzing production performance records and data; use SAP to transact work orders and compile data.
  • Maintains safe and clean work environment by educating and directing personnel on the use of all control points, equipment, and resources; maintaining compliance with established policies and procedures.
  • Applies industry knowledge and technical experience to identify and implement process improvements.
  • Contributes to team effort by performing assembly as needed.
  • Conducting training and retraining to ensure line personnel are proficient on assembly and manufacturing processes. Ensures continuity and uniformity of technical proficiency and skills across the team.
  • Maintaining team tools and equipment and ensuring all items are calibrated. Oversees team VMI materials and manages expired materials.
  • Manages team inventory of subassemblies when necessary and thoroughly tracks team inventory counts to assist the Production Supervisor/Manager, Service Manager, and Material Planning Manager.
  • Will manage NCMRs generated by team, assist in drafting NCMRs and conduct basic troubleshooting
  • Will assist Lead and Supervisor with root cause analysis investigations
  • Perform other duties as assigned.
  • Must be available to work overtime as requested by the Supervisor. This may include nights, weekends, and holidays during times critical to our business such as month-end, quarter-end, and year-end

Qualifications
  • Minimum of 4 years production experience required, preferably in the medical device industry
  • Strong communication skills, both written and oral, including the ability to translate and converse about technical and analytical issues to technical and non-technical contacts
  • Strong technical PC skills
  • Proficient with Microsoft Office suite including Access, Excel, and Word
  • SAP experience preferred
  • Ability to work all shifts (up to 12 hours), depending on business needs
  • Ability to interact and supervise members in a team environment
  • Ability to work independently and to adapt to consistently changing priorities
  • High School Diploma, GED, or equivalent background

Additional Requirements:

Responsible for performing all duties in compliance with FDA's Quality System Regulation (QSR), ISO13485, the Canadian Medical Device Regulations, and all other international regulatory requirements with which Allergan complies.

Significant Work Activities
Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)
Travel
No
Job Type
Experienced
Schedule
Full-time
Job Level Code
IC
Equal Employment Opportunity
At AbbVie, we value bringing together individuals from diverse backgrounds to develop new and innovative solutions for patients. As an equal opportunity employer we do not discriminate on the basis of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information gender identity or expression, sexual orientation, marital status, protected veteran status, or any other legally protected characteristic.