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Manufacturing Associate II
Manufacturing Associate IIAbbVie • North Chicago, Illinois, USA
Manufacturing Associate II

Manufacturing Associate II

AbbVie • North Chicago, Illinois, USA
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Under some supervision manages Production projects including the introduction of new projects and technology into Production and Manufacturing Improvement. Works in concert with peers in other departments to meet project timelines. Responsible for tracking the transfer implementation and monitoring of projects. Uses SAP PI POMS and other systems programs and databases to input verify monitor and analyze pertinent data.

Responsibilities

  • Transfers methods into Production instructions to allow for successful performance of scheduled campaigns.
  • Schedules work tasks with limited assistance to support project / campaign timelines. Drafts diverse scope and complexity documents. Circulates documents to reviewers with limited assistance responds to comments and questions. Manages document review and approval to meet project timelines.
  • Directs changeover activities with assistance.
  • Exercises judgment within generally defined procedures and practices to determine appropriate action. Tracks ongoing problems and gathers information for analysis. Analyze data to develop solutions to general-level problems. Presents a potential solution to management / senior personnel and with assistance creates an implementation plan.
  • Applies knowledge experience and technical skills to understand specific site objectives to provide support to Production initiatives to execute systems and procedures efficiently and compliantly evaluates systems for improvement potential. Works within established systems to improve Good Manufacturing Practices (GMP) compliance.
  • Works on problems of moderate complexity where analysis of situations requires evaluation of several factors.
  • Works under general supervision. Follows established procedures. Decisions are reviewed for soundness of technical judgment.
  • Coordinates activities of sub group and actively works under other sub-groups. Provides technical direction and training to less senior personnel.
  • Frequently interacts with subordinates and functional peer groups. Interaction normally requires the ability to gain cooperation of others conducting presentations of technical information concerning specific projects schedules etc.

Qualifications :

  • Bachelors Degree or equivalent required.
  • At least 5 years experience in all aspects of manufacturing / production processes with good writing skills.
  • Knowledge of media / buffer preparation cell culture or purification of biological drugs is required for specific biologics sites.
  • Computer and scheduling proficiency.
  • A working knowledge of safety quality systems and current Good Manufacturing Practices as applied to equipment and process steps in area of responsibility is required. Familiarity with pertinent regulatory filings. Proficiency with tech transfer process and familiarity with equipment and facilities validation.
  • Must be flexible to handle multiple tasks including ability to handle pressure in a professional manner. Effectively work in a team environment. Maintain high level of energy and professionalism on the job. Build effective working relationships with customers co-workers cross-functioned groups and management.
  • 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 short-term incentive programs.

    Note : No amount of pay is considered to be wages or compensation until such amount is earned vested and determinable. The amount and availability of any bonus commission incentive benefits or any other form of compensation and benefits that are allocable to a particular employee remains in the Companys sole and absolute discretion unless and until paid and may be modified at the Companys sole and absolute discretion consistent with applicable law.

    AbbVie is an equal opportunity employer and is committed to operating with integrity driving innovation transforming lives and serving our community. Equal Opportunity Employer / Veterans / Disabled.

    US & Puerto Rico only - to learn more visit  & Puerto Rico applicants seeking a reasonable accommodation click here to learn more :

    Work :

    No

    Employment Type : Full-time

    Key Skills

    Lean Manufacturing,Six Sigma,Continuous Improvement,ISO 9001,Lean Six Sigma,Management Experience,Manufacturing & Controls,5S,Manufacturing Management,Kaizen,Chemistry,Manufacturing

    Experience : years

    Vacancy : 1

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