Manufacturing Associate II (Sunday to Wednesday, 4:00pm - 2:30am)
Worcester, MA, United Statesfull time
On Site
entry
H1B: yes
AbbVie Manufacturing Associate II manages production projects and manufacturing improvements under some supervision. The role involves using SAP, LIMS, PI, and other systems to input, verify, monitor, and analyze 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.
Bachelor’s 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.
Qualification
Bachelor’s Degree or equivalentGood writing skillsKnowledge of media/buffer preparation
Required
Bachelor’s Degree or equivalent
At least 5 years’ experience in all aspects of manufacturing/production processes
Good writing skills
Knowledge of media/buffer preparation, cell culture or purification of biological drugs
