Manufacturing Associate I/II- Investigation Writer

Employer
AbbVie
Location
Worcester, Massachusetts, USA
Posted
Feb 20, 2018
Ref
1800653
Required Education
Bachelors Degree
Position Type
Full time
Key Responsibilities Include:
  • Candidate will be primarily responsible for investigation writing. This experience is required
  • 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 ABC Production objectives, to provide support to Production initiatives, to execute systems and procedures efficiently and compliantly, evaluates systems for improvement potential. Use standard practices to ensure inter-group consistency. 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.


*Level will be determined based on education & years of experience*
Qualifications:
  • Bachelor's Degree or equivalent required.
  • At least 3+ years of 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.
  • 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.
Experience with Investigation Writing required. Candidate will be largely responsible for this.
Equal Opportunity Employer Minorities/Women/Veterans/Disabled