Process Development Technician in Andover, MA

  • Title: Process Development Technician
  • Code: RCI-32525-1
  • RequirementID: 121110
  • Location: Andover, MA 01810
  • Posted Date: 09/16/2024
  • Duration: 12 Months
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  Job Description

Schedule: Rotating 2nd shift. 1-wk Tuesday/Wednesday/Saturday/Sunday - 2-wk: Monday/Thursday/Friday 2-pm - 2am 

 

Education And Experience

 Must-Have

  • High School Diploma or GED

Nice-to-Have

  • Bachelor's Degree
  • Basic mechanical knowledge and experience in using hand tools.
  • Manufacturing experience in a Good Manufacturing Practices (cGMP) or another regulated environment.

 Position Summary

Cell Culture Technician:

Technical Operations 1
Scope of Team Interaction

  • Accountable for own results
  • Manages own time and professional development
  • Resource Management
  • Works as team member
  • Learns team effectiveness and communication skills
  • Breadth and Depth of Knowledge
  • Develops and applies fundamental knowledge and skills in procedures, techniques, tools, materials and/or equipment needed for position
  • Focused on a limited range of activities
  • Complexity of Technical Knowledge
  • Completes routine tasks consisting of a series of prescribed steps within agreed timeframe
  • Tasks may be embedded in Standard Operating Procedures, operational and technical work practices and guidelines
  • Learns to identify process issues
  • Innovation and Risk-Taking
  • Demonstrates receptiveness to new processes and ideas
  • Knowledge Sharing
  • Learns the work processes and the business within own area
  • Complexity of Problem Solving
  • Identifies and solves routine problems that involve direct application of skills/knowledge in a structured environment
  • Seeks the input and assistance of others
  • Impact of Decisions
  • Decisions impact own work
  • Judgment
  • Significant reliance on supervisor
  • Does not require deviation from established and well-defined procedures and practices
  • Consults with others to ensure quality of judgment
  • Direction Received
  • Completes assignments under close supervision and/or detailed instruction in a structured environment
  • Review of Work
  • Work is closely reviewed
  • Compliance
  • Learns and is accountable for adhering to Client standards, guidelines and values

 Organizational Relationships

  • Functional support groups include Quality Assurance, Quality Control, Validation, Tech Transfer, and Quality Engineering.

  Impact of Decisions

  • Decisions impact own work

 Judgment

  • Significant reliance on supervisor
  • Does not require deviation from established and well-defined procedures and practices
  • Consults with others to ensure quality of judgment
  • Direction Received
  • Completes assignments under close supervision and/or detailed instruction in a structured environment

 Review of Work

  • Work is closely reviewed

 Compliance

  • Learns and is accountable for adhering to Client standards, guidelines and values

Technical Skills Requirements

  • Basic understanding of Good Manufacturing Practices (GMP)

Physical Position Requirements

  • Requires the moving of heavy equipment and the ability to lift ~50 pounds. The incumbent needs to take the necessary safety precautions when working with pressurized systems, steam, and corrosive chemicals.
  • The incumbent is required to attain detail knowledge of the operational equipment.
  • The incumbent will be required to solve problems regarding site assessment, specific units used in Biopharmaceutical manufacturing.
  • The incumbent must be able to express ideas into SOPs, MFRs and be able to use a multitude of programs including Excel, Word, Power Point, etc.

 



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