Job Description
Qualifications
1 year of experience in a GMP-regulated industry (Biotech, Pharma, Medical Device)
High School Diploma or equivalent with a passion for Sciences
Over 1 year of experience in a GMP-regulated industry
Ability to comfortably lift up to 40 lbs
Experience in following Standard Operating Procedures (SOPs
Responsibilities
Conduct weekly and monthly walkthroughs to ensure areas are maintained safely and in compliance with regulations
Keep the process area organized and ensure production areas are stocked with necessary supplies
Apply general knowledge of aseptic techniques
Perform troubleshooting activities in accordance with Standard Operating Procedures (SOPs)
Execute both routine and non-routine production operations according to the manufacturing schedule
Document operations in Batch Production Records (BPR), Solution Records (SLR), Logbooks, and Forms, adhering to Good Documentation Practices (GDP)
Review and verify pages in BPRs, SLRs, Logbooks, and Forms
Work safely, promptly reporting any safety issues and risks to management
Provide equipment training as a qualified trainer
Maintain an up-to-date training folder for relevant processes
Be available to work at least four holidays throughout the calendar year
Job description
Responsibilities:
• Conduct weekly and monthly walkthroughs to ensure areas are maintained safely and in compliance with regulations.
• Keep the process area organized and ensure production areas are stocked with necessary supplies.
• Apply general knowledge of aseptic techniques.
• Perform troubleshooting activities in accordance with Standard Operating Procedures (SOPs).
• Execute both routine and non-routine production operations according to the manufacturing schedule.
• Document operations in Batch Production Records (BPR), Solution Records (SLR), Logbooks, and Forms, adhering to Good Documentation Practices (GDP).
• Review and verify pages in BPRs, SLRs, Logbooks, and Forms.
• Work safely, promptly reporting any safety issues and risks to management.
• Provide equipment training as a qualified trainer.
• Maintain an up-to-date training folder for relevant processes.
• Be available to work at least four holidays throughout the calendar year.
Qualifications:
• 1 year of experience in a GMP-regulated industry (Biotech, Pharma, Medical Device)
• High School Diploma or equivalent with a passion for Sciences
• Associate or bachelor’s degree in biology, Biochemistry, Molecular Biology, or a related field preferred
• Over 1 year of experience in a GMP-regulated industry.
• Ability to comfortably lift up to 40 lbs.
• Experience in following Standard Operating Procedures (SOPs
1 year of experience in a GMP-regulated industry (Biotech, Pharma, Medical Device)
High School Diploma or equivalent with a passion for Sciences
Over 1 year of experience in a GMP-regulated industry
Ability to comfortably lift up to 40 lbs
Experience in following Standard Operating Procedures (SOPs
Responsibilities
Conduct weekly and monthly walkthroughs to ensure areas are maintained safely and in compliance with regulations
Keep the process area organized and ensure production areas are stocked with necessary supplies
Apply general knowledge of aseptic techniques
Perform troubleshooting activities in accordance with Standard Operating Procedures (SOPs)
Execute both routine and non-routine production operations according to the manufacturing schedule
Document operations in Batch Production Records (BPR), Solution Records (SLR), Logbooks, and Forms, adhering to Good Documentation Practices (GDP)
Review and verify pages in BPRs, SLRs, Logbooks, and Forms
Work safely, promptly reporting any safety issues and risks to management
Provide equipment training as a qualified trainer
Maintain an up-to-date training folder for relevant processes
Be available to work at least four holidays throughout the calendar year
Job description
Responsibilities:
• Conduct weekly and monthly walkthroughs to ensure areas are maintained safely and in compliance with regulations.
• Keep the process area organized and ensure production areas are stocked with necessary supplies.
• Apply general knowledge of aseptic techniques.
• Perform troubleshooting activities in accordance with Standard Operating Procedures (SOPs).
• Execute both routine and non-routine production operations according to the manufacturing schedule.
• Document operations in Batch Production Records (BPR), Solution Records (SLR), Logbooks, and Forms, adhering to Good Documentation Practices (GDP).
• Review and verify pages in BPRs, SLRs, Logbooks, and Forms.
• Work safely, promptly reporting any safety issues and risks to management.
• Provide equipment training as a qualified trainer.
• Maintain an up-to-date training folder for relevant processes.
• Be available to work at least four holidays throughout the calendar year.
Qualifications:
• 1 year of experience in a GMP-regulated industry (Biotech, Pharma, Medical Device)
• High School Diploma or equivalent with a passion for Sciences
• Associate or bachelor’s degree in biology, Biochemistry, Molecular Biology, or a related field preferred
• Over 1 year of experience in a GMP-regulated industry.
• Ability to comfortably lift up to 40 lbs.
• Experience in following Standard Operating Procedures (SOPs
💡 Quick Summary
Seeking a career-building opportunity? The Manufacturing Technician position is now open for candidates interested in the Operator & Technician Jobs sector. This role in Boston offers a professional environment and growth potential.
Requirement Snapshot: Candidates should possess basic communication skills, a proactive attitude, and the ability to work in a team. Experience in Operator & Technician Jobs is a plus.
