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Operate a variety of manufacturing equipment including tanks, filtration systems, CIP/SIP skids, agitators, autoclaves, glass washers, and testing devices. This is a hands-on opportunity for individuals interested in working in a GMP-regulated environment, with exposure to advanced production systems, cleanroom operations, and continuous process improvement.

HOUR

Manufacturing Associate I / II (All Shifts)Location: Near Stockbridge, MA Pay Rate: $19.00 - $35.00 per hour (based on experience) Employment Type: Full-Time | Multiple Shifts Available Position OverviewOur growing client is seeking Manufacturing Associates (Level I & II) to support production operations across multiple shifts. This role is responsible for executing manufacturing processes, operating equipment, and ensuring compliance with strict quality and regulatory standards.This is a hands-on opportunity for individuals interested in working in a GMP-regulated environment, with exposure to advanced production systems, cleanroom operations, and continuous process improvement. Key ResponsibilitiesProduction & Process Operations<ul style="margin-bottom:0in;margin-top:0in"><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">Perform manufacturing activities in assigned areas following SOPs, batch records, and GMP standards</li><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">Support routine production, start-ups, changeovers, and technology transfer activities</li><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">Prepare buffers, media, and other solutions according to detailed procedures</li></ul> Equipment Operation<ul style="margin-bottom:0in;margin-top:0in"><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">Operate a variety of manufacturing equipment including tanks, filtration systems, CIP/SIP skids, agitators, autoclaves, glass washers, and testing devices</li><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">Work with manual, semi-automated, and fully automated aseptic filling lines</li><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">Monitor equipment performance and report issues as needed</li></ul> Cleanroom & Aseptic Work<ul style="margin-bottom:0in;margin-top:0in"><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">Perform aseptic operations in controlled cleanroom environments</li><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">Follow strict contamination control procedures and gowning requirements</li></ul> Documentation & Compliance<ul style="margin-bottom:0in;margin-top:0in"><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">Complete all required documentation accurately and in compliance with cGMP standards</li><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">Maintain logbooks, batch records, and production documentation</li><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">Ensure work areas remain audit-ready at all times</li><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">Comply with FDA, OSHA, and other regulatory requirements</li></ul> Collaboration & Communication<ul style="margin-bottom:0in;margin-top:0in"><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">Work closely with team members to complete process steps safely and efficiently</li><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">Communicate any issues, deviations, or process changes to supervisors</li><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">Adapt to changing production schedules and priorities</li><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">Provide feedback and suggestions for process improvements</li></ul> Training & Development<ul style="margin-bottom:0in;margin-top:0in"><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">Complete all required training and maintain up-to-date training records</li><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">Follow established procedures and continuously develop technical skills</li></ul> QualificationsManufacturing Associate I:<ul style="margin-bottom:0in;margin-top:0in"><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">0-2 years of experience in a manufacturing or GMP environment preferred</li><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">Associate or Bachelor's degree in a science-related field or equivalent experience</li></ul> Manufacturing Associate II:<ul style="margin-bottom:0in;margin-top:0in"><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">3-4 years of experience in a GMP or regulated manufacturing environment preferred</li><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">Bachelor's degree in a science-related field or equivalent experience</li></ul> General Requirements:<ul style="margin-bottom:0in;margin-top:0in"><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">Basic understanding of FDA cGMP regulations</li><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">Strong attention to detail and ability to follow detailed instructions</li><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">Good written and verbal communication skills</li><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">Basic computer skills (Word, PowerPoint, etc.)</li><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">Ability to accurately complete documentation</li><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">Ability to work independently and as part of a team</li></ul> Physical & Work Requirements<ul style="margin-bottom:0in;margin-top:0in"><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">Ability to work in a 24/7 shift-based environment, including nights, weekends, and off-hours</li><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">Ability to stand or sit for extended periods</li><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">Ability to lift and carry up to 50 pounds</li><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">Ability to work in cleanroom environments while wearing required PPE</li><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">Adequate visual and auditory acuity for monitoring processes and equipment</li></ul> To see a full listing of all our open positions, please visit:  https://www.redshiftrecruiting.com/jobs-hiring-near-me redShift Recruiting is the region's premier recruiting agency with over 100 years of combined experience in the recruiting field. We specialize in permanent, temporary, and temp-to-hire positions. Our superior service combined with our highly qualified and carefully selected bank of candidates sets us apart.

redShift Recruiting

Manufacturing Associate

Asepsis

Auditory

Autoclave

CIP (Clean-in-Place)

Cleanroom

Communication Skills

Computer Skills

Current Good Manufacturing Practice (cGMP)

Detail Oriented

Documentation

FDA (Food and Drug Administration)

FDA Requirements

GMP (Good Manufacturing Practices)

Lift/Move 50 Pounds

Maintain Compliance

Manufacturing

Manufacturing Equipment

Manufacturing/Industrial Processes

Microsoft PowerPoint

Microsoft Word

OSHA

Operational Support

Operations Processes

Performance Analysis

Presentation/Verbal Skills

Procedure Development

Process Improvement

Process Management

Production Schedule

Production Support

Production Systems

Recruiting/Staffing Agency

Regulations

Regulatory Requirements

SIP (Sterilization-in-Place)

Standard Operating Procedures (SOP)

Startup

System Operations

Writing Skills

SmartSearch

ADAPTED_NOW

Equipment OperationOperate a variety of manufacturing equipment including tanks, filtration systems, CIP/SIP skids, agitators, autoclaves, glass washers, and testing devices. This is a hands-on opportunity for individuals interested in working in a GMP-regulated environment, with exposure to advanced production systems, cleanroom operations, and continuous process improvement.

Manufacturing Associate I / II (All Shifts) Location: Near Stockbridge, MA Pay Rate: $19.00 - $35.00 per hour (based on experience) Employment Type: Full-Time | Multiple Shifts Available Position Overview Our growing client is seeking Manufacturing Associates (Level I & II) to support production operations across multiple shifts. This role is responsible for executing manufacturing processes, operating equipment, and ensuring compliance with strict quality and regulatory standards. This is a hands-on opportunity for individuals interested in working in a GMP-regulated environment, with exposure to advanced production systems, cleanroom operations, and continuous process improvement. Key Responsibilities Production & Process OperationsPerform manufacturing activities in assigned areas following SOPs, batch records, and GMP standards Support routine production, start-ups, changeovers, and technology transfer activities Prepare buffers, media, and other solutions according to detailed procedures Equipment OperationOperate a variety of manufacturing equipment including tanks, filtration systems, CIP/SIP skids, agitators, autoclaves, glass washers, and testing devices Work with manual, semi-automated, and fully automated aseptic filling lines Monitor equipment performance and report issues as needed Cleanroom & Aseptic WorkPerform aseptic operations in controlled cleanroom environments Follow strict contamination control procedures and gowning requirements Documentation & ComplianceComplete all required documentation accurately and in compliance with cGMP standards Maintain logbooks, batch records, and production documentation Ensure work areas remain audit-ready at all times Comply with FDA, OSHA, and other regulatory requirements Collaboration & CommunicationWork closely with team members to complete process steps safely and efficiently Communicate any issues, deviations, or process changes to supervisors Adapt to changing production schedules and priorities Provide feedback and suggestions for process improvements Training & DevelopmentComplete all required training and maintain up-to-date training records Follow established procedures and continuously develop technical skills Qualifications Manufacturing Associate I:0-2 years of experience in a manufacturing or GMP environment preferred Associate or Bachelor's degree in a science-related field or equivalent experience Manufacturing Associate II:3-4 years of experience in a GMP or regulated manufacturing environment preferred Bachelor's degree in a science-related field or equivalent experience General Requirements:Basic understanding of FDA cGMP regulations Strong attention to detail and ability to follow detailed instructions Good written and verbal communication skills Basic computer skills (Word, PowerPoint, etc.) Ability to accurately complete documentation Ability to work independently and as part of a team Physical & Work RequirementsAbility to work in a 24/7 shift-based environment, including nights, weekends, and off-hours Ability to stand or sit for extended periods Ability to lift and carry up to 50 pounds Ability to work in cleanroom environments while wearing required PPE Adequate visual and auditory acuity for monitoring processes and equipment To see a full listing of all our open positions, please visit: https://www.redshiftrecruiting.com/jobs-hiring-near-me redShift Recruiting is the region's premier recruiting agency with over 100 years of combined experience in the recruiting field. We specialize in permanent, temporary, and temp-to-hire positions. Our superior service combined with our highly qualified and carefully selected bank of candidates sets us apart.

Redshift Recruiting LLC

This is an excellent opportunity for individuals interested in building a career in manufacturing, particularly within a GMP-regulated environment, with hands-on exposure to advanced equipment and cleanroom operations. Our growing manufacturing client is seeking motivated Manufacturing Technicians (Level I & II) to support production operations within a regulated environment.

Manufacturing Technician I / II (3 Shifts Available)Location: Near Stockbridge, MA Pay Rate: $19.50 - $24.00 per hour Employment Type: Full-Time | Multiple Shifts (24/7 Operation) Position OverviewOur growing manufacturing client is seeking motivated Manufacturing Technicians (Level I & II) to support production operations within a regulated environment. These roles are responsible for executing manufacturing processes, maintaining compliance with strict quality standards, and supporting production efficiency across multiple shifts.This is an excellent opportunity for individuals interested in building a career in manufacturing, particularly within a GMP-regulated environment, with hands-on exposure to advanced equipment and cleanroom operations.Key ResponsibilitiesProduction & Process Operations<ul style="margin-bottom:0in;margin-top:0in"><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">Perform manufacturing tasks in assigned production areas following established procedures</li><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">Prepare buffers, media, and other solutions according to batch records and written instructions</li><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">Operate a variety of process equipment including tanks, filtration systems, autoclaves, agitators, and cleaning systems (CIP/SIP)</li><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">Support start-ups, changeovers, and technology transfer activities</li></ul> Aseptic & Cleanroom Work<ul style="margin-bottom:0in;margin-top:0in"><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">Perform aseptic operations in controlled cleanroom environments</li><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">Operate manual, semi-automated, and fully automated filling lines</li><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">Follow strict contamination control and sterile processing procedures</li></ul> Documentation & Compliance<ul style="margin-bottom:0in;margin-top:0in"><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">Accurately complete all required documentation in accordance with GMP standards</li><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">Follow all Standard Operating Procedures (SOPs) and batch records</li><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">Ensure work areas remain audit-ready at all times</li><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">Comply with all applicable regulations including FDA, OSHA, and safety standards</li></ul> Collaboration & Communication<ul style="margin-bottom:0in;margin-top:0in"><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">Work closely with team members to complete process steps efficiently and safely</li><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">Communicate issues, deviations, or process concerns to supervisors</li><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">Adapt to changing production schedules and priorities</li><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">Provide input and suggestions for process improvements</li></ul> Training & Development<ul style="margin-bottom:0in;margin-top:0in"><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">Participate in all required training programs</li><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">Maintain up-to-date training records and certifications</li><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">Continuously develop technical knowledge and manufacturing skills</li></ul> QualificationsManufacturing Technician I:<ul style="margin-bottom:0in;margin-top:0in"><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">0-1 year of experience in a manufacturing or GMP environment preferred</li></ul> Manufacturing Technician II:<ul style="margin-bottom:0in;margin-top:0in"><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">1-2 years of experience in a GMP or regulated manufacturing environment preferred</li></ul> General Requirements:<ul style="margin-bottom:0in;margin-top:0in"><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">High school diploma or GED required</li><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">Basic understanding of FDA cGMP regulations preferred</li><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">Strong attention to detail and ability to follow detailed instructions</li><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">Basic computer skills (Word, PowerPoint, etc.)</li><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">Strong written and verbal communication skills</li><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">Ability to accurately document processes and production activities</li><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">Ability to read and write in English</li></ul> Physical & Work Requirements<ul style="margin-bottom:0in;margin-top:0in"><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">Ability to work in a 24/7 production environment, including nights, weekends, or off-shifts as needed</li><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">Ability to stand or sit for extended periods</li><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">Ability to lift and carry up to 50 pounds</li><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">Comfortable working in cleanroom environments with required PPE</li><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;margin-left:0in;line-height:115%;font-size:16px;font-family:'aptos' , sans-serif">Good visual and auditory acuity for monitoring equipment and processes</li></ul> To see a full listing of all our open positions, please visit:  https://www.redshiftrecruiting.com/jobs-hiring-near-me redShift Recruiting is the region's premier recruiting agency with over 100 years of combined experience in the recruiting field. We specialize in permanent, temporary, and temp-to-hire positions. Our superior service combined with our highly qualified and carefully selected bank of candidates sets us apart.

Manufacturing Technician

English Language

High School Diploma

Quality Metrics

Training Program

Manufacturing Technician I / II (3 Shifts Available) Location: Near Stockbridge, MA Pay Rate: $19.50 - $24.00 per hour Employment Type: Full-Time | Multiple Shifts (24/7 Operation) Position Overview Our growing manufacturing client is seeking motivated Manufacturing Technicians (Level I & II) to support production operations within a regulated environment. These roles are responsible for executing manufacturing processes, maintaining compliance with strict quality standards, and supporting production efficiency across multiple shifts. This is an excellent opportunity for individuals interested in building a career in manufacturing, particularly within a GMP-regulated environment, with hands-on exposure to advanced equipment and cleanroom operations. Key Responsibilities Production & Process OperationsPerform manufacturing tasks in assigned production areas following established procedures Prepare buffers, media, and other solutions according to batch records and written instructions Operate a variety of process equipment including tanks, filtration systems, autoclaves, agitators, and cleaning systems (CIP/SIP) Support start-ups, changeovers, and technology transfer activities Aseptic & Cleanroom WorkPerform aseptic operations in controlled cleanroom environments Operate manual, semi-automated, and fully automated filling lines Follow strict contamination control and sterile processing procedures Documentation & ComplianceAccurately complete all required documentation in accordance with GMP standards Follow all Standard Operating Procedures (SOPs) and batch records Ensure work areas remain audit-ready at all times Comply with all applicable regulations including FDA, OSHA, and safety standards Collaboration & CommunicationWork closely with team members to complete process steps efficiently and safely Communicate issues, deviations, or process concerns to supervisors Adapt to changing production schedules and priorities Provide input and suggestions for process improvements Training & DevelopmentParticipate in all required training programs Maintain up-to-date training records and certifications Continuously develop technical knowledge and manufacturing skills Qualifications Manufacturing Technician I:0-1 year of experience in a manufacturing or GMP environment preferred Manufacturing Technician II:1-2 years of experience in a GMP or regulated manufacturing environment preferred General Requirements:High school diploma or GED required Basic understanding of FDA cGMP regulations preferred Strong attention to detail and ability to follow detailed instructions Basic computer skills (Word, PowerPoint, etc.) Strong written and verbal communication skills Ability to accurately document processes and production activities Ability to read and write in English Physical & Work RequirementsAbility to work in a 24/7 production environment, including nights, weekends, or off-shifts as needed Ability to stand or sit for extended periods Ability to lift and carry up to 50 pounds Comfortable working in cleanroom environments with required PPE Good visual and auditory acuity for monitoring equipment and processes To see a full listing of all our open positions, please visit: https://www.redshiftrecruiting.com/jobs-hiring-near-me redShift Recruiting is the region's premier recruiting agency with over 100 years of combined experience in the recruiting field. We specialize in permanent, temporary, and temp-to-hire positions. Our superior service combined with our highly qualified and carefully selected bank of candidates sets us apart.

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Manufacturing AssociateredShift Recruiting

Manufacturing AssociateRedshift Recruiting LLC

Manufacturing TechnicianredShift Recruiting

Manufacturing TechnicianRedshift Recruiting LLC

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