Manufacturing Associate

0–2 years of experience in a GMP environment, or proven ability in an approved laboratory under minimal supervision, preferred; associate's or bachelor's degree in a science-related discipline, or equivalent GMP experience OR. Key Responsibilities Operate process equipment such as tanks, clean-in-place skids (CIP/SIP), agitators, filtration devices, autoclaves, glass washers, integrity testing equipment, and other small equipment.

Manufacturing Associate (All Shifts)
Pay: $28–$35/hour
Location: Near Stockbridge, MA
 
About the Role
Our client is looking for a Manufacturing Associate to perform production operations across assigned areas of the facility. This role supports start-up, changeovers, technology transfer, and routine manufacturing activities, working within a GMP-regulated production environment.
 
Key Responsibilities

• Operate process equipment such as tanks, clean-in-place skids (CIP/SIP), agitators, filtration devices, autoclaves, glass washers, integrity testing equipment, and other small equipment
• Operate manual, semi-automatic, and fully automatic isolator-based aseptic filling lines
• Perform aseptic operations in clean room environments
• Prepare buffers, media, and other solutions, following written procedures and batch records
• Perform process steps in coordination with other associates, asking for help as needed to avoid performing steps without proper training or qualification
• Adhere to scheduling changes and respond appropriately
• Communicate with the supervisor regarding work orders or shifts in process parameters
• Provide input and suggestions to help improve processes
• Follow all GMP and EHS procedures
• Attend and complete all assigned training, and keep your training plan accurate and up to date
• Complete all required documentation per GMP practices
• Help keep manufacturing areas in a state of audit readiness
• Perform production operations following written SOPs and batch records in accordance with GMPs
• Conduct business responsibly and in compliance with applicable state, FDA, OSHA, and HIPAA regulations
• Other duties as assigned

 
Qualifications
 0–2 years of experience in a GMP environment, or proven ability in an approved laboratory under minimal supervision, preferred; associate's or bachelor's degree in a science-related discipline, or equivalent GMP experience OR
3–4 years of experience in a GMP environment, or proven ability in an approved laboratory under minimal supervision, preferred; bachelor's degree in a science-related discipline, or equivalent GMP experience

A degree in another discipline, or the absence of a degree, may be considered if sufficient technical depth has been achieved through professional experience.
 
Additional Requirements

• Understanding of basic FDA cGMP regulations
• Strong verbal and written communication skills
• Basic software application skills (Word, PowerPoint)
• Ability to follow detailed processing instructions
• Ability to accurately complete all necessary documentation
• Satisfactory audio-visual acuity
• Ability to read and write English
• Familiarity with technical issues in the assigned area
• Ability to work shifts covering a 24/7 operation, including off hours as applicable
• Ability to sit or stand for prolonged periods of time
• Ability to lift and carry materials weighing up to 50 lbs

 
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.