Find Jobs
Find Jobs Near You – Available Work in Your Location
Skip to job details
S
Spherion
production associate.
Career Insights for Production Worker
See where this job fits in the broader career landscape. Knowing your career path helps you see what's possible from here.
Scorecard
Based on Massachusetts data
Review key factors to help you decide if this role fits your goals. How is this calculated?
What they do
A Production Worker performs a variety of duties in a factory. Operates machinery, manages distribution and provides quality control inspection.
$43,246 / year median in Massachusetts
+9% projected growth
Job Description
Job details Summary Spherion $28.00 - $29.00 per hour Temp to Perm 7:00 AM - 7:00 PM Industry manufacturing & production (Production Occupations) Reference number S_179260 Job details Spherion is seeking a reliable Production Associate to support manufacturing operations in a GMP-controlled environment. This position will perform production activities, maintain accurate documentation, inspect finished products, and follow established quality, safety, and cleanroom procedures.
Perform manufacturing activities in accordance with GMP and safety requirements.
Maintain accurate inventory records, batch records, and manufacturing documentation.
Inspect finished products to ensure they meet established specifications.
Assist with batch record reconciliation and preventative maintenance activities.
Follow Good Documentation Practices (GDP) and data integrity requirements.
Assist with nonconformance and CAPA-related activities.
Identify and report safety, quality, equipment, or production issues requiring escalation.
Complete required training and assist with training other employees after achieving full training status.
Maintain a clean, organized, and safe work environment.
Follow cleanroom gowning, PPE, safety, and other site-specific requirements.
Use computers and manufacturing systems for daily documentation and transactions.
Spend approximately 90% of the workday in manufacturing suites. experience 1-4 years skills Previous cGMP manufacturing experience.
Biopharmaceutical manufacturing experience.
Experience working in a controlled cleanroom environment.
Experience with batch records and GMP documentation.
Experience with manufacturing equipment and automated systems.
Experience with preventative maintenance activities.
Experience with CAPA, nonconformance, or quality systems. qualifications High school diploma or equivalent.
Minimum 1 year of experience in manufacturing, production, operations, laboratory, or a related field.
Knowledge of GMP and workplace safety practices.
Ability to follow detailed procedures and work instructions.
Ability to accurately complete manufacturing and quality documentation.
Ability to learn new equipment, processes, software, and tools.
Ability to identify and escalate quality, safety, or production concerns.
Ability to work with minimal to moderate supervision.
Effective written and verbal communication skills.
Ability to read and review documentation for extended periods.
Ability to work in a cleanroom and follow gowning procedures.
Ability to wear required PPE and follow GMP requirements. education High School share this job. send via e-mail print it
Responsibilities:
... Follow work instructions and standard operating procedures to complete production assignments. Perform manufacturing activities in accordance with GMP and safety requirements. Maintain accurate inventory records, batch records, and manufacturing documentation. Inspect finished products to ensure they meet established specifications. Assist with batch record reconciliation and preventative maintenance activities. Follow Good Documentation Practices (GDP) and data integrity requirements. Assist with nonconformance and CAPA-related activities. Identify and report safety, quality, equipment, or production issues requiring escalation. Complete required training and assist with training other employees after achieving full training status. Maintain a clean, organized, and safe work environment. Follow cleanroom gowning, PPE, safety, and other site-specific requirements. Use computers and manufacturing systems for daily documentation and transactions. Spend approximately 90% of the workday in manufacturing suites.Working hours:
7:00 AM - 7:00PM Skills:
Previous cGMP manufacturing experience. Biopharmaceutical manufacturing experience. Experience working in a controlled cleanroom environment. Experience with batch records and GMP documentation. Experience with manufacturing equipment and automated systems. Experience with preventative maintenance activities. Experience with CAPA, nonconformance, or quality systems.Education:
High School Experience:
1-4 yearsQualifications:
High school diploma or equivalent. Minimum 1 year of experience in manufacturing, production, operations, laboratory, or a related field. Knowledge of GMP and workplace safety practices. Ability to follow detailed procedures and work instructions. Ability to accurately complete manufacturing and quality documentation. Ability to learn new equipment, processes, software, and tools. Ability to identify and escalate quality, safety, or production concerns. Ability to work with minimal to moderate supervision. Effective written and verbal communication skills. Ability to read and review documentation for extended periods. Ability to work in a cleanroom and follow gowning procedures. Ability to wear required PPE and follow GMP requirements. Spherion West Springfield, MA, The Top-Rated Staffing Agency in Your Area! Looking for your next job? Visit us, call, or text today for personalized job matching and immediate interviews.Apply now:
www.spherion.com/apply/75808 Stay connected! Follow us on Facebook, Instagram, LinkedIn, and TikTok to learn more about Spherion West Springfield, MA, and discover your next opportunity.Email:
wspringfield@spherion.comPhone:
(413) 781-4120 Spherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temp-to-perm or direct hire opportunities, no one works harder for you than Spherion.Equal Opportunity Employer:
Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Spherion, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact Callcenter@spherion.com. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Spherion offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility). It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Show less Show more Spherion is seeking a reliable Production Associate to support manufacturing operations in a GMP-controlled environment. This position will perform production activities, maintain accurate documentation, inspect finished products, and follow established quality, safety, and cleanroom procedures.Responsibilities:
Follow work instructions and standard operating procedures to complete production assignments. Perform manufacturing activities in accordance with GMP and safety requirements. Maintain accurate inventory records, batch records, and manufacturing documentation. Inspect finished products to ensure they meet established specifications. Assist with batch record reconciliation and preventative maintenance activities. Follow Good Documentation Practices (GDP) and data integrity requirements. Assist with nonconformance and CAPA-related activities. Identify and report safety, quality, equipment, or production issues requiring escalation. Complete required training and assist with training other employees after achieving full training status. Maintain a clean, organized, and safe work environment. Follow cleanroom gowning, PPE, safety, and other site-specific requirements. ... Use computers and manufacturing systems for daily documentation and transactions. Spend approximately 90% of the workday in manufacturing suites.Working hours:
7:00 AM - 7:00PM Skills:
Previous cGMP manufacturing experience. Biopharmaceutical manufacturing experience. Experience working in a controlled cleanroom environment. Experience with batch records and GMP documentation. Experience with manufacturing equipment and automated systems. Experience with preventative maintenance activities. Experience with CAPA, nonconformance, or quality systems.Education:
High School Experience:
1-4 yearsQualifications:
High school diploma or equivalent. Minimum 1 year of experience in manufacturing, production, operations, laboratory, or a related field. Knowledge of GMP and workplace safety practices. Ability to follow detailed procedures and work instructions. Ability to accurately complete manufacturing and quality documentation. Ability to learn new equipment, processes, software, and tools. Ability to identify and escalate quality, safety, or production concerns. Ability to work with minimal to moderate supervision. Effective written and verbal communication skills. Ability to read and review documentation for extended periods. Ability to work in a cleanroom and follow gowning procedures. Ability to wear required PPE and follow GMP requirements. Spherion West Springfield, MA, The Top-Rated Staffing Agency in Your Area! Looking for your next job? Visit us, call, or text today for personalized job matching and immediate interviews.Apply now:
www.spherion.com/apply/75808 Stay connected! Follow us on Facebook, Instagram, LinkedIn, and TikTok to learn more about Spherion West Springfield, MA, and discover your next opportunity.Email:
wspringfield@spherion.comPhone:
(413) 781-4120 Spherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temp-to-perm or direct hire opportunities, no one works harder for you than Spherion.Equal Opportunity Employer:
Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Spherion, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact Callcenter@spherion.com. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Spherion offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility). It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Show less Show more key responsibilities Follow work instructions and standard operating procedures to complete production assignments.Perform manufacturing activities in accordance with GMP and safety requirements.
Maintain accurate inventory records, batch records, and manufacturing documentation.
Inspect finished products to ensure they meet established specifications.
Assist with batch record reconciliation and preventative maintenance activities.
Follow Good Documentation Practices (GDP) and data integrity requirements.
Assist with nonconformance and CAPA-related activities.
Identify and report safety, quality, equipment, or production issues requiring escalation.
Complete required training and assist with training other employees after achieving full training status.
Maintain a clean, organized, and safe work environment.
Follow cleanroom gowning, PPE, safety, and other site-specific requirements.
Use computers and manufacturing systems for daily documentation and transactions.
Spend approximately 90% of the workday in manufacturing suites. experience 1-4 years skills Previous cGMP manufacturing experience.
Biopharmaceutical manufacturing experience.
Experience working in a controlled cleanroom environment.
Experience with batch records and GMP documentation.
Experience with manufacturing equipment and automated systems.
Experience with preventative maintenance activities.
Experience with CAPA, nonconformance, or quality systems. qualifications High school diploma or equivalent.
Minimum 1 year of experience in manufacturing, production, operations, laboratory, or a related field.
Knowledge of GMP and workplace safety practices.
Ability to follow detailed procedures and work instructions.
Ability to accurately complete manufacturing and quality documentation.
Ability to learn new equipment, processes, software, and tools.
Ability to identify and escalate quality, safety, or production concerns.
Ability to work with minimal to moderate supervision.
Effective written and verbal communication skills.
Ability to read and review documentation for extended periods.
Ability to work in a cleanroom and follow gowning procedures.
Ability to wear required PPE and follow GMP requirements. education High School share this job. send via e-mail print it
Benefits
- 401(k) Plans
- Dental Insurance
- Disability Insurance
- Life Insurance