QC/QA Inspector II

Randstad USA; Worcester (MA); On-site; USD 34,000 - 39,000; Full time

Job summary

Randstad USA in Worcester, MA is seeking a QA/QC Inspector II for a 2nd shift assignment to support quality operations in a fast-paced GMP environment. This on-site role focuses on data reviews, archiving lab records, and ensuring regulatory compliance.

The ideal candidate has a scientific background or equivalent QA/QC experience, with hands-on use of EMPOWER and A280/Solo VPE instrumentation. Strong organization and teamwork are essential for daily project targets.

Qualifications

• Bachelor's degree in a scientific field or High School Diploma with 5+ years QA/QC experience in pharmaceutical/biologics.
• Hands-on experience with EMPOWER and A280 / Solo VPE instrumentation.
• Demonstrated background working within a fast-paced GMP environment.
• Strong organizational and time management abilities.

Responsibilities

• Review laboratory test data on- and off-the-floor per GMP regulations.
• Archive data and support administrative duties using the RIMS system, including logbook management and document scanning.
• Conduct data mining projects and manage laboratory records with strict attention to quality.
• Maintain a safe, compliant work environment by adhering to procedures and safety requirements.
• Collaborate with cross-functional team members to achieve daily operational and project targets.

Skills

GMP

QA

QC

Education

Bachelor's degree in a scientific field

High School Diploma with 5+ years QA/QC experience

Tools

EMPOWER

A280 / Solo VPE instrumentation

Job description

job summary:

• A Top-Tier Global Pharma Leader in Worcester, MA is seeking a detailed-oriented QA-QC Inspector II for a 2nd shift role (Sunday-Thursday, 2:00 PM-10:30 PM). This onsite opportunity focuses on performing low-complexity data reviews, archiving lab records, and supporting quality operations in a fast-paced GMP environment.

location: Worcester, Massachusetts
job type: Contract
salary: $25.00 - 28.77 per hour
work hours: 9 to 5
education: High School
responsibilities:

• Perform routine on-the-floor and off-the-floor reviews of laboratory test data in compliance with GMP regulations.
• Archive data and support administrative duties using the RIMS system, including logbook management and document scanning.
• Conduct data mining projects and manage laboratory records with strict attention to quality standards.
• Maintain a safe, compliant work environment by adhering to procedural and safety requirements.
• Collaborate with cross-functional team members to achieve daily operational and project targets.

qualifications:

• Required:
  • Bachelor's degree in a scientific field (or High School Diploma with 5+ years of QA/QC experience in pharmaceutical/biologics).
  • Hands-on experience with EMPOWER and A280 / Solo VPE instrumentation.
  • Demonstrated background working within a fast-paced GMP environment.
  • Strong organizational and time management abilities.
• Preferred:
  • Experience with LIMS systems.

#LI-MH1
skills: Good Manufacturing Practices (GMP), Quality Assurance (QA), Quality Control (QC)
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 Randstad, 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 [e-mail].
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, Randstad 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).
This posting is open for thirty (30) days.
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.

• Required:

  • Bachelor’s degree in a scientific field (or High School Diploma with 5+ years of QA/QC experience in pharmaceutical/biologics).

  • Hands-on experience with EMPOWER and A280 / Solo VPE instrumentation.

  • Demonstrated background working within a fast-paced GMP environment.

  • Strong organizational and time management abilities.

• Preferred:

  • Experience with LIMS systems.

#LI-MH1