Job Description
Job Descriptionjob summary:
Join a leading manufacturing team in Framingham, MA as a Quality Inspector I and play a key role in maintaining critical laboratory operations. This onsite, first-shift position (Wednesday-Saturday, 8:30am-7:00pm) offers a stable schedule and the opportunity to work in a highly regulated, fast-paced environment that supports career growth in the pharmaceutical or biotech industry.
Ideal for detail-oriented individuals with strong Microsoft Office skills, this role involves sample coordination, documentation, and maintaining quality standards in compliance with CGMP. While a high school diploma is required, candidates with GMP or lab experience-or a science degree-are strongly encouraged to apply. With free onsite parking and the opportunity to relocate at your own expense, this is a solid stepping stone into the world of quality and compliance.
location: Framingham, Massachusetts
job type: Contract
salary: $25.00 - 28.50 per hour
work hours: 8 to 4
education: High School
responsibilities:
- Receive, document, and dispose of samples in the Quality Control laboratory according to SOPs and CGMP standards.
- Coordinate the distribution of samples to various testing laboratories and maintain detailed tracking records.
- Perform accurate data entry and filing of laboratory documentation to ensure data integrity and traceability.
- Manage laboratory reserve samples and ensure proper labeling, storage, and retrieval processes.
- Order and maintain inventory of laboratory supplies to support uninterrupted lab operations.
- Clean, store, and organize laboratory glassware following safety and cleanliness protocols.
- Update and maintain laboratory databases to track the completion of sample and documentation-related tasks.
qualifications:
Required Skills:
- High school diploma or equivalent.
- Experience with Microsoft Office Suite, especially Excel and Word.
- Detail-oriented with strong organizational skills.
- Authorized to work in the U.S. without sponsorship now or in the future (no visa sponsorship available).
- Ability to work independently under general supervision and in compliance with CGMPs.
Preferred Skills:
- At least 1 year of experience in a GMP (Good Manufacturing Practices) environment.
- Bachelor's degree in a science-related field (microbiology, chemistry, or similar).
- Laboratory experience or background in quality control processes.
- Familiarity with data entry and maintaining laboratory documentation.
skills: Quality control, SOP, Quality Assurance, Chemistry, Microbiology, GMP (Good Manufacturing Practice)
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 HRsupport@randstadusa.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, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (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.