QC Raw Materials Associate I (2nd Shift)

job summary:
Step into a crucial hands-on quality control role where your daily work directly ensures the safety and efficacy of life-saving products. Working on our 2nd shift team, you will take ownership of raw material sampling and release, utilizing advanced analytical tools and precise techniques in a modern laboratory environment.

Shift: 2 nd shift / 12pm-8pm, Monday through Friday

location: Norwood, Massachusetts
job type: Contract
salary: $35 - 42 per hour
work hours: 9 to 5
education: Bachelors

responsibilities:

• Requesting, sampling, and shipping of raw materials
• Sample coordination including cross functional collaboration with internal and external labs
• Supporting domestic and international sample shipments
• Supporting testing for methods including pH, conductivity, TruScan RM spectroscopy, appearance, and dimensional verification
• Inspect product and raw material retain samples.
• LIMS (LabVantage) sample logging and result entry
• Raw material and consumable component inspection and release
• Clean room gowning and aseptic techniques.
• Managing/stocking of QC lab supplies and routine lab cleaning.
• Complete and maintain cGMP documentation for work performed.
• Maintain a safe laboratory working environment.
• Foster a positive and inclusive work culture that promotes collaboration, innovation, and continuous improvement.
• Follow all relevant GxP regulations, guidelines, and company policies to ensure compliance with regulatory and internal requirements.
• Execute tasks precisely as defined in internal guiding documents including but not limited to standard operating procedures (SOPs) and work instructions.
• Follow Good Documentation Practices and Data Integrity requirements to ensure data, documentation, and records are completed and maintained for use by the business and available to support audits or inspections.
• Complete training in assigned required learning plan according to the defined timing and the prescribed requalification cadence.

 
qualifications:
Required:

• BS in a relevant scientific discipline.
• 0-2 years with BS or 3+ experience in GMP QC laboratory setting.
• Demonstrated aptitude or ability to learn
• Strong understanding of GxP Regulations, with a proactive team-oriented approach.

#LI-KH1

skills: Quality control, GMP (Good Manufacturing Practice), LIMS (Laboratory Information Management System




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 View email address on us.fitly.work.




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.