Raw Materials Associate

tsu.edu; Norwood (MA); On-site; USD 34,000 - 41,000; Full time

Job summary

tsu.edu in Norwood, MA is seeking a Raw Materials Associate I to perform QC raw material activities in support of GMP manufacturing. The role pays $25-$30 per hour on a 6+ month contract and requires a BS in a scientific discipline.

You will handle sampling, shipping, testing, documentation, and compliance with GxP and cGMP, while maintaining a safe lab and contributing to continuous improvement.

Qualifications

• GxP regulations familiarity for QC workflows.
• Demonstrated ability to learn new methods quickly.
• Collaborative mindset in cross-functional teams.

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 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.

Skills

GxP Regulations knowledge

Aptitude to learn

Team collaboration

Education

BS in a relevant scientific discipline

Job description

Title: Raw Materials Associate I
Location: Norwood, MA
Pay: $25-30/hr
Contract: 6+ months

Job Summary

The individual in this role will perform QC Raw Material activities in support of GMP Manufacturing and potentially support special projects as assigned.

Job 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.

Education & Qualifications

• 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.