Location Requirements: On site in Braintree, MA

Pay Rate: $30/hr max pay

W2 contract only - no C2C or 1099

Duration: 6+ months, possible temp to hire

Required Skills

• ISO 13485 exp preferred, along with ISO 7 and 8 cleanroom
• ISO 5 is even better

Must Have:

• Environmental Monitoring
• Water Monitor & Collecting
• Performing tests in the lab and familiar with aseptic techniques
• Microsoft Office experience - Advanced/Proficient
• Exp with Bioburden testing is great

Responsibilities:
* Responsible for performing Microbiological testing such as Bioburden, Endotoxin, Growth promotion testing, TOC & Conductivity testing, sending samples for Microbial ID testing and other micro testing.
* Perform Environmental monitoring of clean rooms including Viables and Non-viables testing and responsible of water samples collection and testing.

• Working knowledge of aseptic techniques and provides database support, generates reports, and analyzes the data as needed.
• Inspection and testing of raw materials, in-process, and final product testing.
• Assist in trending environmental monitoring data. Report and investigate any monitoring excursions.
• Monitors equipment and instrumentation used daily to ensure proper operation and calibration.
• Maintains a working inventory of all components, materials and solutions as needed.
• Develops and revises SOPs & Forms
• Responsible for identifying and alerting supervisor of issues on instruments and/or test executions; makes initial recommendations for possible solutions and/or corrective actions.
• Assist in Out of Specification (OOS) Investigations, Non-conformances, and Corrective Action/Preventive Actions (CAPAs).
• Assists in the writing and updating of Microbiological test procedures, protocol, logbooks, and checklists.
• Assist as needed in test method validation, investigation studies or other product development studies.
• Assist in preparing for and participating in FDA audits, customer audits, etc.

Qualifications:

• Bachelor's degree in Microbiology, Biology, or a relevant scientific discipline.
• A minimum of 2-4 years' experience in a medical device, pharmaceuticals, Quality/Regulatory Compliance, or other cGMP regulated product preferred environment.
• Familiarity with application of FDA and/or ISO quality standards in a government regulated industry. Quality Certification (e.g., CQE, CQA, Six Sigma) preferred.
• Proficient computer competence, including experience with database and Microsoft Office software to create reports, spreadsheets, analyze data and prepare presentations.
• Experience with performing Microbiological assays in cGMP compliance lab and understanding of aseptic techniques.
• Working knowledge of standard laboratory practices and safety.
• Ability to follow instructions precisely, recognize deviations, and recommend corrective action.
• Experience working in ISO Class 7 & 8 cleanrooms preferred.

Impellam Group and its brands are equal-opportunity employers committed to diversity and inclusion. All qualified applicants will receive consideration without regard to race, color, religion, gender, sexual orientation, pregnancy or maternity, national origin, age, disability, veteran status, or any other factor determined to be unlawful under applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application, interview process, pre-employment activity, and the performance of crucial job functions.

If you require additional disability considerations, modifications, or adjustments please let us know by contacting HR-InfoImpellamNA@impellam.com or fill out this form to request accommodations.