Environmental Monitoring and Utilities Monitoring Technical Support, Quality Con
Atrium, Boston, MA, United States
EM/UM Technical Support, Quality Control Microbiology
The Environmental Monitoring and Utilities Monitoring Technical Support role will provide technical support for the EM/UM team as a Subject Matter Expert (SME). This role will serve as a key resource within the organization, providing technical expertise in the areas of EM/UM sampling, testing, aseptic processing, and contamination control in accordance with regulatory standards. This role reports to the Associate Director of Quality Control in Cell and Genetic Therapies (VCGT).
On‑site role.
12‑month contract with the chance to extend.
Key Duties and Responsibilities
Demonstrates a strong understanding of sampling and microbiological testing methodologies, including but not limited to EM, UM, Bioburden, Endotoxins, Sterility, Gram Stain, and Identification program per relevant regulatory standards.
Hands‑on experience in the handling of microbiology lab instruments, i.e., Vitek, Endosafe, BacT, MALDI-TOF, and Isolator.
Organize, plan, and support team members with technical questions and problem‑solving to ensure group efficiency and accountability.
Ensure compliance with current Good Manufacturing Practices (cGMP), as well as Health, Safety, and Environmental policies per Vertex standards.
Provide subject matter expertise in Out‑of‑Specification (OOS) and Out‑of‑Trend (OOT) investigations.
Manages deviations and Corrective and Preventative Action (CAPA) implementation associated with Microbiological methodologies.
Support laboratory inspections and audits, including addressing follow‑up actions and ensuring continuous improvement.
Collaborate with cross‑functional teams, including Manufacturing, Quality Assurance, Regulatory CMC, and Analytical Development, to ensure alignment and effective communication between teams.
Assist with document revisions.
Knowledge and Skills
Extensive knowledge and experience of Quality Control methods and compendial requirements, including but not limited to (Sterility, Endotoxin, Environmental monitoring, ID, APS/PAQ processes).
Strong understanding of Aseptic processing and contamination control strategies in manufacturing facilities.
Extensive experience working in a GMP environment.
Strong communication and scientific writing.
Experience with electronic systems such as LIMS and Quality Management Systems (Veeva) preferred.
Education and Experience
Bachelor’s degree in Microbiology or related field.
A minimum of 7 years of industry experience in Microbiology in a Biotechnology and/or Cell and Gene therapy organization.
Pay Range
$60/HR – $70/HR
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The Environmental Monitoring and Utilities Monitoring Technical Support role will provide technical support for the EM/UM team as a Subject Matter Expert (SME). This role will serve as a key resource within the organization, providing technical expertise in the areas of EM/UM sampling, testing, aseptic processing, and contamination control in accordance with regulatory standards. This role reports to the Associate Director of Quality Control in Cell and Genetic Therapies (VCGT).
On‑site role.
12‑month contract with the chance to extend.
Key Duties and Responsibilities
Demonstrates a strong understanding of sampling and microbiological testing methodologies, including but not limited to EM, UM, Bioburden, Endotoxins, Sterility, Gram Stain, and Identification program per relevant regulatory standards.
Hands‑on experience in the handling of microbiology lab instruments, i.e., Vitek, Endosafe, BacT, MALDI-TOF, and Isolator.
Organize, plan, and support team members with technical questions and problem‑solving to ensure group efficiency and accountability.
Ensure compliance with current Good Manufacturing Practices (cGMP), as well as Health, Safety, and Environmental policies per Vertex standards.
Provide subject matter expertise in Out‑of‑Specification (OOS) and Out‑of‑Trend (OOT) investigations.
Manages deviations and Corrective and Preventative Action (CAPA) implementation associated with Microbiological methodologies.
Support laboratory inspections and audits, including addressing follow‑up actions and ensuring continuous improvement.
Collaborate with cross‑functional teams, including Manufacturing, Quality Assurance, Regulatory CMC, and Analytical Development, to ensure alignment and effective communication between teams.
Assist with document revisions.
Knowledge and Skills
Extensive knowledge and experience of Quality Control methods and compendial requirements, including but not limited to (Sterility, Endotoxin, Environmental monitoring, ID, APS/PAQ processes).
Strong understanding of Aseptic processing and contamination control strategies in manufacturing facilities.
Extensive experience working in a GMP environment.
Strong communication and scientific writing.
Experience with electronic systems such as LIMS and Quality Management Systems (Veeva) preferred.
Education and Experience
Bachelor’s degree in Microbiology or related field.
A minimum of 7 years of industry experience in Microbiology in a Biotechnology and/or Cell and Gene therapy organization.
Pay Range
$60/HR – $70/HR
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