Adicet Bio Inc.
Quality Control Microbiology Associate
Adicet Bio Inc., Redwood City, California, United States, 94061
Quality Control Microbiology AssociateThe Quality Control (QC) Microbiology Associate is an energetic and entry-level individual with a background in microbiology, biology, or other related fields of science. The Quality Control Microbiology Associate is responsible for collecting environmental monitoring and personnel monitoring samples in the cleanroom in accordance with SOP, and cGMP guidelines.
Key responsibilities:
Perform environmental monitoring (EM) in cleanrooms and controlled areas.
Complete documentation for QC activities including EM data, material preparation, equipment logs and inventory logs.
Draft and review data reports.
Perform microbial isolations and identifications.
Write and revise QC specific procedures .
Generate EM trend reports.
Write/participate in EM investigations, deviation, and CAPAs.
Maintenance of the laboratory, supplies, and equipment.
QUALIFICATIONS:
BS in biological sciences or a related field is required.
1-3 years of relevant academic and industry experience in a manufacturing environment.
Familiarity with cleanroom environment is desirable.
Familiarity with data processing software such as Excel, Word, PowerPoint is desirable.
Familiarity with microbiology is desirable.
Ability to operate for lengthy periods of time while gowned in cleanroom is expected.
Experience in drafting of documents such as SOPs or reports is desirable.
Ability to work both independently and in a team environment, multitask and meet deadlines in a fast-paced environment.
High initiative, organized, and conscientious record keeping skills, strong attention to detail.
Excellent verbal and written communication skills.
Ability to utilize troubleshooting and problem-solving skills.
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Key responsibilities:
Perform environmental monitoring (EM) in cleanrooms and controlled areas.
Complete documentation for QC activities including EM data, material preparation, equipment logs and inventory logs.
Draft and review data reports.
Perform microbial isolations and identifications.
Write and revise QC specific procedures .
Generate EM trend reports.
Write/participate in EM investigations, deviation, and CAPAs.
Maintenance of the laboratory, supplies, and equipment.
QUALIFICATIONS:
BS in biological sciences or a related field is required.
1-3 years of relevant academic and industry experience in a manufacturing environment.
Familiarity with cleanroom environment is desirable.
Familiarity with data processing software such as Excel, Word, PowerPoint is desirable.
Familiarity with microbiology is desirable.
Ability to operate for lengthy periods of time while gowned in cleanroom is expected.
Experience in drafting of documents such as SOPs or reports is desirable.
Ability to work both independently and in a team environment, multitask and meet deadlines in a fast-paced environment.
High initiative, organized, and conscientious record keeping skills, strong attention to detail.
Excellent verbal and written communication skills.
Ability to utilize troubleshooting and problem-solving skills.
#J-18808-Ljbffr