QC Microbiologist
- Employer
- Actalent
- Location
- Lower Chichester, Pennsylvania, US
- Salary
- Competitive
- Closing date
- Jul 4, 2022
View more
- Sector
- Consultancy/Private Sector
- Field
- Conservation science
- Discipline
- Other
- Salary Type
- Salary
- Employment Type
- Full time
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Overview
The Contract Quality Control Analyst will support quality control testing operations. The quality control testing programs include in-process and final drug product microbial testing such as bioburden, endotoxin, gram stain, environmental monitoring, and sterility techniques.
Specific Responsibilities:
Education and Qualifications:
Expected hours of work:
Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. Were supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
The Contract Quality Control Analyst will support quality control testing operations. The quality control testing programs include in-process and final drug product microbial testing such as bioburden, endotoxin, gram stain, environmental monitoring, and sterility techniques.
Specific Responsibilities:
- Perform daily cGMP quality control laboratory microbiological testing activities
- Perform data analysis and result reporting of microbiology assays to support product lot release with adherence to turnaround times
- Perform all activities with respect to cGMP compliance
- Support thorough cGMP investigations for out-of-specification test results
- Support technical problem solving
- Support product stability programs including execution of stability testing, stability data analysis, and final reporting of stability data
- Operate at a consistent and exemplary level of efficiency, producing high quality and accurate results
Education and Qualifications:
- Bachelors degree in a relevant discipline (biological sciences or equivalent)
- Minimum one (1) year of experience in the pharmaceutical industry within a Quality Control role; experience with cell therapy products is a plus
- Successfully interface with multi-disciplined teams
- Extremely detail-oriented with strong technical skills
- Ability to effectively manage multiple priorities involving aggressive timelines at a high level of productivity
- High level of ownership and accountability
- Demonstrate sense of urgency; ability to recognize time sensitivity
Expected hours of work:
- Weekend shift
- Wednesday to Saturday
- 10 hours/4 days
- 10AM - 8PM
About Actalent:
Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. Were supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
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