Microbiologist
Microbiologist
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$ 21 - 38
1 Vacancy
Job Description
Job Overview:
Executes the activities of QC Microbiology Laboratory by following approved microbiological and chemical test procedures and ensuring their delivery in an accurate and timely manner following proper safety precautions.
Responsibilities:
Provides QC microbiology support to the Aseptic Manufacturing and validation process.
Performs Microbiological Tests and studies by following the established procedures referenced in the official sources.
Collection of water samples for testing (WFI DI Raw)
Collection of samples (Raw Materials Excipients Validation In-process and Finished product samples) for microbiological/chemical testing.
Conducts validations studies and routine tests related to Bioburden Tests Bacterial Endotoxin Tests Particulate Matter Test and Sterility Tests.
Preparation of microbiological media and diluents by following laboratory procedures
Quality Control Testing of microbiological media and reagents.
Environment Monitoring of Aseptic / Non-aseptic Manufacturing areas and Trending of microbial data obtained from EM/Utilities/Raw Materials/In-process and finished products testing and preparing the periodical summary report.
Maintenance of Laboratory inventory and cleanliness of the Laboratory.
Responsible for maintaining the microbiology isolates obtained from EM and Utility Monitoring Program.
Follow established health and safety procedures and policies related to QC Microbiology Laboratory operations. Perform other related duties as and assigned by Microbiology Laboratory Management.
Perform other duties as assigned.
Qualifications:
A.S. in a life sciences discipline and 2 years of relevant experience working in cGMP cleanrooms and QC Microbiology lab B.S / M.S. in a life sciences discipline and 0-2 years of relevant experience working in cGMP cleanrooms and QC Microbiology or equivalent combination of education training and professional experience that provides the individual with the required knowledge skills and abilities.
Demonstrates flexibility in following unique campaign requirements that may include off-hour and weekend work.
Demonstrate thorough understanding of QC Microbiology Laboratory Operations and Sterility Assurance program.
Demonstrate the ability to establish good working relationships with other departments including vendors colleagues and subordinates.
Demonstrates the appropriate technical knowledge necessary to make sound decisions on development issues with minimal supervision.
Demonstrate the ability to analyze data and information and assess and resolve complex problems/issues as .
Must be able to comprehend and follow all applicable SOPs.
Demonstrate knowledge and experience with electronic Quality Management Systems such as MasterControl and Trackwise.
Demonstrate solid understanding of the current federal local and international regulations regarding the production testing and release of drug substances and products.
Good understanding of cGMPs industry and regulatory standards and guidelines.
Demonstrate familiarity with Microsoft programs like Word Excel PowerPoint Project Teams Outlook etc.
Demonstrate the ability to portray the appropriate level of integrity and professionalism.
Demonstrate the ability to communicate effectively with management staff regulators and client representatives in written and verbal formats.
Demonstrate the ability to complete tasks accurately and according to established and shifting timelines.
Demonstrate the ability to make quality scheduling resource allocation and priorities decisions.
Energetic execution-focused self-motivated and organized individual who is accustomed to working in a deadline-focused high-pressure entrepreneurial environment.
Results-oriented and efficient.
Creative and open-minded who fosters an environment in which sharing of ideas is encouraged.
Demonstrate the ability to work closely with a diverse customer and employee base (internally and externally).
Demonstrate the ability to work well in a cross-functional team environment.
Must communicate fluently in English and have legible handwriting.
Physical Demands:
Ability to travel between and within facilities to visit staff operations and projects as needed.
Ability to sit stand climb stairs and climb ladders to mezzanines (when necessary).
Ability to lift up to 40 pounds on occasion.
Ability to use PPE (safety shoes goggles respirators gloves etc. when necessary).
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Jabil including its subsidiaries is an equal opportunity employer and considers qualified applicants for employment without regard to race color religion national origin sex sexual orientation gender identity age disability genetic information veteran status or any other characteristic protected by law.
Accessibility Accommodation
If you are a qualified individual with a disability you have the right to request a reasonable accommodation if you are unable or limited in your ability to use or access site as a result of your disability. You can request a reasonable accommodation by sending an e-mail to or calling with the nature of your request and contact information. Please do not direct any other general employment related questions to this e-mail or phone number. Please note that only those inquiries concerning a request for reasonable accommodation will be responded to.#whereyoubelong
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Employment Type
Full-Time
