What are the responsibilities and job description for the Microbiology Technician position at WhiteCrow Research?
About WhiteCrow
We are global talent research, insight, and sourcing specialists with offices in the UK, USA, Singapore, Malaysia, Hong Kong, Dubai, and India. Our international reach has helped us to understand and penetrate specialist markets at a global level. In addition to this, our service is also extended to complement our client’s in-house talent acquisition teams.
About our client
Our client is a global injectables company headquartered in Bengaluru, India, with a strong presence across Asia, Europe, and the USA, and is expanding rapidly into new markets. The company focuses on developing value-added sterile injectables that address critical gaps in healthcare delivery.
By enhancing hospital workflows, reducing wastage of key resources, and improving operational efficiency, our client plays a vital role in supporting healthcare professionals. A robust and reliable supply chain further ensures consistent access to essential medications for patients worldwide.
As a Microbiology Technician, you will be responsible for...
- Performing routine environmental monitoring (viable and non-viable) in classified cleanroom areas (Grade A/B/C/D), including surface and personnel monitoring. Manufacturing is performed inside isolators with surrounding grade C environment.
- Collecting and testing samples from water systems (e.g., purified water, WFI), compressed gases, and other utilities per GMP and site procedures.
- Supporting aseptic process simulations (media fills), including preparation, execution, and recovery/interpretation of microbiological data.
- Performing microbiological tests such as bioburden, endotoxin (LAL), and sterility testing for raw materials, in-process samples, and finished products.
- Preparing microbiological media, perform growth promotion testing, and maintain inventory of reagents and supplies.
- Maintaining laboratory notebooks, logs, and electronic systems in a compliant and organized manner, ensuring adherence to data integrity standards.
- Supporting qualification and validation activities including cleanroom and utility qualifications, method validations, and EM qualification mapping.
- Assisting in investigations related to microbial excursions or deviations and contribute to the development and implementation of CAPAs.
- Supporting microbiology lab startup activities including equipment qualification, SOP development, and execution of technical transfer protocols.
- Following all safety, quality, and regulatory policies, and maintain compliance with cGMP, USP, EU Annex 1, and other applicable guidelines.
What you already have...
Qualifications/Experience:
- Associate’s or bachelor’s degree in microbiology, Biology, Life Sciences, or a related field.
- 1–3 years of microbiology laboratory experience in a GMP-regulated pharmaceutical or biotechnology manufacturing environment.
- Experience working in sterile environments or supporting aseptic processes preferred.
- Familiarity with environmental monitoring equipment (e.g., particle counters, air samplers), microbiological techniques, and lab instrumentation.
- Knowledge of cGMPs, data integrity principles, and microbiological standards (USP <61>, <62>, <71>, <85>, <1116>).
Skills/Competencies:
- Strong attention to detail and commitment to data accuracy and integrity.
- Ability to work independently while collaborating effectively within a team
- Good time management and organizational skills to support multiple tasks and priorities.
- Proficient in the use of Microsoft Office and basic laboratory software systems.
- Willingness to work flexible shifts or weekends to support aseptic operations and testing schedules, as needed.
- A proactive and patient-focused mindset with a strong sense of ownership and compliance.