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Those who join Emergent BioSolutions feel a sense of ownership about their future. You will excel in an environment characterized by respect, innovation and growth opportunities. Here, you will join passionate professionals who advance their scientific, technical and professional skills to develop products designed-to protect life.
ANALYST I, QC LAB SERVICES - MICROBIOLOGY (Multiple Positions)
Term positions available beginning in March 2021 for 6 months with the potential for term extensions or permanent positions
THE COMPANY
Emergent BioSolutions is dedicated to one simple mission—to protect and enhance life.
As a global specialty pharmaceutical company, Emergent offers specialized products to healthcare providers and governments to address medical needs and emerging health threats.
We value the diversity that each employee brings, and while we look for people who share our Core Values, we thrive on difference as well. With hundreds of talented employees working around the globe, Emergent is a growing organization with a wide variety of scientific, technical and professional career opportunities worldwide.
THE OPPORTUNITY
The Analyst I, QC Laboratory Services performs GMP compliant testing as required to support the facility environment and filling process, Raw Material testing, In-process, Finished Product release & Stability or nonclinical/ clinical studies. The Analyst I also perform testing required to support assay and process validations. He/She will perform testing to support release of lab specific material (media, standards).
Essential Functions
Perform routine laboratory procedures including analyzing and reviewing data
Receive and test samples
Receive, prepare, test, release materials used for QC testing (for example: media, standards)
Document laboratory work consistent with GxP requirements
Maintain laboratory records and inventory for supplies and reagents
Perform preventative maintenance on laboratory equipment in accordance with established procedures.
Perform detailed technical and data integrity review of QC data as required
Adhere to all effective TMD’s/SOPs and safety requirements and document laboratory work consistent with cGMP requirements
Initiate investigation reports attaching required documentation
Maintain a clean and sanitary work area in accordance with standard laboratory practice and procedures
Prepare and Autoclave supplies and garbage
Model the organizational core values through day-to-day actions
**EDUCATION, EXPERIENCE & SKILLS**:
Bachelor’s Degree in a scientific discipline
Under two years’ experience in a pharmaceutical cGMP environment
Basic knowledge of Microsoft Office - Word, Excel
Basic knowledge of pharmaceutical GLPs and GMPs
Knowledge of laboratory techniques and safety precautions
WHMIS and biohazard safety awareness
Ability to work in a fast paced and highly regulated environment
Able to multi-task and adapt to changing priorities
Competent in laboratory safety and generally-accepted lab practice, including maintaining adequate written laboratory records
Able to communicate and articulate information in both written and verbal forms
Strong organizational and interpersonal skills; can work collaboratively with others.
Able to interpret analytical data
