Research Associate II
LGC Group•Gaithersburg, MD
•$27 - $37•Onsite
About The Position
The Research Associate II will support the research and development of new precision diagnostic products for LGC Clinical Diagnostics. This role involves independently performing routine and non-routine applications of cellular/molecular genetic technology to quantitate and manipulate genetic material.
Requirements
- A Bachelor's degree with at least 2 years of industry experience
- Experience in Molecular Biology techniques such as DNA/RNA Purification and quantitation, PCR (Endpoint or Real time PCR), DNA/RNA electrophoresis.
- Basic cell culture and aseptic techniques
- Experience in writing and executing protocols
- Software experience: Excel, Word and PowerPoint.
- Analytic skills: Perform preliminary data interpretation/analysis. Follow SOPs.
Nice To Haves
- Master’s degree in Biochemistry or Molecular Biology or a related field
- Critical thinker who can analyze date and respond quickly to manage projects.
- Ability to manage and complete projects as assigned.
- Capability of working with multiple departments to achieve project related goals.
- Ability to work independently with minimal supervision.
- Strong organizational skills
- Engaged and committed team professional who is committed for product integrity.
- Passion for continuous improvement.
- Can work on diverse projects and is willing to reprioritize them as needed
- Collaborates effectively with others
- Independent thinker and self-learner
Responsibilities
- Manufacture intermediate level stock products using batch records and standard operating procedures.
- Perform general molecular techniques such as plasmid purification, gel-electrophoresis, RNA transcription, and bacterial culturing.
- Perform nucleic acid analysis (RNA/DNA integrity analysis, real time qPCR, digital PCR) and analyze results.
- Organize projects and data using Excel, Word, PowerPoint and a document control system.
- Work with supervisor to plan and execute new projects as assigned according to the timelines and ensure documentation meets GLP/GMP requirements.
- Record test results and data records, seek appropriate approval and file according to established procedures.
- Maintain, calibrate and operate equipment according to established protocols. Monitor equipment for appropriate operation within set parameters and refer abnormal results to lab management.
- Work in collaboration with the Quality Assurance group to fulfil Quality Management Goals and proactively address problems under an ISO quality system.
- Plan for raw material requirements by maintaining appropriate inventory of reagents and ordering reagents as needed through an ERP system (SAP).
- Maintain a clean and safe lab environment.
Benefits
- Competitive compensation with strong bonus program
- Comprehensive medical, dental, and vision benefits for employees and dependents
- FSA/HSA Pre-tax savings plans for health care, childcare, and elder care
- Deductible Buffer Insurance and Critical Illness Insurance
- Great gym onsite!
- 401(k) retirement plan with matching employer contribution
- Company-paid short- and long- term disability, life insurance, and employee assistance program
- Flexible work options
- Pet Insurance for our furry friends
- Enhanced Parental leave of 8 additional weeks
- PTO that begins immediately
- Town Hall monthly meeting onsite/virtual, Cheer program where employees are recognized for outstanding work, Companywide social events, frequent catered lunches and much more!
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
