Research Associate II
LGC Clinical Diagnostics•Gaithersburg, MD
•$27 - $37•Onsite
About The Position
Advance LGC Clinical Diagnostics purpose of understanding disease by supporting the research and development of new precision diagnostic products. Support includes 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
Mid Level
