Quality Control (QC) Environmental Monitoring (EM) Specialist

Camris•Silver Spring, MD

4d•Onsite

About The Position

We are seeking a Quality Control (QC) Environmental Monitoring (EM) Specialist to support the Pilot Bioproduction Facility (PBF) at the Walter Reed Army Institute of Research (WRAIR) in Silver Spring, Maryland. PBF is a one-of-a-kind cGMP-compliant pharmaceutical manufacturing facility engaging in next-generation development for cutting-edge companies and government agencies. The professionals at PBF are engaging in trailblazing endeavors every day. Most exciting, the end products vary, so every year brings multiple opportunities for professional enrichment in original projects. CAMRIS International, LLC, is a dynamic medical research and development firm that achieves innovative solutions to health and development challenges through high-quality, cost-effective programs and research management services. We combine our proven systems with today's most effective, evidence-based best practices. Our core practice areas include vaccine research, development, and production; microbiology and infectious disease research; biodefense; clinical research; global health security; and HIV/AIDS programs. Our employees enjoy a collegial environment where individual contributions matter at all levels. At CAMRIS, you will notably improve the lives of people at home and abroad.

Requirements

BA/BS degree in a science field (preferably chemistry, biochemistry, biology, microbiology, or engineering) and four years of experience in a regulated laboratory environment or an equivalent combination of credentials and experience.
Skills in using various types of analytical techniques and laboratory equipment.
Excellent computer skills, including Microsoft Office software such as Word and Excel.
Knowledge of complex scientific/office procedures and techniques relating to the position.
Strong communication skills, including the ability to explain and teach methodologies.
Ability to work independently following specific technical training.
Must be currently eligible to work in the United States without visa sponsorship and have lived in the United States for three of the past five years if a non-US citizen.

Nice To Haves

Experience with technical writing and LIMS is a plus.
Knowledge of aseptic technique, cGMP, cGLP, or FDA regulations a plus.

Responsibilities

Execute analytical and microbiological testing on in-process materials and finished vaccine products, including (but not limited to): Growth media growth promotion, Microbial seed viability, Microbial identification, Gram Stain, Protein concentration, Visual Inspection.
Environmental monitoring of production clean rooms.
Sampling and testing the in-house purified water, WFI, and clean steam.
Sampling and testing of the in-house compressed gas system.
Assist senior associates on lab projects as requested and work on specialty projects as assigned.
Order supplies and perform basic laboratory equipment care.
Participate in SOP revision or authoring of new SOPs as required.
Responsible for limited data review and trend analysis as requested.
Train staff as requested.
Provide all job-related progress reports or technical reports, as requested, in a timely manner.
Maintain a safe workplace, ensuring that they know and observe appropriate safety and occupational health rules and regulations.
The employee must attend safety training relative to their position and report any infractions of safety procedures to the facility Safety Officer.
Performs other duties as assigned.