Job summary
Job post source
This job is directly from CAMRIS
Job overview
The Quality Control Scientist role at CAMRIS supports the Pilot Bioproduction Facility at WRAIR, leading analytical testing and quality control to ensure compliance and scientific rigor in pharmaceutical manufacturing.
Responsibilities and impact
The scientist will lead QC analytical efforts including method development, validation, transfer, equipment management, data analysis, and mentoring junior staff to support drug development and regulatory compliance.
Compensation and benefits
CAMRIS offers a comprehensive benefits package including medical, dental, vision insurance, FSAs, HSA, life and disability insurance, 401(k) with match, tuition reimbursement, paid time off, and other employee support programs.
Experience and skills
Candidates need a master's degree with 10 years pharma analytical experience or equivalent, expertise in GMP analytical methods, PCR, UPLC, LC-MS, ELISA, LIMS proficiency, and leadership skills; a PhD and CGE/cIEF experience are preferred.
Career development
The role offers opportunities for professional enrichment through diverse projects at a cutting-edge cGMP facility and mentoring responsibilities for junior scientists.
Work environment and culture
CAMRIS promotes a collegial environment valuing individual contributions, with a focus on impactful health and development work globally.
Company information
CAMRIS International is a medical research and development firm specializing in vaccine research, biodefense, infectious diseases, and global health programs, supporting government and commercial clients.
Team overview
The position is within the ASAT team at the Pilot Bioproduction Facility, working cross-functionally with quality assurance and external partners like CDMOs.
Job location and travel
The job is located at the Walter Reed Army Institute of Research in Silver Spring, Maryland, within a cGMP-compliant pharmaceutical manufacturing facility.
Application process
Applicants must submit their resume online at CAMRIS.com and complete a Public Trust-level background check as part of the federal contract requirements.
Unique job features
This role is distinguished by its involvement in next-generation pharmaceutical manufacturing, complex analytical method leadership, and work in a unique government-affiliated cGMP facility.
Company overview
CAMRIS is a global development and research firm that provides innovative solutions in health, agriculture, economic development, and humanitarian assistance. They generate revenue through government contracts, primarily with agencies like USAID and the Department of Defense, offering services such as project design, implementation, and evaluation. Founded in 1955, CAMRIS has a long history of contributing to international development and has built a reputation for using evidence-based approaches to improve outcomes in challenging environments.
How to land this job
Position your resume to highlight leadership in analytical method development, method transfer, and validation within cGMP environments, emphasizing experience with PCR, UPLC, LC-MS, ELISA, and mRNA characterization technologies.
Focus on showcasing expertise in LIMS platforms, especially LabVantage, and your role in process optimization, equipment lifecycle management, and regulatory compliance including FDA and ICH guidelines.
Apply through multiple channels including CAMRIS's official website (www.CAMRIS.com), LinkedIn job postings, and relevant pharmaceutical industry job boards to maximize application visibility.
Connect with current CAMRIS employees in the Analytical Sciences and Technology or Quality Control divisions on LinkedIn; start conversations by referencing recent CAMRIS projects at the Walter Reed Army Institute of Research or asking about their experience working in a cGMP-compliant pilot bioproduction facility.
Optimize your resume for ATS by incorporating keywords such as 'method transfer,' 'analytical testing,' 'cGMP,' 'LIMS,' 'FDA compliance,' 'stability testing,' and specific equipment names like 'Quant Studio 5/7' and 'CGE/cIEF' to ensure your resume passes initial electronic screenings.
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