Job summary
Job post source
This job is directly from CAMRIS
Job overview
The GMP Senior Project Manager at CAMRIS leads project management for the Pilot Bioproduction Facility, overseeing biologics development and manufacturing projects to ensure timely, high-quality delivery.
Responsibilities and impact
The role involves managing project schedules, reporting performance, leading team meetings, coordinating client interactions, resource planning, risk evaluation, process improvement, and building the PMO from the ground up.
Compensation and benefits
CAMRIS offers a comprehensive benefits package including medical, dental, vision insurance, FSAs, HSA, life and disability insurance, legal services, pet insurance, 401(k) with match, tuition reimbursement, paid time off, holidays, bonding leave, and a referral bonus program.
Experience and skills
Candidates need a BS/BA and 12 years in biologics development or manufacturing, proficiency in MS Project and Microsoft Office tools, operational excellence knowledge, and US work eligibility; PMP, cost analysis, CDMO, capital project management, SmartSheet, and leadership experience are preferred.
Career development
The job offers professional enrichment through diverse projects and mentoring junior staff, with opportunities to grow the PMO and develop leadership skills.
Work environment and culture
CAMRIS promotes a collegial environment valuing individual contributions, focused on impactful health and development solutions globally.
Company information
CAMRIS International is a medical research and development firm specializing in vaccine research, infectious diseases, biodefense, clinical research, and global health security, delivering innovative, cost-effective programs.
Team overview
The candidate will join the PMO team supporting the Pilot Bioproduction Facility, collaborating closely with government and private clients and internal teams to manage over 20 projects.
Job location and travel
The position is based at the Walter Reed Army Institute of Research in Silver Spring, Maryland, with no specific mention of remote work or travel requirements.
Application process
Applicants must submit resumes online at www.CAMRIS.com and undergo a Public Trust-level background check as part of the federal contract requirements.
Unique job features
This role is unique in building the PMO from scratch at a cutting-edge cGMP pharmaceutical manufacturing facility engaged in next-generation biologics projects.
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 your extensive experience managing biologics development or manufacturing projects, emphasizing your proficiency with MS Project, SmartSheet, and resource planning tools relevant to GMP environments.
Emphasize leadership skills in building and scaling Project Management Offices (PMO), your ability to manage complex schedules, budgets, and cross-functional teams, and your experience with operational excellence and process standardization.
Apply through multiple channels including the CAMRIS corporate website and LinkedIn to maximize your visibility and chances of selection for the GMP Senior Project Manager role.
Connect with current CAMRIS employees in the Pilot Bioproduction Facility or Project Management divisions on LinkedIn to gain insights and express your enthusiasm; use ice breakers like commenting on CAMRIS’s innovative work in biologics manufacturing or asking about their experiences working on government contracts.
Optimize your resume for ATS by incorporating keywords from the job description such as 'GMP', 'biologics development', 'MS Project', 'SmartSheet', 'PMO', 'resource planning', and 'operational excellence' to ensure it passes initial screenings effectively.
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