We help prepare for today's challenges and tomorrow's threats.
Gaithersburg, Maryland
At Emergent, our mission is to protect and save lives. For over 25 years, we’ve been at work preparing those entrusted with protecting public health. We deliver protective and life-saving solutions for health threats like smallpox, mpox, botulism, Ebola, anthrax and opioid overdose emergencies. To learn more about how we help prepare communities around the world for today’s health challenges and tomorrow’s threats, visit our website and follow us on LinkedIn, X, Instagram, Apple Podcasts and Spotify. Please note: It has come to our attention that there may be people posing as Emergent recruiters and hiring managers online, offering fraudulent opportunities to job seekers. Emergent will never ask for any financial commitment from a candidate as a pre-employment requirement. Learn more about recruitment fraud and how to protect yourself here: https://bit.ly/recruitment-fraud
On-site · Winnipeg
Manage deviations and corrective and preventive actions, including investigations, product impact assessments, root cause analysis, and review and approval of records. Support quality systems and improvement projects, participate in inspections and audits, and represent Quality Assurance in cross-functional teams while ensuring GMP and procedural compliance.
On-site · Winnipeg
The Specialist I, Quality Compliance supports regulatory inspections, manages internal audits, and oversees corrective and preventive actions (CAPAs). They also maintain regulatory intelligence, manage product complaints, and ensure site-wide adherence to cGxP requirements.
On-site · Winnipeg
The Analyst II will lead and execute the transfer, validation, and optimization of analytical and biological test methods within a regulated laboratory. They will interpret complex data and collaborate cross-functionally to ensure all methods remain compliant with regulatory expectations and GMP standards.
On-site · Winnipeg
The Analyst III leads the transfer, validation, and lifecycle management of analytical and biological test methods within a regulated laboratory. They provide scientific leadership for complex projects while mentoring junior staff and ensuring compliance with GMP requirements.
On-site · Winnipeg
The Analyst I performs routine GMP-compliant laboratory testing to support raw material, in-process, and finished product release. They are also responsible for maintaining laboratory records, equipment, and inventory while adhering to safety and regulatory guidelines.
On-site · Winnipeg
Lead the Engineering, Facilities, and Validation (EFV) team at the site while serving as a member of the Site Leadership Team. Ensure operational excellence, regulatory compliance, and the successful execution of capital projects and validation master plans.
On-site · Winnipeg
The Specialist I, QA Operations provides quality oversight for lot release, operational compliance, and quality systems to ensure GMP adherence. They manage deviations, CAPAs, and change controls while partnering with cross-functional teams to maintain inspection readiness.
On-site · Winnipeg
This role supports validation efforts for equipment, facilities, and computer systems to ensure compliance with GxP requirements. The specialist will lead validation projects, conduct data integrity assessments, and provide technical guidance to improve quality processes.
On-site · Winnipeg
The Analyst I performs GMP-compliant laboratory testing to support raw material, in-process, and finished product release. They are also responsible for maintaining laboratory records, equipment, and inventory while adhering to safety and regulatory guidelines.
On-site · Winnipeg
The Packaging & Inspection Assistant is responsible for the packaging, inspection, and labeling of pharmaceutical products in compliance with cGMP standards. They also maintain production areas according to 6S standards and operate packaging machinery.
On-site · Winnipeg
The Specialist provides technical expertise to support manufacturing, aseptic filling, and packaging departments, including troubleshooting and quality investigations. They also manage technology transfers for new products and processes while ensuring compliance with cGMP standards.
On-site · Winnipeg
The Specialist provides technical expertise to manufacturing and packaging departments by leading investigations, troubleshooting production issues, and executing corrective actions. They are also responsible for authoring batch records, standard operating procedures, and facilitating continuous improvement initiatives.
On-site · Winnipeg
The Specialist, MS&T provides technical expertise to production departments by leading investigations, troubleshooting process concerns, and executing corrective actions. They also author batch records, conduct statistical process control, and implement continuous improvement initiatives.
On-site · Winnipeg
The Director of Operational Excellence leads the site's transformation roadmap by implementing Lean principles and building organizational capability. They partner with the site leadership team to optimize value streams, improve operational performance, and foster a culture of continuous improvement.
On-site · Winnipeg
The Packaging & Inspection Assistant is responsible for the packaging, inspection, and labeling of specialty pharmaceutical products in compliance with cGMP standards. They also maintain production areas, operate packaging machinery, and identify process improvements to ensure quality and accuracy.
On-site · Winnipeg
Lead the technology transfer of products and platforms into the cGMP environment and manage a results-driven team for process monitoring and trend analysis. Collaborate with manufacturing operations to drive process improvements, troubleshoot processing issues, and ensure regulatory compliance.
On-site · Winnipeg
The Specialist I, Quality Control is responsible for designing microbiology protocols, managing CAPAs, deviations, and change controls, and performing environmental monitoring assessments. They also serve as a contamination control strategy SME and provide technical support for cross-functional projects and audits.
On-site · Winnipeg
The Director of Quality Assurance leads QA Operations, Quality Systems, and Validation for the Winnipeg site to ensure compliance with GMP and health authority requirements. This role provides strategic leadership for inspection readiness, risk management, and the escalation of significant quality issues.
On-site · Winnipeg
The Manufacturing Associate supports the filling of specialty pharmaceutical products while ensuring compliance with cGMP standards. Responsibilities include operating machinery such as freeze dryers and sterilizers, documenting procedural steps, and maintaining clean production areas.
On-site · Winnipeg
Lead and manage multiple complex engineering capital projects simultaneously while ensuring alignment with company strategies and compliance expectations. Facilitate project execution through cross-functional team leadership, vendor management, and oversight of design, procurement, and commissioning activities.
