Posted 29 days ago
Specialist I, Quality Compliance
@ Emergent Biosolutions
Winnipeg, Manitoba
Overview
Emergent Biosolutions is hiring a Specialist I, Quality Compliance in Winnipeg to support regulatory inspections, customer audits and internal audits. The role plans and leads internal audits, manages CAPAs and audit responses, and maintains the site's regulatory intelligence program. Requires a bachelor's degree in science and at least five years in regulated life sciences, four of them in quality assurance.
Responsibilities:
- Plan and conduct internal quality system audits
- Lead cross-functional audit teams
- Manage CAPAs and verify their effectiveness
- Support regulatory inspections and post-inspection follow-up
- Oversee product complaints and inquiries
Requirements summary:
- Bachelor's degree in science or related field
- Five years in regulated life sciences, four in quality assurance
- Strong knowledge of cGMP and GxP regulations
- Experience conducting audits and supporting regulatory inspections
- Proven technical writing skills
Tools & skills
Source and dates
Employer career site / ATS feed · successfactors
- Employer posting date
- 2026-10-14
- First seen by our source
- 2026-10-15
- Source record updated
- 2026-10-15
These dates describe the source record, not a live verification that the employer is still hiring. Check the original posting.
Job details
| Seniority | Mid level |
| Department | Quality assurance |
| Experience | 5+ years |
| Work setting | Office, Laboratory, Plant or factory |
| Position | Sitting and standing |
| Physical demands | physical low · computer high |
| Languages | English |
| Education | Bachelor’s degree (required) |
| Fields of study | Science |
| Perks mentioned | Flexible hours |
Summary and details written by AI from the posting; the employer’s posting is the authority.
Emergent Biosolutions
Saved company profile
Historical company information from a saved The Jobs API profile (LinkedIn/Crunchbase fields). It is not live-verified; figures may have changed. Missing values remain unknown.
Protecting against emerging global health threats.
Full company description
At Emergent, we develop, manufacture, and deliver protections against public health threats. For more than two decades, we’ve been at work defending people from things we hope will never happen — so that we’re prepared, just in case they ever do. 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:
- LinkedIn followers
- 49,609
- People associated on LinkedIn
- 1,369
- Reported office locations
- 300 Professional Dr, Gaithersburg, Maryland 20879, US
- 155 Innovation Dr, Winnipeg, MB R3T 5Y3, CA
- 3500 N Martin Luther King Jr Blvd, Lansing, Michigan 48906, US
- 50 Shawmut Rd, Canton, Massachusetts 02021, US
- 401 Plymouth Rd, Plymouth Meeting, Pennsylvania 19462, US
- Earlsfort Terrace, Dublin City, County Dublin D02, IE
- Business categories
- Health Care
- Biotechnology
- Life Science
- Manufacturing
- Pharmaceutical
- Other recorded names
- Emergent Biosolutions
- Emergent BioSolutions
- Specialties
- Manufacturing
- Partnering
- M&A
- Devices Development
- Vaccine Development
- Therapeutics Development
- and Contract Development and Manufacturing
- Profile identifies a recruitment agency
- No
- Reported total investment
- 286,500,000
Currency and observation date were not supplied; this is not a current valuation or a funding round.
At Emergent, we develop, manufacture, and deliver protections against public health threats. For more than two decades, we’ve been at work defending people from things we hope will never happen — so that we’re prepared, just in case they ever do. 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…
| Field | Value |
|---|---|
| Industry | Biotechnology Research |
| Company size | 501-1,000 employees |
| Headquarters | Gaithersburg, Maryland |
| Organization type | Public Company |
| Year founded | 1998 |
| Specialties | ManufacturingPartneringM&ADevices DevelopmentVaccine DevelopmentTherapeutics Developmentand Contract Development and Manufacturing |
| Open jobs on Jobsy | 15 |
| View page |
Preparedness today, safer tomorrow.
Emergent is a leading public health company that delivers protective and life-saving solutions to
communities around the world. Here, you will join passionate professionals where our culture is informed by our values and commitment to protecting and saving lives.
Job Summary
The Specialist I, Quality Compliance is responsible for supporting and representing Emergent during regulatory inspections, customer audits, and internal audits. This includes coordinating audit and inspection activities, managing preparation and logistics, developing written responses, and ensuring timely completion of audit-related corrective and preventive actions (CAPAs).
The role is responsible for planning, conducting, and reporting internal audits; managing audit responses and CAPAs; and maintaining the site's regulatory intelligence and surveillance program. The position supports compliance with cGxP requirements and other applicable regulations and quality system activities at the Winnipeg site.
In addition, provides oversight of product complaints and inquiries, annual product quality reviews (APQRs), and quality agreements, ensuring adherence to regulatory, corporate quality requirements and established procedures.
Responsibilities
• Plan, schedule, and conduct internal quality system audits in accordance with the approved audit schedule, including review of previous audits, regulatory inspections, procedures, processes, and operational activities.
• Lead cross-functional audit teams, providing guidance, training, and day-to-day direction throughout the audit lifecycle.
• Prepare comprehensive audit plans, consolidate audit observations, and author clear and concise audit reports.
• Evaluate documentation, records, processes, and personnel practices to assess compliance with GxP requirements, regulatory expectations, and internal standards.
• Partner with functional area management to discuss audit findings, establish corrective actions, and drive timely resolution of identified compliance gaps.
• Verify CAPA effectiveness to ensure sustainable compliance improvements.
• Draft, review and maintain Quality Technical Agreements with customers and clients.
• Collect, analyze, and trend compliance metrics; prepare reports and present compliance performance and improvement initiatives during Management Review meetings.
• Support regulatory inspections through inspection readiness activities, participation in inspections, and coordination of post-inspection follow-up activities.
• Maintain current knowledge of applicable GxP regulations, industry standards, and regulatory trends, serving as a compliance subject matter expert for the site.
• Provide compliance assessments, recommendations, and guidance to support business operations and quality system effectiveness.
• Lead or participate in cross-functional projects as assigned, acting as the Quality Assurance representative and providing compliance expertise.
• Provide oversight and management of the site’s product inquiry and product complaint programs, ensuring investigations and responses are completed in accordance with regulatory and company requirements.
• Support continuous improvement initiatives aimed at enhancing quality systems, inspection readiness, and overall compliance performance.
The above statements are intended to describe the general nature of work performed by those in this job. It is not an exhaustive list of all duties, and other duties may be assigned.
Education, Experience & Skills
• Bachelor’s degree in Science or related degree
• Minimum of five (5) years of experience in the pharmaceutical, biotechnology, or other regulated life sciences industry with at least at least 4 years of experience within Quality Assurance or related Gxp function.
• Industry certifications or diplomas in Quality Management, Auditing, and/or Quality Systems considered an asset.
• Demonstrated experience conducting internal audits, managing CAPAs, and supporting regulatory inspections.
• Strong knowledge of cGMP and other applicable GxP regulations and quality systems.
• Excellent analytical, critical thinking, and problem-solving skills, with the ability to assess strengths, risks, and gaps within systems and processes.
• Demonstrated ability to work independently while effectively collaborating across departments and organizational levels.
• Excellent interpersonal and communication skills, including the ability to influence stakeholders and effectively navigate challenging discussions.
• Strong organizational skills with the ability to manage multiple priorities, analyze large volumes of information, and make sound compliance-based decisions.
• Proven technical writing skills, including the preparation of audit reports, compliance assessments, CAPAs, and quality agreements.
• Ability to make sound decisions regarding complex compliance-related issues with minimal supervision.
• Demonstrated accountability, professionalism, and commitment to quality and compliance excellence.
• Experience with aseptic manufacturing processes, cleanroom operations, and gowning qualification programs preferred.
• High level of personal and departmental accountability and responsibility.
• Strong understanding of pharmaceutical regulations and guidance, including ICH guidelines (Q1-Q14, as applicable), 21 CFR Parts 11, 210, 211, 600, and 640, Health Canada GUI-0001, and current industry trends.
• Experience supporting regulatory inspections by Health Canada, FDA, EMA, or other global regulatory authorities.
There are physical/mental demands and work environment characteristics that must be met by an individual to successfully perform the essential functions of the job. This information is available upon request from the candidate.
As part of our team, you'll join talented and inspiring colleagues whose sense of purpose complements your own. We offer highly diverse career opportunities, a supportive culture, competitive salaries, flexible work arrangements and an extensive benefits package. Information submitted will be used by Emergent BioSolutions for activities related to your prospective employment. Emergent BioSolutions respects your privacy and any use of the information submitted will be subject to the terms of our Privacy Policy.
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