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Analyst , QC Laboratory Services

Job in Winnipeg, Manitoba, A3C, Canada
Listing for: Emergent BioSolutions
Full Time position
Listed on 2026-07-21
Job specializations:
  • Quality Assurance - QA/QC
Job Description & How to Apply Below
Position: Analyst I, QC Laboratory Services
Emergent is a leading public health company that delivers protective and life‑saving solutions to communities around the world.

Job Summary
The Analyst I, QC Laboratory Services performs GMP compliant testing as required to support Raw Material testing, In‑process, Finished Product release & Stability or non‑clinical/clinical studies. The Analyst I also performs testing required to support assay and process validations and to support release of lab specific material (media, standards).

Responsibilities

Perform routine laboratory testing procedures including analyzing and reviewing data

Receive and test samples within required time frames

Receive, prepare, test, and release materials used for QC testing (e.g., media, standards, biological indicators, cultures, etc.)

Document laboratory work consistent with GDP and GxP requirements

Maintain laboratory records, ensuring documents are reconciled and filed immediately after completion

Maintain inventory of supplies, reagents, standards, solutions, cultures, etc. required to perform testing

Perform preventative maintenance on laboratory equipment

Maintain a clean and sanitary work area in accordance with standard laboratory practice and procedures

Contribute to investigations to aid in determination of root cause

Adhere to all effective TMDs/SOPs and safety requirements

Maintain the lab and testing following applicable regulations and guidelines, including but not limited to USP, EP, GMP, FDA, Health Canada, and EU requirements

Work effectively and productively with other team members and on independent assignments

Prepare and autoclave supplies and garbage

Education, Experience & Skills

University degree or technical diploma in microbiology, biology or related field of study

Experience in a pharmaceutical cGMP environment is an asset, but is not required

Basic knowledge of Microsoft Office – Word, Excel

Basic knowledge of pharmaceutical GLPs and GMPs

Knowledge of laboratory techniques and safety precautions

WHMIS and biohazard safety awareness

Ability to work in a fast‑paced and highly regulated environment

Able to multi‑task and adapt to changing priorities

Competent in laboratory safety and generally accepted lab practice, including maintaining adequate written laboratory records

Able to communicate and articulate information in both written and verbal forms

Strong organizational and interpersonal skills; can work collaboratively with others

Able to interpret analytical data

Ability to pass pre‑employment medical and background check

Benefits

Competitive salaries

Flexible work arrangements

Extensive benefits package

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