AI Biotech Job Matching

QA/QC Analyst Jobs in Biotech & Pharma — Ranked by Qualification

Quality assurance and quality control roles are among the most stable career paths in pharmaceutical and biotech manufacturing. These positions are ranked by how well a science graduate with GMP/GLP exposure qualifies for each one.

5 matched roles shown
$68k average salary
AI-scored by qualification match

Ranked Roles — Best Match First

Each role is scored based on how well a typical qa qc analyst jobs candidate qualifies. Upload your resume to get scores based on your specific background.

QC Analyst I — Analytical Testing

Apotex Inc. · Toronto, ON
89 match
💼 Full-time 💰 $54k–$70k ⏱️ 1–3 years
✓ HPLC, dissolution, and GMP documentation experience are the full requirement for this role — met by most analytical chemistry graduates.
HPLCDissolution TestingGMPUSP MethodsLIMSOOS Investigations
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QA Associate — Batch Record Review

Novo Nordisk · Mississauga, ON / Plainsboro, NJ
85 match
💼 Full-time 💰 $58k–$75k ⏱️ 1–2 years
✓ Batch record review requires GMP awareness and documentation skills — accessible with a science degree and any GMP coursework or co-op.
Batch Record ReviewGMPDeviation ManagementSOP WritingChange Control
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Microbiological QC Analyst

Halo Labs / Eurofins Pharma · Multiple Canada / USA
83 match
💼 Full-time 💰 $52k–$68k ⏱️ 1–2 years
✓ Microbiology degree with aseptic technique experience directly qualifies for environmental monitoring, bioburden, and endotoxin testing roles.
Environmental MonitoringBioburden TestingEndotoxin (LAL)Sterility TestingAseptic Technique
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QA Specialist — Regulatory Compliance

Sanofi · Toronto, ON / Bridgewater, NJ
74 match
💼 Full-time 💰 $68k–$88k ⏱️ 3–5 years
✓ Regulatory compliance QA roles require 3+ years of GMP documentation experience, CAPA management, and Health Canada / FDA audit experience.
⚠ Missing: Regulatory submission experience
FDA 21 CFRHealth Canada GMPCAPAAudit PrepRisk AssessmentICH Q10
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QC Analyst — Biologics (ELISA / Bioassay)

Biogen · Research Triangle Park, NC
80 match
💼 Full-time 💰 $65k–$84k ⏱️ 1–4 years
✓ ELISA and bioassay skills from academic or industry lab experience, combined with GMP documentation training, meet the core requirements for biologics QC.
ELISABioassayHPLCGMPProtein CharacterizationUSP <1030>
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See Which of These You Actually Qualify For

Upload your resume and our AI scores every open biotech role against your specific background — showing your interview probability before you apply.

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Most In-Demand Skills for These Roles

These are the skills that appear most frequently in job postings and determine your match score.

GMP Documentation
SOP Writing & Review
CAPA Management
Deviation Handling
Change Control
LIMS / QMS Software
Batch Record Review
Environmental Monitoring
Risk Assessment (FMEA)
Regulatory Submissions (IND/NDA)
ICH Guidelines
Audit Preparation

Salary Ranges

Typical compensation in Canada and the US. Actual offers vary by location, company size, and experience level.

Entry Level
$50k
0–2 years experience
Mid Level
$68k
2–5 years experience
Senior Level
$95k
5+ years experience

Who Should Apply

Candidates most likely to qualify for these roles.

Science graduates with a degree in biology, chemistry, biochemistry, or pharmaceutical sciences who have exposure to GMP or GLP principles (through coursework, co-op, or prior employment). Understanding of regulatory frameworks (Health Canada, FDA 21 CFR Part 11) increases match scores significantly at the senior level. CAPA, deviation management, and documentation control are core skills — some companies provide foundational GMP training for entry-level hires.