Top 52 Biotechnology Jobs in Beaverton, Or

Senior QA Specialist, Plasmid Manufacturing
Novel Biotechnology USA, Inc —Vancouver, WA
- $75,000 - $80,000 a year
- Full-time
- US work authorization
- In-person
- Senior level
- Health insurance
- Dental insurance
Quick Apply
Territory Rep – BioPharma
Prism Biotech —Portland, OR
- $86,745 - $117,997 a year
- Full-time
- Mid-level
- Analysis skills
- Experience equivalent to degree accepted
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Special Agent: STEM—Physical Sciences Background
Federal Bureau of Investigation —Portland, OR
- $103,236 - $133,200 a year
- Full-time
- Mid-level
- Analysis skills
- Bachelor's degree
9d
Microbiologist
Element Materials Technology —Portland, OR
- Organizational skills
- 1 year
- Communication skills
Telehealth Genetic Counselor
Natera —Portland, OR
- $101,200 - $126,500 a year
- Spanish
- Google Workspace
- HIPAA
- Commuter assistance
- Health insurance
Primary Care Pharma Rep
Prism Biotech —Gresham, OR
- $86,985 - $118,237 a year
- Full-time
- Primary Care
- Organizational skills
- Leadership
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Project Manager - 29998_G
BEPC Inc —Hillsboro, OR
- $50 - $55 an hour
- Contract
- 5 years
- Engineering
- Mid-level
- Health insurance
- Dental insurance
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Senior/Principal Manufacturing Asset Engineer, HTO
Genentech —Hillsboro, OR
- $80,500 - $176,000 a year
- Online Application
- Bachelor of Science
- 8 years
- Analysis skills
Senior Medical Science Liaison, Rare Disease - PNW
Acadia Pharmaceuticals Inc. —Portland, OR
- $181,300 - $226,600 a year
- Medicine
- Microsoft Excel
- Microsoft Outlook
- Paid parental leave
- Employee stock purchase plan
8d
Protein Scientist
Twist Bioscience —Wilsonville, OR
- Mid-level
- SQL
- Continuous improvement
Quick Apply
Global MSAT Senior DP Product Steward
Genentech —Hillsboro, OR
- $114,400 - $212,400 a year
- Online Application
- 7 years
- Management
- Bachelor of Science
National Strategic Accounts Sr Manager
Adaptive Biotechnologies —Portland, OR
- $168,000 - $252,000 a year
- Online Application
- Remote
- Up to 50% travel
- 5 years
- Bachelor of Science
Director, Market Access Payer Accounts
Summit Therapeutics —Portland, OR
- $197,000 - $246,500 a year
- 5 years
- Bachelor's degree
- Travel
Quick Apply
2d
Skeletal Dysplasia Account Manager - Seattle, WA/Portland, OR
BridgeBio Pharma —Portland, OR
- $155,000 - $210,000 a year
- Full-time
- Hybrid work
- Bachelor of Science
- Analysis skills
- Bachelor's degree
- Commuter assistance
- Health savings account
8d
Regional Account Manager, IgAN Nephrology, Portland, OR
Alexion Pharmaceuticals,Inc. —Portland, OR
- Clean driving record
- 5 years
- Master's degree
Experienced Testifying Expert | Biomechanics
Explico —Portland, OR
- Research
- Analysis skills
- Mentoring
- Disability insurance
- Health insurance
Special Agent: STEM—Physical Sciences Background
Federal Bureau of Investigation —United States
- $103,236 - $133,200 a year
- Full-time
- Mid-level
- Analysis skills
- Bachelor's degree
9d
Biostatistician - AI Trainer
micro1 —United States
- $60 - $65 an hour
- Contract
- Remote
- 5 years
- No experience needed
- Analysis skills
- Flexible schedule
8d
Field Reimbursement Manager - Kidney (East Texas-Louisiana)
Vertex Pharmaceuticals —United States
- $136,000 - $204,000 a year
- Full-time
- Microsoft Excel
- Microsoft Outlook
- 5 years
- Loan repayment program
- Health insurance
Senior Medical Science Liaison (Nephrology) - Lower Manhattan, Brooklyn, Staten Island, Long Island
Vertex Pharmaceuticals —United States
- $171,300 - $256,900 a year
- Full-time
- English
- Mentoring
- Data entry
- Loan repayment program
- Health insurance

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biotechnology jobs near beaverton, or

Senior QA Specialist, Plasmid Manufacturing

Novel Biotechnology USA, Inc
Vancouver, WA

Quick Apply

Job Details

Full-time
$75,000 - $80,000 a year

Benefits

Health insurance
Dental insurance
401(k)
Paid time off
Vision insurance

Qualifications

Document control experience within pharmaceutical industry
Preventive action implementation
Production deviation management
Corrective and preventive actions (CAPA)
Manufacturing facility experience
Production validation processes
Quality assurance experience within pharmaceutical industry
Quality audits
Commissioning phase involvement
Regulatory compliance analysis
Supplier quality assurance (SQA)
Pharmaceutical manufacturing facility experience

Full Job Description

Senior QA Specialist, Plasmid Manufacturing

About the company

The next wave of genetic medicine depends on better DNA. At Novel Bio, we're making that possible. We're a team of DNA artists, experts, and problem solvers who saw a biotech bottleneck and decided to fix it. From our headquarters in Vancouver, Washington (in the heart of the Pacific Northwest) our advanced manufacturing technology delivers high-yield, high-purity plasmid DNA: the foundation for fast-growing markets in cell and gene therapies, RNA therapeutics, and vaccines. We support our partners at every stage, from early R&D through clinical.

About the role

We are building a cGMP plasmid DNA production facility supplying critical raw material and intermediates for cell and gene therapy. Our facility design is being finalized now, and our quality system is being expanded. We are looking for an experienced, hands-on QA professional with direct plasmid DNA manufacturing experience to help us build our quality operation the right way: pragmatically, phase-appropriately, and in compliance with cGMP.

This is a rare opportunity to shape a quality system and facility from an early stage rather than inherit one. You will do the day-to-day work of QA while also advising on how we establish our QMS, facility, and processes to meet GMP requirements for plasmid manufacturing. You will provide leadership and oversight for the Quality Management System and ensure compliance with approved Quality Manual requirements and procedures. You'll thrive here if you are energized by a fast-moving startup environment, confident enough to help us get things right the first time, and comfortable rolling up your sleeves for both strategic and routine work.

What you'll do

Perform core QA activities: batch record review, deviation and CAPA management, product disposition, change control, and supplier quality.
Advise on the build-out of our quality management system, facility, and manufacturing processes to meet phase-appropriate GMP requirements for plasmid DNA production.
Apply risk-based, phase-appropriate judgment to help us translate regulatory expectations into practical, right-sized quality practices, avoiding both under-compliance and unnecessary gold-plating.
Contribute to validation strategy and execution, including facility, equipment, process, and cleaning validation.
Support internal and external audits and inspection readiness.
Author, review, and improve SOPs, policies, and batch records.
Apply Quality Risk Management tools including FMEA.
Lead and support qualification and validation activities including IQ/OQ/PQ.
Ensure effective document control, records retention, and good documentation practices.
Lead deviation investigations, root cause analysis, and CAPA implementation.
Support GMP training programs and training effectiveness.
Serve as QA approver for procedures, protocols, reports, and training records as authorized.
Support development of quality agreements.
Support oversight of laboratory controls, calibration and maintenance programs, manufacturing, and supplier qualification.

What you bring

Direct, hands-on QA experience in a cGMP plasmid DNA production environment. (This is essential.)
Strong working knowledge of GMP regulations and guidance as they apply to plasmid DNA as a raw material/intermediate for cell and gene therapy, and the judgment to apply them in a phase-appropriate, risk-based way.
Experience across core QA disciplines: batch record review, deviations/CAPA, change control, disposition, supplier quality, and validation.
Experience authoring commissioning, qualification, and validation (CQV) documentation, including validation master plans (VMPs), user requirement specifications, and IQ/OQ/PQ protocols and reports.
Comfort operating in an early-stage, resource-constrained, and occasionally chaotic startup environment.
Confidence and communication skills to advise senior stakeholders and influence how we set things up.
Willingness to be reachable after hours in the event of a manufacturing emergency. (Not a shift role; occasional only.)

Benefits

Health insurance
Vision insurance
Dental insurance
Paid time off and sick leave
401(k)

Pay: $75,000.00 - $80,000.00 per year

Benefits:

401(k)
Dental insurance
Health insurance
Paid time off
Vision insurance

Application Question(s):

How many years experience do you have in a cGMP plasmid DNA production environment?
If selected, how soon will you be able to start this role?

Ability to Relocate:

Vancouver, WA 98683: Relocate before starting work (Required)

Work Location: In person

Quick Apply

Refine Your Search

biotechnology jobs in beaverton, or

Senior QA Specialist, Plasmid Manufacturing

Territory Rep – BioPharma

Special Agent: STEM—Physical Sciences Background

Microbiologist

Telehealth Genetic Counselor

Primary Care Pharma Rep

Project Manager - 29998_G

Senior/Principal Manufacturing Asset Engineer, HTO

Senior Medical Science Liaison, Rare Disease - PNW

Protein Scientist

Global MSAT Senior DP Product Steward

National Strategic Accounts Sr Manager

Director, Market Access Payer Accounts

Skeletal Dysplasia Account Manager - Seattle, WA/Portland, OR

Regional Account Manager, IgAN Nephrology, Portland, OR

Experienced Testifying Expert | Biomechanics

Special Agent: STEM—Physical Sciences Background

Biostatistician - AI Trainer

Field Reimbursement Manager - Kidney (East Texas-Louisiana)

Senior Medical Science Liaison (Nephrology) - Lower Manhattan, Brooklyn, Staten Island, Long Island

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