ZipRecruiter

Log In

1

Biotech Manufacturing Jobs in Bothell, WA (NOW HIRING)

Synkriom

Be Seen First

Cell Therapy Manufacturing Associate with Biotech experience

Bothell, WA · On-site

$15 - $20/hr

The primary purpose of the Manufacturing Associate role is to complete production assignments with high quality and timely output in a cellular therapeutic manufacturing environment. *Duties ...

Synectics Inc

MANUFACTURING ASSOCIATE

Bothell, WA · On-site

$17.28 - $21.95/hr

Works on routine manufacturing assignments per written procedures, where ability to recognize ... Biotech or clinical lab experience is nice to have * Schedule: Shift Timing- Alt Wed - Sat, 0500 ...

next page

Showing results 1-20

All JobsBiotech Manufacturing JobsBiotech Manufacturing Jobs in Bothell, WA

Biotech Manufacturing information

See Bothell, WA salary details

$13

$23

$37

How much do biotech manufacturing jobs pay per hour?

As of Jun 23, 2026, the average hourly pay for biotech manufacturing in Bothell, WA is $23.69, according to ZipRecruiter salary data. Most workers in this role earn between $18.56 and $26.49 per hour, depending on experience, location, and employer.

What is the difference between Biotech Manufacturing vs Biotech Quality Control?

AspectBiotech ManufacturingBiotech Quality Control
CredentialsTypically requires a degree in biotech, biology, or chemistrySimilar credentials, often with additional certifications in quality assurance
Work EnvironmentProduction floors, laboratories, cleanroomsLaboratories, testing facilities, quality assurance labs
Employer & Industry UsageManufacturing plants, biotech companies, pharmaceutical firmsQuality assurance departments within biotech and pharma companies
Common Search & ComparisonBiotech Manufacturing vs Biotech Quality Control

Biotech Manufacturing focuses on producing biotech products, involving process development and production. Biotech Quality Control emphasizes testing and ensuring product quality, often working closely with manufacturing but with a focus on compliance and standards.

What are some common challenges faced in biotech manufacturing, and how can new team members prepare for them?

In biotech manufacturing, common challenges include maintaining strict quality standards, adhering to complex regulatory requirements, and troubleshooting equipment or process issues. New team members can prepare by familiarizing themselves with Good Manufacturing Practices (GMP), developing strong attention to detail, and being proactive in learning about the latest industry protocols. Teamwork is essential, as much of the work involves cross-functional collaboration with quality assurance, engineering, and research departments to ensure smooth production and compliance.

What are the key skills and qualifications needed to thrive in Biotech Manufacturing, and why are they important?

To excel in Biotech Manufacturing, a background in biology, chemistry, or engineering with knowledge of GMP (Good Manufacturing Practices) is typically required. Familiarity with bioprocessing equipment, laboratory information management systems (LIMS), and relevant certifications such as Six Sigma or ASQ is often expected. Attention to detail, problem-solving abilities, and strong teamwork skills help professionals stand out in this environment. These competencies are crucial for ensuring safe, efficient, and compliant production of biotechnological products.

What is manufacturing in biotech?

Manufacturing in biotech involves producing biological products such as vaccines, therapies, or enzymes through controlled processes like fermentation or cell culture. Biotech manufacturing requires strict adherence to Good Manufacturing Practices (GMP), quality control, and often involves specialized equipment and cleanroom environments. Biotech manufacturing roles may also require knowledge of process development, validation, and regulatory compliance.

How is biotechnology used in manufacturing?

Biotech manufacturing involves using living organisms, such as bacteria or cells, to produce products like pharmaceuticals, enzymes, and biofuels. Biotech manufacturing technicians and scientists often work with bioreactors, sterile environments, and quality control processes to ensure product safety and efficacy.

What is the highest paying job in biotech?

In biotech manufacturing, senior roles such as Director of Manufacturing, Vice President of Manufacturing, or Chief Operating Officer typically have the highest salaries. These positions require extensive experience, leadership skills, and often advanced degrees or specialized certifications, and they oversee large teams and complex production processes.

What is biotech manufacturing?

Biotech manufacturing is the process of producing products using biological systems or living organisms, such as bacteria, yeast, or mammalian cells. This field is crucial for making pharmaceuticals, vaccines, enzymes, and other biological products on a large scale. Biotech manufacturing involves a combination of biology, chemistry, and engineering to ensure products are made efficiently, safely, and to high quality standards. It is a key part of the biotechnology industry and is vital for developing new medical treatments and therapies.

How to get into biotech manufacturing?

To enter biotech manufacturing, candidates typically need a background in biology, chemistry, or related fields, often requiring a bachelor's degree or higher. Gaining experience through internships or entry-level positions, developing skills in laboratory techniques and GMP (Good Manufacturing Practice), and obtaining certifications such as cGMP training can improve job prospects. Familiarity with manufacturing equipment and attention to quality control are also important for success in this field.
What are the most commonly searched types of Biotech Manufacturing jobs in Bothell, WA? The most popular types of Biotech Manufacturing jobs in Bothell, WA are:
What job categories do people searching Biotech Manufacturing jobs in Bothell, WA look for? The top searched job categories for Biotech Manufacturing jobs in Bothell, WA are:
What cities near Bothell, WA are hiring for Biotech Manufacturing jobs? Cities near Bothell, WA with the most Biotech Manufacturing job openings:
Biotech Manufacturing jobs near you
Infographic showing various Biotech Manufacturing job openings in Bothell, WA as of June 2026, with employment types broken down into 83% Full Time, 12% Part Time, 3% Contract, and 2% Nights. Highlights an 81% Physical, 4% Hybrid, and 15% Remote job distribution, with an average salary of $49,268 per year, or $23.7 per hour.

PHARMACEUTICAL - SR. CQV Manager/Lead

MMR Consulting

Seattle, WA • On-site

Other

Posted 7 days ago

Job description

Previous Pharmaceutical/Biotech experience is mandatory for this role
(Commissioning, Qualification & Validation - Pharmaceutical Manufacturing)
The work will require 90% travel to work in Denver/Boulder, Raleigh, midwest, Philadelphia, Portland, or other locations.
MMR Consulting is an engineering and consulting firm specializing in the pharmaceutical and biotechnology industries. Its services include Engineering, Project Management, and Validation.
MMR Consulting has offices in Canada, USA, and Australia.
This is an outstanding opportunity to join our growing team, where the successful candidate will work with a group of engineers involved in the design, commissioning & qualification, start-up and project management of various processes, systems, and facilities. The ideal candidate should possess leadership skills to lead teams of intermediate & junior engineers.
This role is for Sr. CQV Manager/Lead will require to lead commissioning, qualification, and validation activities for pharmaceutical manufacturing capital projects and operational initiatives. This individual will oversee cross-functional CQV execution for GMP-regulated facilities, utilities, equipment, automation systems, and manufacturing processes while ensuring compliance with FDA, cGMP, and global regulatory standards.
The ideal candidate will possess strong pharmaceutical project leadership experience within biotech, sterile manufacturing, fill-finish, API, or biologics environments and will serve as a key liaison between engineering, quality, validation, manufacturing, and external vendors. This role requires the ability to manage project schedules, budgets, risks, resources, and validation deliverables in support of facility expansions, new product introductions, and operational readiness initiatives.
Key Responsibilities
  • Lead all CQV project activities for pharmaceutical and biotech manufacturing projects.
  • Develop and manage CQV strategies, project plans, schedules, budgets, and resource allocation.
  • Coordinate commissioning and qualification activities for:
    • Process equipment
    • Clean utilities
    • HVAC systems
    • Automation and control systems
    • Manufacturing and packaging lines
  • Ensure compliance with FDA, cGMP, ISPE, GAMP, and corporate quality standards.
  • Oversee execution of:
    • FAT/SAT protocols
    • IQ/OQ/PQ protocols
    • Validation documentation
    • Deviations and CAPAs
    • Change controls
  • Collaborate with Quality Assurance, Engineering, Manufacturing, Automation, and Regulatory teams to support project milestones and inspection readiness.
  • Manage third-party CQV consultants, contractors, and vendors.
  • Provide risk assessments and mitigation strategies to maintain project timelines and compliance objectives.
  • Support startup, operational readiness, and technology transfer activities.
  • Present project status updates and KPI reporting to senior leadership and stakeholders.

Required Experience
  • Minimum 8-12 years of experience in pharmaceutical, biotech, or life sciences industries.
  • Minimum 5 years of direct CQV project management experience within GMP-regulated manufacturing environments.
  • Proven experience managing large-scale capital projects, facility expansions, or greenfield startup projects.
  • Strong experience with commissioning and qualification of:
    • Cleanrooms
    • Process equipment
    • Utilities
    • Automation systems
    • Manufacturing processes
  • Experience authoring and reviewing validation lifecycle documentation.
  • Demonstrated success leading cross-functional teams and managing multiple project workstreams simultaneously.
  • Experience supporting FDA audits and regulatory inspections.
  • Background in biologics, sterile fill-finish, vaccine, API, or aseptic manufacturing environments strongly preferred.

Required Qualifications
  • Bachelor's degree in Engineering, Life Sciences, Pharmaceutical Sciences, or related technical discipline.
  • Strong understanding of:
    • cGMP regulations
    • FDA validation requirements
    • ISPE Baseline Guides (inc. C&Q) and ASTM E2500 GUIDE
    • GAMP 5 principles
  • Proficiency with project management methodologies, scheduling tools, and reporting systems.
  • Excellent communication, leadership, and stakeholder management skills.
  • Ability to work effectively in fast-paced, highly regulated project environments.

Preferred Qualifications
  • Digital Validation software experience (i.e. Kneat or equivalent)
  • PMP certification preferred.
  • Experience with DeltaV, MES, SCADA, or other pharmaceutical automation platforms.
  • Familiarity with Kneat, TrackWise, Veeva, or electronic validation systems.
  • Previous consulting or EPCM experience is a plus.
  • Lean Six Sigma certification preferred.

Compensation: 120,000$ - 150,000$ based on experience.
Equal Employment Opportunity and Reasonable Accommodations
MMR Consulting is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. Our hiring decisions are based on merit, qualifications, and business needs. We are committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please let us know the nature of your request.

Apply