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Pharmaceutical Development Jobs in Seattle, WA (NOW HIRING)

Inizio

Pharmaceutical District Manager

Seattle, WA · On-site

$160K/yr

Alora Pharmaceuticals is a fully integrated company dedicated to the development, manufacturing, and promotion of specialty products across the U.S. With strong brand and generic franchises and ...

Septodont

Territory Manager - Seattle, WA

Seattle, WA · On-site

$85K/yr

At Septodont, a global leader in dental products and a key player in pharmaceutical development and contract manufacturing (CDMO), we are proud to work every day to improve patients' health and well ...

Pharmacy Careers

Oncology Pharmacist

Redmond, WA · On-site

Oncology Pharmacist - Advance Your Career in Cancer Care Are you a pharmacist passionate about ... Stay current with oncology drug developments, clinical guidelines, and emerging therapies. What You ...

Pharmacy Careers

Oncology Pharmacist

Mill Creek, WA · On-site

Oncology Pharmacist - Advance Your Career in Cancer Care Are you a pharmacist passionate about ... Stay current with oncology drug developments, clinical guidelines, and emerging therapies. What You ...

New

MultiCare

Pharmacist

Puyallup, WA · On-site

$63.75 - $76.50/hr

Manufacture nonstandard pharmaceutical preparations when required and maintain appropriate records * Supervise support personnel and assumes responsibility for final check of all completed work ...

Seattle Children's

Pharmacist, Retail

Bellevue, WA · On-site

$68.75 - $103.12/hr

... development across all scheduled outpatient service locations. Required Education and Experience ... Detailed working knowledge of USP 795, USP 797, and USP 800 pharmaceutical compounding safety ...

MultiCare

Pharmacist NRU

Bonney Lake, WA · On-site

$75.89 - $101.98/hr

Manufacture nonstandard pharmaceutical preparations when required and maintain appropriate records ... development to invest in you. Well-being and support Generous PTO, Code Lavender and Employee ...

MultiCare

Pharmacist

Auburn, WA · On-site

$72.97 - $98.05/hr

Manufacture nonstandard pharmaceutical preparations when required and maintain appropriate records ... Competitive tuition assistance, award-winning residencies, fellowships and career development to ...

MultiCare

Pharmacist

Tacoma, WA · On-site

$75.89 - $101.98/hr

Manufacture nonstandard pharmaceutical preparations when required and maintain appropriate records ... Competitive tuition assistance, award-winning residencies, fellowships and career development to ...

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Showing results 1-20

All JobsPharmaceutical Development JobsPharmaceutical Development Jobs in Seattle, WA

Pharmaceutical Development information

See Seattle, WA salary details

$26.7K

$77.9K

$149.1K

How much do pharmaceutical development jobs pay per year?

As of Aug 6, 2026, the average yearly pay for pharmaceutical development in Seattle, WA is $77,862.00, according to ZipRecruiter salary data. Most workers in this role earn between $39,800.00 and $101,300.00 per year, depending on experience, location, and employer.

What is a pharmaceutical development?

A Pharmaceutical Development job involves researching, formulating, and optimizing new drug products to ensure safety, efficacy, and regulatory compliance. Professionals in this role work on drug formulation, process development, and scale-up for manufacturing. They collaborate with scientists, regulatory teams, and production staff to bring medications from the lab to market. This field requires strong knowledge of chemistry, biology, and regulatory requirements.

What are the key skills and qualifications needed to thrive in pharmaceutical development?

To thrive in Pharmaceutical Development, you need a strong background in pharmaceutical sciences, chemistry, or related fields, often supported by an advanced degree (MS or PhD) and experience in drug formulation and testing. Proficiency in analytical instrumentation (e.g., HPLC, GC), regulatory compliance systems, and Good Laboratory Practice (GLP) certifications are highly valued. Strong project management, problem-solving abilities, and effective communication skills set top performers apart. These competencies ensure the development of safe, effective pharmaceuticals while navigating complex regulatory requirements and cross-functional team dynamics.

What does a pharmaceutical development professional do?

Professionals in Pharmaceutical Development typically oversee the formulation and optimization of new drug products, conduct lab-based experiments, and analyze test data to ensure product efficacy and safety. They frequently collaborate with cross-functional teams such as quality assurance, regulatory affairs, and manufacturing to advance each stage of product development. Regular responsibilities also include drafting technical reports, maintaining detailed laboratory documentation, and supporting regulatory submissions. The role often requires balancing hands-on lab work with strategic planning, ensuring that all processes comply with industry standards and regulations.

What are popular job titles related to Pharmaceutical Development jobs in Seattle, WA? For Pharmaceutical Development jobs in Seattle, WA, the most frequently searched job titles are:
What job categories do people searching Pharmaceutical Development jobs in Seattle, WA look for? The top searched job categories for Pharmaceutical Development jobs in Seattle, WA are:
Pharmaceutical Development jobs near you
Infographic showing various Pharmaceutical Development job openings in Seattle, WA as of August 2026, with employment types broken down into 60% Full Time, 10% Part Time, and 30% Contract. Highlights an 80% In-person, and 20% Remote job distribution, with an average salary of $77,862 per year, or $37.4 per hour.

QC Chemist IV (Method Tranfer, Method Validation) / Pharma Industry

Pioneer Data

Bothell, WA • On-site

Contractor

Re-posted 9 days ago

Job description

Position Details:
Our client, a world-leading Pharmaceutical Company in Bothell, WA is currently looking for a QC Chemist IV to join their expanding team.
Job Title: QC Chemist IV (Method Tranfer, Method Validation) / Pharma Industry
Duration: 12 months contract, extendable up to 48 months
Location: Bothell, WA
Note:
The client has the right-to-hire you as a permanent employee at any time during or after the end of the contract.
You may participate in the company group medical insurance plan
Job Description:

Quality Control Chemist

Role Summary:
This position serves as a quality control expert within the Quality Control Sciences and Validation group, providing critical support for analytical method transfer and validation activities across global pharmaceutical operations. 
The role requires an individual contributor who can independently manage complex technical projects while ensuring compliance with current Good Manufacturing Practices and regulatory standards. 
This scientist will serve as a technical authority for method transfer initiatives, working across multiple internal and external testing sites to support drug development programs. 
The position demands strong analytical expertise combined with excellent project management capabilities to coordinate deliverables and maintain timelines. 
Success in this role requires the ability to balance multiple priorities while maintaining rigorous attention to detail and scientific integrity throughout all validation and transfer activities.
 
Responsibilities:
Support Project Leads for method transfer and validation activities internally and externally for assigned pharmaceutical development programs
Author and review protocols and reports for method transfer, method validation, method bridging, and other technical development documentation associated with analytical methods
Plan and track method transfer and validation deliverables to ensure timely completion of project milestones
Collaborate and interact with internal global quality control testing sites and laboratories, external testing sites, project leads, and functional representatives
Review method transfer and validation assays, perform data verification, conduct non-routine data mining, and execute in-depth data analysis
Represent quality control in intra-department projects and initiatives or cross-functional teams in support of program and company goals
 
Skills:
Expertise in designing and evaluating method validation and transfer studies including partial re-validation, co-validation, and cross-validation approaches
Technical writing skills for authoring analytical methods, validation protocols, and transfer study reports
Expert knowledge of scientific principles and expertise with monoclonal antibodies, antibody-drug conjugates, vaccines, and gene therapy products
Strong analytical mindset and technical skills in analytical methods and plate-based methods, with preference for analytical separation method experience including size exclusion chromatography, imaged capillary isoelectric focusing, and capillary electrophoresis sodium dodecyl sulfate
Project management skills with demonstrated experience managing multiple projects simultaneously
Strong data interpretation, method troubleshooting skills, and sound scientific judgment
Excellent time management skills with attention to detail and commitment to achieving team and individual goals
Strong communication skills to lead teams and influence leaders or cross-functional team members
Understanding of regulatory guidance and requirements pertaining to method transfer, method validation, and regulatory submissions
 
Experience:
8-10 years of relevant experience in pharmaceutical or biological drug product development, analytical chemistry, or quality control within a regulated biotechnology or pharmaceutical company
Progressive levels of responsibility throughout career demonstrating increasing technical and leadership capabilities
 
Qualifications:
Bachelor's degree in analytical chemistry, biology, biochemistry, pharmaceutical science, or related technical discipline in life sciences
Post-graduate degree in a related field is preferred
This is an exceptional opportunity to join a leading pharmaceutical organization where you will play a pivotal role in ensuring the quality and regulatory compliance of critical analytical methods that support life-saving therapies. 
You will work at the intersection of science and quality, collaborating with talented professionals across global sites while contributing to innovative drug development programs that make a real difference in patients' lives.