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Remote Antibody Jobs (NOW HIRING)

Jade Biosciences

Jade's pipeline also includes JADE201, an afucosylated anti-BAFF-R monoclonal antibody, as well as ... This is a fully remote role, preferably based on the U.S. West Coast, with occasional domestic and ...

Jade Biosciences

$135K - $155K/yr

Jade's pipeline also includes JADE201, an afucosylated anti-BAFF-R monoclonal antibody, as well as ... Strong communication skills This is a remote role; periodic travel to team and company events is ...

Invivyd

Strategic Account Manager, Miami

Miami, FL · On-site +1

... antibody being investigated for the prevention of COVID-19. Be part of making a difference. Be part of Invivyd. Location: Remote (Miami) Position Summary: At Invivyd, we're building a new category of ...

Invivyd

... antibody being investigated for the prevention of COVID-19. Be part of making a difference. Be part of Invivyd. Location: Remote - Geography based Do you have a consistently strong record of sales ...

Argenx

Associate Director, Medical Writing

$164K - $225K/yr

Our unique antibody engineering technologies combined with the complementary expertise of our ... Strong preference for individuals located on the East Coast** #LI-Remote For applicants in the ...

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Remote Antibody information

What is the difference between Remote Antibody vs Remote Immunoassay Technician?

AspectRemote AntibodyRemote Immunoassay Technician
Required CredentialsBachelor's in Biology, Biochemistry, or related field; laboratory experienceSimilar credentials; often requires certification in immunoassay techniques
Work EnvironmentRemote research, data analysis, and documentationRemote lab testing, sample processing, and assay setup
Industry UsageBiotech, pharmaceutical, research institutionsClinical labs, diagnostics companies, research facilities
Common Search/ComparisonYesYes

Remote Antibody and Remote Immunoassay Technician roles share similar educational backgrounds and industry settings. However, Remote Antibody focuses more on research and development of antibodies, while Remote Immunoassay Technicians primarily perform lab testing and sample analysis. Both roles are essential in biotech and clinical industries, often requiring comparable skills and certifications.

What cities are hiring for Remote Antibody jobs? Cities with the most Remote Antibody job openings:
What are the most commonly searched types of Antibody jobs? The most popular types of Antibody jobs are:
What states have the most Remote Antibody jobs? States with the most job openings for Remote Antibody jobs include:
What job categories do people searching Remote Antibody jobs look for? The top searched job categories for Remote Antibody jobs are:
Remote Antibody jobs near you
Infographic showing various Remote Antibody job openings in the United States as of July 2026, with employment types broken down into 92% Full Time, 4% Part Time, 1% Temporary, 2% Contract, and 1% Summer. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution.

Director, GMP Quality Assurance

Jade Biosciences

On-site, Remote

Full-time

Posted 17 days ago

Job description

About Jade Biosciences
Jade Biosciences is a clinical-stage biotechnology company focused on developing best-in-class therapies that address critical unmet needs in autoimmune diseases. Jade's lead candidate, JADE101, targets the cytokine APRIL, and is currently being evaluated in a Phase 1 clinical trial for the treatment of immunoglobulin A nephropathy. Jade's pipeline also includes JADE201, an afucosylated anti-BAFF-R monoclonal antibody, as well as JADE301, an undisclosed antibody candidate, both currently in preclinical development. Jade was launched based on assets licensed from Paragon Therapeutics, an antibody discovery engine founded by Fairmount. For more information, visit JadeBiosciences.com and follow the Company on LinkedIn.
Role Overview
The Director, GMP Quality Assurance (QA) provides QA support across Jade's product pipeline across various stages of development. This role serves as a key partner to CMC and cross-functional teams, offering QA expertise, guidance and risk-based input to support development and product quality strategies.
The role provides QA oversight of contract manufacturers (CMOs) and service providers supporting cell bank, drug substance (DS), drug product (DP), finished drug product (FDP) packaging and labeling, and product distribution, ensuring alignment with GMP requirements and Jade quality standards.
Additionally, the position coordinates day-to-day GMP quality activities for outsourced manufacturing, including the intake, routing, tracking, and timely archival of quality records such as batch disposition, deviations, CAPAs, change controls, expiry/retest extensions, and product complaints. The Director collaborates with internal and external stakeholders to support timely, compliant documentation and batch release decisions. Additionally, the role may also support other QA Leads to promote cross-program alignment, consistency in QA practices, and balanced workload distribution.
This is a fully remote role, preferably based on the U.S. West Coast, with occasional domestic and international travel. The position reports to the Senior Director, GMP Quality Assurance.
Key Responsibilities
  • Serve as the QA lead for assigned GMP-related activities including quality oversight of CDMOs, tech transfer, scale-up, manufacturing (cell bank, DS, DP, FDP), and disposition of clinical materials
  • Quality reviewer and approver for quality records such as change controls, CAPAs, deviations, temperature excursions, product complaints, expiry/retest, stability protocols/reports, master batch records, method qualifications, etc.
  • Collaborate with CMC, Supply Chain, Analytical Development and Program Management to ensure on-time delivery of products and compliance with all relevant cGMP regulations and guidelines as they pertain to manufacturing and supply operations
  • Supports archival of documents/records, quality metrics and develop/maintain QA related tracking logs
  • Work directly with operating entities (internal and CMOs) to ensure that product(s) meet all required quality standards and specifications
  • Supports management of Quality Agreements, including project coordination, cross-functional review, and approval workflows
  • Represent the Quality function in product development (CMC) teams to provide proactive quality guidance and decisions
  • Influence other functional departments to ensure that CMOs achieve and maintain the appropriate levels of GMP compliance and provide the highest level of quality services to Jade
  • Lead quality risk management activities to proactively identify, assess, and mitigate GMP-related risks across manufacturing and supply operations
  • Facilitate resolution of quality issues with internal and external parties in a timely manner
  • Coordinate communications with CMOs and internal technical product teams on quality issues
  • Review CMC sections of regulatory filings, as needed
  • Collaborate cross-functionally with CMC, Regulatory, Clinical Supply Chain, and Program Leadership teams to ensure quality is embedded across development and manufacturing activities
  • Participate in and support regulatory authority inspections and internal audits
  • Supports development/maintenance of Quality SOPs
  • Contribute to the development and maintenance of a positive team-focused company culture
  • Other duties, as assigned

Qualifications
  • Bachelor's degree and 15 years of experience or a master's degree with 12+ years of experience in scientific discipline or comparable experience
  • 10+ years of experience in GMP Quality Assurance at an operational level supporting manufacturing and quality control in a pharmaceutical or biotech environment
  • Experience with all phases of development (Ph 1-4 including commercial)
  • In-depth knowledge and full understanding of GMP FDA, EMA regulations, device and combo product related guidelines, and other ICH guidelines
  • Ability to research and interpret international GMP related regulations and guidance
  • Experience managing CDMOs
  • Experience related to managing technology transfer, scale up, and validation
  • Experience supporting regulatory authority/notified body inspections
  • Experience supporting regulatory submissions (e.g. IND, BLA) and responses to health authority queries (e.g., FDA, EMA)
  • Strategic thinker with a hands-on approach; comfortable balancing long-term planning with day-to-day execution
  • Proven experience developing strong partnerships with cross functional key stakeholders to ensure that strategic business goals are met through the sharing of knowledge and teamwork
  • Must have excellent verbal, written, interpersonal and organizational skills
  • Strong communication and influencing skills, as well as problem solving ability to evaluate quality matters and make decisions utilizing risk-based approach
  • Must be self-motivated with the ability to thrive in a fast-paced, ambiguous environment while managing competing priorities
  • Excellent computer skills with working knowledge of MS Office such as Word and Excel, Visio and Adobe Acrobat professional, and familiarity with SharePoint
  • Commitment to fostering a diverse and inclusive workplace

Position Location
This is a remote role; up to 15% travel to team and company events is required.
The anticipated salary range for candidates for this role is $210,000 - $235,000. The final salary offered will depend on several factors, which may include, but not limited to, relevant years of experience, educational background, and geography.
As part of the I-9 verification of authorization to work in the United States, Jade Bioscience participates in E-Verify. To learn more about E-Verify please review this poster.
Jade Biosciences is proud to be an Equal Opportunity employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law.

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