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Remote Bioassay Scientist Jobs (NOW HIRING)

Rothe Development, Inc.

Data Curator (Remote)

Familiarity with Open Science Principles. Preferred Qualifications: * Industry or academic experience in one or more bioimaging or other bioassay modalities (e.g., microscopy, micro-computed ...

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Remote Bioassay Scientist information

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$83.5K

$127K

$171K

How much do remote bioassay scientist jobs pay per year?

As of Sep 7, 2026, the average yearly pay for remote bioassay scientist in the United States is $127,031.00, according to ZipRecruiter salary data. Most workers in this role earn between $109,000.00 and $143,500.00 per year, depending on experience, location, and employer.

What is a remote bioassay scientist?

A Remote Bioassay Scientist is a professional who designs, conducts, and analyzes biological assays (bioassays) to evaluate the effects of substances, such as drugs or chemicals, on living organisms or cells, while working from a remote location. These scientists typically collaborate with research teams, interpret experimental data, and ensure compliance with scientific and regulatory standards. Remote Bioassay Scientists use digital tools and communication platforms to manage experiments, share results, and contribute to research projects without being physically present in a laboratory. Their work is crucial in pharmaceutical, biotechnology, and environmental science fields.

What are the key skills and qualifications needed to thrive as a remote bioassay scientist, and why are they important?

To thrive as a Remote Bioassay Scientist, you need a solid background in biology or biochemistry, experience with assay development and validation, and a relevant degree such as a BS, MS, or PhD. Familiarity with laboratory information management systems (LIMS), data analysis software, and common bioassay platforms is typically required, along with certifications in laboratory best practices. Strong problem-solving abilities, attention to detail, and effective communication are essential soft skills for collaborating with remote teams and troubleshooting experiments. These competencies ensure accurate experimental results, efficient workflow, and successful collaboration in a remote scientific environment.

What are the main challenges of working as a remote bioassay scientist, and how can they be addressed?

Working remotely as a Bioassay Scientist often presents challenges such as coordinating experimental workflows without direct access to lab facilities and maintaining seamless communication with on-site teams. To address these challenges, remote scientists typically focus on experimental design, data analysis, and protocol optimization, collaborating closely with laboratory staff via virtual meetings and digital data-sharing platforms. Establishing clear documentation and regular check-ins helps ensure project timelines are met and results are accurately interpreted. Staying organized and proactive in communication are key to thriving in a remote bioassay role.

What is the difference between Remote Bioassay Scientist vs Remote Laboratory Technician?

AspectRemote Bioassay ScientistRemote Laboratory Technician
Required CredentialsBachelor's/Master's in Biology, Biochemistry, or related field; experience in bioassaysAssociate's or Bachelor's in Laboratory Science or related field; basic lab skills
Work EnvironmentResearch labs, pharmaceutical companies, biotech firms (remote options available)Laboratories, clinical settings, manufacturing facilities (remote roles less common)
Industry UsageUsed in biotech, pharma, research institutionsUsed in clinical labs, manufacturing, quality control

The Remote Bioassay Scientist and Remote Laboratory Technician roles share some foundational lab skills and industry settings, but the Bioassay Scientist typically requires more advanced education and focuses on designing and analyzing bioassays, often in research or development contexts. The Laboratory Technician generally performs routine testing and sample processing, with less emphasis on experimental design.

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Remote Bioassay Scientist jobs near you
Infographic showing various Remote Bioassay Scientist job openings in the United States as of August 2026, with employment types broken down into 1% Internship, 1% As Needed, 91% Full Time, 4% Part Time, and 3% Contract. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $127,031 per year, or $61.1 per hour.

Director, Analytical Development and Validation, Tech Ops (Biologics)

Oruka Therapeutics

Remote

$213K - $240K/yr

Full-time

Re-posted 29 days ago

Job description

Job Title: Director, Analytical Development and Validation, Tech Ops (Biologics)     

Location: Hybrid - Waltham, MA. Candidates will be required to be in-office 3 days/week. Remote may be considered.        

Role Overview:

The Director of Analytical Development and Validation will provide scientific and strategic leadership for late-stage analytical activities supporting the development, validation, and lifecycle management of biologic drug products, with a focus on monoclonal antibodies. This role will lead method validation and comparability efforts in support of BLA/MAA submissions, process changes, and commercial readiness, while partnering closely with CMC, Quality, Regulatory Affairs, and external partners.

The ideal candidate is a hands-on leader with deep expertise in analytical method validation, device functional testing, regulatory expectations for late-stage biologics, and the ability to guide teams through complex technical and compliance-driven milestones. This role is highly visible within the CMC team and a pivotal addition to our growing organization where you will play an integral role in supporting multiple programs' analytical activities in support of releasing supplies for clinical trials and preparing for commercialization across US, Canada and EU.

Key Responsibilities: 
  • Lead late-stage analytical development activities for biologics, including method transfer & validation for release, stability, characterization and device functional testing assays.
  • Provide subject matter expertise for ICH Q2/Q14, USP/EP/JP, and global regulatory expectations related to analytical methods.
  • Oversee validation of assays including potency/bioassays, purity and impurities (SEC, CE-SDS, icIEF, HPLC), identity, characterization, residuals and device functional testing.
  • Experience with PFS and Autoinjector functional testing is required, including validation per ISO guidance(s).
  • Drive analytical strategies to support BLA/MAA submissions, post-approval changes, and comparability studies.
  • Partner with Process Development, Manufacturing, Quality, and Regulatory to support late-stage development, tech transfer, and commercial launch readiness.
  • Support analytical risk assessments, control strategy development, and lifecycle management activities.
  • Serve as analytical lead for regulatory interactions, including agency questions and inspections.
  • Build, mentor, and lead a high-performing analytical development team (internal and/or external).
  • Set technical direction, priorities, and timelines for late-stage analytical deliverables.
  • Manage and provide technical oversight to CDMOs and contract laboratories.
  • Review and approve protocols, validation reports, development reports, and regulatory documentation.
  • 10-20% travel is required for this role.
Qualifications: 
  • Experience with monoclonal antibodies and PFS/Auto Injectors is a requirement.
  • Director: Master's (10+ years) or PhD (7+ years) with experience in a scientific discipline with relevant experience in analytical development and/or QC.
  • Relevant industry experience in method development, qualification, validation and method transfer in support of ongoing development and/or commercialization of biologics.
  • Experience with methods including but not limited to U/HPLC, Capillary Electrophoresis, Spectrophotometer, Bioassay (ELISA and Cell-Based), device functional testing per ISO guidance.
  • Deep understanding of ICH guidelines for method development/qualification and validation as well as regulatory expectations in US, Canada and EU.
  • Experience managing multiple stability studies, protocol development and performing trending analysis, OOS/OOT investigations, root cause analysis, etc.
  • Experience with late-phase comparability studies, especially geared toward commercialization.
  • Experience in authoring/contributing to regulatory filings, specifically Module 3 for analytical methods and stability studies
  • Demonstrated track record of successful tech transfers between CDMOs with an eye towards late-stage development and commercial launch.
  • Excellent writing, organization, communication and people management skills with the ability to work effectively with a diverse group of internal and external stakeholders.
  • Must have a creative and strategic attitude with the ability to work in a fast-paced environment.

Compensation:

  • An appropriate financial package will be developed for the successful candidate to include a competitive base salary and equity, with a performance-related bonus opportunity.
  • The anticipated salary range for candidates, who will work in Waltham, MA is $213,000-240,000. The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Oruka is a multi-state employer and this salary range may not reflect positions that work in other states.

We're looking forward to hearing how you can contribute to our team and mission. Join us in shaping the future of our company and making a real impact every day.

Apply