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Bio Reference Laboratories Jobs (NOW HIRING)

Neion Bio

Scientist, Analytical Development

New York, NY · On-site

$130/hr

About Neion Bio Neion Bio is harnessing nature's best molecular factory, the chicken egg, to make ... Select and manage CROs and specialized analytical laboratories, including drafting scopes of work ...

New

Neion Bio

Scientist, Analytical Development

New York, NY · On-site

$130/hr

About Neion Bio Neion Bio is harnessing nature's best molecular factory, the chicken egg, to make ... Select and manage CROs and specialized analytical laboratories, including drafting scopes of work ...

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How much do bio reference laboratories jobs pay per hour?

As of Jul 11, 2026, the average hourly pay for bio reference laboratories in the United States is $17.78, according to ZipRecruiter salary data. Most workers in this role earn between $14.42 and $19.23 per hour, depending on experience, location, and employer.

What are some common challenges faced by laboratory technicians at Bio Reference Laboratories, and how can they be managed?

Laboratory technicians at Bio Reference Laboratories often work in a fast-paced, high-volume environment, requiring careful attention to detail and strict adherence to safety protocols. Managing time efficiently and maintaining accuracy while processing large numbers of samples can be challenging, especially during peak testing periods. Effective communication with colleagues and supervisors helps ensure proper workflow and minimizes errors. Continued training and staying updated on new testing methodologies also support technicians in overcoming these challenges and maintaining high-quality results.

What is the difference between Bio Reference Laboratories vs Medical Laboratory Technicians?

AspectBio Reference LaboratoriesMedical Laboratory Technicians
CredentialsMedical Laboratory Technicians typically require an associate degree in medical laboratory technology and certificationSame as above, often requiring certification
Work EnvironmentClinical laboratories, hospitals, diagnostic labsHospital and diagnostic lab settings, performing tests under supervision
Industry UsageUsed by diagnostic labs like Bio Reference Laboratories for testing servicesCommonly employed within labs including Bio Reference Laboratories

Bio Reference Laboratories and Medical Laboratory Technicians work closely in diagnostic testing environments. While Bio Reference Laboratories is a diagnostic company providing testing services, Medical Laboratory Technicians are the professionals performing the laboratory tests. Both roles require similar credentials and work in comparable settings, making them closely related in the healthcare industry.

Who owns BioReference laboratories?

BioReference Laboratories is owned by OPKO Health, a healthcare company that acquired the laboratory in 2015. As a major reference laboratory, it provides diagnostic testing services across various medical fields and employs licensed professionals and advanced laboratory equipment.

Is BioReference legit?

BioReference Laboratories is a reputable clinical laboratory that provides diagnostic testing services. It is a well-established company accredited by relevant health authorities, ensuring quality and compliance in its operations.

What are the career options in a laboratory?

Career options in a laboratory include roles such as laboratory technician, medical technologist, research scientist, and laboratory supervisor. These positions typically require relevant education, technical skills, and familiarity with laboratory equipment and safety protocols.

What are Bio Reference Laboratories?

Bio Reference Laboratories is a clinical laboratory company that provides a wide range of diagnostic testing services to physicians, hospitals, clinics, and other healthcare providers. They specialize in routine and specialized laboratory tests, including blood work, pathology, genetic testing, and COVID-19 diagnostics. The company operates numerous patient service centers and offers advanced laboratory information systems to ensure timely and accurate results. Bio Reference Laboratories is known for its commitment to quality, innovation, and supporting healthcare professionals with reliable laboratory data.

What are the key skills and qualifications needed to thrive as a laboratory technician at BioReference Laboratories, and why are they important?

To thrive as a laboratory technician at BioReference Laboratories, you need a background in biological sciences, laboratory procedures, and a relevant associate's or bachelor's degree. Familiarity with laboratory information systems (LIS), automated analyzers, and quality control protocols is typically required. Attention to detail, strong organizational skills, and effective communication help ensure accuracy and collaboration in a fast-paced environment. These skills are vital for delivering reliable test results and maintaining high standards of patient care and laboratory safety.

What is a BioReference lab?

A BioReference lab is a clinical laboratory that performs diagnostic testing on biological samples such as blood, urine, or tissue. Laboratory technicians and scientists working there analyze samples using specialized equipment and follow strict quality standards to support patient diagnosis and treatment.
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Bio Reference Laboratories jobs near you
Associate Director, Analytical Development & QC

Associate Director, Analytical Development & QC

Formation Bio

Boston, MA • On-site

Full-time

Re-posted 8 days ago

Job description

About Formation Bio
Formation Bio is a tech and AI driven pharma company differentiated by radically more efficient drug development.
Advancements in AI and drug discovery are creating more candidate drugs than the industry can progress because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately limit the number of new medicines that can reach patients, Formation Bio, founded in 2016 as TrialSpark Inc., has built technology platforms, processes, and capabilities to accelerate all aspects of drug development and clinical trials. Formation Bio partners, acquires, or in-licenses drugs from pharma companies, research organizations, and biotechs to develop programs past clinical proof of concept and beyond, ultimately helping to bring new medicines to patients. The company is backed by investors across pharma and tech, including a16z, Sequoia, Sanofi, Thrive Capital, John Doerr, Spark Capital, SV Angel Growth, and others.
You can read more at the following links:
  • Our Vision for AI in Pharma
  • Our Current Drug Portfolio
  • Our Technology & Platform

At Formation Bio, our values are the driving force behind our mission to revolutionize the pharma industry. Every team and individual at the company shares these same values, and every team and individual plays a key part in our mission to bring new treatments to patients faster and more efficiently.
About the Position
We are seeking a highly motivated, self-driven and detail-oriented Associate Director of Analytical Development and Quality Control to join our CMC team. This role will provide broad exposure across Formation Bio's portfolio, requiring the ability to flex between small molecule and biologics programs at different phases of development in an outsourced development model, requiring strong technical skillset, vendor management, and the ability to balance scientific rigor with program timelines.
You will play a key role in providing technical leadership as a subject matter expert for the development, optimization, and validation of drug substance and drug product analytical methods to support outsourced development and manufacturing of small molecule and biologics programs including but not limited to proteins, monoclonal antibodies, and vaccines. In this role you will also oversee all Formation Bio stability programs and closely collaborate with CMC, QA, and Regulatory teams.
Responsibilities
  • In close collaboration with CDMOs and contract testing laboratories, lead development, optimization and validation of phase-appropriate analytical methods for small molecule and biologics drug substances and drug products.
  • Manage testing (in-process, release, stability) at CDMOs and contract testing laboratories.
  • Provide technical oversight for method transfers, comparability assessments, and laboratory readiness.
  • Lead selection, qualification, and ongoing performance management of external analytical vendors.
  • Oversee and manage Formation Bio's stability studies across all programs, including review and approval of stability protocols and review and trending of stability data to support shelf-life and retest dating. Track and publish stability program metrics. Act as the primary contact for stability-related inquiries.
  • Oversee and manage Formation Bio's critical reagents and reference standards inventory and testing.
  • Lead investigations of release and stability OOS and OOT results, deviations, CAPAs and change controls.
  • Author and review analytical sections of CMC documents, including protocols, reports, and regulatory submissions.
  • Author and review of SOPs and work instructions.
  • Closely collaborate with CMC, QA, and Regulatory teams.

About You
  • Analytical Chemistry, Biochemistry, Molecular Biology, or a related discipline Master's degree with 5+ years or Bachelor's Degree with 8+ years of relevant small molecule and biologics analytical development and QC experience.
  • Proven ability to operate effectively in a fast-paced, virtual, and outsourced development environment.
  • Highly organized with a track record of managing multiple priorities across programs in an outsourced development model.
  • Strong scientific judgment with the ability to independently assess data quality, identify risks, and recommend mitigation strategies.
  • Ability to communicate complex analytical concepts clearly to both technical and non-technical stakeholders.
  • Collaborative mindset with a strong sense of ownership and accountability.
  • Extensive hands-on experience developing, optimizing, and validating analytical methods for release and stability testing of small molecules and biologics.
  • Hands-on experience with analytical methods pertinent to bilogics (qPCR, IEF, UHPLC, MS, CE, SDS-PAGE, ELISA, peptide mapping, glycan analysis, etc.) and small molecules (UHPLC, IC, GC, IR, UV, KF, PSD, dissolution, etc.).
  • Experience with authoring and reviewing technical documents such as test methods, method development reports, validation protocols, validation reports, specification justification reports, retest and shelf-life memos, and SOPs.
  • Experience with designing stability studies and performing stability data trending according to applicable guidances.
  • Strong working knowledge of Smartsheet and JMP.
  • Thorough understanding of ICH, FDA, EMA guidances and GMP requirements governing process development, manufacturing, and stability.
  • Ability to travel domestically and internationally up to 25% of the time.

Total Compensation Range: $177,500 - $232,000
Compensation Individual compensation is determined by several factors, including role scope, geographic location, and skills & experience. Your offer will reflect where you fall within the range based on these considerations. In addition to base salary, we offer equity, comprehensive benefits, and generous perks. If the posted range doesn't match your expectations, we still encourage you to apply!
Where We Hire Formation Bio is prioritizing hiring in key hubs, primarily the New York City and Boston metro areas, with a hybrid model requiring 3 days per week in office. Applicants from the Research Triangle (NC) and San Francisco Bay Area may also be considered. Please apply only if you reside in these locations or are willing to relocate
Equal Opportunity Formation Bio is committed to building a diverse and inclusive team. We are an equal opportunity employer and welcome candidates from all backgrounds. All qualified applicants will receive consideration for employment without regard to race, color, creed, religion, national origin, ancestry, sex (including pregnancy, childbirth, breastfeeding, and related medical conditions), gender identity or expression, sexual orientation, age, disability, genetic information, marital status, military or veteran status, or any other characteristic protected by federal, state, or local law.

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