Bioanalytical Scientist Job at SRG (Alderley Edge)

Scientist I / Scientist II, Bioanalytical

Arrowhead Pharmaceuticals is seeking a Scientist I/II to join the BioAnalytical ...

Location

United States , Madison

Salary:

90000.00 - 110000.00 USD / Year

Arrowhead Pharmaceuticals, Inc

Expiration Date

Until further notice

Requirements

Bachelor’s degree with 5+ years, or Master’s degree with 3+ years, of relevant experience in the pharmaceutical or CRO industry
Demonstrated experience in method development using diverse analytical platforms, with deep expertise in ligand‑binding assays for immunogenicity assessment
Proven project‑management skills with the ability to prioritize multiple tasks and meet deadlines
Strong organizational skills with excellent attention to detail, and adherence to good documentation practices
Excellent oral and written communication skills
Self‑motivated team player who thrives in a fast-paced, dynamic, multidisciplinary, and matrixed environment

Job Responsibility

Work independently or in collaboration with senior scientists to support project planning for bioanalytical activities, including critical reagent generation and the ADA method development, optimization, and qualification
Lead assigned projects, perform or oversee non-GxP and GxP ADA validations and sample analysis from early to late development, both internally and with external partners. Conduct data analysis and interpretation as needed
Track progress against project timelines, prepare routine status updates, and effectively communicate progress, challenges, and mitigations to management and cross‑functional project teams
Collaborate and support internal bioanalysis team on data review and inventory management
Stay current with evolving methodologies, and regulatory expectations related to ADA assessment, particularly for oligonucleotide therapeutics
Manage multiple projects concurrently and prioritize work effectively in a fast‑paced environment

What we offer

competitive salaries and an excellent benefit package

Fulltime

Intern - Bioanalytical Scientist [LCMS]

Labcorp is seeking a Bioanalytical LCMS Scientist Intern to join our team in Sin...

Location

Singapore , Singapore

Salary:

Not provided

Life Science Talent

Expiration Date

Until further notice

Requirements

Bachelor's degree in Biotechnology, Chemistry or Biomedical Sciences
3 months or more experience with hands-on wet chemistry experiment

Job Responsibility

GLP (good laboratory practice) and GCP (good clinical practice) training
Extract analytes from complicated matrix using various techniques, e.g., PPT, LLE, SLE, SPE
Operation of Liquid Chromatography with Tandem Mass Spectrometry (LC-MS/MS)
Sets up, operates and performs routine and non-routine maintenance on general equipment
Performs a full method validation
Evaluates data for report preparation and experiment modification as directed
Performs sample analysis for samples from clinical trial
Assists in setting up method development

Fulltime

Bioanalytical Portfolio Scientist

In this vital role you will serve as the technical subject matter expert for out...

Location

United States

Salary:

109020.15 - 147497.85 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree OR Master's degree and 2 years of regulated commercial scientific laboratory experience OR Bachelor's degree and 4 years of regulated commercial scientific laboratory experience OR Associate's degree and 8 years of regulated commercial scientific laboratory experience OR High school diploma / GED and 10 years of regulated commercial scientific laboratory experience

Job Responsibility

Serve as the technical subject matter expert for outsourced methods and is responsible to ensure adequate method validation and optimal method performance at CROs
Provides scientific and technical oversight for the transfer, validation, and execution for pharmacokinetic (PK) assays, ensuring adherence to sponsor requirements and current regulatory guidance on bioanalytical assays (e.g. FDA, ICH, EMEA, NMPA)
Leads the transfer and validation of PK assays at external CROs using ligand-binding, ELISA, ECL, LC-MS/MS and hybrid methodologies
Collaborates closely with internal bioanalytical subject matter experts to understand critical attributes of the PK method to ensure successful assay transfer and validation
Monitors assay performance over time and provides input for troubleshooting and continuous improvement efforts
Accountable for method lifecycle management, including review of method validation plans, protocols, reports, and qualification/bridging of reagents and reference material
Reviews analytical data, method protocol, validation/sample analysis plans, reports, and other study documentation for scientific accuracy and consistency with GLP/GCP documentation standards and current regulatory guidance
Works with cross functional partners from CROs to navigate issue resolution and escalation utilizing the governance structure
Provides subject matter expertise during supplier evaluation and monitoring activities
Follows and contributes to guidance documents and SOPs

What we offer

A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
Stock-based long-term incentives
Award-winning time-off plans
Flexible work models where possible

Fulltime

Scientist, LCMS PK Bioanalytical

An exciting opportunity is available for a Scientist to join the PK LCMS group i...

Location

United States , Andover

Salary:

79400.00 - 128500.00 USD / Year

Pfizer

Expiration Date

Until further notice

Requirements

MS with 4 to 6 years of relevant work experience, ideally mostly in industry (or BS/BA with 6 to 8 years of experience)
Expertise in development, characterization, and implementation of bioanalytical LCMS assays
Experience in the operation and troubleshooting of LCMS instrumentation and associated operating/data analysis software including Skyline, Analyst, Sciex OS and Xcalibur
Hands-on experience of biological sample preparation procedures for quantitative LCMS assays on biotherapeutics
Knowledge of writing scripts to set up methods for automated liquid handler system
Knowledge of protein biochemistry of therapeutic antibodies, fusion proteins or ADCs

Job Responsibility

Responsible for the development, qualification and implementation of PK/PD assays using mass spectrometry in support of discovery and preclinical projects
Works with group leads or other discovery and regulated bioanalytical team members and project team members to accomplish goals
Participates in technology development and implementation by exploring new workflows, including automation, high throughput sample preparation and instrumentation in protein quantitation, to expand the group’s PK LCMS bioanalytical capabilities
Participate in all phases of mass spectrometry laboratory operations including technology evaluations, the development of sample preparation and separation methods, data analysis, interpretation, reporting and follow up discussions with the project teams on utilizing the data in appropriate decision making
Ensure all tasks and responsibilities are carried out according to scientific and ethical standards e.g. responsible for electronic notebook record keeping
QC and peer review of data and reports

What we offer

401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution
paid vacation, holiday and personal days
paid caregiver/parental and medical leave
health benefits to include medical, prescription drug, dental and vision coverage
bonus target of 7.5% of the base salary
Relocation assistance may be available

Fulltime

Scientist Laboratory Technician (QC Bioanalytical Lab)

The integrated Biologics Analytical Department provides support to the Biotechno...

Location

Switzerland , Schachen, Lucerne

Salary:

Not provided

Randstad

Expiration Date

June 30, 2026

Requirements

Education as a laboratory technician EFZ or a scientific bachelor’s degree
Work experience in a GMP laboratory
Ability to communicate and document in English
Strong team player, demonstrating mutual respect

Job Responsibility

Execution of analytical testing of drug substance release, stability and characterization for biologics under GMP/GDP
Support of analytical method validation and transfers, write technical protocols and report
Troubleshoot methods to ensure seamless method qualification & execution in the laboratory
Support equipment maintenance, calibration and qualification & periodic review
Works in accordance with applicable internal company regulations: safety, health and environmental protection
Improvement of methods and troubleshooting around equipment and procedures
Release and stability testing of biologics to determine relative potency according to cGMPs
Documentation of activities in an electronic laboratory notebook according to cGMPs
Supporting equipment maintenance and calibration activities

Fulltime

New

Scientist Bioanalytics & Pharmacokinetics

Location: Heidelberg, Germany (on site) Start Date: October 2026 Responsibilit...

Location

Germany , Heidelberg

Salary:

Not provided

VERAXA Biotech GmbH

Expiration Date

Until further notice

Requirements

Ph.D. in Life Sciences, Bioengineering, Pharmacology or related subject area with 3+ years of pharmaceutical development experience in pharma, biotech, or a CRO, with a focus on pharmacokinetics and bioanalytics
Experience with designing, optimizing, qualifying, and validating bioanalytical assays using ECL-based immunoassays (Meso Scale Discovery) and ELISA platforms to support PK/TK assessments, including solid understanding of respective regulatory guidelines
Strong laboratory skills, including the ability to independently execute the bioanalysis of primary samples, handling of biological fluids/matrices (biosafety level S1+ S2) and training of technical assistants in respective assays
Experience in maintaining laboratory notebooks and conducting data-fitting using commercially available software packages such as GraphPad Prism
Training in PK data analysis and interpretation and PK/PD modeling, using industry standard software packages e.g. Phoenix WinNonlin
Excellent verbal & written communication and presentation skills
Commitment to fostering a strong quality-driven culture
Fluency in English (spoken and written) is required
Knowledge in R would be beneficial
German skills are a plus

Job Responsibility

Support anti-idiotypic antibody generation at external CROs and characterization efforts
Plan, conduct, evaluate, and qualify bioanalytical assays (focus on ligand binding assays) in-house, at the highest level of scientific integrity
Arrange assay transfers to clinical CROs and validate methods according to regulatory standards for use in FIH studies
Support in the design and interpretation of external non-clinical in vivo PK studies (GLP and non-GLP) for large molecule drug candidates (ADCs and TCEs)
Apply PK and PBPK models using in vivo study data from different species, employing industry-standard software
Prepare expert reports, scientific documents, and presentations in English
Work collaboratively within project teams and communicate efficiently with multidisciplinary teams to design and prosecute studies in line with the strategic direction of the projects

Fulltime

Senior Associate (In Vivo Pharmacokinetics and Drug Metabolism)

We are seeking a highly motivated, detail-oriented, and collaborative Senior Ass...

Location

United States , Thousand Oaks

Salary:

79424.85 - 107457.15 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

Master's degree
Bachelor's degree with a minimum of 2 years of rodent laboratory animal research experience
Associate's degree with a minimum of 4 years of rodent laboratory animal research experience
High school diploma / GED with a minimum of 6 years of rodent laboratory animal research experience

Job Responsibility

Support senior team members in the execution of preclinical in vivo PKDM-BA studies using mouse and rat models
Assist with routine handling, restraint, husbandry support, and dosing of mice and rats through multiple administration routes including intravenous (IV), oral gavage (PO), subcutaneous (SC), and intraperitoneal (IP)
Perform biological sample collection from rodents including blood, plasma, serum, urine, feces, and tissue specimens under the guidance of experienced scientists and study leads
Conduct clinical observations, monitor rodent health and welfare, and accurately document findings in accordance with study protocols and institutional guidelines
Support rodent necropsy procedures, tissue collection and processing, and basic surgical manipulations as directed by senior staff
Prepare study materials, dosing formulations, laboratory supplies, and associated documentation to facilitate efficient study execution
Maintain accurate, organized, and compliant experimental records and laboratory documentation
Assist with laboratory organization, equipment readiness, and inventory management of research consumables and animal study supplies
Adhere to institutional animal care and use guidelines, SOPs, and laboratory safety procedures
Collaborate effectively with scientists, veterinarians, and laboratory staff to support research timelines and study objectives

What we offer

A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
Stock-based long-term incentives
Award-winning time-off plans
Flexible work models where possible

Fulltime

Principal Scientist: PKDM-BA (Small molecule bioanalysis group lead)

At Amgen, our shared mission—to serve patients—drives all that we do. It is key ...

Location

India , Hyderabad

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree PhD OR PharmD OR MD and relevant post-doc where applicable and xx years of directly related experience
Master’s degree and xx years of directly related experience
Bachelor’s degree and xx years of directly related experience

Job Responsibility

Lead and mentor a team of scientists in the design, execution, and interpretation of bioanalytical studies
Develop, validate, and implement bioanalytical methods for quantitative measurement of drug candidates, metabolites, and biomarkers in biological matrices
Perform and supervise quantitative bioanalysis using LC-MS/MS and other advanced analytical platforms
Handle and process complex biological matrices (e.g., plasma, tissue homogenates, urine, bile) with robust extraction procedures to ensure accurate and reproducible results
Apply sound knowledge of extraction techniques (e.g., protein precipitation, liquid-liquid extraction, solid-phase extraction) to optimize bioanalytical workflows
Ensure compliance with regulatory guidelines and maintain high-quality documentation
Collaborate with PKDM project team representatives and BA scientists located at our US sites and ensure integration of bioanalytical data into project decision-making
Ensure data quality, integrity, reproducibility, and timely delivery of results while maintaining safety standards across all workflows
Mentor and develop team members, promoting a culture of scientific rigor and innovation
Contribute to strategic planning and allocation of bioanalytical resources

Fulltime

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Bioanalytical Scientist

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