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

Scientist III - Regulated Immunogenicity & Molecular Bioanalytics - FSP

We are looking to fill a Scientist III – Regulated Immunogenicity and Molecular ...

Location

United States , Springhouse

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

Experience executing routine molecular assays, data interpretation, and quality control techniques for technologies including nucleic acid extraction, qPCR/dPCR, and NGS (Illumina platform)
Ability to follow established procedures, and strong attention to detail
Strong verbal and written communication skills with the ability to deliver ideas to an interdisciplinary team
Proven experience thinking critically and ability to solve complex technical issues
Competent individual that maintains full accountability for data generated and can work collaboratively in an organized setting
Proficient in the use of Microsoft Office, and electronic laboratory notebooks
Scientist 3: B.S./B.A. 3-5 years of experience or MS 1-2 years of experience

Job Responsibility

Ability to generate quality experimental data
Communicates results and provides unsolicited ideas to team and project lead through meetings and in reports
Provide input as a collaborating scientist on method development reports and test method optimization, qualification and validation
Strong organizational and project management skills
Demonstrates urgency and sensitive to meet project timelines

What we offer

full benefits, sick time, 401K, paid holidays, and paid time off

Fulltime

Manager, Bioanalytical Services

Manager, Bioanalytical Services- Full-Time, Onsite; Whitesboro, New York. ICON p...

Location

United States , Whitesboro

Salary:

100472.00 - 125590.00 USD / Year

iconplc

Expiration Date

Until further notice

Requirements

Bachelor’s or advanced degree in Biochemistry, Pharmacology, or a related field
Proven experience in bioanalytical services, laboratory management, or a related role, with a strong understanding of GLP and regulatory requirements
Excellent leadership and team management skills, with the ability to oversee complex laboratory workflows
Strong problem-solving and organizational skills, with a focus on delivering high-quality data under tight deadlines
Effective communication and collaboration skills, with experience working in cross-functional project teams

Job Responsibility

Managing the day-to-day operations of the bioanalytical laboratory, ensuring timely and accurate analysis of clinical samples
Leading a team of scientists and lab technicians, providing mentorship and guidance to maintain high performance and scientific integrity
Overseeing the development and validation of bioanalytical methods in compliance with GLP and regulatory standards
Collaborating with cross-functional teams, including clinical and regulatory teams, to ensure alignment of bioanalytical activities with project goals
Ensuring all laboratory processes adhere to quality control procedures and regulatory requirements, and implementing continuous improvement initiatives

What we offer

Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being
Life assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others

Fulltime

Scientific Associate Director - Pharmacokinetics and Drug Metabolism

In this vital and exciting role, you will oversee Pharmacokinetics and Drug Meta...

Location

India , Hyderabad

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

PhD in Pharmacokinetics, Pharmaceutical Sciences, Engineering, or related fields with equivalent professional degrees and 12+ years of experience in the Biotechnology/Pharmaceutical Industry
Solid technical experience with the application of SM in vitro/in vivo ADME and pharmacokinetics fundamentals to drug discovery projects
Ability to drive the progression of SM discovery and development within project teams
Expertise with in vitro ADME, in vivo ADME, PK/PD etc
Experience in supporting preclinical components of regulatory documentations
Excellent interpersonal, technical, and communication skills
Past experience as a laboratory scientist in a pharma or biotech environment
Excellent written and oral communication skills, attention to detail and accuracy, and interpersonal skills
Record of scientific contributions through peer-reviewed articles and external presentations

Job Responsibility

Lead/mentor a team of scientists involved in ADME characterization of small molecules
Directly responsible for leading a team of scientists involved in undertaking mechanistic in vitro ADME assays
Develop/implement novel tools to efficiently support mechanistic ADME work
Oversee activities/establish workflows for small molecule bioanalytical and ADME screening teams
Serving as a subject matter expert of small molecule ADME to support the programs and recommend strategies to PKDM project team representatives to reduce/mitigate risks due to metabolism
Collaborate with scientists across our PKDM scientific community
Leveraging specialized ADME/PK skills such as in vitro ADME, in vivo ADME, biotransformation, PK/PD, to impact project progression and decision-making
Contributing to the analysis of pre-clinical ADME and PK data for IND and NDA filings and documenting these analyses in appropriate reports
Building close relationships with partner functions

Bioanalytical Scientist

SRG

Location:
United Kingdom , Alderley Edge

Category:
Research and Development

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
January 30, 2026

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