Scientist - Analytical Development Job at SRG (Speke, Liverpool)

Scientist - Analytical Development

The Flu Biopharmaceutical Development (Flu-BPD) group is a multi-disciplinary sc...

Location

United Kingdom , Speke, Liverpool

Salary:

16.77 - 17.77 GBP / Hour

SRG

Expiration Date

Until further notice

Requirements

Minimum of science degree or equivalent in Biochemistry, Virology or other science related field
Previous experience of stability development or proven experience of troubleshooting stability indicating assays, ideally within a biopharma setting
Laboratory experience is essential

Job Responsibility

Perform development activities for the performance of a variety of stability studies, including the setting up of required studies and the analysis of the data from these studies
Perform development of a stability accelerated model
Perform development activities for stability indicating assays, including developing novel techniques for the department and / or troubleshooting existing assays
Contribute and function effectively in a key development project, generating high quality, accurate data to support the project
Makes detailed observations, analyses data, and interprets results
Present findings at internal meetings and supports the preparation of technical reports, summaries, protocols and manuscripts
Ensure the effective technical transfer of any developed assays through to the Quality control function
Continue to support new assays until they become routine, business as usual activities
Laboratory maintenance - housekeeping self-inspections and stock control - re-order schedules and communication with key suppliers
Laboratory documentation of results is accurate, neat and timely, to include investigations

Fulltime

Scientist II/Sr. Scientist I, Analytical Research and Development

We are seeking a Scientist II/ Senior Scientist I with hands‑on experience in ph...

Location

United States , Cambridge

Salary:

130000.00 - 180000.00 USD / Year

Beam Therapeutics

Expiration Date

Until further notice

Requirements

Degree in a relevant discipline (biochemistry, biotechnology, biological sciences, bioengineering, or related fields)
Minimum PhD with 2+ years or BS/MS with 10-15 years industry experience
Must have hands-on experience on analytical method development, optimization, qualification, and testing at GMP or non-GMP environments, supporting clinical phase programs
Experience with analysis of RNAs, proteins, protein conjugates, lipids, and lipid nanoparticles (LNPs) is highly desirable
Extensive experience with at least one or several of the analytical techniques is required: HPLC (RP, IPRP, SEC, IEX), capillary gel electrophoresis, ELISA
Experience with qPCR, DNA and RNA extraction, western blotting, UV spectrophotometry, DLS, MALS, mass spectrometry, and compendial testing will be a plus
Experience with analytical CMC development, method transfer, and QC technical support is highly desirable
A good understanding of ICH Q2 and Q14, with working knowledge on analytical Quality by Design concept
Familiarity with data analysis software such as Openlab, Chromeleon, and statistical software such as JMP
Team player with excellent oral and written communication skills

Job Responsibility

Lead early through late phase method development, optimization, and transfer for lot release, stability, and characterization of drug substances, critical materials, and drug products
Establish technical leadership as subject matter expert in multiple analytical techniques during method development and transfer and provide technical troubleshooting support when needed
Work with cross-functional groups including Research & Development, Quality Control, and Process Development teams to participate in various aspects of method development, transfer, characterization, comparability, and investigation
Coordinate routine sample testing including requests from Research and Development groups and Process Development teams
Author and review SOPs, technical reports, and assist in the preparation of CMC regulatory submissions
Analyze, track, and trend data to monitor analytical assays and ensure consistency in assay performance
Maintaining detailed documentation of experiments in ELN system
Adapting to a fast-paced, dynamic research environment
Mentor and train junior scientists
Living Beam Therapeutics core values

Fulltime

Research & Development Analytical Scientist

At Argenta, we partner with our customers to take animal health solutions from m...

Location

United States , Shawnee

Salary:

Not provided

Argenta

Expiration Date

Until further notice

Requirements

Bachelor’s degree in science related field
Previous experience in pharmaceutical industry, animal health industry or related field preferred
Previous experience in analytical pharmaceutical development preferred
Strong oral and written communication skills
Ability to work independently and handle multiple projects and able to adapt to rapidly changing priorities
Ability to work with outside customers and clients

Job Responsibility

Conduct qualitative and quantitative chemical analysis and experiments for active pharmaceutical ingredients and pharmaceutical products as per project requirements
Assist in the development of new products and processes as per compliance and regulatory requirements
Assist with the technology transfer (methods and products) from Argenta Research into Argenta Manufacturing
Support the Research & Development efforts of the company by providing scientific and technical support for the development of new products
Create and maintain activity plans for assigned projects
Generate, document and review technical data for internal reports, client reports and CMC regulatory support documents

Fulltime

Analytical Development Scientist

Analytical Development Scientist. Provide measurement science to generate and im...

Location

United Kingdom , Huddersfield

Salary:

17.91 - 18.91 GBP / Hour

SRG

Expiration Date

Until further notice

Requirements

Degree (BSc, MSc, or equivalent) in Chemistry or Analytical Chemistry with a proven track record in analytical method development
Knowledge of HSE systems, QA procedures, and compliance responsibilities
Comprehensive experience with chemical and physical analytical techniques such as LC, GC, MS, NMR, FTIR, SEM, EDS, and PSD
Strong background in analytical chemistry, critical data analysis (statistics/DoE), method development, calibration, modelling, validation, and technical transfer
Significant experience supporting manufacturing operations including process monitoring, data analysis, troubleshooting, and implementing process improvements
Problem Solving: Ability to analyse complex problems and generate creative, original solutions
Management: Strong time management, work planning (>4 weeks), team coordination, and meeting management skills
Laboratory/Analytical: Comprehensive practical and theoretical knowledge
Research Skills: Literature/database searching, and ability to interpret complex information
Communication: Clear verbal, written, and presentation skills

Job Responsibility

Provide measurement science to generate and improve manufacturing processes for new and existing products through improved understanding
Support manufacturing processes and projects to meet business targets
Utilise laboratory and plant information efficiently to identify improvements and implement change in line with good change‑management principles and procedures
Collaborate with internal and external partners to deliver analytical aspects of process development and manufacturing support
Remain up to date with scientific developments and proactively identify opportunities to apply them to project work
Plan, manage and conduct non‑routine chemical and physical analysis, analytical development, and process analytical technology projects to support new and existing manufacturing processes
Provide expertise and advice in Analytical Chemistry to both local and global teams under guidance of the Specialist Team Leader
Support development of other scientists in analytical techniques and best practices
Use knowledge and experience to improve safe ways of working in partnership with Departmental Safety Leadership teams
Manage, record and communicate activities in compliance with site, company, and regulatory requirements

Senior Scientist, Analytical Development and Quality Control

The Senior Scientist, Analytical Development and Quality Control will support an...

Location

United States , Waltham

Salary:

115000.00 - 140000.00 USD / Year

Kailera Therapeutics

Expiration Date

Until further notice

Requirements

PhD with a minimum of 6 years, MS with a minimum of 10 years, or BS with a minimum of 12 years of experience in analytical development and quality control within the pharmaceutical or biotech industry
Proven experience with peptides and small molecules in both injectable and solid oral dosage forms
Experience managing outsourced activities with CDMOs
Strong expertise in analytical techniques such as HPLC, UPLC, MS, GC, and spectroscopic methods
Knowledge of regulatory requirements (FDA, EMA) and ICH guidelines related to analytical development
Proven effective communication and interpersonal skills
Ability to work effectively in a fast-paced, collaborative environment

Job Responsibility

Participate in the assessment and selection of Contract Development and Manufacturing Organizations (CDMOs)
Oversee analytical activities conducted by these CDMOs to ensure external partners fulfill technical needs and quality standards
Perform detailed review and provide data integrity oversight of data generated at CDMOs
Ensure appropriate methods are developed and implemented for drug substance and drug product based on identified critical quality attributes
Provide oversight of phase-appropriate method validation activities in alignment with current regulatory requirements
Oversee stability programs to support product retest, shelf-life, and expiration dating
Contribute to the preparation of data summaries and reports, and data review of regulatory submissions (INDs, NDAs, IMPDs)
Ensure analytical methods and data meet regulatory requirements, generate data to justify specification limits, and assess trends in stability data
Ensure all analytical activities comply with GMP, ICH guidelines, and other relevant regulations
Participate in internal and external investigations of quality events (e.g., deviations, CAPAs, OOS, etc.)

What we offer

comprehensive health coverage
flexible time off
paid holidays
year-end shutdown
monthly wellness stipend
generous 401(k) match
tuition reimbursement
commuter benefits
disability and life insurance
annual bonus opportunities

Fulltime

Senior Scientist I/II - Analytical Development (CMC)

The Senior Scientist will be responsible for managing analytical development, gu...

Location

United States , Brisbane

Salary:

150000.00 - 176000.00 USD / Year

Mammoth Biosciences

Expiration Date

Until further notice

Requirements

PhD in Analytical Chemistry, Pharmaceutical Sciences, Biochemistry, or related field with 3+ years of relevant industry experience
MS with 6 years of experience in a biotech/pharma setting
Scientist II: PhD + 5 years minimum experience or MS + 8 years minimum experience
Strong working knowledge of oligo/mRNA-LNP related analytical methods
Hands-on expertise with relevant analytical techniques for gene/cell therapies or complex biologics (e.g., HPLC, LC-MS, DLS, UV, ELISA, qPCR/ddPCR, particle/aggregate characterization, and/or enzymatic assays)
Strong understanding of ICH guidelines, phase-appropriate method validation, and regulatory expectations
Proven track record of guiding method qualification and validation in early phase settings
Experience managing analytical workflows at CDMO/CTLs
Excellent problem-solving, communication, and cross-functional collaboration skills
Ability to regularly work onsite at our Brisbane, CA location

Job Responsibility

Support analytical method development and implementation, both internally and via contract labs, to support the characterization, release testing, and stability of CRISPR-based drug substance and drug product
Establish internal capabilities for select analytical assays in R&D labs, including method qualification and troubleshooting for nucleases, guide RNAs, and delivery vehicles
Manage relationships with external testing labs (CTLs) and manufacturing partners (CDMOs) to ensure method development, validation, and transfer meet project timelines and regulatory expectations
Draft and review protocols, reports, and method qualification and validation documentation in compliance with ICH and relevant regulatory guidelines
Provide technical leadership on assay design and analytical strategy, ensuring methods are phase-appropriate, scalable, and tailored for novel CRISPR-based genetic medicines
Support preparation of CMC documentation for regulatory submissions (e.g., INDs)
Evaluate and implement emerging analytical technologies that align with ultracompact CRISPR platform and pipeline needs
Help build and mentor a small team as the company scales

What we offer

Company-paid health/vision/dental benefits
Unlimited vacation and generous sick time
Company-sponsored meals and snacks
Wellness, caregiver and ergonomics benefits
401(k) with company matching

Fulltime

Analytical Chemistry Development Scientist 1

Looking for local candidates, contract position, potential long term depending o...

Location

United States , Salt Lake City

Salary:

25.00 - 28.00 USD / Hour

MillenniumSoft Inc

Expiration Date

Until further notice

Requirements

Experience / understanding of working in a lab
Lab work experience a strong plus
Ability to write detailed technical protocols and reports
Strong communication skills
Strong ability to learn
Bachelor’s degree or higher in a STEM major (Examples: Chemistry, chemical engineering, biomedical engineering, materials science)
Need US Citizens Or GC Holders Only

Job Responsibility

Provide technical skill, analytical testing, and engineering support for design and development activities for various medical device products
Support current products in roles of quality, research & development, pilot-scale manufacturing, supply continuity, and cost improvement
Focus will be on analytical chemistry and chemical work in the lab
Execute technical and cross-functional project work

Fulltime

Analytical Chemistry Development Scientist

This is a full-time contract position, with potential for long-term engagement, ...

Location

United States , Salt Lake City

Salary:

Not provided

MillenniumSoft Inc

Expiration Date

Until further notice

Requirements

Bachelor’s degree in Chemistry, Chemical Engineering, Biomedical Engineering, Materials Science, or related field
Experience or understanding of lab work is required, with hands-on lab experience strongly preferred
The ability to write detailed technical protocols and reports is advantageous
Strong communication skills
Strong learning ability
Proficiency in analytical chemistry and/or in vitro biological testing
Understanding of lab protocols and procedures
Strong written and verbal communication skills
Ability to learn quickly and adapt to new tasks

Job Responsibility

Provide technical support for technology development in medical device products, including research & development and pilot-scale manufacturing projects
Conduct analytical chemistry and/or in vitro biology work using lab instruments
Execute technical and cross-functional project tasks
Follow standard operating procedures (SOP) and test methods
Coordinate lab maintenance activities
Perform other duties as directed by the Supervisor to support business operations

Fulltime

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Scientist - Analytical Development

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