Scientist I Job at Danaher Corporation (Pensacola)

Scientist I

We are looking for a Scientist l to join our winning laboratory team rated by Fo...

Location

United States , Whitesboro

Salary:

46864.00 - 58580.00 USD / Year

iconplc

Expiration Date

Until further notice

Requirements

Bachelors in Biology, Chemistry, or Biotechnology
ability to work in a fast paced collaborative environment
effective communication skills
attention to detail
ability to organize and prioritize work

Job Responsibility

Developing and performing assays on biological samples from pre-clinical and clinical trials
validating the quantification of Biomarkers, New Chemical and Biological Entities in tissues, biological fluids or chemical matrices
performing assays for routine batch analysis of Biomarkers, NCE and NBE in biological fluids/chemical matrix involving simple to complex analytical techniques
performing laboratory work to FDA and international regulatory GLP and GCP standards

What we offer

Various annual leave entitlements
range of health insurance offerings
competitive retirement planning offerings
Global Employee Assistance Programme, LifeWorks
life assurance
flexible country-specific optional benefits including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments

Fulltime

Scientist I

Responsible for performing routine testing of in-process and finished product sa...

Location

United States , Canton

Salary:

45000.00 - 67000.00 USD / Year

Fagron

Expiration Date

Until further notice

Requirements

Bachelor of Science degree in a biological science with 3-5 years progressive laboratory experience
Excellent verbal and written communication skills
Planning and organizational skills
Must successfully execute requirements to achieve ISO 5 environment gown certification
Trained in cGMP
Ability to work interdepartmentally and communicate effectively
Excellent attention to detail
Ability to excel in a fast pace environment
Excellent organization skills
Ability to prioritize tasks

Job Responsibility

Performs routine testing of in-process and finished products and provides support for protocols for product validation and environmental monitoring
Performs AQL visual inspection
Performs microbial enumeration and gram staining, and growth promotion testing
Performs duties related to sample receipt, shipping to contract laboratories, and disposal of sample retains
Must be able to understand and follow good documentation practices
Assists Scientist / Lead Scientist / Senior Scientist with test method validations and special projects
Monitors and tracks microbiological test results
Conducts routine entries for summaries of test results for trend analysis
Promptly reports data discrepancies and out of limits conditions to supervision
Provides edits for standard operating procedures for microbiology test procedures

What we offer

Competitive salary
Comprehensive benefits
Performance package
Ability to be part of an international leader in an expanding industry

Fulltime

Scientist I

Responsible for performing routine testing of in-process and finished product sa...

Location

United States , Canton

Salary:

45000.00 - 67000.00 USD / Year

Fagron

Expiration Date

Until further notice

Requirements

Bachelor of Science degree in a biological science with 3-5 years progressive laboratory experience
Excellent verbal and written communication skills are essential
Planning and organizational skills necessary for primary responsibilities
Must successfully execute requirements to achieve ISO 5 environment gown certification as required by supervision
Trained in cGMP
Ability to work interdepartmentally and communicate effectively with various departments
Excellent attention to detail
Ability to excel in a fast pace environment
Excellent organization skills
Ability to prioritize tasks

Job Responsibility

Performs routine testing of in-process and finished products and provides support for protocols for product validation and environmental monitoring
Performs AQL visual inspection
Performs microbial enumeration and gram staining, and growth promotion testing, as needed
Performs duties related to sample receipt, shipping to contract laboratories, and disposal of sample retains
Must be able to understand and follow good documentation practices
Assists Scientist / Lead Scientist / Senior Scientist with test method validations and special projects related to environmental monitoring or sterility testing
Monitors and tracks microbiological test results
Conducts routine entries for summaries of test results for trend analysis
Promptly reports data discrepancies and out of limits conditions to supervision
Provides edits for standard operating procedures for microbiology test procedures as well as other Quality Control documentation

What we offer

Competitive salary
Comprehensive benefits
Performance package
Ability to be part of an international leader in an expanding industry

Fulltime

Scientist I

Responsible for performing routine testing of in-process and finished product sa...

Location

United States , Canton

Salary:

45000.00 - 67000.00 USD / Year

Fagron

Expiration Date

Until further notice

Requirements

Bachelor of Science degree in a biological science with 3-5 years progressive laboratory experience
Excellent verbal and written communication skills
Planning and organizational skills
Must successfully execute requirements to achieve ISO 5 environment gown certification
Trained in cGMP
Ability to work interdepartmentally and communicate effectively with various departments
Excellent attention to detail
Ability to excel in a fast pace environment
Excellent organization skills
Ability to prioritize tasks

Job Responsibility

Performs routine testing of in-process and finished products and provides support for protocols for product validation and environmental monitoring
Performs AQL visual inspection
Performs microbial enumeration and gram staining, and growth promotion testing
Performs duties related to sample receipt, shipping to contract laboratories, and disposal of sample retains
Must be able to understand and follow good documentation practices
Assists Scientist / Lead Scientist / Senior Scientist with test method validations and special projects related to environmental monitoring or sterility testing
Monitors and tracks microbiological test results
Conducts routine entries for summaries of test results for trend analysis
Promptly reports data discrepancies and out of limits conditions to supervision
Provides edits for standard operating procedures for microbiology test procedures as well as other Quality Control documentation

What we offer

Competitive salary
Comprehensive benefits
Performance package
Ability to be part of an international leader in an expanding industry

Fulltime

Scientist I

The Scientist I position embraces our safety-driven culture in all responsibilit...

Location

United States , Lexington

Salary:

Not provided

Valvoline

Expiration Date

Until further notice

Requirements

Minimum B.S. in Chemistry, Chemical Engineering, or related scientific field required
Experience in lab operations and EHS program management, preferably in a manufacturing or industrial laboratory environment
Excellent oral and written communication skills required
Multi-tasker and problem-solver
Attention to detail and desire to complete quality work products
Ability to work well with others and comprehend instruction quickly
Strong attention to detail with excellent organizational and documentation skills
Ability to work independently and as part of a collaborative team
Effective problem-solving and critical thinking skills
Strong commitment to safety, quality, and laboratory best practices

Job Responsibility

Runs laboratory equipment as trained
Prepares product blends under supervision
Documents laboratory data in notebook and spreadsheets
Performs calculations as directed and in teams
Performs a variety of specific tasks under close supervision which involve a series of detailed steps
Collects and evaluates data
Reviews, interprets, and analyzes data for technical, quality and compliance to protocols, methods, SOPs, client criteria, and Good Laboratory Practices (GLP)
Provides straightforward solutions to problems using readily available clear and direct references
Assists Scientists/Researchers on projects
Run product demonstration to customers under direction

What we offer

Health insurance plans (medical, dental, vision)
Health Savings Account (with employer base deposit and match)
Flexible spending accounts
Competitive 401(k) with generous employer base deposit and match
Incentive opportunity
Life insurance
Short and long-term disability insurance
Paid vacation and holidays
Employee Assistance Program
Employee discounts

Scientist I

Scientist I; Onsite, Whitesboro, New York- Full-Time. ICON plc is a world-leadin...

Location

United States , Whitesboro

Salary:

46864.00 - 58580.00 USD / Year

iconplc

Expiration Date

Until further notice

Requirements

Bachelors in Biology, Chemistry, or Biotechnology
Ability to work in a fast paced collaborative environment
Familiarization with basic laboratory operations is preferred
Knowledge of binding assay formats and platforms
Effective communication skills
Attention to detail
Ability to organize and prioritize work

Job Responsibility

Developing and performing assays on biological samples from pre-clinical and clinical trials
Validating the quantification of Biomarkers, New Chemical and Biological Entities in tissues, biological fluids or chemical matrices
Performing assays for routine batch analysis of Biomarkers, NCE and NBE in biological fluids/chemical matrix involving simple to complex analytical techniques
Performing laboratory work to FDA and international regulatory GLP and GCP standards

What we offer

Very competitive salary packages
Annual bonuses
Range of health-related benefits to employees and their families
Competitive retirement plans
Life assurance
Various annual leave entitlements
Global Employee Assistance Programme, LifeWorks
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments

Fulltime

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

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

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Scientist I / Scientist II, Bioanalytical

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

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