Scientist II, Chemistry Job at MillenniumSoft Inc (Research Triangle Park)

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

New

Medical Laboratory Scientist II - Chemistry

Join a team that’s setting the standard for safety and quality. Every day as a Q...

Location

United States , Royal Oak

Salary:

Not provided

Quest Diagnostics

Expiration Date

Until further notice

Requirements

One (1) year full-time experience or training (high complexity testing) in a clinical laboratory setting
BS/BA in Medical Technology, Chemistry or Biology, or Associates degree in a Laboratory Science or Medical Technology, or Previously qualified as a Technologist under 42 CFR 493. 1433 published in March 14, 1990
Foreign educated candidates must provide a detailed credential evaluation from IERF (International Education Research Foundation)
United States-educated candidates must provide a detailed original transcript
Proven leadership and problem-solving skills
Must be detail-oriented, have the ability to work independently, establish work priorities and to handle several tasks simultaneously for maximum department efficiency
Interpersonal skills necessary to deal courteously and effectively with supervisors, co-workers and clients
Communication skills necessary to handle telephone inquiries from clients
Ability to deal with client information in a confidential manner
Proficiency in Microsoft Office (Word, Excel and Outlook) and Laboratory Information Systems

Job Responsibility

Perform test procedures of moderate/high complexity requiring the exercise of independent judgement and responsibility in those specialties in which they are qualified
Must demonstrate proficiency in all areas of testing and be proficient troubleshooting all applicable instruments/procedures in the department
Provides support to the department in the areas of quality control, troubleshooting complex problems, customer support, instrument and equipment maintenance, staff training, process improvement and the completion of special projects as assigned
Perform and report on assigned analytical tests in accordance with applicable Standard Operating Procedures (SOP) ensuring that applicable quality control requirements are met
Actively support and comply with laboratory policies and procedures for specimen handling and processing, test analysis, reporting and maintaining records of patient test results
Adhere to analytical schedules to maintain turnaround time of results including STATS or critical results to clients
Ensure reagents/test kits have received dates, expiration dates and if applicable opened dates
Perform and document QC analysis to ensure accuracy of clinical data and proper instrument function. Make quality control decisions regarding the disposition of an assay or test
Responsible for informing supervisory personnel of all problems associated with the proper performance of test procedures
Report any actual or potential deviation from standard or accepted testing procedures and cooperate fully with any investigation of same

What we offer

Day 1 Medical, supplemental health, dental & vision for FT employees who work 30+ hours
Best-in-class well-being programs
Annual, no-cost health assessment program Blueprint for Wellness®
healthyMINDS mental health program
Vacation and Health/Flex Time
6 Holidays plus 1 "MyDay" off
FinFit financial coaching and services
401(k) pre-tax and/or Roth IRA with company match up to 5% after 12 months of service
Employee stock purchase plan
Life and disability insurance, plus buy-up option

Fulltime

Scientist II

The Scientist II embraces our safety driven culture in all tasks and demonstrate...

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
3+ years of experience in analyzing aqueous samples utilizing chromatography equipment and/or previous experience supporting manufacturing in professional laboratory environments
Experience with development of analytical test methods, and laboratory methods a plus
Experience managing complex projects and working on tight deadlines
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
Ability to work independently and as part of a collaborative team
Effective problem-solving and critical thinking skills

Job Responsibility

Runs laboratory equipment as trained and prepares product blends as guided
Collects and evaluates data, utilizing lab notebooks and laboratory information management systems
Reviews, interprets, and analyzes the data for technical, quality, SOPs, client criteria, and Good Laboratory Practices (GLP)
Provides straightforward solutions to problems using readily available clear and direct references
Assists the team on projects including projects with cross functional groups
Write reports summarizing data and on the projects provided
Maintain instruments through routine calibration, troubleshooting, and preventive maintenance
Participate in continuous improvement initiatives for efficiency, accuracy, and method development
Support daily housekeeping, chemical inventory management, and waste disposal in compliance with safety regulations
Demonstrate a strong commitment to laboratory safety, including proper use of PPE, safe chemical handling, and adherence to OSHA/EPA regulations

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

Fulltime

Scientist II

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

Location

United States , Whitesboro

Salary:

56704.00 - 70880.00 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

Under general supervision, develop and perform assays on biological samples from pre-clinical and clinical trials
Validate the quantification of Biomarkers, New Chemical and Biological Entities in tissues, biological fluids or chemical matrices
Perform assays for routine batch analysis of Biomarkers, NCE and NBE in biological fluids/chemical matrix involving simple to complex analytical techniques
Perform 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
Range of health insurance offerings
Global Employee Assistance Programme, LifeWorks
Flexible country-specific optional benefits

Fulltime

Scientist, Product Transfer II

This position is responsible for Product Transfer activities including creation ...

Location

United States , Stillwater, Minnesota

Salary:

70000.00 - 86000.00 USD / Year

Diasorin

Expiration Date

Until further notice

Requirements

Bachelor’s or Master's degree in Chemistry, Biology, Medical Technology OR related science field or a 2 year degree (i.e. MLT) with equivalent experience
5+ Years of related laboratory experience or demonstrated competence within the in-vitro diagnostic industry
Comprehensive understanding of immunology and immunoassay technology and systems
Ability to work in a regulated industry
Working knowledge of general lab equipment (e.g. pH meter, balances, mixers, etc.)
Knowledge of good manufacturing practices (GMP)
Knowledge of statistical analysis and reporting methods
Ability to train and mentor team members on basic group procedures and tasks
Ability to train and mentor team members in higher level skills
Proven ability to work with minimal supervision

Job Responsibility

Work in conjunction with Product Development in creation of all documentation for LIAISON® Reagent Manufacturing and Quality Control for new products. Create part numbers for new products in the design cycle
Create routings for new part numbers created in design cycle
Aid in creation of part numbers and routings for newer team members
Manufacture new Internal Controls for product in the design cycle
Serve on Core Teams for assigned development projects
Perform material processing and reagent formulation for bulk intermediates and components
Determine reprocessing need for calibrator, controls and conjugates, with assistance
Maintain clean work space in QC and Reagent Prep labs, consistent with Good Laboratory Practices (GMP)
Contribute to group Reagent Prep and QC duties, including lab and equipment maintenance
Utilize basic SAP (kitting, ordering to Cost Center, assign expiration dates, etc.) to ensure correct dating, accounting and flow through facility

What we offer

comprehensive plan of health benefits
retirement and financial wellbeing
time off programs
wellbeing support and perks
may be eligible to participate in an annual incentive program

Fulltime

Associate Scientist II

This is where your work makes a difference. At Baxter, we believe every person—r...

Location

United States , Round Lake

Salary:

80000.00 - 120000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

Bachelor’s degree or equivalent experience in a relevant scientific field (e.g., chemistry, pharmaceutical sciences) with at least 2+ years of proven experience
Experience working with analytical chemistry instruments such as HPLC, pH meters, UV spectroscopy, titrations, particle analysis, TOC, flame photometry, and sample extraction techniques
Proficiency in a regulated environment and strong technical problem-solving skills
Excellent oral and written communication skills, strong analytical abilities, and keen attention to detail
Experience with Electronic Lab Notebooks and pharmaceutical GMP laboratories is preferred
Experience with Empower software is advantageous
Ability to manage multiple tasks concurrently and efficiently
Strong laboratory/technical, writing, and computer skills
Ability to effectively coordinate and communicate complex information with managers and peers

Job Responsibility

Conduct critical chemical and physical analyses on finished product R&D stability samples, and support testing of raw materials and other R&D initiatives
Act as a study director for studies, independently evaluating results and determining their impact
Provide training and supervision to junior members within the laboratory
Review test data meticulously, perform documentation reviews in LIMS and other computerized systems
Apply sophisticated laboratory instrumentation and computer systems for data collection and recording
Participate in validations and transfers, ensuring compliance with regulatory standards
Perform detailed chemical assays
Complete all testing, including special project/protocol testing, in a timely manner
Maintain data integrity and ensure compliance with company SOPs, FDA regulations, and other quality standards
Collaborate with various departments to solve problems, boost efficiency, improve quality, and provide outstanding product support

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer
Medical and dental coverage that start on day one
Insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
Employee Stock Purchase Plan (ESPP)
401(k) Retirement Savings Plan (RSP)
Flexible Spending Accounts

Fulltime

Associate Scientist II

This is where your work makes a difference. At Baxter, we believe every person d...

Location

United States , Round Lake

Salary:

80000.00 - 120000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

Bachelor’s degree or equivalent experience in a relevant scientific field (e.g., chemistry, pharmaceutical sciences) with at least 2+ years of proven experience
Experience working with analytical chemistry instruments such as HPLC, pH meters, UV spectroscopy, titrations, particle analysis, TOC, flame photometry, and sample extraction techniques
Proficiency in a regulated environment and strong technical problem-solving skills
Excellent oral and written communication skills, strong analytical abilities, and keen attention to detail
Experience with Electronic Lab Notebooks and pharmaceutical GMP laboratories is preferred
Experience with Empower software is advantageous
Ability to manage multiple tasks concurrently and efficiently
Strong laboratory/technical, writing, and computer skills
Ability to effectively coordinate and communicate complex information with managers and peers

Job Responsibility

Conduct critical chemical and physical analyses on finished product R&D stability samples, and support testing of raw materials and other R&D initiatives
Act as a study director for studies, independently evaluating results and determining their impact
Provide training and supervision to junior members within the laboratory
Review test data meticulously, perform documentation reviews in LIMS and other computerized systems
Apply sophisticated laboratory instrumentation and computer systems for data collection and recording
Participate in validations and transfers, ensuring compliance with regulatory standards
Perform detailed chemical assays
Complete all testing, including special project/protocol testing, in a timely manner
Maintain data integrity and ensure compliance with company SOPs, FDA regulations, and other quality standards
Collaborate with various departments to solve problems, boost efficiency, improve quality, and provide outstanding product support

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer
Medical and dental coverage that start on day one
Insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
Employee Stock Purchase Plan (ESPP)
401(k) Retirement Savings Plan (RSP)
Flexible Spending Accounts

Fulltime

Medical Laboratory Scientist II

Baptist Health is looking to add a highly motivated and skilled Medical Laborato...

Location

United States , Jacksonville

Salary:

Not provided

Baptist Health (Florida)

Expiration Date

Until further notice

Requirements

Licensed as a Medical Technologist in the State of Florida
Licensed in the areas of Chemistry and Hematology
Trained in chemistry, coagulation, urinalysis, hematology and some serology
Strong critical-thinking and laboratory background
Associate's Degree
Less than 1 year Medical Technologist Experience
Licensed Clinical Laboratory Technician Required

Job Responsibility

Maintaining expertise and performing technical, specimen collection/processing, LIS, general department, and clerical functions in laboratory areas where applicable
Maintaining records of performance as defined in the SOP manuals
Supervision by Director and Section Supervisors
can perform all responsibilities without on-site supervision
Supervising MLTs as General Supervisor and serving as Charge Technologist in the absence of other lab supervisors or MTs
May instruct new employees and students
Rounding to other Baptist Health laboratory locations to perform safety and quality assurance audits

What we offer

$500 Sign-On Bonus
Mileage reimbursement provided
No weekends or holidays

Parttime

Scientist II, Chemistry

MillenniumSoft Inc

Location:
United States , Research Triangle Park

Category:
Research and Development

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
January 11, 2026

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