Laboratory Analyst Job at Bureau Veritas Certification CZ, s.r.o. (Sainte-Foy)

Laboratory Analyst

Join Galp and bring your curiosity and passion every day. With a customer-centri...

Location

Portugal , Matosinhos

Salary:

Not provided

Galp

Expiration Date

Until further notice

Requirements

Customer orientation and attention to detail
Teamwork skills, initiative, team spirit, and energy
Positive and assertive communication
Strong analytical and problem-solving skills
Organizational and operational response capabilities
English proficiency – Intermediate level (reading/writing/speaking)
IT/technology knowledge, Excel, and Power BI (preferably at an intermediate or advanced level)

Job Responsibility

Perform tests and daily operations, ensuring continuous improvement, compliance with procedures and regulations, and improved service levels
Conduct tests for Interlaboratory Testing Programs, ensuring the maintenance and demonstration of competence
Carry out activities related to quality control and the creation of lubricant product prototypes, characterizing them
Support and respond to audits of the Accredited Laboratory System under the ISO/IEC 17025 standard
Prepare work documents such as operational procedures or assist in regulatory updates
Ensure the quality and validity of produced results and equipment control
Monitor and track equipment performance
Assist in the implementation of new techniques or technologies
Identify opportunities and improvement actions (in operational efficiency, safety, environment, and quality) or help ensure their implementation

What we offer

Competitive salary and bonus scheme
Health and life insurance for you and your family
Meal allowance

Fulltime

Laboratory Analyst I

We're looking for a hands-on, detail-oriented Laboratory Technician to join our ...

Location

United States , Kansas City

Salary:

45000.00 - 46000.00 USD / Year

Beacon Hill

Expiration Date

Until further notice

Requirements

Bachelor's degree in Chemistry, Chemical Engineering, or a related field preferred
Experience supporting R&D, formulation, or process development is highly desirable

Job Responsibility

Prepare, test, and evaluate lab-scale samples to support new product development and customer-driven projects
Operate, troubleshoot, and maintain laboratory and pilot-scale equipment to ensure smooth daily operations
Support scale-up and process development through data collection, material testing, and documentation
Record all experimental data, observations, and calculations accurately in both written and electronic lab notebooks
Perform stoichiometric and chemical calculations using manual and digital tools
Conduct research to help identify solutions, improve formulations, and optimize manufacturing processes
Follow all EHS (Environmental, Health & Safety) standards, SOPs, and lab safety protocols
Work closely with scientists, engineers, and production teams to achieve project goals

What we offer

Be part of a collaborative, innovative team developing cutting-edge products
Gain exposure to state-of-the-art lab and process technologies
Enjoy career growth opportunities and hands-on learning in a supportive environment

Fulltime

Laboratory Analyst & Operations Administrator

As the Laboratory Analyst & Operations Administrator, you will support the day t...

Location

Ireland , Athy

Salary:

Not provided

AXEREAL SCA

Expiration Date

Until further notice

Requirements

Degree in Food Science, Chemistry, Biology, or related discipline
Experience in laboratory operations including equipment calibration, chemical stock management, and sample analysis
Knowledge of food safety and compliance standards (HACCP, GMP, ISO)
Proficiency in data management systems such as JDE and MAPPS
Experience in quality testing methods for malt and barley (e.g., COA generation, intake testing)
Strong communication skills for daily meetings, audits, and customer interactions
Organizational and administrative ability to manage data, generate POs, and support stock management
Attention to detail to ensure compliance, testing accuracy, and reliable reporting
Ability to work collaboratively with production, commercial, and supply chain teams
Problem-solving mindset demonstrated through participation in RCFAs and quality investigations

Job Responsibility

Support the day to day running of the lab and the coordination of intake operations prior to, during and post-harvest
Ensure all lab equipment is maintained, cleaned and tested appropriately
Assist the Production Manager with tasks such as plant and process checks, administration, BOPEX meetings, preparation and participation in other audits and site visits
Work closely with Plant & Production Manager to ensure health & safety is the top priority on site
Collaborate with Production Manager and Quality Team to maintain food safety compliance
Support monthly due diligence testing program to uphold compliance standards
Participation in RCFAs (Root Cause Failure Analysis)
Conduct GEMBA walks to monitor workplace practices and safety
Day-to-day running of the lab ensuring smooth operations
Support malt analysis & COA generation (Certificates of Analysis)

What we offer

Attractive salary and benefits package
Career opportunities internationally
Focus on flexibility, inclusion, collaboration and health and wellbeing

Fulltime

Laboratory Analyst & Operations Administrator

As the Laboratory Analyst & Operations Administrator, you will support the day t...

Location

Ireland , Athy

Salary:

Not provided

AXEREAL SCA

Expiration Date

Until further notice

Requirements

Degree in Food Science, Chemistry, Biology, or related discipline
Experience in laboratory operations including equipment calibration, chemical stock management, and sample analysis
Knowledge of food safety and compliance standards (HACCP, GMP, ISO)
Proficiency in data management systems such as JDE and MAPPS
Experience in quality testing methods for malt and barley (e.g., COA generation, intake testing)
Strong communication skills for daily meetings, audits, and customer interactions
Organizational and administrative ability to manage data, generate POs, and support stock management
Attention to detail to ensure compliance, testing accuracy, and reliable reporting
Ability to work collaboratively with production, commercial, and supply chain teams
Problem-solving mindset demonstrated through participation in RCFAs and quality investigations

Job Responsibility

Work closely with Plant & Production Manager to ensure health & safety is the top priority on site
Collaborate with Production Manager and Quality Team to maintain food safety compliance
Support monthly due diligence testing program to uphold compliance standards
Participation in RCFAs (Root Cause Failure Analysis)
Conduct GEMBA walks to monitor workplace practices and safety
Day-to-day running of the lab ensuring smooth operations
Support malt analysis & COA generation (Certificates of Analysis)
Maintain, clean, and test all lab equipment regularly
Assist with department samples for standardisation
Ensure process machines are calibrated and fit for use (e.g., Agri Check, FOSS 1241)

What we offer

attractive salary and benefits package
career opportunities internationally
focusing on flexibility, inclusion, collaboration and health and wellbeing

Fulltime

Lab Analyst

Airswift has been tasked by one of our major chemical manufacturing clients to f...

Location

United States , No Trees, Texas

Salary:

Not provided

Airswift Sweden

Expiration Date

Until further notice

Requirements

Associate's Degree in Chemistry or related field, two year Lab Tech program or equivalent education with a minimum 2 years of college chemistry and 1 year of college math or equivalent work experience
Must be knowledgeable in analytical methods and functions and be able to perform mathematical calculations
Must be able to work, overtime, weekends, callouts, and holidays as necessary
High proficiency in Microsoft applications (such as Word, Excel, PowerPoint and Outlook)
Excellent written and verbal communication skills
Ability to read, write and speak in English
Excellent interpersonal skills including the ability to work as part of a team
Must possess valid driver’s license
Must be able to lift 50 lbs, climb ladders and stairs
Walking, bending, stooping is required

Job Responsibility

Maintain protection of the environment and the health and safety of our employees, customers, and the communities in which we operate and/or transport our products, as our highest priority
Perform routine analyses, including control samples and calibration checks, without supervision
Provide laboratory support including (but not limited to): preparation of equipment and reagents, storage of samples, packaging and shipping samples, stockroom/supplies, sampling, and instrument and method maintenance
Troubleshoot, repair, and adjust instruments and methods, coordinating with instrument service representatives when necessary
Maintain analytical data and Lab operating statistical record, to support plant operations and customer specification requirements
Analyze & document raw materials, in-process and finished products in accordance with Laboratory Standard Operating Procedures
Assure that the plant is furnished with sample analysis for process control decisions and technical studies in a timely, accurate manner
Be thoroughly familiar with and able to operate instrumentation such as analytical balances, automatic titrators, ICP, particle size distribution analyzer, ion chromatograph (IC), and gas chromatographs
Participate in learning and incorporating new technologies into the laboratory processes as directed by management

What we offer

Health, Dental, Vision, 3% matching 401k, 2 weeks of PTO and paid holidays

Fulltime

Systems Analyst

We are looking for a dedicated Systems Analyst to join our team in Dallas, Texas...

Location

United States , Dallas

Salary:

Not provided

Robert Half

Expiration Date

Until further notice

Requirements

Bachelor’s degree in healthcare, IT, or a related field
Master’s degree is preferred
Certification as a Medical Technologist or Medical Lab Technician is advantageous
At least two years of experience in a hospital or clinical setting is preferred
Epic Beaker certification in Clinical and Anatomic Pathology is required or must be obtained within nine months of hiring
Proficiency in system analysis and technical troubleshooting is essential
Prior experience with Epic system builds, training, and support is highly desirable
Familiarity with tools such as Active Directory, Microsoft SQL Server, and IBM systems

Job Responsibility

Lead regular status meetings and provide updates to stakeholders while mentoring analysts on application workflows
Organize discovery sessions to identify operational requirements and propose effective solutions
Investigate and resolve system issues, recommending corrective actions to improve functionality
Collaborate with IT teams to implement technical solutions and enhance system performance
Support integration efforts between Epic Beaker and third-party applications, utilizing tools like Data Innovations Instrument Manager
Develop and maintain Reporting Workbench reports to provide actionable insights from laboratory data
Ensure system documentation is accurate, comprehensive, and up-to-date
Coordinate testing, upgrades, and go-live activities for Epic systems to ensure smooth transitions
Maintain Epic Master Training environment and deliver user training to ensure effective system utilization

What we offer

medical
vision
dental
life and disability insurance
401(k) plan

Fulltime

Senior QC Analyst

At Target Healthcare Group, we are pioneers in the pharmaceutical industry, comm...

Location

Salary:

Not provided

360 Resourcing Solutions

Expiration Date

Until further notice

Requirements

Bachelor’s or Master’s degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related field
Minimum 5–8 years of QC laboratory experience in the pharmaceutical or biopharmaceutical industry
Strong working knowledge of analytical techniques such as HPLC, GC, UV-Vis, FTIR, TOC and dissolution
Proven experience in method validation, instrument troubleshooting, and data integrity compliance
Excellent understanding of cGMP, GLP, and regulatory requirements
Strong attention to detail and analytical thinking
Proficiency in laboratory software including Chromeleon
Strong communication, leadership, and mentoring skills
Ability to work independently and manage multiple priorities under tight timelines

Job Responsibility

Perform qualitative and quantitative chemical and microbiological analyses of raw materials, in-process samples, finished products, and stability samples using validated methods (e.g., HPLC, GC, UV, FTIR, Dissolution)
Review and verify analytical data, ensuring accuracy, completeness, and compliance with cGMP and SOPs
Lead out-of-specification (OOS), out-of-trend (OOT), and deviation investigations, including root cause analysis and CAPA development
Support release testing and timely completion of batch records to ensure uninterrupted product supply
Participate in method validation, method transfer, and equipment qualification activities
Develop and optimise analytical methods as required to support new product development or process changes
Troubleshoot complex analytical and instrumentation issues independently and provide guidance to peers
Ensure all activities comply with cGMP and ICH, and other applicable regulatory guidelines
Prepare, review, and maintain laboratory documentation including test records, logbooks, and SOPs
Support internal and external audits and respond to audit findings

What we offer

Active Social and charity committee
Cycle to Work Scheme
Electric Vehicle Scheme
Eye Care Vouchers

Quality Control Analyst

3rd shift position (10pm-6:30am). Must be able to train for the first month on 1...

Location

United States , Miami

Salary:

Not provided

Beacon Hill

Expiration Date

Until further notice

Requirements

Bachelor’s Degree (BA/BS) in Chemistry or related field
Less than one year testing of chemicals/pharmaceutical products
Must be able to read and understand analytical procedures
Must be able to effectively communicate results, problems, or issues, in English verbally as well as in writing
Must be computer literate
Must be precise and consistent in day-to-day analysis, easily trainable, and ready to learn
Must be able to work in a team environment and be flexible to easily adapt to changes in assignments
Must follow safe practices as identified in appropriate SDS while working with chemicals and must follow applicable state and federal regulations
Must possess a working knowledge of analytical chemistry techniques, such as analytical weighing, quantitative transfer, preparation of quantitative solutions, analytical dilutions, spectrophotometric analytical techniques, dissolution and drug release, disintegration, moisture determination (Karl Fischer, Coulometric, LOD), thin-layer chromatographic technique, gas chromatographic techniques, HPLC, and measuring physical parameters (bulk and tapped densities, and particle size by sieve analysis)
Must be able to follow compendial (USP/EP/BP/JP) procedures for wet chemical tests

Job Responsibility

Performs professional, technical laboratory functions
The QC Analyst I – is an entry-level role in the analytical Quality Control responsible for performing testing of raw materials, in-process and finished pharmaceutical dosage forms, products on stability, cleaning verification samples following written procedures and applicable SOPs, to clearly document activities performed during testing and to calculate and report results on applicable specification documents
Performs physical and chemical analysis of raw materials, components, in-process and finished pharmaceutical products, including products on stability, according to written methods or compendial methods as applicable, material specifications, using analytical techniques such as IR spectroscopy, UV-Vis spectroscopy, and chromatographic techniques adhering to company policies as identified in standard operating procedures (SOPs)
Prepares samples for analysis involving thorough cleanliness and complex steps for analysis using chromatographic techniques and other analytical techniques as applicable in compliance with cGMP and current safety regulations
Creates and maintains laboratory record documentation in compliance with regulatory requirements
Actively participates in investigation of laboratory results, when required
Prepares volumetric test solutions following USP or in-house methods for wet chemical tests, standardizes such solutions as required, standardizes API for use as in-house reference standard as assigned

Fulltime

Laboratory Analyst

Bureau Veritas Certification CZ, s.r.o.

Location:
Canada , Sainte-Foy

Category:
Research and Development

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
March 13, 2026

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Location:Canada , Sainte-Foy

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Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:March 13, 2026

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Location:
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Contract Type:
Not provided

Job Posted:
March 13, 2026