Water Quality Analyst Job at Massachusetts Municipal Association (Maynard)

Environmental Laboratory Analyst - Water Quality

We are looking for an Environmental Laboratory Analyst – Water Quality to join o...

Location

Portugal , Sacavém

Salary:

Not provided

EDP

Expiration Date

Until further notice

Requirements

Bachelor's or Master's degree in Chemistry, Chemical Engineering, Biochemical Engineering, or related fields
Preferably 2–5 years of experience in environmental or water quality laboratories
Strong motivation for laboratory-based work in the field of water quality monitoring
Solid knowledge of laboratory chemistry techniques and analytical methods
Experience with instrumental and bench analytical techniques
Good data analysis, interpretation, and reporting skills
Proficiency with standard computer tools for data processing and reporting
Team-oriented mindset and good collaboration skills
Availability to occasionally participate in field sampling campaigns at locations distant from the laboratory

Job Responsibility

Perform water sampling activities in rivers, reservoirs, and other environmental monitoring locations
Conduct laboratory analysis of collected samples according to accredited procedures and defined analytical parameters
Apply a range of chemical and instrumental analytical techniques for water quality assessment
Analyse and interpret laboratory results, ensuring accuracy and compliance with quality standards
Prepare technical reports and support environmental monitoring activities
Collaborate closely with multidisciplinary teams in laboratory and field activities

Fulltime

Analyst, Quality Control, Microbiology

In this essential role, you will serve as the Microbiology Quality Control Analy...

Location

United Kingdom , Oxford

Salary:

Not provided

Moderna

Expiration Date

Until further notice

Requirements

BSc in a relevant scientific discipline with 5 years Quality Control experience in a cGMP organization with a focus on Microbiology
Hands-on experience of various Microbiology testing techniques and analyses (e.g. Vitek, Isolator Technology, Bioburden, BET, Sterility, others)
Working knowledge of relevant and current FDA, EU, ICH guidelines and regulations preferred
Working experience in a GMP environment
Ability to collaborate effectively in a dynamic, cross-functional matrix environment
Ability to efficiently prioritise and complete multiple projects and tasks in a fast-paced environment
Proven ability to conduct investigations

Job Responsibility

Conducting routine environmental monitoring (EM) and sampling of critical utilities such as water systems in a GMP manufacturing facility
Executing microbiological analyses including TOC, Conductivity, Bioburden, Endotoxin, Sterility, and other GMP QC methods
Supporting GMP testing for product release, stability, and validation samples
Preparing, shipping, and receiving contract laboratory samples, including those for microbiological identification
Participating in new microbiological method transfers in collaboration with Analytical Sciences & Technology (AS&T) teams
Supporting development, implementation, and maintenance of laboratory systems in line with cGMP expectations
Performing general laboratory support activities including reagent preparation, equipment maintenance, and housekeeping
Participating in audit readiness activities, including support to internal and external audit teams
Assisting in equipment and method qualifications, and potentially troubleshooting assay methods and instrumentation
Drafting and revising SOPs, protocols, reports, and contributing to quality system documentation (e.g., deviations, CAPAs, EM excursions, and change controls)

What we offer

Best-in-class healthcare, plus voluntary benefit programs
A holistic approach to well-being with access to fitness, mindfulness, and mental health support
Family building benefits, including fertility, adoption, and surrogacy support
Generous paid time off, including vacation, bank holidays, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown
Savings and investments to help you plan for the future
Location-specific perks and extras

Fulltime

Analyst III, Quality Lab-Microbiology

This position is responsible for conducting microbiological in support of manufa...

Location

United States , Hayward

Salary:

88000.00 - 121000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

B.S. degree in Microbiology, Biology, or related science experience
with minimum of 5 years' experience, or Master's Degree in Chemistry or biological science with 1-4 years' experience
Knowledge of microbiology and environmental monitoring (Endotoxin, Bioburden, and EM monitoring test)
Demonstrates some knowledge of assays/equipment in functional area
Computer literate and competent with a general knowledge of word processing and spreadsheets (such as Microsoft Office)
Proficient use of laboratory equipment and tools
Must be detail-oriented, conscientious, and responsible
Must have effective verbal and written communication skills
Some knowledge of applicable CTP/SOPs, EHS requirements, FDA Regulations application of CGMP/GDPs
Must be able to learn new computer systems and programs in a timely manner

Job Responsibility

Conduct Microbiological analysis on raw materials, initial, in-process and final products, and samples collected from the environmental monitoring programs at manufacturing facility
Testing as required supporting Endotoxin testing, Bioburden analysis, microbial identifications, biological indicators, growth promotion, water
Will be required to read microbial plates and interpret test results
Perform microbial and particulate monitoring of clean rooms throughout the facility. May be responsible for overseeing daily workflow of assigned area
Performs weekly Real Time Risk Assessments (RTRA) to identify potential contamination issues in cleanrooms
Perform equipment maintenance and calibrations as required
Maintain regulatory compliance through established programs for lab testing, training, SOPs, and validation
Write and execute validations for manufacturing processes and laboratory instruments and methods
Work on special projects / protocol testing that involves new methods and instrumentation. Complete all testing, including special project / protocol testing in a timely and appropriate manner
Investigate deviations and write nonconformance documents

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), with the ability to purchase company stock at a discount
401(k) Retirement Savings Plan (RSP), with options for employee contributions and company matching
Flexible Spending Accounts

Fulltime

Analyst Iii, Quality Lab-Microbiology

This is where you make a difference in our patients’ safety. As a member of the ...

Location

United States , Hayward

Salary:

88000.00 - 121000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

B.S. degree in Microbiology, Biology, or related science experience
with minimum of 5 years’ experience, or Master’s Degree in Chemistry or biological science with 1-4 years’ experience.
Knowledge of microbiology and environmental monitoring (Endotoxin, Bioburden, and EM monitoring test)
Demonstrates some knowledge of assays/equipment in functional area. Computer literate and competent with a general knowledge of word processing and spreadsheets (such as Microsoft Office).
Proficient use of laboratory equipment and tools. Must be detail-oriented, conscientious, and responsible. Must have effective verbal and written communication skills. Some knowledge of applicable CTP/SOPs, EHS requirements, FDA Regulations application of CGMP/GDPs.
Must be able to learn new computer systems and programs in a timely manner.
Strong leadership, organization and time management skills.
Attention to detail and ability to prioritize multiple tasks in a timely manner.
Effective organizational skills and ability to plan and suggest resolutions to technical problems.
Strong data analysis and report writing skills.

Job Responsibility

Conduct Microbiological analysis on raw materials, initial, in-process and final products, and samples collected from the environmental monitoring programs at manufacturing facility.
Testing as required supporting Endotoxin testing, Bioburden analysis, microbial identifications, biological indicators, growth promotion, water.
Perform microbial and particulate monitoring of clean rooms throughout the facility.
Performs weekly Real Time Risk Assessments (RTRA) to identify potential contamination issues in cleanrooms.
Perform equipment maintenance and calibrations as required.
Maintain regulatory compliance through established programs for lab testing, training, SOPs, and validation.
Write and execute validations for manufacturing processes and laboratory instruments and methods.
Work on special projects / protocol testing that involves new methods and instrumentation.
Investigate deviations and write nonconformance documents
Lead and/or actively contribute to a team setting within the laboratory to increase efficiency, solve problems, generate cost savings, improve quality, and provide new 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

Analyst III, Quality Lab-Microbiology

This is where you make a difference in our patients’ safety. As a member of the ...

Location

United States , Hayward

Salary:

88000.00 - 121000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

B.S. degree in Microbiology, Biology, or related science experience
with minimum of 5 years’ experience, or Master’s Degree in Chemistry or biological science with 1-4 years’ experience
Knowledge of microbiology and environmental monitoring (Endotoxin, Bioburden, and EM monitoring test)
Demonstrates some knowledge of assays/equipment in functional area
Computer literate and competent with a general knowledge of word processing and spreadsheets (such as Microsoft Office)
Proficient use of laboratory equipment and tools
Must be detail-oriented, conscientious, and responsible
Must have effective verbal and written communication skills
Some knowledge of applicable CTP/SOPs, EHS requirements, FDA Regulations application of CGMP/GDPs
Must be able to learn new computer systems and programs in a timely manner

Job Responsibility

Conduct Microbiological analysis on raw materials, initial, in-process and final products, and samples collected from the environmental monitoring programs at manufacturing facility
Testing as required supporting Endotoxin testing, Bioburden analysis, microbial identifications, biological indicators, growth promotion, water
Will be required to read microbial plates and interpret test results
Perform microbial and particulate monitoring of clean rooms throughout the facility
May be responsible for overseeing daily workflow of assigned area
Performs weekly Real Time Risk Assessments (RTRA) to identify potential contamination issues in cleanrooms
Perform equipment maintenance and calibrations as required
Maintain regulatory compliance through established programs for lab testing, training, SOPs, and validation
Write and execute validations for manufacturing processes and laboratory instruments and methods
Work on special projects / protocol testing that involves new methods and instrumentation

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), with the ability to purchase company stock at a discount
401(k) Retirement Savings Plan (RSP), with options for employee contributions and company matching
Flexible Spending Accounts

Fulltime

Senior Quality Control Analyst

We are looking for a highly skilled, hands-on Senior Quality Control Analyst to ...

Location

Canada , Vancouver

Salary:

88000.00 - 110000.00 CAD / Year

AbCellera Biologics

Expiration Date

Until further notice

Requirements

Deep, hands-on Microbiology experience in a regulated (GMP) QC environment
Experience mentoring or leading team members working within microbiology labs or cleanroom/controlled environments
8+ years of hands-on QC microbiology experience in a GMP setting
Bachelor’s degree in Microbiology or a related life sciences field
Clear communication, collaboration, and calm, structured decision-making under pressure
Strong ownership, accountability, and a solutions-focused mindset
Organized, detail-oriented, and committed to inspection readiness and data integrity
Thrives in an environment requiring in-lab leadership, cross-functional coordination, and prioritization of operational needs

Job Responsibility

Leading Microbiology operations, including bioburden, endotoxin, microbial ID, growth promotion, EM sampling, water testing, and trending
Troubleshooting microbiological assays, contamination events, and EM deviations, ensuring timely and compliant resolution
Providing daily in-lab mentorship to the QC team, fostering strong technique, aseptic practices, and microbiological best practices
Ensuring microbiology labs and adjacent QC spaces remain inspection-ready, including GMP housekeeping and equipment readiness
Coordinating stability pulls, sample preparation, testing, and data tracking across QC programs
Overseeing sample receipt, chain-of-custody, aliquoting, storage conditions, and distribution workflows
Supporting routine sampling, testing, and trending of Utilities (WFI, clean steam, compressed gases) with appropriate documentation
Reviewing micro data packages, protocols, reports, and testing documentation for accuracy and adherence to ALCOA++ principles

What we offer

Equity
Annual bonus dependent on team and company performance
6% (non-match) RRSP contribution
CAD $1,500 annual Active Lifestyle Allowance
Annual vacation
Professional development opportunities
Comprehensive health benefits
Scientific and technical mentorship
Strong sense of community and connections through work, clubs, and socials

Fulltime

New

Data and Technology Manager

4Creeks is seeking a Data & Technology Manager to support the Water Consulting T...

Location

United States , Visalia

Salary:

30.00 - 40.00 USD / Hour

4Creeks, Inc.

Expiration Date

Until further notice

Requirements

Bachelor's degree in Data Science, Information Systems, Computer Science, Engineering, Analytics, or a related field (or equivalent experience)
Experience managing and organizing large datasets and data systems
Strong coding and scripting experience for automation and data analysis (Python, SQL, R, or similar)
Experience developing workflows, dashboards, or user-facing analytical tools
Strong understanding of database systems, data structures, and data management best practices
Excellent analytical, organizational, and problem-solving skills
Strong communication skills with the ability to translate technical concepts into practical solutions

Job Responsibility

Develop and manage systems for organizing, storing, and maintaining large regulatory and monitoring datasets, including groundwater basin data, water quality records, and compliance reporting data for programs such as SGMA and ILRP
Establish standards and best practices for data governance, quality control, and accessibility across water policy and regulatory projects
Design scalable processes for collecting and integrating data from California state sources
Support policy analysis, regulatory compliance, and client reporting through structured data management and efficient delivery of actionable information
Utilize Python, SQL, R, or similar languages to automate regulatory reporting workflows, compliance tracking, and monitoring data processing
Build tools, scripts, and dashboards that support SGMA compliance reporting, ILRP field data analysis, and water quality trend tracking
Reduce manual effort in recurring data tasks across water programs
Research and implement modern tools and platforms that improve data organization and analytical capability for water policy and regulatory work
Stay current on emerging technologies, AI-driven tools, and data infrastructure relevant to the California water sector
Recommend solutions that enhance team productivity and support client deliverables

What we offer

Full employee health coverage (50% coverage for dependents)
Company 401(k) contribution
Participation in the Employee Stock Ownership Program (ESOP)
Performance bonuses

Fulltime

Process Development Principal Scientist

Location

United States , Thousand Oaks

Salary:

148363.00 - 171657.00 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

PHD degree or (foreign equivalent) in analytical chemistry, chemistry, or related field & 3 years of experience in the job offered or in a process development-related occupation. Position requires 3 years of experience in the following: 1. Mass spectrometry knowledge in mechanism of different ionization techniques, configuration of mass spectrometry platforms by different vendors including Waters, Thermo Fisher, or Agilent, and gas-phase ion chemistry for structural elucidation
2. Sample preparation including liquid-liquid extraction and solid phase microextraction for qualitative and quantitative analysis of both small molecules and large molecules
3. Analytical techniques including FT-IR (Fourier-transform infrared spectroscopy), NMR (nuclear magnetic resonance), and UV (ultraviolet–visible spectroscopy)
4. Chromatography and related separation techniques including RP-HPLC (reversed phase high-performance liquid chromatography) and GC (gas chromatography)
5. High-throughput analysis in processing multidimensional mass spectrometry-based data and implementing statistical analysis and interpreting statistical results
and 6. Software applications including ChemDraw, Xcalibur, or ChemStation and programming language for data processing including Python or Matlab.

Job Responsibility

Lead analytical method development, validation and trouble-shooting for drug substances and drug products and in-process testing for synthetic small molecules and/or synthetic peptide testing and characterization
Define analytical control strategies and implement methodologies for development of late phase clinical programs
Collaborate closely with drug substance and drug product process development colleagues to achieve project objectives
Lead and mentor a group of analysts in supporting process development
Provide career development guidance to the team members
Provide concise summary to cross-functional leadership for endorsement of key decisions
Oversee activities at contract manufacturing and testing sites
Author technical reports and analytical Chemistry, Manufacturing and Controls (CMC) sections in regulatory documents
Address analytical and product quality inquiries from health authorities
Supervises direct reports

What we offer

stock
retirement
medical
life and disability insurance
eligibility for an annual bonus
Retirement and Savings Plan with generous company contributions
group medical, dental and vision coverage
life and disability insurance
flexible spending accounts
discretionary annual bonus program

Fulltime

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Water Quality Analyst

Job Description

Job Responsibility

Requirements

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