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<h3>Job Description</h3>
Job Description
Are you detail-oriented and passionate about maintaining high-quality standards in a fast-paced environment? We're looking for a fill-time Post Processing Technician I to join our team in the Processing Department. Available shifts include Monday through Friday 7:30AM - 4:00PM or Friday through Monday 7:00AM - 5:30PM. This position plays a vital role in supporting the post-processing process, ensuring compliance, and maintaining product quality from start to finish. If you're excited to work with a dedicated team in a dynamic setting, this could be the perfect opportunity for you!
As a Post Processing Technician I, you will be responsible for performing routine tasks across all processing areas, working under the guidance of the Processing Supervisor and Post Processing Technician III. Your responsibilities will include conducting green waste disposal processes, trimming batches by hand and machine, and assisting with the dry and cure processes. You'll play a role in maintaining quality control measures, ensuring batches meet product standards, and supporting inventory management by keeping accurate records. In addition, you will be expected to keep your workspaces and machinery clean, sanitized, and organized to maintain operational efficiency.
Previous experience is preferred but not required. The ideal candidate will have a keen eye for detail and the ability to focus on sensitive and complex tasks. Strong verbal and written communication skills, flexibility, and adaptability are essential to succeed in this role. You must be able to stand for extended periods, lift up to 50 lbs occasionally, and perform manual tasks requiring fine motor skills. Safety is a priority, and you will be required to maintain balance while using ladders or performing tasks such as stooping, kneeling, or reaching.
If you're ready to be part of a supportive team in an evolving environment and are excited about contributing to our post-processing process, we encourage you to apply today!

Post Processing Technician 1

<h3>Job Description</h3>
Job Description
Job Title: Analytical Chemist
Job Description
Support, lead, and develop the Research and Development (R&amp;D) team to create innovative new products. Engage in field testing, scale-up processes, and the development of new polymers, adhesives, epoxies, and other coatings.
Responsibilities
<ul>
<li>Lead and support the R&amp;D team in creating new products.</li>
<li>Perform field testing and scale-up processes.</li>
<li>Develop new polymers, adhesives, epoxies, and other coatings.</li>
<li>Drive continuous improvement activities within the R&amp;D department.</li>
<li>Manage product development projects and ensure timely delivery.</li>
<li>Ensure adherence to regulatory standards in R&amp;D for coatings and adhesives.</li>
</ul>
Essential Skills
<ul>
<li>Expertise in chemistry and analytical chemistry.</li>
<li>Proficiency in research and development processes.</li>
<li>Experience with scale-up, polymer chemistry, and epoxy.</li>
<li>Understanding of adhesives and raw material testing.</li>
<li>Experience in polymer synthesis.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Masters or PhD in Chemistry, Materials Science, or Chemical Engineering.</li>
<li>5+ years of experience leading R&amp;D teams.</li>
<li>Knowledge of regulatory standards for coatings and adhesives.</li>
</ul>
Work Environment
The role requires working 100% onsite at the Westwood facility. 
Job Type &amp; Location
This is a Permanent position based out of Westwood, Massachusetts.
Pay and Benefits
The pay range for this position is $125000.00 - $140000.00/yr.
They have full vision, dental, health, and vacation. They have great benefits for medical leave as well.
Workplace Type
This is a fully onsite position in Westwood,MA.
Application Deadline
This position is anticipated to close on Oct 31, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

Analytical Chemist

<h3>Job Description</h3>
Job Description
Job Title: Clean Room Assembler
As a Clean Room Assembler, you will be responsible for assembling product parts on the assembly line in accordance with production guidelines. You will also perform spot checks of products to ensure adherence to approved quality standards.
Responsibilities
<ul>
<li>Assemble assigned product parts on the assembly line following production guidelines.</li>
<li>Perform spot checks of products to ensure adherence to approved quality standards.</li>
<li>Notify management of product discrepancies or equipment malfunctions.</li>
<li>Adhere to established company policies and procedures, paying special attention to safety regulations.</li>
<li>Wear personal protective equipment in accordance with training guidelines.</li>
<li>Perform other related duties as assigned.</li>
</ul>
Essential Skills
<ul>
<li>Must have microscope experience </li>
<li>Must have previous manufacturing experience </li>
<li>Comfortable using tweezers, cutters, wire strippers, and adhesives.</li>
<li>Strong attention to detail and mechanical assembly skills.</li>
</ul>
Pay and Benefits
The pay range for this position is $22.00 - $24.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
 • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in NASHUA,NH.
Application Deadline
This position is anticipated to close on Nov 7, 2025.
About Aerotek:
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meets their goals, skills and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role solving for companies’ construction, manufacturing and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are everything spirit to the test as your career continues to grow.
Aerotek offers weekly pay, employee benefits including medical, dental &amp; vision, life insurance, health advocacy and employee assistance programs, a 401(k) plan, and employee discounts.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
Company DescriptionWe know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow. 
<h3>Company Description</h3>
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow.

Clean Room Assembler

<h3>Job Description</h3>
Job Description
Job Title: Analytical Chemist
Job Description
Support, lead, and develop the Research and Development (R&amp;D) team to create innovative new products. Engage in field testing, scale-up processes, and the development of new polymers, adhesives, epoxies, and other coatings.
Responsibilities
<ul>
<li>Lead and support the R&amp;D team in creating new products.</li>
<li>Perform field testing and scale-up processes.</li>
<li>Develop new polymers, adhesives, epoxies, and other coatings.</li>
<li>Drive continuous improvement activities within the R&amp;D department.</li>
<li>Manage product development projects and ensure timely delivery.</li>
<li>Ensure adherence to regulatory standards in R&amp;D for coatings and adhesives.</li>
</ul>
Essential Skills
<ul>
<li>Expertise in chemistry and analytical chemistry.</li>
<li>Proficiency in research and development processes.</li>
<li>Experience with scale-up, polymer chemistry, and epoxy.</li>
<li>Understanding of adhesives and raw material testing.</li>
<li>Experience in polymer synthesis.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Masters or PhD in Chemistry, Materials Science, or Chemical Engineering.</li>
<li>5+ years of experience leading R&amp;D teams.</li>
<li>Knowledge of regulatory standards for coatings and adhesives.</li>
</ul>
Work Environment
The role requires working 100% onsite at the Westwood facility. 
Job Type &amp; Location
This is a Permanent position based out of Westwood, Massachusetts.
Pay and Benefits
The pay range for this position is $125000.00 - $140000.00/yr.
They have full vision, dental, health, and vacation. They have great benefits for medical leave as well.
Workplace Type
This is a fully onsite position in Westwood,MA.
Application Deadline
This position is anticipated to close on Nov 3, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

<h3>Job Description</h3>
Full-Service Clinical Laboratory | CAP &amp; CLIA Accredited
Are you ready to take the next step in your laboratory career? A full-service clinical laboratory is seeking a full-time Laboratory Supervisor to oversee the microbiology and molecular departments.
This is an excellent opportunity to grow in a collaborative, supportive environment that values professional development, recognition, and career advancement.
Position Highlights:
<ul>
<li>
Permanent, full-time role primarily on day shift&nbsp;
</li>
<li>
Lead a CAP- and CLIA-accredited laboratory committed to excellence
</li>
<li>
Work in a culture that fosters challenge, growth, and recognition
</li>
</ul>
Qualifications:
<ul>
<li>
Bachelor’s Degree in Medical Technology/MLS&nbsp;or related field
</li>
<li>
ASCP Certification (MT/MLS/M/SM/MB) required
</li>
</ul>
Compensation &amp; Benefits:
<ul>
<li>
Highly competitive hourly rate
</li>
<li>
Comprehensive benefits package including:
<ul>
<li>
Medical, dental, and vision insurance
</li>
<li>
Prescription drug coverage
</li>
<li>
Generous PTO
</li>
<li>
Life insurance
</li>
<li>
Flexible Spending Account (FSA)
</li>
<li>
401(k) retirement plan and more!
</li>
</ul>
</li>
</ul>
Apply today or reach out directly to Andrea at <a href="mailto:andrea@ka-recruiting.com" target="_blank">andrea@ka-recruiting.com</a>&nbsp;or call/text 617-746-2745
ACC 10311051

Microbiology or Molecular Lab Supervisor on Day Shift

<h3>Job Description</h3>
NEW Microbiology and/or Molecular Technologist opening at a full service clinical laboratory! This laboratory is fully accredited by CAP and CLIA. They are looking to hire a permanent and full time Medical Technologist/MLS on DAY Shift! This laboratory offers a culture where there are ample opportunities for challenge, growth and recognition!
For consideration, applicants must have either a Bachelor's Degree in Medical Technology/MLS and/or an AS Degree in Medical Laboratory Science/Medical Laboratory Technician AND ASCP Certification as a MT/MLS, MB, SM/M or&nbsp;MLT. This position is Monday through Friday Day or Evening Shift! New graduates and experienced candidates are both encouraged to apply!
This laboratory is offering a highly competitive hourly rate and a top notch benefits package! Benefits include medical, dental, vision, prescription drug, generous PTO, life insurance, FSA, 401K and more!
Interested? Apply below or contact Andrea at <a href="mailto:andrea@ka-recruiting.com" target="_blank">andrea@ka-recruiting.com</a> or 617-746-2745.
ACC 10311201

Microbiology and Molecular Technologist OR Technician on Day Or Evening Shift

<h3>Job Description</h3>
Job Description
Research Scientist– Oncology Translational Research (Onsite – Cambridge, MA)&nbsp;
We are seeking a Research Scientist– Oncology Translational Research for a global pharmaceutical client. You will join the Translational Research team within the Oncology Thematic Research Center in Cambridge, MA. You will work broadly with the research organization to support drug discovery programs, by conducting experimental work in a translational setting, including developing and implementing cutting-edge technology and novel cellular, molecular, and biochemical assays in cancer research and deliver data for Oncology TRC programs.&nbsp;
This is a 40-hour per-week, 12-month contract (extensions possible), 100% onsite role in Cambridge, MA&nbsp;
Work hours/schedule: M - F, typical work hours are 9:00am to 5:00pm&nbsp; Parking Fee: Candidates must be agreeable with the $20/day parking fee at Cambridge Crossings.&nbsp;
This is a W2 role as a Stage 4 Solutions employee. Health benefits and a 401K are offered.&nbsp;
Responsibilities:&nbsp;&nbsp;
<ul>
<li>
Design, optimize, and set up high-throughput screening cellular assays to characterize drug responses and combinations in various in vitro oncology models.&nbsp;
</li>
</ul>
<ul>
<li>
Conduct molecular, biochemical and related assays including qPCR, ELISA, Western blot, immunostaining and basic microscopy.&nbsp;
</li>
</ul>
<ul>
<li>
Develop biomarker, pharmacodynamic and target engagement assays.&nbsp;
</li>
</ul>
<ul>
<li>
Execute, troubleshoot and interpret scientific experiments with some supervision.&nbsp;
</li>
</ul>
<ul>
<li>
Effectively communicate and document experimental procedures, analyze results and data through study reports and internal meetings.&nbsp; &nbsp;
</li>
</ul>
Requirements:&nbsp;&nbsp;
<ul>
<li>
3+ years of experience in conducting cancer cell line and primary cell culture, expansion and functional assays.&nbsp;
</li>
</ul>
<ul>
<li>
Experienced in the design and development of cell-based and molecular assays in a high-throughput manner.&nbsp;
</li>
</ul>
<ul>
<li>
Drug combination screen&nbsp;
</li>
</ul>
<ul>
<li>
Experience performing analysis of protein and DNA/RNA samples using a variety of methodologies including but not limited to western blot, flow cytometry, qPCR, MSD/ELISA, RNAi, CRISPR.&nbsp;
</li>
</ul>
<ul>
<li>
Proficiency in utilizing software such as Graph Pad, Microsoft Office, etc. for data analysis and figure generation is required.&nbsp;
</li>
</ul>
<ul>
<li>
BS or MS Degree.&nbsp;
</li>
</ul>
Please submit your resume to our network at <a href="https://www.stage4solutions.com/careers/" target="_blank">https://www.stage4solutions.com/careers/</a> (please apply to the Research Scientist– Oncology Translational Research (Onsite – Cambridge, MA) role).&nbsp;
Please feel free to forward this project opening to others who may be interested.&nbsp;
Stage 4 Solutions is an equal-opportunity employer. We celebrate diversity and are committed to providing employees with an inclusive environment that is free of discrimination and harassment. All employment decisions are based on the job requirements and candidates’ qualifications, without regard to race, color, religion/belief, national origin, gender identity, age, disability, marital status, genetic information, or other applicable legally protected characteristics.&nbsp;
Compensation: $45hr. - $50.91/hr.&nbsp;
#LI-SW1&nbsp;&nbsp;&nbsp;

Research Scientist- Oncology Translational Research (Onsite - Cambridge, MA)

<h3>Job Description</h3>
Job Description
Job Title: Biologist Location: Boston, MA 02210 Work Schedule: Monday–Friday, 8:00 AM – 5:00 PM
Job Overview:
We are seeking a highly motivated Biologist to join our Downstream Process Development team. The candidate will contribute to the purification and characterization of viral vectors, biologics, or recombinant proteins, supporting process development and manufacturing activities.
Key Responsibilities:
<ul>
<li>
Execute purification processes including affinity chromatography (e.g., AVB, CaptureSelect) and ion-exchange chromatography (AEX, CEX).
</li>
<li>
Operate AKTA systems (Avant, Pure, or Pilot) for small- to large-scale purification runs.
</li>
<li>
Perform tangential flow filtration (TFF) for buffer exchange and product concentration.
</li>
<li>
Support experimental design, data collection, and documentation following GMP/GLP guidelines.
</li>
<li>
Troubleshoot and optimize purification processes.
</li>
<li>
Analyze samples using relevant methods (UV, SDS-PAGE, ddPCR, ELISA, HPLC).
</li>
<li>
Collaborate cross-functionally with upstream, analytical, and manufacturing teams.
</li>
<li>
Maintain lab equipment, buffers, column inventory, and compliance with safety standards.
</li>
</ul>
Qualifications:
Education:
<ul>
<li>
Master’s degree in Biochemistry, Chemical Engineering, Biotechnology, or related field.
</li>
</ul>
Experience:
<ul>
<li>
Minimum 2 years of hands-on purification experience in academic or industry settings.
</li>
</ul>
Technical Skills:
<ul>
<li>
Strong experience with ion-exchange and affinity chromatography.
</li>
<li>
Familiarity with buffer preparation.
</li>
<li>
Knowledge of basic analytical methods for product characterization.
</li>
</ul>
Soft Skills:
<ul>
<li>
Strong attention to detail and excellent documentation habits.
</li>
<li>
Effective communication and teamwork skills.
</li>
<li>
Ability to manage multiple tasks and meet project timelines.
</li>
</ul>
Preferred Qualifications:
<ul>
<li>
Experience in AAV or other viral vector purification.
</li>
<li>
Experience with AKTA systems and Unicorn software.
</li>
</ul>

Purification Scientist - Biologics / Viral Vectors

<h3>Job Description</h3>
Job DescriptionSalary: 
Description: 
We are seeking an experienced Quality Control Microbiologist to join Marianas Technical Operations organization, advancing personalized medicine and radiopharmaceuticals. This person will be responsible for routine microbiological testing including environmental monitoring, environmental monitoring performance qualifications, growth promotion, bioburden, endotoxin, and sterility testing to support product release. In addition to supporting routine testing, this role will ensure that work is completed with SOPs and adheres to strict quality standards.
 
Illustrative Breadth of Responsibilities:
<ul>
<li>Perform environmental monitoring and environmental monitoring performance qualifications (viable, non-viable, and surface monitoring) of classified areas and maintain database of recovered data and isolates to actively trend EM data.</li>
<li>Perform bioburden, endotoxin, and sterility testing to support product release.</li>
<li>Conduct growth promotion testing and release of media.</li>
<li>Ensures aseptic operator qualification and process simulations are performed aseptically according to GMP compliance.</li>
<li>Microbial enumeration and data analysis from microbiological testing.</li>
<li>Experienced with raw material testing is considered a plus.</li>
<li>Identifying, investigating, and resolving microbial action limits, Out of Specification (OOS) results, and deviations.</li>
<li>Maintain laboratory equipment in accordance with internal procedures.</li>
<li>Adhere to SOPs to ensure high quality standards.</li>
<li>Track progress against project timelines, generate regular status updates, and communicate progress and risks to management.</li>
<li>Adhere to safe laboratory practices.</li>
<li>Multi-task across several projects and manage time effectively to achieve results.</li>
<li>Perform other duties as assigned.</li>
</ul>
Requirements/Skills:
<ul>
<li>Bachelors degree in microbiology or related field with a minimum of two years of experience working in a GMP environment in the pharmaceutical or biotechnology industry. Experience working with radiopharmaceuticals will be considered as a plus.</li>
<li>Experience with cGMP and GMP regulations.</li>
<li>Commitment to maintain data integrity through strict adherence to standardized procedures and relevant compliance requirements.</li>
<li>Good understanding of the radiation safety regulations and guidelines is preferred.</li>
<li>Comfortable handling radioactivity and follow proper ALARA (As Low As Reasonably Achievable) technique Strong communication skills, with motivation to work effectively and cooperatively with others, and to establish and maintain good working relationships.</li>
</ul>
Mariana Oncologys Principles
<ul>
<li>Building a Legacy</li>
<li>Execution Excellence</li>
<li>Courage of our Convictions</li>
</ul>

Quality Control Analyst II, Microbiology

<h3>Job Description</h3>
Job DescriptionSalary: $50K - $55K 
Gloucester Marine Genomics Institute (GMGI) is an exciting independent research institute addressing critical challenges facing our oceans, human health, and the environment through innovative scientific research and education. GMGI is looking for a Research Associate to join our team studying the biology of exceptionally long-lived marine animals. Our goal is to translate evolutionary insights from these exceptional animals into interventions that promote human healthspan and combat age-related diseases, using zebrafish as a development platform. This position will conduct zebrafish genetics work and husbandry, testing these evolutionary targets to extend healthy functionality. This project will use modern genetic editing techniques and apply new assays to modulate and test the molecular mechanisms of aging.
The ideal candidate will have experience with aquatic husbandry, standard molecular biology techniques, excellent communication skills, attention to detail, and the ability to work with a multi-disciplinary team of collaborators. This is an extraordinary opportunity for a dynamic and motivated individual to learn a powerful genetic model and to advance aging research in an entrepreneurial and exciting work environment.
 
Responsibilities:
<ul>
<li>Standard molecular biology and genetics experimental research.</li>
<li>Contribute to the maintenance of the aquatic facility, including feeding, water quality, and health monitoring.</li>
<li>Contribute to the generation and maintenance of transgenic zebrafish lines, including microinjection, mutant screening, and genotyping.</li>
<li>Apply assays to quantify biological aging in zebrafish, including taking tissue samples, performing histology, and compound neuro-muscular functionality.</li>
<li>Maintain a comprehensive electronic lab notebook.</li>
<li>Contribute to grant proposals and publications, and present results at lab meetings and other venues.</li>
<li>Participate in institutional fund-raising activities and community outreach activities.</li>
</ul>
 
Qualifications:
<ul>
<li>BS or MS in genetics, molecular or cell biology, or related field, with lab experience.</li>
<li>Experience with standard molecular biology techniques such as DNA/RNA isolation, PCR/qPCR, molecular cloning, and CRISPR gene editing.</li>
<li>Experience with the husbandry of aquatic models.</li>
<li>Experience with zebrafish and histology is desirable.</li>
<li>Ability to work independently to design and execute experiments</li>
<li>Strong data analysis skills using standard bioinformatic and statistic software packages</li>
<li>Attention to detail and strong problem-solving skills</li>
<li>Excellent organization skills and the ability to multi-task in a fast-paced environment</li>
<li>Excellent communication and teamwork skills.</li>
<li>Enthusiasm and commitment to GMGIs mission for science and education.</li>
</ul>
This position will report to the Research Scientist.
 
It's our goal as an employer to provide an enriching and supportive environment for our employees. We are proud to offer a benefit package that includes:
Health and Dental Insurance
Medical and Dependent Flex Spending Accounts
Long Term Disability
Life Insurance
Paid Time Off
403(b) Retirement Plan
12 Paid Holidays
Applicants must be authorized to work in the US.
 
About GMGI 
Gloucester Marine Genomics Institute (GMGI) was launched in 2013 in the belief that the ocean represents a new source of opportunity. As a not-for-profit whose ambitious mission is to address critical challenges facing our oceans, human health and the environment through innovative scientific research and education GMGI is demonstrating that there is vast potential in marine science discovery powered by genomics.
GMGI is proud to be an equal opportunity employer, and all aspects of employment are based on merit, competence, performance and business need.
In addition to researching diversity in our oceans, GMGI is committed to supporting diversity in our workforce and classrooms. We know that having varied backgrounds and experiences stimulates discussion and new ideas. We are committed to taking action on diversity, equity, and inclusion through providing substantial training opportunities to increase our self-awareness as an organization and building a team of staff and students from uniquely different backgrounds. Please visit our website for more information: <a href="http://www.gmgi.org" target="_blank">www.gmgi.org</a>

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