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job_organization_name

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<h3>Job Description</h3>
Job Description
CHEMICAL OPERATOR
Our company is currently seeking a skilled and experienced PETN Chemical Operator for our explosive manufacturing facility. The ideal candidate will have some mechanical and chemical experience, excellent communication skills, and a high degree of mechanical and chemical aptitude. The successful applicant will be responsible for operating production line equipment, handling and packaging finished goods, loading raw materials, monitoring the production process, operating loading machinery, maintaining work area and equipment, carrying out basic quality and testing checks, data logging, and reporting any issues with equipment directly to supervision. The applicant must be willing and able to cross-train into all positions within the PETN process. The applicant must understand and follow Standard Operating Procedures (Work Instructions) and production directives without deviation. Must be able to lift up to 50 lbs., sit, stand, climb stairs and qualify for all required PPE.
ABOUT AUSTIN POWDER
Austin Powder manufactures a full line of industrial explosives and provides blasting services to customers in the quarrying, mining, construction, and oil and gas industries -- all for the purpose of providing aggregate, energy, and mineral products to consumers.
Our values of commitment to safety, attention to detail, and the power of family are the very bedrock upon which our company's culture is built. We truly value our team which is why we offer competitive opportunities for career growth and advancement.
WORK EXPERIENCE / REQUIREMENTS
<ul>
<li>Must have basic understanding of computers</li>
<li>Must be able to handle working in chemical manufacturing environment</li>
<li>Must be self-starter capable of working in team or sole contributor</li>
<li>Good organization and record keeping skills</li>
<li>Excellent communication skills</li>
<li>Must be able to lift 50 lbs</li>
<li>Ability to work overtime when applicable</li>
<li>Swing Shift 12 hour shift schedule</li>
</ul>
EDUCATION REQUIREMENTS
<ul>
<li>Minimum of a high school education or equivalent mandatory</li>
</ul>
PREFERRED EXPERIENCE
<ul>
<li>1 year of experience in Chemical Operations</li>
<li>Previous working experience with Process Safety Management</li>
<li>Explosive or chemical manufacturing</li>
<li>Mechanically inclined</li>
<li>Previous working experience with Microsoft Word, Excel</li>
</ul>
ARE YOU READY TO JOIN OUR TEAM?
If you feel that you would be right for this night shift position, please fill out our initial 3-minute, mobile-friendly application so that we can review your information. We look forward to meeting you!
This contractor and subcontractor shall abide by the requirements of 41 CFR 60-1.4(a), 60-300.5(a) and 60-741.5(a). These regulations prohibit discrimination against qualified individuals based on their status as protected veterans or individuals with disabilities, and prohibit discrimination against all individuals based on their race, color, religion, sex, sexual orientation, gender identity, national origin, and for inquiring about, discussing or disclosing compensation. Moreover, these regulations require that covered prime contractors and subcontractors take affirmative action to employ and advance in employment individuals without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.
 

 Job Posted by ApplicantPro

Chemical Operator

<h3>Job Description</h3>
Job Description
About Certified Group
 At Certified Group, we deliver expert solutions and rigorous testing our customers can trust—on time, every time—so the world can have confidence in what it consumes. As a leading North American provider of laboratory testing, regulatory consulting, and certification and audit services, Certified Group brings together trusted brands including Food Safety Net Services (FSNS), FSNS Certification &amp; Audit, Certified Laboratories, EAS Consulting Group, and Labstat International Inc.
We support a wide range of industries, including food &amp; beverage, dietary supplements &amp; NHPs, cosmetics, OTC and personal care products, tobacco, nicotine, cannabis, and hemp.
We are united by a shared culture and core values: Start with the Customer, Drive to Deliver, Commit to Safety and Quality, and Believe in the Team—including believing in you.
The Opportunity
 We are seeking a Lab Services Supervisor to play a critical leadership role within our laboratory operations. This position is ideal for a hands-on leader who is passionate about training, quality, and developing high-performing teams.
In this role, you will oversee and deliver laboratory training, mentor staff, and partner closely with management to ensure operational excellence, regulatory compliance, and a positive, professional work environment. 
Key Responsibilities
<ul>
<li>Lead, deliver, and oversee training for new and current laboratory personnel. </li>
<li>Mentor and coach team members, providing ongoing performance feedback and development support. </li>
<li>Evaluate training effectiveness and manage corrective action plans when needed. </li>
<li>Maintain a collaborative, respectful, and safety-focused workplace culture.</li>
<li>Ensure compliance with the FSNS Quality Manual, SOPs, QC standards, and ISO 17025 guidelines. </li>
<li>Conduct internal audits related to training and test performance. </li>
<li>Maintain trainer qualifications and required certifications.</li>
<li>Process samples and perform testing as needed across multiple laboratory areas. </li>
<li>Maintain the ability to perform all functions reporting to the supervisor. </li>
<li>Oversee test results and reporting, including communication of out-of-specification results. </li>
<li>Address client needs in collaboration with the Management Team.</li>
<li>Work closely with Operations and Technical Managers to support lab priorities and schedules. Identify opportunities to improve operational efficiency through effective training. </li>
<li>Stay current with industry trends, scientific literature, and professional development opportunities.</li>
<li>Promote and uphold safety standards for yourself and others. Ensure proper use of PPE and adherence to laboratory safety protocols.</li>
</ul>
Education &amp; Experience
<ul>
<li>Bachelor’s degree in Life Sciences or a related field required. </li>
<li>Master’s degree in Life Sciences or a related field preferred. </li>
<li>Minimum of two years of analytical laboratory experience and at least one year of experience managing or supervising personnel, or an equivalent combination of education and experience. </li>
<li>Familiarity with GMP, OSHA, FDA, BAM, APHA, and Compendium methods is required. </li>
<li>Working knowledge of LIMS and Microsoft Office is required.</li>
</ul>
Skills &amp; Competencies
<ul>
<li>Strong written, verbal, and interpersonal communication skills. </li>
<li>Excellent organizational and time-management abilities. </li>
<li>Critical thinking and independent problem-solving skills. </li>
<li>Ability to interpret written, verbal, and visual instructions. </li>
<li>Comfortable working in a fast-paced, deadline-driven environment.</li>
<li>Ability to lead and supervisor a team.</li>
</ul>
 Sunday -Thursday Sunday shift starting at 10am Monday-Thursday shift starting at 2pm

Laboratory Services Supervisor

<h3>Job Description</h3>
Job DescriptionSalary: $115,000/$130,000 per year 
Join Us at Oxford Biotherapeutics (OBT)
Oxford Biotherapeutics (OBT) is a clinicalstage biotechnology company developing innovative antibodybased therapeutics for the treatment of cancer. You will contribute directly to the preclinical development of our immunooncology pipeline.
Our proprietary OGAP platform, the worlds largest cancerspecific membrane protein library enables the discovery of novel, highly tumourspecific antigens for firstinclass ADC, Bispecific Tcell Engager (BITE), and CARbased therapeutics. Our lead asset, OBT076, is in Phase 1b clinical development, supported by a strong internal and partnered pipeline with leaders such as Roche, Boehringer Ingelheim, and Zymeworks.
 
Learn more at <a href="http://www.oxfordbiotherapeutics.com" target="_blank">www.oxfordbiotherapeutics.com</a>.

About the Role
As an Antibody Discovery Associate Scientist/Scientist, you will play a key role in discovering both tool and therapeutic antibodies using stateoftheart in vivo and in vitro approaches. Youll collaborate closely with crossfunctional teams, contribute to experimental design, and help drive projects forward in a fastpaced, highly innovative environment.
 
This role is an excellent fit for someone who is proactive, detailoriented, scientifically curious, and excited to work on cuttingedge antibody discovery pipelines.

Key Responsibilities
<ul>
<li>Single Bcell discovery: Plan and execute multiparameter flow cytometry for antigenspecific Bcell sorting; recover paired VH/VL sequences using singlecell RTPCR; perform molecular cloning and antibody expression for rapid screening.</li>
<li>Molecular recovery &amp; sequencing: Develop and perform workflows for RTPCR/PCR, barcoding, and amplicon QC; prepare NGS libraries and support sequencing for deep repertoire capture.</li>
<li>Repertoire mining &amp; clonal analysis: Analyse BCR repertoires (VDJ assignment, CDR annotation), perform clonal clustering and lineage inference, and identify promising antibodies using developability/sequenceliability assessments.</li>
<li>Highthroughput screening (HTS): Run ELISA, Octet, and cellbased assays to assess specificity, affinity, and expression levels.</li>
<li>Antibody characterisation: Perform kinetics and epitope binning (BLI/SPR), assess crossreactivity and affinity maturation, and contribute to mechanismofaction assays.</li>
<li>Data analysis &amp; reporting: Own QC, analysis, and visualisation of experimental data; prepare clear written summaries and present findings to internal and external partners.</li>
<li>Operational excellence: Maintain highquality scientific records, support workflow optimisation, and uphold lab safety and data integrity.</li>
</ul>

Knowledge, Experience &amp; Skills
Required
<ul>
<li>BS/MS/PhD in Immunology, Molecular Biology, Biochemistry, Cell Biology, or a related field. BS/MS: 35 years handson experience in antibody discovery (industry preferred) PhD: 12 years experience</li>
<li>Experience with flow cytometry/FACS for antigenspecific Bcell sorting (SONY sorter experience a plus)</li>
<li>Proficiency in singlecell RTPCR, PCR, cloning, expression, and sequence analysis</li>
<li>Experience with NGS workflows library prep, indexing, QC and repertoire analysis tools (e.g., MiXCR, IgBLAST, PipeBio)</li>
<li>Familiarity with SPR/BLI for kinetics and epitope binning</li>
<li>Competence in data analysis software such as FlowJo, Geneious Prime, Biacore/Octet, and GraphPad Prism</li>
<li>Strong written and verbal communication skills</li>
</ul>
 
Preferred
<ul>
<li>Experience with CRISPR gene editing</li>
<li>Understanding of antibody developability assessment</li>
</ul>

Benefits
We care deeply about the wellbeing of our employees and their families. Our comprehensive benefits include:
<ul>
<li>Medical, dental, and vision insurance for employees and dependents</li>
<li>Flexible Spending Account (FSA)</li>
<li>ShortTerm Disability (STD), LongTerm Disability (LTD), Basic Life &amp; AD&amp;D, and Supplemental Life insurance</li>
<li>401(k) plan</li>
<li>120 hours of Paid Time Off + 5 sick days per year</li>
<li>11 public holidays</li>
<li>Annual bonus program</li>
<li>Employee referral bonus program</li>
<li>New hire stock options</li>
</ul>

Equal Opportunities Statement
OBT is an equal opportunity employer. We welcome applicants of all backgrounds and do not discriminate on the basis of race, colour, religion, gender, sexual orientation, gender identity or expression, national origin or ancestry, age, disability, marital status, or veteran status. All qualified applicants will receive fair consideration for employment.

Why Join Us
At OBT, we foster a culture grounded in innovation, scientific excellence, and collaboration. Colleagues describe our environment as friendly, supportive, and hardworking, where people trust one another and share a commitment to making meaningful impact.
We value diverse perspectives and believe our strength comes from working together with curiosity, respect, and a shared purpose.

Antibody Discovery Associate Scientist/Scientist

<h3>Job Description</h3>
Job Description
Adesis Inc. - a subsidiary of Universal Display Corporation (Nasdaq: OLED), a global leader in organic light emitting diodes - is a premier contract development and manufacturing organization (CDMO) accelerating our clients’ success in the biotech, pharmaceutical and specialty chemistry industries through our innovative chemistry and solutions. Adesis Inc. encompasses almost 100,000 square feet of state-of-the-art laboratory and manufacturing space in two U.S. locations - New Castle and Wilmington, DE, centrally located in the Mid-Atlantic biotech/ pharmaceutical hub. Our business model provides clients with organic chemistry services in three areas: early-stage research, scale-up and development, and specialty manufacturing. We specialize in organic and organometallic synthesis, from milligrams to multi-kilogram quantities, and our exceptional technical team prides ourselves in our ability to solve challenging chemistry problems for our growing client base. Adesis is an extraordinary company looking for extraordinary talent! Our mission is to accelerate our clients’ success through innovative chemistry and solutions, and we offer promising careers in an inclusive work environment aligned with our values of innovation, ownership and integrity.

Job Summary: The manufacturing Process Chemist works both independently and as part of a team to assist in the development, optimization, and technology transfer of commercial manufacturing compounds. The position involves set-up, use, and cleaning of various laboratory equipment as well as running established protocols with the guidance of chemists and senior technical staff. 
Key Responsibilities:
<ul>
<li>
Develop robust processes for the target compounds to ensure safe and reproducible processes.
</li>
<li>
Develop alternate synthetic routes to target molecules and modify reactants and/or equipment as required.
</li>
<li>
Solve complex chemical problems which may arise during process development, optimization or scale up of processes.
</li>
<li>
Understand the concepts of reaction kinetics, design of experiments, solubility and crystallization, mass transfer, heat transfer and process safety to ensure critical process parameters are identified.
</li>
<li>
Accountable for documentation to ensure the consistent manufacture of products; including batch records, production instructions, and development / qualification reports.
</li>
<li>
Performs other related duties as assigned by Management. Technical and Specialized Equipment:
</li>
</ul>
<ul>
<li>
NMR
</li>
<li>
(UP)LC/MS
</li>
<li>
EasyMax, PolyBLOCK
</li>
<li>
Jacketed reactors
</li>
<li>
GC/MS
</li>
<li>
Automated Chromatography Systems
</li>
<li>
Hydrogenation equipment
</li>
</ul>

Required Qualifications:
<ul>
<li>
BS or MS in Chemistry or related field required. 
</li>
<li>
At least 2 - 5 years’ experience in technical production, R&amp;D, and/or new product development experience required. 
</li>
<li>
Ability to define problems, collect data, establish facts, and draw valid conclusions. Interpretation of technical instructions from disparate information sources, and deal with several abstract and concrete variables.
</li>
<li>
Ability to work within a fast-paced, dynamic and team environment.
</li>
<li>
Working knowledge of ISO-9001, cGMP, and/or ICH Q7 in pharma or chemical regulated environments preferred.
</li>
<li>
Knowledge of Process Improvement methodology (ie., Lean Manufacturing, Six Sigma, and/or TOC) a plus.
</li>
<li>
Experience with or ability to master the use of modern research tools such as EasyMax, PolyBlock, Continuous Flow Reactors, and in-situ process monitoring a plus.
</li>
<li>
Strong computer skills in standard &amp; scientific systems, such as Microsoft Word, Excel, PowerPoint, ChemDraw, Reaxys and Scifinder.
</li>
</ul>
Current Benefits at Adesis:
<ul>
<li>
Competitive base salary and annual bonus program
</li>
<li>
Medical/Prescription Drug coverage, Dental, and Vision for employees and family
</li>
<li>
Option between Flexible Spending account (FSAs) or Health Savings Account (HSA) 
</li>
<li>
Group Term Life insurance, short term disability, and long-term disability benefits for employees
</li>
<li>
Employee Stock Purchase Plan (ESPP)
</li>
<li>
401(k) company contribution
</li>
<li>
Annual charitable matching gift
</li>
<li>
Generous Paid Time Off
</li>
</ul>
Annual compensation range: $65k-75k

Process Chemist

<h3>Job Description</h3>
Job DescriptionDIHO Consulting USA is seeking a Geotechnical Engineer on behalf of our client for their Southeast Louisiana Area offices.
The successful candidate will provide engineering and consulting services for a wide variety of projects and clients, primarily in the Energy Market Sector. Our client offers training and support necessary for career advancement, with the objective of developing the candidate into a departmental management role. Their Southeast Louisiana operations are well established in the local market and have an experienced engineering support staff in place.
We are looking for a candidate with excellent communication skills, a strong desire for career advancement, and sound leadership qualities.
Responsibilities
<ul>
<li>Prepare technical proposals.</li>
<li>Execute geotechnical engineering project assignments.</li>
<li>Work with and provide mentorship to engineering support staff.</li>
<li>Manage and coordinate geotechnical field and laboratory assignments.</li>
<li>Perform engineering analyses and prepare reports.</li>
<li>Maintain client expectations for project quality and schedule.</li>
</ul>
Requirements
<ul>
<li>Bachelors Degree in Civil Engineering.</li>
<li>PE License or active EIT Certification.</li>
<li>Excellent written and verbal communication skills.</li>
</ul>
Benefits
This position includes a comprehensive benefits package provided by our client, which includes:
<ul>
<li>Flexible work schedule.</li>
<li>Health, Vision, Dental, Disability, and Life Insurance.</li>
<li>401(k) Retirement Program with up to 4% employer match after eligibility period.</li>
<li>120 hours of Paid Time Off (PTO) annually.</li>
<li>9 company-paid holidays.</li>
</ul>

Geotechnical Engineer

<h3>Job Description</h3>
Job Description
Chemical Operator – Fort Mill, SC
Schedule:
<ul>
<li>Full-Time (40 hours/week)</li>
<li>3rd Shift: 12-hour schedule (2-2-3 rotation)</li>
<li>Hours: 7:00 PM – 7:00 AM</li>
<li>Must be available every other weekend</li>
</ul>
Pay:
<ul>
<li>Starting at&nbsp;$20.00/hour and up, based on experience</li>
</ul>
Benefits:
<ul>
<li>401(k)</li>
<li>Holiday Pay</li>
<li>Medical Insurance</li>
</ul>
About the Company
Join one of America’s leading custom and toll manufacturers of specialty organic chemicals. We produce organic intermediates, polymers, and colorants for customers around the world. We’re growing and looking for a reliable&nbsp;Chemical Operator&nbsp;to join our team!
Job Summary
As a Chemical Operator, you’ll be responsible for:
<ul>
<li>Mixing and blending chemicals</li>
<li>Following batch sheets for daily tasks</li>
<li>Performing general labor duties as needed</li>
</ul>
What We’re Looking For
<ul>
<li>Team-oriented and self-motivated</li>
<li>Willing to learn and accept training</li>
<li>Detail-focused with mechanical/electrical aptitude</li>
<li>Experience as a Chemical Operator is a plus, but not required</li>
</ul>
Requirements
<ul>
<li>Good problem-solving and time management skills</li>
<li>Familiarity with PPE (including respirators)</li>
<li>Ability to read batch sheets and MSDS</li>
<li>Previous experience in chemical manufacturing is a plus</li>
</ul>

<h3>Job Description</h3>
Job Description
Arrowhead Pharmaceuticals, Inc. (Nasdaq: ARWR) is a clinical stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead's RNAi-based therapeutics leverage this natural pathway of gene silencing.
Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.
Arrowhead's corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI &amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI. Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need. 
The Position
The Associate Manufacturing Scientist I (third shift) will involve assisting in the synthesis and subsequent purification steps of large scale oligonucleotides. The operator must comply with GLP/GMP protocols and be able to follow all association SOPs and work instructions when performing and documenting operations.
3rd shift work hours are 10 pm – 8:30 am and includes a 15% shift differential.
Responsibilities
<ul>
<li>Follow batch records, SOPs, and work instructions to detail</li>
<li>Document all operations in batch records and notebooks</li>
<li>Comply with GMP protocols</li>
<li>Assist other chemists within the CMC group during synthesis and chromatography of oligonucleotides including:
<ul>
<li>Reagent solution preparation</li>
<li>Column Packing</li>
<li>Mobile phase preparation</li>
<li>Fraction collection</li>
</ul>
</li>
<li>Operate TFF to desalt purified RNA solutions</li>
<li>Operate a lyophilizer and package solid drug substance</li>
<li>Execute processes as part of a team to ensure production timelines are kept and quality product is produced</li>
<li>Maintain a clean work space</li>
<li>Maintain safety by wearing required personal protective equipment</li>
</ul>
Requirements
<ul>
<li>BS or MS in chemistry, biochemistry, engineering, or related scientific field</li>
<li>Entry level to 3 years experience in a similar position</li>
<li>Good verbal and written communication skills</li>
<li>Ability to work in a team environment</li>
<li>Ability to pay attention to detail</li>
</ul>
Preferred
<ul>
<li>Experience working in a GMP setting with controlled documentation</li>
</ul>
Wisconsin pay range $70,000—$83,000 USD
Arrowhead provides competitive salaries and an excellent benefit package. 
All applicants must have authorization to work in the US for a company. 
California Applicant Privacy Policy

Associate Manufacturing Scientist II (3rd Shift)

<h3>Job Description</h3>
Job Description
Position Summary
We are looking for an Intern for the Economic Competitiveness Division, VEDP’s internal strategy team, during the summer of 2026 (10 weeks). This self-starting individual should be seeking on-the-job experience in economic development, policy development, and strategic analysis. Interns will complete a project and develop a presentation to be shared with staff at the end of the internship. They will be part of an organization-wide cohort, providing networking and professional development opportunities throughout the summer.
Duties:
<ul>
<li>Research policies and evaluate their potential benefit to Virginia’s economic competitiveness by reading, summarizing, and synthesizing relevant literature </li>
<li>Analyze quantitative data and present data analysis in a visually compelling format </li>
<li>Assist in designing and developing reports for economic development stakeholders </li>
<li>Engage with executive staff and key stakeholders on relevant research, including presenting research or updates on key projects </li>
<li>Assist in other project-related tasks as needed </li>
</ul>
Knowledge and Skills Required:
<ul>
<li>Interest in economics, business, public policy, or state government </li>
<li>Excellent planning, organizational, and communication skills</li>
<li>Excellent analytical and problem-solving skills</li>
<li>Effective time management skills</li>
<li>Proficiency with Microsoft Office</li>
<li>Basic to advanced data analysis experience with Excel </li>
<li>Previous research and data experience (preferred but not required) </li>
</ul>
Qualifications Preferred: 
Pursuit of a bachelor’s or graduate degree in social science (economics, public policy, or political science), mathematics, data analytics, business, or related field is preferred. 
This position will be full-time, hybrid – working a minimum of 40 hours per week: 24 hours per week (3 days: typically, Tuesday-Thursday) in our Richmond office and up to 16 hours per week (2 days) from home.
All candidates must apply through our website <a href="https://www.vedp.org/careers" target="_blank">https://www.vedp.org/careers</a>
Internship Period: June 1, 2026 – August 6, 2026 (10 weeks)
Salary: Undergrad Students - $15 per hour, Graduate Students - $17 per hour 
Application Deadline: February 6, 2026

VEDP is an Equal Opportunity Employer. All applicants are considered for employment without regard to race, sex, color, national origin, religion, sexual orientation, gender identity or expression, age, veteran status, political affiliation, genetics, or against otherwise qualified individuals with disabilities. It is VEDP’s intent that its employment and personnel policies and practices conform to all applicable federal, state, and local laws and regulations regarding non-discrimination and affirmative action. Applicants requiring more information or requiring assistance may contact VEDP Human Resources at 1-804-545-5634 or <a href="mailto:vedphr@VEDP.org" target="_blank">vedphr@VEDP.org</a>. TDD 1-800-828-1120.

Economic Competitiveness Intern

<h3>Job Description</h3>
Job Description
WGNSTAR is a dynamic and growing company with a global footprint. Primarily focused on the semiconductor industry, we provide a platform for you to expand your career with knowledge gained on the job training, and tailored development. We know we need talented people like you that hold similar values, which is why we do not put limits on learning, development, industry, and personal growth. Start your path to a WGNSTAR career today!&nbsp;
Schedule: Compressed 12hr Shift – Nightshift Pay Rate: $25 - $29 Hourly DOE&nbsp; Location: Hillsboro, OR Position Type:&nbsp;Full Time Benefits: This position is eligible for WGNSTAR’s full benefits package, including Medical, Dental, Vision, and 401(k). Additional benefits are listed at the end of this posting. &nbsp; Principal Duties and Responsibilities:
<ul>
<li>May operate metrology tools including electron microscopes, Focused Ion Beam and additional lab equipment to complete analytical requests in the client lab</li>
<li>May perform tests and sampling to include setup and operation of metrology equipment&nbsp;</li>
<li>Will utilize client software and equipment to complete tasks, support processes and product tracking&nbsp;</li>
<li>May provide reports and results of sampling and experiments&nbsp;</li>
<li>May perform PM, troubleshooting and minor maintenance of lab equipment&nbsp;</li>
</ul>
Requirements:
<ul>
<li>Excellent communication, lab protocol and time management skills&nbsp;</li>
<li>Must support 12hr compressed work week schedule&nbsp;</li>
<li>Familiarity with semiconductor manufacturing environment, processes and equipment&nbsp;</li>
<li>Direct experience using metrology &nbsp;and/or electron microscopy equipment&nbsp;</li>
<li>A.S or B.S. degree in STEM or related scientific fields&nbsp;</li>
</ul>
Physical Effort/Activities: May be required to walk up to 5+miles per day, able to be on feet for 8-10 hrs at a time, ability to&nbsp;bend, twist, push/pull, crouch, kneel in confined spaces, work at heights, on a ladder, and lift up to 50 pounds. The physical demands described above are representative of those that must be met by an employee to successfully perform the essential functions of this job.
Additional Benefits: Paid Vacation, Select Holidays, Overtime Opportunities, On-site Facilities &amp; Career Development Opportunities.&nbsp;
The people who thrive most at WGNSTAR are those individuals who perform well in a team environment, enjoy interacting and engaging with several different stakeholders, and adapt quickly to changing environments, while leveraging their skills, quality, and knowledge to drive themselves and their teams towards continuous improvement and success.&nbsp;
This job description is intended to convey information essential to understanding the scope of the job and the general nature and level of work performed by job holders within this job. This job description is not intended to be an exhaustive list of qualifications, skills, efforts, duties, responsibilities or working conditions associated with the position.&nbsp;
 This position is not eligible for visa sponsorship. All applicants must be legally authorized to work in the United States without the need for current or future sponsorship (e.g., H-1B, O-1, etc). Additionally, WGNSTAR does not participate in the STEM OPT extension program for this role. Equal opportunities and Social Governance
WGNSTAR is an Equal Opportunity Employer, drug free workplace, and complies with ADA regulations as applicable.
WGNSTAR places an immense emphasis on equal employment, encourages diversity in the workplace, and applies an open-door policy for inclusion of all employees. Our diversity program encourages people from any gender, background, ethnicity, culture, education, and experience to join the company and more importantly build a career through employee development.
Through our Global wellness programs, WGNSTAR ensures our employees and families have access to a full range of wellness services through our Employee Assistance Program (EAP). In the communities that surround our business operations, we support individual and group sponsorships for local sports and those that are vulnerable in society.
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Metrology Technician III - Nightshift Only

<h3>Job Description</h3>
Job Description
RMB ENVIRONMENTAL LABORATORIES
JOB DESCRIPTION
Sample Receiving and Microbiology Analyst
DEPARTMENT: 
Laboratory
EXEMPTION STATUS:
Non-exempt / Hourly
POSITION LOCATION:
Shafer, MN
DATE PREPARED:
December 2025
POSITION STATUS
Full – time MONDAY - FRIDAY 
POSITION SUMMARY
Duties include receipt of client samples, unpacking coolers of containers and logging samples into a Laboratory Information Management System (LIMS). Additional responsibilities include working in the microbiology laboratory to assist with basic water sample testing for coliform bacteria.
DUTIES &amp; RESPONSIBILITIES
<ul>
<li>Ability to follow standard operating procedures, computer data entry with attention to detail and ability to multitask. Must be able to lift 50 pounds.</li>
<li>Environmental sample receipt from clients and work order submittal into Laboratory LIMS system; Evaluation and distribution of daily laboratory work orders to analysts.</li>
<li>Distribution of sampling supplies to clientele and field personnel,</li>
<li>Maintain sample work order productivity by evaluating receiving samples; the samples are selected and grouped by parameter to expedite analysis and minimize turn-around-time. Rush service samples, as well as those with short holding times, are prioritized and analyzed accordingly.</li>
<li>Ensure sample compliance with EPA regulated sample collection, storage, and transportation guidelines; by providing accurate sampling guidance and education to clients; consulting with clients to ensure adherence with field and laboratory quality assurance measures; and providing proper guidance of standard operating procedure and EPA methodologies as applicable to sample receipt operations,</li>
<li>Conflict resolution and troubleshooting by consulting with clientele, assigned project manager, and/or Laboratory Director,</li>
<li>Maintain confidential sample and client information in the Laboratory Information Management System (LIMS),</li>
<li>Provide billing with work orders, as applicable,</li>
<li>Maintain laboratory sample collection supply inventory by checking stock to determine inventory levels and anticipating supply needs.</li>
<li>Maintain professional and technical knowledge by reviewing current EPA and RMB standard operating procedures, requirements, and guidelines, reviewing internal laboratory quality control and assurance procedures, • Maintain safety of the workplace and coordinate with Facilities Manager and Laboratory Director to maintain compliance with laboratory and OSHA requirements,</li>
</ul>
EDUCATION &amp; EXPERIENCE
The type of formal education and type/amount of experience that would typically be needed to successfully perform in the position.
<ul>
<li>Experience in Laboratory setting is welcomed.</li>
</ul>
KNOWLEDGE, SKILLS &amp; ABILITIES
<ul>
<li>Skills – Measurable or observable behavior while performing a cognitive or manual activity, such as skill in word processing.</li>
<li>Ability – Natural (perhaps innate) talents or gained capabilities, such as ability to follow procedures.</li>
<li>Quality control and quality assurance understanding</li>
<li>Safety conscience </li>
<li>Current technology and trends </li>
<li>Express ideas clearly, concisely, and effectively orally and in writing</li>
<li>Exercise appropriate judgment in answering questions and releasing information; analyze and project consequences of decision and/or recommendations.</li>
<li>Communicate effectively with a variety of individuals representing diverse cultures and backgrounds and function calmly in situations which require high degree of sensitivity, tack, and diplomacy.</li>
<li>An ability to plan, organize and prioritize work.</li>
</ul>
WORKING CONDITIONS
<ul>
<li>The environment in which the position functions and the frequency of exposure, such as frequent exposure;</li>
</ul>
Exposure to Sulfuric Acid, Nitric Acid, Potassium Iodide and Starch solution. Employees must follow safety measures. Frequent: walking, standing, bending, and twisting of neck, bending, and twisting of waist, lifting and carrying objects weighing up to 15 pounds, lifting of up to 50 lbs. Occasional: sitting, repetitive use of hands to operate instruments, computers, printers, copiers.
EEO Statement
RMB Environmental Laboratory is an Equal Opportunity Employer and will not discriminate against any applicant for employment on the basis of race, age, religion, sex, veterans, individuals with disabilities, sexual orientation, or gender identity.
Note: Job Descriptions are not exhaustive lists of all skills, responsibilities, or efforts associated with a job. They reflect principal job elements essential for performing the job and evaluating performance. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of the position.
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