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<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
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
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 Summer Intern, Mechanistic Pharmacology - Cellular Trafficking &amp; Assay Development will support discovery research efforts within Arrowhead Pharmaceuticals by contributing to ongoing studies focused on RNAi-based therapeutics. This internship provides hands-on laboratory experience, exposure to experimental design, and opportunities to develop scientific communication skills while working closely with experienced scientists. 
This is an 11-week Summer Internship Program paying $21.00 per hour and requires full-time, onsite work five days per week at the designated location.
Responsibilities
<ul>
<li>Complete onboarding activities including shadowing team members, skill assessments, learning core laboratory techniques, and reviewing foundational scientific background.</li>
<li>Execute one of two predefined research projects within the Mechanistic Pharmacology group.</li>
<li>Perform experiments to interrogate constraints on TRiM platform efficacy using techniques such as
<ul>
<li>mammalian cell culture</li>
<li>dose-response curve generation,</li>
<li>Quantitative PCR (qPCR)</li>
<li>fluorescence-based uptake assessment (microscopy or flow cytometry)</li>
<li>cellular fractionation</li>
<li>western blotting.</li>
</ul>
</li>
<li>Analyze experimental data and maintain a well-organized laboratory notebook in Benchling.</li>
<li>Participate in group discussions, literature review, and hypothesis generation.</li>
<li>Present project updates in weekly group meetings.</li>
<li>Prepare final deliverables, including a scientific poster and a ~20-minute presentation summarizing project objectives, results, and learnings.</li>
</ul>
Requirements:
<ul>
<li>Currently enrolled in a bachelor's degree program at an accredited university or college and majoring in a scientific discipline such as Biochemistry, Biology, Chemistry, or Engineering.</li>
<li>Excellent verbal and written communication skills, including comfort presenting in group settings.</li>
<li>Strong problem-solving and organizational skills.</li>
<li>Proficiency in Microsoft Office applications.</li>
<li>Ability to lift up to 40 lbs.</li>
<li>Willingness and ability to spend 75% of the workday walking the facility and 25% at a desk.</li>
</ul>
Preferred:
<ul>
<li>Fundamental understanding of cell biology and biochemical principles.</li>
<li>Previous laboratory experience and familiarity with basic lab techniques.</li>
<li>Curiosity, enthusiasm for discovery science, and willingness to learn new approaches and techniques.</li>
</ul>
Wisconsin pay range $9,240—$9,240 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

Summer Intern, Mechanistic Pharmacology - Cellular Trafficking & Assay Development

<h3>Job Description</h3>
Job Description
 
$500 Sign-On Bonus

At CHT USA, we foster a supportive workplace with competitive benefits, including medical, vision, dental, and life insurance starting on day 31. Our 401(k) plan allows participation the first of the month after three months of employment, with a 3% company-paid contribution and full vesting from eligibility. We offer opportunities for growth, and we’d love to hear from you!
Are you ready to take your career to the next level? We're looking for a dedicated Chemical Operator to join our team! In this role, you'll operate equipment and semi-automatic systems to transform chemicals into high-quality products. 

Apply Today! 
 
Take advantage of our $500 sign-on bonus and 6% shift premium as you advance your career with us. Your future starts here!

Key Responsibilities:
<ul>
<li>Follow initiatives to enhance quality, cleanliness, safety, and productivity while reducing costs.</li>
<li>Gain expertise in operating equipment through hands-on training.</li>
<li>Collaborate with the QC lab and R&amp;D teams.</li>
<li>Build production batches and maintain accurate batch paperwork.</li>
<li>Load and unload chemicals, operate pumps and filters, and monitor temperatures and run speeds.</li>
<li>Troubleshoot basic equipment issues and submit repair work orders.</li>
<li>Maintain a safe and organized work area, following 6S principles.</li>
<li>Work together with your team to achieve key performance indicators (KPIs) and perform other assigned duties.</li>
</ul>

Qualifications:
<ul>
<li>High school diploma or GED.</li>
<li>1-3 years of related operator experience preferred.</li>
<li>Forklift certification required (or ability to obtain within 90 days).</li>
<li>Ability to lift 50 pounds and work independently on daily tasks.</li>
<li>Familiarity with ERP solutions (e.g., SAP, Sage, Microsoft Dynamics) preferred.</li>
</ul>

Personal Attributes:
<ul>
<li>Strong interpersonal and communication skills.</li>
<li>Effective multitasker with excellent organizational and time-management abilities.</li>
<li>Eager to learn and collaborate with diverse team members.</li>
</ul>

If you're ready to make an impact and grow your career in a dynamic environment, we want to hear from you! Apply today to join our team and take advantage of the $2000 sign-on bonus!

Chemical Operator - 1st Shift

<h3>Job Description</h3>
Job Description

Septerna is a biotechnology company based in South San Francisco, CA on a mission to develop life-changing medicines for patients with the vision to become the industry-leading G protein-coupled receptor (GPCR)-focused drug discovery company. The company's Native Complex Platform™ recapitulates GPCRs with their native structure, function, and dynamics outside of the cellular context. This approach enables novel access to modern structural and screening technologies used in industrial-scale drug discovery for the entire class of GPCRs. Septerna has an emerging pipeline of GPCR-targeted small molecule programs with potential for growth to target many GPCRs that have been undruggable and unexploited to date.
We are excited to expand our multidisciplinary team of individuals focused on creating revolutionary medicines to address the unmet needs of patients. At Septerna we strive to embrace diversity of thought, expertise, and background through collaboration. To join our ambitious team, be prepared to bring your real self to work every day; grow and learn from a talented team of drug hunters, scientists, and business professionals; and contribute your passion, creativity, and energy to accomplish our mission. We share a fearless pursuit of ground-breaking innovations and cultivate an environment where our employees succeed by learning from each other and working as a team.
We are committed to the development of meaningful therapeutics for patients with indications of high unmet need. This is a tremendous opportunity to work with talented individuals on the frontlines of therapeutic discovery and development. You will directly help move therapies through preclinical research, positioning them for success in the clinic. The successful candidate will add their passion, unique talents, and expertise to a dynamic team motivated to discover new disease-modifying therapeutics for patients in a fast-paced environment.
For more information see: <a href="http://www.septerna.com" target="_blank">www.septerna.com</a>.
THE ROLE
The Research Associate will primarily be responsible for the development and conduct of in vivo, ex vivo, as well as in vitro studies to support the advancement of Septerna's small molecule drug discovery pipeline. They will work independently and collaboratively in an inter-disciplinary setting to design and execute experiments in preclinical models to understand in vivo pharmacology, establish PK/PD relationships, and inform the efficacy of Septerna's therapeutic candidates. They will help generate and analyze functional in vitro and in vivo data to determine the therapeutic mechanism of action, and rank candidates for preclinical development. They may also engage in biomarker discovery efforts by utilizing a variety of in vivo and ex vivo models to enable and inform effective therapeutic development.
We are committed to the development of meaningful therapeutics for patients with indications of high unmet need. This is a tremendous opportunity to work with talented individuals on the frontlines of therapeutic discovery and development. You will help move therapies through preclinical development, positioning them for success in the clinic. The successful candidate will add their passion, unique talents, and expertise to a dynamic team on the frontlines of innovative therapeutic development.
The position is based in South San Francisco, CA.
*Title commensurate with experience
Key Responsibilities include but are not limited to: 
<ul>
<li>Design and execute in vivo pharmacology studies to understand therapeutic mechanism in relevant disease models</li>
<li>Generate, analyze, document, and help interpret data to establish functional PK/PD relationships</li>
<li>Work collaboratively with in vivo, in vitro and ex vivo models to determine the mechanism of action of drug candidates. </li>
<li>Will require some weekend work</li>
<li>Be a member of multiple project teams and present results in lab, team and department meetings</li>
<li>Perform in literature searches, read and interpret papers to help design and trouble-shoot in vivo, ex vivo and in vitro experiments</li>
<li>Help in authoring in vivo pharmacology study designs, protocols, and reports to support regulatory filings</li>
<li>Follow all company policies/practices, and maintain accurate records and notebooks</li>
</ul>
REQUIRED EDUCATION, SKILLS &amp; EXPERIENCE 
<ul>
<li>BSc/Masters in Pharmacology, Toxicology, or related biological science</li>
<li>1-3 years direct hands-on experience with in vivo studies or disease models in academia or the biotechnology and pharmaceutical industries</li>
<li>Ability to be hands on and work directly with rodent models for dosing (PO, SC, IP, IV) and blood collection</li>
<li>Experience working with other scientists to analyze, interpret, and present data</li>
<li>Ability to collaborate in writing protocols and trouble-shooting biological experiments</li>
<li>Detail-oriented and organized, with strong interpersonal skills for clear and effective communication – ability to proactively engage and collaboration with colleagues</li>
</ul>
PREFERRED SKILLS &amp; EXPERIENCE
<ul>
<li>Experience working with primary cells or ex vivo models</li>
<li>Experience working with generation of surgical models in rodents (e.g. osmotic minipump implantation or stereotaxic surgery)</li>
<li>Previous work on therapeutic discovery and development programs in the field of endocrine and metabolic diseases</li>
<li>Experience working with vendors and CROs to execute studies, analyze data, and generate reports</li>
<li>ELN experience with Benchling and data analysis with GraphPad Prism</li>
</ul>
The anticipated salary range for candidates who will work in South San Francisco, CA is $70,000 - $85,000. Individual pay may vary based on additional factors, including, and without limitation, job-related skills, experience, work location and relevant education or training. Septerna's compensation package also includes benefits, stock options, and annual target bonus for full-time positions. 
Note to Employment Agencies: Please do not forward any agency resumes. The company will not be responsible for any fees related to resumes that are unsolicited. We are an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. Septerna participates in the E-Verify program. California Consumer Privacy Act Privacy Notice For Job Applicants. If you are a California resident, click here for our CCPA Notice.

Research Associate, In Vivo Pharmacology

<h3>Job Description</h3>
Job Description
Polymer Chemist or Engineer – Advanced Composites &amp; Resin Formulation
????&nbsp;Location: North Houston, TX (On-site, Full-Time)
If you have hands-on&nbsp;manufacturing&nbsp;experience in composites — especially&nbsp;pultrusion&nbsp;or filament winding — and&nbsp;a strong&nbsp;understanding of polymer chemistry or formulation, we want to hear from you.
This is a great opportunity to join a growing technical team that’s working on advanced materials for critical infrastructure. The company is scaling quickly and is positioned for long-term growth in its market. This role will make direct, visible contributions to product innovation, material performance, and the overall success of the organization.
What We’re Looking For
Let’s keep this clear: we’re trying to find someone who has:
<ul>
<li>Strong experience with composites, ideally in&nbsp;filament winding, pultrusion, or RTM</li>
<li>Some&nbsp;polymer&nbsp;chemistry background&nbsp;— ideally hands-on with&nbsp;polyurethanes, thermosets, or resin formulation</li>
<li>The ability to work cross-functionally with R&amp;D, quality, and production teams</li>
<li>Comfort working in a lab setting, testing environment, and production-adjacent spaces</li>
</ul>
This role sits at the intersection of&nbsp;materials science,&nbsp;applied chemistry, and&nbsp;advanced manufacturing. The team is open to candidates who are stronger in one area and developing in the other — so don’t self-select out if you’re missing a box or two.
What You’ll Be Doing
<ul>
<li>Formulating and optimizing&nbsp;polyurethane resin systems&nbsp;for use in composite manufacturing</li>
<li>Supporting composite production processes (e.g.,&nbsp;filament winding,&nbsp;RTM,&nbsp;pultrusion)</li>
<li>Running tests and analyzing data from&nbsp;DSC,&nbsp;FTIR,&nbsp;DMA, chemical titration, etc.</li>
<li>Collaborating with technical, engineering, and production teams to move formulas from lab to line</li>
<li>Evaluating raw materials, documenting experimental results, and contributing to product development cycles</li>
<li>Staying up to date on material trends and sustainability practices — low-carbon sourcing, recycling, etc.</li>
</ul>
Minimum Qualifications
<ul>
<li>Bachelor’s degree in Chemistry, Polymer Science, Chemical Engineering, or a related field</li>
<li>3+ years of relevant experience with&nbsp;composite materials,&nbsp;polyurethanes, or&nbsp;thermoset systems</li>
<li>Familiarity with lab instrumentation and composite testing methods</li>
<li>Ability to manage projects, troubleshoot formulations, and communicate technical findings clearly</li>
</ul>
Bonus if You Have
<ul>
<li>Experience with&nbsp;fire performance,&nbsp;color science, or&nbsp;coatings</li>
<li>Background in scaling formulations from lab to full-scale production</li>
<li>Exposure to aerospace or defense-related composite materials</li>
</ul>
A Few Final Notes
Before applying, please take a moment to review the role and expectations carefully. This is a&nbsp;high-impact, hands-on&nbsp;role with visibility across the organization. If you're experienced in composites, and you have some grounding in polymer formulation — or vice versa — this could be a strong fit.
We know this combination is rare, and the team is open to seeing candidates who are stronger in one area than the other.
If that sounds like you, apply now. We'd love to learn more.

Polymer Chemist

<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 Analytical Chemist I will support the Quality Control laboratory by performing analytical testing of raw materials, in-process samples, intermediates, and finished products. The technician will ensure compliance with ISO-9001 Standards, internal procedures, and client-specific requirements while maintaining accurate documentation and supporting laboratory operations. Essential Duties and Responsibilities Include the following. Other duties may be assigned.
<ul>
<li>
Perform routine analytical testing using techniques such as HPLC, GC, LC-MS, UV-Vis, FTIR, and wet chemistry methods.
</li>
<li>
Execute raw material, in-process, release, and stability testing in accordance with SOPs and regulatory guidelines.
</li>
<li>
Prepare, standardize, and document test solutions and reagent.
</li>
<li>
Calibrate and maintain analytical instruments; promptly report malfunctions.
</li>
<li>
Maintain accurate laboratory records in compliance with Good Documentation Practices (GDP).
</li>
<li>
Identify and correct problems with instruments in QC lab. Identify and communicate problems and solutions related to process, procedure, and materials to Analytical team lead and QC Chemists.
</li>
<li>
Maintain cleanliness and organization of lab by following safety, regulatory, and chemical hygiene plan
</li>
<li>
Perform daily record keeping in electronic lab notebook,
</li>
<li>
Responsible for properly managing the generation and accumulation of hazardous and non-hazardous waste
</li>
<li>
Assist in OOS/OOT investigations and support root cause analysis.
</li>
<li>
Attend and participate in QC Team meetings. Develop team skills.
</li>
<li>
Participate in continuous improvement initiatives to optimize laboratory efficiency and data integrity.
</li>
</ul>

Required Qualifications
<ul>
<li>
Bachelor’s degree in chemistry, Pharmaceutical Sciences, or related field.
</li>
<li>
QC analytical laboratory experience in a pharmaceutical, biotech, or CDMO environment, preferred.
</li>
</ul>

Technical Skills:
<ul>
<li>
Hands-on experience with HPLC, GC, and spectroscopic techniques.
</li>
<li>
Familiarity with cGMP, ICH, and USP/EP guidelines preferred.
</li>
<li>
Strong analytical and problem-solving skills with attention to detail.
</li>
</ul>

Other Skills:
<ul>
<li>
Proficiency in Microsoft Office and laboratory data systems (e.g., Empower, Open Lab CDS, Mass hunter and LIMS) is a plus.
</li>
<li>
Excellent written and verbal communication skills.
</li>
<li>
Strong organizational skills and ability to work both independently and in a team setting.
</li>
</ul>

Current Benefits at UDC:
<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

Analytical Chemist

<h3>Job Description</h3>
Job Description
Duties:
<ul>
<li>Perform environmental monitoring of cleanrooms</li>
<li>Collect water samples to ensure all sample collected per schedule and tested on time</li>
<li>Perform and review microbiological assays such as Gram Stain, Endotoxin, Sterility, Microbial Identification, Growth Promotion, Bioburden and Plate Reading</li>
<li>Perform and review visual inspection of final product</li>
<li>Data entry and trend data as needed and prepare slides for management</li>
<li>Assist in investigations regarding out of specifications (OOS) results, address and manage deviations related to micro procedures</li>
</ul>
 
Qualifications:
<ul>
<li>&nbsp;AA Degree and 1+ years’ experience in Microbiology lab/Environmental Monitoring OR</li>
<li>HS Degree and 2+ years’ experience in Microbiology lab/Environmental Monitoring </li>
<li>Experience in the application of microbiological techniques such as environmental air monitoring, water testing, surface monitoring</li>
<li>Experience in aseptic techniques and clean room operations</li>
<li>Ability to gown for entry into Aseptic core and supporting areas, and lift approximately 25 lbs.</li>
<li>Ability to pass vision exam for visual inspection</li>
<li>Knowledge of GMP, SOPs and quality control processes for commercial manufacturing</li>
</ul>
 
Why Choose R&amp;D Partners?
As an employee, you have access to a comprehensive benefits package including:
<ul>
<li>Medical insurance – PPO, HMO &amp; HSA</li>
<li>Dental &amp; Vision insurance</li>
<li>401k plan</li>
<li>Employee Assistance Program</li>
<li>Long-term disability</li>
<li>Weekly payroll</li>
<li>Expense reimbursement</li>
<li>Online timecard approval</li>
</ul>
&nbsp;
Pay Scale:
$48,000 (Dependent on Experience)
&nbsp;
R&amp;D Partners is a global functional service provider and strategic staffing resource specializing in scientific, clinical research &amp; engineering. We provide job opportunities within major pharmaceutical, biopharmaceutical, biotechnology, and medical device companies.
&nbsp;
R&amp;D Partners is an equal-opportunity employer.
Company DescriptionR&amp;D Partners is a national staffing firm focused in the areas of: Scientific, Clinical Research and Engineering. Our team offers well over 200 years of combined staffing experience providing consulting, direct hire &amp; outsourcing solutions with our west coast offices in San Francisco, Redwood City and San Diego, CA and our east coast offices located in Harrisburg, PA and Tampa, FL. The cornerstone of our success: a knowledgeable and experienced recruiting team. Our life sciences recruiters, clinical research recruiters and engineering recruiters are uniquely specialized. After a detailed assessment of our clients’ needs, we can then identify appropriate candidates utilizing our established network of professionals. R&amp;D Partners takes a proactive approach to recruiting, establishing relationships with experienced passive candidates so when the time is right, we can combine our candidates’ talents with our clients’ opportunities. 
<h3>Company Description</h3>
R&amp;D Partners is a national staffing firm focused in the areas of: Scientific, Clinical Research and Engineering. Our team offers well over 200 years of combined staffing experience providing consulting, direct hire &amp; outsourcing solutions with our west coast offices in San Francisco, Redwood City and San Diego, CA and our east coast offices located in Harrisburg, PA and Tampa, FL.\r\n\r\nThe cornerstone of our success: a knowledgeable and experienced recruiting team.\r\n\r\nOur life sciences recruiters, clinical research recruiters and engineering recruiters are uniquely specialized. After a detailed assessment of our clients’ needs, we can then identify appropriate candidates utilizing our established network of professionals. R&amp;D Partners takes a proactive approach to recruiting, establishing relationships with experienced passive candidates so when the time is right, we can combine our candidates’ talents with our clients’ opportunities.

Quality Control Microbiology Tech

<h3>Job Description</h3>
Job Description
Responsibility/Requirements:
· Perform analysis of plating solutions
· Treat batch tanks
· Assist in trouble shooting issues, as they arise
· Perform ICP, titration and dilutions for chemical analysis, will train
· Perform tank maintenance
· Responsible for accurate data entry into True Chem software, will train
· Operate forklifts
· Focus on 6S practices
· High responsibility to safety issues
· Observes all company policies and procedures
· Maintain high level of performance
· Actively participate in continuous improvement initiatives by identifying and providing suggestions on areas of improvement.
· High school diploma or equivalent
· 1-2 years of lab or chemical experience preferred
· Must be proficient in the use of computers and programs
· Able to lift 55 pounds as a part of daily routine
· Licensed Waste Water Treatment Operator preferred
· Ability to work with and move drums up to 850 lbs using a drum dolly and totes using forklift in tight areas
3rd shift hours: Sunday - Wednesday – 8:00 pm – 6:30 am (4 day, 10 hour shifts)
Training:
The employee will train on 1st shift for approximately 2-3 weeks.
Benefits:
60 days - Insurance Benefits available (Medical, Dental, Vision, &amp; Life)
90 days – 401K/Roth
Vacation and Flex Time
Holiday Pay
Payday every Friday!
&nbsp;
Company DescriptionElectro-Spec is a diversified automated electroplating company that utilizes PLC automation for many of its processes. (i.e. Gold, Silver, Nickel, Tri-M3, Electroless Nickel, and Passivation) We are a dynamic company, well known in the plating industry for the high quality work we have produced in Indiana since 1959. We have a casual, team-oriented work environment; we also provide opportunities for career growth and advancement to employees at all levels at both locations. 
<h3>Company Description</h3>
Electro-Spec is a diversified automated electroplating company that utilizes PLC automation for many of its processes. (i.e. Gold, Silver, Nickel, Tri-M3, Electroless Nickel, and Passivation) We are a dynamic company, well known in the plating industry for the high quality work we have produced in Indiana since 1959. We have a casual, team-oriented work environment; we also provide opportunities for career growth and advancement to employees at all levels at both locations.

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