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city

state

<h3>Job Description</h3>
Job Description
Duties:
<ul>
<li>Operate and monitor chemical processing equipment to ensure optimal performance and safety.</li>
<li>Conduct routine inspections of machinery and equipment to identify any issues or maintenance needs.</li>
<li>All operators are expected to work as a team and use consensus decision making to achieve departmental goals and objectives.</li>
<li>Maintain accurate records of production data, including batch numbers, quantities, and quality control measures.</li>
<li>Collaborate with team members to implement lean manufacturing practices for improved efficiency.</li>
<li>Read and act upon daily area operating instructions. Provide feedback to supervision on operational issues, related to process conditions, improvement ideas, operational instructions, etc.</li>
<li>Provide shift change relief. Conduct hourly (minimal requirement) tours of manufacturing area to ensure good operating condition of all equipment. Identify and resolve mechanical and/or process-related issues.</li>
<li>Check levels, temperatures, pressures etc. Communicate findings to supervision. Collect and analyze process samples. Record results on prescribed schedule.</li>
<li>Work regularly assigned shifts and provide a fair and equitable amount of overtime for co-worker absences, illnesses, vacations, holidays, etc.</li>
<li>Assist in materials handling, including the safe transport of chemicals within the facility.</li>
<li>Adhere to all safety protocols and SOP guidelines to maintain a safe working environment.</li>
<li>Participate in training programs to enhance skills related to machining, fabrication, and forklift operation.</li>
</ul>
Qualifications:
<ul>
<li>High school diploma or equivalent required</li>
<li>Process Technology degree or certification</li>
<li>Ability to read, write, and speak English fluently</li>
<li>2-3 years' experience working with machinery, mechanical, and chemical processes</li>
<li>No fear of heights or confined spaces</li>
<li>Experience with materials handling techniques and safety practices.</li>
<li>Proficient computer skills, the ability to use process control software and enter data</li>
<li>Ability to perform mathematical calculations</li>
<li>Ability to complete Hazmat training</li>
<li>Strong problem-solving skills and the ability to troubleshoot equipment issues effectively.</li>
<li>Commitment to maintaining high standards of safety and quality throughout all operations.</li>
<li>Possess a valid driver's license</li>
<li>Must have clarity of vision at 20 feet or more and at 20 inches or less.</li>
<li>Able to judge distances and space relationships.</li>
<li>Peripheral vision is needed while eyes are fixed.</li>
<li>Eye adjustment is used in doing near point work. Able to identify and distinguish colors.</li>
<li>Express ideas by spoken word, as well as perceive the nature of sounds.</li>
<li>Must be able to speak and hear other plant employees, vendors, customers, etc.</li>
</ul>
Preferred Qualifications:
<ul>
<li>Associate degree in chemistry or related field</li>
<li>Lean manufacturing experience</li>
<li>boiler experience</li>
<li>Certified forklift operator</li>
<li>3-5 years' experience as a process/chemical operator</li>
<li>Pipefitting experience</li>
<li>Experience in instrumentation &amp; industrial electrical components</li>
</ul>
Environmental Conditions:
<ul>
<li>Job duties occur both inside and outside. There is exposure to extreme temperatures, moisture, humidity, and loud noises</li>
<li>Gases, dust, odors, fumes, and mists associated with normal chemical plant operation may be present</li>
<li>In production areas employees must wear company supplied protective equipment such as hard hat, safety glasses, respirator, gloves, slickers, and boots</li>
<li>Must be able to climb stairs, bend, stoop, walk, twist, grasp, pull, push, reach overhead, and lift up to 50 pounds</li>
</ul>
Benefits:
<ul>
<li>401(k)</li>
<li>401(k) matching</li>
<li>Dental insurance</li>
<li>Employee assistance program</li>
<li>Flexible spending account</li>
<li>Health insurance</li>
<li>Health savings account</li>
<li>Life insurance</li>
<li>Paid time off</li>
<li>Parental leave</li>
<li>Safety equipment provided</li>
<li>Vision insurance</li>
</ul>
Join us as we strive for to maintain a safe, efficient, and welcoming environment for all!
 12 hour rotating shifts Overtime as needed Call in as needed

Chemical Operator

<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
Qualis LLC is seeking a Scientist/Engineer II at Wright-Patterson AFB, OH for the TMAS Range Task Order. This position supports the 96th Test Group Aerospace Survivability and Safety Operating Location's (704 TG/OL-AC) Landing Gear Test Facility (704 TG/OL-ACL). Duties for this position include responsibility for Research, Development, Test and Evaluation (RDAT&amp;E) for aircraft and space vehicle flight hardware qualification.

Essential Duties:
<ul>
<li>Evaluates customer test requirements for aircraft landing gear, tires, wheels, brakes, or components;</li>
<li>Prepares test procedures based on established test method or Design of Experiment (DOE) principals;</li>
<li>Oversight and monitoring of testing and assists when needed;</li>
<li>Reviews and analyzes test data and may adjust test program parameters based on actual results;</li>
<li>Provides daily/weekly progress reports, as needed;</li>
<li>Prepares written test reports;</li>
<li>Assists in the preparation of briefings and presentations to government working levels and senior government officials and communicates effectively with both technical and non-technical customers;</li>
<li>Performs test system engineering analysis and participates in determining requirements for upgrades to facility electrical, mechanical, hydraulic, and/or computer equipment</li>
<li>Develop and use plans to execute and track project/program performance.</li>
<li>Advocate, plan, and direct testing at facilities for understanding and qualification of flight hardware.</li>
<li>Develop, apply, assess, and improve rules/tools to predict and compare test results.</li>
<li>Assess technical, financial, and schedule performance using agreed upon metric.</li>
<li>Communicate and comply with all relevant Federal and local safety, security and interpersonal relations policies, regulations, and procedures.</li>
</ul>

Required Qualifications:
<ul>
<li>Bachelor's degree from an accredited engineering school and up to three (3) years related engineering experience, or a master's degree from an accredited engineering school.</li>
<li>Experience specifically in the area of aerospace vehicle equipment design, structural fatigue and dynamometer testing, and quality assurance; specifically aircraft landing gear, tires, wheels, and brakes required. Comparable experience and qualifications will be considered in lieu of the specific experience mentioned. State registration as an Engineer-in-Training or as a Professional Engineer is desirable.</li>
<li>Applicants must be able to communicate effectively in English, both orally and in writing, and must have interpersonal skills allowing them to interact effectively with government officials and contractors.</li>
<li>Experience with Microsoft Office applications, including Word, Excel, and Project; technical editing; and data management is highly preferred. Experience with MATLAB, Solid Works and other engineering tools is desirable.</li>
<li>Must have the ability to pass a NACI (National Background Check with Inquiries)</li>
<li>Must have the ability to travel 5% of the time.</li>
</ul>
 
Benefits
Qualis LLC is committed to hiring and retaining a diverse and talented workforce who can contribute to the mission and vision of the Company. Our employees are our greatest asset and we promote a positive work environment, teamwork, professional growth, innovation, community involvement, flexible scheduling and a family-friendly work environment.
Equal Opportunity Employer/M/F/Vet/Disabled and a Participant in E-Verify

Scientist/Engineer II

<h3>Job Description</h3>
Job Description
The European Institute of Policy Research and Human Rights is a prestigious institution that offers cutting-edge online programs designed to educate future leaders in policy research, human rights, and related disciplines. Our mission is to deliver world-class skill enhancing programs to candidates globally, equipping them with the knowledge and skills to influence policy and drive positive change in their communities.
Applications are invited for Senior Research Fellowship (for candidates enrolled / passed Masters / Doctoral in any discipline).
Program Overview
<ul>
<li>Learn and follow our methodology to draft research paper in one of the researchable areas. (No prior experience in research paper writing is required, Candidates will receive comprehensive mentorship and guidance throughout the process / tenure.) Program Certification fee of Eur498 is applicable. As a Certified Senior Research Fellow is a significant achievement a valuable addition to your CV that can impress future employers, universities, or scholarship committees. It helps set you apart with a unique edge.</li>
</ul>
What You'll Do:
<ul>
<li>Learn and Lead Groundbreaking Research: Know how to Tackle important policy issues and devise groundbreaking solutions.</li>
<li>Collaborate with Experts</li>
<li>Strategic Analysis: Utilize data to create influential policy recommendations.</li>
<li>Publish &amp; Impact: Contribute your findings to esteemed academic and policy publications.</li>
</ul>
Candidate will be choosing one of the researchable research areas for their research.
Research papers produced by candidates will be published with a Digital Object Identifier (DOI), ensuring the work is uniquely identifiable and accessible through our open-source publication portal.
Eligibility Criteria / Who Can Apply:
<ul>
<li>Open to candidates who are currently enrolled in or have completed a Masters or Doctoral program. Candidates enrolled or passed Bachelor degree but not enrolled in Masters are not eligible to apply.</li>
<li>Applicants from all academic disciplines are welcome, including but not limited to Law, Human Rights, International Relations, Management, Political Science, Social Sciences, Engineering, Medicine, Business, and related fields.</li>
<li>Working / non working professionals in any sector are encouraged to apply. This includes lecturers, professors, advocates, medical professionals, journalists, engineers, historians, managers, environmental scientists, government officials, social activists, and those involved in politics or any relevant field.</li>
<li>Candidates must demonstrate the ability to work independently in a virtual environment and effectively meet deadlines.</li>
</ul>
How to Apply
Interested candidates should submit their updated CV.
Shortlisted candidates will be contacted with complete details.
Note: Applicants are advised to submit only one application. Multiple applications for different positions or locations may result in the cancellation of all submitted applications.

(SRFP)-Research Fellow-Senior (Code:EU7255)

<h3>Job Description</h3>
Job DescriptionPoultry Science Technician Pay Range: $65,000 - $90,000/Year Who is Nova-Tech Engineering? Headquartered in Willmar, MN, Nova-Tech Engineering is a growing, dynamic company founded in 1992 that began as one person’s passion to benefit the agricultural industry.&nbsp; Through innovative process automation technology, the company engineers and manufactures products that serve over 500 commercial poultry hatcheries in over 65 countries worldwide.&nbsp; Nova-Tech houses every aspect of its business on the MinnWest Technology Campus, including a manufacturing facility located just steps away from our engineering and drafting teams. Walking from building to building, you can observe our whole process, from concept to final product. What we’re looking for:
<ul>
<li>Gain perspective from U.S.-based veterinarians on Nova-Tech Poultry processes and future opportunities.</li>
<li>Assess treatments and processes to promote “best for the bird.”</li>
<li>Provide training to internal team members and customers on best practices for poultry health and welfare.</li>
<li>Support regional business managers and account managers through technical expertise and collaborative problem-solving.</li>
<li>Assist research and development teams with projects and testing as needed.</li>
<li>Develop and maintain a global network to collaborate with industry professionals and identify emerging challenges and opportunities.</li>
<li>Travel regularly to hatcheries and farms domestically and occasionally internationally to collaborate and understand market challenges.</li>
<li>Attend industry seminars and tradeshows regularly; represent Nova-Tech and present to large groups as needed.</li>
<li>Create detailed reports summarizing findings for internal and customer leadership.</li>
<li>Work with Nova-Tech Poultry leadership to identify solutions and innovations while supporting Nova-Tech Engineering’s mission, vision, and values.</li>
</ul>
 What you’ll do: The Poultry Science Technician will collaborate with veterinarians, hatcheries, farms, and internal teams to assess poultry treatments and processes, promote bird welfare, and identify opportunities for innovation. This position will support Regional Business Managers and Account Managers by evaluating treatments and training team members and customers on best practices. Additionally, the Poultry Science Technician will assist research and development teams as needed, develop a global network to identify market challenges, and represent Nova-Tech at industry seminars and tradeshows. The ideal candidate will be comfortable presenting to large groups and building relationships across the poultry industry. Other key areas include:
<ul>
<li>Bachelor’s degree in Poultry Science, Animal Science, or related field (Master’s Degree preferred) with 3+ years of relevant experience.</li>
<li>Knowledge of Nova-Tech Poultry products preferred.</li>
<li>In-depth knowledge of the poultry industry domestically and globally, including bird testing, observation, and data-driven decision making.</li>
<li>Proven leadership, communication, and interpersonal skills with the ability to influence, train, and provide constructive feedback.</li>
<li>Excellent problem-solving, analytical, and technical skills with a collaborative, team-oriented mindset.</li>
<li>Comfortable presenting to large audiences at seminars, trade shows, and customer meetings.</li>
<li>Ability to work effectively across cultures and build strong relationships with customers and partners globally.</li>
<li>Commitment to fostering a culture of stewardship with our customers and partners.</li>
<li>Self-starter with the ability to prioritize, handle multiple demands, and maintain attention to detail in a deadline-oriented environment. </li>
<li>Microsoft Office proficiency, with CRM and project management tools experience preferred. </li>
<li>Ability to travel domestically and internationally; valid driver’s license and passport required.</li>
</ul>
 Our location: In 2005, Nova-Tech partnered with Life-Science Innovations to buy a 37-building, 110-acre historic hospital facility in Willmar from the State of Minnesota. &nbsp;Since that time, we have developed the resulting MinnWest Technology Campus into the largest privately owned technology park in the country.&nbsp;Willmar, MN is a bustling community located less than two hours from Minneapolis and one hour from St. Cloud known for its lakes and vibrant entertainment. Things to check out: Willmar Stingers, Willmar WarHawks, Little Crow Ski Team, Green Lake and boat cruises, Glacial Lakes State Trail, Dorothy A. Olson Aquatic Center, The Barn Theatre, Sibley State Park, Robbins Island, Destination Playground, YMCA, Ridgewater College, area golf courses and simulators, local breweries, restaurants, and shopping. Why join our team? Nova-Tech Engineering offers a flexible, collaborative, and productive work environment focusing on culture and strengths.&nbsp; We’ve worked hard to create our unique culture and seek team members who match our core values so we can continue to create revolutionary solutions that advance our customers’ ability to feed the world. The MinnWest Technology Campus offers a wide array of on-site amenities including a cafeteria, pool, fitness center, gymnasium, meeting spaces, daycare center, and more!&nbsp;We offer competitive wages with generous paid time off and benefits starting day one!&nbsp;Learn more at&nbsp;<a href="http://www.nteglobal.com.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&amp;nbsp" target="_blank">www.nteglobal.com.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&amp;nbsp</a>; To Apply or Further Inquire Contact: Rachel Weiss | Talent Acquisition <a href="mailto:Rachel.Weiss@nteglobal.com" target="_blank">Rachel.Weiss@nteglobal.com</a> (320) 222-9790 &nbsp;
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Poultry Science Technician

<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
This position 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.
Responsibilities
<ul>
<li>Follow batch records, SOPs, and work instructions to detail</li>
<li>Document all operations in batch records and logbooks</li>
<li>Comply with GMP protocols</li>
<li>Operate large scale oligonucleotide manufacturing equipment (i.e. oligonucleotide synthesizer, purification skid, tangential flow filtration system, lyophilizer, ChemGlass reactors, pH/conductivity meters, peristaltic pumps, etc.)</li>
<li>Assist other chemists within the Manufacturing group during synthesis and purification of oligonucleotides including:
<ul>
<li>Reagent solution preparation</li>
<li>Mobile phase preparation</li>
<li>Column Packing</li>
<li>Fraction collection</li>
</ul>
</li>
<li>Perform oligonucleotide/intermediate analysis via LCMS</li>
<li>Communicate with cross-functional groups such as Process Development, Analytical Development, Quality Control, Quality Assurance, etc.</li>
<li>Maintain a clean work space</li>
<li>Maintain safety by wearing required personal protective equipment</li>
<li>Track and update raw material usage in D365 ERP software</li>
<li>Act as production campaign lead</li>
<li>Assist with new personnel training</li>
</ul>
Requirements:
<ul>
<li>Bachelor's degree in a scientific field OR appropriate work experience</li>
<li>Entry level to 2 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 and controlled documentation</li>
</ul>
Wisconsin pay range $63,000—$73,000 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 I

<h3>Job Description</h3>
Job DescriptionChemical Operator
BestLogic Staffing is recruiting for a Chemical Operator.
Shift Hours:11 pm - 7 am 
Position Summary The Chemical Operator is responsible for the safe operation of equipment in a manufacturing facility, material handling, quality control, accurate recordkeeping, and maintaining housekeeping standards while following company policies and safety procedures.
Essential Functions
<ul>
<li>Operate and monitor plant systems (feeds, temperatures, pressures)</li>
<li>Follow procedures and instructions from Leads and Managers.</li>
<li>Sample, test, and record process streams per quality requirements.</li>
<li>Accurately weigh and add raw materials; monitor inventory.</li>
<li>Load finished products into bulk tankers, totes, and drums.</li>
<li>
Assist with maintenance preparations.
</li>
<li>
Maintain housekeeping and Good Manufacturing Practices.
</li>
<li>Support compliance with OSHA, EPA, PSM, and safety policies.</li>
<li>
Input data into ERP system and complete logs/forms.
</li>
<li>
Provide improvement suggestions to management.
</li>
<li>
Participate in EHS and training programs.
</li>
<li>
Must be willing to work overtime, nights, and weekends.
</li>
<li>
Other duties as assigned.
</li>
</ul>
Skills &amp; Qualifications
<ul>
<li>High school diploma required; community college certificate preferred.</li>
<li>0-5 years of chemical or manufacturing experience (certificate in Chemical Plant Technician training may substitute).</li>
<li>
Basic Microsoft Office 365 skills.
</li>
<li>Knowledge of hazardous materials handling, OSHA/EPA compliance, and emergency response training.</li>
<li>
Strong mechanical aptitude and troubleshooting skills.
</li>
<li>Ability to work effectively in teams and interact with all plant levels.</li>
<li>
Full professional English proficiency (written &amp; verbal).
</li>
<li>
Flexible schedule availability.
</li>
</ul>
About BestLogic Staffing
BestLogic Staffing is a top staffing firm partnering with some of the largest names in various industries. Our professional recruitment teams place talented individuals at client locations worldwide, providing hundreds of exciting career opportunities!
To learn more about our process or speak with a recruiter directly, call 1-866-585-8055.
BestLogic Staffing is an equal-opportunity employer.

Chemical Operator (3rd shift)

<h3>Job Description</h3>
Job DescriptionSalary: $100,000 - $115,000K/year 
If youre a Senior Research Associate or Associate Scientist with handson antibody discovery experience and a drive to advance new therapeutics, wed love to hear from you!
 
 
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
The Antibody Discovery Research Associate will support early-stage therapeutic and tool antibody programs by performing experiments that contribute to antibody generation using single B cell platforms, screening, and lead candidate selection.
 
The ideal candidate is highly organized, detail-oriented, and comfortable working in a fast-paced, collaborative research environment.
 
Key Responsibilities
<ul>
<li>Perform hands on antibody discovery work flows including cell culture, multi colour flow cytometry to sort and analyse rare immune cell populations.</li>
<li>Develop, optimize and perform screening cell-based functional assays.</li>
<li>Characterize antibodies by performing Elisa, SPR, BLI (Octet), Western blot.</li>
<li>Maintenance of cell lines, freezing, thawing, expansion.</li>
<li>Perform molecular biology tasks like PCR, cloning, transfection, sequence analysis, RNA/DNA purification methods, gel extraction as needed.</li>
<li>Ensure all experimental work complies with established protocols and SOPs.</li>
<li>Maintain accurate and detailed experimental records and record all experimental data into Electronic Notebook.</li>
<li>Contribute to troubleshooting, optimization, and continuous improvement of discovery workflows</li>
<li>Compiling and analysing data by FlowJo, GraphPad Prism, and Excel.</li>
<li>Conduct analysis and effectively communicate results and present data at internal meetings.</li>
<li>Collaborate with cross functional teams to align with project goals.</li>
<li>Committed to fostering an inclusive, collaborative, and innovative research environment.</li>
</ul>

Please note the roles and responsibilities for the position include but are not limited to the above.
 
Knowledge, Experience &amp; Skills
Required
<ul>
<li>BS. or M.S. in Molecular Biology, Immunology, Bioengineering, Biochemistry, or related field with 5+&gt; years of experience working in a lab setting (industry experience preferred).</li>
<li>Experience with antibody discovery platforms including single B cell, hybridoma, or display technologies.</li>
<li>Proficiency in mammalian cell culture, in vitro assay development and flow cytometry.</li>
<li>Strong organizational skills, attention to detail and ability to work independently and collaboratively.</li>
<li>The ability to be a team player and collaborate with colleagues is critical.</li>
</ul>

Preferred
<ul>
<li>Strong understanding of B cell biology.</li>
<li>Experience working with antibody sequences, including CDR identification and diversity analysis</li>
<li>Hands-on experience with multi-color flow cytometry including panel design, staining, compensation, and data analysis/interpretation</li>
<li>Hands on experience with BLI or SPR.</li>
<li>Assay development and characterising antibodies using cell-based assays and flow cytometry.</li>
<li>Comfortable working with high-throughput screening tools or automation.</li>
<li>Experience with cell engineering technologies, such as transfection, electroporation, lentiviral transduction, and CRISPR.</li>
<li>Experience with high-throughput antibody expression &amp; purification.</li>
<li>Experience with cytotoxicity assays using T cell engagers</li>
<li>Innovative, detail-oriented, and quality-driven with a proactive mindset.</li>
<li>Exceptional communication and interpersonal skills; able to translate complex data for diverse audiences.</li>
<li>Highly motivated self-starter with scientific curiosity and a roll-up-your-sleeves attitude.</li>
<li>Flexible and eager to learn new methods and optimize workflows.</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 asfriendly, 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.

Senior RA/Associate Scientist

<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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