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city

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<h3>Job Description</h3>
Job DescriptionJob Title: Chemist - Architectural PaintJob Description
Join our dynamic team as a Chemist in the Architectural Paint division, where you will be instrumental in testing and developing new paint materials. Your role will involve mixing chemicals and additives to create innovative architectural paint, ensuring that quality standards are met and environmental impacts are considered.
Responsibilities
<ul>
<li>Test new architectural paint materials within a laboratory setting.</li>
<li>Mix chemicals and additives to create architectural paint, ensuring quality standards and environmental considerations are met.</li>
<li>Select appropriate resins, pigments, additives, and solvents to achieve desired paint properties such as adhesion, durability, color, and gloss.</li>
<li>Conduct laboratory testing including viscosity, draw downs on different substrates, stain resistance, and application testing.</li>
<li>Provide technical support for key innovation projects and customer services.</li>
<li>Ensure lab safety by following general safety procedures.</li>
<li>Perform hands-on work in the lab to deliver reliable results.</li>
<li>Collaborate with scientists and technicians to plan and execute technical lab work.</li>
</ul>
Essential Skills
<ul>
<li>Proficiency in chemistry, particularly in paint and coating.</li>
<li>Knowledge of polymer chemistry.</li>
<li>Experience with viscosity, application testing, draw down, and stain resistance.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Diploma with 5+ years of hands-on paint/coating lab experience.</li>
<li>Associates degree with 2+ years of hands-on paint/coating lab experience.</li>
<li>Bachelor's degree with co-op or industrial internship preferred.</li>
<li>Experience in making paint or coatings, with a preference for architectural paint.</li>
<li>Experience conducting lab testing such as viscosity and application testing.</li>
<li>Knowledge of rheology and viscosity.</li>
</ul>
Work Environment
Work within the Applications Lab, a specialized environment that fosters innovation and technical excellence. You will be part of a team that is committed to developing cutting-edge solutions in architectural paint, with access to expert training and tutoring.
Job Type &amp; Location
This is a Contract to Hire position based out of Wilmington, DE.
Pay and Benefits
The pay range for this position is $26.00 - $32.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Wilmington,DE.
Application Deadline
This position is anticipated to close on Jan 23, 2026.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

Paint Chemist

<h3>Job Description</h3>
Job DescriptionAerotek is Hiring Cleanroom Technicians
📍 Allentown, PA
&amp;#x1F4B0; Pay: $22–$28/hr (based on experience) + 15% Night Shift Differential
⏱ Shifts:
<ul>
<li>Day Shift: 6:00 AM – 6:00 PM</li>
<li>Night Shift: 6:00 PM – 6:00 AM</li>
</ul>
Why You’ll Love This Opportunity
<ul>
<li>Great Pay + Built‑In Overtime with 12‑hour shifts</li>
<li>Choose the Shift That Fits Your Schedule – day or night</li>
<li>Clean, Modern Facility – full cleanroom gear provided</li>
<li>Convenient On‑Site Amenities including cafeteria and breakroom</li>
<li>Real Career Growth in a fast‑expanding semiconductor industry</li>
</ul>
What You’ll Do
<ul>
<li>Operate advanced equipment used in semiconductor processing</li>
<li>Perform photolithography, etching, substrate cleaning, and related tasks</li>
<li>Set up and maintain manual and computer‑controlled machinery</li>
<li>Work as part of a team to process wafers and optical components</li>
<li>Monitor quality and make adjustments as needed</li>
<li>Maintain a clean, safe, and organized workspace</li>
</ul>
What We’re Looking For
<ul>
<li>High school diploma or GED</li>
<li>Basic Microsoft Excel &amp; Word skills</li>
<li>Ability to stand for long periods and lift up to 20 lbs</li>
<li>Strong manual dexterity; comfortable using microscopes</li>
<li>Reliable, motivated, and eager to learn new technical skills</li>
</ul>
Ready to Step Into a High‑Tech Career?
<ul>
<li>If you’re looking for stable work, long‑term growth, and a clean, modern environment—this is the place to start.</li>
</ul>
Job Type &amp; Location
This is a Contract to Hire position based out of Breinigsville, PA.
Pay and Benefits
The pay range for this position is $22.50 - $30.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Breinigsville,PA.
Application Deadline
This position is anticipated to close on Jan 23, 2026.

About Aerotek:
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meets their goals, skills and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role solving for companies’ construction, manufacturing and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are everything spirit to the test as your career continues to grow.
Aerotek offers weekly pay, employee benefits including medical, dental &amp; vision, life insurance, health advocacy and employee assistance programs, a 401(k) plan, and employee discounts.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
Company DescriptionWe know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow. 
<h3>Company Description</h3>
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow.

Cleanroom Technician

<h3>Job Description</h3>
Job DescriptionCompany Description 
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;<a href="http://www.abbvie.com" target="_blank">www.abbvie.com</a>. Follow @abbvie on&nbsp;X,&nbsp;Facebook,&nbsp;Instagram,&nbsp;YouTube,&nbsp;LinkedIn&nbsp;and&nbsp;Tik Tok.
Job Description 
Purpose:
Leads cross-functional collaborations on identifying and developing consumer eyecare products (artificial tears, gels and ointments). Leads the direction, planning, and interpretation of clinical trials or research activities within consumer eye care innovation of one or more programs. Participates in and may lead cross-functional teams to generate, deliver, and disseminate high-quality data supporting consumer eye care product scientific and business strategy.
Responsibilities:
•Serves as an in-house expert in identification and development of consumer eye care products. As required by program needs, in partnership with Discovery, Translational, and CMC colleagues contribute to design and implement translational strategies. May participate in or lead clinical development contributions to due diligence or other business development activity.
• Serves as a champion for innovation in consumer eye care. Actively solicits opinion leader interactions related to the disease area(s); partners with Medical Affairs, Commercial and other functions in these activities as required, consistent with corporate policies, to ensure that broad cross-functional perspectives are incorporated into Clinical Development Plans and protocols as appropriate.
•Leads and demonstrates ownership of the design and implementation of multiple clinical development programs (or one large, complex program) in support of the overall product development plan, based on strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie’s customers, markets, business operations and emerging issues. Oversees project-related education of investigators, study site personnel and AbbVie study staff.
•May have responsibility for leading clinical study teams, monitoring overall study integrity and review, interpretation and communication of accumulating data pertaining to safety and efficacy of the molecule. Along with Clinical Operations, is responsible for ensuring agreed-upon study enrollment and overall timelines for key deliverables.
•Primary responsibility for and ownership of design, analysis, interpretation and reporting of scientific content of protocols, Investigator Brochures, Clinical Study reports, regulatory submissions and responses and other program documents.
•May oversee the work of Medical and/or Scientific Directors and of Clinical Scientists working on the same or related programs.
•May serve on or co-chair Integrated Evidence Strategy Team(s), with responsibility for development of a rigorous, cross-functionally-aligned, vetted Clinical Development Plan with full consideration of contingencies and alternative approaches. In the role of Co- Chair, responsibilities may include supervision of matrix team members; serving as Clinical Research representative to lend clinical development or medical expertise to Asset Development Teams (ADTs).
•Stays abreast of professional information and technology through conferences, medical literature and other available training, to augment expertise in the therapeutic area. May represent AbbVie at key external meetings.
•Responsible for understanding the regulatory requirements related to the clinical studies and global drug development and accountable for complying with those requirements. Serves as a clinical representative for key regulatory discussions.
•Ensures adherence to Good Clinical Practices, pharmacovigilance standards, standard operating procedures and to all other quality standards in conducting research.
Qualifications 
•Bachelors degree in the sciences; advanced degree (e.g., MS, PhD, OD, MD, PharmD) preferred.
•At least 8 years of product development experience with 5 years of experience in consumer eye care in the pharmaceutical industry, academia, or equivalent.
•Direct experience in leading cross-functional and translational development preferred.
•Ability to run a complex clinical research program independently.
•Proven leadership skills and ability to bring out the best in others on a cross-functional global team. Must be able to lead through influence.
•Ability to interact externally and internally to support a global scientific and business strategy.
•Extensive knowledge of clinical trial methodology, regulatory and compliance requirements governing clinical trials and experience in development of clinical strategy and the design of study protocols.
•Must possess excellent oral and written English communication skills.
•Ability to exercise judgment and address complex problems and create solutions for one or more projects.
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or&nbsp;local law:&nbsp;​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company&nbsp;believes in&nbsp;good faith it will pay for this role at the time&nbsp;of this posting based on the job grade for this position.&nbsp;Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and&nbsp;we&nbsp;may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the&nbsp;future. ​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),&nbsp;medical/dental/vision&nbsp;insurance and 401(k) to eligible&nbsp;employees.​
</li>
<li>
This job is eligible to participate in our short-term incentive&nbsp;programs.&nbsp;​
</li>
<li>
This job is eligible to participate in our long-term incentive&nbsp;programs​
</li>
</ul>
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and&nbsp;determinable.&nbsp;The amount and availability of any bonus,&nbsp;commission, incentive, benefits, or any other form of&nbsp;compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and&nbsp;absolute&nbsp;discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with&nbsp;applicable law.&nbsp;
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" target="_blank">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.ht…</a>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
<a href="https://www.abbvie.com/join-us/reasonable-accommodations.html" target="_blank">https://www.abbvie.com/join-us/reasonable-accommodations.html</a>

Senior Scientific Director, Clinical Development - Consumer Eye Care Product Development

<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
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
Our client, leading leader in biotechnology and diagnostics, is looking for Chemist/Scientist based out of Indianapolis, IN. If you are interested in discussing further, please review the details below. 
 
Duration: Long term contract (Possibility of further extension) 
Pay Rate: $45/hr on W2 DOE 
 
Job Summary: 
Executes all pre-clinical scientific research and/or development strategies in research and development. Investigates the feasibility of applying a wide variety of scientific principles and concepts to potential inventions, products and problems. Plans and executes laboratory research. Maintains broad knowledge of state-of-the-art principles and theories. The Opportunity:
As a Scientist, you will provide testing support for product and process research and development (including design, development, analysis, troubleshooting, etc). You will apply sound experimental design, perform complex scientific research to support research and development of product formulations and/or analytical methods. Possess an in-depth knowledge and experience in the field of analytical chemistry, electrochemistry, biosensors, in-vitro diagnostics, and/or biomedical engineering. Your duties will be dynamic and complex often involving research, analysis, and solution development. 
Qualifications: 
· Applies deep and intensive knowledge of scientific principles. 
· Performs laboratory based studies and experimentation to generate data relevant to various product development projects specifically, the Diabetes Care portfolio. 
· Test and assess innovative technologies as part of our Research and Early Development Scouting efforts.
· Bachelor’s degree in Chemistry, Biochemistry, or a related Life Sciences field with 5 years of relevant experience or Master of Science/PhD with 2 years of relevant experience
· 2+ years of experience in, biomedical or analytical chemistry 
· 2+ years of experience in the field of biosensors 
 
Preferred: 
· More than 5 years of progressive work experience in an appropriate scientific field. 
· Previous Lab based role / safety focused role 
 
If interested, please send your updated resume at <a href="mailto:hr@dawarconsulting.com" target="_blank">hr@dawarconsulting.com</a>/<a href="mailto:akansha@dawarconsulting.com" target="_blank">akansha@dawarconsulting.com</a>

Chemist/Scientist

<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>
</ul>
<ul>
<li>Prepares test procedures based on established test method or Design of Experiment (DOE) principals;</li>
</ul>
<ul>
<li>Oversight and monitoring of testing and assists when needed;</li>
</ul>
<ul>
<li>Reviews and analyzes test data and may adjust test program parameters based on actual results;</li>
</ul>
<ul>
<li>Provides daily/weekly progress reports, as needed;</li>
</ul>
<ul>
<li>Prepares written test reports;</li>
</ul>
<ul>
<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>
</ul>
<ul>
<li>Performs test system engineering analysis and participates in determining requirements for upgrades to facility electrical, mechanical, hydraulic, and/or computer equipment</li>
</ul>
<ul>
<li>Develop and use plans to execute and track project/program performance.</li>
</ul>
<ul>
<li>Advocate, plan, and direct testing at facilities for understanding and qualification of flight hardware.</li>
</ul>
<ul>
<li>Develop, apply, assess, and improve rules/tools to predict and compare test results.</li>
</ul>
<ul>
<li>Assess technical, financial, and schedule performance using agreed upon metric.</li>
</ul>
<ul>
<li>Communicate and comply with all relevant Federal and local safety, security and interpersonal relations policies, regulations, and procedures.</li>
</ul>
Requirements
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>
</ul>
<ul>
<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>
</ul>
<ul>
<li>Applicants must have interpersonal skills allowing them to interact effectively with government officials and contractors.</li>
</ul>
<ul>
<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>
</ul>
<ul>
<li>Must have the ability to pass a NACI (National Background Check with Inquiries)</li>
</ul>
<ul>
<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
POSITION SUMMARY:
The Senior Design Transfer Scientist will be responsible for facilitating the transition of products from Development to Operations. The Sr. Scientist will plan, execute, implement, and document all design transfer activities for an IVD/PMA assay under design control, for next generation sequencing (NGS) assays. The successful candidate will work within the R&amp;D and collaborate cross-functionally with members of operations, bio-development, bioinformatics, quality, regulatory affairs, and clinical affairs.
The Sr. Scientist is expected to divide time between working in the lab and at the desk and providing training and guidance to junior team members in their creation of design transfer documentation and execution of NGS experiments to support in vitro diagnostic (IVD) design transfer. The candidate will maintain a broad knowledge of state-of-the-art principles and theories. This role will also support regulatory IVD and PMA submissions from a design transfer perspective. The ideal candidate will be an enthusiastic, flexible team member who learns quickly, enjoys multi-tasking and most importantly, has an interest in our company and our products. 
PRIMARY RESPONSIBILITIES:
<ul>
<li>Conduct risk assessments (FMEA) to identify gaps in the process and come up with a strategy to make it compliant with IVD standards</li>
<li>Design and develop manufacturing, QC and commercial operations processes</li>
<li>Plan and execute laboratory research in relation to manufacturing scale up and improving process capability</li>
<li>Assure experimental quality through sound experimental design; utilizes DOE, Cpk analysis, Gage R&amp;R and assists in the design of experiments for others</li>
<li>Plan and conduct stability studies with assistance from junior team members</li>
<li>Lead cross functional efforts in establishing supply chain for raw materials and consumables and propose improvements</li>
<li>Attend core team meetings, serve as a voice of operations and liaison between R&amp;D and Operations</li>
<li>Lead test method developments and characterizations</li>
<li>Conduct studies to generate specifications</li>
<li>Set process and test method specifications based on statistical analysis</li>
<li>Lead test method validations and process validations</li>
<li>Set up product structures (BOMs), write SOPs, manufacturing and QC documents etc</li>
<li>Write various protocols and reports</li>
<li>Significant role in PMA submission, audit prep and qualification of suppliers and manufacturing processes</li>
<li>Present status update, data and proposals in various forums to technical and non-technical audiences</li>
<li>Lead junior members of the team</li>
</ul>
QUALIFICATIONS: 
<ul>
<li>Bachelor's degree plus 10 years of relevant experience OR a Master's degree with 7 years of experience OR PhD with 4 years of experience required</li>
<li>Strong scientific background in molecular and cell biology, Biotechnology, or Biochemistry</li>
</ul>
KNOWLEDGE, SKILLS, AND ABILITIES:
<ul>
<li>Extensive knowledge of design control</li>
<li>Experience working to policies; procedures and international quality standards or in a highly regulated industry</li>
<li>Knowledge of quality and regulatory standards and requirements (ISO, CLSI, FDA) is a must</li>
<li>Ability to follow and establish SOPs and in-depth knowledge of GLP/GMP guidelines</li>
<li>Experience authoring study plans, protocols and study reports is highly desired.</li>
<li>Adept with Excel and basic statistical analysis</li>
<li>Hands-on experience with statistical tools such as Minitab or JMP</li>
<li>Supervise junior scientists and team members in their experimental execution and technical documentation</li>
<li>Experience with nucleic acid technologies relating to NGS, PCR, qPCR and multiplex PCR</li>
<li>Hands-on experience with NGS and DNA/RNA molecular biology is preferred</li>
<li>IVD product development experience is a plus</li>
<li>Very strong analytical and problem-solving skills</li>
<li>Strong interpersonal and communication skills</li>
</ul>

Compensation &amp; Total Rewards 
This range reflects a good-faith estimate of the base pay we reasonably expect to offer at the time of hire. Final compensation will vary based on experience, qualifications, and internal equity considerations.
This position is also eligible for additional compensation and benefits through Natera's robust Total Rewards program, including:
<ul>
<li>
Annual performance incentive bonus
</li>
<li>
Long-term equity awards
</li>
<li>
Comprehensive health benefits (medical, dental, vision)
</li>
<li>
401(k) with company match
</li>
<li>
Generous paid time off and company holidays
</li>
<li>
Additional wellness and work-life benefits
</li>
</ul>

Compensation Range $122,100—$152,700 USD
OUR OPPORTUNITY
Natera™ is a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women's health, and organ health. Our aim is to make personalized genetic testing and diagnostics part of the standard of care to protect health and enable earlier and more targeted interventions that lead to longer, healthier lives.
The Natera team consists of highly dedicated statisticians, geneticists, doctors, laboratory scientists, business professionals, software engineers and many other professionals from world-class institutions, who care deeply for our work and each other. When you join Natera, you'll work hard and grow quickly. Working alongside the elite of the industry, you'll be stretched and challenged, and take pride in being part of a company that is changing the landscape of genetic disease management.
WHAT WE OFFER
Competitive Benefits - Employee benefits include comprehensive medical, dental, vision, life and disability plans for eligible employees and their dependents. Additionally, Natera employees and their immediate families receive free testing in addition to fertility care benefits. Other benefits include pregnancy and baby bonding leave, 401k benefits, commuter benefits and much more. We also offer a generous employee referral program!
For more information, visit <a href="http://www.natera.com" target="_blank">www.natera.com</a>.
Natera is proud to be an Equal Opportunity Employer. We are committed to ensuring a diverse and inclusive workplace environment, and welcome people of different backgrounds, experiences, abilities and perspectives. Inclusive collaboration benefits our employees, our community and our patients, and is critical to our mission of changing the management of disease worldwide.
All qualified applicants are encouraged to apply, and will be considered without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, age, veteran status, disability or any other legally protected status. We also consider qualified applicants regardless of criminal histories, consistent with applicable laws.
If you are based in California, we encourage you to read this important information for California residents. 
Link: <a href="https://www.natera.com/notice-of-data-collection-california-residents/" target="_blank">https://www.natera.com/notice-of-data-collection-california-residents/</a>
Please be advised that Natera will reach out to candidates with a @natera.com email domain ONLY. Email communications from all other domain names are not from Natera or its employees and are fraudulent. Natera does not request interviews via text messages and does not ask for personal information until a candidate has engaged with the company and has spoken to a recruiter and the hiring team. Natera takes cyber crimes seriously, and will collaborate with law enforcement authorities to prosecute any related cyber crimes.
For more information: - BBB announcement on job scams - FBI Cyber Crime resource page

Senior Design Transfer Scientist

<h3>Job Description</h3>
Job Description
Polymer Chemist or Engineer – Advanced Composites &amp; Resin Formulation

Polymer Chemist

<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!

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