field_job_employment_type

field_job_occupational_field_parents_all

job_organization_name

city

state

<h3>Job Description</h3>
Founded over 35 years ago, First Quality is a family-owned company that has grown from a small business in McElhattan, Pennsylvania into a group of companies, employing over 5,000 team members, while maintaining our family values and entrepreneurial spirit. With corporate offices in New York and Pennsylvania and 8 manufacturing campuses across the U.S. and Canada, the companies within the First Quality group produce high-quality personal care and household products for large retailers and healthcare organizations. Our personal care and household product portfolio includes baby diapers, wipes, feminine pads, paper towels, bath tissue, adult incontinence products, laundry detergents, fabric finishers, and dishwash solutions. In addition, we manufacture certain raw materials and components used in the manufacturing of these products, including flexible print and packaging solutions.
 
Guided by our values of humility, unity, and integrity, we leverage advanced technology and innovation to drive growth and create new opportunities. At First Quality, you’ll find a collaborative environment focused on continuous learning, professional development, and our mission to Make Things Better®.
 
We are seeking an Associate Product Development Scientist for our First Quality Products site located in McElhattan, PA.
 
This position is responsible for creating, developing, and implementing new and proprietary designs of absorbent-related product systems based upon business, customer, and consumer needs as well as provide support for the needs of present product systems to assure competitive performance and value.
 
Principal Accountabilities/ Responsibilities:
<ul>
<li>Participate as a member of the Product Development team; execute projects in timely, diligent, safe, and professional manner, and contribute to the growth of the team and department.</li>
<li>Design new products and product improvements to meet business and consumer needs.</li>
<li>Develop new and improved materials and technologies with suppliers, and ensure all new raw materials obtain proper safety testing and clearance.</li>
<li>Use basic Design of Experiments (DOE) techniques to develop experimental plans.</li>
<li>Support the existing business product cost improvements through product redesigns.</li>
<li>Provide technical support to reduce consumer complaints.</li>
<li>Support corporate proprietary technology by documenting and patenting novel ideas.</li>
<li>Develop new test methods to better predict and understand product performance in use.</li>
<li>Work with more senior scientist or manager to help set project objectives.</li>
<li>Coach and develop indirect reports to enhance team performance towards department objectives.</li>
</ul>
 
Education and experience requirements:
<ul>
<li>Four-year technical degree (e.g. Chemistry, Chemical Engineering, Mechanical Engineering, Material Science Engineering) or equivalent; additional business studies preferred.</li>
<li>3+ years in R&amp;D inventing, developing, and implementing new products.</li>
<li>Knowledge of and experience with developing product systems for the retail market, preferably hygiene products.</li>
<li>Knowledge of materials used in retail absorbent products (e.g. pulp, super absorbent polymers, nonwovens).</li>
<li>Working knowledge of consumer product converting technologies for pulp, paper, and nonwoven materials.</li>
<li>Experience with the process of searching, evaluating, and filing patents.</li>
<li>Experience providing direction for the physical testing of hypotheses, resulting in specific conclusions and recommendations.</li>
<li>Able to speak, read and write the English language and have strong oral and written communication skills.</li>
<li>Good analytical skills, with working knowledge of basic statistics.</li>
<li>Good computer skills in Microsoft Office program.</li>
<li>Able to travel ~20-30% to US and International for product and process trials.</li>
</ul>
 
What We Offer You
We believe that by continuously improving the quality of our benefits, we can help to raise the quality of life for our team members and their families. At First Quality you will receive:
<ul>
<li>Competitive base salary and bonus opportunities</li>
<li>Paid time off (three-week minimum)</li>
<li>Medical, dental and vision starting day one</li>
<li>401(k) with employer match</li>
<li>Paid parental leave</li>
<li>Child and family care assistance (dependent care FSA with employer match up to $2500)</li>
<li>Bundle of joy benefit (year's worth of free diapers to all team members with a new baby)</li>
<li>Tuition assistance</li>
<li>Wellness program with savings of up to $4,000 per year on insurance premiums</li>
<li>...and more!</li>
</ul>
 
First Quality is committed to protecting information under the care of First Quality Enterprises commensurate with leading industry standards and applicable regulations. As such, First Quality provides at least annual training regarding data privacy and security to employees who, as a result of their role specifications, may come in to contact with sensitive data.
 
First Quality is an Equal Opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, sexual orientation, gender identification, or protected Veteran status.
 
For immediate consideration, please go to the Careers section at <a href="http://www.firstquality.com" target="_blank">www.firstquality.com</a> to complete our online application.

Associate Product Development Scientist

<h3>Job Description</h3>
Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Aldevron, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.&nbsp;
You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.
At Aldevron, we deliver world-class CDMO services that accelerate the development of groundbreaking therapies. Our mission is to be the engine of innovation for genomic medicine pioneers. As a member of our team, you’ll help bring life-changing innovations to life—impacting millions around the world. We bring together deep scientific expertise, an unwavering commitment to quality, and a collaborative spirit to drive progress. Whether you're launching your career or bringing years of experience, we value the unique perspective you bring. Join us and become part of a mission-driven team advancing science and unlocking human potential—one discovery at a time.
Learn about the Danaher Business System which makes everything possible.
The Sr Scientist/Sr. Engineer - RNA role is responsible for overseeing multiple new technical transfer activities involving Drug Substance and Drug Product program life cycles from development through clinical and commercial applications from both internal and external sending parties with a specialization in RNA Drug Substance.
This position reports to the Manager of RNA Technical Operations and is part of the Technical Operations Department located in Fargo, ND and will be an on-site role.&nbsp;
In this role, you will have the opportunity to:
<ul>
<li>
Design, execute and oversee new process unit operations and bring innovative ideas to troubleshoot problems
</li>
<li>
Lead and facilitate the onboarding of technical transfers throughout the product life cycle and steer later phase application programs to meet clinical standards
</li>
<li>
Mentor other teammates in Tech Ops and other crossfunctional teams through training of innovative initiatives, optimizations, and unit operations
</li>
<li>
Execute and lead change controls, quality event investigations, and support process qualification/validation initiatives
</li>
<li>
Steer both internal and external parties as the subject matter expert (SME) providing technical support in a timely manner to drive on time delivery and right first time metrics
</li>
</ul>
The essential requirements of the job include:
<ul>
<li>
BS degree in biology, molecular biology, biochemistry, chemistry, or related discipline with 6+ years of experience.
</li>
<li>
MS degree in biology, molecular biology, biochemistry, chemistry, or related discipline with 3+ years of experience.
</li>
<li>
PhD in biology, molecular biology, biochemistry, chemistry, or related discipline with 3+ years of experience.
</li>
<li>
Experience in leading RNA technical transfer projects through manufacturing, experimental design, and data analysis life cycles in a cGMP environment
</li>
<li>
Ability to apply critical thinking and oversee multiple projects in flight with robust knowledge of processes and procedures required to lead end to end programs throughout the products life cycle.
</li>
</ul>
It would be a plus if you also possess previous experience in:
<ul>
<li>
Working knowledge of current industry drug substance and drug product regulatory guidelines
</li>
</ul>
Aldevron, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it’s a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info.
#LI-LM3
Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. 
For more information, visit <a href="http://www.danaher.com" target="_blank">www.danaher.com</a>. 
Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. 
The U.S. EEO posters are available here.
We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact:1-202-419-7762 or <a href="mailto:applyassistance@danaher.com" target="_blank">applyassistance@danaher.com</a>.

Sr Scientist/Sr. Engineer - RNA

<h3>Job Description</h3>
Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Beckman Coulter Life Sciences, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.
You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.
At Beckman Coulter Life Sciences, we know time is the most critical facet in the laboratory today: time to get life-saving therapies to patients faster; reclaiming time by automating tedious manual workflows; and saving time spent addressing erroneous or complex results.
We are partners in time and accelerate answers to critical questions through the power of automation. We develop innovations for scientists by scientists, with many of our 3,300+ global colleagues coming from the laboratory.
It’s all part of our time-tested approach to bringing meaningful innovations at the speed of life since 1935. And we’re just beginning. Working together, let’s put our time and talents together to advance human health for tomorrow.
Learn about the Danaher Business System which makes everything possible.
In this role, you will have the opportunity to: 
<ul>
<li>
Lead and execute Sustaining projects across&nbsp;several cross-functional teams composed of multiple internal functions including Product Development, Procurement, Quality, Regulatory, Supply chain and Marketing.
</li>
<li>
Ensure &nbsp;manufacturing readiness for New Product Introduction (NPI) projects, ensuring seamless transfer from development to production.
</li>
<li>
Collaborate cross-functionally with R&amp;D, Procurement, Quality, and Supply Chain to define requirements&nbsp; for formulation, packaging, and process requirements for NPI projects.
</li>
<li>
Support design transfer by translating product requirements into manufacturing workflows, including creation of process documentations such as assembly drawings/Product Master record, work instructions, Bill of Materials (BOMs), and routings for reagent manufacturing.
</li>
<li>
Apply technical knowledge to support root-cause analysis, implement corrective actions, and sustainment as part of continuous improvement efforts.&nbsp;
</li>
</ul>
The essential requirements of the job include:
<ul>
<li>
BS degree in Life Sciences , molecular Biology, biochemistry, bioengineering or closely related discipline with 5+ years’ experience in reagent manufacturing within a regulated industry such as life sciences or medical devices.
</li>
<li>
In depth understanding of design controls and best practices for reagent manufacturing.
</li>
<li>
Demonstrated ability to organize, prioritize, plan, and execute multiple large-scale projects from definition through implementation, coordinating with cross-functional internal teams and third-party contractors
</li>
<li>
Strong problem-solving skills, adaptability to changing priorities, and to deliver results to meet project timelines.
</li>
<li>
Familiarity with ERP systems (e.g. Oracle) and willingness to travel up to 10%, as needed, for supplier or inter-site collaboration.
</li>
</ul>
#LI-PRO-KRISH
Beckman Coulter Life Sciences, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it’s a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info.
Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. 
For more information, visit <a href="http://www.danaher.com" target="_blank">www.danaher.com</a>. 
Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. 
The U.S. EEO posters are available here.
We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact:1-202-419-7762 or <a href="mailto:applyassistance@danaher.com" target="_blank">applyassistance@danaher.com</a>.

Sr. Reagent Manufacturing Scientist

<h3>Job Description</h3>
Ecolab, the global leader in premium cleaning, sanitizing and maintenance products and services for the hospitality, institutional and industrial markets is seeking a Chemical Plant Operator / Mixer. This role is responsible for mixing chemical batches by following standard formulas, applicable instructions and current standard operating procedures.
What’s in it For You: 
<ul>
<li>
The opportunity to take on some of the world’s most meaningful challenges, helping customers achieve clean water, safe food, and healthy environments
</li>
<li>
The ability to make an impact and shape your career with a company that is passionate about growth
</li>
<li>
The support of an organization that believes it is vital to include and engage diverse people, perspectives, and ideas to achieve our best
</li>
<li>
Comprehensive benefits package starting day one of employment including medical, dental, vision, matching 401k, company paid pension, stock purchase plan, tuition reimbursement and more!
</li>
</ul>
Click Here to see our benefits.
What You Will Do: 
<ul>
<li>
Review daily mix schedules and ensure the raw materials required are available
</li>
<li>
Follow mix instructions and accurately add raw materials to the mixes manually, using pumps or mixing systems
</li>
<li>
Mix batches using variable agitation
</li>
<li>
Perform routine observation of the product during the mixing and filling process to ensure batch quality. Report any out-of-spec raw material, premises, or mixed batches and consults with Quality personnel on any batch adjustments.
</li>
<li>
Properly cleans out all mix tanks
</li>
<li>
Operate fork trucks, palletizers, scales, pumps, and other material handling equipment to transport raw material and finished product
</li>
<li>
Perform building and equipment preventative maintenance
</li>
<li>
Perform other duties as assigned
</li>
</ul>
Position Details:
<ul>
<li>
Plant location: Montgomery, AL
</li>
<li>
Work week and shift: Monday - Friday, Rotating Shifts
</li>
<li>
Compensation package offered: $23.17/ per hour
</li>
</ul>
Minimum Qualifications: 
<ul>
<li>
High School diploma or GED
</li>
<li>
1 year of previous experience working in a chemical and/or manufacturing environments
</li>
<li>
1 year of experience understanding systems, pumps, read meters, basic Quality Control data, and track mixing and quality information (mix logs, batch adjustments, etc.)
</li>
<li>
1 year experience performing basic Quality Control tests (take samples, perform pH tests)
</li>
<li>
&nbsp;Excellent attention to detail; must be able to simultaneously mix several tanks and accurately complete related documents
</li>
<li>
Ability to read and match numbers on shipping records, labels, raw materials, and finished goods
</li>
<li>
No Immigration Sponsorship available for this opportunity
</li>
</ul>
Physical Demands: 
<ul>
<li>
Must be able to lift/carry 50lbs
</li>
<li>
Must be able to participate in respirator fitness, if required
</li>
<li>
Must be able to pass a drug screen and physical exam
</li>
</ul>
Preferred Qualifications: 
<ul>
<li>
Basic knowledge of chemistry
</li>
<li>
Ability to work in a fast-paced environment
</li>
<li>
&nbsp;Excellent organizational skills and ability to multitask
</li>
<li>
&nbsp;Excellent communication skills and the ability to work as part of a team
</li>
</ul>
Annual or Hourly Compensation Range:
$23.17 ph Many factors are taken into consideration when determining compensation, such as experience, education, training, geography, etc. We comply with all minimum wage and overtime laws.
Benefits&nbsp;
Ecolab provides the following benefits: medical, dental, vision, life insurance, accident insurance, critical illness insurance, hospital indemnity insurance, auto insurance, home insurance, pet insurance, identity theft protection, short-term and long-term disability, 401k, pension plans, retirement health care benefits, short-term incentives, vacation (12 days), holidays, parental leave, employee stock purchase plans&nbsp;(Full-Time Associates), discount on day care services and caregiver services, adoption assistance, group legal services, employee assistance program, employee discount program, and education assistance program,&nbsp;on-Site childcare and fitness facilities may be available at select Ecolab locations.&nbsp;Click here for additional benefits information. If you are viewing this posting on a site other than our Ecolab Career website, view our benefits at&nbsp;jobs.ecolab.com/working-here.
Potential Customer Requirements Notice
To meet customer requirements and comply with local or state regulations, applicants for certain customer-facing roles may need to:
- Undergo additional background screens and/or drug/alcohol testing for customer credentialing.
- Be fully vaccinated for COVID-19, including a booster if eligible, unless a religious or medical accommodation is requested by the applicant and approved by Ecolab.
Americans with Disabilities Act (ADA)&nbsp;
Ecolab will provide reasonable accommodation (such as a qualified sign language interpreter or other personal assistance) with our application process upon request as required to comply with applicable laws. If you have a disability and require accommodation assistance in this application process, please visit the Recruiting Support link in the footer of each page of our career website.&nbsp;&nbsp;
 
Our Commitment to a Culture of Inclusion &amp; Belonging \nAt Ecolab, we believe the best teams are inclusive. We are on a journey to create a workplace where every associate can grow and achieve their best. We are committed to fair and equal treatment of associates and applicants and recruit, hire, promote, transfer and provide opportunities for advancement based on individual qualifications and job performance. In all matters affecting employment, compensation, benefits, working conditions, and opportunities for advancement, we will not discriminate against any associate or applicant for employment because of race, religion, color, creed, national origin, citizenship status, sex, sexual orientation, gender identity and expressions, genetic information, marital status, age, disability, or status as a covered veteran.
\n
In addition, we are committed to furthering the principles of Equal Employment Opportunity (EEO) through Affirmative Action (AA). 
\n
We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance, the San Francisco Fair Chance Ordinance, and the New York City Fair Chance Act.

Chemical Plant Operator I

<h3>Job Description</h3>
Company Description
Accu Reference Medical Lab is a state-of-the-art medical testing laboratory service that offers a comprehensive range of tests for the diagnosis, screening, and evaluation of diseases and health conditions. The lab is certified under the federal government’s Clinical Laboratory Improvement Amendments (CLIA) and operates in compliance with all governmental regulations. The laboratory uses the latest diagnostic technology and continually updates its services as new tests become available. Our experienced technicians ensure the most accurate and precise testing results, and we consistently strive for quality improvement through robust techniques and technological advancements. Accu Reference Medical Lab is an equal opportunity employer.
 
JOB DESCRIPTION:
 
The Supervisor plans, organizes, schedules, and directs the Pre-Analytical department to meet established turnaround time and maintain budget.&nbsp;Provides direct on-site supervision of the day-to-day operation including adjustment of workforce scheduling, specimen workflow, quality, compliance, and adherence to department/company policies.&nbsp;
 
QUALIFICATIONS:
 
1.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Education: High School/equivalent required.&nbsp;(College degree a plus).
2.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Excellent organizational, communication, leadership and problem-solving skills.
3.&nbsp;&nbsp;&nbsp;Minimum 3 years clinical laboratory experience in supervisory role (Pre-Analytical Experience preferred). 
4.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Experience with production workflow management.
 
JOB RESPONSIBILITIES:
 
1.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Devotes time to evaluate specimen workflow to maintain adequate turnaround time and improve shift/employee productivity
2.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Maintain adequate staffing by interviewing, hiring, training, and performing the competency. &nbsp;&nbsp;
3.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Perform the scheduling, planning, staffing, and monitoring of workflow based on specimen delivery flow to meet established goals.
4.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Provide employee development. 
5.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Procure appropriate department supplies.
6.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Provides supervision and leads the Pre-Analytical Department.
7.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Serve as a resource for problem solving and process improvement of all established goals.&nbsp;
8.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Investigates and documents non-conforming events as necessary.&nbsp;
9.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Recommends process improvement ideas.
10.&nbsp; Uses effective two-way communication with employees and management. 
11.&nbsp; Supports, implements, and ensures compliance with all department/company policies.
12.&nbsp; Monitors and ensures implementation of processes to meet established goals.
13.&nbsp; Ensures compliance by conducting audits.
14.&nbsp; Interacts with internal and external customers to ensure proper specimen handling.
15.&nbsp; Participates in the updating of departmental standard operating procedures to accurately reflect the current practices.
16.&nbsp; Reviews employee timecards for attendance and overtime.
17.&nbsp; Motivates and develops staff. Coordinates training and feedback for employee development.

Pre-Analytical Supervisor - night shift

<h3>Job Description</h3>
Position:&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;MRI Scientist – Sequence Development
Location:&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Oakwood Village, OH&nbsp;
About ViewRay Systems
ViewRay Systems, Inc. is a technology company seeking to provide the global radiation therapy community with advanced medical instruments incorporating the most capable and highest level of technology possible. Our belief is that only significant technological innovation can enable society to conquer disease. Our mission is to dare to change the paradigms of medicine and solve “impossible” technical problems to enable clinicians to effect a cure to save precious human lives, mitigate pain and suffering, and enhance quality of life. Our vision is to become the world’s leader in producing highly-effective innovative technology to cure cancer.&nbsp;
ViewRay Systems designs, manufactures, and markets the MRIdian A3i® radiation therapy system. The MRIdian A3i system is designed to treat patients with the smallest radiation therapy margins available&nbsp;&nbsp;with the highest patient throughput demonstrated for the most complicated cases&nbsp;&nbsp;
 
The MRIdian A3i system treats by aligning the sharpest radiation therapy beam on the market to diagnostic quality magnetic resonance images (MRIs) of the patient, adapts the treatment plan to the reality of the patient, and then uses the real-time MRIs to control the beam and record real-time doses delivered to the patient.&nbsp;
If you are driven by a passion for innovation and want to be part of a team that is changing the world, we invite you to explore the opportunities available at ViewRay Systems.
Job Description:
ViewRay is currently looking for a motivated MRI Physicist experienced in sequence development who will share our passion for conquering cancer and help us develop our groundbreaking MRI guided Radiation Therapy system. The ideal candidate is an adept problem solver and leader that can work through technical challenges and employ pragmatic solutions.&nbsp;
 
Responsibilities:
•\tDevelop innovative high speed imaging techniques that approach real-time imaging in both 2D and 3D space.
•\tDevelop fast imaging techniques, tailored for the radiation therapy space, that will provide the required definition while increasing patient throughput.
•\tDevelop new calibration sequences and workflow on a new MRI platform.
•\tWork with a cross-functional team of engineers and scientists to translate promising prototypes into product while leading technical/clinical risk retirement.
•\tProvide technical expertise and support for projects with internal and external collaborators.
 
Required Qualifications:
•\tPh.D. in Physics / Electrical Engineering / Biomedical Physics / Biomedical Engineering, or equivalent.
•\tStrong background in MR physics and pulse sequence design.
•\tExpertise in MR imaging techniques and clinical applications.
•\tExperience in working with internal and external partners.
•\tSubstantial experience in C++/C software design, implementation, and coding.
•\tExperience using Matlab for signal and image processing.
•\tAbility to work independently, prioritize, and take initiative
•\tAbility to multi-task and follow through.
•\tDetail-oriented and organized.
•\tSkilled in MS office software applications (PowerPoint, Word, Excel).
 
Valued Qualifications:
•\tDesire and bandwidth to expand to other disciplines.
•\tExperience with E&amp;M modeling.
 
Job Type: Full-time&nbsp;
Pay: Commensurate with experience&nbsp;
Ability to Relocate: Cleveland, OH 44128: Relocate before starting work (Required)&nbsp;
Work Location: In person in Cleveland, OH: Relocate before starting work (Required)&nbsp;
Benefits:&nbsp;
<ul>
<li>Health, dental, and vision insurance&nbsp;</li>
<li>401K Contribution Plan&nbsp;</li>
<li>Paid time off and flexible schedule&nbsp;</li>
<li>Office stocked with snacks, drinks, and occasional catered meals&nbsp;</li>
</ul>
 
Email inquiries to <a href="mailto:careers@viewraysystems.com" target="_blank">careers@viewraysystems.com</a>&nbsp;
 
ViewRay Systems, Inc. is an Equal Opportunity Employer and does not discriminate on the basis of race, religion, color, creed, national origin, gender, age, sexual orientation, status as a protected disabled or Vietnam Era Veteran, disability, or any other legally protected status.&nbsp;

MRI Scientist - Sequence Development

<h3>Job Description</h3>
POSITION SUMMARY
 
The Chemist will provide analytical support for QC testing of antibiotic products which include raw materials, in-process samples, stability samples, validation samples, product surveillance, and finished products according to Quality Assurance standard procedures, as assigned. Assist with development and validation of chemical assays. Assist with installing, validating, and trouble-shooting new and existing equipment, including automated systems, as assigned. Accurately generate and document all analytical test results per written procedures and corporate policies and support management in the evaluation and review of all test results and investigations as needed.
 
ROLES &amp; RESPONSIBILITIES:
 
<ul>
<li>Maintains the QC laboratories to comply with cGMP and US Antibiotics standards of safety, quality, and cleanliness.</li>
<li>Follows all safety precautions and guidance from training sessions, chemical hygiene plan, MSDSs (Material Safety Data Sheets), and other technical literature and resources.</li>
<li>Performs efficient and reliable analytical tests following validated procedures for raw material, in process, validation, product surveillance, finished product, stability, water, and environmental samples, as assigned.</li>
<li>Documents all results in accordance with cGMPs and written procedures.</li>
<li>Troubleshoots and solves problems with assays and laboratory equipment and reports all observations.</li>
<li>Strictly follows written procedures to minimize analytical variability. Recommends any potential improvements or changes to methods and lab operations (changes implemented via the change control process).</li>
<li>Interprets analytical results correctly, notifying supervision promptly of any situation that indicates analytical issues or product issues.</li>
<li>Participates in analytical method validations or transfers as required.</li>
<li>Performs satisfactorily on all analyst qualification studies, indicating technical proficiency.</li>
<li>Plans, performs, and documents non-routine tests (or special studies) and investigations under the direction of supervisor and/or manager.</li>
<li>Evaluates and utilizes state-of-the-art equipment, including automated systems and computerized systems to perform and document testing and meet the goals of improved performance, including reliability and efficiency.</li>
<li>Maintains and improves proficiency of technical skills through training.</li>
<li>Conducts special studies in accordance with protocols and direction of management. Prepares well-documented reports of results.</li>
<li>Carries out other departmental duties as deemed appropriate by supervisor/manager.</li>
<li>Reviews (i.e., validates) analytical test results for other laboratory personnel, as required.</li>
<li>Assists supervision in conducting analytical failure investigations, as required, following all procedures.</li>
<li>Calibrates and maintains assigned laboratory equipment as needed according to schedules and procedures, documenting all results.</li>
<li>Assists with equipment qualification testing as required by management.</li>
<li>Assists with sampling tasks as required.</li>
<li>Ensures that testing of products manufactured at the facility is performed per approved procedures and appropriate regulations and those lab operations conform to company standards for safety and performance.</li>
<li>Reports all test results and any concerns with accuracy of analytical data and/or any issues that may impact product quality, efficacy, safety, or purity.</li>
<li>Supports production needs by efficient laboratory turnaround of samples with right-first-time testing.</li>
<li>Evaluates test results versus established test criteria and/or product specifications.</li>
<li>Must be able to follow procedures for investigative analytical results as required.</li>
<li>Advises, in a technical role, less-experienced staff, notifying supervisor or manager of problems/issues or additional training needs.</li>
<li>Initiates ideas for operational changes and continuous improvement in laboratory, within constraints of policies and procedures to improve cGMP compliance, efficiency, cost, and performance.</li>
<li>Must be able to assure the accuracy and integrity of analytical results/documentation generated. Exercises careful attention to testing procedures, and sampling handling and preparation as to avoid known degradation failure modes for materials under test, and to documentation.</li>
</ul>
 
EDUCATION, WORK EXPERIENCE, CERTIFICATIONS:
<ul>
<li>BS/BA degree in Chemistry (or related science) or equivalent related analytical experience.</li>
<li>Minimum of 0-5 years of analytical experience in pharmaceutical industry and/or other scientific experience.</li>
<li>Strong knowledge/experience of cGMPs in areas beyond QC laboratory.</li>
</ul>
 
KNOWLEDGE, SKILLS, AND ABILITIES:
 Skills/Abilities:
<ul>
<li>Demonstrate ability to perform a wide variety of chemical, instrumental, and chromatographic analyses in an efficient, reliable, and safety conscious manner.</li>
<li>Advanced computer skills.</li>
<li>Appropriate interpersonal and leadership skills</li>
<li>Strong verbal communication skills and technical writing skills.</li>
<li>Ability to prioritize and decide appropriate course of actions for routine issues.</li>
<li>Ability to recognize possible compliance, technical, or safety-related issues and notify supervisor or manager promptly.</li>
<li>Ability to suggest appropriate corrective and/or preventive action(s) and assist with implementation.</li>
<li>Ability to work in a multi-disciplinary team environment</li>
<li>Demonstrate visual acuity per SOP requirements</li>
</ul>
Required Knowledge:
<ul>
<li>Understanding of analytical techniques, test methodology, method development, method validation and reporting for data integrity.</li>
<li>Comprehensive skills related to chemical, instrumental, chromatographic analysis, Operational Excellence, statistical applications and tools</li>
<li>Understanding of equipment installation, validation, calibration, and troubleshooting, etc.</li>
<li>Strong knowledge of cGMPs, USP and FDA’s laboratory related requirements.</li>
</ul>

Chemist

<h3>Job Description</h3>
Duration : 12 Months
Description:
A Product Development Scientist role involves a wide range of activities, including developing and optimizing new product formulations and processes, conducting laboratory testing and evaluations. Key responsibilities include batching several iterations, ensuring technical accuracy in product development through stability studies, and documentation. Working with the team, time management, attention to detail, strong analytical skills, strong communication, following the timeline.
Consumer Products - Skin Health
BA Degree
2 to 4 years’ experience
Will need to go between Summit and Skillman office, 830-5
 
Skills required:
documentation work
organizing samples, delivering samples
batching exp
2 years of formulation exp
Skillman for batching - 5 days a week - majority of the role is in Skillman
paperwork done in summit (1 day in summit)
4 days Skillman and 1 day summit (depend on the workload and paperwork)
Timings : 8:30-5- Flexible
basic lab instruments
intern exp will also work
making 2 batches a day and 8 batches a week
 
About US Tech Solutions:
US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit <a href="http://www.ustechsolutions.com" target="_blank">www.ustechsolutions.com</a>.
US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
 
Recruiter Details:
Name: I.Prudvi kumar
Email: <a href="mailto:prudvi.k@ustechsolutionsinc.com" target="_blank">prudvi.k@ustechsolutionsinc.com</a>
Internal Id: 25-50776

Formulation Scientist

<h3>Job Description</h3>
Amber Bio is a biotechnology company pioneering new gene editing modalities using multi-kilobase edits to reach previously undruggable patient populations. Founded by pioneers in the CRISPR field from leading institutions for gene editing research, the company is developing a first-of-its-kind RNA editing platform that can correct thousands of bases at once, thereby correcting genetic mutations safely and reversibly. If you are interested in building a new frontier in genetic medicine, we welcome you to apply.
 
Job Description: Research Associate III/ Senior Research Associate (Biodesigner), Assay Development / Bioanalytical Development
 
Position Overview: The Research Associate III/ Senior Research Associate in Assay Development and Bioanalytical Development will play a critical role in the development, qualification, and validation of bioanalytical methods to support our RNA editing programs. The successful candidate will work under the guidance of an assay development scientist to develop custom assays for the analysis of samples, including AAVs, cells, and tissues. This role also involves drafting key documents such as Standard Operating Procedures (SOPs) and method development reports.
 
Key Responsibilities:
<ul>
<li>Method Development, Qualification, and Validation:</li>
<li>Support the development, qualification, and validation of bioanalytical methods in accordance with regulatory guidelines.</li>
<li>Develop, optimize, and execute robust bioanalytical methods for the characterization, release, and stability testing of Amber's gene therapy. </li>
<li>Sample Analysis:</li>
<li>Support drug absorption, distribution, metabolism, and excretion studies.</li>
<li>Perform analysis of AAVs, cells, and tissues to support various stages of research and development.</li>
<li>Lead efforts to streamline and optimize sample storage and processing, as well as establishing and maintaining critical reagent stocks and cell banks.</li>
<li>Documentation Reporting:</li>
<li>Draft and review key documents such as SOPs, method development, and sample analysis reports.</li>
<li>Maintain accurate and detailed records of all experiments and analyses.</li>
<li>Collaboration &amp; Communication</li>
<li>Collaborate with manufacturing and preclinical teams to support pipeline needs.</li>
<li>Communicate and present findings clearly to internal stakeholders.</li>
</ul>
 
Qualifications:
<ul>
<li>B.A./B.S. or M.S. in Molecular Biology, Biochemistry, Analytical Chemistry, or a related field.</li>
<li>3+ years of experience in bioanalytical and assay development in the biotechnology or pharmaceutical industry.</li>
<li>Demonstrated strong proficiency in a wide range of molecular biology techniques such as molecular cloning, DNA/RNA extractions, RT-qPCR, ddPCR, and ELISA.</li>
<li>Experience with cell-based assays and detection methods such as fluorescence, luminescence, and ECL.</li>
<li>Hands-on experience using laboratory automated systems (e.g., liquid handlers, extraction robotics, etc.).</li>
<li>Background in RNA-based therapies is highly desirable.</li>
<li>Experience writing SOPs and reports supporting IND filings (e.g. development, qualification sample analysis reports, etc.)</li>
<li>Knowledge of FDA and ICH guidelines for method development, qualification, and validation. </li>
<li>Prior history in compiling and analyzing data and generating reports that are routinely presented to project teams.</li>
<li>Ability to work effectively in a collaborative, fast-paced environment.</li>
</ul>
 
Preference will be given to those who display:
 
<ul>
<li>High motivation, with a strong work ethic and dedication to generating impact.</li>
<li>Attention to detail, with the ability to extract deep insights from data.</li>
<li>Ability to go from ideation to data in an independent fashion.</li>
<li>Long-term personal vision with defined career goals.</li>
<li>Team-oriented thinking.</li>
<li>Demonstrated excellence in small team environments, including a “no task is too small” attitude. </li>
</ul>
 
If you have a passion for advancing gene editing technologies and desire to be part of a pioneering biotech company, we encourage you to apply and join our ambitious team.
 
Please apply directly through LinkedIn.
 
Amber Bio is an equal-opportunity employer and encourages applications from candidates of diverse backgrounds. We value diversity and are committed to creating an inclusive and supportive work environment for all employees.

Research Associate III/ Senior Research Associate (Biodesigner), Assay Development / Bioanalytica...

<h3>Job Description</h3>
Our pharmaceutical client is seeking a Principal Scientist who will be responsible for evaluating and interpreting analytical results, as well as developing, validating, and transferring analytical methods for APIs, intermediates, and raw materials. If you are someone who wants to be apart of a highly technical environment with a lot of growth, this role may be the one for you! 
Responsibilities:
<ul>
<li> Safely and effectively develop, establish, and validate analytical testing methodologies used to control raw materials, production intermediates, and final products</li>
<li> Actively participate in teams assembled to investigate and solve analytical technical issues within Analytical Development, Chemical Development, Process Support Group and Quality Control.</li>
<li> Perform analytical chemistry assays based on new and existing methodologies</li>
<li> Operate analytical instrumentation such as HPLC, GC, GC/MS, FTIR, Titrator, Particle Size Analyzer </li>
<li> Write technical reports to document analytical methods</li>
<li> Maintain laboratory notebooks documenting work</li>
<li> Maintain compliance with GMP SOPs and DEA regulations</li>
<li> Transfer documented analytical methods to the QC and Process Support Group departments</li>
<li> Set up new or existing analytical methods for compound identification, purity and potency testing.</li>
<li> Coordinate off-site testing as necessary</li>
<li> Conduct testing of analytical samples for the Chemical Development Department as needed.</li>
<li> Qualify reference materials.</li>
<li> May also perform other duties as required.</li>
</ul>
Qualifications:
<ul>
<li>Ph.D. in Chemistry or related field with minimum 6 years of experience or M.S. in Chemistry or related field with minimum 10 years of experience or B.S. degree in Chemistry or related field with 14 years of experience in lab environment, pharmaceutical experience preferred.</li>
</ul>

12,477 Science Jobs