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city

state

<h3>Job Description</h3>
Job Description
CHA Hollywood Presbyterian (CHA HPMC) is a nationally recognized acute care facility that has been caring for the Hollywood community and Los Angeles Areas since 1924.
Join our Global Network and be a CHA Global Ambassador 
CHA HPMC is also a part of the world-renown CHA Health System (CHS). CHS has CHA University which consists of 14 education institutions including medical school, nursing school and pharmacy. CHA global network operates 81 hospitals and specialty clinics, 30 research and 31 bio/pharmaceutical/healthcare companies with 14,000 employees in seven countries.
Our New Facility is seeking for Top Talents
The best women’s hospital in Los Angeles is looking for current RN candidates to staff Operating Room, Emergency Department, Labor &amp; Delivery and Mother-Baby care units to be housed in our expanding new patient tower facility scheduled to open next year. Come be a part of this dedicated and caring team right in the heart of Hollywood.
 
Perform high complexity clinical laboratory procedures to include Aerobic and Anaerobic bacteriology, molecular microbiology and mycology .Possess ability to exercise good independent judgment. Assumes responsibilities for daily department operations and Quality control management in compliance of Hospital policy and procedure and applicable regulatory requirement (State and Federal laws). Assist Laboratory Director in process improvement, operational efficiency, high quality of service and strategic planning to meet operational needs.
Summary:
<ul>
<li>Demonstrating ability to engage in regular and continuous decision making having an impact on people, costs and quality of service</li>
<li>Exercising responsibility for recommending personnel actions, hiring, disciplinary, dismissal, appraising performance, and training. May include staff adjustments during census drops</li>
<li>Be able to delegate, but assume full responsibility for valid results and review</li>
<li>Is familiar with laws and regulations for state and federal agencies, and College of American Pathologist (CAP).</li>
<li>On a documented schedule, reviewing and assuming responsibility for maintaining required department documents/files and procedure manuals</li>
<li>Developing new procedures and updates old procedures as needed. Rotating through weekend call with other Supervisors</li>
<li>Demonstrating knowledge of laboratory computer system regarding ordering, reporting, and verifying results and downtime computer procedures</li>
<li>Setting up quality control standardization and calibration procedures that monitor instruments applying acceptability criteria.</li>
<li>Executing predefined plans of action in response to quality control and documents actions</li>
<li>Troubleshooting malfunctioning test systems/instruments.</li>
<li>Instituting corrective action for any problems in the laboratory.</li>
<li>Processing samples and orders based on physician request</li>
<li>Performing inventories and maintains reasonable supplies.</li>
<li>Demonstrating knowledge of age specific care, including but not limited to, identifying the need for additional safety measures, physiological normal values/readings; and assessing skin integrity, behavior, motor skills and/or activities that place patients at risk as well as communicates effectively in a clear, concise, understandable manner. Applicable for the populations checked: Infant ( x) Pediatric (x ) Adult (x ) Geriatric ( x)</li>
<li>Incorporates HPMC mission of “quality care with compassion and respect” into daily performance of job functions.</li>
<li>Communicates problems/concerns to the Clinical Laboratory and Pathology Services Director.</li>
<li>Responds acceptably to priority specifications for tests</li>
</ul>
Professional Requirements:
<ul>
<li>Reports to work on time and as scheduled, completes work within designated time</li>
<li>Uses computerized time clock correctly.</li>
<li>Completes departmental and hospital-wide in-services, competencies and Health Stream assignments in a timely fashion.</li>
<li>Attends staff meetings and actively participates, reads and returns all staff meeting minutes.</li>
</ul>
 
Minimum Education:
<ul>
<li>Bachelor's degree in biological science or related field.</li>
</ul>
Preferred Education:
<ul>
<li>N/A</li>
</ul>
Minimum Work Experience and Qualifications:
<ul>
<li>Ability to communicate effectively verbally and in writing.</li>
<li>Must be able to work in a union environment.</li>
<li>Masters Degree or Equivalent experience preferred</li>
</ul>
Preferred Work Experience and Qualifications:
<ul>
<li>Three to five years’ experience in Microbiology section preferred.</li>
<li>Two years supervisory experience preferred</li>
</ul>
Required Licensure, Certification, Registration or Designation:
<ul>
<li>MT (ASCP) certification.</li>
<li>California Clinical Laboratory Scientist license.</li>
<li>Current Los Angeles County Fire Card required (within 30 days of employment)</li>
</ul>
 Shift: Days Hours: Varied Shift Hours: Varied Weekly Hours: 40 Type: Exempt FTE: 1.0

Microbiology CLS Supervisor Full Time Day

<h3>Job Description</h3>
Job Description
Job Summary:
We are seeking a Medical Physicist to join our Radiation Oncology team. You will support therapeutic radiation services by ensuring equipment compliance, maintaining QA/QC protocols, participating in patient treatment planning, and supporting brachytherapy and advanced procedures (SRS, SBRT, HDR, TBI).
This role is critical in maintaining safety, compliance, and optimal treatment delivery for cancer patients.
 
Qualifications:
Required:
<ul>
<li>Master’s Degree in Medical Physics or related field</li>
<li>ABR Certification or ABR eligible</li>
<li>BLS/CPR Certification</li>
<li>Experience in radiation equipment QA/QC and treatment planning</li>
</ul>
Preferred:
<ul>
<li>3+ years experience in clinical Radiation Oncology</li>
<li>Experience with HDR brachytherapy, prostate seed implantation, and dosimetry review</li>
</ul>
 
Key Responsibilities:
<ul>
<li>Perform QA/QC on linear accelerators, CT, HDR, and treatment planning systems</li>
<li>Collaborate with Radiation Oncologists and Dosimetrists to ensure accurate treatment plans</li>
<li>Conduct weekly chart reviews and participate in patient chart rounds</li>
<li>Support brachytherapy services (HDR and LDR) and prostate seed implants</li>
<li>Assist in advanced procedures including SRS, SBRT, TBI, and respiratory gating</li>
<li>Maintain documentation for compliance with NRC and state regulations</li>
<li>Participate in departmental radiation safety and provide annual in-service training</li>
</ul>
 
Why Join Us?
<ul>
<li>Collaborative, mission-driven team</li>
<li>Access to state-of-the-art technology</li>
<li>Opportunity to contribute to cutting-edge radiation therapy treatments</li>
</ul>
Company DescriptionInSync Consulting Services is a staffing agency specializing in Healthcare, Commercial, and EOR staffing services. 
<h3>Company Description</h3>
InSync Consulting Services is a staffing agency specializing in Healthcare, Commercial, and EOR staffing services.

Medical Physicist

<h3>Job Description</h3>
Job DescriptionCertified Group is committed to delivering expert solutions and quality testing our customers can feel confident in – on time, every time – so the world can trust in what it consumes. As a leading North American provider of laboratory testing, regulatory consulting, and certification &amp; audit services, Certified Group includes Food Safety Net Services (FSNS), FSNS Certification &amp; Audit, Certified Laboratories, EAS Consulting Group, and Labstat International Inc. Certified Group provides analytical testing and regulatory guidance services in the food &amp; beverage, dietary supplements &amp; NHP, cosmetics, OTC, personal care, tobacco, nicotine, cannabis, and hemp industries. 
 
We are currently looking for a Chemist to join our growing team!
 
ESSENTIAL RESPONSIBILITIES
<ul>
<li>Perform analysis using one or more of the following techniques: GC, LCMS, GCMS, GC, HPLC, ICP/MS, ICP-OES, UV-VIS, FTIR, Titration, Gravimetric Analysis, or other techniques, as appropriate in a timely fashion maintaining a high level of quality.</li>
<li>Prepare analytical standards.</li>
<li>Perform daily balance, temperature and monthly pipette verification.</li>
<li>Perform sample processing in accordance with standard operating procedures. </li>
<li>Perform sample preparation.</li>
<li>Successfully participate in proficiency testing.</li>
<li>Calibrate and maintain analytical instruments.</li>
<li>Participate in relevant ISO QA/QC activities and documentation thereof</li>
<li>Prepare standards and maintain inventory.</li>
<li>Effectively participate in proficiency testing as required by ISO17025 and other accrediting/certifying bodies.</li>
<li>Maintain analytical and quality records as required for accreditation/certification and related to analytical work and instrument maintenance.</li>
<li>Submit accurate and timely reports based on the analysis.</li>
<li>Identify results that require further investigation or discussion with the Department Manager/Supervisor.</li>
<li>Participate in OOS investigation and/or CAPA when necessary.</li>
<li>Plan and perform work to meet deadlines and expected turn-around times.</li>
<li>Perform routine diagnosis, troubleshooting and maintenance of equipment.</li>
<li>Learn new techniques and technologies as appropriate.</li>
<li>Works effectively with other departments.</li>
<li>Provide training to new chemists when needed. </li>
<li>Other duties as required.</li>
</ul>
MINIMUM QUALIFICATIONS
<ul>
<li>BA/BS degree in Chemistry related field, or 1 year of relevant work experience</li>
<li>Knowledge of GMP GLP GDP </li>
<li>Strong relevant quantitative skills</li>
<li>High level of computer skills and familiarity with data acquisition software</li>
<li>Strong trouble-shooting and problem-solving skills</li>
<li>High level of computer literacy</li>
<li>Good conceptual basis in analytical chemistry</li>
<li>Proven ability to perform standard chemical laboratory techniques </li>
</ul>
Benefits: 
<ul>
<li>Progressive 401k Retirement Savings Plan</li>
<li>Employer Paid Short- Term and Long-Term Disability, and Life Insurance</li>
<li>Group Medical</li>
<li>Tuition Reimbursement</li>
<li>Flexible Spending Accounts</li>
<li>Dental</li>
<li>Paid Holidays and Time Off</li>
<li>Many positions which qualify for the company bonus program</li>
</ul>
 
Certified Group values diversity in its workforce. The company is firmly committed to a policy of Equal Opportunity and will administer its policies in a manner that treats each employee and applicant for employment on the basis of merit. Certified Group will take affirmative action to seek out qualified applicants without regard to race, color, religion, sex, national origin, age, handicap, or veteran status.

Chemist

<h3>Job Description</h3>
Job Description
Castle Biosciences Earns "Top Workplaces USA Award" for Phoenix, Pittsburgh, and Friendswood!
You won't find a work culture and benefits package like ours every day. Come join our team and a group of colleagues who love working at Castle!
 Learn more at <a href="http://www.CastleBiosciences.com" target="_blank">www.CastleBiosciences.com</a>
Castle Biosciences Inc. is growing, and we are looking to hire a R&amp;D, Senior Scientist, Pipeline working from our Friendswood, TX office and may also consider Pittsburgh @Nova Place location as a secondary location option, with a start date on or before December 1, 2025.
Why Castle Biosciences?
Exceptional Benefits Package:
<ul>
<li>Excellent Annual Salary </li>
<li>20 Accrued PTO Days Annually + 10 Paid Holidays</li>
<li>401K with 100% Company Match up to 6%</li>
<li>3 Health Care Plan Options + Company HSA Contribution</li>
<li>Company Stock Grant Upon Hire</li>
</ul>
A DAY IN THE LIFE OF AN R&amp;D Senior Scientist, Pipeline
The Senior Scientist, Pipeline, will work with R&amp;D colleagues to evaluate, develop, and validate clinical devices and molecular biomarkers that enhance disease diagnosis, prognosis, and prediction of therapy response. This role focuses on identifying opportunities for new clinical devices and tests, collaborating with cross-functional teams to develop business cases, project plans, and study protocols. The Senior Scientist will also support the Clinical Research team in organizing, auditing, and interpreting data from ongoing studies to build validity and utility evidence for current and pipeline tests. Additionally, this position will collaborate across Castle Biosciences to produce key scientific materials, including publications, abstracts, slide decks, and other literature used for internal training and external education.
REQUIREMENTS
<ul>
<li>Master's or PhD in life sciences or a bachelor's degree with a minimum of 3 years of postgraduate medical writing experience in life sciences or industry equivalent in the biotech sector.</li>
<li>PhD level training in the life sciences, with a focus on oncology</li>
<li>The ability to successfully communicate and teach in a complex and competitive environment.</li>
<li>Strong interpersonal, organizational, and communication skills, written and oral.</li>
<li>Demonstrated team player.</li>
</ul>
TRAVEL
<ul>
<li>10% travel required.</li>
</ul>
SCHEDULE
<ul>
<li>Monday - Friday, in-office 5 days a week from 9:00 am to 5:30 pm, exempt position, working from the Pittsburgh, PA @ Nova Place office or Friendswood, TX office occasionally.</li>
<li>Off-hour work will be required to facilitate communication and meet deadlines.</li>
</ul>
READY TO JOIN OUR BIOTECH TEAM?
We truly appreciate your time. If this feels like the right opportunity for you, we'd love for you to complete our mobile-friendly application. We're excited to learn more about you and look forward to connecting soon!
Castle Biosciences Awards and Research Developments!

WORK AUTHORIZATION
All candidates must be legally authorized to work in the United States. Currently, Castle Biosciences does not sponsor H1B visas, OPT, or other employment-related visa's.
ABOUT CASTLE BIOSCIENCES INC.
At Castle, it all comes down to people. After all, disease doesn't just happen - it happens to people. We believe that disease management and treatment decisions can be better informed through a person's unique biology, which is revealed through the scientific rigor of our innovative, laboratory-developed tests. We are committed to empowering healthcare providers and patients with the goal of improved outcomes. 
Every employee at Castle has an impact on patient care, and we work to ensure that everyone finds their work to be both challenging and rewarding. We behave with integrity and treat our colleagues with respect and kindness. Our culture fosters an environment of trust, transparency, and collaboration. We prioritize and encourage internal growth and professional development.
Castle Biosciences is an equal opportunity employer as to all protected groups, including protected veterans and individuals with disabilities. 
If you have a disability and you believe you need a reasonable accommodation in order to search for a job opening or to submit an online application, please e-mail <a href="mailto:ReasonableAccommodationsRequest@castlebiosciences.com" target="_blank">ReasonableAccommodationsRequest@castlebiosciences.com</a>.
This email was created exclusively to assist disabled job seekers whose disability prevents them from being able to apply online. Only messages left for this purpose will be returned. Messages left for other purposes, such as following up on an application or technical issues not related to a disability, will not receive a response.
** No third-party recruiters, please Job Posted by ApplicantPro

Senior Scientist, Pipeline (FWD)(PIT)

<h3>Job Description</h3>
Job Description
Flourish Research is looking for motivated, talented, creative individuals who want to learn and grow in their careers while contributing to research that changes lives!&nbsp;&nbsp;We offer an excellent comprehensive benefits package, a supportive and collaborative work environment, and endless growth opportunities. We are actively hiring Clinical Research Assistants at our Covina site location. This location has been serving the Greater LA community since 2010 and specializes in Cardiovascular and Metabolic clinical trials. The&nbsp;Research Assistant&nbsp;is to assist under the direct supervision of the Site Director or Clinical Research Coordinator (CRC) in clinic supporting activities and perform duties and procedures related to the start-up, conduct, and close-out phases of clinical research protocols&nbsp;while providing an impeccable patient experience in every single interaction. Shift:&nbsp; Monday-Friday, 8:30 AM - 5 PM (occasional weekends) Location:&nbsp;&nbsp;315 N 3rd Ave #103, Covina, CA 91723 Compensation:&nbsp; $23-$33/hr - depending on experience Benefits:&nbsp; Health, dental, and vision insurance plans, 401(k) with 4% match, tuition reimbursement, parental leave, referral program, employee assistance program, life insurance, disability insurance, and 15 days of PTO + 10 company holidays. RESPONSIBILITIES
<ul>
<li>Professionally represent Flourish Research in all interactions with patients, sponsors, and clinical partners.</li>
<li>Review study protocols and support protocol-specific patient visits and procedures.</li>
<li>After training, accurately document patient assessments, observations, and test results per protocol and regulations.</li>
<li>Obtain and document informed consent in accordance with federal, IRB, and GCP requirements.</li>
<li>Help recruit, screen, schedule, and follow up with study subjects to meet enrollment and visit timelines.</li>
<li>Maintain complete and accurate source documents, CRFs/eCRFs, and other study records.</li>
<li>Protect patient and study confidentiality and promptly report adverse events to appropriate team members.</li>
<li>Assist with investigational product and study supply accountability and documentation.</li>
<li>Communicate regularly with the Team Lead, CRCs, Site Director, PI, and study team and document as required.</li>
<li>Participate in required training, stay current on regulations, and perform duties safely, efficiently, and as assigned.</li>
<li>Other duties as assigned by leadership</li>
</ul>
QUALIFICATIONS
<ul>
<li>Associate's degree in Science or equivalent clinical research experience; Bachelor’s degree preferred.</li>
<li>1–3+ years of experience in clinical or biological research.</li>
<li>ECG, phlebotomy, and other protocol-related technical skills preferred.</li>
<li>Solid understanding of clinical research methods and GCP/regulatory concepts.</li>
<li>Strong oral and written communication skills; able to collaborate across research teams.</li>
<li>Proficient with Office 365 and general computer applications.</li>
<li>Demonstrates professionalism, strong work ethic, integrity, and attention to detail.</li>
<li>Adaptable team player who can take on additional tasks, support process improvements, and help train new hires.</li>
</ul>
Flourish Research offers an excellent comprehensive benefits package, a supportive and collaborative work environment, and endless growth opportunities. Apply today to learn more about how you can join us in our mission to save and improve the lives of others! Flourish Research is where clinical trials thrive. Flourish Research represents one of the industry's most progressive and diversified clinical trial companies with robust capabilities in the therapeutic areas of cardiology/metabolic disorders/renal, CNS, pulmonology, and vaccines. At Flourish Research, we strive toward excellence. In clinical trials and healthcare, excellence means everyone deserves the best care, regardless of their race, color, gender identity, religion, ethnicity, physical abilities, age, sexual orientation, or veteran status. We embrace employees, customers, and patients from these underrepresented groups to help make this vision a reality. Flourish Research is driven by a diverse and inclusive community of passionate people who are committed to improving the quality of life of communities around the world. Flourish is committed to a safe work environment where all employees, customers, and patients are included, and treated with dignity and respect. Flourish Research strives to build an organization that attracts and leverages diversity in our staff, which reflects the diversity of our local communities. We promote education, acceptance, and inclusion because there is beauty in diversity. The more diversity we have in our team, the more unique perspectives, and ideas we share, and the better prepared we are to serve our communities. WE SEE YOU. WE ARE YOU. WE EMBRACE YOU. WE CELEBRATE YOU! It is the policy of Flourish Research not to discriminate against any applicant for employment, or any employee because of age, color, sex, disability, national origin, race, religion, or veteran status.
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tiZG3JD4Jk

Research Assistant

<h3>Job Description</h3>
Job Description
Entry Level Chemist needed in Mansfield, TX!
Part Time Opportunity
Description:
<ul>
<li>Perform Analytical Testing on R&amp;D Products</li>
<li>Keep Laboratory clean</li>
<li>Follow all regulatory guidelines</li>
</ul>
Pay:&nbsp;20.00-24.00 hourly depending on experience
Instrumentation/Testing:
<ul>
<li>Titrations</li>
<li>Ph</li>
<li>Viscosity testing</li>
<li>GC</li>
</ul>
Schedule:&nbsp;up to 20 hours a week, schedule is flexible
Contract:&nbsp;12-18 months
Education/Experience:
<ul>
<li>BS in Chemistry - New graduates welcome</li>
</ul>
Job Type &amp; Location
This is a Contract position based out of Mansfield, TX.
Pay and Benefits
The pay range for this position is $18.00 - $24.00/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 Mansfield,TX.
Application Deadline
This position is anticipated to close on Dec 18, 2025.
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.

Entry Level Chemist

<h3>Job Description</h3>
Job Description
Chemical Blender - $20 - $25/hr
Hours: 8am-5pm
We are searching for a Chemical Blender for a company located in Anaheim, CA.
Responsibility:
<ul>
<li>Sets up and starts all packaging operations under their responsibility.</li>
<li>Obtains and understands all documentation for packaging batches.</li>
<li>Pumping and gravity feeding chemicals into specific containers in predetermined quantities. Operates heavy equipment (Forklift; reach and sit down, pumps, hoses, valves, scales, etc.) safely.</li>
<li>Pulls product for work orders and blends and loads, labels, and packages as necessary and completes all required paperwork.</li>
<li>Operates heavy equipment (forklift; reach and sit down, pumps, hoses, valves, scales, etc.) safely</li>
<li>Knowledgeable in DOT/OSHA requirements for Hazardous Materials</li>
</ul>
Qualifications:
<ul>
<li>2-5 years prior chemical manufacturing</li>
<li>Must be able to pass respirator fit test</li>
<li>Ability to lift up to 50 lbs</li>
<li>Strict adherence to PPE requirements at all times</li>
<li>Pass live scan, drug screen, and extensive background check</li>
</ul>
How to Apply:
Choose from one of the following application methods:
<ul>
<li>Email your resume <a href="mailto:toJobs.Lakewood-CerritosCA@expresspros.com" target="_blank">toJobs.Lakewood-CerritosCA@expresspros.com</a></li>
<li>Call our office at (866) 949-4894</li>
<li>Submit your online application at<a href="http://www.expresspros.com/lakewoodcerritosca/" target="_blank">www.expresspros.com/lakewoodcerritosca/</a></li>
<li>Visit our office at 7077 Orangewood Ave., Suite 128, Garden Grove, CA 92841</li>
</ul>
About Us:
Express works with job seekers to help find the right job for their skills and experience. As one of the leading staffing companies in North America, we’re ready to help you take the next step in your career. Whether you are ready for a full-time position, looking for part-time work, or want a more flexible schedule, Express has a wide range of jobs available including:
<ul>
<li>Administrative</li>
<li>Light Industrial</li>
<li>Skilled Trades</li>
<li>Professional positions</li>
</ul>
We are an equal opportunity employer and value diversity, fostering an inclusive workplace for all. Our hiring decisions are based on merit, and we do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, disability status, or genetic information.

Chemical Blender Operator

<h3>Job Description</h3>
Job DescriptionAbout the role:
As a Senior Chemical Engineer, you will provide chemical engineering support at a manufacturing and chemical process facility for equipment, systems and processes for use in commercial nuclear power industry following established practices. The plant is governed under OSHA's Process Safety Management regulation.
You will report to the Senior Manager of Engineering and be located at Ogden, UT. You will support this role 100% onsite.
 Key Responsibilities:
<ul>
<li>Provide direct, daily technical engineering support for manufacturing and chemical operations and maintenance.</li>
<li>Assume lead technical responsibility for design and implementation of new or modified systems. This includes specification of new processes and equipment designs, as well as, overseeing and coordinating installation, fabrication, testing and qualification of new equipment or processes. Ensure compliance to safety and regulatory requirements.</li>
<li>Apply engineering to identify causes of failures in systems and recommended resolutions.</li>
<li>Validate PFD, P&amp;IDs, process design basis and process control requirement.</li>
<li>Participate in process hazard analyses and implement recommendations to reduce the hazards at the facility.</li>
<li>Analyze and recommend use of technological innovations in material, machinery, manufacturing, and chemical processing techniques to solve complex manufacturing and equipment issues.</li>
<li>Develop methods in materials, equipment, and process designs .</li>
<li>Perform engineering calculations to support equipment and process designs including mass and energy balances.</li>
<li>Assume a project leadership role in coordinating efforts of capital projects including coordination across multiple departments to implement project scope, schedule, and capital spending targets.</li>
<li>Address customer and regulatory requirements and concerns.</li>
</ul>
 Qualifications:
<ul>
<li>B.S. in Chemical Engineering</li>
<li>Demonstrated experience in troubleshooting processes and equipment.</li>
<li>5+ Years of engineering experience in a chemical plant</li>
<li>Experience with ChemCAD/ASPEN or equivalent</li>
<li>Working knowledge of PSM/RMP and Process Hazard Analysis</li>
<li>Teamwork skills – including leadership and participation</li>
</ul>

Senior Chemical Engineer

<h3>Job Description</h3>
Job Description
OLH Technical Services, LLC (OLH), a subsidiary of Three Saints Bay, LLC, and a Federal Government Contractor industry leader, is seeking a Forensic DNA Examiner in Quantico, VA.
Position Overview: The Forensic DNA Examiner provides a wide range of forensic examination services in forensic disciplines, including DNA databasing that support the Federal Government. The examiner shall also assist in instrument calibration and validation in compliance with Unit specific and QA standards and policies.
Position Responsibilities:
<ul>
<li>
Specific duties may include, but are not limited to:
<ul>
<li>
Receive and account for boxes of evidence and related materials from contributors.
</li>
<li>
Visually inspect and process evidence and related materials for mitochondrial and/or nuclear DNA as appropriate; isolate and collect materials for analysis from appropriate areas of various evidentiary materials; prepare samples for instrumental analysis, and associate samples with other existing submissions (as appropriate).
</li>
<li>
Make an initial determination of the types of samples suitable for analysis and select appropriate protocols for conducting the examination of materials.
</li>
<li>
Conduct DNA examinations on items of evidence.
</li>
<li>
Calibrate instruments used for forensic examinations and analysis
</li>
<li>
Use LIMS for evidence inventory, tracking, and flow.
</li>
<li>
Maintain proper chain-of-custody of all forensic material under examination.
</li>
<li>
Follow all QA/QC procedures, protocols and adhere to laboratory division policies and procedures related to its accreditation and safety standards.
</li>
<li>
Conduct DNA analysis and comparisons of profiles or sequences as appropriate.
</li>
<li>
Author forensic reports to include all laboratory note and supporting documentation.
</li>
<li>
Provide all generated profiles or sequences in a format necessary for inclusion, storage, and searching of the appropriate DNA databases.
</li>
<li>
Provide all generated profiles or sequences in a format necessary for inclusion, storage, and searching of the appropriate DNA databases.
</li>
<li>
Conduct technical and administrative reviews of all work.
</li>
<li>
Support activities, functions, or duties, as defined in future projects, including future task orders.
</li>
<li>
Research, develop, and author whitepapers and information papers, as required.
</li>
<li>
Perform duties related to safety requirements.
</li>
<li>
Utilize excellent customer relation skills and the ability to effectively communicate with contributors, team members, management, and other partners.
</li>
</ul>
</li>
<li>DNA Examiner personnel must successfully complete an internal training program.</li>
</ul>
Position Requirements:
<ul>
<li>
Education: B.S. degree in biology, chemistry, or related field of Biological Science from accredited university/college.
</li>
<li>
Experience: At least one (1) year as a DNA Examiner in an accredited forensic laboratory.
</li>
<li>
Skills: Knowledge of related sciences such as biochemistry, chemistry, physics, molecular biology, genetics, and mathematics. Basic knowledge of quality control measures to effectively evaluate scientific data resulting from DNA analysis. Knowledge of the uses of computers and the ability to manipulate data for basic statistic evaluation and display.
</li>
</ul>
Position is Located in Quantico, VA
Apply at:&nbsp;<a href="https://phg.tbe.taleo.net/phg01/ats/careers/v2/viewRequisition?org=GATEWAYVENT&amp;cws=55&amp;rid=5114&nbsp;&nbsp;&amp;nbsp" target="_blank">https://phg.tbe.taleo.net/phg01/ats/careers/v2/viewRequisition?org=GATE…</a>;
VEVRAA Federal Contractor
 Three Saints Bay, LLC and its subsidiaries offer a team-oriented working environment and the opportunity to work with exceptional, dedicated industry professionals. We offer our employees a comprehensive benefits package and the opportunity to take part in exciting projects with government and commercial clients, both domestic and international.
 We are an Equal Opportunity Employer. We invite resumes from all interested parties without regard to race, color, sex, sexual preference, religion, creed, national origin, age, genetic information, marital or veteran status, disability, or any other category protected by federal, state, or local law.

Forensic Scientist - Biologist / DNA (5114)

<h3>Job Description</h3>
Job Description
Job description:
What you’ll do: As a Senior Scientist, you will contribute directly as well as guide others to: identify new opportunities, create new material technologies, and commercialize novel materials.
Duties / Responsibilities of this position:
<ul>
<li>Identify and create new technologies in structural and/or environmental sealing polymeric materials and processes through a technically fundamental approach.</li>
<li>Develop fundamental knowledge on the relationship of materials, processes, structures, and properties.</li>
<li>Lead a set of R&amp;D personnel to independently plan and execute research and development projects to explore new technologies, products, or modes of problem solution.</li>
<li>Provide mentorship to less-experienced associates.</li>
<li>Generate and interpret data in context of problem resolution and effectively communicate findings and direction to other departments in the organization.</li>
<li>Maintain and expand expertise in a set of scientific areas, including physical, chemical, analytical, or formulation principles and methods.</li>
<li>Help develop mechanistic understanding of current products and processes.</li>
<li>Cultivate global collaboration in the internal and external scientific community.</li>
<li>Support patent activities through filing activities, patent surveillance, and defense of our intellectual property.</li>
<li>Serve as a champion of safety practices in the laboratory and office environments.</li>
<li>Provide leadership to technicians and specialists.</li>
<li>Very competent with self-directed work.</li>
<li>Construction, maintenance, and safety responsibilities for laboratory workspace and equipment.</li>
</ul>
Job Requirements:
Knowledge/Skills/Abilities:
· BS with 10+ years of product development experience, MS with 5+ years of product development experience, or PhD in the sciences, typically in chemistry or material science.
· At least 5 years of experience leading and mentoring research and development personnel toward the identification and development of new technologies in a business setting.
Select skills in technical/scientific disciplines, as required.
· Very adept at maintaining and improving safety requirements in the laboratory and work space.
· Select skills in technical/scientific disciplines, as required.
· Versed in scientific methods, laboratory apparatus, and communication skills.
Core Competencies:
· Performance Driven
· Communication
· Customer Centric
· Passion/Values
· Innovation
· Safety/Sustainability
· Collaboration
· Leadership
Physical Demands Analysis:
<ul>
<li>Occasional lifting up to 30 lbs.</li>
<li>Occasional carrying up to 30 lbs.</li>
<li>Occasional pushing/pulling up to 30 lbs.</li>
<li>Frequent fine finger movement and handling materials</li>
<li>Frequent gripping and reaching</li>
<li>Occasional climbing stairs/step ladder</li>
<li>Continuous sitting</li>
<li>Continuous use of computer monitor, keyboard, and computer mouse</li>
<li>Frequent standing and walking</li>
<li>Occasional bending, stooping, twisting or balancing</li>
<li>Rare crawling, kneeling, and crouching</li>
</ul>
Environmental Conditions:
<ul>
<li>Inside Work – continuous</li>
<li>Outside Work – rare</li>
<li>Hot/Cold – occasional</li>
<li>Humid/Dry – occasional</li>
<li>Dust/Vapor Fumes – occasional</li>
<li>Hazardous Machines – occasional</li>
<li>Moving Objects – occasional</li>
<li>Sharp hand tools – occasional</li>
<li>Loud Noise – occasional</li>
<li>Working alone – frequent</li>
<li>May be required to wear the following Personal Protective Equipment (PPE): Safety Glasses, Gloves, Sleeves, and Respirator (Dust Mask).</li>
</ul>
Job Type: Full-time
Benefits:
<ul>
<li>401(k)</li>
<li>401(k) matching</li>
<li>Dental insurance</li>
<li>Health insurance</li>
<li>Life insurance</li>
<li>Paid time off</li>
<li>Retirement plan</li>
<li>Tuition reimbursement</li>
<li>Vision insurance</li>
</ul>
Company DescriptionSTART - Specialized Talent Acquisition Recruiting Team. We offer 24/7 staffing services to the Metro Detroit Area. 
<h3>Company Description</h3>
START - Specialized Talent Acquisition Recruiting Team. We offer 24/7 staffing services to the Metro Detroit Area.

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