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<h3>Job Description</h3>
Job Description 
Position Purpose and Objectives
The Analytical Chemist job duties consist of the technical aspects of the department in support of directions from the QC Analytical Lab Supervisor and the Quality Operations Manager. He/She is responsible for ensuring regulatory compliance to FDA Guidelines (DSHEA), customer requirements, and departmental function. The primary responsibility is to develop and validate analytical methods for various dietary finished product matrixes and train analysts and chemists. He/She will support analytical testing of incoming raw materials, in-process samples, stability, and finished goods within the QC Laboratory.
Essential Job Functions
<ul>
<li>Coordinate the testing of raw materials and finished goods with outside labs when required, and allocate results of said testing to the necessary persons.</li>
<li>Develop and perform analytical methods based on adaptations of USP, AOAC, NSF, or other industrial resources.</li>
<li>Write SOPs and methods to meet cGMP’s and GLP.</li>
<li>Validate and qualify laboratory methods including writing of protocols and reports.</li>
<li>Train chemists and analysts on laboratory methods &amp; procedures when requested.</li>
<li>Assist and supervise incoming raw materials and finished product analytical analysis.</li>
<li>Perform daily testing of incoming samples using wet chemical and instrumental techniques, as needed.</li>
<li>Maintain and record analytical data within prescribed notebooks.</li>
<li>Compile analytical testing data and issue testing justification documentation.</li>
<li>Compile lab results and issue completed worksheets for final review.</li>
<li>Prepare various laboratory reagents as required for daily operations.</li>
<li>Order and stock all lab supplies required for operation while keeping cost down through effective sourcing and purchasing.</li>
<li>Ensure accuracy and completeness of all QC logbooks and binders.</li>
<li>Provide peer review of other chemists’ work as needed.</li>
<li>Ensure that the QC lab is kept in good repair.</li>
<li>Communicate issues and non-conformances to the QC Analytical Lab Supervisor and Quality Operations Manager immediately.</li>
<li>Conduct Lab Investigations for all unexpected results.</li>
</ul>
Knowledge, Skills, and Abilities Required
<ul>
<li>Must be Proficient in PC functions, (WORD, EXCEL, ACCESS, POWERPOINT, etc.) and Empower software.</li>
<li>Must be well organized and detail oriented.</li>
<li>Demonstrate good verbal and written communication skills.</li>
<li>Be familiar with and demonstrate excellent advanced laboratory problem solving skills.</li>
<li>Must be experienced in advanced laboratory testing methods.</li>
<li>Must be knowledgeable in HPLC configuration including column designs, flow rates, reagent variabilities, wavelengths, and detectors.</li>
<li>Must be knowledgeable in solubility factors, oil products, water-based products, and oil/water emulsions and the impacts to testing formulations of these designs.</li>
<li>Must demonstrate Good Laboratory Practice in completing daily work assignments.</li>
<li>Competent in performing mathematical and scientific calculations as they relate to job function. Communication and management skills.</li>
<li>Ability to manage, carry out, and prioritize analytical functions.</li>
<li>Ability to see areas that need improvement and to address them.</li>
</ul>
Supervisory Responsibility
<ul>
<li>Responsible for ensuring all requirements for Analytical functions are met.</li>
<li>Responsible for providing an evaluation of the technical performance of analytical chemists as requested.</li>
</ul>
Working Conditions
<ul>
<li>Working functions are generally limited to the QC lab with some facility work at times.</li>
</ul>
Minimum Qualifications
<ul>
<li>BS Degree in chemistry, analytical chemistry, instrumental analysis, physical chemistry (or extensive analytical laboratory experience in lieu of degree) . </li>
<li>10 years previous laboratory experience.</li>
<li>Driven, intelligent, and motivated to succeed and improve.</li>
<li>Extensive Analytical (HPLC) analysis experience </li>
<li>Excellent people skills, and ability to function under pressure.</li>
</ul>
Success Factors
<ul>
<li>Driven and motivated.</li>
<li>Technical leadership. </li>
<li>Intelligent and displays aptitude.</li>
<li>Problem solving skills. </li>
<li>Detail oriented. </li>
<li>Self-motivated team player. </li>
<li>Well organized. </li>
<li>Willingness to cooperate and work with other departments.</li>
</ul>
Benefits
<ul>
<li>Retirement plan 401(k) - 401(k) matching</li>
<li>Dental, Vision, Health, Short/long term disability and Life insurance</li>
<li>Paid time off</li>
<li>Holiday</li>
</ul>

QC Analytical Chemist

<h3>Job Description</h3>
Job Description
NOVA Engineering &amp; Environmental is seeking an experienced Senior Geotechnical Engineer (PE) to join our Fort Lauderdale, FL office. The ideal candidate will have a strong background in Geotechnical Engineering, Construction Materials Testing, and Special Inspections on a wide variety of projects. This role involves acting as a senior project manager and technical reviewer for technical reports after they are sent to clients, ensuring accuracy and compliance with industry standards.
NOVA works on a diverse range of projects including commercial, industrial, retail, government, office, transportation, and residential developments. Our team is dedicated to delivering high-quality solutions and exceptional client service.
Key Responsibilities:
<ul>
<li>Lead and manage geotechnical engineering projects from inception to completion.</li>
<li>Conduct and oversee special inspections and construction materials testing projects.</li>
<li>Review and approve technical reports for both geotechnical engineering and construction materials testing projects, ensuring they meet client and regulatory requirements.</li>
<li>Provide expert guidance and mentorship to junior engineers and technical staff.</li>
<li>Collaborate with project managers and clients to develop project scopes, budgets, and schedules.</li>
<li>Ensure all projects comply with local, state, and federal regulations.</li>
<li>Participate in business development activities, including proposal preparation and client presentations.</li>
</ul>
Qualifications:
<ul>
<li>Professional Engineer (PE) license is required.</li>
<li>Bachelor's degree in Civil Engineering, Geotechnical Engineering, or a related field.</li>
<li>Minimum of 5 years of experience in geotechnical engineering, special inspections, and construction materials testing.</li>
<li>Strong knowledge of industry standards and regulations.</li>
<li>Excellent written and verbal communication skills.</li>
<li>Proven ability to manage multiple projects and meet deadlines.</li>
<li>Strong analytical and problem-solving skills.</li>
<li>Proficiency in relevant engineering software and tools.</li>
</ul>
Benefits &amp; Perks:
<ul>
<li>Comprehensive group medical insurance, including health, dental and vision</li>
<li>Opportunity for professional growth and advancement</li>
<li>Certification reimbursement and incentive program</li>
<li>Paid time off</li>
<li>Company–observed paid holidays</li>
<li>Company paid life insurance for employee, spouse and children</li>
<li>Company paid short term disability coverage</li>
<li>Other supplemental benefit offerings including long-term disability, critical illness, accident and identity theft protection</li>
<li>401K retirement with company matching of 50% on the first 6% of employee contributions</li>
<li>Wellness program with incentives</li>
<li>Employee Assistance Program</li>
</ul>
NOVA is an Equal Opportunity Employer. All qualified candidates are encouraged to apply. NOVA does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, ancestry, marital status, veteran status or any other characteristic protected by law.
About Nova:
Established in 1996, NOVA was originally founded to provide Environmental Consulting, Geotechnical Engineering, and Construction Materials Testing and Inspection services to the design and construction community, largely in the southeastern United States. Since our founding, NOVA has added additional service lines such as Facilities and Building Envelope, Forensics, Municipal and more. We are dedicated to providing a wide variety of projects and services with an emphasis on collaboration and safety. We offer a stimulating and inspiring work environment where our employees are recognized for their efforts and achievements and are mentored for professional growth.
Currently, NOVA employs 650+ personnel in 18 offices serving clients throughout the southeastern United States and beyond. Our firm has professional and administrative support staff that includes registered professional engineers, registered professional geologists, environmental scientists, registered roof observers, LEED accredited professionals, soil/foundation engineers, laboratory specialists, materials technicians, ICC-certified inspectors, NICET-certified technicians, and AWS-certified welding inspectors. NOVA’s facilities include AASHTO-accredited laboratories in soils, concrete, aggregate and hot-mix asphalt testing/inspection. We also have CCRL-inspected laboratories for concrete sampling, curing, and testing. NOVA will continue to expand its reach and reputation as a leader in the testing, inspection, and consulting fields with a strong legacy of quality and integrity by promoting our best internal resources and recruiting a diverse culture of valued and exceptional talent.
#LI-JT

Senior Geotechnical Engineer (PE)

<h3>Job Description</h3>
Job DescriptionDocumentation Specialist/QA Support
Job Description
This individual plays a vital role in performing and assisting in coordinating resource allocation to conduct stability administration activities, ensuring accuracy and compliance against pre-defined standards and specifications. This role is essential for maintaining the integrity of all records in accordance with cGMP requirements and providing effective coordination and support for both external and internal audits.
Responsibilities
Organizing and Tracking Samples:
<ul>
<li>Help manage and schedule stability tests (how products hold up over time).</li>
<li>Make sure everything is done accurately and on time.</li>
</ul>
Handling Paperwork and Records:
<ul>
<li>Keep track of documents and make sure they follow strict rules (cGMP).</li>
<li>Store and manage records properly so they’re easy to find and audit.</li>
</ul>
Supporting Audits:
<ul>
<li>Help prepare for inspections from internal teams or outside agencies.</li>
<li>Make sure everything is in order and compliant.</li>
</ul>
Monitoring Product Stability:
<ul>
<li>Track how products perform over time (Real Time Stability).</li>
<li>Spot trends or issues using basic data analysis.</li>
</ul>
Reporting Issues Quickly:
<ul>
<li>If something goes wrong (like a failed test), report it in the system within one business day.</li>
</ul>
Helping Improve the Lab:
<ul>
<li>Take part in projects to make the lab run better or more efficiently.</li>
</ul>
Keeping the Workplace Safe:
<ul>
<li>Follow safety rules while making sure the work meets quality standards</li>
</ul>
Essential Skills
<ul>
<li>Proficiency in laboratory operations.</li>
<li>Experience with audit processes.</li>
<li>Knowledge of stability testing and document control.</li>
<li>Ability to track follow-up activities associated with Real Time Stability.</li>
<li>Skill in trending and statistical analysis of stability data.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Experience with resource allocation to conduct stability administration activities.</li>
<li>Capability to ensure accuracy and compliance against pre-defined standards and specifications.</li>
</ul>
Work Environment
The Laboratory Associate will work in a laboratory/office environment. The schedule is Monday to Friday, 8 AM to 5 PM
Pay and Benefits
The pay range for this position is $17.00 - $18.00/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 Ormond Beach,FL.
Application Deadline
This position is anticipated to close on Sep 22, 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.

Laboratory Associate

<h3>Job Description</h3>
Job Description
A&nbsp;healthcare facility&nbsp;in&nbsp;City,&nbsp;State, is in need of a Locum Medical Physicist to join its Radiation Oncology team and provide physics consultation to all Radiation Oncology personnel concerning aspects of patient care and treatment.&nbsp;Insert statement(s) about key responsibilities/requirements specific to to client, team, or requirements.
 
Requirements
X Education Level&nbsp;in Medical Physics
X Certification / License
X&nbsp;years of experience
X state license (if required by state)
Current RAM license (if applicable)
Strong presentation skills, ability to communicate effectively to a group via phone/face to face
Strong technical aptitude
Strong analytical, math, physics skills, including data collection, problem-solving
The ability to resolve complex technical issues independently
Self-motivated, organized
Detail-oriented
Possess strong time management skills
Other requirements specific to job/client
 
Estimated Pay
We provide a competitive range of compensation for this position. Actual compensation is influenced by a wide array of factors including, but not limited to, skill set, level of experience and specific office location.&nbsp;It is possible that this position can be hired outside of the salary range based on experience.
 
Benefits of Working with Epic OncologyStaffing
Competitive Compensation
Travel and Lodging Support
Per Diem Allowances
Weekly Direct Deposit
Online Access to Your Payroll Account
Health Insurance, Including Dental and Vision Options
Life Insurance Options
401k Matching Program
Experienced Radiation Oncology Recruiters
Deep networks to connect you with the most up-and-coming, recognized positions in your field
Exclusive searches with direct connections to decision makers
 
About Epic Oncology Staffing
With more than 20 years of experience in improving the efficiency of oncology departments, Epic Oncology Staffing has become a prominent name in Radiation Oncology Services across the nation. We have successfully placed over 10,000 healthcare professionals, which is a testament to our expertise. Our unique partnership approach enables our placement experts to gain a deep understanding of our candidates' career goals and objectives, allowing us to identify the ideal opportunities for them.
 
﻿If you are interested in this job opportunity, please apply now or contact us for more information.
 
 
By applying for this position, you agree that any calls from Epic Staffing Group and its subsidiaries may be monitored or recorded for training and quality assurance purposes.
Epic Staffing Group provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, housing, age, disability or genetics.
We will consider all qualified applicants for employment, including those with criminal histories, in a manner consistent with the requirements of applicable federal, state, and local laws.

Physicist

<h3>Job Description</h3>
Job DescriptionDescription:
Provides microbiological support for all manufacturing and support activities. Participates in activities such as environmental monitoring, media fills, microbiological and chemical sampling of utilities and services, and other tasks as assigned. Performs microbiological and related testing including, but not limited to, bio burden BET, MLT, Microbial Identification, Sterility, TOC, pH, Conductivity, Utility Monitoring, and Growth Promotion. Perform quarterly and annual data analysis, archiving and trending of Environmental Monitoring and utilities data. Serves as mentor to member(s) of the Microbiology staff. 
Requirements:
<ul>
<li>Understand and perform microbiological techniques including, but not limited to, Bio burden, Sterility, Endotoxin, TOC, Water Testing, Environmental Monitoring, Growth Promotion and visual inspections.</li>
<li>Create or revise departmental SOPs.</li>
<li> Maintain the quarterly report for the Microbiology lab tracking all Alerts, Actions, or OOS.</li>
<li>Perform all relevant microbiology tests and reports</li>
<li>Maintain, review and approve all equipment log books associated with the Microbiology Lab.</li>
<li>Keep Microbiology area in a tidy, organized and in a sanitary condition at all times.</li>
<li>Ensure that all supplies related to microbiological monitoring and testing are maintained in sufficient quantities and within shelf-life.</li>
<li>Create, execute and compile verification protocols and reports related to Microbiology.</li>
<li>Leads laboratory investigations for out of specification (OOS) microbiological testing results, and other microbiological laboratory non-conformances.</li>
<li>Prepare deviations, investigations, OOS, change control, work orders and test reports.</li>
<li>Excellent verbal and written communication skills.</li>
<li>Assist in ordering/inventory of lab supplies.</li>
<li>Subject Matter Expert regarding aseptic technique and processing and contributes to related training.</li>
<li>Optimize procedures and methods in relation to microbiological monitoring.</li>
<li>Maintains microbiological results and reports, tracks, trends and metrics ad hoc and per established schedules.</li>
<li>Monitor compendia and other standards to ensure procedures and processes are current with industry standards.</li>
<li>At the request of Quality Assurance Department, assist in vendor audits.</li>
<li>Maintains currency with FDA, EMA and other CGMP standards and industry trends. </li>
</ul>
Education and Experience Required:
<ul>
<li>B.S. in a scientific discipline. </li>
<li>Minimum 3 to 5 years working in a FDA/EMA regulated environment. </li>
<li>Excellent writing skills, judgment, integrity, investigation (as in OOS), ability to work independently.</li>
</ul>
This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee. Duties, responsibilities and activities may change or new ones may be assigned at any time with or without notice.

Microbiologist I

<h3>Job Description</h3>
Job DescriptionDescription:
Job purpose
 
The Quality Control Microbiologist (QCM) is responsible for performing and managing quality control testing results for human tissue donors, recovered, and acquired tissue, and final processed grafts. Must perform applicable QC testing and related functions in accordance with standard operating procedures, all applicable federal and state regulatory and accrediting standards requirements. Communicates directly with contracted laboratories and internal departments to ensure testing results are available, accurate and communicated in a timely manner.
 
Duties and responsibilities
 
<ol>
<li>Perform Quality Control (QC) testing of tissue samples including, but not limited to, Cell Viability testing, bioburden of recovery cultures, sterility testing, in-process bioburden, method suitability, gram staining, biochemical testing, and microbial identification using VITEK 2.</li>
<li>Perform QC release testing of microbiology media, materials, and reagents. </li>
<li>Review test results and manage Biomaterial Tracking System (BTM) according to internal standard procedures to ensure proper management, tracking, and disposition of grafts. </li>
<li>Communicates directly with outside laboratories (if needed) to obtain records and internally with Operations and Quality Assurance to ensure appropriate samples are available for testing and results are properly communicated. </li>
<li>Maintain proper documentation and trend analysis of QC test results.</li>
<li>Support environmental monitoring (EM) of the facility by reading environmental monitoring plates, processing samples for identification, maintain records and trend analysis.</li>
<li>Support water system testing of the facility by testing for total organic carbon (TOC), bioburden, endotoxin, and conductivity. Reading plates and processing samples for identification.</li>
<li>Perform laboratory cleaning and maintenance of equipment as needed. </li>
<li>Support and execute qualification / validation protocols of QC testing methods as applicable.</li>
<li>Review testing reports, protocols, and procedures to ensure compliance with internal requirements and applicable regulations.</li>
<li>Assist Manager in maintaining the laboratory stock of media and reagents and ordering laboratory supplies.</li>
<li>Participate in the on-call weekend alternating schedule.</li>
</ol>
General Responsibilities
<ol>
<li>Create, review, and edit QC procedures according to AATB, FDA and USP guidelines.</li>
<li>Maintain knowledge of appropriate federal and state regulatory and statutory requirements as well as accrediting body requirements.</li>
<li>Responsible for reporting all variances, errors, and deviations to QA management.</li>
<li>Participate in the investigation complaints and deviations including the formulation and implementation of corrective actions.</li>
<li>Participate in audits and inspections, as needed.</li>
<li>Maintain trend analysis and metrics of testing results.</li>
<li>Support accreditation and licensing activities.</li>
<li>Perform other duties as assigned by the QC Manager and/or Director of Quality Control.</li>
</ol>
 
Requirements:
Qualifications
 
Education/Experience: Bachelor’s in Science, Microbiology degree preferred or Associate in Science with two years of experience. An equivalent combination of education and experience in a regulated environment (e.g., Biologics, Microbiology, Pharmaceutical, etc.) will be considered. 
 
Laboratory Skills: Aseptic techniques, bioburden, sterility, growth promotion, gram staining, microbial identification, and microbiology testing. 
 
Other Skills: Excellent interpersonal, verbal, and written communication skills required. 
Must demonstrate excellent organizational and record keeping skills. 
Must be detail oriented with the ability to multi-task in a high-pressure environment. 
Must gain knowledge of all regulations, laws, and/or standards that govern the tissue banking industry within the first year of employment. 
Computer and Equipment: Proficient in Microsoft Office. 
Working knowledge of Vitek® 2, Sievers M9 Laboratory TOC Analyzer, Conductivity Meter and Cell Analyzers. 
 
 
Working conditions
 
Primarily, a fast pace, lab-oriented work environment. Evening and weekend work may be required.
 
Physical requirements
 
While performing the duties of this job, the employee is regularly required to sit or stand for prolonged periods of time. The employee may occasionally be required to pull, lift and/or move up to 20 pounds.
 
Direct Reports
No direct reports.

Quality Control Microbiologist

<h3>Job Description</h3>
Job DescriptionDescription:
Bauer Foundation Corp. (BFC) is a Florida corporation and the U.S. subsidiary of the world-wide operating Bauer Group based in Schrobenhausen, Germany. The Bauer Group is a world- renowned foundation contractor, designer, and builder of the world’s finest foundation equipment.
 
BFC, as part of the Bauer construction division, is a leader in the execution of complex excavation pits, ground improvement, deep foundations, and vertical seals, utilizing the most up to date equipment and installation techniques. Bauer Foundation Corp. provides all types of foundation solutions and services for industrial, commercial, residential, and governmental construction projects. Bauer Foundation Corp. promotes Bauer services and technology throughout the entire United States.
 
BFC is looking for a dynamic individual with experience as an Estimating Manager, in the special foundation industry. If you have a passion for progress, we want to hear from you!
 
Reports to: Operations VP and CEO
Location: Odessa Corporate office
Schedule: 8a-5p M-F with travel as needed
 
Job Summary:
The Estimating Manager manages the estimating function and develops standards, procedures, tools, and methodologies to produce cost estimates for technical projects based on work scope, specifications, and proposal or contract requirements. 
This position is responsible for calculating civil construction cost estimates, and you will be involved in the planning, development, negotiation, and contract execution of a project.
 
 
Requirements:
Supervisory Responsibilities:
• Oversees the operations of the Estimating department.
 
 
Responsibilities of this Position:
• Determining the total cost of materials, equipment, utilities, and labor for construction projects.
• Assess cost effectiveness of products, projects or services, tracking actual costs relative to bids as the project develops.
• Researching construction documents and analyzing specifications.
• Preparing estimates for planning, organizing, and scheduling project work.
• Managing pre-qualification and pre-bid submissions.
• Preparing estimates to meet project goals, such as setting work hours, sequencing tasks, obtaining materials, and securing the best deals with vendors and subcontractors.
• Ensuring that relevant documents and budgets are submitted before a bid deadline.
• Regularly reporting to Senior Leadership and keeping clients updated on the project status.
• Preparing estimates to meet project goals, such as setting work hours, sequencing tasks, obtaining materials, and securing the best deals with vendors and subcontractors.
• Ensuring that relevant documents and budgets are submitted before a bid deadline.
• Regularly reporting to Senior Leadership and keeping clients updated on the project status.
• Facilitate turning over the project to the Operations Team after project award.
• Identify and implement improvements to processes, procedures, and products.
• Establish preliminary project schedules.
• Maintain records of all project details and documentation, including contracts, bids, and correspondence.
• Manage a team of Estimators to ensure efficient and effective work performance.
• Ensure contractors comply with safety standards and local regulations.
• Perform other duties as assigned.
 
 
Qualifications and Requirement:
• Bachelor’s degree in Civil Engineering, Construction Management, or similar field.
• Minimum 10 years of estimating and/or project management experience particularly in heavy civil and special foundations.
• Ability to work closely with other project teams and stakeholders.
• Extensive knowledge of best industry practices and standards.
• Strong analytical skills
• Excellent communication skills
• Strong attention to detail
• Ability to read, understand and organize construction plans and specifications
• Strong organizational and problem-solving skills
• Ability to work independently and with minimal structure while exercising great judgment
• Strong ability to multitask, prioritizes, and works well under pressure to meet established deadlines
• Advanced knowledge in Microsoft Office (Excel, Access, Project, Power Point, Word, Outlook).
 
Compensation and benefits:
Competitive salary; commensurate with experience.
 
Benefit packages available – health insurance, life insurance, short-term disability, 401(k) plan with employer match, paid holidays and vacation, paid parental leave, and tuition assistance
 
Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor an employment Visa at this time.
 
BAUER Foundation Corp. is a DFWP and 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 veteran status.
 
#LI-DNI

Estimating Manager - Geotechnical Foundations

<h3>Job Description</h3>
Job DescriptionDescription:
Summary/Objective Lab Section Supervisors plan, manage and supervise the activities of Medical Laboratory Assistants and Technicians. In addition to performing the same essential job functions as the Technologist/Technician, Supervisors also make schedules, purchase supplies, maintain equipment inventory, and evaluate staff job performance.
Essential Functions
<ul>
<li>Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.</li>
<li>Assures quality control and quality assurance programs meet requirements set forth by all regulatory agencies</li>
<li>Performs and supervises all routine and complex tests as ordered by the clinician</li>
<li>Develops and updates department policy and procedure manuals</li>
<li>Establishes and reviews that a scheduled preventive maintenance program is performed and documented on all equipment and testing systems</li>
<li>Assures that Proficiency Testing surveys are performed and reported accurately and timely. Provides appropriate documentation of corrective action for results outside of acceptable limits</li>
<li>Provides technical support and information to other laboratory staff members and clinicians</li>
<li>Resolve problems and issues as they arise and keeps Laboratory Manager and Director of Laboratory Services informed of such situations</li>
</ul>
Supervisory Responsibility
This position manages Medical Laboratory Technologists, Medical Laboratory Technicians, and Laboratory Assistants and is responsible for the performance management of the employees within the department.
<ul>
<li>Work Environment &amp; Physical Demands Lifting – Must be able to lift above shoulder height up to 10 lbs. as needed. In addition, must be able to lift up to 30 lbs. on a daily basis, multiple times a day replacing instrumentation reagents. For items weighing more than 30 lbs., a dolly or cart must be utilized.</li>
<li>Pushing/Pulling – Must be able to push/pull up to 30 lbs. on a daily basis. For items weighing more than 30 lbs., a dolly or cart must be utilized.</li>
<li>Carry weight, lift – Must be able to carry reagents to instrumentation weighing up to 30 lbs. on a daily basis. For items weighing more than 30 lbs., a dolly or cart must be utilized.</li>
<li>Bending/Twisting/Stooping – Must be able to bend/twist/stoop to replace reagents, remove instrumentation waste, file racks of specimens, and in storing of supplies</li>
<li>Sitting/Standing – Must be able to constantly stand and walk for several hours in duration. Sitting is appropriate based on workload volume and particular testing being performed (example – microscopic work)</li>
<li>Smells – Ability to tolerate strong odors when disposing of specimens or reagents</li>
<li>Dexterity – Must be able to perform a large amount of repetitive hand movements by utilizing computers and opening/closing specimen containers</li>
</ul>
Travel Based on staffing needs, staff may be required to commute to other regional laboratories to provide laboratory coverage which may also require changing work hours, additional shifts and/or weekends.
Requirements:
 
Required Education and Experience Bachelor of Science Degree in Medical Technology or related science degree along with the successful completion of an approved formal training program in Medical Technology.
Preferred Education and Experience A minimum of 6 years experience as a Medical Technologist plus previous experience as a general supervisor in a clinical laboratory setting in the related specialty.
Additional Eligibility Qualifications
Active State of Florida Supervisor’s license in Hematology, Chemistry, Serology, Microbiology, and Molecular Pathology. Complete knowledge of Quality Assurance, Quality Control, and Proficiency testing programs. Complete understanding of compliance with all regulatory agencies along with the applicable State and Federal laws and regulations governing the practice of the Laboratory.

LAB SECTION SUPERVISOR - FULL TIME

<h3>Job Description</h3>
Job DescriptionDescription:
 An excellent opportunity exists to work for a government contractor with competitive compensation and work-life balance. Posterity Group is seeking experienced Therapeutic Medical Physicist with the West Palm Beach VA Medical Center. 
 
Duties include but are not limited to:
<ul>
<li>Performs the clinical practice of therapeutic medical physics in its entirety with considerable discretion and independent judgment.</li>
<li>Oversees the chain of events from image acquisitions to treatment verification and delivery to assure consistent geometry and optimal treatment delivery.</li>
<li>Provides assessments and monitoring of image quality throughout this chain of events.</li>
<li>Acquires and stores data for treatment plans such that the information is secure and retrievable</li>
<li>Designs and/or oversees the design, and fabrication of treatment aids and beam modifies as needed.</li>
<li>Calculates and/or supervises the calculation of dose distributions and machine settings for patient treatments.</li>
<li>Establishes protocols to ensure high quality patient dosimetry and determination of actual delivered dose.</li>
</ul>
Requirements:
Education. Master's degree or higher in a physics, science, or engineering discipline recognized by an accredited college or university with at least 30 semester hours in medical physics, health physics, radiological science, physics, engineering, chemistry, or biology; or an equivalent foreign degree and coursework substantiated by the National Association of Credential Evaluation Services. 
Board Certification. Persons hired or reassigned to TMP positions in the VHA must be board certified in the field of therapeutic medical physics by an approved certifying body. The board certificate must be current and the applicant must abide by the certifying body's requirements for continuing education. 
Approved Certifying Bodies(a) The American Board of Radiology (ABR) in any of the following field titles:
<ul>
<li>1. Therapeutic Medical Physics</li>
<li>2. Therapeutic Radiologic or Therapeutic Radiological Physics</li>
<li>3. Radiologic Physics or Radiological Physics</li>
</ul>

Therapeutic Medical Physicist

<h3>Job Description</h3>
Job DescriptionDescription:
Attention all hearing conservationists, we are calling on you to help us provide services to our Military Service members. CAOHC is required.
We will primarily work weekends, with some occasional weekdays on an "as needed basis".
We provide health readiness services to meet the medical and dental requirements to maintain a deployable military force for the following:
<ul>
<li>U.S. Army Reserve (USAR)</li>
<li>Army National Guard (ARNG)</li>
<li>U.S. Navy Reserve (USNR)</li>
<li>U.S. Marine Forces Reserve (MARFORRES)</li>
<li>U.S. Coast Guard Reserve (USCGR)</li>
<li>Air National Guard (ANG)</li>
<li>U.S. Air Force Reserve (USAFR)</li>
</ul>
Responsibilities:
<ul>
<li>Perform manual audiograms and evaluations.</li>
<li>Review test results for quality control, contrast, detail, and adequate demonstration of hearing.</li>
</ul>
Requirements:
<ul>
<li>Current certification as a hearing technician or occupational hearing conservationist</li>
<li>Experience within the last two years working as a Audiology Technician</li>
<li>Experience working with military - preferred</li>
<li>CAOHC is required</li>
<li>Experience working with DOEHRS and BENSON software - preferred</li>
<li>CPR/BLS certification is preferred</li>
<li>Proficient with computer programs</li>
</ul>
With over three decades of experience, we are a trusted industry leader. Our experienced team of clinicians and logistics professionals are dedicated and strive to do the right thing for our partners and their members every time. Because of this commitment, we’ve set a new standard of care delivery through our fixed-clinic, mobile treatment center, telemedicine, and portable deployment models.
Join our team and become a part of a bridge for better health.
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If you are made a conditional offer of employment, you will be required to undergo background check (including criminal record check) and drug screening. We use E-Verify in our hiring process.
DOCS Health is committed to ensuring equal employment opportunity. All employment decisions, policies, and practices are in accordance with applicable federal, state, and local anti-discrimination laws. DOCS Health will not engage in or tolerate unlawful discrimination (including any form of unlawful harassment) on account of a person's sex (including pregnancy), age, race, color, religion, national origin, ancestry, citizenship, physical or mental disability, sexual orientation, gender nonconformity, status as a transgender individual, gender identity, genetic information, marital status, family responsibility, armed services, or any other status protected by law.

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