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city

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<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.
________________________________________
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.

Hearing Conservationist - RHRP

<h3>Job Description</h3>
Date Posted: 2025-09-05 Country: United States of America Location: HFL04: ASG Jacksonville-Blount Island 6061 BF Goodrich Blvd , Jacksonville, FL, 32226 USA Position Role Type: Onsite U.S. Citizen, U.S. Person, or Immigration Status Requirements: The ability to obtain and maintain a U.S. government issued security clearance is required. U.S. citizenship is required, as only U.S. citizens are eligible for a security clearance Security Clearance: DoD Clearance: Secret Our Engineered Polymer Products division, located in Jacksonville, Florida, is a leading manufacturer of advanced, high-performance composite and elastomeric structures for U.S. Navy surface ships and submarines. Whether in the air or underwater, we're pushing the limits of innovation. Collins Aerospace will always be a place where people can come together and make a difference. Want to join us on this important journey. Collins Aerospace is looking for a motivated Quality Engineer - Metrology to join our dynamic team. You will need to be a curious and relentless problem solver bringing your skills and abilities to bear on issues and opportunities arising on our legacy programs. 
<ul>\n
<li>The position is working Onsite at our Blount Island Jacksonville FL facility</li>
\n
<li>Relocation Assistance will be provided.</li>
\n</ul>
\n What You Will Do 
<ul>\n
<li>Perform three-dimensional inspection utilizing Spatial Analyzer software in addition to various traditional metrology tools for in-process inspections and alignments of large complex naval parts.</li>
\n
<li>Write measurement scripts within Spatial analyzer.</li>
\n
<li>Evaluate and prepare metrology reports for customer deliverables.</li>
\n
<li>Independently work and communicate with operations, engineering, management, and other disciplines to ensure timely delivery of measurement results.</li>
\n
<li>Interface with all levels of management and coworkers to resolve technical/quality issues related to internal and external product and process quality performance.</li>
\n
<li>Be the voice of the customer in a manufacturing setting.</li>
\n
<li>Write and help support standard work.</li>
\n
<li>Work alongside existing Quality Engineers to develop an understanding of program requirements and Engineering methodology for future program support.</li>
\n
<li>Perform root cause analysis for non-conformities and improvement process</li>
\n
<li>Support audits in compliance with AS9100 and ISO9001</li>
\n
<li>Investigate the root cause of customer escapes and non-conformances and determine appropriate corrective/preventive actions.</li>
\n
<li>Complete and maintain customer documentation.</li>
\n</ul>
\n Qualifications You Must Have 
<ul>\n
<li>Typically requires Bachelor's degree in Science, Technology, Engineering or Mathematics (STEM)) and a minimum of 2 years of Quality Assurance or/and Quality Control experience OR</li>
\n
<li>Advanced Degree in a related field and minimum 1 year of experience</li>
\n
<li>Experience with GD&amp;T</li>
\n
<li>Able to be flexible around shifts, for training and to maintain workflow, to include overtime.</li>
\n
<li>Experience with ERP Systems</li>
\n
<li>U.S. citizenship is required, as only U.S. citizens are authorized to access information under this program/contract</li>
\n</ul>
\n Qualifications We Prefer 
<ul>\n
<li>Ability to obtain, organize and analyze quality data.</li>
\n
<li>Manage multiple competing priorities simultaneously.</li>
\n
<li>Excellent communication skills, both verbal and written, internal and external.</li>
\n
<li>Basic computer and scripting skills</li>
\n
<li>Experience in SAP</li>
\n
<li>Experience in an AS9100 certified environment or similar operating system certifications (IATF16949, ISO-9001-2015, etc.)</li>
\n</ul>
\n What We Offer 
<ul>\n
<li>Medical, dental, and vision insurance</li>
\n
<li>Three weeks of vacation for newly hired employees</li>
\n
<li>Generous 401(k) plan that includes employer matching funds and separate employer retirement contribution, including a Lifetime Income Strategy option</li>
\n
<li>Tuition reimbursement program</li>
\n
<li>Student Loan Repayment Program</li>
\n
<li>Life insurance and disability coverage</li>
\n
<li>Optional coverages you can buy pet insurance, home and auto insurance, additional life and accident insurance, critical illness insurance, group legal, ID theft protection</li>
\n
<li>Birth, adoption, parental leave benefits</li>
\n
<li>Ovia Health, fertility, and family planning</li>
\n
<li>Adoption Assistance</li>
\n
<li>Autism Benefit</li>
\n
<li>Employee Assistance Plan, including up to 10 free counseling sessions</li>
\n
<li>Healthy You Incentives, wellness rewards program</li>
\n
<li>Doctor on Demand, virtual doctor visits</li>
\n
<li>Bright Horizons, child and elder care services</li>
\n
<li>Teladoc Medical Experts, second opinion program</li>
\n
<li> And more!</li>
\n</ul>
\n Learn More &amp; Apply Now Collins Aerospace, a Raytheon Technologies company, is a leader in technologically advanced and intelligent solutions for the global aerospace and defense industry. Collins Aerospace has the capabilities, comprehensive portfolio, and expertise to solve customers' toughest challenges and to meet the demands of a rapidly evolving global market. Our Advanced Structures team leverages advanced materials and additive manufacturing to develop complex interior and exterior solutions. These solutions ensure structural integrity of the aircraft, help aircraft take off and land, stay trim in the air, move forward, carry cargo and conduct rescues. We delight our customers with superior products and best-in-class service. Our global team is committed to continuous improvement - we work hard to make our solutions lighter-weight, stronger and more technically advanced, so that plane travel can be safer, more affordable, and more sustainable in the years to come. We are looking for the best and brightest to fly and land with us! WE ARE REDEFINING AEROSPACE. Please ensure the role type (defined below) is appropriate for your needs before applying to this role. Onsite: Employees who are working in Onsite roles will work primarily onsite. This includes all production and maintenance employees, as they are essential to the development of our products. Regardless of your role type, collaboration and innovation are critical to our business and all employees will have access to digital tools so they can work with colleagues around the world - and access to Collins sites when their work requires in-person meetings. At Collins, the paths we pave together lead to limitless possibility. And the bonds we form - with our customers and with each other -- propel us all higher, again and again. The salary range for this role is 66,000 USD - 130,000 USD. The salary range provided is a good faith estimate representative of all experience levels. RTX considers several factors when extending an offer, including but not limited to, the role, function and associated responsibilities, a candidate's work experience, location, education/training, and key skills. Hired applicants may be eligible for benefits, including but not limited to, medical, dental, vision, life insurance, short-term disability, long-term disability, 401(k) match, flexible spending accounts, flexible work schedules, employee assistance program, Employee Scholar Program, parental leave, paid time off, and holidays. Specific benefits are dependent upon the specific business unit as well as whether or not the position is covered by a collective-bargaining agreement. Hired applicants may be eligible for annual short-term and/or long-term incentive compensation programs depending on the level of the position and whether or not it is covered by a collective-bargaining agreement. Payments under these annual programs are not guaranteed and are dependent upon a variety of factors including, but not limited to, individual performance, business unit performance, and/or the company's performance. This role is a U.S.-based role. If the successful candidate resides in a U.S. territory, the appropriate pay structure and benefits will apply. RTX anticipates the application window closing approximately 40 days from the date the notice was posted. However, factors such as candidate flow and business necessity may require RTX to shorten or extend the application window. RTX 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, age, disability or veteran status, or any other applicable state or federal protected class. RTX provides affirmative action in employment for qualified Individuals with a Disability and Protected Veterans in compliance with Section 503 of the Rehabilitation Act and the Vietnam Era Veterans' Readjustment Assistance Act. Privacy Policy and Terms: Click on this link to read the Policy and Terms

Quality Engineer/Metrology

<h3>Job Description</h3>
Job Description For more than 65 years, HEICO Corporation has thrived by serving niche segments of the aviation, defense, space and electronic industries by providing innovative and cost-saving products and services. HEICO's high energy culture focuses our Team Members' on providing high quality products and services to our customer base. Our leadership approach creates a dynamic environment that continually challenges our Team Members to perform at their best. For four consecutive years, Forbes Magazine ranked HEICO as one of the 200 "Best Small Companies." HEICO Corporation offers competitive compensation, paid vacation and holidays, an excellent 401K plan with company match, and medical, dental, life, and disability insurance. ROLE : The Senior CMM Programmer/ Metrology Technician is primarily responsible for assisting Project Engineers with reverse engineering, production support and development of inspection plans. Will create inspection programs for CMM using PC-DMIS and perform first-article inspection of assigned components. ESSENTIAL DUTIES AND RESPONSIBILITIES include the following: 
<ul>
<li> Programming, validation and operation of all metrology equipment, including CMM, Video Measure Machine, Optical/laser Scanners, Form Tracer and Layout </li>
<li> Collaborate with Engineering to develop reverse engineering dimensional data and provide </li>
<li> feedback on dimensioning of engineering drawings </li>
<li> Provide technical assistance to inspection as necessary </li>
<li> Assist with supplier dimensional correlation issues </li>
<li> Advise on selection and application of inspection equipment </li>
<li> Ability to perform job duties with no supervision </li>
<li> Perform other duties, as assigned </li>
</ul>
\n Requirements EDUCATION : 
<ul>
<li> High School Diploma or GED Equivalent Required </li>
<li> Associates or Bachelors preferred with formal training in CMM programming and GD&amp;T preferred </li>
</ul>
 EXPERIENCE: 
<ul>
<li> 5+ years related work experience required </li>
<li> Layout inspection experience required </li>
<li> Ability to validate all inspection methods </li>
<li> Detailed working knowledge of ASME Y14.5 GD&amp;T and drawing interpretation required </li>
<li> Experience with PC-DMIS CMM inspection software is required. </li>
<li> Solidworks or other 3D CAD experience desired </li>
<li> Strong work ethic (flexibility to work occasional long hours) </li>
<li> Must have a high attention for detail and accuracy </li>
<li> Must work well with others and be flexible in handling multiple tasks </li>
<li> Assist all departments with challenging inspection methodologies </li>
<li> Training in Geomagic and experience with optical (blue light or equiv.) scanner technology highly preferred </li>
<li> Practiced in self verification/validation of methods and measurements </li>
</ul>
 CERTIFICATES, LICENSES, REGISTRATIONS: ASQ Certified Quality Technician Preferred SPECIALIZED KNOWLEDGE OR ABILITIES : 
<ul>
<li> Language: English, Ability to read, analyze, and interpret general relevant periodicals, professional journals, technical procedures, or governmental regulations. Ability to write reports, business correspondence, and procedure manuals. Ability to effectively present information and respond to questions from groups of managers, clients, associates, customers, and the general public. </li>
<li> Computer Skills: MS Office including Excel, 3D CAD experience (Pro-E, Solidworks, etc.), PC DMIS </li>
<li> Mathematical Skills: Ability to work with mathematical concepts such as probability and statistical inference, and fundamentals of plane and solid geometry and trigonometry. Ability to apply concepts such as fractions, percentages, rations, and proportions to practical situations. </li>
<li> Reasoning Abilities: Ability to define problems, collect data, establish facts, and draw valid conclusions. Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables </li>
</ul>
 PHYSICAL DEMANDS : Ability to access surface plates and equipment from multiple angles to accommodate widely varying components. Frequent use of hands to finger, handle, or feel parts is required. Bending and twisting occasionally. Lifting required up to 50 pounds. Specific vision abilities required by this job include close vision, color vision, peripheral vision, depth perception, and ability to adjust focus. WORK ENVIRONMENT: Office / Laboratory environment, phone/computer work, low noise level except when on the manufacturing floor where it will be medium to high level

Senior Metrologist

<h3>Job Description</h3>
Job DescriptionActalent is Hiring a Team of Analytical Scientists // First and Second Shift!Job Description
We are seeking a dedicated Associate Scientist to perform routine tests of finished products, stability samples, raw materials, and CV samples. The role involves assays, chromatographic purity, and content uniformity analysis using UV and HPLC, and particle size distribution using various techniques. This position requires working in a regulated laboratory environment, adhering to in-house monographs and USP standards.
Responsibilities
<ul>
<li>Perform routine tests on finished products, stability samples, raw materials, and CV samples using UV and HPLC.</li>
<li>Evaluate test results and decide on the acceptability of samples.</li>
<li>Maintain accurate lab notebooks and complete analytical reports, summaries, and proper documentation in compliance with SOPs.</li>
<li>Ensure laboratories are maintained with good housekeeping practices and are in compliance with cGMP.</li>
<li>Ensure notebooks are reviewed promptly according to SOPs.</li>
<li>Analyze and interpret results in written and oral formats.</li>
<li>Assist in the training of new analysts.</li>
<li>Conduct laboratory investigations and initiate Quality Events, CAPA, and Change Controls as needed.</li>
<li>Follow all SOPs and Safety Guidelines to ensure compliance with a cGMP environment.</li>
</ul>
Essential Skills
<ul>
<li>Proficiency in HPLC, UPLC, and UV-Vis.</li>
<li>Strong experience in chemistry and analytical techniques.</li>
<li>Experience with SOPs and GMP compliance.</li>
<li>Ability to analyze and interpret data accurately.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Bachelor's degree in Chemistry or related scientific field with 1-2 years of pharmaceutical analysis experience, or Master's degree with 1 year of experience.</li>
<li>Ability to manage problems involving several concrete variables in standardized situations.</li>
<li>Competence in performing necessary computations and interpreting graphs.</li>
<li>Working knowledge of instrumentation software used in laboratories.</li>
</ul>
Work Environment
This position is based in a lab environment regulated by FDA and GMP standards. Work schedule is 1st shift 8am-5pm OR 2nd shift 2pm-11pm, with all training taking place during the first shift.
Pay and Benefits
The pay range for this position is $29.00 - $35.00/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 Coral Springs,FL.
Application Deadline
This position is anticipated to close on Sep 16, 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.

Associate Scientist

<h3>Job Description</h3>
Job DescriptionpcActalent is Hiring a Team of Analytical Scientists // First and Second Shift!Job Description
We are seeking a dedicated Associate Scientist to perform routine tests of finished products, stability samples, raw materials, and CV samples. The role involves assays, chromatographic purity, and content uniformity analysis using UV and HPLC, and particle size distribution using various techniques. This position requires working in a regulated laboratory environment, adhering to in-house monographs and USP standards.
Responsibilities
<ul>
<li>Perform routine tests on finished products, stability samples, raw materials, and CV samples using UV and HPLC.</li>
<li>Evaluate test results and decide on the acceptability of samples.</li>
<li>Maintain accurate lab notebooks and complete analytical reports, summaries, and proper documentation in compliance with SOPs.</li>
<li>Ensure laboratories are maintained with good housekeeping practices and are in compliance with cGMP.</li>
<li>Ensure notebooks are reviewed promptly according to SOPs.</li>
<li>Analyze and interpret results in written and oral formats.</li>
<li>Assist in the training of new analysts.</li>
<li>Conduct laboratory investigations and initiate Quality Events, CAPA, and Change Controls as needed.</li>
<li>Follow all SOPs and Safety Guidelines to ensure compliance with a cGMP environment.</li>
</ul>
Essential Skills
<ul>
<li>Proficiency in HPLC, UPLC, and UV-Vis.</li>
<li>Strong experience in chemistry and analytical techniques.</li>
<li>Experience with SOPs and GMP compliance.</li>
<li>Ability to analyze and interpret data accurately.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Bachelor's degree in Chemistry or related scientific field with 1-2 years of pharmaceutical analysis experience, or Master's degree with 1 year of experience.</li>
<li>Ability to manage problems involving several concrete variables in standardized situations.</li>
<li>Competence in performing necessary computations and interpreting graphs.</li>
<li>Working knowledge of instrumentation software used in laboratories.</li>
</ul>
Work Environment
This position is based in a lab environment regulated by FDA and GMP standards. Work schedule is 1st shift 8am-5pm OR 2nd shift 2pm-11pm, with all training taking place during the first shift.
Pay and Benefits
The pay range for this position is $29.00 - $35.00/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 Sunrise,FL.
Application Deadline
This position is anticipated to close on Sep 8, 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.

HPLC Associate Scientist

<h3>Job Description</h3>
The Orlando VA is seeking a BC/BE Rheumatology Section Chief.
Recruitment/Sign-on Bonus Available Student Loan Reimbursements Quality of Life VA/Federal Benefits.
The Rheumatology Department at the Orlando VA Sunshine Healthcare System is a well-established trained staff seeking a board certified/board eligible rheumatology physician. Successful completion of a U.S. Fellowship in Rheumatology is strongly preferred.
The Chief will be responsible for leading the Division of Rheumatology at the Orlando VA Healthcare System.
<ul>
<li>Direct and develop the clinical, educational and research activities of the VA Rheumatology Division.</li>
<li>Provide clinical care in the outpatient rheumatology clinics and on the inpatient rheumatology consultation service as well as the inpatient Medicine teaching service.</li>
<li>Provide a rich educational environment for students, residents and fellows and promote scholarly activities.</li>
<li>Promote and expand research opportunities and recruit additional investigators in clinical, translational, and basic science.</li>
<li>Mentor and support faculty in their clinical, educational and research pursuits.</li>
</ul>
The VA Orlando Healthcare System provides an excellent compensation and benefits package commensurate with qualifications and experience. Unrestricted licensure in any state and US citizenship is required.
VA physicians practice medicine more and spend less time on business tasks. Enjoy an environment that supports an interdisciplinary care team approach delivering state-of-the-art medicine using some of the most advanced medical technologies in the Nation. Plus, VA offers an unparalleled variety of practice options in research, academia, and administration. VA ensures and encourages a healthy work/life balance through predictable scheduling, reduced paperwork, elimination of billing hassles and lifts the burden of liability coverage.
If interested, please e-mail your CV.

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