chemical lab supervisor

Henkel

<div><div><h4 class="jobSectionHeader">About this Position
</h4>This role is responsible for ensuring product quality and regulatory compliance through testing of materials, supporting quality investigations, maintaining lab standards, and driving process improvements within the quality department. 
 
<h4 class="jobSectionHeader">What you&acute;ll do
</h4><ul><li>Perform standard quality control testing on incoming raw materials, semi-finished goods, and finished goods.
</li><li>Comply with all Health, Safety, and Environmental (SHE) rules, procedures, and regulations.
</li><li>File and maintain retain samples, dispose of old retain samples, and maintain a clean working environment.
</li><li>Assist Quality Engineers with complaint investigations and provide appropriate training to internal customers in the SHEQ area.
</li><li>Identify and implement opportunities for process optimization within the quality department.
</li><li>Develop tests and report on formulations, executing lab testing and generating test data and documentation. Communicate with various internal functions and execute the implementation of regulation changes.
</li></ul><h4 class="jobSectionHeader">What makes you a good fit
</h4><ul><li>Bachelor&rsquo;s degree in chemistry, Chemical Engineering, or Analytical Chemistry (master&rsquo;s degree is a plus).</li><li>
3 to 5 years of experience in chemical laboratories within FMCG, chemical, or manufacturing industries, preferably including at least 2 years in a leadership or supervisory role</li><li>
Fluent level of English is required.</li><li>
Ability to train, mentor, and evaluate lab technicians and analysts.</li><li>
Solution-Oriented, analytical and structured.</li></ul>
<h4 class="jobSectionHeader">Some perks of joining Henkel
</h4><ul><li>Flexible work scheme with flexible hours, hybrid work model, and work from anywhere policy for up to 30 days per year</li><li>
Diverse national and international growth opportunities</li><li>
Globally wellbeing standards with health and preventive care programs</li><li>
Gender-neutral parental leave for a minimum of 8 weeks</li><li>
Employee Share Plan with voluntary investment and Henkel matching shares</li><li>
Comprehensive Health Insurance for employee + dependents</li><li>
Employee Assistance Programme provides a wide range of mental health and wellbeing benefits</li></ul>
At Henkel, we come from a broad range of backgrounds, perspectives, and life experiences. We believe the uniqueness of all our employees is the power in us. Become part of the team and bring your uniqueness to us! We look for a diverse team of individuals who possess different backgrounds, experiences, personalities and mindsets.</div></div>

Quality Lead - Chemical lab

Curaleaf

<div><div>At Curaleaf, we're redefining the cannabis industry with a strong commitment to quality, expertise, and innovation. As a leading global cannabis provider, our brands&mdash;including Curaleaf, Select, and Grassroots&mdash;offer premium products and services in both medical and adult-use markets.

Join us at Curaleaf to be part of a high-growth, purpose-driven company that champions corporate social responsibility through our Rooted in Good initiative, supporting community outreach and positive change. Here, you'll have the opportunity to make a meaningful impact, drive innovation, and help shape the future of cannabis.</div> 


Job Type: Full Time, Exempt 
Shift: Days, Monday through Friday

POSITION SUMMARY:

The Lab Manager oversees and maintains all oil production, medication formulating, and testing throughout the Processing Suite. Leadership and supervision extend to all oil production steps, analytical testing, formulation of medications, and all associated departmental functions. Also, provide leadership guidance and assistance as required in all Post-Harvest and Filling/Packaging operations. The Lab Manager must monitor and maintain the production facility in accordance with the State regulations and standards set by the company. 


ESSENTIAL DUTIES AND RESPONSIBILITIES:
<ul>
<li>Full scientific oversight of the Labs and all processes</li>
</ul><ul><li>Manage extraction process, purification process, formulation process, and analytical testing in their entirety</li>
</ul><ul><li>Build a strong high functioning team and manage through both engagement and accountability</li>
</ul><ul><li>Recruit new talent Hire all new staff from Extraction Technicians through Chemists</li>
</ul><ul><li>Complete employee evaluations and performance-based coaching</li>
</ul><ul><li>Resource planning and staff scheduling</li>
</ul><ul><li>Develop and oversee all applicable training programs</li>
</ul><ul><li>Capacity and production planning for departments based on constraints and calculated requirements</li>
</ul><ul><li>Validations and qualifications of SOPs, equipment, and methods</li>
</ul><ul><li>Conducting IQ OQ PQ projects for new equipment</li>
</ul><ul><li>Complete R&amp;D projects as required for product and process expansion</li>
</ul><ul><li>Create and track all department metrics and KPIs (focusing on safety, quality, and productivity)</li>
</ul><ul><li>Liaison with Corporate applicable SMEs</li>
</ul><ul><li>Engineer technical solutions for departmental expansion</li>
</ul><ul><li>Execute on short-term projects as well as long-term vision for the departments</li>
</ul><ul><li>Maintain all cGMPs based on set facility standards</li>
</ul><ul><li>Conduct quality-based investigations and create CAPAs</li>
</ul><ul><li>Write and review all department specific SOPs, Work Instructions, Forms, or other technical and controlled documents</li>
</ul><ul><li>Implement continuous improvement initiatives including six sigma and 5S</li>
</ul><ul><li>Managing procurement process of department and maintain an OPEX budget</li>
</ul><ul><li>Ensure all associated personnel are trained in and comply with all New York DOH applicable regulations</li>
</ul><ul><li>Ensure processing operation is fully compliant with state regulations and state/federal law</li>
</ul><ul><li>Assure that operation adheres to all business and industry license requirements</li>
</ul><ul><li>Cannabis industry specific processes related to Post-Harvest (drying, curing, trimming), Processing (extraction, purification, formulation, filling, and packaging), Kitchen Formulation (edibles) and Analytical Testing (potency reporting)</li>
</ul><ul><li>QA/QC duties that require analytical testing for quality and consistency; data review and analysis of HPLC and GC equipment</li>
</ul><ul><li>Oversight of highly sophisticated CO2 based extraction equipment; Processing concentrates and extracts with heat and pressure</li>
</ul><ul><li>Operating, maintaining, repairing and adjusting laboratory equipment such as winterizers, pumps, balances, centrifuges, roto-evaporates, decarb ovens, stills, homogenizers, and another laboratory equipment</li>
</ul><ul><li>Storing supplies and equipment, disposal of waste according to guidelines, and keeping laboratory, storerooms, harvest rooms, and working areas immaculate</li>
</ul><ul><li>Able to process samples by collection, extraction, preparing for analysis, and quantifying results</li>
</ul><ul><li>Scientific laboratory procedures and techniques as used in a chemistry laboratory including methods of measurements</li>
</ul><ul><li>Health and safety practices and precautions (including HazCom) applicable to a laboratory and manufacturing</li>
</ul><ul><li>Development of automation tools specifically related to filling and packaging (injectors, cappers, de-dusters, case counters, box erectors, carton sealers, labelers, etc.)</li>
</ul><ul><li>Maintaining strict inventory compliance and records of all controlled substances tracked through BioTrackTHC</li>
</ul><ul><li>Travel Requirements:</li>
</ul><ul><li>Perform other duties as assigned.</li></ul> 


Supervisory Responsibilities:

This position directly supervises the work activities of others and is accountable for the management of others, through a subordinate supervisor, concerning selection, recommending termination, performance appraisal, and professional development. 


QUALIFICATIONS:

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. 


Minimum Qualifications:
<ul>
<li>Ability to lift up to 50 lbs. and complete repetitive tasks as required</li>
</ul><ul><li>BS/BA Degree or greater in a related field with at least 3 years' experience in a pharmaceutical lab or highly regulated manufacturing/production setting</li>
</ul><ul><li>Scientific writing for processes, training, and procedures which require technical documentation</li>
</ul><ul><li>Strong verbal and communication skills</li>
</ul><ul><li>Ability to work in a cross-functional team environment</li>
</ul><ul><li>Knowledge of Microsoft Office Suite with strong abilities within Excel</li></ul> 


Preferred Qualifications:
<ul>
<li>Degree in Chemistry or Chemical Engineering preferred</li>
</ul><ul><li>Analytical Lab experience with HPLC and GC analysis highly preferred</li>
</ul>
Physical Demands

While performing the duties of this job, the employee is regularly required to stand; walk; use hand to finger, handle or feel; reach with hands and arms; climb or balance; stoop, kneel, crouch or crawl; and talk or hear. Employee is exposed to moving mechanical parts, fumes or airborne particles and toxic or caustic chemicals. The employee must frequently lift and/or move up to 50 or more pounds and regularly move up to 25 pounds. The noise level in the work environment is normal. Work Environment

The noise level in the work environment is normal. The employee is frequently exposed to an environment of natural chemical fumes, herbal aromas, airborne particles, exposed to wet and/or humid conditions. Employee will have moderate exposure to conditions such as dust and particles that affect the respiratory system, eyes, or the skin, depending on department job assignments. Personal Protective Equipment is provided for employees to utilize<div> 
What We Offer:
<ul>
<li>Career Growth Opportunities</li>
<li>Competitive Pay and Benefits</li>
<li>Generous PTO and Parental Leave</li>
<li>401(K) Retirement Plan</li>
<li>Life/ Disability Insurance</li>
<li>Community Involvement</li>
<li>Referral Bonuses and Product Discounts</li>
</ul>
Benefits vary by state, role type, and eligibility.
Follow us on Social Media: 
Instagram: @curaleaf.usa 
Twitter: @Curaleaf_Inc 
LinkedIn: Curaleaf LinkedIn

Curaleaf Holdings, Inc. (TSX: CURA) (OTCQX: CURLF) (&quot;Curaleaf&quot;) is a leading international provider of consumer products in cannabis with a mission to enhance lives by cultivating, sharing, and celebrating the power of the plant. As a high-growth cannabis company known for quality, expertise and reliability, the Company, and its brands, including Curaleaf, Select, Grassroots, Find, and Anthem provide industry-leading service, product selection and accessibility across the medical and adult-use markets. Curaleaf International is powered by a strong presence in all stages of the supply chain. Its unique distribution network throughout Europe, Canada and Australasia brings together pioneering science and research with cutting-edge cultivation, extraction and production. Home | Curaleaf | Cannabis with Confidence

Our Vision: To be the world's leading cannabis company by consistently delivering superior products and services and driving the global acceptance of cannabis.

Our Values:
<ul>
<li>Lead and Inspire.
</li><li>Commit to Win.
</li><li>ONE Curaleaf.
</li><li>Driven to Deliver Excellence.
</li></ul>Curaleaf is an equal opportunity employer. Curaleaf recruits, employs, trains, compensates, and promotes regardless of race, religion, color, national origin, gender identity, sexual orientation, physical ability, age, veteran status, and other protected status as required by applicable law.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

Individuals adversely impacted by the war on drugs are encouraged to apply.

Current Curaleaf employees should apply for open positions through our Internal Job Board, which can be accessed via the link on The Leaf.</div></div>

Processing Lab Manager

Kennametal

<div>About Kennametal
With over 85 years as an industrial technology leader, Kennametal Inc. delivers productivity to customers through materials science, tooling and wear-resistant solutions. Customers across aerospace and defense, earthworks, energy, general engineering and transportation turn to Kennametal to help them manufacture with precision and efficiency. Learn more at kennametal.com. Follow @Kennametal: Instagram, Facebook, LinkedIn and YouTube.
Job Title: Quality Supervisor 
Location: Huntsville, AL 
The Lab Supervisor is responsible for managing the daily operations of the Lab. This person will promote Kennametal's management-based safety culture within the lab. This person should be able to perform analysis on Tungsten, Tungsten Carbide, and Molybdenum products using a variety of testing equipment and instrumentation as needed. This individual maintains the integrity of testing methods for finished, in-process, and raw materials, as well as, maintaining the testing results for the environmental concern of the facility. 
Duties and Responsibilities:<ul><li>
Assigns tasks and duties to Lab personnel as needed.</li><li>
Trains and coaches Lab technicians and personnel.</li><li>
Responsible for procedure development as assigned by the Quality Manager.</li><li>
Evaluates all types of test data as required, make decisions for re-testing, and evaluate unexpected or questionable data.</li><li>
Responsible for incorporating new instrumentation or instrument upgrades as assigned by the Quality Manager.</li><li>
Develops, tests, and documents testing methods for instrument upgrades/new instrumentation. Trains lab personnel on new instrument operations.</li><li>
Assures proper care of instrumentation. Monitors instrument maintenance, responsible for instrument repair and preventative maintenance.</li><li>
Is responsible for revising departmental ISO documentation as assigned by the Quality Manager.</li><li>
Completes internal quality audits as assigned by the Quality Manager.</li><li>
May serve as a team leader or facilitator for process improvement, cost reduction, and lean manufacturing programs.</li><li>
Perform other related duties as assigned.</li></ul> 
Equipment Used: A wide variety of testing equipment and instrumentation including:<ul><li>
Analytical balances</li><li>
Light and electron microscope imaging systems.</li><li>
Metallography sample preparation. Metallurgical testing.</li><li>
AA, XRF, and DCP spectrometers</li><li>
Malvern Particle distribution analyzers</li><li>
Physical testing apparatus: FSSS, Ro-Tap (Sieve analysis), Hall Flow, Powder Density.</li><li>
Carbon, Sulfur, Oxygen, and Nitrogen analysis instrumentation.</li><li>
Microwave Digestion system</li><li>
Sintering furnace operation; CNC press operation.</li></ul> 
Skills/Knowtedge Required:<ul><li>
Supervisory and Leadership skills</li><li>
Knowledge of measuring and testing techniques.</li><li>
Advanced mathematical skills</li><li>
Knowledge of inorganic chemistry, knowledge of metallurgy is preferred. Excellent written and oral communication skills.</li><li>
Highly competent in using Microsoft programs. Able to analyze network programs supporting lab and manufacturing processes to improve efficiency and test data distribution.</li><li>
Must be detail-oriented and able to work under pressure in a demanding fast-paced environment.</li><li>
Basic knowledge of manufacturing processes</li></ul> 
Experience Guidelines:
Bachelor of Science Degree in Chemistry or Engineering preferred. Preference will be given to candidates with previous supervisory experience in a powder processing environment. 
To be considered for this position, you must be legally authorized to work in the US (excluding Optional Practice Testing) and not require sponsorship now or in the future. 
 Kennametal Inc. is an Equal Employment Opportunity employer</div>

Quality Lab Supervisor

Falcon Laboratory LLC

We are seeking an experienced Civil Laboratory Supervisor to oversee laboratory operations related to construction materials testing. The successful candidate will be responsible for supervising lab staff, ensuring compliance with industry standards, maintaining equipment, and delivering accurate and timely test results to support civil engineering and construction projects.Key Responsibilities<ul><li>Supervise daily operations of the civil/materials testing laboratory</li><li>Ensure testing is performed in accordance with ASTM, AASHTO, BS, or relevant standards</li><li>Manage and train laboratory technicians and junior staff</li><li>Review, verify, and approve test results and reports</li><li>Coordinate sampling, testing schedules, and resource allocation</li><li>Maintain laboratory equipment, calibration records, and inventory</li><li>Ensure compliance with QA/QC procedures, safety regulations, and accreditation requirements</li><li>Communicate test results and technical findings with engineers, clients, and project teams</li><li>Assist in audits and implement corrective actions when required</li></ul>Job Types: Full-time, Permanent

Laboratory Supervisor

Unilever

<div><div>ABOUT UNILEVER</div>
With 3.4 billion people in over 190 countries using our products every day, Unilever is a business that makes a real impact on the world. Work on brands that are loved and improve the lives of our consumers and the communities around us. We are driven by our purpose: to make sustainable living commonplace, and it is our belief that doing business the right way drives superior performance. At the heart of what we do is our people &ndash; we believe that when our people work with purpose, we will create a better business and a better world.
At Unilever, your career will be a unique journey, grounded in our inclusive, collaborative, and flexible working environment. We don&rsquo;t believe in the &lsquo;one size fits all&rsquo; approach and instead we will equip you with the tools you need to shape your own future.
JOB PURPOSE
Unilever is the place where you can bring your purpose to life with the work that you do &ndash; creating a better business and a better world. If you are an experienced Microbiologist and Hygienist, then this role is just for you!
WHAT WILL YOUR MAIN RESPONSIBILITIES BE<div>
Ensure that all incoming raw materials and all outgoing packed products meet Unilever standards. Monitor and identify substandard situations / processes in terms of manufacturing hygiene compliance on site. Act as a reference for microbiological and hygienic standards and behavior on site. 
 
Key Responsibilities: 
<ul><li>Product Safety</li><li>Is responsible for the identification and monitoring of microbiological standards.</li><li>Develops and reviews the incoming raw material and outgoing product test regime and monitors the program, recommending corrective action where required.</li><li>Tests and releases raw materials to the factory, WIP and finished products based on the successful test results.</li><li>Conducts analysis of development samples, packed products and consumer complaint sample and recommends changes to processes.</li><li>Validates and verifies effectiveness of cleaning processes and procedures and recommends corrective action where required</li><li>Identifies behaviors that will impact microbiologically on raw materials, product or WIP, equipment etc and recommends relevant actions</li><li>Coordinate training and awareness of site teams of microbiology, its implications and controls.</li><li>Hygiene</li><li>Ensures that the manufacturing process is hygienic and microbiologically safe for the production, by monitoring the implementation of appropriate and sustainable hygiene program is in place.</li><li>Conducts Hygiene and Food Safety audits and together with the Quality manager and Production team identify suitable corrective action plans.</li><li>Ensures that immediate corrective action is implemented in the case of non-conformance and possible risk to product safety.</li><li>Conducts hygiene audits of the factory environment, site canteens and ablutions, people and 3rd Party, makes recommendations with respect to changes that need to be made to management or the maintenance department.</li><li>Stock Returns</li><li>Conduct relevant micro tests trade returns, raw materials, in-process and packed product that may be substandard or over age.</li><li>Makes stock return judgement based on the micro safety of the products and recommends the necessary action in line with site and Company policy.</li><li>Co-ordinates the paperwork and supervises the physical action to ensure the follow through of recommendation</li><li>Other</li><li>Lead lab analysts and microbiologists in MPC Factory</li><li>Co-ordinates and monitors site pest control program (internal and external)</li><li>Overall responsibility for running of the Chemical and Micro laboratory.</li><li>Provides representation for Microbiology on the HACCP team.</li><li>Co-ordinates all investigations into Micro incidents.</li><li>Generates reports as and when required to provide consumer safety information to the business/ site</li></ul></div>
WHAT YOU NEED TO SUCCEED
Experiences &amp; Qualifications<ul><li>Diploma in Chemical Institute - Bachelor of Agriculture - Bachelor of Science</li><li>Knowledge of Microsoft Office (Word, excel, PowerPoint and Outlook)</li><li>Understanding of HACCP requirements</li></ul>
Skills<ul><li>Strong Communications skills</li><li>Problem solving skills</li><li>Managing Conflict</li><li>Managing &amp; Leading Change</li><li>Knowledge of product packaging and manufacturing processes.</li><li>Expert background in chemicals.</li><li>Knowledge of quality systems.</li></ul>
Leadership<ul><li>
You are energized by delivering fantastic results. You are an example to others &ndash; both your results and your resilience. You are constantly on the lookout for better ways to do things, engaging and collaborating with others along the way.</li><li>
As an individual you are the one responsible for your own wellbeing and delivering high standards of work. You must also focus on the Consumer and what they need. You are humble and have your head up, looking around to interpret evidence and data smartly, spot issues and opportunities to make things better.</li></ul><ul><li>
Critical SOL (Standards of Leadership) Behaviors<ul><li>
PASSION FOR HIGH PERFORMANCE: Takes personal responsibility and accountability for execution and results. Has an owner&rsquo;s mindset, using data and insight to make decisions.</li><li>
PERSONAL MASTERY: Sets high standards for themselves. Actively builds own wellbeing and resilience.</li><li>
CONSUMER LOVE: Whatever their role, always looks for better ways to serve consumers. Invests time inside and outside to understand the needs of consumers.</li><li>
PURPOSE &amp; SERVICE: Has humility, understanding that leadership is service to others, inside and outside Unilever.</li><li>
AGILITY: Explores the world around them, continually learning and developing their skills.</li></ul></li></ul>
Unilever embraces diversity and encourages applicants from all walks of life! This means giving full and fair consideration to all applicants and continuing development of all employees regardless of age, disability, gender reassignment, race, religion or belief, sex, sexual orientation, marriage and civil partnership, and pregnancy and maternity.
Unilever is an organisation committed to equity, inclusion and diversity to drive our business results and create a better future, every day, for our diverse employees, global consumers, partners, and communities. We believe a diverse workforce allows us to match our growth ambitions and drive inclusion across the business. At Unilever we are interested in every individual bringing their &lsquo;Whole Self&rsquo; to work and this includes you! Thus if you require any support or access requirements, we encourage you to advise us at the time of your application so that we can support you through your recruitment journey.
#LI-DNP</div>

Quality Labs Supervisor

Calderys

<div>
 
 Responsibilities
 
 
 
 <ul>
 <li>
 Meeting the EHS protocols &amp; regulatory norms in force
 </li>
 <li>
 To check and control quality parameters of the Raw materials &amp; Semi- finished products and finished product.
 </li>
 <li>
 Data entry in computer
 </li>
 <li>
 Quality and Process control activities during shift operation ( 1st /2nd/ 3rd).
 </li>
 <li>
 Testing of BD, CCS , PLC, Thermal Conductivity, Flexural strength and other specific tests for refractory materials as applicable.
 </li>
 <li>
 Handling quality complaints.
 
 
 </li>
 </ul>
 
 Requirements
 
 
 
 <ul>
 <li>
 B.Sc. / M.Sc. in Chemistry, preferably with specialization in Inorganic or Analytical Chemistry.
 </li>
 <li>
 2&ndash;5 years of experience in a refractory, ceramics, or related materials lab.
 </li>
 <li>
 Familiarity with ISO 9001, ASTM standards, and refractory material specifications.
 </li>
 <li>
 Strong attention to detail, analytical skills, and understanding of QA documentation.
 
 
 </li>
 </ul>
 
 Calderys Group
 
 
 
 Calderys is a leading global solution provider for industries operating in high temperature conditions . The Group specializes in thermal protection for industrial equipment with a wide range of refractory products, and advanced solutions to enhance steel casting, metallurgical fluxes and molding processes.
 
 
 As an international business with a presence in more than 30 countries and a strong footprint in the Americas through the brand HWI, a member of Calderys, we offer our employees a world of opportunity.
 
 
 With a legacy of over 150 years, and an unwavering commitment to excellence, we continue to shape our future through teamwork, customer-centricity and a proactive mindset. We are the vital partner of all high temperature industries and our purpose places sustainability and innovation at the heart of our business. It reflects our reason for existing: to support our customers building a better world through sustainable solutions.
 
 
 Our values are a driving force in this purpose: We are tenacious, accountable, multicultural and authentic..
 
 
 In our company, performance is recognized and learning is promoted. Our services and solutions depend upon the expertise and commitment of our employees. So we ensure that they have the scope and opportunities to develop their potential within a diverse, inclusive and collaborative setting. It is an environment for people to grow, where every day is a new day and more exciting than the last.
 
 
 Calderys - Forged in legacy. Fueled by excellence.
 
 
 For more information, please visit Calderys.com
</div>

Lab. Supervisor/Chemist, BRW

Sonora Quest Laboratories

<div>Primary City/State:
Phoenix, Arizona
Department Name:
General Lab-Days-Ref Lab
Work Shift:
Day
Job Category:
Lab
POSITION SUMMARY
 
This position performs waived and non-waived tests as defined by CLIA &lsquo;88 in an accurate and timely manner with supervision. Assists with department compliance with all pertinent laboratory accrediting agencies and regulatory requirements (e.g., CLIA &rsquo;88, JCAHO, CAP, OSHA). Personnel report to department supervisor. May be responsible for the collection, receipt, and processing of biological specimens into the laboratory.
Performs all functions according to established policies, procedures, regulatory and accreditation requirements, as well as applicable professional standards.
KNOWLEDGE, SKILLS AND ABILITIES
<ul><li>Must exhibit personal maturity and responsibility.
</li><li>Excellent reading, writing and math abilities.
</li><li>Communicates effectively in oral and written formats sufficient to demonstrate comprehension.
</li><li>Ability to perform detailed work; work with frequent interruptions, multi-task, problem solve and memorization.
</li><li>Ability to take direction and assimilate instructions quickly.
</li><li>Detail oriented and exceptional organizational skills.
</li><li>Basic computer skills.
</li><li>Must exhibit skills in exceptional customer service, good performance review and passing on-site competency evaluation and /or assessment as defined by the department.
</li></ul>MINIMUM QUALIFICATIONS
<ul><li>Applicant must meet one of the following criteria to qualify:
<ul><li>Associate degree in a laboratory science (chemical or biological science) or medical laboratory technology from an accredited institution, or
</li><li>Bachelor&rsquo;s degree in chemical or biological science (transcripts will be reviewed to determine eligibility).
</li><li>Equivalent laboratory training and experience meeting the requirements defined in the CLIA regulation 42CFR493.1489 , or
</li><li>Meet other criteria defined in 42CFR493.1489 or 42CFR493.1491 (including US military medical laboratory procedures training courses)
</li></ul></li><li>Individuals working in the state of Nevada or California are required to maintain their certification throughout their time in position.
</li><li>Foreign educated candidates must provide a detailed credential evaluation from IERF (International Education Research Foundation) or other nationally recognized credentialing agency for review to determine eligibility and translated diploma.
</li><li>Demonstrated competency in phlebotomy in departments where applicable.
</li></ul>PREFERRED QUALIFICATIONS
<ul><li>MLT certification (ASCP, AMT, HEW, AAB).
</li><li>Basic knowledge of specimen requirements and knowledge of medical terminology.
</li><li>Previous experience with phlebotomy and processing.
</li><li>Additional related education and/or experience.</li></ul> 
Our organization supports a drug-free work environment.</div>

Medical Lab Technician I

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