chemical lab supervisor

St. Charles Health System

<div>Salary Range: $89,752 - $134,617
 
Laboratory Supervisor for Madras 
(Full-Time, Days)
ST. CHARLES HEALTH SYSTEM
JOB DESCRIPTION
TITLE: Laboratory Supervisor (Redmond/Madras/Prineville)
REPORTS TO POSITION: Manager, Laboratory Northern Campuses
DEPARTMENT: Laboratory
DATE LAST REVIEWED: January 14, 2020
OUR VISION: Creating America&rsquo;s healthiest community, together
OUR MISSION: In the spirit of love and compassion, better health, better care, better value
OUR VALUES: Accountability, Caring and Teamwork
DEPARTMENT SUMMARY: The laboratory departments provide many services to our multi-hospital organization and outreach community including: blood collection, processing, testing, and reporting of results, spanning all disciplines of laboratory medicine.
POSITION OVERVIEW: The Laboratory Supervisor at St. Charles Health System &ndash; is a working supervisor that ensures and maintains service quality in all phases of testing in one or more Laboratories within the St. Charles Health System. This position is responsible for staffing and daily operations of the Laboratory. This position directly manages caregivers in the Laboratory.
ESSENTIAL FUNCTIONS AND DUTIES:
Actively and cooperatively participates as a member of the laboratory leadership team to maintain safe, efficient, and compliant SCHS operations and services.
Performs the duties and functions of a Medical Laboratory Scientist/Technologist. 60% Bench duties.
Monitors the accuracy, quality and timeliness of services provided in one or more technical disciplines. Ensure that services are performed and delivered in compliance with all regulatory, legal and organizational requirements.
Performs personnel supervisory functions, 40% Supervisory duties, including coaching, education, staff development, competency assessment and annual evaluations. Monitor, oversee and adjust staffing/scheduling to ensure safe and efficient Laboratory operations.
Works collaboratively with Director to create and manage quarterly budget for the assigned lab.
Assists with capital requests, workflow planning, and evaluation/analysis of new tests or instruments.
Responsible for coordinating new caregiver orientation, training and initial competency assessment.
Responsible for annual technical and phlebotomy competencies for staff. Ensuring all required records are updated and placed into personnel files in a timely manner.
Provides technical consultation, education, and decision support for technical staff, clinicians, clients and customers at assigned hospital.
Maintains and updates, when necessary, applicable procedures, quality system records and proficiency testing records.
Ensures instrument to instrument comparisons are performed, documented and reviewed in a timely fashion and linearity studies are performed as required by regulatory agencies and as indicated by QC.
Directs, coaches and monitors the performance of all direct reports, to develop and maintain a high performance team that meets organizational and Laboratory goals.
Monitors and ensure all direct reports are current with regulatory compliance and safety requirements. Implements and manages all organizational safety directives and goals.
Provides and oversees team&rsquo;s delivery of customer service in a manner that promotes goodwill, is timely, efficient and accurate.
Conducts all activities with the highest standards of professionalism and confidentiality. Complies with all applicable laws, regulations, policies and procedures, supporting the health system&rsquo;s corporate integrity efforts by acting in an ethical and appropriate manner, reporting known or suspected violations of applicable rules, and cooperating fully with all company investigations and proceedings.
Supports the vision, mission and values of the organization in all respects.
Supports Value Improvement Practice (VIP- Lean) principles of continuous improvement with energy and enthusiasm, functioning as a champion of change.
Provides and maintains a safe environment for caregivers, patients and guests.
May perform additional duties of similar complexity within the organization, as required or assigned. 
EDUCATION
Required: Bachelor&rsquo;s degree in related field required. Graduate of an approved school of MLS/MT in accordance with the ASCP is required.
Preferred: N/A
LICENSURE/CERTIFICATION/REGISTRATION
Required: Current Oregon drivers&rsquo; license required or the ability to obtain upon hire and the ability to meet SCHS driving requirements. Ability to travel to all SCHS worksites.
Current national certification or licensure at the Technologist/Scientist level by one or more of the following accredited credentialing agencies: ASCP, AMT, AAB, HEW and California Department of Health Services. Acceptable credentials: MLS (ASCP), MT (ASCP), BB (ASCP), H (ASCP), C (ASCP), M (ASCP), MB (ASCP), SBB (ASCP), SC (ASCP) , SM (ASCP), SI (ASCP), MT (AMT), MT (HEW), MT (AAB), CLS
Preferred: Experience with process improvement methodologies
EXPERIENCE
Required: Minimum two (2) years of experience as a laboratory generalist. Intermediate to advanced proficiency in Microsoft applications (Word, PowerPoint, Excel and Access), database management, document preparation and project presentations.
Preferred: Minimum one year of previous laboratory leadership preferred. Experience leading team meetings, dissemination of organizational information (e.g. QA, QC, Process Improvement.
PERSONAL PROTECTIVE EQUIPMENT
Must be able to wear appropriate Personal Protective Equipment (PPE) required to perform the job safely.
PHYSICAL REQUIREMENTS:
Continually (75% or more): Use of clear and audible speaking voice and the ability to hear normal speech level.
Frequently (50%): Sitting, keyboarding operation
Occasionally (25%): Standing and walking lifting/carrying/pushing or pulling 1-10 pounds, grasping/squeezing, operation of a motor vehicle
Rarely (10%): Bending, stooping/kneeling/crouching climbing stairs climbing ladder/step-stool (varies by area) , reaching overhead lifting/carrying/pushing or pulling 11-25 pounds.
Exposure to Elemental Factors
Rarely (10%): chemical solution
Blood-Borne Pathogen (BBP) Exposure Category
Risk for Exposure to BBP
.
Schedule Weekly Hours:
40
Caregiver Type:
Regular
Shift:
First Shift (United States of America)
Is Exempt Position?
Yes
Job Family:
SUPERVISOR
Scheduled Days of the Week:
Variable with Call
Shift Start &amp; End Time:
Variable</div>

Laboratory Supervisor - Madras

University Health

<div><h1 class="jobSectionHeader">Laboratory Supervisor</h1>
<h2 class="jobSectionHeader">Position Summary:</h2>

Join our team as a Laboratory Supervisor, where you'll play a key leadership role in ensuring high-quality, timely, and accurate laboratory testing. Working closely with the Laboratory Manager, you'll help oversee daily operations, ensure compliance with accreditation and regulatory standards, and support staff development. Your expertise in laboratory science will guide technical operations, while your leadership will foster a collaborative and productive environment.
<h2 class="jobSectionHeader">
Key Responsibilities:</h2>
<ul><li> Supervise and coordinate daily activities within the clinical laboratory.</li></ul>
<ul><li> Ensure timely and precise test results in compliance with federal, state, and accreditation standards.</li></ul>
<ul><li> Assist with staffing, training, and performance evaluations.</li></ul>
<ul><li> Collaborate across departments to prioritize workflow and maintain quality standards.</li></ul>
<ul><li> Apply advanced scientific knowledge within your specialty area to support excellence in patient care.</li></ul>
<h2 class="jobSectionHeader">
Qualifications:</h2>
<ul><li> Education: Bachelor&rsquo;s degree in Medical Technology or a related science (biological, chemical, or medical) from an accredited institution, plus completion of a structured clinical program (CAHEA-approved).</li></ul>
<ul><li> Experience: Minimum of 2 years in a clinical laboratory setting, with at least 1 year in a specific department.</li></ul>
<h2 class="jobSectionHeader">
Histology Applicants:</h2>
<ul><li> Bachelor of Science in Histotechnology preferred.</li></ul>
<ul><li> Completion of an accredited histology program and certification as a Histotechnician required.</li></ul>
<h2 class="jobSectionHeader">
Licensure/Certification (One of the Following Required):</h2>
<ul><li> Certification by ASCP-BOC or AMT in clinical laboratory sciences.</li></ul>
<ul><li> Specialty certification in your laboratory area if not certified as a Medical Laboratory Scientist.</li></ul>
<ul><li> Histocompatibility Specialist certification (ACHI).</li></ul>
<ul><li> Certified Histotechnician or Cytotechnologist by a recognized agency.</li></ul>
<h2 class="jobSectionHeader">
Why Join Us?</h2>
<ul><li> Supportive leadership and collaborative team environment.</li></ul>
<ul><li> Opportunities for professional growth and continuing education.</li></ul>
<ul><li> Be part of a mission-driven organization committed to excellence in patient care and laboratory innovation.</li></ul></div>

Laboratory Supervisor

Indus Food Preserving co.

We are seeking a dedicated Lab Incharge to oversee our Seasoning and Flavors laboratory. The ideal candidate will ensure quality, consistency, and compliance with all food safety standards while leading the lab team efficiently. Freshers with relevant educational background are encouraged to apply.Key Responsibilities:Supervise daily laboratory operations for seasoning and flavors production.Ensure compliance with food safety and quality standards (HACCP, ISO, etc.).Conduct tests, quality checks, and analysis of raw materials, in-process samples, and finished products.Maintain accurate lab records, reports, and documentation.Train, guide, and manage lab staff to improve efficiency and accuracy.Collaborate with production and R&amp;D teams for product development and troubleshooting.Ensure proper calibration and maintenance of lab instruments.Qualifications &amp; Skills:Bachelor&rsquo;s degree in Food Science, Chemistry, or related field.# Freshers with strong educational background in relevant fields are welcome.# Knowledge of food quality standards, testing methods, and laboratory practices is a plus.Leadership potential and willingness to learn.# Attention to detail and analytical mindset.# Good communication skills.Location: Korangi Industrial Area (Residents Only) Gender: Only FemaleJob Type: Full-timePay: Rs50,000.00 - Rs60,000.00 per monthWork Location: In person

Lab Incharge – Seasoning & Flavors(Korangi Industriale Area)

SCADA Industries (Pvt) Ltd

Job Title: Lab ChemistLocation: Port Qasim, Karachi Job Type: Full-TimeCompany Overview SCADA Industries (Pvt.) Ltd. is a rapidly expanding specialty chemical manufacturer serving the textile and industrial sectors.Position OverviewWe are hiring Lab Chemists for QA/QC operations. Applicants with BE Chemical Engineering or MSc (Organic/Applied Chemistry) are encouraged to apply. The role involves laboratory analysis, raw material screening, physical/chemical testing, and quality control of textile-related chemicals.Key Responsibilities <ul><li>Laboratory-based development work for textile chemicals</li><li>Perform quantitative and qualitative testing of dyes, chemicals and auxiliaries</li><li>Conduct raw-material inspection and in-process quality control</li><li>Contribute to new product development &amp; finished product evaluation</li><li>Establish and maintain SOPs for equipment operation &amp; chemical handling</li><li>Conduct physical and chemical analysis to validate product performance</li><li>Operate colour-measurement instruments (DataColor/Spectrophotometer)</li><li>Maintain QC documentation, calibration logs, and batch-testing reports</li></ul>We Are Looking For<ul><li>BE Chemical Engineering/MSc Organic or Applied Chemistry</li><li>Experience Fresh to 2 Years in laboratory of chemical vesting environment</li><li>Strong analytical approach with attention to detail</li><li>Interest in formulation work, dye analysis, and chemical evaluation</li><li>Good documentation, reporting and communication skills Internship or Final-Year Project related to chemicals or textiles is a plus</li></ul>What We Offer<ul><li>Direct mentorship under senior lab and dye technologists</li><li>Career progression path: QC Chemist Lab Engineer Technical Lead</li><li>Exposure to QA, R&amp;D, and product development workstreams</li><li>A learning-oriented environment with strong growth potential</li></ul>How to Apply<ul><li>Email your CV to: hr@scadachem.com</li></ul>Job Types: Full-time, FresherApplication Question(s):<ul><li>In which area do you live? Current Address?</li><li>What is your current Salary?</li><li>What is your expected Salary?</li><li>Your age?</li><li>Do you have ever worked in Chemical Lab Testing?</li><li>Your Qualification and specialization?</li></ul>Education:<ul><li>Bachelor's (Required)</li></ul>Experience:<ul><li>Chemical Lab Testing: 1 year (Required)</li></ul>Location:<ul><li>Karachi (Required)</li></ul>Willingness to travel:<ul><li>100% (Required)</li></ul>Work Location: In person

Lab Chemist / Quality Control Officer

USALCO

<div>The statements below are intended to describe the general nature and level of work being performed by associates assigned to this job. This job description is not intended to be an exhaustive list of all responsibilities and skills required of associates so classified.
USALCO Baltimore Plant, LLC is a major unit within the manufacturing network of a leading provider of aluminum-based component products used in water treatment, pulp and paper manufacturing, the making of catalysts for oil refining, the housing market and other sectors. The right individual will have a can-do attitude, the ability to be part of a team while operating independently and consistently performs to very high standards.
JOB SUMMARY:
The person in this role will safely perform laboratory duties that include, but are not limited to, performing analytical tests of intermediate and finished products, reporting results to production supervisors and managers, to maintain quality standards. Responsibilities will include performing routine chemical testing in accordance with Certificates of Analysis, including: pH, acid value, solids and other standard analytical tests as required, labeling samples and reagents, cataloging, organizing, and sorting samples, reagents, equipment, data, and documents. The position requires a motivated, detail oriented, and results driven team player who:<ul><li>
Incorporates safety and quality into every decision while performing day-to-day activities,</li><li>
Effectively communicates with Supervisor and peers,</li><li>
Can understand laboratory testing procedures and equipment in a lab environment.</li><li>
Carry out general laboratory and office tasks to ensure smooth daily operations</li></ul><ul><li>
Will actively seek out opportunities for lab organization, safety, and cleanliness</li><li>
Effectively utilize ERP software to electronically prepare and manage certificate of analysis, prepare shipping documents, and track product quality data.
</li></ul>The employee in this position will be a positive-natured, task-oriented individual. The employee is responsible for the safe and efficient operation of laboratory equipment. The person must possess excellent verbal and non-verbal communication skills necessary to keep Supervisor and peers informed of progress and problems. This person must be personally and professionally motivated to work constructively with team members at all levels within the company, to execute job responsibilities.
ROLES AND RESPONSIBITIES:<ul><li>
Ability to wear appropriate Personal Protective Equipment required for the job.</li><li>
Performing analytical tests of intermediate and finished products</li></ul><div>
<ul><li>Enter Certificate of Analysis (COA) data into internal systems with accuracy and attention to detail</li></ul>
<ul><li>Track product analytical testing data electronically.
</li></ul><ul><li>Calibrating laboratory equipment.</li></ul>
<ul><li>Assist with creating quality paperwork required for shipments (BOL, COA, etc.)</li></ul>
<ul><li>Organizing and cataloging laboratory samples.</li></ul>
<ul><li>Properly disposing of chemicals no longer needed.</li></ul>
<ul><li>Cleaning &amp; organizing laboratory spaces.</li></ul>
<ul><li>Assist operations with tracking and electronically entering product batch information into ERP system.
</li></ul><ul><li>Maintaining positive relationship with production personnel and lab vendors.</li></ul>
<ul><li>Taking inventory of and maintaining stock of equipment and supplies.</li></ul>
<ul><li>Apply all plant safety rules, work guidelines, practices, and procedures.</li></ul>
<ul><li>Assist in development and apply improvements in processes, equipment, and procedures.</li></ul>
<ul><li>Perform other duties as assigned in support of business goals and objectives.</li></ul></div>
MINIMUM QUALIFICATIONS:
KNOWLEDGE AND SKILLS<ul>
<li>Requires planning skills to prioritize daily process operation.</li>
<li>Strong organizational skills and attention to detail
</li><li>Knowledge of laboratory safety and operating procedures.</li>
<li>Must be dependable, flexible, and organized.</li>
<li>Requires good interpersonal and communication skills.</li>
<li>The ability to clearly and succinctly communicate with others, both verbally and in written form.</li>
<li>Strong Analytical and Mathematical aptitude.</li>
<li>Strong written and verbal communication skills</li><li>
Proficiency with standard office software and data entry</li></ul>
EDUCATION:<ul><li>
High School Diploma or GED</li></ul>
EXPERIENCE:<ul><li>
Experience performing basic chemical tests (pH, Acid Value, Solids, etc.) preferred</li><li>
Chemical or manufacturing experience, preferred</li></ul>
ESSENTIAL FUNCTIONS:<ul>
<li>Must be proficient in conducting titration.</li><li>
Routinely stand 80% of shift</li><li>
Work both indoors and outdoors during all seasons</li></ul></div>

Lab Technician

Syngene International Limited

<div>
 Date: 23 Dec 2025
 
 
 Location:
 
 
 Bangalore, KA, IN, 560099
 
 
 Division: Dedicated Centre
 
 
 
 Job Title:
 
 Process Development Scientist-ADC
 
 
 
 Job Location:
 
 Bengaluru
 
 
 
 About Syngene:
 
 Syngene (www.syngeneintl.com) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply.
 
 
 At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures and SOPs, in letter and spirit
 
 
 
 Mandatory expectation for all roles as per Syngene safety guidelines
 
 
 
 <ul>
 <li>
 Overall adherence to safe practices and procedures of oneself and the teams aligned
 </li>
 <li>
 Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company&rsquo;s integrity &amp; quality standards
 </li>
 <li>
 Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times.
 </li>
 <li>
 Ensuring safety of self, teams and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times in the workplace.
 </li>
 <li>
 Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self
 </li>
 <li>
 Compliance to Syngene&rsquo; s quality standards at all times
 
 
 </li>
 </ul>
 
 Core Purpose Of The Role
 
 
 
 Personnel handling this profile will be responsible for performing reactions as per the requirement of the project. They are also responsible for documenting the observations in relevant notebooks. They are to follow instructions from the supervisor and work in a group (or individually) to accomplish the tasks in a timely and efficient manner.
 
 
 
 Key Responsibilities
 
 
 
 <ul>
 <li>
 Perform chemical reactions for the process development of Antibody Drug Conjugates (ADC) that connect an antibody with a potent drug (payload) through a chemical bond in HPAPI facility or in ADC lab. Thereby, suitable prior experience is highly desirable.
 </li>
 <li>
 The selected candidate would handle highly potent active pharmaceutical ingredients (HPAPIs) and cytotoxic compounds.
 </li>
 <li>
 Perform synthetic chemistry reactions, reaction work-ups, purification of the compounds by column chromatography, crystallization, re-crystallization techniques, preparative TLC and operating lab instruments.
 </li>
 <li>
 Ensure that the samples generated during the course of synthesis are given for analysis and record subsequent results obtained and update the supervisor / group leader on the progress of synthesis and ensure samples are packed appropriately for shipment
 </li>
 <li>
 Record the observations of experiment/reaction, results, utilization of resources and other activities related to the reaction in the laboratory or e-notebook following guidelines and in timely manner and ensure that the same is handled safely and confidentially.
 </li>
 <li>
 Ensure that the instrument / equipment are calibrated, undergone preventive maintenance and are kept clean before use and in case of any breakdown, report to maintenance immediately.
 </li>
 <li>
 Ensure that they know the MSDS of the chemicals they are handling and aware of emergency response procedures in case of accidental spillage, leakage or fire and ensure proper waste segregation as per EHS norms.
 </li>
 <li>
 Follow EHS and quality system requirements at all times in the workplace ensuring individual safety and lab safety.
 </li>
 <li>
 Attend all mandatory trainings and update training records as and when trainings are completed.
 </li>
 <li>
 Ensure confidentiality at all times.
 
 
 </li>
 </ul>
 
 Syngene Values:
 
 Follow safety and data integrity guideline.
 
 
 All employees will consistently demonstrate alignment with our core values:
 
 
 <ul>
 <li>
 Excellence
 </li>
 <li>
 Integrity
 </li>
 <li>
 Professionalism
 
 
 </li>
 </ul>
 
 Education:
 
 M.Sc with hands on experience in process chemist in an industry setting
 
 
 
 Equal Opportunity Employer
 
 
 
 It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities.
</div>

Process development Scientist-ADC

Glenmark Pharmaceuticals

<div>Glenmark Pharmaceuticals Inc., USA is a subsidiary of Glenmark Pharmaceuticals Ltd., a leading player in the discovery of new molecules &ndash; both New Chemical Entities (NCE's) and New Biological Entities (NBEs'), with eight molecules in various stages of clinical development. Glenmark Pharmaceuticals Inc., USA is a fast growing and robust US generics business, with plans to move into the innovative market as well. The USA subsidiary also markets APIs to regulated and semi-regulated countries. 
 
POSITION SUMMARY:
This position is for a highly motivated member of the Quality Control (QC) Lab at the Monroe manufacturing facility, reporting to the QC Manager. Primary responsibilities for this position will be: perform QC analysis in compliance to cGMP in line with standards prescribed by USFDA. Maintain compliance to data integrity and cGMP in QC lab in line with standards prescribed by USFDA. Perform IOQ/Calibration for instruments in QC lab at Monroe with guidance of CQA. Execute and complete procedures and systems for RM, PM, FD and in process testing in QC lab. Provide information, data for evaluation and execution of stability study as per Quality and regulatory requirement. Timely complete testing and ensure compliance during analytical TT and AMV performed in QC lab. Able to be a qualified trainer for QC related systems and SOP&rsquo;s and responsible that personnel are appropriately trained.
OVERALL JOB RESPONSIBILITIES:
<ul><li>Be cost effective and vigilant of laboratory reagents, glassware, etcetera to ensure department is within the Revenue and Capex Budget as per spent analysis project.</li>
<li>Provide feedback to management with laboratory standard hours for financial prudence in resource planning, allocation and manpower to ensure within approved budgets while building best in class quality processes and systems at site.</li>
<li>Execute and maintain quality system controls to ensure no critical and major market complaints.</li>
<li>Take appropriate steps to reduce wastages and losses in the analysis process and build improved efficiency</li>
<li>Perform day to day activities for the chemical laboratory which shall include testing of in- process, RM, PM and FP samples, Swab sample and Tech Transfer (as applicable).</li>
<li>Ensuring compliance to systems and procedures throughout product lifecycle.</li>
<li>Communicate with Supervisor and/or report any preparations or data that may result in an Incidence &amp; OOS.</li>
<li>Ensure that the QC Laboratory is in a ready state of compliance for internal and external audits.</li>
<li>Execute technology transfer of analytical methods for new products. Execute cleaning validation of new products.</li>
<li>Assist in the monitoring of changes in the monographs Pharmacopoeia requirements, Regulatory agencies recommendations and implement the same in QC Lab.</li>
<li>Apply CAPA for Lab failures in OOS.</li>
<li>Prepare in timely fashion updating and revision of SOP, specification, STP and any other documents</li>
<li>Assist in timely completion of Tech Transfer of Finished products.</li>
<li>Ensure training of QC staff</li>
<li>Perform the Tracking System Deployment for Stability Samples/ Process Validation Samples etc.</li>
<li>Perform the Training Tracking Tool/Software for QUALITY Assurance and Quality Control.</li>
</ul>
Education :
B.Sc. in Chemistry with concentration in Biochemistry
Experience:
<ul><li>1-3 years in the field of Pharmaceutical (manufacturing facility).</li><li>Background in the functional areas of Quality Control in Stability, Finished Goods and some Raw Materials with a some experience in R&amp;D.</li></ul>
Extensive knowledge in general laboratory equipment including but not limited to: HPLC, UV-Vis and FTIR.
Knowledge and Skills :
Knowledge of cGMP, Validations and Qualifications, regulatory guidelines, US Pharmacopoeias, Internal auditing, Handling of regulatory Inspections, well acquainted with QMS, well versed with Change control/deviations and market compliant management system. 
 
Skills in coordination of calibration and preventative maintenance services, including but not limited to: setting up vendor contracts, processing quotes, generating purchasing orders and handling vendor invoices. 
 
Technical writing skills to generate SOPs and serve as the Subject Matter Expert. 
 
Began training under Six Sigma and Project Management.
Support the Management to organize and maintain the QC team, good communications skills, front runner, and GMP trainer.
Other requirements (licenses, certifications, specialized training)
Will be an added advantage if the individual has dealt with multiple audits personally.</div>

Quality Control Analyst

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