chemistry quality control technician

SCADA Industries (Pvt) Ltd

<p><b>Job Title: </b>Lab Chemist</p><p><b>Location:</b> Port Qasim, Karachi<br/><b>Job Type:</b> Full-Time</p><p><b>Company Overview </b></p><p>SCADA Industries (Pvt.) Ltd. is a rapidly expanding specialty chemical manufacturer serving the textile and industrial sectors.</p><p>Position Overview</p><p>We are hiring <b>Lab Chemists</b> for QA/QC operations. Applicants with <b>BE Chemical Engineering or MSc (Organic/Applied Chemistry)</b> are encouraged to apply. The role involves laboratory analysis, raw material screening, physical/chemical testing, and quality control of textile-related chemicals.</p><p><b>Key Responsibilities </b></p><ul><li>Laboratory-based development work for textile chemicals</li><li>Perform <b>quantitative and qualitative testing</b> of dyes, chemicals and auxiliaries</li><li>Conduct raw-material inspection and <b>in-process quality control</b></li><li>Contribute to new product development &amp; finished product evaluation</li><li>Establish and maintain <b>SOPs for equipment operation &amp; chemical handling</b></li><li>Conduct <b>physical and chemical analysis</b> 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><p><b>We Are Looking For</b></p><ul><li>BE Chemical Engineering/MSc Organic or Applied Chemistry</li><li>Experience <b>Fresh to 2 Years</b> 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><p><b>What We Offer</b></p><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><p><b>How to Apply</b></p><ul><li>Email your CV to: hr@scadachem.com</li></ul><p>Job Types: Full-time, Fresher</p><p>Application Question(s):</p><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><p>Education:</p><ul><li>Bachelor's (Required)</li></ul><p>Experience:</p><ul><li>Chemical Lab Testing: 1 year (Required)</li></ul><p>Location:</p><ul><li>Karachi (Required)</li></ul><p>Willingness to travel:</p><ul><li>100% (Required)</li></ul><p>Work Location: In person</p>

Lab Chemist / Quality Control Officer

RICI

<p><b>Chemical Quality Assurance Officer / Engineer</b></p><p><b>Department</b></p><p>Quality / Laboratory / Compliance</p><p><b>Reports To</b></p><p>Quality Manager / Laboratory Manager</p><p><b>Job Purpose</b></p><p>To ensure that all chemical testing, laboratory activities, and quality systems comply with <b>applicable standards, regulatory requirements, and internal procedures</b>, ensuring accuracy, reliability, and integrity of results.</p><p><b>Key Responsibilities</b></p><p><b>Quality System &amp; Compliance</b></p><ul><li>Implement, maintain, and improve the <b>Quality Management System (QMS)</b> in line with <b>ISO 17025 / ISO 9001</b>.</li><li>Ensure laboratory compliance with <b>accreditation body requirements</b> and regulatory standards.</li><li>Control and maintain <b>quality documents</b>, SOPs, work instructions, and forms.</li><li>Manage <b>non-conformities</b>, root cause analysis, corrective and preventive actions (CAPA).</li></ul><p><b>Internal Audits &amp; Assessments</b></p><ul><li>Plan and conduct <b>internal audits</b> and follow up on findings.</li><li>Support <b>external audits</b> (accreditation, regulatory, client audits).</li><li>Monitor audit action plans and verify effectiveness.</li></ul><p><b>Laboratory Quality Control</b></p><ul><li>Review and approve <b>test methods, validation/verification data</b>, and uncertainty calculations.</li><li>Monitor <b>QC activities</b> such as blanks, standards, spikes, duplicates, control charts, and PT/ILC results.</li><li>Investigate <b>out-of-specification (OOS)</b> and abnormal results.</li></ul><p><b>Proficiency Testing &amp; Method Performance</b></p><ul><li>Coordinate <b>Proficiency Testing (PT)</b> and Inter-Laboratory Comparisons (ILC).</li><li>Evaluate PT results and initiate corrective actions when required.</li><li>Ensure ongoing <b>method performance monitoring</b>.</li></ul><p><b>Training &amp; Competence</b></p><ul><li>Maintain <b>training and competency records</b> for laboratory personnel.</li><li>Identify training needs and support technical competency assessments.</li></ul><p><b>Equipment &amp; Calibration</b></p><ul><li>Ensure <b>calibration, verification, and maintenance</b> of laboratory instruments.</li><li>Review calibration certificates and traceability to national/international standards.</li></ul><p><b>Data Integrity &amp; Reporting</b></p><ul><li>Ensure <b>accuracy, traceability, and integrity</b> of laboratory data.</li><li>Review and approve <b>test reports</b> before release (where applicable).</li><li>Ensure compliance with data integrity principles (ALCOA+).</li></ul><p><b>Qualifications &amp; Experience</b></p><p><b>Education</b></p><ul><li>Bachelor&rsquo;s degree in <b>Chemistry, Analytical Chemistry, Chemical Engineering</b>, or related field.</li></ul><p><b>Experience</b></p><ul><li>2&ndash;5 years experience in <b>chemical laboratory QA/QC</b> or quality systems.</li><li>Hands-on experience with <b>ISO 17025</b> (strongly preferred).</li></ul><p><b>Skills &amp; Competencies</b></p><ul><li>Strong knowledge of <b>chemical testing techniques</b> (ICP, GC, IC, titration, wet chemistry, etc.).</li><li>Understanding of <b>quality control tools</b> and statistical concepts.</li><li>Excellent documentation and report-writing skills.</li><li>Strong analytical, problem-solving, and attention to detail.</li><li>Ability to work independently and with cross-functional teams.</li></ul><p>Job Type: Full-time</p>

QA/QC -Chemcal Lab

Horizon Biolabs Pvt Ltd

<p><b>Job Description</b></p><p>Horizon Biolabs Pvt Ltd. is a GLP compliant <b>Pharmaceutical Testing Laboratory </b>located in Hyderabad , India . We are industry-leading global provider of laboratory testing services in Chemical and Microbiological segments across the pharmaceutical , Biotech , medical devices and packaging Industries .</p><p><b>We are looking for :</b></p><p>Candidate with Msc/Bsc/Bpharm/Mpharm having minimum 03-05 years of experience in any reputed Pharma Testing Lab/ CRO /Pharmaceutical Industry as a Sr.QC Analyst.</p><p>About the job</p><p>The Quality Control Analyst will report to the Manager of Quality.</p><p><b>Experience</b></p><ul><li>3+ years of QC lab experience in CRO/pharmaceutical industry in a cGMP environment is required.</li><li>Must have hands on experience on HPLC/GC (Gas Chromatography)</li><li>Method Development/validation experience desirable.</li></ul><p>Education</p><ul><li>Bachelor&rsquo;s /Masters degree in Science related field required.</li></ul><p>Job Type: Full-time</p><p>Schedule:</p><ul><li>Day shift</li></ul><p>Education:</p><ul><li>Msc/M Phrama/B Pharma/Bsc(Chemistry)</li></ul><p>Experience:</p><ul><li>total work: 03-05 years (Required)</li><li>Candidates from QC lab experience in CRO/pharmaceutical industry in a cGMP environment is required.</li></ul><p>Job Type: Full-time</p><p>Benefits:</p><ul><li>Provident Fund</li></ul><p>Location:</p><ul><li>Hyderabad, Telangana (Preferred)</li></ul><p>Work Location: In person</p><p>Job Type: Full-time</p><p>Benefits:</p><ul><li>Provident Fund</li></ul><p>Application Question(s):</p><ul><li>Are you currently staying in Hyderabad?</li><li>Are you having QC lab experience in CRO/pharmaceutical industry in a cGMP environment?</li><li>are you ready to join immediately?(within 7 days)</li></ul><p>Work Location: In person</p><p>Job Type: Full-time</p><p>Benefits:</p><ul><li>Provident Fund</li></ul><p>Work Location: In person</p>

QC Analyst-HPLC,GC

CAPTEK Softgel International

Become part of a team that champions wellness worldwide. CAPTEK® Softgel International is a global leader in the development and production of high-quality nutraceutical supplements. As a contract manufacturer organization (CMO), we collaborate with innovators from some of the world’s most successful brands.
<br><br>
<b>Summary:</b> The Quality Control Chemist III plays a senior role in the Quality Control (QC) laboratory, responsible for leading complex analytical testing and providing cross-functional support for the testing and release of raw materials and finished goods. In addition to performing advanced chemical analyses, the Chemist III supports the QC Supervisor with daily operations, mentoring junior chemists, and ensuring compliance with cGMP regulations. This role bridges technical execution with leadership by ensuring timely, accurate testing while driving continuous improvement in quality systems.
<br><br>
<b>Essential Duties and Responsibilities:</b><br>
<ul>
<li>Perform advanced analytical testing on raw materials and finished goods using High-Performance Liquid Chromatography (HPLC), Gas chromatography (GC), Ultraviolet and Visible (UV-Vis), Fourier Transform Infrared Spectroscopy (FTIR), Atomic Absorption Spectrometry (AA), and other techniques, ensuring data accuracy and compliance with established specifications.</li>
<li>Lead investigations of out-of-specification (OOS) results, including root cause analysis and documentation of corrective actions.</li>
<li>Review and approve analytical data and Certificates of Analysis (CoAs) for accuracy and completeness prior to supervisor sign-off.</li>
<li>Provide technical support and guidance to QC Chemists I and II, ensuring adherence to SOPs, test methods, and good documentation practices.</li>
<li>Collaborate with the QC Supervisor to coordinate daily sample flow, prioritizing testing schedules for raw material (RM) and finished goods (FG) to meet production and release timelines.</li>
<li>Support the Supervisor in ensuring timely review and disposition of RM and FG, including the verification of data used for release decisions.</li>
<li>Assist in training QC staff on new test methods, instruments, and safety procedures.</li>
<li>Acts as a liaison between the QC lab and other departments (QA, Production, Planning and Purchasing) for RM/FG testing needs, troubleshooting, and process improvements.</li>
<li>Troubleshoot OOS results on raw materials with vendors, including coordinating retesting, reviewing vendor CoAs, and collaborating on corrective actions to ensure material compliance and timely resolution.</li>
<li>Troubleshoot finished goods OOS results and escalate findings through proper Quality management channels, involving Sales and Business teams as necessary, based on management's approval.</li>
<li>Perform method development and validation as needed, with documentation aligned to regulatory and internal standards.</li>
<li>Participate in internal and external audits, provides data and justifications as needed.</li>
<li>Assist in the maintenance, calibration, and troubleshooting of laboratory instruments.</li>
<li>Support contract testing coordination with third-party labs for specialized assays or confirmatory testing.</li>
<li>Draft and revise SOPs, test methods, and other controlled documents.</li>
<li>Work closely with the QC Supervisor/Quality Management to manage the workflow for raw material and finished good testing, ensuring timely completion and release.</li>
<li>Participate in cross-functional meetings with QA, Production, and Purchasing to align testing priorities with business needs.</li>
<li>Assist RM/FG CoAs approvals and releases materials/products as needed.</li>
<li>Lead continuous improvement initiatives to enhance testing efficiency, reduce errors, and streamline processes.</li>
<li>Engage in interdepartmental collaboration to resolve technical issues affecting RM/FG quality, including non-conformance investigations.</li>
<li>Generates appropriate and complete finished product Certificates of Analysis per product requirement and verifying finished product CoA claims as accurate, true, and complete.</li>
<li>Prepares sample, solvents/reagents, and systems for testing, calculates data and results, documents the entire procedure, disposes and safely cleans up solutions in the hazardous chemicals waste (under the hood), discards all disposables in appropriate waste containers and properly and safely cleans all glassware, work-stations, and apparatus/equipment used.</li>
<li>Safely and appropriately uses tools such as scalpels, glassware, dishes, weighing dishes, pipets, burets, volumetric flasks, ovens, furnaces, stirrers/heat-plates, ultrasonicators, baths, balances, titrators, chemically resistant containers, graduated cylinders, beakers, spectrophotometer cuvettes and permanent markers.</li>
<li>Ensure lab compliance with cGMP, safety, and environmental regulations, including proper chemical handling and waste disposal.</li>
<li>Safely uses reagents (substance or compounds) such as water, acids and bases of varying concentration, buffers, and solvents ranging from weak to strong that are added to a system in order to bring about a chemical reaction or to see if a reaction, interaction, or separation occurs.</li>
<li>Obtains sample and checks sample label and appearance to make sure that the sample is correct. Accurately weigh, label, log and document all samples and in-use apparatus, tools, equipment/instruments, and solvents/regents.</li>
<li>Adheres to all safety, cGMP, and Captek's Standard Operating Procedures, particularly those of the 6 series, while par-taking in the accountability of all QC staff to do the same.</li>
<li>Quality Control Chemist III must have the ability to be flexible, handle multiple projects simultaneously and adapt to increased business demands.</li>
<li>Perform additional duties as assigned.</li>
</ul>
<b>Qualifications:</b><br>
<ul>
<li>5+ years of experience in a cGMP-regulated QC laboratory, with a focus on raw material and finished product testing.</li>
<li>Proficient with advanced analytical instruments (HPLC, GC, UV-Vis, FTIR, AA) and method troubleshooting.</li>
<li>Experience leading technical teams or mentoring junior chemists.</li>
<li>Strong technical writing, problem-solving, and data analysis skills.</li>
<li>Excellent communication skills, with the ability to work cross-functionally.</li>
<li>Knowledge of regulatory requirements (21 CFR Part 111, USP, FDA) in dietary supplements or pharmaceutical industries is a plus.</li>
</ul>
<b>Education/Experience:</b><br>
Bachelor’s degree in Chemistry, Biochemistry, or related scientific field (required); Master’s degree preferred.
<br><br>
<b>Work Environment:</b><br>
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.
<br><br>
While performing the duties of this job, the employee is occasionally exposed to work near moving mechanical parts, fumes, or airborne particles and risk of electrical shock. The noise level in the work environment is usually moderate.
<br><br>
<b>Physical Demands:</b><br>
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.
<br><br>
Physical demands require sitting for extended periods of time, walking, bending, reaching, carrying, and occasionally lifting and/or moving objects up to 25 pounds. Specific vision abilities required by this job include Close vision, Peripheral vision, and the ability to adjust focus. While performing the duties of this job, the employee is occasionally required to use hands to finger, handle, or feel; reach with hands and arms; climb or balance; stoop, kneel, crouch, or crawl and talk or hear.
<br><br>
<b>EEOC Statement:</b><br>
CAPTEK is an equal employment opportunity employer. In order to provide equal opportunities to all individuals, employment decisions will be based on merit, qualifications, and abilities, not on any mental or physical disability. We comply with the law regarding reasonable accommodation for disabled employees and applicants.
<br><br>
We do not discriminate on the basis of actual or perceived race, color, national origin, ancestry, sex (which includes pregnancy, childbirth, breastfeeding and medical conditions related to pregnancy, childbirth or breastfeeding), reproductive health decisions, gender, gender identity, gender expression, religious creed, disability (mental and physical) including HIV and AIDS, medical condition (cancer and genetic characteristics ), genetic information, age, marital status, sexual orientation, military and veteran status, or any other characteristic protected by federal, state or local law. Our management team is dedicated to this policy with respect to recruitment, hiring, placement, promotion, transfer, training, compensation, benefits, employee activities and general treatment during employment.
<br><br>
Thank you for your interest in joining the CAPTEK team. You will be contacted shortly if your application is selected.

Quality Control Chemist III

Energy Northwest

<div><div>It's fun to work in a company where people truly BELIEVE in what they are doing!</div><div></div><div><i>
We're committed to bringing passion and customer focus to the business.</i></div><div></div><div><br>
GENERAL SUMMARY<br>
<br>
Perform special and routine chemistry tasks, such as chemical and radiochemical analyses, instrument calibrations, data review; attend training, and other tasks as assigned. Function as a plant Emergency Response Team Member (ERO qualified). Function as a Fire Brigade Member (Fire Brigade qualified).<br>
<br>
PRINCIPAL ACCOUNTABILITIES<br>
<br>
Work independently on tasks for which qualified, such as:</div><ul><li><div>
Routine sampling of plant systems to ensure compliance with chemistry control guidelines and proper chemical control.</div></li><li><div>
Special sampling of plant systems to ensure compliance with chemistry control guidelines and proper chemical control.</div></li><li><div>
Surveillance sampling of plant systems to ensure compliance with chemistry control guidelines and proper chemical control.</div></li><li><div>
Perform data review and provide necessary corrective actions as needed.</div></li><li><div>
Troubleshooting and calibrations on laboratory instrumentation.</div></li><li><div>
System chemical additions.</div></li><li><div>
Radiological surveys as permitted by the RWP.</div></li><li><div>
Inventories of laboratory chemicals and equipment, and hazardous waste satellite areas.</div></li><li><div>
Revisions of procedures, lesson plans, and OJT guides.</div></li><li><div>
Initiate Condition Reports to document adverse issues, such as out of specification chemistry results, equipment problems, procedure issues, safety concerns, etc.</div></li><li><div>
Initiate Work Requests to address equipment/housekeeping issues.</div></li><li><div>
Participate in the laboratory quality control program and cross check programs.</div></li><li><div>
Function as a Fire Brigade member.</div></li><li><div>
Function as the OSC Chemistry Technician for the Emergency Response Organization.</div></li><li><div>
Perform other tasks as assigned.</div></li></ul><div><br>
Training Accountabilities:</div><ul><li><div>
Attend/participate in Chemistry Technician training (Note - percent of time will vary based on in grade level).</div></li><li><div>
Participate in Fire Brigade training and drills.</div></li><li><div>
Participate in ERO training and drills.</div></li></ul><div><br>
REQUIRED EDUCATION &amp; EXPERIENCE<br>
<br>
Placement in grade:</div><div>
75% - Associate's degree with no related experience;</div><div>
80% - Bachelor's degree with no related experience, OR Associate's degree with one year related experience;</div><div>
85% - Bachelor's degree with one year related experience, OR Associate's degree with two years related experience;</div><div>
90% - Bachelor's degree with two years related experience, OR Associate's degree with three years related experience, OR six years Navy experience, achieving a rank of E5 or below, with ELT Qualifications;</div><div>
95% - Bachelor's degree with three years related experience, OR Associate's degree with four years related experience, OR six years Navy experience, achieving a rank of E6 or above, with ELT Qualifications. Note: Bachelor's or Associate's degree must be in Science/Engineering/Math from an accredited college or university.</div><div></div><div>
Starting Pay Range:</div><div></div>
$47.09 - $59.65 Hourly<div></div><div>
This is a bargaining unit position. The selected candidate's starting hourly rate will be based on qualifications in accordance with the Collective Bargaining Unit Agreement.</div><div></div><div>
Incentive Compensation</div><div>
This role is eligible to participate in our annual incentive plan. Incentives are earned based on employee performance against defined metrics and company goals.</div><div></div><div>
Benefits</div><div>
Energy Northwest (EN) offers a highly competitive and substantial benefits package which allows qualifying employees (and their families) to enroll in medical, dental, vision, and basic life insurance. Other voluntary benefits may include flexible spending accounts, tuition reimbursement, supplemental life insurances, credit monitoring, and identity theft insurance. EN offers three retirement programs to qualifying employees including a matching 401(k) deferred compensation plan, the Washington State Pension Plan (PERS), and a 457(b) savings plan. Qualifying employees will also accrue 160 hours of personal time per year and nine paid holidays throughout the calendar year.</div><div></div><div>
We are an Equal Opportunity Employer and do not discriminate due to race, color, age, gender, gender identity, sexual orientation, ethnicity, religion, national origin, veteran status or on the basis of disability.</div><div></div><div><div>
EEO is the law, click here to learn more</div>.</div></div><div></div>

Chemistry Technician - In Grade

White Mastery Systems

<ul><li><b>Lab Technician/Assistant:</b> Supports senior scientists, prepares samples, runs tests, maintains equipment.</li><li><b>Quality Control Analyst:</b> Tests products (pharma, food, etc.) to ensure they meet quality standards.</li><li><b>Chemist (Analytical, Production):</b> Analyzes substances, refines products, develops formulations, ensures safety.</li><li><b>Research Scientist (Junior):</b> Assists in developing new products and expanding knowledge.</li><li><b>Pharmaceutical Sales/Medical Rep:</b> Promotes drugs to healthcare professionals using chemistry knowledge.</li></ul><p>Job Types: Full-time, Permanent, Fresher</p><p>Pay: ₹18,219.09 - ₹42,634.41 per month</p><p>Benefits:</p><ul><li>Health insurance</li><li>Paid sick time</li><li>Paid time off</li><li>Provident Fund</li></ul><p>Work Location: In person</p>

BSc chemistry

Strahl & Pitsch LLC

<p><b>QC Chemist Job Summary:</b></p><p>The QC Chemist is responsible for performing qualitative and quantitative chemical analyses of raw materials, in-process samples, and finished products to ensure compliance with internal specifications, regulatory standards, and customer requirements. The role ensures product quality, supports manufacturing processes, and maintains laboratory accuracy and compliance.</p><p><b>Key Responsibilities:</b></p><p>&middot; Equipment - Set up, operate, calibrate, and maintain laboratory instruments and equipment, and troubleshoot any malfunctions.</p><p>a. GC</p><p>i. Learning/creating methods</p><p>ii. Data Analysis</p><p>iii. Writing the methods</p><p>iv. Performing routine maintenance on the equipment</p><p>v. Monitoring and ordering required supplies</p><p>b. Rheometer</p><p>i. Researching valuable methods/calculations of transforming rheometric data to S&amp;P useful information and results.</p><p>c. DSC</p><p>i. Running tests and analyzing the data.</p><p>ii. Maintenance</p><p>d. General equipment maintenance &ndash; contacting suppliers to resolve equipment issues.</p><p>&middot; Support Production</p><p>a. Quality testing (including but not limited to) Titrations, melting points, penetrations, etc.</p><p>b. Strahl Building In-Process tests</p><p>i. Checking pails</p><p>ii. Candelilla peroxide check, etc.</p><p>c. Setting up Strahl Building production testing (when necessary)</p><p>d. Fill in for Lab Tech (when necessary) including morning production checks and testing, filtering, bleaching.</p><p>e. Tanker sampling/testing</p><p>&middot; Environmental Monitoring swabbing (Monthly + Food Production)</p><p>&middot; Blending and testing of samples in assistance of investigation, non-conforming product disposition.</p><p>&middot; General lab procedure updates.</p><p>&middot; Performing the quality updates for change controls (ie. Formula update)</p><p>&middot; Assisting Research Manager with projects, evaluation documents.</p><ul><li>Assist with product research and testing to support investigations and management requests to make commercial decisions.</li><li>Ensure compliance with Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), and standard operating procedures (SOPs).</li><li>Investigate out-of-specification (OOS) and out-of-trend (OOT) results and assist in root cause analysis.</li><li>Maintain laboratory safety, cleanliness, and proper disposal of chemical waste.</li><li>Support internal and external audits (e.g., FDA, ISO, cGMP inspections).</li><li>Strong problem-solving, critical thinking, attention to detail, and communication skills are vital.</li><li>Ability to summarize data and present it to Senior and Executive Management</li><li>Comply with safety and regulatory requirements.</li><li>Other duties as considered necessary to support Quality, Lab and R&amp;D</li></ul><p>Job Type: Full-time</p><p>Pay: $29.00 per hour</p><p>Expected hours: 40 per week</p><p>Benefits:</p><ul><li>401(k) matching</li><li>Dental insurance</li><li>Health insurance</li><li>Life insurance</li><li>Paid time off</li><li>Vision insurance</li></ul><p>Work Location: In person</p>

Quality control chemist

Search 10000+ Chemistry quality control technician jobs near you this January. New roles added regularly across leading industries. Apply today.