qc chemist

Pk Navratana Agritech Pvt.Ltd

Requirement . a biotechnologists, microbiologists, agricultural scientists, and PhD doctors.<ul><li>State-of-the-Art Labs: They possess bio and chemical labs for quality assurance and product development.</li><li>Product Focus: Developing micronutrients, bio-fertilizers, organic fertilizers, plant growth promoters, and insecticide product .</li><li>Qualification should be B.Sc. Chemistry or M.Sc. Chemistry in Agriculture field. </li><li>Must have minimum 2 years experience in an agriculture company.</li><li>Applied only boys from Uttar Pradesh </li></ul>Job Type: Full-timePay: From ₹20,000.00 per monthBenefits:<ul><li>Flexible schedule</li><li>Internet reimbursement</li><li>Paid time off</li></ul>Education:<ul><li>Master's (Preferred)</li></ul>Work Location: In person

QC Chemist

Rawabi Integrated Gas Company

Job Description<ul><li>Responsible for both gas and bulk products quality analysis and certification.</li><li>Incoming inspection of raw materials and outsourced products.</li><li>In-process inspection in the gas plants.</li><li>Carry out Final product analysis of all gas products.</li><li>Report failure rate to the concerned immediately and support for the necessary action.</li><li>Maintaining all QC documents relevant to ISO 9001 QMS & ISO 17025</li><li>Responsible for maintaining all analytical equipments and instruments.</li><li>Responsible for housekeeping and safety in Q.C laboratory and premises.</li><li>Carryout in process product quality inspection in coordination with plant operators.</li><li>Inform QC manager about failure rate of products.</li><li>Ensure all equipments (Gas analyzers / G.C's) are being calibrated at regular interval and intact.</li><li>Maintain analysis reports.</li><li>Follow-up quality standards set by the company.</li><li>Measure / monitor KPI's</li><li>Any other tasks assigned by Quality control Manager</li></ul>Skills<li>University degree in Chemistry (Bachelor / Master)</li><li>Minimum 5 years' experience in Quality control functions at manufacturing industries, industrial gas,field experience is an added advantage.</li><li>Professional knowledge of Laboratory analytical equipments, instruments and chemicals</li><li>Technical / analytical ability to execute.</li><li>Self-motivated</li><li>Good computer skills such as MS office and other software knowledge and experience</li><li>Fluent in English and local language</li>EducationBachelor in ChemistryApply Now

Quality Control (QC) Chemist

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

Strahl & Pitsch LLC

QC Chemist Job Summary: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.Key Responsibilities:&middot; Equipment - Set up, operate, calibrate, and maintain laboratory instruments and equipment, and troubleshoot any malfunctions.a. GCi. Learning/creating methodsii. Data Analysisiii. Writing the methodsiv. Performing routine maintenance on the equipmentv. Monitoring and ordering required suppliesb. Rheometeri. Researching valuable methods/calculations of transforming rheometric data to S&amp;P useful information and results.c. DSCi. Running tests and analyzing the data.ii. Maintenanced. General equipment maintenance &ndash; contacting suppliers to resolve equipment issues.&middot; Support Productiona. Quality testing (including but not limited to) Titrations, melting points, penetrations, etc.b. Strahl Building In-Process testsi. Checking pailsii. Candelilla peroxide check, etc.c. Setting up Strahl Building production testing (when necessary)d. Fill in for Lab Tech (when necessary) including morning production checks and testing, filtering, bleaching.e. Tanker sampling/testing&middot; Environmental Monitoring swabbing (Monthly + Food Production)&middot; Blending and testing of samples in assistance of investigation, non-conforming product disposition.&middot; General lab procedure updates.&middot; Performing the quality updates for change controls (ie. Formula update)&middot; Assisting Research Manager with projects, evaluation documents.<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>Job Type: Full-timePay: $29.00 per hourExpected hours: 40 per weekBenefits:<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>Work Location: In person

Quality control chemist

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.
 
Summary: 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.
 
Essential Duties and Responsibilities: 
<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>
Qualifications: 
<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>
Education/Experience: 
Bachelor’s degree in Chemistry, Biochemistry, or related scientific field (required); Master’s degree preferred.
 
Work Environment: 
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.
 
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.
 
Physical Demands: 
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.
 
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.
 
EEOC Statement: 
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.
 
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.
 
Thank you for your interest in joining the CAPTEK team. You will be contacted shortly if your application is selected.

Quality Control Chemist III

Eli Lilly

<div>At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We&rsquo;re looking for people who are determined to make life better for people around the world.
Organization Overview:
At Lilly, we serve an extraordinary purpose. We make a difference for people around the globe by discovering, developing and delivering medicines that help them live longer, healthier, more active lives. Not only do we deliver breakthrough medications, but you also can count on us to develop creative solutions to support communities through philanthropy and volunteerism.<div>
Key Objectives /Deliverables: 
<ul><li>Understand the scientific principles required for manufacturing and testing of</li></ul>
intermediates and bulk drug substances, including the interaction of the chemistry and 
equipment. 
<ul><li>Develop, monitor, and appropriately react to established statistically based metrics in</li></ul>
real-time to assess analytical vs. process variability and capability. 
<ul><li>Provide technical support to non-routine (e .g., deviation ) investigations including the</li></ul>
preparation as required of relevant technical documents, such as: Change Controls, 
Regulatory Submissions, Deviations, Validation Protocols, Tickets, Procedures, PFDs, 
Periodic Quality Evaluations, etc. 
<ul><li>Support production floor operations through change proposals, investigations, and</li></ul>
deviation root cause analysis. 
<ul><li>Maintain and improve quality systems including method remediation.</li><li>Participate in self-assessments and regulatory agency inspections.</li><li>Ensure internal and external quality and supply commitments are met.</li><li>Manage the review and retention of cGMP documents.</li><li>Must follow data integrity practices and procedures. (ALCOA + principles ).</li></ul></div><div>
Basic Requirements: 
<ul><li>Bachelor&rsquo;s Degree in a science related field.</li></ul></div><div>
Additional Preferences: 
<ul><li>Demonstrated strong problem solving and analytical thinking skills.</li><li>Understanding of statistical tools and analysis.</li><li>Excellent interpersonal skills and networking skills.</li><li>Experience in QA, QC, Manufacturing, Tech Services, or Regulatory Affairs.</li><li>Demonstrated strong written and verbal communications skills.</li><li>Strong attention to detail.</li><li>Ability to organize and prioritize multiple tasks.</li><li>Experience and knowledge of cGMP requirements.</li></ul></div><ul><li>Familiarity with wet chemistry techniques, HPLC, GC, FTIR, UV/Vis, Titrations</li></ul><div>
Other Information: 
<ul><li>Must complete applicable Learning Plan.</li><li>Tasks require entering manufacturing and laboratory areas which require wearing appropriate PPE.</li><li>Overtime or on-call hours may be required in order to meet business needs.</li><li>Unless approved by leadership, Chemist-QC-IAPI is considered an on-site position.</li><li>Must adhere to policies and guidelines outlined in the employee handbook and Red Book.</li></ul></div>
The job specification is intended to provide a general overview of the job requirements at the time it was prepared. The job requirements of any position may change over time and may include additional responsibilities not specifically described in the job specification. As always, you should consult with your supervision regarding your actual job responsibilities and any related duties that may be required for the position.
Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.
Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status. 
Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women&rsquo;s Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Learn more about all of our groups.
Actual compensation will depend on a candidate&rsquo;s education, experience, skills, and geographic location. The anticipated wage for this position is
$65,250 - $169,400
Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly&rsquo;s compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.
#WeAreLilly</div>

Chemist - QC-IAPI

Ticktix Solutions Pvt Ltd

<ul><li>Analytical Chemist: Responsible for determining the chemical composition of substances using techniques like HPLC, GC, and NMR spectroscopy, ensuring quality, safety, and regulatory compliance in pharmaceuticals, food safety, forensics, and environmental science.</li><li>Quality Control/Quality Assurance (QC/QA) Specialist: Performs chemical tests on raw materials and finished products to ensure safety and compliance with standards in pharmaceuticals, cosmetics, and food production industries.</li><li>Research Scientist: Works in R&amp;D labs to develop new chemicals, materials, and sustainable solutions, contributing to drug discovery, eco-friendly materials, and advanced polymers.</li><li>Environmental Chemist: Focuses on pollution control, waste management, and green chemistry, analyzing environmental samples and developing eco-friendly solutions.</li></ul>Job Types: Full-time, Permanent, Fresher, InternshipPay: ₹18,209.10 - ₹22,609.14 per monthBenefits:<ul><li>Health insurance</li><li>Paid sick time</li><li>Paid time off</li><li>Provident Fund</li></ul>Work Location: In person

Bsc chemistry

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