quality control scientist

Novel Microdevices

<div>Position Title: Staff Scientist &ndash; Assay Development, Quality, and Manufacturing Support 
Department: R&amp;D / Quality / Manufacturing 
Reports To: VP of Assay Development and Chief Operating Officer 
Position Summary

The Scientist will play a key role in supporting the development, validation, and manufacturing of Novel Microdevices&rsquo; molecular diagnostic assays and reagents. This cross-functional position bridges R&amp;D, Quality Control, and Manufacturing, ensuring that new assays and production lots meet performance, consistency, and regulatory requirements.

The ideal candidate is a hands-on scientist who enjoys both bench-level experimentation and structured quality processes, thrives in a fast-paced startup environment, and contributes to the continuous improvement and commercialization of diagnostic products. 

Key Responsibilities
<ul>
<li>Assay Development &amp; Verification
<ul><li>Support R&amp;D in the design, optimization, and verification of new molecular diagnostic assays (e.g., qPCR, nucleic acid extraction, reagent formulation).</li>
<li>Conduct feasibility, design transfer, and V&amp;V (Verification &amp; Validation) testing to ensure product performance and regulatory compliance.</li>
<li>Perform analytical testing to assess assay sensitivity, specificity, reproducibility, and robustness.</li>
<li>Analyze, interpret, and present experimental data to cross-functional teams.</li>
</ul>Reagent &amp; Manufacturing Support
<ul><li>Collaborate with Manufacturing to scale reagent formulations, optimize processes, and ensure lot-to-lot consistency.</li>
<li>Conduct in-process, release, and stability testing on raw materials, intermediates, and finished products.</li>
<li>Develop and refine SOPs, batch records, and test methods for reagent preparation and product release.</li>
<li>Support troubleshooting of reagent production issues and contribute to process improvements.</li></ul> 
 
<ul><li>Execute and document QC methods in compliance with ISO 13485, FDA 21 CFR Part 820, and IVDR standards.</li>
<li>Support method validation, transfer, and verification in alignment with CLSI and internal quality requirements.</li>
<li>Participate in investigations of nonconformances, OOS/OOT events, and CAPA development.</li>
<li>Ensure accurate and complete documentation consistent with design control, traceability, and QMS standards.</li>
</ul>Cross-Functional Collaboration
<ul><li>Work closely with QA, R&amp;D, and Operations to support technology transfer and readiness for scale-up.</li>
<li>Provide technical input for product characterization, design reviews, and risk assessments (ISO 14971).</li>
<li>Train and mentor laboratory staff on analytical methods, data integrity, and best practices.</li>
</ul>Contribute to continuous improvement initiatives to strengthen product performance and operational efficiency.</li></ul> 


Minimum Qualifications
<ul>
<li>PhD or Master&rsquo;s degree in Molecular Biology, Biochemistry, Biotechnology, or a related life science field, or equivalent experience in assay development or molecular diagnostics; with at least 2 years of relevant experience; 
OR 
Bachelor&rsquo;s degree in a related discipline with at least 5 years of relevant experience in assay development, molecular biology, or quality control within a regulated IVD or life sciences environment.</li>
<li>Hands-on experience with qPCR and molecular assay techniques, including nucleic acid extraction, amplification, or detection.</li>
<li>Working knowledge of ISO 13485, FDA 21 CFR Part 820, or similar quality management systems.</li>
<li>Strong experimental design, troubleshooting, and data analysis skills.</li>
<li>Excellent documentation, organization, and communication skills with a proven ability to collaborate across R&amp;D, Manufacturing, and QA/QC.</li></ul> 


Preferred Qualifications
<ul>
<li>Experience in IVD assay development and design transfer from prototype to production.</li>
<li>Familiarity with reagent formulation, lyophilization, or stability studies.</li>
<li>Prior involvement in V&amp;V studies, design control documentation, or regulatory submissions.</li>
<li>Knowledge of statistical tools for data trending and method validation (e.g., JMP, Minitab, or equivalent).</li>
<li>Exposure to risk management (ISO 14971) and document control systems.</li></ul></div>

Staff Scientist – Assay Development, Quality, and Manufacturing Support

Herbalife

<div>Overview:
<h2 class="jobSectionHeader">Position summary statement:</h2><div>
The Scientist, Document Control validates raw material specifications meet Herbalife Nutrition and regulatory standards. Collaborate with teams for timely raw material change approvals. This offers an outstanding chance to pioneer nutrition innovation and enhance product quality and compliance!</div><h2 class="jobSectionHeader">
Detailed responsibilities/duties:</h2><ul><li>
Conduct a technical assessment of raw material documents to verify suitability for Inner and/or Outer Nutrition.</li><li>
Collaborate and offer mentorship to Document Sourcing (Corporate and Regional) teams concerning queries associated with raw material specifications, documentation, and Agile procedures.</li><li>
Formulate, evaluate, and adjust raw material specifications in an Agile context following existing requirements and regulations through collaboration with Research and Development (Tech Ops, Formulation), Global Regulatory Affairs and Product Compliance (Corporate and Regional), Quality Control (QC), Product Science, and Transportation teams.</li><li>
Route raw material change requests and change orders in Agile, securing timely approvals from various departments.</li><li>
Assess raw materials used in new formulas or formula revisions, ensuring that the raw materials and suppliers meet the standards for contract manufacturers.</li><li>
Communicate with Global Regulatory Affairs and Product Compliance (Corporate and Regional) regarding specific country testing requirements, as necessary.</li><li>
Address problems concerning raw material specifications through cooperation with raw material suppliers or contract manufacturers.</li><li>
Support and offer mentorship to the Document Sourcing team.</li><li>
Notify contract manufacturers of any modifications in raw material specifications.</li><li>
Keep detailed records regarding raw materials.</li><li>
Perform other responsibilities as assigned.</li></ul><h2 class="jobSectionHeader">
Required qualifications:</h2><div>
Skills:</div><ul><li>
Fundamental understanding of raw material documents and processes.</li><li>
High degree of attention to detail for identifying document acceptability.</li><li>
Driven to deliver results and demonstrate a track record of meeting objectives.</li><li>
Strong customer service and relationship management skills.</li><li>
Strong written and verbal communication abilities to facilitate productive teamwork across diverse departments.</li><li>
Strong analytical skills for accomplishing changes.</li><li>
Outstanding planning and interpersonal abilities to manage multiple tasks.</li><li>
Proficiency in Microsoft Office.</li><li>
Great teammate with flexibility and adaptability to changes.</li></ul><h2 class="jobSectionHeader">
Experience:</h2><ul><li>
4-5 years of experience in Quality Assurance or Quality Control within an FDA regulated sector (21-CFR- Food, Dietary Supplement, or Drug).</li><li>
Previous experience conducting laboratory tests in the Food, Dietary Supplement, Pharmaceutical, or Environmental sectors.</li></ul><h2 class="jobSectionHeader">
Education:</h2><ul><li>
Bachelor&rsquo;s degree in a scientific field or equivalent experience.</li></ul></div>

Scientist, Document Control - India

Natera

<div>
 
 Position Summary
 
 
 
 We are seeking a meticulous and dedicated Scientist for reagent development and quality control assay development. The Scientist will join a cross-functional team of assay development scientists, bioinformaticians, and engineers who are tasked with developing the scalable and robust platforms that underlie many of Natera&rsquo;s clinical assays. In this role, the Scientist will contribute to new product development by characterizing reagent performance and risks, establishing quality control assays and manufacturing processes, and transferring the assays and processes to Operations. Candidates must have experience with reagent development and laboratory automation for next-generation sequencing-based clinical assays in an R&amp;D setting.
 
 
 
 Primary Responsibilities
 
 
 
 <ul>
 <li>
 Plan, manage, and execute projects to meet requirements and timelines.
 </li>
 <li>
 Develop and optimize reagents (enzymes, buffers, oligonucleotides, etc.) for use in NGS-based clinical assays.
 </li>
 <li>
 Independently design and execute experiments for characterizing reagent performance, formulation, stability, and manufacturing tolerance.
 </li>
 <li>
 Design, develop, and validate quality control assays and associated analysis pipelines for incoming and manufactured reagents, either independently or in collaboration with other assay development scientists, automation engineers, and bioinformaticians.
 </li>
 <li>
 Perform data analysis, interpret results, and decide on next steps.
 </li>
 <li>
 Document results, author SOPs, and coordinate tech transfer to the Operations team.
 </li>
 <li>
 Perform other duties as assigned.
 
 
 </li>
 </ul>
 
 Qualifications
 
 
 
 <ul>
 <li>
 Bachelor&rsquo;s degree in molecular biology, biochemistry, or closely related field with 6+ years experience in assay development for the life science industry
 </li>
 <li>
 Master&rsquo;s degree in molecular biology, biochemistry, or closely related field with 4+ years experience in assay development for the life science industry.
 </li>
 <li>
 Doctorate in molecular biology, biochemistry, or closely related field with 1+ years experience in assay development for the life science industry.
 
 
 </li>
 </ul>
 
 Knowledge, Skills, And Abilities
 
 
 
 <ul>
 <li>
 History of success in reagent development or quality control assay development in an R&amp;D environment.
 </li>
 <li>
 Extensive hands-on experience with various molecular biology techniques including but not limited to: next generation sequencing, PCR/qPCR, and nucleic acid extraction and quantification.
 </li>
 <li>
 Strong understanding of molecular biology and the chemistry underlying nucleic acid extraction, PCR, library preparation, and next-generation sequencing.
 </li>
 <li>
 Ability to independently perform moderate to high complexity experiments either manually or with liquid handler support.
 </li>
 <li>
 Must be able to independently design and execute experiments, interpret results, and decide on next steps.
 </li>
 <li>
 Must have experience working with next-generation sequencing data and performing data analysis in Excel, JMP, or similar software.
 </li>
 <li>
 Must have good communication and time management skills.
 </li>
 <li>
 Coding proficiency (Python or R) is a plus.
 </li>
 <li>
 Liquid handler method development experience is a plus.
 
 
 </li>
 </ul>
 The pay range is listed and actual compensation packages are based on a wide array of factors unique to each candidate, including but not limited to skill set, years &amp; depth of experience, certifications and specific office location. This may differ in other locations due to cost of labor considerations.
 
 
 San Carlos, CA
 
 
 $108,800&mdash;$135,950 USD
 
 
 
 OUR OPPORTUNITY
 
 
 
 Natera&trade; is a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women&rsquo;s health, and organ health. Our aim is to make personalized genetic testing and diagnostics part of the standard of care to protect health and enable earlier and more targeted interventions that lead to longer, healthier lives.
 
 
 The Natera team consists of highly dedicated statisticians, geneticists, doctors, laboratory scientists, business professionals, software engineers and many other professionals from world-class institutions, who care deeply for our work and each other. When you join Natera, you&rsquo;ll work hard and grow quickly. Working alongside the elite of the industry, you&rsquo;ll be stretched and challenged, and take pride in being part of a company that is changing the landscape of genetic disease management.
 
 
 
 What We Offer
 
 
 
 Competitive Benefits - Employee benefits include comprehensive medical, dental, vision, life and disability plans for eligible employees and their dependents. Additionally, Natera employees and their immediate families receive free testing in addition to fertility care benefits. Other benefits include pregnancy and baby bonding leave, 401k benefits, commuter benefits and much more. We also offer a generous employee referral program!
 
 
 For more information, visit www.natera.com.
 
 
 Natera is proud to be an Equal Opportunity Employer. We are committed to ensuring a diverse and inclusive workplace environment, and welcome people of different backgrounds, experiences, abilities and perspectives. Inclusive collaboration benefits our employees, our community and our patients, and is critical to our mission of changing the management of disease worldwide.
 
 
 All qualified applicants are encouraged to apply, and will be considered without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, age, veteran status, disability or any other legally protected status. We also consider qualified applicants regardless of criminal histories, consistent with applicable laws.
 
 
 
 If you are based in California, we encourage you to read this important information for California residents.
 
 
 
 Link: https://www.natera.com/notice-of-data-collection-california-residents/
 
 
 Please be advised that Natera will reach out to candidates with a @natera.com email domain ONLY. Email communications from all other domain names are not from Natera or its employees and are fraudulent. Natera does not request interviews via text messages and does not ask for personal information until a candidate has engaged with the company and has spoken to a recruiter and the hiring team. Natera takes cyber crimes seriously, and will collaborate with law enforcement authorities to prosecute any related cyber crimes.
 
 
 
 For More Information
 
 
 
 <ul>
 <li>
 BBB announcement on job scams
 </li>
 <li>
 FBI Cyber Crime resource page
 </li>
 </ul>
</div>

Scientist R&D, Reagent Development

Piramal Pharma Solutions

<div>
 
 
 POSITION SUMMARY:
 
 Piramal Pharma Solutions&rsquo; HPAPI Research and Manufacturing facility, located in Riverview, Michigan, is seeking a qualified Quality Control Chemist to join our Quality Control team. The Quality Control Chemist is responsible for providing analytical chemistry support for the facility.
 
 
 
 
 
 
 
 To perform this position 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:
 
 
 
 
 
 
 <ul>
 <li>
 Shall adhere to all applicable regulatory requirements, including FDA, EPA, OSHA, and related safety, health and environmental procedures, policies and practices.
 </li>
 <li>
 Consistent support and practice of all Piramal Pharma Solutions mission, vision, and values.
 </li>
 <li>
 Identify and protect the original technical information as part of the company property.
 </li>
 </ul>
 
 
 
 
 
 KEY RESPONSIBILITIES:
 
 
 <ul>
 <li>
 Support manufacturing operations through the testing of raw materials and starting materials as required to meet production timelines.
 </li>
 <li>
 Perform cleaning verifications on multi-use equipment using approved methods.
 </li>
 <li>
 Test reference standards and stability samples.
 </li>
 <li>
 Document sample preparation, equipment set-up, and test results in laboratory notebooks or other appropriate test record forms. Verify data with second quality team member as required. Maintain all records as required to maintain compliance.
 </li>
 <li>
 As required, test intermediates and final products to meet production timelines/client requirements.
 </li>
 <li>
 Assist in the revision of documentation as required.
 </li>
 <li>
 Participate in quality unit projects, including but not limited to supplier certification, methods development, methods validation and training of both quality unit members as appropriate.
 </li>
 <li>
 Provide support in the maintenance and calibration of laboratory analytical instrumentation.
 </li>
 <li>
 Assist in the maintenance of the QC laboratory through routine housekeeping, as well as keeping personal bench area and desk organized.
 </li>
 <li>
 As required, perform routine testing on the water system (DI, ice, potable, and QC water), and prepare reports as needed.
 </li>
 </ul>
 
 
 
 
 
 EDUCATION/EXPERIENCE:
 
 
 <ul>
 <li>
 Bachelor&rsquo;s degree in Chemistry or Biochemistry or equivalent.
 </li>
 <li>
 One (1) year of experience in pharmaceutical quality control or equivalent is preferred
 </li>
 <li>
 Familiarity with analytical testing and instrumentation.
 </li>
 </ul>
 
 
 
 
 
 JOB COMPENTENCIES:
 
 
 <ul>
 <li>
 Excellent organizational and planning skills.
 </li>
 <li>
 Strong written, verbal, and interpersonal communication skills.
 </li>
 <li>
 High attention to detail.
 </li>
 <li>
 Demonstrated strong analytical skills, and the ability to work independently against multiple deadlines.
 </li>
 </ul>
 
 
</div>

Quality Control Chemist

Sandoz

<div>Your Key Responsibilities:
Your responsibilities include, but not limited to:
<ul><li>Independently plan, organize, perform and document scientific experiments /GMP testing /manufacturing plant activities under minimal supervision; handle several activities at a time
</li><li>-Take over responsibility for and utilize special tools /equipment or specialized facilities as an expert; schedule and perform maintenance and qualification of instruments / equipment -Proactively identify conflict situations and contribute to solutions
</li><li><ul><li>Work according to appropriate standards for quality, ethics, health, safety, environment protection, and information security; lead initiatives to ensure continuous improvement. Documentation of raw data, evaluate and interpret results; propose and actively support the design of next experiments.
</li></ul></li><li>Review and verify raw data generated by others; approval of tests / experiments performed by others. Write protocols, scientific reports or lab procedures based on templates or SOPs under minimal supervision. For technical development units: Develop new methods or optimize existing methods/processes (lab or plant); contribute to development and implementation of new technologies
 </li><li>-For GMP units: ensure compliance to cGMP -For technology-focused roles: Perform information and literature searches under minimal guidance. Actively foster knowledge exchange.
</li><li>Train and coach associate scientists, technicians, temporary employees and employees under training / education -For project-focused role: Participate in function-specific sub teams and fulfill assigned project tasks and responsibilities under supervision -Uses professional concepts and company's policies and procedures to solve a wide range of difficult problems in imaginative and practical ways.
</li><li>Contributes to some cost center goals and objectives -Design, plan and perform / supervise scientific experiments and contribute to project related scientific /technical activities under minimal supervision (e.g., interpret and report results, generate and evaluate data, draw relevant conclusions, optimize existing methods / processes).
</li><li>Establish innovative solutions for verification and control of critical quality attributes, critical material attributes or critical process parameter in cooperation with other colleagues. Establish control procedures and specifications and review test procedures. Generate scientific documents to hand over to internal and / or external partners (e.g., MST, TechOps, authorities, external companies) and support generation of international registration documents under minimal supervision.
</li><li>If assigned this task, maintenance of infrastructure / equipment and required investments (e.g. system ownership) -Generate lab procedures or SOP&rsquo;s, generate protocols and reports -Lead technical meetings during product development at the local level as well as on the level of SDC network -Report and present scientific /technical results internally and contribute to publications, presentations and patents.
</li></ul>What you&rsquo;ll bring to the role:
<h3 class="jobSectionHeader">Essential Requirements:
</h3><ul><li>M Pharm with 2-5 years' experience or PhD with 1-3 years' experience
</li><li>Functional Breadth.
</li><li>Operations Management and Execution.
</li><li>Collaborating across boundaries. 
</li></ul>Skills:
<ul><li>Environment.
</li><li>Experiments Design.
</li><li>Health And Safety (Ehs).
</li><li>Laboratory Equipment.
</li><li>Manufacturing Process.
</li><li>Materials Science.
</li><li>Process Simulation.
</li><li>Project Management.
</li><li>Sop (Standard Operating Procedure).
</li><li>Technical Writing.
</li></ul><h3 class="jobSectionHeader">Why Sandoz?
</h3>Generic and Biosimilar medicines are the backbone of the global medicines industry. Sandoz, a leader in this sector, provided more than 900 million patient treatments across 100+ countries in 2024 and while we are proud of this achievement, we have an ambition to do more!
With investments in new development capabilities, production sites, new acquisitions, and partnerships, we have the opportunity to shape the future of Sandoz and help more patients gain access to low-cost, high-quality medicines, sustainably.
Our momentum is powered by an open, collaborative culture driven by our talented and ambitious colleagues, who, in return for applying their skills experience an agile and collegiate environment with impactful, flexible-hybrid careers, where diversity is welcomed and where personal growth is supported!
Join us!</div>

Scientist - Pharmaceutical Development

ALI BIN ALI

<div>
 
 
 &middot;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Coordinates with the production department for QC related issues
 
 
 &middot;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Interacting with plant visitors as and when required.
 
 
 &middot;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Solves basic quality problems within prescribed guidelines to ensure final product integrity
 
 
 &middot;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Prepares the Beverage mixing units and Filler ready by carrying out sanitation activities prior to daily production run.
 
 
 &middot;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; During production perform all the specified Laboratory tests on line samples at the frequency specified in PI Quality manual.
 
 
 &middot;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Documents obtained test results in the quality sheets as mentioned in the PI manual.
 
 
 &middot;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Performs quality test on PET blown bottles according to the procedures and frequency specified in PI Quality manual.
 
 
 &middot;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Monitors finished product packaging integrity/date coding.
 
 
 &middot;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Calibrates and documents the Lab equipments per frequency specified in the PI Quality manual.
 
 
 &middot;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Controls and monitors syrup preparation and prepare control drinks.
 
 
 &middot;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Ensures all arrived raw material are within specifications by performing quality checks and document the results.
 
 
 &middot;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Ensures QC. Tests are performed at correct frequency at CO2 plant.
 
 
 &middot;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Administrates the concentrate storage, rotation &ldquo;FIFO&rdquo; and expiring units.
 
 
 &middot;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Monitors the proper operation of syrup mixing, sugar addition, and final syrup specifications.
 
 
 &middot;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Maintains treated water within specification as outlined in the PI manual.
 
 
 &middot;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Reports to maintenance department any equipment -malfunctions.
 
 
 &middot;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Strictly adheres to Food safety and Hygiene policy &amp; procedures
 
 
 &middot;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Steam boiler, monitors the chemicals dosage and analyzes the Boiler water for conformity
 
 
 &middot;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; In the water treatment, carry out annual carbon filter discharge and re-charge as per schedule
 
 
 &middot;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Carries out quality tests on all inbound imported CSD and reports to next level.
 
 
 &middot;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Ensures that proper housekeeping has been carried out in the plant.
 
 
</div>

Cargill

<div>
 Job Purpose and Impact
 
 
 The Assistant Manager - QC will provide expertise with all daily operations in quality control laboratories. In this role, you will support the buildup and maintenance of the rapid technology platform by providing reliable accurate analytical figures as well as perform validation and troubleshooting of new analytical methods to ensure they meet the requirements and deadlines.
 
 
 Key Accountabilities
 
 
 <ul>
 <li>
 Provide analytical support to Rapid Technology Application platform by releasing precise and accurate results and ensure scope of testing parameter is sufficient to build MPA module.
 </li>
 <li>
 Provide ongoing technical support to stakeholders, investigate quality problems and deliver improvement actions with follow up.
 </li>
 <li>
 Perform method validation and verification to roll out new testing method in the lab.
 </li>
 <li>
 Document standard operating procedures, identify possible trends in testing results with data analysis software and provide input to team members to improve quality control system.
 </li>
 <li>
 Organize and maintain accurate and pertinent data, including spreadsheets, graphs and reports.
 </li>
 <li>
 Maintain systems and techniques for reporting data across functional areas.
 </li>
 <li>
 Organize and participate ring tests with the goal to check and control methods and equipment.
 </li>
 <li>
 Handle basic issues and problems under direct supervision, while escalating more complex issues to appropriate staff.
 </li>
 <li>
 Other duties as assigned
 
 
 </li>
 </ul>
 
 Qualifications
 
 
 
 Minimum Qualifications
 
 
 <ul>
 <li>
 Bachelor's degree in a related field or equivalent experience
 
 
 </li>
 </ul>
 
 Preferred Qualifications
 
 
 
 <ul>
 <li>
 "Able to work independently, possess positive working attitude with high initiative level, and communicate effectively"
 </li>
 <li>
 Necessary English reading capacity
 </li>
 <li>
 Experience with chemical analysis (preferable)- oils and fats, starch, sweeteners, etc.
 </li>
 <li>
 Knowledge in calibrate, maintain and troubleshoot various analytical instruments such as GC, HPLC, AAS, ICP, NIR etc
 </li>
 <li>
 Able to demonstrate sound understanding of Statistical Process Control (SPC), method validation and report writing
 </li>
 <li>
 Minimum of Three years of working experience in the Food industry Lab
 </li>
 </ul>
</div>

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