analytical lab analyst

Inland Empire Paper Co

<div>Company Description 
Inland Empire Paper Company, operating in Millwood Washington since 1911, strives to be the industry leading custom ground-wood paper supplier through highly efficient production methods, first-in-class customer service, and market defining employee capabilities. We offer well-paying jobs with excellent benefits at a place you can make a long term career. 
Job Description 
IEP is seeking a Laboratory Analyst to be the primary responsibility for the routine functions of the IEP Lab. This role supports IEP&rsquo;s production and environmental goals through the collection and analysis of samples using standardized laboratory test procedures. Previous lab experience is not necessarily required, but qualified candidates must be able to learn and comprehend unfamiliar test methods quickly. Candidates must also show a commitment to excellence by continually improving laboratory technique and demonstrating attention to detail. This role is also responsible for the basic administration of related laboratory functions such as equipment maintenance, supplies inventory, disposal, and documentation.
Responsibilities:<ul><li>
Collect pulp, paper, and water samples from all areas of the manufacturing process, and conduct analyses in accordance with standardized methods.</li><li>
Perform all quality assurance and quality control (QA/QC) procedures as required by the analytical method, lab accreditation requirements, or IEP policy. Recognize and take corrective action when QA/QC requirements are not being met.</li><li>
Maintain and administrate a clean and organized work space.</li><li>
Keep inventory for laboratory supplies and place orders for laboratory and other related mill functions. Conduct periodic audits of existing inventory.</li><li>
Keep up-to-date records of all laboratory Safety Data Sheets (SDS). Handle the disposal of waste material in accordance with State law.</li><li>
Maintain all laboratory equipment, including scheduling preventative maintenance and calibrations. Establish and keep current equipment documentation and maintenance records.</li><li>
Follow and execute IEP policy for laboratory accreditation. Pass an initial demonstration of capability (IDC) and validate with ongoing proficiency testing (PT).</li><li>
Commission, as needed, new laboratory analyses or laboratory equipment, including writing Standard Operating Procedures (SOPs).</li></ul> 

Qualifications 
<ul><li>
Minimum education of high school diploma, or equivalent</li><li>
At least one year of coursework and/or work experience in a laboratory setting</li><li>
Ability to read laboratory procedures and perform all steps</li><li>
Self-motivated to troubleshoot issues related to quality, errors, or equipment</li><li>
Basic proficiency with Microsoft Word and Excel</li><li>
Organizational skills and attention to detail</li><li>
Communication skills</li></ul> 

Additional Information 
<ul><li>
The Laboratory Analyst pay range is $19 to $24 per hour, depending on experience and education.</li><li>
Inland Empire Paper Company continues to offer excellent benefits to employees and their families including medical, dental, vision, life insurance, 401(k) retirement plan, 13 paid holidays per year and 2 weeks of vacation to start (pro-rated first year based on hire date).</li><li>
IEP is a smoke-free and drug-free (including cannabis-free) facility running 24/7.</li><li>
All job offers and subsequent employment are contingent upon a drug screen and background check.</li><li>
Normal work hours are 7 AM to 4 PM, Monday through Friday.</li><li>
Must help cover permit-related testing for holiday weekends.</li></ul> 
Your application to this posting is deemed to be your consent to the collection, use and necessary disclosure of personal information for the purposes of recruitment. Privacy of all applicants and the confidentiality of personal information are respected. Thank you to all applicants for your interest and effort in applying for this position; however, only candidates selected for interviews will be contacted.
To learn more about us visit our website: https://iepco.com/</div>

Laboratory Analyst

ABC Techno Labs India Private Limited

Designation - Analyst (Instrument Lab - LCMS )Experience - 1 - 3 Yrs Location - MumbaiResponsibility &amp; Authority:1. Comply with the laboratory&rsquo;s Quality Policy, Quality Objectives, and Quality Management System (QMS) procedures.2. Perform sample preparation, instrument setup, and testing using LC-MS (Liquid Chromatography&ndash;Mass Spectrometry) as per approved methods and SOPs.3. Ensure that all analyses are carried out accurately, efficiently, and within the specified turnaround time to meet customer and regulatory requirements.4. Calibrate, operate, and maintain the LC-MS and associated instruments (HPLC, balances, pipettes, etc.) as per the preventive maintenance schedule.5. Perform system suitability tests (SST) and instrument performance checks before and during analysis to ensure data reliability.6. Prepare standards, reagents, and mobile phases required for LC-MS analysis in accordance with standard laboratory practices.7. Record all instrument parameters, chromatograms, calibration data, and raw results accurately in analytical worksheets or electronic systems.8. Ensure the integrity, traceability, and confidentiality of test data and analytical results.9. Report test results promptly to the Technical Manager &ndash; Instrumentation, ensuring all documentation is reviewed and approved as per QMS requirements. Assist in method validation, verification, and development activities under the supervision of the Technical Manager.10. Maintain and update the instrument maintenance logbook, calibration records, and performance verification reports.11. Identify any non-conformities or deviations during testing and immediately inform the Technical Manager for corrective and preventive action (CAPA).12. Ensure all chemicals, standards, and reagents are properly labelled, stored, and handled following safety and environmental guidelines.13. Participate in internal quality control (IQC) and proficiency testing (PT) programs to ensure accuracy and consistency of test results.14. Coordinate with other chemists and technical staff to ensure smooth workflow and timely completion of analysis.15. Support internal and external audits by providing relevant records, documents, and technical clarifications.Interested Candidate Contact Person - Suganya - HR, Contact Number - 9600171117Job Types: Full-time, PermanentPay: &#8377;13,000.00 - &#8377;26,000.00 per monthBenefits:<ul><li>Cell phone reimbursement</li><li>Provident Fund</li></ul>Work Location: In person

Analyst (Instrumentation Lab - LCMS)

Colgate-Palmolive

<div>
 No Relocation Assistance Offered
 
 
 Job Number #168581 - Gebze - Kocaeli, Turkey, Turkey
 
 
 
 Who We Are
 
 
 
 Colgate-Palmolive Company is a global consumer products company operating in over 200 countries specialising in Oral Care, Personal Care, Home Care, Skin Care, and Pet Nutrition. Our products are trusted in more households than any other brand in the world, making us a household name!
 
 
 Join Colgate-Palmolive, a caring, innovative growth company reimagining a healthier future for people, their pets, and our planet. Guided by our core values&mdash;Caring, Inclusive, and Courageous&mdash;we foster a culture that inspires our people to achieve common goals. Together, let's build a brighter, healthier future for all.
 
 
 
 Job Summary (with AI &amp; Digital enhancements):
 
 
 
 The Plant Analytical Lab Coordinator is responsible for overseeing the daily operations of the analytical laboratory within the plant, ensuring timely and accurate testing of raw materials, in-process samples, and finished products. This role ensures compliance with safety, regulatory, and quality standards while leading continuous improvement activities&mdash;including the adoption of AI and digital technologies to enhance laboratory efficiency&mdash;and supporting production needs. Additional responsibilities include complaints management, supplier quality, OSQ, mock recovery exercises, KPI reporting, leveraging data analytics, and supporting shop floor training and documentation through digital platforms.
 
 
 
 Key Responsibilities (with suggested AI &amp; Digital details):
 
 
 
 <ul>
 <li>
 Coordinate and monitor daily lab activities, ensuring adherence to quality, safety, and regulatory standards, by utilizing digital dashboards and workflow tools
 </li>
 <li>
 Supervise routine and non-routine analytical testing using appropriate laboratory techniques (e.g., HPLC, GC, FTIR, titration, etc.),
 </li>
 <li>
 Ensure accurate, complete, and timely recording of test results. Utilize Laboratory Information Management Systems (LIMS) and AI-powered data validation tools for review and approval of laboratory data and reports
 </li>
 <li>
 Maintain and update laboratory SOPs, work instructions, and test methods in compliance with internal and regulatory guidelines
 </li>
 <li>
 Maintain compliance with internal procedures, GMP/GLP, ISO, and external regulatory requirements, monitoring this through automated compliance tracking software
 </li>
 <li>
 Participate in internal and external quality and safety audits and support corrective action implementation
 </li>
 <li>
 Manage calibration, maintenance, and qualification of laboratory instruments and equipment
 </li>
 <li>
 Manage laboratory consumables inventory, reagents, and supply procurement
 </li>
 <li>
 Review, approve and ensure accuracy of test results and related documentation
 </li>
 <li>
 Train and mentor laboratory analysts and technicians on procedures, safety and quality requirements
 </li>
 <li>
 Lead or support investigations and root cause analyses for out-of-specification or non-conformance results
 </li>
 <li>
 Manage and coordinate complaints management processes, including investigation, documentation, and resolution of product quality issues
 </li>
 <li>
 Drive supplier quality management, including evaluation, qualification, performance monitoring, and resolution of supplier quality issues
 </li>
 <li>
 Plan and lead mock recovery exercises to ensure readiness and compliance with product recall requirements
 </li>
 <li>
 Compile and report quality Key Performance Indicators (KPIs), including lab performance, complaint trends, audit outcomes and quality improvements
 </li>
 <li>
 Support shop floor training activities by providing mandatory quality trainings to operations personnel and ensuring competency
 </li>
 <li>
 Collaborate with production, engineering, R&amp;D, and other teams on quality-related projects and problem-solving
 </li>
 <li>
 Support continuous improvement initiatives in the lab and across the site&rsquo;s Quality Management System, promoting the adoption of AI and digital solutions
 </li>
 <li>
 Maintain a clean, organized, and safe laboratory environment
 
 
 </li>
 </ul>
 
 Required Qualifications (with digital skills addition):
 
 
 
 <ul>
 <li>
 Bachelor&rsquo;s or Master&rsquo;s degree in Chemistry, Microbiology, Food Science, or related scientific disciplines
 </li>
 <li>
 Minimum 3 years&rsquo; experience in a quality laboratory or quality assurance role, preferably in a manufacturing environment
 </li>
 <li>
 Hands-on experience with analytical instrumentation (e.g., HPLC, GC, UV-Vis, FTIR, etc.)
 </li>
 <li>
 Strong knowledge of quality systems, documentation practices, and regulatory standards (GMP, GLP, ISO, etc.)
 </li>
 <li>
 Fluency in English
 </li>
 <li>
 Excellent organizational, written, communication, and problem-solving skills
 </li>
 <li>
 Experience working in cross-functional teams
 </li>
 <li>
 Good knowledge of MS Office, Google tools, and experience with digital lab management systems
 </li>
 <li>
 Ability to lead, supervise, and train laboratory personnel, including the use of digital training platforms
 </li>
 <li>
 Experience with complaints management, supplier quality, shop floor training, documentation control, audits, and root cause analysis preferred
 
 
 </li>
 </ul>
 
 Preferred Qualifications (enhanced):
 
 
 
 <ul>
 <li>
 Experience in a manufacturing or plant environment.
 </li>
 <li>
 Familiarity with LIMS (Laboratory Information Management Systems) or quality management software
 </li>
 <li>
 Experience with regulatory audits and external customer or supplier audits
 </li>
 <li>
 Experience with statistical quality control and performance measurement is a plus
 
 
 </li>
 </ul>
 
 Perks Of Role
 
 
 
 <ul>
 <li>
 International Working Environment
 </li>
 <li>
 Shuttle Services (From Anatolian Side of Istanbul and Kuru&ccedil;e&scedil;me on the Izmit side)
 </li>
 <li>
 Comprehensive Medical/Life insurance coverage
 </li>
 <li>
 24/7 Employee Assistance Program
 
 
 </li>
 </ul>
 
 Disclaimer - Interested candidates are requested to upload their resumes drafted in English language only.
 
 
 
 
 Our Commitment to Inclusion
 
 
 
 Our journey begins with our people&mdash;developing strong talent with diverse backgrounds and perspectives to best serve our consumers around the world and fostering an inclusive environment where everyone feels a true sense of belonging. We are dedicated to ensuring that each individual can be their authentic self, is treated with respect, and is empowered by leadership to contribute meaningfully to our business.
 
 
 
 Equal Opportunity Employer
 
 
 
 Colgate is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, colour, religion, gender, gender identity, sexual orientation, national origin, ethnicity, age, disability, marital status, veteran status (United States positions), or any other characteristic protected by law.
 
 
 Reasonable accommodation during the application process is available for persons with disabilities. Please complete this request form should you require accommodation.
 
 
 <ul>
 <li>
 site
 
 
 </li>
 </ul>
</div>

Plant Analytical Lab Coordinator

Dr. Reddy's Laboratories

<div>
 
 Dr. Reddy&rsquo;s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because
 
 Good Health Can&rsquo;t Wait
 
 .
 
 
 
 
 We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries.
 
 
 
 
 For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. As the pharmaceutical industry evolves and undergoes disruption, we see an opportunity &ndash; to strengthen our core further (the next steps) and to build the future (the new bets).
 
 
 
 
 &lsquo;The Next and the New&rsquo; is how we aim to continue to be the partner of choice &ndash; purpose-driven, future-ready and sustainable. Our aim is to reach over 1.5 Bn+ patients across the world by 2030 by growing our core businesses and building for the future with sustainability at the core of our purpose and strategy. Sustainability for us means operating in a manner that respects people, planet and purpose &ndash; helping us conserve precious resources, serve our patients, create value for stakeholders, give back to society, fulfil our potential and maintain our integrity and transparency
 
 
 
 
 Dr Reddy&rsquo;s maintains a work environment, free from discrimination and is an equal opportunity employer. We are committed to employ &amp; nurture all qualified diverse workforce without regard to race, colour religion, nationality, sex, age, disability status, genetics, sexual orientation, gender expression, citizenship or any other characteristic or classification protected by applicable law(s) of the country we operate in. We treasure every talent, and recognize merit and diversity in our organization.
 
 
 
 
 
 
 Job Description
 
 
 
 
 
 Job Summary
 
 
 
 We are seeking a dynamic and experienced Analytical Specialist in Active Pharmaceutical Ingredient (API) MSc business for employing advanced analytical techniques to characterize and elucidate the structure and properties of various materials at a molecular and atomic level. You will play a crucial role in driving research and development initiatives by providing in-depth insights into complex materials through the application of cutting-edge analytical methodologies.
 
 
 
 
 
 
 
 Roles &amp; Responsibilities
 
 
 
 &bull; You will be responsible for working on new product development, addressing regulatory deficiency queries, and leveraging filings. Your role involves ensuring the qualification of reference/working standards, developing analytical methods, conducting validations, and transferring methods to QC.
 
 
 &bull; You will be responsible for developing and validating analytical methods, preparing method development and validation reports, and conducting online sample analysis for product development. Your role includes compiling forced degradation studies and identifying unknown impurities.
 
 
 &bull; You will compile stability data for completed projects, analyse product strategy, efficiency, and cross-functional issues in Analytical Research and Development (AR&amp;D). Your role involves visualizing developmental needs, understanding process scalability, and ensuring the procurement of necessary laboratory supplies.
 
 
 &bull; You will be responsible for maintaining lab equipment according to Good Laboratory Practices (GLP), investigating abnormal results in collaboration with group leaders, and ensuring calibration of instruments as per the schedule. Your role includes adhering to safety and environmental protocols, keeping the work area clean, and maintaining well-organized documentation.
 
 
 &bull; You will be responsible to employ advanced analytical techniques such as spectroscopy Nuclear Magnetic Resonance (NMR), Fourier Transform Infrared Spectroscopy (FTIR), Ultraviolet- Visible Spectroscopy (UV-Vis), mass spectrometry, Gas chromatography (GC), high-performance liquid chromatography HPLC), electron microscopy transmission electron microscope (TEM) and the scanning electron microscope (SEM), X-ray diffraction, and other specialized techniques to analyse and characterize materials.
 
 
 &bull; You will be responsible for trouble shooting for products from lab development stage to plant scale up using various analytical techniques.
 
 
 &bull; You will be Supporting complex generic projects by generating knowledge of Reference listed Drug (RLD) through reverse engineering and develop strategy to prove pharmaceutical sameness.
 
 
 &bull; You will be responsible for Coaching, Mentoring and training the scientists and members of the team.
 
 
 
 
 
 
 Qualifications
 
 
 
 
 
 Educational qualification:
 
 MS in Pharmaceutical Analysis/Post Graduation in Pharma/Physics
 
 
 
 Minimum work experience:
 
 5-10 years of experience
 
 
 
 Skills &amp; attributes:
 
 
 
 
 Technical Skills
 
 
 
 &bull; Hands on experience in Reverse Engineering of drug products
 
 
 &bull; Experience in Nuclear Magnetic Resonance (NMR), Fourier Transform Infrared Spectroscopy (FTIR), Ultraviolet- Visible Spectroscopy (UV-Vis).
 
 
 &bull; Knowledge on Morphology Analysis, Image Analysis and Optical Microscopy.
 
 
 &bull; Understanding and experience on Gas chromatography (GC) or high-performance liquid chromatography HPLC) method development and method validations.
 
 
 &bull; Hands on experience in liquid chromatography mass spectrometry (LCMS)/ liquid chromatography-high resolution mass spectrometry (LC-HRMS)
 
 
 &bull; Experience in electron microscopy, Transmission Electron Microscope (TEM) and the Scanning Electron Microscope (SEM)
 
 
 &bull; Knowledge on competitive strategies for technology innovation and Analytical Equipment.
 
 
 &bull; Proficiency in data analysis, interpretation, and statistical tools.
 
 
 
 
 
 
 
 Behavioral Skills
 
 
 
 &bull; Excellent communication and interpersonal skills.
 
 
 &bull; Ability to work with cross functional teams.
 
 
 &bull; Strong analytical and problem-solving abilities.
 
 
 &bull; Leadership skills to motivate and mentor the team.
 
 
 
 
 
 
 Additional Information
 
 
 
 
 
 About the Department
 
 
 
 
 
 
 Integrated Product Development Organisation
 
 
 
 
 
 We integrate our deep science capabilities and cutting-edge technology to develop innovative, accessible and affordable therapies for patients worldwide. We are a science-driven, innovation-focused pharmaceutical company committed to accelerating access to healthcare solutions to patients around the world. We have End to end capabilities in API, Formulations, Clinical, Intellectual Property and Regulatory Affairs. We are serving 55+ markets including USA, Canada, Europe, China, LATAM, ASEAN and all Emerging Markets with innovative and generic products ranging from Active pharmaceutical ingredients (API), Oral formulations, Parenteral (Injectables, Opthalmics) &amp; Other dosages
 
 
 Our product development efforts drive a portfolio of more than 1,000 products Enabled by our robust R&amp;D team consisting of more 200 scientists and functional experts and more than 150 doctorates, we have filed 1,071 patents and also published over 1,000 papers for peer review over the years.
 
 
 
 
 
 Benefits Offered
 
 
 
 At Dr. Reddy&rsquo;s we actively help to catalyse your career growth and professional development through personalised learning programs.
 
 
 The benefits you will enjoy at Dr. Reddy&rsquo;s are on par with the best industry standards. They include, among other things and other essential equipment, joining &amp; relocation support, family support (Maternity &amp; Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself.
 
 
 
 
 
 Our Work Culture
 
 
 
 Ask any employee at Dr. Reddy&rsquo;s why they come to work every day and they&rsquo;ll say, because Good Health Can&rsquo;t Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and we&rsquo;re always attuned to the new and the next to empower people to stay fit. And to do this, we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system, they can make magic.
 
 
 For more details, please visit our career website at
 
 https://careers.drreddys.com/#!/
 
 
</div>

Analytical Scientist

Ideal Option and Ideal Balance

<div>Description:

Location: Renton, WA
Compensation: $21.60/hr
Schedule: 7:30 AM - 4:00 PM Tuesday - Saturday
Training Schedule: 8:00 AM - 4:30 PM Monday - Friday
Ideal Option has been working on the front lines of the opioid epidemic since our first clinic opened in 2012. With more than 65 clinics across 10 states, we continuously strive to be the nation&rsquo;s leading provider of low-barrier evidence-based treatment for opioid use disorder. We are looking for a Laboratory Analyst 2 to join our growing team and help us in our vision to give back lives, reunite families, and heal communities that are suffering from the devastating effects of substance use disorder.
We value our patients and our employees!
We treat our employees like we would want to be treated ourselves: with respect and compassion.
Below are some specifics on what Ideal Option offers and the role.
The Role:
As a Laboratory Analyst 2, you play a key role in performing a variety of moderate and waived testing to include screening toxicology drug analysis, in a clinic or laboratory setting. Additional responsibilities include:<ul><li>
Analyzes patient specimens by performing and verifying diagnostic medical laboratory tests and following department protocols.</li><li>
Makes independent decisions relating to patient testing and prioritization of testing.</li><li>
Processes, packages, and ships specimens to be transported to the main laboratory for further testing.</li><li>
Performs and reports quality control on all instrumentation before reporting test results following established quality control policies and procedures.</li><li>
Performs preventative maintenance and troubleshooting on a variety of instruments and equipment and documents appropriately.</li><li>
Verifies all normal and abnormal results, correlates abnormal test results with other patient data, seeks pathologist or manager consultation if necessary, and notifies appropriate medical staff of test results.</li><li>
Maintains patients' medical records and verifies accuracy.</li><li>
Assists in ordering laboratory supplies and necessities to maintain appropriate level of inventory.</li><li>
Performs and reports routine and STAT laboratory tests of moderate complexity.</li><li>
Complies with national PHI laws including HIPAA and 42 CFR Part 2.</li><li>
Maintains continual sustained attendance.</li><li>
Other duties as assigned.</li></ul>
Benefits:
At Ideal Option, we offer our employees a competitive and comprehensive benefits program to recognize how important you are to the company.<ul><li>Medical, vision, and dental</li><li>Short-term and long-term disability options</li><li>Life insurance</li><li>Employee Assistance and Life Assistance programs</li><li>A 401K retirement program</li><li>Pet Insurance</li><li>Paid time off and paid holidays</li></ul>
Requirements:

Minimum Requirements:<ul><li>
Associate or bachelor's degree in science with at least 24 semester hours in Biology, Chemistry, Medical Laboratory Science or a combination.</li><li>
Attention to detail, specimen processing, immunoassay instrumentation.</li></ul>
Preferred<ul><li>
1 year experience in a clinical laboratory setting.</li></ul></div>

Laboratory Analyst 2

Luminol Biopharma Pvt Ltd

Job Title: Junior/Mid-Level Analyst &ndash; HPLC, UV, Dissolution, Assay, RS, and Method Validation Company: KMS Healthcare Pvt. Ltd. Department: Quality Control / Analytical R&amp;D Experience: 2-10 years in pharmaceutical analysisJob Summary:We are seeking an experienced Analyst with expertise in HPLC, UV-Vis spectroscopy, dissolution testing, assay, related substances (RS), and method validation as per ICH guidelines. The candidate will be responsible for conducting analytical testing, preparing protocols/reports, and ensuring compliance with regulatory standards.Key Responsibilities:1. Analytical Testing &amp; Instrumentation:<ul><li>Perform routine and non-routine analysis using HPLC, UV-Vis, dissolution apparatus, and other lab instruments.</li><li>Conduct assay, related substances (RS), dissolution, and stability testing as per pharmacopeial methods (USP/EP/BP/IP).</li><li>Troubleshoot and maintain analytical instruments (HPLC, UV spectrophotometer, dissolution apparatus).</li></ul>2. Method Validation &amp; Transfer:<ul><li>Prepare and execute method validation/verification protocols (Accuracy, Precision, Linearity, Specificity, LOD/LOQ, Robustness) as per ICH Q2(R1).</li><li>Support method transfer activities between labs or sites.</li></ul>3. Documentation &amp; Compliance:<ul><li>Prepare analytical reports, validation protocols, and reports in compliance with GMP/GLP.</li><li>Review and ensure data integrity (ALCOA+ principles).</li><li>Follow SOPs, pharmacopeial guidelines (USP/EP), and ICH requirements.</li></ul>4. Regulatory &amp; Audits:<ul><li>Support regulatory submissions (ANDAs, DMFs) with analytical data.</li><li>Participate in internal/external audits (FDA, WHO, MHRA).</li></ul>5. Cross-Functional Collaboration:<ul><li>Work with QA, R&amp;D, and production teams for investigations (OOS/OOT, deviations).</li><li>Train junior analysts on analytical techniques and compliance.</li></ul>Qualifications &amp; Skills:<ul><li>Education: Bio Technology/ M.Sc./B.Pharm/M.Pharm in Chemistry/Pharmaceutical Sciences.</li><li>Experience: 2-10 years in pharmaceutical QC/ADL labs, with hands-on experience in:</li><li>HPLC/UPLC (Method development/validation preferred).</li><li>UV-Vis spectroscopy, dissolution testing (Apparatus I/II).</li><li>Assay, RS, forced degradation studies.</li><li>Regulatory Knowledge: ICH, USFDA, GMP, GLP.</li><li>Software: Empower, LabSolutions, Dissolution software.</li><li>Soft Skills: Detail-oriented, problem-solving, teamwork.</li></ul>Preferred:<ul><li>Experience in oral solid dosages (tablets/capsules).</li><li>Knowledge of impurity profiling, stability studies (ICH Q1A).</li></ul>Why Join Us?<ul><li>Opportunity to work in a GMP-compliant lab with advanced instrumentation.</li><li>Career growth in analytical development/validation.</li><li>Exposure to global regulatory standards.</li></ul>Job Type: Full-timeLocation:Door No.6, Kamarajar St, East Tambaram, Selaiyur, Chennai, Tamil Nadu 600059Note:&middot; Experience in the relevant/same field.Please Share resume Mobile # +91 9500112999 (WhatsApp)Job Types: Full-time, PermanentPay: &#8377;35,000.00 - &#8377;70,000.00 per monthBenefits:<ul><li>Provident Fund</li></ul>Work Location: In person

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</div></div><div>Genel Nitelikler<ul><li>&Uuml;niversitelerin U&ccedil;ak, Uzay veya Makine M&uuml;hendisli&#287;i b&ouml;l&uuml;mlerinden mezun,</li><li>Statik, Dinamik, Titre&#351;im ve Mukavemet konular&#305;nda sa&#287;lam temellere sahip,</li><li>Yap&#305;sal Analiz konusunda tercihen en az 2 y&#305;l tecr&uuml;beye sahip,</li><li>Yayg&#305;n yap&#305;sal analiz programlar&#305;ndan en az birisinde (ABAQUS, ANSYS, NASTRAN vb.) tecr&uuml;be sahibi,</li><li>Karma&#351;&#305;k geometrileri analize haz&#305;rlama konusunda tecr&uuml;beye sahip,</li><li>&#304;leri seviyede MS Office bilgisine sahip,</li><li>&#304;leri seviyede &#304;ngilizce bilgisine sahip,</li><li>Karma&#351;&#305;k analiz s&uuml;re&ccedil;lerine sistematik ve tutarl&#305; &ccedil;&ouml;z&uuml;mler getirebilen,</li><li>Bireysel ve tak&#305;m halinde verimli &ccedil;al&#305;&#351;abilen,</li><li>Yo&#287;un i&#351; temposuna uyum sa&#287;layabilen,</li></ul>
&ldquo;Yap&#305;sal Analiz M&uuml;hendisi&rdquo; aray&#305;&#351;&#305;m&#305;z bulunmaktad&#305;r.
Tercih Sebepleri<ul><li>U&ccedil;u&#351; Mekani&#287;i ve U&ccedil;u&#351; Y&uuml;kleri konular&#305;nda bilgi sahibi olmak,</li><li>Kompozit malzeme &ouml;zellikleri, laminasyon planlar&#305; ve analiz s&uuml;re&ccedil;leri hakk&#305;nda tecr&uuml;be sahibi olmak,</li><li>Bilimsel programlama dillerinden en az birisine hakim olmak,</li><li>Yap&#305;sal analiz kodu geli&#351;tirmesinde bulunmu&#351; olmak.</li></ul></div></div><div></div>

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