analytical technician

eCom Solutions Inc

Job Title: Laboratory TechnicianDuration: Continued As Needed &ndash; No End Date - (Temporary with Potential for Full-Time Hire)Shift: Mon-Fri 8am-4pm or 9am-5pmInterview Process: Video interview/In PersonWe are seeking a detail-oriented and motivated Laboratory Technician to support our Research &amp; Development (R&amp;D) Labs, including the New Product Development, Second Sourcing, and Value Engineering teams. This is a temporary position with the potential for a full-time opportunity based on performance and business needs.In this role, you will perform analytical testing on ingredients and finished products using a variety of advanced laboratory instruments. You&rsquo;ll also manage shelf-life and accelerated aging studies, contributing valuable data to our R&amp;D initiatives. Once trained, the ideal candidate will be able to work independently and maintain a high level of accuracy and attention to detail.Key Responsibilities:<ul><li>Conduct analytical testing of ingredients, powders, ready-to-drink beverages, and sports nutrition bars using equipment such as:</li><li>Dynamic Light Scattering Particle Size Analyzer</li><li>Dynamic Vapor Sorption (DVS)</li><li>Polarized Light Microscope</li><li>Rheometer</li><li>Differential Scanning Calorimeter (DSC)</li><li>Shear Cell</li><li>Other advanced lab instruments</li><li>Prepare and monitor ingredient and product samples for accelerated aging and shelf-life studies, and perform testing at designated intervals.</li><li>Record, organize, and format data using Microsoft Office tools (Excel, Word, PowerPoint).</li><li>Gain proficiency in software specific to each analytical instrument used in the lab.</li></ul>Qualifications: Minimum Requirements:Associate&rsquo;s degree in Food Science, Nutrition, Biology, Chemistry, or a related scientific field.Preferred Qualifications:Bachelor&rsquo;s degree in Food Science, Nutrition, Biology, Chemistry, or a related field.<ul><li>1&ndash;2 years of relevant laboratory experience in an academic or industrial setting.</li><li>Experience with advanced analytical instrumentation and laboratory best practices.</li></ul>Job Type: ContractPay: $24.47 - $30.00 per hourBenefits:<ul><li>Dental insurance</li><li>Health insurance</li></ul>Work Location: In person

Lab Technician

Eurofins

<div>Company Description 
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic, and labelling is accurate.
Eurofins is dedicated to delivering testing services that contribute to the health and safety of society and the planet, and to its corporate responsibility to protect the environment and ensure diversity, equity, and inclusion across the entire network of Eurofins companies. 
Job Description 
Come Join the leader in Environment Testing. Eurofins Environment Testing has a fulltime entry level opportunity with full benefits. The Laboratory Technician I, using general laboratory methods, techniques, equipment, and instrumentation in compliance with Eurofins Environment Testing America&rsquo;s Quality Assurance programs and standard operating procedures, supports laboratory operations through general maintenance of laboratory and supply storage areas, equipment, instruments, and supplies.
Shift &amp; Hours: Position is full time, Wednesday-Sunday 12:00pm-9:00pm
Compensation (DOE) - $17.50/hourly Plus 15% shift ($20.13/hour) differential when on shift and Full Benefits
Essential Duties and Responsibilities<ul><li>
Performs routine lab tasks that provide experience and familiarization with methods, practices, and programs. These include:<ul><li>
Preparation of samples using standard techniques</li><li>
Performing chemical analysis using standard techniques</li><li>
Calculating data</li><li>
Recording and reporting data and any unusual test occurrences to the supervisor</li><li>
Performing routine instrument maintenance</li></ul></li><li>
Responsible for performing job functions in compliance with EHS and QA standards</li><li>
Responsible for general housekeeping in his/her work area</li><li>
Ability to become trained and competent on complex instrumentation including but not limited to gas chromatography, gas chromatography/mass spectrometry, atomic absorption, ICP, and instrument specific data systems.</li></ul>
Secondary Duties<ul><li>
Works under close supervision using routine and standard methods</li><li>
Aliquots and weighs samples</li><li>
Washes glassware</li></ul> 

Qualifications 
Requirements<ul><li>
Education: High school Chemistry coursework a must, basic laboratory experience</li><li>
Experience: Laboratory experience helpful Previous production-oriented work helpful (awareness and ability to meet deadlines)</li><li>
Authorization to work in the United States indefinitely without restriction or sponsorship</li><li>
Final candidates must pass a pre-employment background check and drug screen</li><li>
Must have a valid US drivers license without recent incident.</li><li>
Professional working proficiency in English is a requirement, including the ability to read, write and speak in English.</li><li>
Perform other duties as assigned</li></ul>
Knowledge<ul><li>
Analytical and/or General Science &#61623; Scientific methods and method compliance</li><li>
Strong Mathematics background</li><li>
Knowledge of Standard Operating Procedures</li><li>
Knowledge of laboratory procedures</li><li>
Laboratory safety rules and chemical hazards</li></ul>
Skills<ul><li>
General knowledge of chemistry and/or general science</li><li>
Basic mathematical skills</li><li>
Production work</li><li>
Good organizational skills</li><li>
Good communication skills</li><li>
Problem solving skills</li><li>
Ability to muti-task</li><li>
Quick learner</li><li>
Work independently</li><li>
Work within time constraints</li></ul>
Abilities<ul><li>
Use calculator/mathematical formulas and concepts</li><li>
Complete work within time and quality constraints</li><li>
Work independently following written or verbal instructions</li><li>
Cooperate and coordinate both orally and in writing</li><li>
Follow and learn appropriate protocols in one or more of the following disciplines:<ul><li>
Organic preparation</li><li>
Metals preparation and analysis</li><li>
Gas Chromatography</li><li>
Gas Chromatography/Mass Spectrometry</li><li>
Radio Chemistry</li><li>
Wet Chemistry</li><li>
High Resolution preparation and analysis</li><li>
Low Resolution preparation and analysis</li></ul></li></ul>
Physical Requirements<ul><li>
Lifting and Carrying: Lifting up to 50 pounds and carrying up to 30 pounds when moving samples and disposing of waste</li><li>
Pushing and Pulling: Pushing and pulling up to 200 pounds when moving sample carts and gas tanks</li><li>
Body Positions: Approximately 60% of time standing when analyzing samples, 10% walking when moving about laboratory, and 30% sitting when working at computer, doing paper work, or analyzing samples. These percentages vary significantly Page 4- Analyst I depending upon duties being performed. Must be able to sit, stand, or stoop for long periods of time.</li><li>
Body Movements: Stooping, kneeling, crouching, and reaching when getting samples and performing analyses</li><li>
Smelling: For unusual odors, leakage, contamination</li><li>
Hand Use: Handling samples, operating instruments, data entry</li><li>
Hearing: Conversational hearing ability</li><li>
Vision: Performing analyses, viewing computer screen, doing paperwork</li><li>
Speaking: Conversational speaking ability.</li></ul>
This position description is written as a guideline to inform employees of what is generally expected of them at each job level. The description is not intended to be all encompassing or limiting in any manner; rather, it is hoped it will add understanding and better reflect the work performed at all levels of employment. Duties and responsibilities other than those listed may be included as needed within the work group or the company as a whole. 
Additional Information 
Please note - Eurofins Environment Testing (USA) provides a compensation range for informational purposes, the actual base salary may vary based upon, but not limited to, relevant experience and skill set, base salary of internal peers, business sector, and geographic location.
As a Eurofins employee, you will become part of a company that has received national recognition as a great place to work. We offer excellent full-time benefits including comprehensive medical coverage, life and disability insurance, 401(k) with company match, paid holidays, paid time off, and dental and vision options.
We support your development! Do you feel you don&rsquo;t match 100% of the requirements? Don&rsquo;t hesitate to apply anyway! Eurofins companies are committed to supporting your career development.
We embrace diversity! Eurofins network of companies believe in strength and innovation through diversity, being an Equal Opportunity Employer. We prohibit discrimination against employees or applications based on gender identity and/or expression, race, nationality, age, religion, sexual orientation, disability, and everything else that makes employees of Eurofins companies unique.
Sustainability matters to us! We are well on our way to achieving our objective of carbon neutrality by 2025, through a combination of emission reduction and compensation initiatives. We encourage our laboratory leaders to make sustainable changes at their local level, and in addition to their initiatives we also count on our dedicated carbon reduction team to help us to achieve this goal!
Find out more in our career page: https://careers.eurofins.com/
Company description: Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.
The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in discovery pharmacology, forensics, advanced material sciences and Eurofins Scientific 2/2 March 2023 agroscience contract research services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
In over 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralised and entrepreneurial network of ca. 900 laboratories in 61 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.
In 2022, Eurofins generated total revenues of EUR 6.7 billion, and has been among the best performing stocks in Europe over the past 20 years.
We do not offer Visa Sponsorship for this role.
Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.<div></div>
Eurofins USA Environment Testing is a Disabled and Veteran Equal Employment Opportunity employer.</div>

Lab Technician (Weds-Sun 12pm-9pm) - Metals Prep, Environmental Testing

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

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

Catalent Pharma Solutions

<div>Analytical Chemist II
Position Summary
Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually. Catalent is committed to a Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer and Catalent employee.
Catalent&rsquo;s Greenville, N.C. facility specializes in end-to-end turn-key solutions for oral solid dosage forms, including integrated formulation development, analytical services, commercial manufacturing, and packaging. This state-of-the-art facility has had over $100M of investments in recent years and features fit-for-scale capacity with potent handling capabilities, ideal for orphan or targeted drug development.
The Analytical Chemist II is responsible for independently performing routine and non-routine analytical testing in support of pharmaceutical products following all applicable safety, quality, and regulation requirements. Under general supervision, the Analytical Chemist II will author standard operating procedures, analytical testing procedures, final submission ready documents, and create document templates for use by junior team members.
This position is 100% on-site at the Greenville site.
The Role<ul><li>
Independently perform routine and complex testing for chromatographic and spectrophotometric methods (HPLC, GC, UV) of analysis for excipients, new chemical entities and/or drug products.</li><li>
Compare laboratory data against specifications and trend data where applicable to determine if results meet requirements.</li><li>
Interpret data and make recommendations to management for improvement or potential concerns.</li><li>
Create report templates and/or enter data into established reports/templates or software-based systems.</li><li>
With guidance, propose applicable specifications based on data obtained in support of certain programs.</li><li>
Ensure proper usage, care, and return of calibration standards including, but not limited to, reference standards, timers, thermometers, and instrumentation.</li><li>
Ensure accuracy of testing by following method/standard instructions and adhering to internal SOPs to eliminate the potential for repeat testing, deviations, and investigations.</li><li>
Direct and assist in laboratory personnel training when required.</li><li>
All other duties as assigned.</li></ul>
The Candidate<ul><li>
Associate degree in Biotechnology, Chemistry or equivalent science degree with 4 years of professional experience in pharmaceutical analytical chemistry or;</li><li>
BS or BA degree in a science-related field (e.g. Biology, Chemistry, Pharmaceutical Sciences) with 3 years of professional experience in pharmaceutical analytical chemistry or;</li><li>
Master&rsquo;s degree in a science-related field with 2 years of professional experience in pharmaceutical analytical chemistry.</li><li>
2 years HPLC and GC experience required.</li><li>
Experience in a Catalent analytical laboratory in a role that is independent and proficient in chromatography and data review as well as troubleshooting and technical understanding may be substituted for 2 years of professional experience.</li><li>
Position requires the ability to lift 10-50lbs, unassisted.</li><li>
Majority of the work day is performed while standing, walking, lifting, pulling, and pushing.</li><li>
Requires bending, squatting, crawling, climbing, and reaching.</li><li>
Some exposure to hazardous chemicals and other active chemical ingredients.</li></ul>
Why You Should Join Catalent<ul><li>
Competitive medical benefits and 401K</li><li>
152 hours of PTO + 8 Paid Holidays</li><li>
Dynamic, fast-paced work environment</li><li>
Opportunity to work on Continuous Improvement Processes</li></ul>
Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.
personal initiative. dynamic pace. meaningful work.
Visit Catalent Careers to explore career opportunities.
Catalent is an Equal Opportunity Employer, including disability and veterans.
If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process. 
Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written &amp; signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.
Important Security Notice to U.S. Job Seekers:
Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond&mdash; it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities.
California Job Seekers can find our California Job Applicant Notice HERE.</div>

Analytical Chemist II

C2HR LLP

We are looking for a dedicated Lab Technician - Female (TUNIS - FILI ) to join our team. As a Lab Technician, you will play a crucial role in conducting various laboratory tests and experiments to support our research and development efforts. Your work will be essential in ensuring the accuracy and reliability of our scientific data, contributing to the overall success of our projects in the Hospital/Health Care industry.As a Lab Technician you will have the opportunity to work on cutting-edge projects that aim to improve healthcare outcomes and advance medical knowledge. Your attention to detail and precision will be key in maintaining the quality standards of our laboratory operations. This role offers a dynamic environment where you can enhance your skills and make a meaningful impact on the healthcare sector.Responsibilities:<ul><li>Performing various laboratory tests and experiments accurately and efficiently.</li><li>Preparing samples, specimens, and equipment for testing.</li><li>Recording and analyzing data with precision and attention to detail.</li><li>Maintaining laboratory equipment and ensuring proper calibration and functioning.</li><li>Following standard operating procedures (SOPs) and safety guidelines at all times.</li><li>Collaborating with other team members to achieve project goals and deadlines.</li><li>Reporting any deviations or issues in test results promptly to the supervisor.</li><li>Assisting in the development and optimization of laboratory procedures.</li></ul>Requirements:<ul><li>Associate degree in a relevant field (e.g., Medical Technology, Biology, Chemistry).</li><li>Proven experience working as a Lab Technician or in a similar role.</li><li>Strong knowledge of laboratory best practices and procedures.</li><li>Ability to operate and maintain laboratory equipment effectively.</li><li>Excellent analytical skills and attention to detail.</li><li>Good communication and teamwork abilities.</li><li>Ability to work independently with minimal supervision.</li><li>Adherence to safety and quality standards in a laboratory setting.</li></ul>Benefits:<ul><li>Accommodation</li><li>Transportation</li><li>Pay -5000 QAR</li></ul>Job Type: Full-time

Lab Technician - Female

Road and Transport, RTA Dubai

Job Title Civil Engineering Technician - Roads and Transport Authority Dubai Job Description Civil Engineering Technician - Roads and Transport Authority Dubai Job Location: Dubai, United Arab Emirates Industry: Government Administration Function: Civil Engineering Technician Gender: Any Candidate Nationality: All Nationalities (Priority for UAE Nationals) Job Type: Full-time Position Overview The Roads and Transport Authority (RTA) in Dubai is looking for a motivated Civil Engineering Technician to join its Right of Way department. This role involves conducting technical inspections, auditing safety compliance, and ensuring adherence to engineering standards within road corridors. What You ll Do * Contribute to developing field survey plans for assessing asset conditions within road corridors * Perform technical and engineering audits on safety standards and specifications for ongoing work * Document field visits using electronic systems for accurate reporting and follow-up actions * Submit proposals for engineering modifications to enhance road and public safety * Verify compliance of traffic diversions with approved engineering plans and permits * Monitor service project work programs within road corridors and report deviations * Follow up on closing damage reports related to road assets and ensure corrective actions * Address and analyze client complaints, taking necessary actions to improve service quality * Coordinate with consultants and contractors to ensure compliance with corrective measures * Implement scheduled technical inspections and monitor compliance with laws and standards Ideal Profile * Bachelor s degree in Civil, Architectural, or Electrical Engineering (0 years of experience) OR * Diploma in Engineering (2 years of experience) OR * Technical/Industrial High School Certificate (3 years of experience) * Strong knowledge of engineering and safety standards in road infrastructure projects * Excellent problem-solving and analytical skills * Ability to work under pressure and manage multiple priorities * Proficient in using technical reporting systems and related software * Strong communication and interpersonal skills

Civil Engineering Technician - Roads and Transport Authority

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