chemistry laboratory technician

Sweeney Analytical Labs LLC

Job Overview We are seeking a highly motivated and detail-oriented Chemical Laboratory Technician to join our quality team. This position will include hands on experience in chromatograph , microbiology and pharmaceutical sample evaluation.Responsibilities<ul><li>Prepare, analyze, and document chemical samples using established laboratory techniques and procedures</li><li>Conduct quality control tests to verify product consistency and compliance with industry standards</li><li>Assist in microbiology, chemistry, and other specialized testing as required</li><li>Ensure laboratory operations adhere to Good Laboratory Practice (GLP), FDA regulations, CGMP (Current Good Manufacturing Practice), and other relevant standards</li><li>Support research &amp; development activities by executing experiments and analyzing data to inform project decisions</li></ul>Skills<ul><li>Strong understanding of laboratory procedures, techniques, and analysis skills across multiple disciplines including microbiology and analytical chemistry.</li><li>Familiarity with GLP, CGMP, FDA regulations, and quality control standards in pharmaceutical manufacturing</li><li>Knowledge of lab terminology</li><li>Proficiency in laboratory techniques such as sample preparation, chemical analysis, microscopy, and data collection methods</li><li>Excellent math skills for precise measurements and data interpretation</li><li>Prior experience in research laboratories or industrial laboratories demonstrating scientific research capabilities</li></ul>Pay: $20.00 - $32.00 per hourExpected hours: 40.0 per weekBenefits:<ul><li>Flexible schedule</li><li>Paid sick time</li><li>Paid time off</li></ul>Education:<ul><li>Bachelor's (Preferred)</li></ul>Experience:<ul><li>cGxP: 1 year (Required)</li></ul>Work Location: In person

Chemical Laboratory Technician

Reliance Industries Limited

<div>
 
 Job Accountabilities
 
 
 
 <ul>
 <li>
 To check the drilling fluid parameters assist in designing the hydraulic programs for hole cleaning and pore pressure.
 </li>
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 To analyse the produced gas and water sample from CBM wells and testing of Prop pant sand for procurement.
 </li>
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 Planning of different cement jobs/ acidisation / cement squeezing.
 </li>
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 To operate and maintenance of all type of laboratory instruments
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 Sampling bonding of prop pant sand and other chemicals &amp; testing of cement sample at factory premises.
 </li>
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 Interaction with the drilling engineer, completion engineer and G&amp;G personnel for better performance
 </li>
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 Quality control of the chemicals for a better performance and cost of the inventory control
 </li>
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 Mud quality and effective drilling operation
 </li>
 <li>
 Maintenance and operating of all types of laboratory equipment
 
 
 </li>
 </ul>
 Quality control testing well / chemicals / produced fluids
 
 
 
 Skill &amp; Competencies
 
 
 
 Good communication skill
 
 
 
 Education Required
 
 
 
 BE (Chemical) / M.Sc. (Chemistry)
 
 
 
 Experience Required
 
 
 
 Minimum 3 years in working experience in upstream (E&amp;P) Oil/Gas
</div>

Chemist Field Operation

Zoetis

<div><div>Lead Laboratory Technician &ndash; Chemistry</div><div>
100% Onsite &ndash; Louisville KY</div><div></div><div> 
Summary:</div><div>
The Lead Laboratory Technician holds a key leadership position within the lab, blending exceptional technical expertise with leadership and communication skills. This role is essential for mentoring and training junior team members, upholding the highest standards of test results, resolving complex issues, assisting the Supervisor in overseeing lab operations, and driving efficiency and cost-effective testing. This role works closely with Supervisors, Managers, and the Medical Team to align lab operations with organizational goals.</div><div></div><div> 
The Lead Technician position requires a complete understanding of all ZRL departmental processes including all safety practices, quality control, and testing procedures from set-up to reporting through the Laboratory Information System (LIS). This position will lead the laboratory through the daily workflow and must be a highly skilled, effective communicator with strong leadership abilities including the ability to handle complex problem-solving tasks including triaging samples and delegation of work. Additionally, The Lead Technician trains colleagues, performs advanced quality control tasks, and manages complex reporting and identification processes.</div><div></div><div> 
Job Duties:</div><div></div><ul><li> 
 Responsible for leading the lab team in strict adherence to all ZRL safety procedures and protocols.</li><li> Assists in overseeing day-to-day lab operations, including inventory management, equipment maintenance, and adherence to safety protocols.</li><li> Ensure all team members participate fully in the implementation of the laboratory and ZRL Quality Control and Assurance protocols.</li><li> Maintain rigorous quality control standards, reviewing and implementing QC plans to ensure accuracy and reliability in lab results.</li><li> Train and mentor team colleagues in the laboratory standard operating procedures for sample set-up, result interpretation, and reporting for all departmental tests.</li><li> Understand and interpret guidelines for results and assist team members with difficult cases.</li><li> Understand and utilize the Laboratory Information System (LIS) including for accessioning, requisition maintenance, test ordering and batch reporting.</li><li> Perform all reporting of results and manager review in LIS.</li><li> Engage with Medical and Leadership colleagues to resolve customer service issues, utilizing Salesforce as needed.</li><li> Operation and maintenance of all laboratory analyzers and equipment.</li><li> Delegate tasks as necessary to maintain a smooth and seamless workflow, even under the pressure of a high-volume testing work environment.</li><li> Engage with Medical and Leadership to improve departmental processes and eliminate waste while maintaining quality.</li><li> Perform literature reviews and additional training to stay current in laboratory Standard Operating Procedures (SOP).</li><li> Understand and ensure team compliance to all EH&amp;S biosafety requirements of the lab.</li><li> Address and resolve complex issues related to samples, instruments, and customer complaints, ensuring minimal disruption to lab operations. Ensures Corrective Actions are being initiated and resolved as problems occur.</li></ul><div></div><div> 
Education/Experience:</div><ul><li> BA/BS in Biology, or a related Science Field with 3+ Years of Diagnostic Laboratory Experience</li><li> Requires subject matter expertise on all major core lab benches (hematology, chemistry, urinalysis etc.)</li><li> Requires experience with 2-3 of the following instruments: Advia 2120i, Immulite 2000 XPi, AU680/5800, Clinitek Advantus, or Stago STarT.</li></ul><div></div><div> 
Technical Skills Required:</div><ul><li> Proficiency in Microsoft Platforms (Teams, Outlook, Word etc.)</li><li> Strong attention to detail and organizational skills.</li><li> Verbal and written communication skills.</li><li> Ability to work in a team environment and collaborate with colleagues.</li><li> Indirect leadership skills and ability to influence others</li><li> Ability to work independently and follow instructions accurately.</li><li> Advanced in all laboratory techniques including staining techniques, biochemical testing, and standard operating procedures for all tests offered.</li><li> Advanced understanding of all reporting guidelines.</li><li> Mentorship and Training</li><li> Problem-Solving</li><li> Operational Management</li><li> Innovation</li></ul><div></div><div> 
Physical Position Requirements:</div><ul><li> Ability to lift up to 50 pounds</li><li> Ability to bend, kneel, stoop, crouch</li><li> Ability to walk, sit, or stand for extended periods</li></ul> 
<div></div>
Full time<div></div>
Regular<div></div>
Colleague<div></div><div>
Any unsolicited resumes sent to Zoetis from a third party, such as an Agency recruiter, including unsolicited resumes sent to a Zoetis mailing address, fax machine or email address, directly to Zoetis employees, or to Zoetis resume database will be considered Zoetis property. Zoetis will NOT pay a fee for any placement resulting from the receipt of an unsolicited resume.</div><div></div><div>
Zoetis will consider any candidate for whom an Agency has submitted an unsolicited resume to have been referred by the Agency free of any charges or fees. This includes any Agency that is an approved/engaged vendor but does not have the appropriate approvals to be engaged on a search.</div><div></div>
Zoetis is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status or any other protected classification. Disabled individuals are given an equal opportunity to use our online application system. We offer reasonable accommodations as an alternative if requested by an individual with a disability. Please contact Zoetis Colleague Services at zoetiscolleagueservices@zoetis.com to request an accommodation. Zoetis also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act. All applicants must possess or obtain authorization to work in the US for Zoetis. Zoetis retains sole and exclusive discretion to pursue sponsorship for the acquisition or maintenance of nonimmigrant status and employment eligibility, considering factors such as availability of qualified US workers. Individuals requiring sponsorship must disclose this fact. Please note that Zoetis seeks information related to job applications from candidates for jobs in the U.S. solely via the following: (1) our company website at www.Zoetis.com/careers site, or (2) via email to/from addresses using only the Zoetis domain of &ldquo;@zoetis.com&rdquo;. In addition, Zoetis does not use Google Hangout for any recruitment related activities. Any solicitation or request for information related to job applications with Zoetis via any other means and/or utilizing email addresses with any other domain should be disregarded. In addition, Zoetis will never ask candidates to make any type of personal financial investment related to gaining employment with Zoetis.</div>

Lead Lab Tech – Chemistry

<div>
 
 Job Accountabilities -
 
 
 
 Support shift in charge for shift co-ordination work.
 
 
 Priorities the samples for testing.
 
 
 Provide right containers to collect samples, identifies right carriers to distribute samples and designate right location for pre-testing storage.
 
 
 Ensure the usability of the chemicals / standards to use in the test and performs the test by following the procedure step by step. Confirms test results by using validation techniques before reporting.
 
 
 Calibration -
 
 
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 Identify the calibrations as per the method protocol and the instruments as per schedule.
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 Prepare calibration and working standards as per requirement.
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 Perform the calibrations as per the method and instrument as per schedule. Standardises the laboratory solutions.
 
 
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 </ul>
 Evaluates performance of additives and process chemicals.
 
 
 Collects samples of raw materials as per the requirement and track the quality of incoming raw material.
 
 
 Timely testing and results reporting of Raw materials, in process, product &amp; trouble shooting samples of all plants.
 
 
 Classify the product grades based on the specification.
 
 
 Detect exceptions or deviations in test results
 
 
 Perform on-spot mitigation in emergency situation under the guidance of the section head
 
 
 Ensure proper sample retention as per defined lab procedure for addressing issues with customers (need based)
 
 
 Dispose left over samples safely as per SOP and co-ordinate with plant and other agencies for further actions.
 
 
 Awareness about Laboratory Quality Systems requirements and good knowledge and skills for LIMS and SAP QM operations for day to day laboratory work.
 
 
 Maintain laboratory inventory (Reagents, Glassware, and Equipment) and raise the requirement for its availability in time.
 
 
 Participate in various audits of lab quality systems including safety.
 
 
 Data Management
 
 
 Comply to quality systems
 
 
 Ensure timely entry approval of test results in LIMS.
 
 
 HSE &amp; other regulatory compliance
 
 
 Stay aware of environmental, site, statutory regulations.
 
 
 Handle chemicals and tools as per safety norms
 
 
 Ensure Good Housekeeping and safe working conditions
 
 
 Follow and enforce applicable HSE procedures/ practices
 
 
 Learning &amp; mentoring
 
 
 Conduct on job training to analysts and new joiners for laboratory analytical work.
 
 
 Conduct on job training to analysts and new joiners for laboratory safety.
 
 
 Business / Function-specific Competencies (Technical /Functional)
 
 
 Participate in external trainings and events as advised by the section head
 
 
 Timely execution of assigned tasks
 
 
 Erratic changes in plans
 
 
 Working with multiple interface such as business, customers, operations, E&amp;M and HSEF
 
 
 Sample management
 
 
 Prioritization of assigned activities
 
 
 HSEF -specific Competencies
 
 
 Fire Safety Management
 
 
 Fire &amp; Gas Detection system
 
 
 Waste Management
 
 
 Integrated Management System
 
 
 RIL HSE Management System
 
 
 HSE Policy, Principles, Standards and Procedures &amp; Practices
 
 
 Emergency Preparedness and response
 
 
 
 Education Qualification-
 
 
 
 B. Sc. Chemistry, Masters preferred
 
 
 
 Experience Required -
 
 
 
 Minimum 5-7 years in QA/QC discipline
</div>

Chemist - PT Lab / Chemical Lab - PSF / PFF / PFY

Lead Candidate

<div>
 
 
 
 QC Chemistry Method Transfer Scientist
 
 
 
 
 
 
 
 
 
 WHO?:
 
 
 
 
 
 
 
 If you&rsquo;re an experienced QC Chemist or Microbiologist looking to take your next steps, this Method Transfer role is a great opportunity!
 
 
 
 
 
 This exciting chance to join the team is offered by INCOG Biopharmaceutical Services, who are continuing to build their state of the art sterile injectable CDMO. Having won the Best Places to Work in Indiana 4 years in a row, INCOG is the perfect place to continue building your career!
 
 
 
 
 
 INCOG Biopharma Services in Indianapolis, IN is hiring a QC Chemistry Method Transfer Scientist who will be working closely with the Senior Director of Quality. They will be instrumental in championing and developing the organization's batch review excellence. This role offers the opportunity to work at INCOG&rsquo;s state-of-art sterile injectable CDMO during an exciting time of growth, contributing towards a better path to market for life-saving drugs.
 
 
 
 
 
 
 
 WHAT?:
 
 
 
 
 
 
 
 This role involves close collaboration with QC leadership and will provide develop and lead the program for performing method transfer for analytical and/or microbiological assays from client laboratories into the INCOG QC Laboratories.
 
 
 
 
 
 The role responsibilities are, but are not limited to:
 
 
 
 
 <ul>
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 Lead the development and implementation of the INCOG QC Method Transfer program for both analytical and microbiological assays.
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 Perform assessments of both incoming client methods and compendial test methods for raw materials, container/closures, API/BDS, in-process, and finished products for suitability with existing INCOG laboratory capabilities to identify if additional chemicals or instruments are required.
 </li>
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 Partner with customers to develop, review, approve, and execute method transfer into the chemistry and/or microbiology laboratory.
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 Collaborate with the Quality Team on building laboratory safety program to ensure a safe and quality-minded environment for all personnel working in the laboratory.
 </li>
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 Advocate for clients by collaborating cross-functionally to schedule microbiological sampling, testing, instruments, and personnel to meet customer needs and timelines.
 </li>
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 Support laboratory investigations using troubleshooting tools to identify errors, and exercise rapid decision making to implement corrective actions during OOS/OOT and other non-conformance events.
 </li>
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 Utilize various paper and automated systems to manage local QC and site policies, procedures, and technical reports throughout document lifecycles including authoring, reviewing, approving, and retiring.
 </li>
 </ul>
 
 
 
 
 
 
 YOU:
 
 
 
 
 
 
 
 Ideally, candidates will have a Bachelor&rsquo;s degree in Biology, Microbiology, Biochemistry, or Chemistry, along with 5 years of GMP manufacturing QC testing of pharmaceuticals.
 
 
 
 
 <ul>
 <li>
 Experience with using laboratory instrumentation from pH/conductivity meters, osmometers, and density meters to more complicated systems used for UHPLC/HPLC, GC, CE, and icIEF analysis.
 </li>
 <li>
 Ability to author scientifically sound SOPs, Work Instructions, Transfer Protocols and Summary Reports
 </li>
 <li>
 Prior leadership experience in GMP QC laboratories supporting pharmaceuticals is preferred but not essential
 </li>
 </ul>
 
 
 
 
 Curious? Send us your resume at apply@leadcandidate.com or you can find more information on our website.
 
 
 
 
 
 
 Don&rsquo;t meet all the requirements? Don&rsquo;t sweat! We&rsquo;re always looking for an excuse to discuss your next opportunity. You might just surprise yourself&hellip;
 
 
 
 
 
 
 
 Lead Candidate wholeheartedly supports Equality and Diversity in employment and opposes all forms of unlawful or unfair discrimination on the grounds of age, disability, sex, gender reassignment, sexual orientation, pregnancy and maternity, race, religion or belief and marriage and civil partnerships.
 
 
</div>

QC Chemistry Method Transfer Scientist

Falcon Laboratory LLC

Job SummaryFalcon Laboratory is seeking an experienced Senior Civil Lab Technician to oversee and perform testing of construction materials including soil, concrete, aggregates, and asphalt. The role involves supervising junior technicians, ensuring compliance with ASTM/AASHTO/BS standards, and maintaining high-quality laboratory operations.Key Responsibilities<ul><li>Perform and supervise laboratory testing of:</li><li>Soil (compaction, CBR, Atterberg limits, sieve analysis, etc.)</li><li>Concrete (slump, compressive strength, flexural strength, mix design support)</li><li>Aggregates (gradation, specific gravity, impact value)</li><li>Asphalt (Marshall stability, bitumen content, extraction tests)</li><li>Ensure all testing is conducted in accordance with ASTM, BS, AASHTO, or relevant local standards.</li><li>Review and verify test results before submission to engineers or clients.</li><li>Supervise and mentor junior lab technicians and assistants.</li><li>Maintain proper calibration and preventive maintenance of lab equipment.</li><li>Prepare and validate laboratory reports and documentation.</li><li>Coordinate with site teams for sampling and testing schedules.</li><li>Assist laboratory manager in audits, accreditation processes, and quality control procedures.</li><li>Ensure compliance with safety and quality management systems.</li></ul>Required Qualifications<ul><li>Diploma or Degree in Civil Engineering or related field.</li><li>2-3+ years of experience in construction materials testing laboratory.</li><li>Strong knowledge of international testing standards (ASTM, AASHTO, BS).</li><li>Experience handling laboratory audits and accreditation requirements (ISO 17025 preferred).</li><li>Proficiency in MS Office and laboratory reporting systems.</li></ul>Job Types: Full-time, Permanent

Civil Laboratory Technician

Kindeva Drug Delivery

Our Work Matters
 At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world.
 
The Impact You Will Make
 Kindeva Northridge is currently seeking a meticulous and detail-oriented Quality Control Laboratory Technician to join our team. The Quality Control Laboratory Technician will play a crucial role in ensuring that our incoming Raw Material and Hard Goods meet quality standards and regulatory requirements. This position requires strong attention to detail, excellent organizational skills, and the ability to perform a variety of quality control tests and inspections. The ideal candidate will be dedicated to maintaining high standards of product quality and safety.
 
Role Responsibilities
 <ul>
<li>Perform routine Quality Control tests on hard goods and packaging components using standard testing methods and instrumentation. Conduct tests to assess product quality and compliance with specifications.</li>
<li>Ensure that samples are properly labeled, handled, and stored to maintain sample integrity and traceability.</li>
<li>Operate laboratory equipment and instrumentation used for Quality Control testing, including spectrophotometers, pH meters, balances, and other analytical instruments. Follow Standard Operating Procedures (SOPs), Work Instruction (WI) and safety protocols for instrument operation.</li>
<li>Record test results, observations, and other relevant data accurately and legibly in laboratory notebooks, worksheets and/or electronic databases. Maintain detailed records of all Quality Control activities in compliance with regulatory requirements and Kindeva policies.</li>
<li>Communicate all non-conformances or atypical results to Quality Control Group Lead and/or Manager in a timely manner.</li>
<li>Document non-conformance in Quality Management System as required.</li>
<li>Support continuous improvement activities within functional group and/or department as needed.</li>
<li>Adhere to all safety regulations and Kindeva policies related to laboratory operations and quality control testing. Follow established protocols for handling hazardous materials, chemical waste disposal, and personal protective equipment (PPE) usage.</li>
<li>Comply with GMPs and department SOPs.</li>
<li>Update or Create documents such as SOPs, WIs or Worksheet/Forms as needed to update or document new procedures.</li>
<li>Work well in both a team and an individual environment.</li>
<li>Maintain flexibility to support unexpected rush material release requests.</li>
</ul>
Basic Qualifications
 <ul>
<li>High school diploma or equivalent required.</li>
<li>Minimum 3 years of experience in a Quality Control or Laboratory Technician role within a manufacturing environment.</li>
<li>Strong attention to detail and ability to follow written and verbal instructions accurately.</li>
<li>Proficiency in basic mathematical calculations and measurement techniques.</li>
<li>Commitment to maintaining a safe work environment and complying with regulatory requirements.</li>
<li>Ability to prioritize and manage multiple assignments while maintaining strong attention to detail</li>
<li>Excellent planning and organization skills required for our fast-paced environment and must be highly motivated, proactive and willing to take on new challenges.</li>
</ul>
Preferred Qualifications
 <ul>
<li>Associate degree or certification in a scientific field.</li>
</ul>
#LI-Onsite
 
California residents should review our Notice for California Employees and Applicants before applying.
 
The expected compensation range for this position represents a good faith estimate. The specific compensation offered to a candidate may vary based on factors including, but not limited to, the candidate’s relevant knowledge, training, skills, work location, and/or experience. In addition, this position may be eligible for a range of benefits (e.g., Medical, Dental, & Vision, Health Savings Accounts, Flexible Spending Accounts, Disability Benefits, Life Insurance, Voluntary Benefits, Paid Absences, and 401k Benefits, etc.).
 
Kindeva does not accept unsolicited assistance from headhunters or recruitment firms for any of our job openings. Any resumes or candidate profiles submitted to Kindeva employees—regardless of format—without a valid, signed agreement and an approved job order from an authorized signatory in Talent Acquisition will be considered the sole property of Kindeva. No fees will be paid in the event that a candidate is hired as a result of an unsolicited resume or referral.
 
Equal Opportunity Employer: 
Kindeva Drug Delivery is an Equal Opportunity/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, Protected Veteran status, sexual orientation, or any other characteristic protected by federal, state or local law.
 
Do you see yourself as part of the Kindeva mission? Click Apply Now Today!

QC Raw Materials Lab Technician

Search 4100+ Chemistry laboratory technician jobs near you this March. New roles added regularly across leading industries. Apply today.