Laboratory Analyst jobs at Occidental Petroleum

Westlake offers you the potential to enrich your work life and career experience in an entrepreneurial environment. We work together to enhance peoples' lives through our products and presence in the communities in which we operate. This position provides analytical support to the Plaquemine Operating Units. DUTIES AND RESPONSIBILITIES May include, but are not limited to, the following: Demonstration of a strong safety mindset through personal behavior and commitment to environmental, health & safety policies. Comply with Laboratory Safety Policy and site HSP's. Participation in the PACE safety culture. Writes permits and work orders in accordance with company environmental, health and safety and operational procedures. Reports injuries, incidents and hazards to supervision as soon as reasonably possible. Conducts tasks and operational duties with appropriate PPE as assigned. Reviews JHA for appropriate PPE needed for routine and non-routine duties. Actively participates in unit safety training and monthly safety modules. Membership on the Emergency Response Team. Analyze raw material, in-process materials, environmental samples and finished products related to sites operational units using Laboratory standard operating procedures and specifications. Review all results and then report them accordingly to the proper operating unit. Input of data into LIMS/SAP. Assist with preventive maintenance of instrumentation. Assist with troubleshooting of instrumentation. Assist with laboratory housekeeping and 5S to maintain clean working environment. Perform assigned duties needed to keep the lab functioning efficiently. Carry out other activities/tasks as needed/assigned by management. EDUCATION, EXPERIENCE AND QUALIFICATIONS Bachelor's degree in chemistry or science/technical field strongly preferred, with a minimum of 12 hours in chemistry course work (applicable experience can be substituted for chemistry course work). Minimum of two years previous laboratory experience required (clinical/research acceptable). Basic laboratory skills such as quantitative and qualitative testing, ability to interpret results. Experience gas or liquid chromatography, ICP and/or discrete liquid analysis a plus Excellent verbal and written communication skills Advanced computer skills, particularly with Microsoft Office Suite, LIMS, SAP and statistical software. Basic troubleshooting skills with the ability to escalate problems Experience with regulatory certifications/accreditations such as ISO 9001, cGMPS, FCC, and ASTM. This position also requires a high degree of organizational skills to be able to meet deadlines. This position requires the ability to work a 12-hour rotating day shift schedule with holidays and weekends. Occasional overtime, nights and callouts will be required as well. PHYSICAL DEMANDS While performing the duties of this job, the employee is frequently required to sit; stand; walk; use hands to touch, handle, or feel; reach with hands and arms; and talk or hear. The employee is occasionally required to stoop, kneel, or crouch. The employee must occasionally lift and/or move up to 10 pounds, and infrequently lift and/or move up to 50 lbs. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception, and ability to adjust focus. The employee must frequently make minor decisions requiring limited judgement, general decisions in the absence of specific directions, and perform activities requiring sustained concentration. WORK ENVIRONMENT The noise level in the work environment is sometimes moderate when working in an office, however, some of the work may be required in the operating units which mandates usage of required PPE including safety glasses, hearing protection, etc. May also result in exposure to outside elements and may require usage of stairs. Travel may occasionally be required. Westlake is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to any characteristics protected by applicable legislation. If you are an active Westlake employee (or an employee of any Westlake affiliates), please do not apply here. You will apply via the Jobs Hub application in Workday.

provides analytical support to the Plaquemine Operating Units. DUTIES AND RESPONSIBILITIES May include, but are not limited to, the following: * Demonstration of a strong safety mindset through personal behavior and commitment to environmental, health & safety policies. * Comply with Laboratory Safety Policy and site HSP's. * Participation in the PACE safety culture. * Writes permits and work orders in accordance with company environmental, health and safety and operational procedures. * Reports injuries, incidents and hazards to supervision as soon as reasonably possible. * Conducts tasks and operational duties with appropriate PPE as assigned. * Reviews JHA for appropriate PPE needed for routine and non-routine duties. * Actively participates in unit safety training and monthly safety modules. * Membership on the Emergency Response Team. * Analyze raw material, in-process materials, environmental samples and finished products related to sites operational units using Laboratory standard operating procedures and specifications. * Review all results and then report them accordingly to the proper operating unit. * Input of data into LIMS/SAP. * Assist with preventive maintenance of instrumentation. * Assist with troubleshooting of instrumentation. * Assist with laboratory housekeeping and 5S to maintain clean working environment. * Perform assigned duties needed to keep the lab functioning efficiently. * Carry out other activities/tasks as needed/assigned by management. EDUCATION, EXPERIENCE AND QUALIFICATIONS * Bachelor's degree in chemistry or science/technical field strongly preferred, with a minimum of 12 hours in chemistry course work (applicable experience can be substituted for chemistry course work). * Minimum of two years previous laboratory experience required (clinical/research acceptable). * Basic laboratory skills such as quantitative and qualitative testing, ability to interpret results. * Experience gas or liquid chromatography, ICP and/or discrete liquid analysis a plus * Excellent verbal and written communication skills * Advanced computer skills, particularly with Microsoft Office Suite, LIMS, SAP and statistical software. * Basic troubleshooting skills with the ability to escalate problems * Experience with regulatory certifications/accreditations such as ISO 9001, cGMPS, FCC, and ASTM. * This position also requires a high degree of organizational skills to be able to meet deadlines. * This position requires the ability to work a 12-hour rotating day shift schedule with holidays and weekends. Occasional overtime, nights and callouts will be required as well. PHYSICAL DEMANDS While performing the duties of this job, the employee is frequently required to sit; stand; walk; use hands to touch, handle, or feel; reach with hands and arms; and talk or hear. The employee is occasionally required to stoop, kneel, or crouch. The employee must occasionally lift and/or move up to 10 pounds, and infrequently lift and/or move up to 50 lbs. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception, and ability to adjust focus. The employee must frequently make minor decisions requiring limited judgement, general decisions in the absence of specific directions, and perform activities requiring sustained concentration. WORK ENVIRONMENT The noise level in the work environment is sometimes moderate when working in an office, however, some of the work may be required in the operating units which mandates usage of required PPE including safety glasses, hearing protection, etc. May also result in exposure to outside elements and may require usage of stairs. Travel may occasionally be required.

Responsibilities Follows defined test plans and datasheets with necessary supervision/support. Evaluates test performance and sample operation to properly evaluate test results. Records and explains test results and completes test report. Serves as Lead for simple test programs as assigned with the necessary assistance. Communicates project status and results as needed. Holds responsibility for defining test plan, report completion and accuracy, meeting of agreed deadlines, and managing project related activities. Examines customer samples and learns to operate appropriate tests for each case with support. Communicates with internal customers during setup and operation to ensure proper evaluation. Directs, builds and/or adapts simple test setups, sample preparations/solutions and instruments to new situations, based on test plans and instructions. Trains other lab staff on these test procedures or instruments. Operates and maintains test instruments appropriately to measure and test samples. Performs maintenance on designated test instruments and laboratory area. For a single testing technology, integrates basic process and instruments improvements into all aspects of the job. Communicates with management and technical staff to provide suggestions for new instruments, processes, and forms to improve accuracy and efficiencies. Understands and follows safe chemical hygiene practices. Read and follow the Underwriters Laboratories Code of Conduct, and follow all physical and digital security practices. Other duties as assigned. #LI-BW1 #LI-Onsite Qualifications Bachelor's degree or diploma from an accredited university through a formal program of study in Chemistry or related discipline including Chemical Engineering, Biochemistry, Organic/Inorganic Chemistry, Material Science but not limited to these disciplines only. Demonstrated ability to manage multiple projects while maintaining high quality and exceptional customer service. Demonstrated ability to successfully partner with Engineering and other Laboratory Personnel to complete projects in a timely manner with high quality. Demonstrated ability to analyze special testing needs. Effective communication skills and ability to interact with customers Demonstrated ability to be innovative and creative Desire to work in a team-oriented environment Ability to use Microsoft Office suite is a must Ability to incorporate automation into day-to-day testing. Total Rewards: We understand compensation is an important factor as you consider the next step in your career . The estimated salary range for this position is $52,900 to $70,500 and is based on multiple factors, including job-related knowledge/skills, experience, geographical location, as well as other factors. This position is eligible for annual bonus compensation with a target payout of 5% of the base salary. This position also provides health benefits such as medical, dental and vision; wellness benefits such as mental and financial health; and retirement savings (401K) commensurate with the standard rewards offered in each individual location or country. We also provide full-time employees with paid time off including vacation (15 days), holiday including floating holidays (12 days) and sick time off (72 hours).

Onsite - Gurnee IL Who We Are: PurposeBuilt Brands, rooted in a legacy dating back to Weiman, stands as a pioneer in crafting top-tier products for specialty surfaces. Our beloved brands, including Weiman, Goo Gone, Green Gobbler, Biokleen, Gonzo, Magic, Wright's, Stone Care International, Urnex, Five Star, and Micro-Scientific, are preferred choices among consumers and seasoned professionals alike. At PBB, we seek to hire employees who bring a level of engagement, drive, and performance that pushes business forward. We work together and are motivated by positive results, while continuously thriving in a scrappy environment. We believe our greatest assets are the talented and passionate employees who are motivated by our purposeful work. Our company may be 60 years old, but the real growth is just getting started. The Role: The Quality Assurance Chemist is responsible for ensuring finished products are made to quality specifications. This position will oversee the quality of a product from raw materials to finished product. The position will also be responsible for ensuring that the quality lab is maintained and sufficient to perform lab testing. The Quality Assurance Chemist will work directly with production, research and development, and supply chain departments. What You Will Do: Perform chemical and microbial testing of batches and make adjustments as needed Inspect raw materials including chemicals, packaging components, and labels Assist Quality Technicians and production with finished product inspections Calibrate and maintain lab equipment Troubleshoot lab equipment Inspect and approve FDA product for release Assist in validation of lab equipment (IQ, OQ, PQ) Assist with product validations Maintain quality assurance lab Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice. What You Will Bring: Bachelor's Degree in a science discipline or equivalent experience 2-5 years previous lab experience Basic understanding of chemistry and laboratory equipment (e.g., pH meter, viscometer, UV-Vis, gas chromatograph, FTIR, auto titrator, etc.). Strong computer skills (proficient in MS Word, Excel, PowerPoint, and use of Access databases). Excellent verbal and written communication skills. Ability to problem solve and good math skills. Strong attention to detail and organizational skills. Understanding of manufacturing processes Hours: Monday - Friday, 5:00 p.m. - 2:00 a.m. Benefits: PBB offers a wide range of benefits because we understand no two employees are the same. We want our employees to feel empowered to set their day up for success, whether that's in the office or remote. What We Offer: Flexible work options (fully remote, hybrid, onsite) Generous paid time off Competitive salaries and bonus incentives 401K company match Competitive medical, dental, & vision insurance Pet insurance Annual fitness stipend Unmatched employee discount on all products Summer Hours LinkedIn learning membership Job Title: Quality Assurance Chemist PBB Job Code: QAC Mercer Job Code: QLT.03.006.P10 FLSA Status: Exempt Reports To: QA Manager Job Function: Quality Work Location: Gurnee IL Travel Required: None

**KNOWLEDGE/ EXPERIENCE/SKILLS:** Typical Requirements: Two or more years of either applicable lab experience or relevant college coursework. Physically capable of working within a laboratory environment on a rotating days schedule. Computer literacy & mechanical aptitude. Strong attention to detail and ability to work independently or as part of a team. Basic skills with Microsoft Excel, Word, Outlook and PowerPoint. Experience with polymer analyses and testing with MFI, Extruder, and DSC is highly desirable. Familiarity with SQC, ISO 9001, ISO 17025 quality systems. **PRINCIPAL ACCOUNTABILITIES:** Accurate, efficient, and un-biased analysis of finished products in a timely manner is high priority. Accountability maintained through the management hierarchy. Control established through the timing & application of documented procedures/methods/protocols and oversight/supervision of activities. This position requires a high level of personal organization and discipline in conducting analyses and logging results on a routine basis. A significant number of inter-departmental activities are reliant upon the accuracy of data collected and reported by this position.

Job Highlights * With support of the Head of Quality Assurance, this position will establish comprehensive maintenance system for analytical instrumentation. * Responsible for troubleshooting, calibration, and stanardization of instruments. * Development and validation of new analytical methods, periodic evaluation of the accuracy and validity of existing tests. * Review and implementation procedures, calibrations, and preventitive maintenance routine. * Source evaluation of raw materials, maintenance and evaluation of raw material records, analysis and disposition of recovered raw materials. * With the support of the Head of Quality Assurance facilitate and monitor sample evaluations. * Provide analytical support for special projects. * All other duties as assigned. Experience / Skills * Minimum of an Associate's degree, Bachelor's preferred, in Chemistry, Analytical Chemistry, or related discipline. * 2 to 5 years of experience in calibration, maintenance, and troubleshooting of analytical equipment. * 2+ years of experience with Agilent GC-FID, GC-MSD, HPLC, ICP-OES and associated software. * Demonstrated method development and validation skills. * Proficiency with Microsoft Office Suite and some familiarity with SAP, LIMS, and QMS. * Must be able to effectively prioritize tasks, work well under time pressure, and possess practical skills to resolve day-to-day laboratory and production operational issues. * Successful candidate will be able to communicate with employees across all departments. Location: Fords Employee Type: Regular Who we are LANXESS is a leading specialty chemicals company with about 12,000 employees in 32 countries. The core business of LANXESS is the development, manufacturing and marketing of chemical intermediates, additives and consumer protection products. LANXESS has achieved leading positions in the Dow Jones Best-in-Class Index and the MSCI ESG and ISS ESG ratings, among others, for its commitment to sustainability. Be part of it! What we offer you * Compensation: We offer competitive compensation packages, inclusive of a global bonus program and an individual performance bonus program. The minimum established pay for this position is $74,500. Please note, the actual compensation may vary based on geographic location, work experience, education, and skill level. * Comprehensive Benefits: We provide a variety of benefits to support your financial security, health and wellbeing including retirement plans, health programs, life insurance and medical care. * Work-Life & Flexibility: We support you in maintaining a balance between working hours and personal life. With our global "Xwork" program, we offer flexible working arrangements in all countries in which we operate. * Training & Development: We are committed to your professional and personal development and encourage you in the ongoing pursuit of education, training and knowledge through both formal and informal learning. * Diversity: LANXESS is an Equal Opportunity Employer and all qualified applicants will receive consideration for employment without regard to race, color, ethnicity, gender, gender identity, sex, sexual orientation, age, social class, physical ability or attributes, religion, national origin, veteran status and political beliefs. LANXESS has a value-based performance culture. We are seeking a range of human interests, backgrounds, and experiences that can be engaged to achieve respect, ownership, trust, professionalism, integrity and healing across all sectors. We are looking to find diverse and talented people to join our team. Studies have shown that some individuals are less likely to apply if they do not meet 100% of the criteria. We are looking to equalize the gap! If you are excited about this role but your past experiences do not align perfectly with every qualification, we encourage you to apply. We will look to assess your talent against our competencies, values and requirements to get the best organizational fit. You might be the right candidate for this or other roles we have available! Join the LANXESS team! Nearest Major Market: New Jersey Job Segment: Chemical Research, QA, Quality Assurance, Chemistry, Instrumentation, Engineering, Quality, Technology, Science

We are Reckitt Home to the world's best loved and trusted hygiene, health, and nutrition brands. Our purpose defines why we exist: to protect, heal and nurture in the relentless pursuit of a cleaner, healthier world. We are a global team united by this purpose. Join us in our fight to make access to the highest quality hygiene, wellness, and nourishment a right and not a privilege. About the role We are searching for a Laboratory Technician to join our Quality team, where innovation and science converge to make a real-world impact. You'll contribute to the growth of our trusted product portfolio, ensuring the highest standards of quality. Your expertise will drive activities from concept to execution, fostering an environment of continuous improvement. If you thrive in a dynamic atmosphere and are looking for a role where your actions directly contribute to the company's success, we would love to see your career success on our team! Your responsibilities * Collect, prepare, and analyze Environmental Monitoring Samples * Analyze raw materials, finished products, and in-process items * Operate, calibrate, and maintain laboratory instrumentation * Utilize laboratory automation and information system * Maintain laboratory compliance with cGMP, Safety and Regulatory requirements * Perform and effectively communicate data analysis in a timely manner to support issue investigations and improvement initiatives * Fill in for team members when necessary to ensure business needs are met * Other duties as assigned The experience we're looking for * Bachelor's degree in a natural science such as Microbiology, Biology or Food Science, etc strongly preferred * Minimum of one (1) year laboratory experience preferred specifically in a quality control environment * Familiar with conventional and rapid microbiological techniques * Previous experience in Microsoft applications required * Excellent administrative skills and strong verbal and written communication * Attention to detail and ability to learn to manage multiple tasks simultaneously * Demonstrated ability to work in a team environment and independently * Must be able to work in a fast-paced laboratory environment using teamwork and interpersonal skills to accomplish goals and provide quick turnaround of test results What we offer With inclusion at the heart of everything we do, working alongside our four global Employee Resource Groups, we support our people at every step of their career journey, helping them to succeed in their own individual way. We invest in the wellbeing of our people through parental benefits, an Employee Assistance Program to promote mental health, and life insurance for all employees globally. We have a range of other benefits in line with the local market. Through our global share plans we offer the opportunity to save and share in Reckitt's potential future successes. For eligible roles, we also offer short-term incentives to recognise, appreciate and reward your work for delivering outstanding results. You will be rewarded in line with Reckitt's pay for performance philosophy. US salary ranges USD 54,000 - 80,000 US pay transparency The base salary range for this role will vary based on experience in job and industry, training and education, skills relevant to the position, and other factors permitted by law. In addition to the base salary, the position is eligible for an annual discretionary bonus, which is subject to change each year. Reckitt offers eligible employees competitive benefits including medical, prescription, dental, vision, and life and disability insurance; paid time off for vacation, sick and Company recognized holidays; a 401(k) plan; 16-week paid parental leave or 26 weeks for the birthing parent; adoption and fertility support; tuition reimbursement; discounts; and much more. Our compensation and benefits packages aim to give our talent the reward, protection, and peace of mind they deserve. If reasonable accommodation is needed to complete your application, please contact *******************************. Reckitt is committed to the full inclusion of all qualified individuals. Equality We recognise that in real life, great people don't always 'tick all the boxes'. That's why we hire for potential as well as experience. Even if you don't meet every point on the job description, if this role and our company feels like a good fit for you, we still want to hear from you. All qualified applicants will receive consideration for employment without regard to age, disability or medical condition; colour, ethnicity, race, citizenship, and national origin; religion, faith; pregnancy, family status and caring responsibilities; sexual orientation; sex, gender identity, gender expression, and transgender identity; protected veteran status; size or any other basis protected by appropriate law. Nearest Major Market: Evansville Job Segment: Lab Technician, Counseling, Nutrition, Healthcare

Job Description Primary Function: Analytical Lab Chemists are responsible for testing analytical lab specimens and analyzing the data to present to both inside and outside parties. Responsibilities: Operation of analytical laboratory equipment. Preparation of exhibits for analytical testing. Maintain accurate & legible records that align with Ampacet's ISO requirements, as well as good documentation practices (GDP). Interface with and support internal & external customers where applicable. Maintains lab and equipment in the highest standards for a clean working environment. Adheres to all safety rules and regulation according to quality and safety policies. Work at a high level of efficiency and productivity to support Ampacet service commitments. Perform additional projects or tasks as assigned by the Lab Manager Maintaining equipment and supplies to provide continuity of workflow. Safeguarding Ampacet property and maintaining security policies. Setting an example by displaying and nurturing a healthy “positive” attitude toward the company. Strive toward continual improvements as they pertain to both personal goals and Ampacet goals. Perform routine maintenance on equipment as necessary Perform routine calibrations in support of the ISO calibration coordinator. Analyze data and write reports for distribution to customers. Help with assigning of projects and signing off on reports. Minimum Qualifications Bachelor's degree in chemistry or a related field of study A candidate without a degree but a minimum of 10 years experience in an analytical lab may be considered. Familiarity with GC-MS, HPLC, FTIR, DSC, TGA, extraction techniques. Ability to demonstrate good math skills. Excellent interpersonal and communication skills. Able to communicate verbally and in writing with a high degree of professionalism. Must be able to interact with all departments within the organization. Experience in JDE, SharePoint, Microsoft Office (Outlook, Word, Excel) and competent with using computers. Ability to work with minimal supervision. Must be able to maintain confidentiality with proprietary formulations. Must be authorized to work in the US without the need for current or future sponsorship for employment visa status. Preferred Qualifications 5 years experience in an analytical lab Organic structure determination / Unknown Analysis MS data evaluation Analytical exepimerntal method development - Especially with Chromotrography Experience with ELSD on HPLC

Red Spot Paint & Varnish was founded in 1903 in Evansville, Indiana. We supply interior and exterior high performance coatings for a world of plastics and automotive markets. We pride ourselves on being a company that has continued to thrive and grow in our community for over 120 years! Red Spot strives to provide an exciting work environment and avenues to give back to our community. If you have a strong desire to work for a leading, global coatings company in the development of new, innovative products, then Red Spot is where you want to be! We are currently seeking a skilled and detail-oriented person to join our Research & Development team as an Analytical Chemist in our Evansville, IN research facility. The main purpose of this position is to analyze, maintain, and/or improve coatings for automotive and non-automotive applications. This includes but is not limited to primers, basecoats, topcoats, and clearcoats. Responsibilities: Perform laboratory testing with high data integrity - to identify and correct technical product and customer issues; conduct necessary testing; evaluates/interprets results, writes clear and concise reports for distribution. Maintain laboratory data systems - to continuously improve on the sort, set in order, standardize, and sustain to all data generated and the connected systems. Maintain laboratory equipment - to be able to independently operate all equipment and its routine repair and maintenance as well as the research to replace said equipment. Capable and flexible, adaptive critical thinking and problem solving. Familiarity with microscope operation and maintenance. Serves as scientific resource to other Red Spot departments - including but not limited to: Paint Production, Technical Sales/Service to ensure manufacture of quality products. Qualifications Bachelor's degree in chemistry or a related science discipline. 0 - 7+ years prior coatings development experience. Ability to problem solve on coatings projects and issues, testing procedures, and instrument management, as well as adequately communicate status with supervisors. Ability to pass Ishihara Test for Color Deficiency. Ability to use advanced instrument software functionality. Ability to speak, read, and write English fluently and/or bilingual. Relevant instrument proficiency and maintenance knowledge preferred. Strong analytical skills. Familiarity with analytical instrument operation (i.e. microscopes) and/or maintenance of these instruments. Ability to concentrate on details and work independently. Ability to learn and apply technical concepts quickly. Knowledge/understanding of general chemical principles/properties. Ability to apply basic statistical techniques. Excellent computer skills - MS Word, Excel Excellent interpersonal skills; capable of relating to individuals at all levels of the organization and externally with customers. Effective oral/written communication skills. Ability to organize and prioritize a variety of projects and multiple tasks in an effective and timely manner. Ability to adhere to all company policies, including safety/environmental procedures and policies. Red Spot offers: Competitive pay commensurate with experience. Comprehensive benefits package including health, dental, and vision insurance. Retirement savings plan (401k) with company match On-site & near site medical clinics at no cost to employees and dependents Paid Holidays and Vacation Time Employee Assistance Program Tuition Reimbursement Long Term Disability Voluntary Life Insurance for employees and dependents Red Spot Paint & Varnish Co., Inc. is an equal opportunity employer. We do not and will not discriminate against any applicant or employee based on race, religion, color, national origin, gender, gender identity, sexual orientation, age, military status, disability, genetic information, citizenship status, or any other basis prohibited by law. Red Spot Paint & Varnish Co., Inc. will comply with its legal obligation to provide reasonable accommodation to qualified individuals and applicants. For more information, visit ************************

Provide technical and analytical support to Sales, Operations, and Quality Control Laboratory. Understand and conduct all activities required of a Quality Assurance Chemist. Become knowledgeable in product formulation, chemistry, and technology. Perform hands on analytical work for assigned projects. Coordinate outside analyses of products and projects as required. Develop reprocessing procedures for non-conforming inventories. Manage laboratory instrument calibration and maintenance. Maintain expertise in the operation and capabilities of analytical instrumentation. Provide oversight for instrument calibration and preventative maintenance schedule. Manage new instrument implementation and installation. Conduct research and development to compliment agriculture, construction, oil field, and surfactant portfolio. Develop and introduce new products, formulations, and analytical methods as requested. Communicate activities and findings routinely. Prepare formal reports on activities and goals. Process and analytical optimization. Develop improved analytical methods. Conduct accuracy and reproducibility studies. Prepare formal method documentation. Provide laboratory personnel training. Assist in resolving discrepancies in process and procedure adjustments. Recommend actions for continuous improvement. Indirect supervision of plant and laboratory personnel will be required during routine execution of job functions. Position can include work duties on evenings, nights and weekends to support production efforts. Maintain active certification in first-aid techniques and administer as needed in site emergencies. All Arclin Personnel are required to participate in all Safety Programs and any site-specific safety training and policies.

The Quality Control Scientist performs laboratory day-today operations, guides and interacts with QC and department personnel to accomplish goals and objectives as directed by supervisor. Other duties include performing raw material testing, final product testing, QC documentation and related GMP activities. What you will do * Maintain and perform daily operations in coordination with the QC Director/Supervisor to include testing of raw material/peptide samples and prioritizing projects * Write and work with other QC Staff and other Department in the creation and approval of control documents such as specifications, SOPs, STMs, etc. * Maintain and perform regular verification of the QC equipment for GMP compliance regularly in coordination with QC Director / Supervisor * Implement and maintain GMP procedures such as following SOP's, Standard Testing Procedures (STP's), written procedure and maintaining proper documentation as necessary for Quality Control * Test, review, and release raw material used in the manufacturing facility for GMP. Performing analytical analysis and reviewing data for completeness and accuracy * Receive, test and release final product peptide manufactured at Bachem * Test and release in-process control samples used in the manufacturing facility for GMP. Performing analytical analysis and reviewing data for completeness and accuracy * Maintain a cGMP quality level of work for the QC operations to include training, documentation and procedural work * Write/revise specifications as necessary, performing analytical analysis and reviewing data for completeness and accuracy * Write standard operating procedures, standard test procedures and other related GMP documentation * Implement and maintain GMP procedures such as following written procedure and maintaining proper documentation as necessary for Quality Control * Perform QC analysis to include: HPLC, UPLC, Water, Mass Spec, UV, GC, melting point, Optical Rotation, TLC and misc. wet chemistry lab work and other related analytical equipment used for control quality of the GMP facility. This work may include calibration and validation of these methods * Control raw material used in the manufacturing facility for GMP to include receiving, quarantine, testing and QC release * Investigate any deviation or out of specification as necessary related to QC work performed as instructed by supervisor * Execute validations as necessary to include QC Analytical methods performed, other validations to support the quality of the manufacturing facility * Follow safety guidelines for handling, disposal and use for a peptide manufacturing company using toxic and/or large volumes of chemicals * Support validation, and stability as necessary to include but not limited to analytical work, documentation and quality GMP procedure Qualifications * Bachelor's degree in chemistry or related field * Master's degree in chemistry or related field (preferred) * Minimum of 1 year experience in GMP pharma/biotech facility * Experience with Equipment Maintenance Programs * Experience with the use of analytical techniques/ instruments, such as, Gas Chromatography (GC), High Performance Liquid Chromatography (HPLC), Karl Fischer (KF), etc. * Excellent written and oral communication skills * Basic computer knowledge, including Microsoft Word, Excel and PowerPoint * Ability to effectively organize, multitask, and work in a fast-paced, deadline driven work environment * Ability to communicate in a proactive and solution-focused manner, including keeping management aware of potential issues * Detail oriented with the ability to troubleshoot and resolve problems * Ability to work independently and manage one's time * Communicate effectively and ability to function well in a team environment * Ability to review Certificate of Analysis for Reagents for the creation of specification documents * Organization skills to support the department in the creation and approval of controlled documents in a timely manner * Flexibility of working hours based on business needs, may include some nights and occasional weekends Base Hourly Range: * Scientist I: $28.90 - $39.73 * Scientist II: $32.41 - $44.56 * Scientist III: $37.65 - $51.78 * Sr. Scientist: $44.85 - $61.67 Placement of new hires in these wage ranges is based on several factors including education, skill sets, experience, and training. Total Rewards We offer all Team Members a total rewards package including competitive pay, annual performance bonus, a generous benefit package with comprehensive Medical/Dental/Vision coverage, 401(k) plan with employer contribution, and paid vacation, personal and sick days. Corporate Social Responsibility Bachem takes responsibility for future generations by a careful handling of resources and avoiding environmental risks. We continually improve our ecological performance and develop and implement new approaches for enhancing employees' environmental awareness. EcoVadis has awarded Bachem Gold Medal status in their assessment of Bachem. Bachem Americas is an Equal Opportunity Employer As an equal opportunity employer, we celebrate the diversity of our team and are committed to building an inclusive workplace where individuals are hired and advanced based on merit, skills, and qualifications. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran status, or other legally protected status. Please note: unsolicited resumes from recruitment agencies will not be considered. Share this job posting by email

Job Summary: The Analytical Chemist is responsible for performing internal analytical tests on seasonings, coating, bakery, and other such farinaceous substances and reporting those results to the formulating Food Scientist. Benefits: Medical Insurance Prescription Drug Plan Dental/Vision Insurance Employee Incentive Plan Flexible Spending Account Cash Accumulation Plan-401K Life/AD&D Insurance Short- Term/Long-Term Disability Vacation Plan Paid Holidays Employee Assistance Program Adoption Assistance Program Tuition Reimbursement Maternity/Paternity Leave Pet Insurance Essential Functions: Maintain flow of incoming samples, outgoing test results, and reports to Scientists or other Technical groups as directed by the R&D Director. This is to be accomplished in a timely and competent manner to meet the requirements of a fast-paced laboratory work environment. Maintain all analytical laboratory equipment, materials, and chemicals associated with the laboratory. Interface with outside laboratories to conduct testing not available in-house. Learn new analytical techniques and equipment technology as purchased or otherwise acquired by the laboratory. Assist in training of new employees on laboratory equipment usage, maintenance, and handling. Operate and maintain a sanitary, safe, and secure laboratory. Perform other duties or special projects as needed. Qualifications: Minimum of an Associate Degree in Laboratory Science and/or 5 years experience in a food, micro, or medical analytical laboratory testing position. Strong communication, interpersonal skills, and general knowledge in Adobe applications, MS Office, AS400, and Lotus Notes. Work Environment: General office setting Periodic exposure to: (1) loud environment, (2) airborne particles with stronger odors associated with spicy food ingredients, (3) cold, hot, wet, and humid conditions, (4) walking and standing on concrete, (5) climbing steps, ladders, (6) standing on elevated surfaces. Fast paced, resource lean environment Salary - $68,000 - $85,000. Disclaimer: The above information on this description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities and qualifications required of employees assigned to this job. New Weds Foods is an Equal Opportunity Employer. Newly Weds Foods will only employ those who are legally authorized to work in the United States without assistance or support from Newly Weds Foods. Any offer of employment is conditional upon the successful completion of a background investigation and drug screen.

Job Description Autocam/NN Inc. is a leading manufacturer of high-performance precision components. We combine innovative thinking with machining technologies to push the boundaries of what is possible. NN's success is based on its talented and empowered team. We are looking for a Chemical Lab Technician to join our team. Chemical Lab Technician Responsibilities: Monitor, evaluate and analyze chemicals used in automotive production processes. Assist and work with team members to obtain effective and efficient production. Measure, record, analyze and maintain chemical concentration requirements needed to achieve effective operational control. Accurately report chemical concentrations using charts and graphs. Conduct project work and research per Chemist's direction. Process parts needing re-work, including deburring and derusting. Evaluate cleaning chemicals. Chemical Lab Technician requirements: Completion of at least 2 years of school towards a chemistry degree.

Perform inspections on raw material, production, shipping, and developmental samples using standard methods. Inspections via physical test and Certificate of Analysis review. Approval of conforming materials to internal and customer requirements. Control non-conforming materials. Recommend any needed adjustments or actions to production based on sample test results, formula guidelines, experience, and other experts as necessary for efficient and timely completion of products meeting customer expectations. Experience and capability to operate a variety of laboratory analytical equipment; including set up, calibration, and maintenance. GC-FID (OpenLab CDS) HPLC (Empower 3) FTIR (Omnic) Flame AAS (Solaar) Auto Titrators (LabX) Viscometers Moisture Analyzers pH Meters Maintain accurate records of all data taken using the LIMS system, batch cards, notebooks, reports, and checklists necessary for the specific type of data being recorded. Capability of using statistical programs to evaluate results. Proficiency in Microsoft Office Suite and Microsoft 365. Ensure accurate and timely delivery of legally binding documents Certificates of Analysis Bills of Lading Collect and maintain samples for inspection, label properly, sort and store for all lots numbers, for required retain period. Participate in continuous improvement activities for laboratory, laboratory/production interactions, and production processes. Including recommending procedure changes, documenting non-conformance incidents, participating in root cause investigations, and actively learning/reviewing analytical test methods and quality protocols. Maintain the laboratory in safe, organized, neat, well stocked, functional condition; including cleaning up work areas, submitting purchase requests for depleted items, prepare replacement stock solutions, maintaining method calibrations, monitoring reagent shelf life, and repairing or notifying others of malfunctioning equipment. Participate in site safety and environmental programs. Perform various clerical duties relating to laboratory responsibilities. Perform laboratory activities as outlined in various ISO and work instruction documents including internal audit responsibilities. Train in and maintain active certification in first-aid techniques. Administer first-aid as needed in site emergencies. Communicate pertinent information to other shifts, staff, and plant personnel on a timely basis. Prepare weekly reports on progress toward yearly goals. Ability to interact and communicate with others effectively, written and oral.

Cargill's size and scale allows us to make a positive impact in the world. Our purpose is to nourish the world in a safe, responsible and sustainable way. Cargill is a family company providing food, ingredients, agricultural solutions and industrial products that are vital for living. We connect farmers with markets so they can prosper. We connect customers with ingredients so they can make meals people love. And we connect families with daily essentials - from eggs to edible oils, salt to skincare, feed to alternative fuel. Our 160,000 colleagues, operating in 70 countries, make essential products that touch billions of lives each day. Join us and reach your higher purpose at Cargill. This position is in Cargill's food and bioindustrial business, where manufacturers, retailers, and foodservice companies rely on us to consistently deliver the products and services they need, and use our technical expertise and market knowledge to develop innovative products. Job Purpose and Impact The Quality Control Chemist will provide expertise with all daily operations in quality control laboratories. In this role, you will develop an in depth understanding of specific systems, ensure that products meet or exceed customer requirements for quality and food safety, and act as backup for FSQR roles including the FSQR Lab Technician. The Chemist I will support the buildup and maintenance of the instrumentation platform by providing reliable accurate analytical figures as well as perform validation and troubleshooting of analytical methods to ensure they meet the requirements. In this role, you will analyze malfunctions of instruments and control systems, determine necessary steps for repair, and work with scientific and analytic food safety and quality computer software, and data management systems. Key Accountabilities Provide ongoing technical support to stakeholders around food safety and quality performance instruments and control systems by investigating quality problems and deliver improvement actions with follow up. Perform general maintenance on equipment and develop new and improved food safety and quality measuring and recording equipment. Perform calibrations on various devices, documenting equipment inspection, testing and repair activities. Perform method validation and verification to roll out new testing method in the lab. Document standard operating procedures, identify possible trends in testing results with data analysis software and provide input to team members to improve quality control system. Organize and maintain accurate and pertinent data, including spreadsheets, graphs, and reports. Provide process improvement support, specialized testing, training, audit systems, analyze data, identify trends, troubleshoot, corrective action and communication regarding processing data and final product. Assess quality parameters and systems including cross checks, raw materials, calibration, maintenance, procedures, food safety, training, auditing and oversight of analytical testing performed in control rooms. PO's and ordering systems Independently solve moderately complex issues with minimal supervision, while escalating more complex issues to appropriate staff, including internal resources and external suppliers. Assist with customer audits, initiatives and follow ups. Provide training, coaching, and mentoring to new team members. Other duties as assigned #LI-Onsite #LI-SM4 Qualifications Minimum Qualifications Bachelor's degree in a related field or equivalent experience. Preferred Qualifications Knowledge in calibrate, maintain and troubleshoot various analytical instruments. Able to work independently and in a team environment, with high initiative level and communicate effectively Proven ability to anticipate, recognize, solve process and laboratory problems. Ability to handle multiple priorities with large projects. Intermediate computer skills Food safety, quality, and regulatory experience Equal Opportunity Employer, including Disability/Vet

We are hiring a Powder Formulation Technician. The Powder Formulation Technician will be responsible for formulation of powdered media. 3rd Shift: 9:00 pm- 5:30 am At FUJIFILM Irvine Scientific (dba FUJIFILM Biosciences), we turn curiosity into breakthroughs that advance the field of life sciences. By offering a comprehensive portfolio of products and services in cell culture media, discovery research reagents, recombinant growth factors and proteins, fine chemicals, and critical assay materials, we partner with the brightest minds in biotech and pharma to tackle the world's biggest health challenges. Imagine being part of a team that enables life-changing discoveries like new vaccines, therapies, and advancements in regenerative medicine. Our culture fosters curiosity, collaboration, and innovation, and we pride ourselves on delivering unparalleled quality and service to our partners. If you're ready to make an impact, your future belongs with us at FUJIFILM Irvine Scientific (dba FUJIFILM Biosciences). Our headquarters in Santa Ana, California, is surrounded by world-class schools, lush parks, and scenic beaches like Laguna and Huntington, making it an ideal place to live, work, and explore. With additional campuses across the US, Europe, China, and Japan, we offer opportunities to make a difference worldwide. Fujifilm is globally headquartered in Tokyo with over 70,000 employees across four key business segments of healthcare, electronics, business innovation, and imaging. We are guided and united by our Group Purpose of "giving our world more smiles." Visit: *************************************************** Job Description Responsibilities: * Formulates Powder media formulas per manufacturing protocols utilizing various weighing equipment such as scales and balance. * Uses Mettler-Toledo IND780 terminal system in conjunction with the SAP ERP system to ensure correct raw materials assigned in the batch record are weighed at the specified quantity. * Suggest changes in departmental procedures and processes (SOPs) as needed. * Performs and documents line clearance at the start of each formulation event. * Maintains all required logs and associated documentation. * Assures that all chemicals are stored and labeled properly. * Performs process scale checks on all required equipment including scales and balances. * Keeps work area, utensils, tanks, mills, and equipment clean and organized. * Ensures that supplies needed such as weigh boats, gloves, lab coats, etc. are well stocked in their designated areas. Orders supplies or informs Lead/Supervisor if supplies need to be ordered. * Follows all safety procedures and works in a safe manner including wearing all required personal protective equipment. * Understands and follows procedures to ensure that chemicals are handled properly. * Good understanding of metric system and its conversions. * Follows and actively participates in sustaining the 6S program in the area. * Other duties as requested by Lead or Supervisor. Required Skills/Education: * High School Diploma or equivalent. * Background in medical devices, diagnostics, food/vitamin processing, or pharmaceuticals. * 1-2 years of hands on experience * General education about chemicals and proper handling (college level science preferred). * Working knowledge of metric system. * Good understanding of current Good Manufacturing Practices (cGMPs). * Ability to speak, read, and write English. * Good oral and written communication skills. Salary and Benefits: * For California, the base salary range for this position is $19.65 - $25.51 per hour. Compensation for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience, location, etc.). * Medical, Dental, Vision * Life Insurance * 401k * Paid Time Off * #LI-onsite EEO Information Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc. ADA Information If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (*******************).

WHO WE ARE We are a company where people matter. We are family driven. We are financially strong. And we are looking for problem-solvers to join our growing team. BENEFITS Up to 10% Retirement Contribution $3,000 sign-on bonus! $600 per Year Wellness Incentive Two Weeks Starting Paid Time Off Medical, Dental, and Vision - Eligible f irst day of the month following hire date. JOIN A TOP WORKPLACE - ******************************************* QC Chemist OPPORTUNITY The primary purpose of this position is to perform required quality control analysis of incoming, manufacturing and outgoing material with authority to make acceptance, production adjustment, and/or rejection decisions. This position may also provide technical support to operations and sales. Hours are for this position are Sunday-Monday 7am -7:30pm and Tuesday- Wednesday from 7am-3:30pm. As QC Chemist, primary responsibilities include: Perform required quality control analysis of incoming, manufacturing and outgoing material with authority to make acceptance, production adjustment, and/or rejection decisions. Record and maintain analysis/records accurately, neatly, legibly and completely. Prioritize daily laboratory activities to meet production schedules. Perform instrument maintenance, calibrations, quality control checks, solution preparations, and solution standardizations. Provide technical support and assistance to operations/production regarding manufacturing adjustment of non-conforming materials and quality issues. Maintain a clean and neat laboratory at all times. Adhere to all safety SOPPs. Initiate corrective actions on identified non-capable procedures or practices. Maintain and properly store sample retains. Communicate to supervisor concerns about standard laboratory procedures, operational problems, quality trends, etc. Maintain a professional attitude and demeanor at all times, treat others with courtesy and respect, and respond to all requests in a professional manner. Promote complete customer satisfaction through quality and service to both internal and external customers. All staff members are responsible for reporting food safety problems to their supervisor or the SQF Practitioner upon observation of a known or potential issue. Uphold Hydrite's Standard of Excellence through a continuous commitment to maintain quality facilities and provide quality products and services to internal and external customers Perform all duties outlined in relevant SOPs and all other duties to be assigned. Participate in RCRA, regulatory, health & safety and process training activities as required. Review changes/additions with your supervisor. Must be RCRA compliant. REPORTING STRUCTURE This position reports to the QC Lab Supervisor. EXPERIENCE AND EDUCATIONAL CRITERIA Bachelor's Degree in Chemistry or related field is required. Must have good communication and interpersonal skills, including the ability to read, write, and speak in English. Proficiency in computer skills and good working knowledge with all MS Office applications. Ability to accurately transfer written and verbal information and documentation and enter data into existing computer system. Must be self-motivated and able to work independently as well as in a group setting. Able to apply mathematical and problem solving skills for resolution. Must possess good laboratory analytical skills. JOB EXPECTATIONS: Uphold Hydrite's Standard of Excellence through a continuous commitment to maintain quality facilities and provide quality products and services to internal and external customers. Participate in RCRA, regulatory, health & safety and process training activities as required. Review changes/additions with your supervisor. Must be RCRA compliant. Regular attendance is essential. Perform all duties outlined in relevant SOPs and all other duties to be assigned. Work with other staff members to maintain workload balances. Provide back-up support as necessary. Support effective communication with all Hydrite departments where responsibilities overlap to ensure success of the branch team. REPORTING STRUCTURE This position reports to QC Lab Supervisor BENEFITS Benefits and perks include 401k and profit sharing, medical/dental/vision/life insurance, paid time off, tuition reimbursement, adoption assistance, legal services insurance, scholarship awards for children of employees, summer picnic, community giving events, free family wellness coaching including nutritionist and fitness coach. WHY HYDRITE? Watch this Why Hydrite video to find out: *************************** WANT TO STAY CONNECTED? FIND US ON SOCIAL MEDIA LinkedIn: linkedin.com/company/hydrite-chemical-co- Facebook: facebook.com/hydrite YouTube:******************************************* Learn more about Hydrite on our website: *********************** Privacy Notice for California Residents: **************************************************************

We have an exciting opportunity at our Carrollton, Texas facility for a QC Chemist. This position serves as a Quality Control Chemist and maintains quality standards by performing analytical testing on incoming and finished products for composition and impurities, as well as recording quality results. In addition, this role will accommodate preparations for new formulations (Gauge studies, method development, instrument installation, etc). Company Overview FUJIFILM Electronic Materials, U.S.A. fuels innovation in the semiconductor industry-where chemistry meets technology. Our advanced materials and formulations enable manufacturers to build the microchips that power Artificial Intelligence, computers, electric vehicles, smartphones, and more. We're a global business-to-business supplier of chemical formulations and advanced materials used for manufacturing and packaging semiconductors. Our chemical formulations allow top manufacturers to produce microchips that both power and connect our digital world. Think you've got what it takes to build a more connected world? Then connect with us today and challenge the boundaries of what's possible-for the world and your future. We have six U.S. manufacturing and Research & Development facilities, located in: Mesa, Arizona; Castroville, California; Hollister, California; Carrollton, Texas; and North Kingstown, Rhode Island-each offering unique local experiences, from vibrant cultural scenes to historic charm. Fujifilm is globally headquartered in Tokyo with over 70,000 employees across four key business segments of healthcare, electronics, business innovation, and imaging. We are guided and united by our Group Purpose of "giving our world more smiles." Visit: *************************************************** Job Description Key responsibilities for this role include: * Responsible for testing and approving raw materials, intermediates, and final products following company processes and procedures via use of lab equipment (eg: GC, Karl Fischer titration, ICP-MS, NVR). * Complete and issue Certificates of Analysis (COA). * Investigate out of specification and out of control results. * Review process control charts and take action as required. * Develop, review, and update laboratory documents and procedures. * Respond to deviations by assessing the impact on product safety and quality. * Instrument validation, troubleshooting, repair, and maintenance. * Laboratory upkeep and cleaning, waste disposal, and gas maintenance. * Maintain safe and healthy work environment by following standards and procedures. * Comply with legal regulations REQUIREMENTS * Requires a Master's degree or BA/BS Chemistry degree and minimum of 1-2 years of experience in the semiconductor or related field or in a production laboratory environment. * Instrumentation and analytical skills experience preferred - wet chemistry techniques, UV-Vis, GC/FID/TCD, IC, HPLC, GFAA, ICP/OES, ICP/MS, FTIR, GC/MS, and liquid particle counters. Additional mass spectroscopy experience a plus. * Ability to multi-task and handle change in priorities. * Strong organization skills, good attention to detail, and the ability to function effectively as part of a cross functional team. * Strong verbal and written communication skills. * Must have excellent computer skills (Word, PowerPoint, Excel and statistical software tools). * Strong troubleshooting skills * Must be able to work 2nd shift. 12:00PM - 9:00PM / Monday thru Friday ADDITIONAL REQUIREMENTS We value a professional, adaptable, and collaborative work environment. The following competencies are essential for success in any role and reflect our commitment to effective teamwork, problem solving, and workplace communication. * Resilience - Ability to adapt to workplace challenges, maintain professionalism, and manage responsibilities effectively. * Communication - Capacity to clearly and professionally exchange ideas, interact respectfully with colleagues and customers, and foster positive workplace relationships. * Reasoning & Decision Making - Ability to analyze information, follow verbal and written instructions, and make logical, sound decisions. * Comprehension - Capability to understand and complete tasks as assigned and solve problems effectively. * Organizational Skills - Competence in managing multiple priorities, maintaining accuracy, and staying focused despite potential workplace distractions. To all agencies: Please, no phone calls or emails to any employee of Fujifilm about this requisition. All resumes submitted by search firms/employment agencies to any employee at Fujifilm via-email, the internet or in any form and/or method will be deemed the sole property of Fujifilm, unless such search firms/employment agencies were engaged by Fujifilm for this requisition and a valid agreement with Fujifilm is in place. In the event a candidate who was submitted outside of the Fujifilm agency engagement process is hired, no fee or payment of any kind will be paid. EEO Information Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc. ADA Information If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (********************************).

Pangea Laboratory seeks a dynamic individual to become an integral part of our Laboratory Operations team! In this role, you will assist with specimen processing and test performance while complying with all regulatory agency guidelines. This role requires knowledge of laboratory procedures, strong attention to detail, and the ability to work effectively both independently and as part of a team. The successful candidate must also adhere to all laboratory health and safety regulations. This position is Monday-Friday from 10:30AM to 7PM onsite in Tustin, CA. Join us in making a meaningful impact! Essential Duties and Responsibilities: Comply with all policies and regulations put in place by Pangea Laboratory, State, Federal, CAP, CLIA, and HIPAA. Complete routine handling, accessioning, and storage of laboratory specimens in accordance with standard operating procedure. Document laboratory information using appropriate information management systems and verify information and discrepancies. Identify and troubleshoot problems in a timely manner and adhere to laboratory procedures when resolving problems. Direct handling of potential hazardous specimens and reagents under safe environment while wearing appropriate PPE. Be familiar with laboratory protocols and procedures for specimen processing, operating equipment and instruments, maintenance of designated laboratory environment and instruments, and data entry. Label and store working reagents and solutions in accordance with standard operating procedure and safety guidelines. Adequately communicate information with team members and management relating to laboratory procedures, equipment, information, issues, etc. Handle light logistical duties, including coordinating the shipping of materials and samples to ensure timely delivery. Ensure testing turnaround time by closely monitoring specimens received and pending processing. Document records in real time using good documentation practices that include but is not limited to department forms, files, and worksheets. Meet or exceed all performance expectations and demonstrate professional working behavior when performing tasks and interacting with team members. Adapt to changes in processes, accepting approved changes and learning new tasks. Follow Pangea Laboratory health and safety policies and procedures and are responsible for reporting violations. Perform other related duties as required or assigned. Education and Experience: 1 year experience in research in the biotech/life sciences industry, or an equivalent combination of education, training, and experience. A Bachelor's or Associate degree in a relevant scientific field (Biology, Chemistry, or a related discipline). General Skills: Have background or basic knowledge in laboratory procedures and guidelines. Have the ability to read, write (legibly), and speak the English language. Strong attention to detail, excellent organizational and time-management skills. Have the ability to quickly understand procedures and be flexible to changes and updates in procedures. Have the ability to troubleshoot and recognize abnormalities then demonstrate proactiveness to address issues in the workflow. Demonstrate autonomy and possess time management skills. Demonstrate ability to prioritize tasks and engage in multi-tasking without sacrificing quality. Computer Skills: Knowledge of basic computer skills such as Microsoft Office Suite to include Excel and Word. Previous experience with Laboratory Information Management Systems, preferred. About Us: Pangea Laboratory is a California-based diagnostics company founded in 2014. We focus on the precise, early detection of emerging diseases. Our mission is to have a positive impact on human life, by providing biomedical communities with reliable and high-quality testing services, delivering the data they need to diagnose and treat diseases in an effective and timely manner. Named a Top Workplace by the OC Register, Pangea Laboratory continues to be a place where employees feel engaged, connected, and energized about their work. If you are passionate about helping people in advancing science and working with awesome teams in a fast-growing company, we want to speak with you! Compensation: The estimated base compensation range for this position is $24 to $28 per hour at the time of posting. Actual compensation details will be provided in writing at the time of offer, if applicable, and is based on several factors we believe fairly and accurately impact compensation, including geographic location, experience, knowledge, skills, abilities, and other job permitted factors. Equal Employment Opportunity Employer: Pangea Laboratory welcomes candidates of all backgrounds. These include sex, age, color, race, religion, marital status, national origin, ancestry, sexual orientation, gender, gender identity, gender expression, physical & mental disability, medical condition, genetic information, military and veteran status, or any other protected status as defined by federal, state, or local law. Location: Onsite - Pangea HQ - 14762 Bentley Cir. Tustin, CA 92780