Medical laboratory scientist jobs in Caguas, PR - 12 jobs

**We believe in the power and joy of learning** At Cengage Group, our employees have a direct impact in helping students around the world discover the power and joy of learning. We are bonded by our shared purpose - driving innovation that helps millions of learners improve their lives and achieve their dreams through education. Cengage Group's portfolio of businesses supports student choice by providing a range of pathways that help learners achieve their goals and lead a choice-filled life. **Our culture values inclusion, engagement, and discovery** Our business is driven by our strong culture, and we know that creating an inclusive workplace is absolutely essential to the success of our company and our learners, as well as our individual well-being. We recognize the value of diverse perspectives in everything we do, and strive to ensure employees of all levels and backgrounds feel empowered to voice their ideas and bring their authentic selves to work. We achieve these priorities through programs, benefits, and initiatives that are integrated into the fabric of how we work every day. To learn more, please see *********************************************************** **What you'll do here:** + Collaborate closely with Product, Build, Sales, and Marketing groups to strengthen a data-driven culture and support customer engagement in research. + Develop evaluation frameworks, study builds, surveys, and other research instruments. + Coordinate data collection and analysis while maintaining scientific rigor. + Apply a strong understanding of data privacy and human-subject research requirements. + Identify patterns and insights through deep triangulation of multiple data sources. + Manage external vendors and partner with internal collaborators to ensure the quality and validity of insights. + Convey findings transparently and purposefully to support consistent product development and successful messaging. + Work with internal and external partners to refine research questions and provide actionable recommendations. + Monitor product implementation and deliver recommendations for ongoing optimization. **Skills you will need here:** + A PhD or Master's degree, or equivalent experience, in Educational Research, Psychology, Program Evaluation, Anthropology, or a related field, together with a strong business approach and interest in technology. + Experience conducting quantitative research and analyzing large datasets, with the ability to develop, lead, and coordinate research studies. + Experience in qualitative research and user-centered approaches, including the capacity to develop and lead open-ended, exploratory research. + Demonstrated experience developing research and evaluation frameworks and managing end-to-end research programs. + Strong project coordination skills; highly collaborative with a problem-solving, achievement-focused approach. + 2-4 years of experience managing research projects in a client services firm, B2C environment, or academic setting. + Preferred experience in Higher Education, K-12, or Career and Professional Education contexts. + Ability to self-manage progress against goals and results, with a high degree of accountability and urgency. + Strong bias for action. + Strong writing and data visualization abilities, capable of preparing and delivering information clearly to various audiences. + Comfort working through ambiguity and seeking answers to complex, open-ended problems. + Ability to work under tight deadlines while maintaining high quality standards. Cengage Group is committed to working with broad talent pools to attract and hire strong and most qualified individuals. Our job applicants are considered regardless of any classification protected by applicable federal, state, provincial or local laws. Cengage is also committed to providing reasonable accommodations for qualified individuals with disabilities including during our job application process. If you are an applicant with a disability and require reasonable accommodation in our job application process, please contact us at accommodations.ta@cengage.com . **About Cengage Group** Cengage Group, a global education technology company serving millions of learners, provides affordable, quality digital products and services that equip students with the skills and competencies needed to be job ready. For more than 100 years, we have enabled the power and joy of learning with trusted, engaging content, and now, integrated digital platforms. We serve the higher education, workforce skills, secondary education, English language teaching and research markets worldwide. Through our scalable technology, including MindTap and Cengage Unlimited, we support all learners who seek to improve their lives and achieve their dreams through education. **Compensation** At Cengage Group, we take great pride in our commitment to providing a comprehensive and rewarding Total Rewards package designed to support and empower our employees. Click here (******************************************************************************************** to learn more about our _Total Rewards Philosophy_ . The full base pay range has been provided for this position. Individual base pay will vary based on work schedule, qualifications, experience, internal equity, and geographic location. Sales roles often incorporate a significant incentive compensation program beyond this base pay range. In this position, you will be eligible to participate in the company's discretionary incentive bonus program. This position's bonus target amount, which is not guaranteed and is dependent on individual performance and overall company results among other factors, is provided below. 10% Annual: Individual Target $77,100.00 - $90,000.00 USD **Cengage Group** , a global education technology company serving millions of learners, provides affordable, quality digital products and services that equip students with the skills and competencies needed to be job ready. For more than 100 years, we have enabled the power and joy of learning with trusted, engaging content, and now, integrated digital platforms. We serve the higher education, workforce skills, secondary education, English language teaching and research markets worldwide. Through our scalable technology, including MindTap and Cengage Unlimited, we support all learners who seek to improve their lives and achieve their dreams through education. **_Warning: Be aware, there has been an increase of targeted recruitment_** **_scams perpetrated by bad actors falsely providing job offers on behalf Cengage Group to candidates as a means of obtaining personal information. Note that Cengage will always interview candidates via live in-person meetings, phone calls and video calls before an offer would be extended. Also, be sure to check that communication is coming from an @cengage.com email address._**

The Alaka'ina Foundation Family of Companies (FOCs) is looking for a Laboratory Technician to support the CDC in San Juan, Puerto Rico. DESCRIPTION OF RESPONSIBILITIES: * The Laboratory Technician will receive samples, verify accompanying information, and accession them electronically into the database. This position labels, sorts, transfers specimens, and runs query lists in order to process specimens daily. The Lab Technician also locates and separates aliquoted specimens that will be processed for testing or shipping. Additional duties may include: * Assist in programming laboratory equipment to conduct necessary diagnostic testing or research. * Perform diagnostic testing, as specified by the Chief of the Laboratory (e.g. ELISA and PCR for detection of human pathogens) proficiently. * Archive specimens that have been completed for testing. * Collect, tabulate, and report test results to database. Conduct assessment of procedures and communicate results to supervisor. * Maintain basic laboratory records of instrument operating procedures and other pertinent data in compliance with Quality Management Standards (QMS) established for CDC laboratories. * Participate in training for use of laboratory equipment and adherence to and QMS standards, safety, select agent, and facility security requirements. REQUIRED DEGREE/EDUCATION/CERTIFICATIONS: Bachelors Degree Required. REQUIRED SKILLS AND EXPERIENCE: Minimum two (2) years' experience as a Laboratory Technician. REQUIRED SECURITY AND CLEARANCE: * Must be a U.S. Citizen * Ability to pass a Tier I background investigation. The Alaka'ina Foundation Family of Companies (FOCs) is a fast-growing government service provider. Employees enjoy competitive salaries; a 401K plan with company match; medical, dental, disability, and life insurance coverage; tuition reimbursement; paid time off; and 10 paid holidays. Kapili Government Services is proud to be an equal opportunity employer. We are an Equal Opportunity/Affirmative Action Employer of individuals with disabilities and veterans. We are proud to state that we do not illegally discriminate in employment decisions on the basis of any protected categories. If you are a person with a disability and you need an accommodation during the application process, please click here to request accommodation. We E-Verify all employees "EOE, including Disability/Vets" OR "Equal Opportunity Employer, including Disability/Veterans" The Alaka`ina Foundation Family of Companies (FOCs) is comprised of industry-recognized government service firms designated as Native Hawaiian Organization (NHO)-owned and 8(a) certified businesses. The Family of Companies (FOCs) includes Ke`aki Technologies, Laulima Government Solutions, Kūpono Government Services, and Kapili Services, Po`okela Solutions, Kīkaha Solutions, LLC, and Pololei Solutions, LLC. Alaka`ina Foundation activities under the 501(c)3 principally benefit the youth of Hawaii through charitable efforts which includes providing innovative educational programs that combine leadership, science & technology, and environmental stewardship. For additional information, please visit ************************** #LI-JS1 #ClearanceJobs

Who are we? For more than 26 years, CorePlus has provided Puerto Rico with anatomical pathology laboratory services and clinical analysis with innovation and precision. Our commitment is, to be a leader in the transformation of pathology to the digital world . In 2020 we deployed our digital pathology platform, being the first organization in Puerto Rico to make the transformation. Known worldwide for operationalizing the use of Artificial Intelligence (AI) in the diagnosis of prostate and breast cancer, CorePlus stands out for being avant-garde. If innovation and compassion appeal to you, we invite you to join our mission and become part of our family; we offer excellent benefits including health plan, dental, vision, 401k, paid vacation, and life insurance. The Position Under direct supervision, the Medical Technologist 1 (MT1) is responsible for the receiving, processing and analyzing of samples. Provides medical information to organizations and establishments to be used to diagnose, treat, and prevent diseases in a clinical and occupational medicine setting. To accurately perform and report all in-house laboratory testing procedures and obtain the necessary specimens for reference laboratory testing, as required. Enhances the efficiency and accuracy of lab testing by maintaining adequate laboratory supplies, by keeping equipment in operational condition and by maintaining a clean and orderly laboratory work area. Assists in the preparation of monthly statistical reports by keeping accurate records on all laboratory procedures performed. Responsibilities Conducts analysis on various body fluids such as urine, whole blood and gynecological samples for clinical and molecular studies. Prepares blood and plasma for a variety of laboratory reference tests. Analyzes and identifies blood and urine cells using a microscope techniques and procedures. Keep laboratory equipment's clean, functional, and calibrated. Completing preventive maintenance requirements; following manufacturer's instructions; troubleshooting malfunctions; calling for repairs; maintaining equipment inventories; evaluating new equipment and techniques. Maintains safe and clean working environment by complying with procedures, rules, and regulations. Organizes laboratory supplies and maintains laboratory inventory records by checking stock to determine inventory level; anticipating needed supplies; expediting orders for supplies; verifying receipt of supplies. Properly and safely disposes of hazardous and infectious waste and materials. Respects patient confidentiality laws. Compiles thorough and professional laboratory reports. Updates and maintains knowledge base by attending workshops, reading, and participating in professional organizations. Ensures accurate laboratory testing by performing phlebotomy on patients when necessary. Prepares reports of technological findings by collecting, analyzing, and summarizing information. Maintains inter- and intradepartmental workflow by fostering a spirit of cooperation. Protects patients and employees by adhering to infection-control and hazardous waste policies and protocols, following identification procedures. Contributes to team effort by accomplishing related results as needed. Maintains quality assurance of the Laboratory by performing proficiency testing. Performs QC reporting. Any other related responsibility not previously described. Requirements and Skills Bachelor's degree in biology Postgraduate in Medical Technology Licensed Medical Technologist ASCP Certified 0-7 years' experience as a Certified Medical Technologist Standardized knowledge in the fields of clinical chemistry, hematology, Phlebotomy, immunology, Microbiology, and urinalysis Knowledge in complex techniques such as PCR and Andrology testing Working Conditions/ Physical Activity: While performing the duties of this job, the employee is regularly required to talk and listen. The employee frequently is required to stand; walk; use hands to finger, handle or feel; and reach with hands and arms. The employee is occasionally required to sit; climb or balance; and stoop, kneel, crouch or crawl. The employee must frequently lift and/or move up to 10 pounds and occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus. CorePlus is an equal employment/affirmative action opportunity employer. It does not discriminate against any qualified person on the basis of sex, race, color, national origin, religion, sexual orientation, age, marital status, mental, physical or sensory disability, or any other classification protected by applicable local, state, federal, and/or international law.

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at *************** Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok. Job Description Performs chemical tests following the established procedures. Responsibilities List up to 10 main responsibilities for the job. Include information about the accountability and scope. * Responsible for performing laboratory analytical tests to the raw materials and finished products following the established parameters(Abbvie policies, FDA, cGMP) and applicable regulations without impact to the manufacturing cycle or the laboratory work flow. * Document the results of the tests and analysis performed accurately. * Perform preventive maintenance and standardize the laboratory equipment. * Participate in the implementation of special projects and test method transfers. * Resolve typical technical problems with minimum intervention of the scientist or others. * Perform changes to existence procedures or create new as required. * Actively participate in training of new employees. * Responsible for the coordination and distribution of tasks when required. * Prepare presentations as required. Qualifications * Associate degree in Natural Sciences with major in Chemistry. * Minimum of two years experience in the pharmaceutical industry or equivalent in an analytical laboratory. * Knowledge and abilities in managing analytical instruments. Additional Information AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more, visit ************************************************************************* US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: *************************************************************

Validation & Engineering Group, Inc. is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, manufacturing operations among other services. Job Description V&EG's Bio Pharma Fair is the exclusive online job fair organized by Validation & Engineering Group, entirely dedicated to professionals in the medical, biomedical, healthcare, pharmaceutical and biotechnological sectors with at least one of these experiences: * Commissioning, qualification, validation * CSV life cycle experience * Automation * QA/QC * Project Management * Facilities/Maintenance Engineering * EHS Qualifications V&EG's Bio Pharma Fair is addressed to young professionals with a biomedical, biotechnological, pharmaceutical, medical and healthcare, medical and biomedical engineering or Science background coming from Puerto Rico and United States . Minimum of three (3) years of experience in the mentioned sectors. Additional Information Positions available for Puerto Rico and The United States. Only candidates that meet the minimum requirements will be considered. Validation and Engineering Group, Inc. is an Equal Employment Opportunity employer.

At **Kelly Science, Engineering, Technology & Telecom (SETT** **)** , we're passionate about helping you find a job that works for you. How about this one? We're seeking an **Laboratory Technician** to work with one of our top global biopharmaceutical clients in the **Barceloneta PR** area. With us, it's all about finding the job that's just right Perform laboratory analytical tests on raw materials and finished products following the established parameters (company policies, FDA, cGMP) and applicable regulations without impact to the manufacturing cycle or the laboratory workflow. Follow Good Manufacturing Practices), safety rules, and Good Laboratory Practices (GLP). **Responsibilities:** * Responsible for performing laboratory analytical tests on the raw materials and finished products following the established parameters (Customer policies, FDA, cGMP) and applicable regulations without impact to the manufacturing cycle or the laboratory workflow. * Document The results of the test and analysis performed accurately. * Perform preventive maintenance and standardize the laboratory equipment. * Participate in the implementation of special projects and test method transfers. * Assure that all samples are collected, tested, and authorized as per the schedule and following applicable procedures. **Qualifications** * Associate or Bachelor degree in Science required, with a major in **Chemistry** * A minimum of two years of experience in the pharmaceutical industry or equivalent in an analytical laboratory.. * Availability to work the third shift, ALL Shifts weekends, and holidays according to business needs. As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here (********************************************************************* for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community. Why Kelly Science & Clinical? Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world's most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals-it's the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed. About Kelly Work changes everything. And at Kelly, we're obsessed with where it can take you. To us, it's about more than simply accepting your next job opportunity. It's the fuel that powers every next step of your life. It's the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year. Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S. Kelly Services is proud to be an Equal Employment Opportunity and Affirmative Action employer. We welcome, value, and embrace diversity at all levels and are committed to building a team that is inclusive of a variety of backgrounds, communities, perspectives, and abilities. At Kelly, we believe that the more inclusive we are, the better services we can provide. Requests for accommodation related to our application process can be directed to Kelly's Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment.

Job Description Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services. We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position: MEC Laboratory Tech I Summary: Perform microbiological testing required for water used in the manufacturing process, raw materials, in process samples and final product following specifications. Perform microbiological testing such as bioburden and endotoxin to water samples used in the product manufacturing process and to the final product. Perform in process product testing such as bioburden, contamination check and endotoxin. Perform all the facilities and utilities environmental monitoring using Climet, RCS, and surface sampling. Perform gowning sampling as part of routine program and for qualification/routine requirements. Follow Good Manufacturing Practices (cGMP), safety rules and Good Laboratory Practices (GLP). Provide support to the manufacturing area during filling process. Responsibilities: • Responsible for performing the environmental monitoring to the manufacturing area and laboratory test (Raw materials, in process sample and finished product) following the established parameters ( policies, FDA, cGMP) and applicable regulations without impact to the manufacturing cycle or laboratory workflow. • Document The results of the test and analysis performed accurately. • Perform maintenance to laboratory equipment. • Identify, collect, and submit samples to the MEC laboratory. • Assure that all samples are collected, tested, and authorized as per schedule and following applicable procedure. • Assist the MEC Laboratory Service, to maintain adequate inventory of materials, reagents, culture media, reference material, and general-purpose material for the operation of the Environmental Control Laboratory. • Complete training and certifications on time as established in the training curriculums. • Control and management for the disposal of domestic, biomedical, and hazardous wastes of the MEC area as applicable, ensuring compliance with Local and Federal regulations following the procedures and policies of the plant, division, and the corporation. • Participate and promote continuous improvement to the Environmental health and safety (EH&S). Qualifications: Associate degree in Natural science with major in Biology, Chemistry, Microbiology and or Minimum of One year of experience in the Pharmaceutical industry or equivalent in a microbiology laboratory. Skills & Experience required for this position Punctual Overtime availability Bilingual (Preferably) Communication Team work Nice to have (but not required) Previous experience preferred but not required In what type of environment would this individual be working? Daily Work Schedule Expectations Candidates must be available to work any shift and Weekends based in business needs Rotating shift every three months. 3 months in 1st shift for training 3 months in 2nd shift 3 months in 3rd shift After completion of 3 shifts, will be assign based in operational needs.. Sunday to Thursday Tuesday to Saturday Holidays will be notify in advance.

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at *************** Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok (******************************* . Job Description Performs chemical tests following the established procedures. Responsibilities List up to 10 main responsibilities for the job. Include information about the accountability and scope. + Responsible for performing laboratory analytical tests to the raw materials and finished products following the established parameters(Abbvie policies, FDA, cGMP) and applicable regulations without impact to the manufacturing cycle or the laboratory work flow. + Document the results of the tests and analysis performed accurately. + Perform preventive maintenance and standardize the laboratory equipment. + Participate in the implementation of special projects and test method transfers. + Resolve typical technical problems with minimum intervention of the scientist or others. + Perform changes to existence procedures or create new as required. + Actively participate in training of new employees. + Responsible for the coordination and distribution of tasks when required. + Prepare presentations as required. Qualifications + Associate degree in Natural Sciences with major in Chemistry. + Minimum of two years experience in the pharmaceutical industry or equivalent in an analytical laboratory. + Knowledge and abilities in managing analytical instruments. Additional Information AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more, visit ************************************************************************* US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: *************************************************************

Job Description Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services. We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position: Lab Tech II Position Description The selected candidate will perform routine analytical testing to support on-site wastewater treatment operations and ensure compliance with local and state regulatory requirements. This role requires the ability to interpret analytical data, coordinate sample testing, and accurately document results using computerized systems. The position is based in laboratory areas and involves close collaboration within a team environment. Key Responsibilities Perform routine analytical testing in support of on-site wastewater treatment operations. Ensure compliance with local and state environmental requirements. Coordinate sample testing activities and input analytical data into computer spreadsheets and laboratory systems. Review and verify analytical data related to finished products and raw materials. Operate analytical laboratory equipment, including analytical balances, total carbon analyzers, spectrophotometers, and pH meters. Interpret test results and support basic data analysis and troubleshooting. Follow laboratory safety, quality, and documentation standards. Support increased workload and volume demands as required by business needs. Required Qualifications Bachelor's degree or Associate degree in Chemistry or a related chemical field. Minimum of 2 years of experience in a pharmaceutical chemical laboratory environment. Strong laboratory skills; experience in wastewater testing is preferred but not required. Experience reviewing analytical data for raw materials and finished products. Proficiency in operating analytical laboratory equipment. Ability to understand, read, and write English. Strong problem-solving skills and attention to detail. Computer proficiency, including data entry and spreadsheet use. Effective verbal and written communication skills. Background in chemical analysis (microbiology experience not required). Work Environment & Schedule Work environment: Laboratory areas; team-based setting. Shift: Primarily second shift; must be flexible to work first or second shift as business needs vary. Schedule may vary from Monday-Friday or Tuesday-Saturday. Overtime is required based on business needs, including approximately one weekend per month. Additional Information On-site position; remote work is not available. Relocation assistance is not provided; candidates must already be local. No travel required. No work with toxins. Interview process: One interview round conducted via Microsoft Teams.

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at *************** Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok. Job Description Performs chemical tests following the established procedures. Responsibilities List up to 10 main responsibilities for the job. Include information about the accountability and scope. Responsible for performing laboratory analytical tests to the raw materials and finished products following the established parameters(Abbvie policies, FDA, cGMP) and applicable regulations without impact to the manufacturing cycle or the laboratory work flow. Document the results of the tests and analysis performed accurately. Perform preventive maintenance and standardize the laboratory equipment. Participate in the implementation of special projects and test method transfers. Resolve typical technical problems with minimum intervention of the scientist or others. Perform changes to existence procedures or create new as required. Actively participate in training of new employees. Responsible for the coordination and distribution of tasks when required. Prepare presentations as required. Qualifications Associate degree in Natural Sciences with major in Chemistry. Minimum of two years experience in the pharmaceutical industry or equivalent in an analytical laboratory. Knowledge and abilities in managing analytical instruments. Additional Information AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more, visit ************************************************************************* US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: *************************************************************

Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services. We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position: Lab Tech II Position Description The selected candidate will perform routine analytical testing to support on-site wastewater treatment operations and ensure compliance with local and state regulatory requirements. This role requires the ability to interpret analytical data, coordinate sample testing, and accurately document results using computerized systems. The position is based in laboratory areas and involves close collaboration within a team environment. Key Responsibilities Perform routine analytical testing in support of on-site wastewater treatment operations. Ensure compliance with local and state environmental requirements. Coordinate sample testing activities and input analytical data into computer spreadsheets and laboratory systems. Review and verify analytical data related to finished products and raw materials. Operate analytical laboratory equipment, including analytical balances, total carbon analyzers, spectrophotometers, and pH meters. Interpret test results and support basic data analysis and troubleshooting. Follow laboratory safety, quality, and documentation standards. Support increased workload and volume demands as required by business needs. Required Qualifications Bachelor s degree or Associate degree in Chemistry or a related chemical field. Minimum of 2 years of experience in a pharmaceutical chemical laboratory environment. Strong laboratory skills; experience in wastewater testing is preferred but not required. Experience reviewing analytical data for raw materials and finished products. Proficiency in operating analytical laboratory equipment. Ability to understand, read, and write English. Strong problem-solving skills and attention to detail. Computer proficiency, including data entry and spreadsheet use. Effective verbal and written communication skills. Background in chemical analysis (microbiology experience not required). Work Environment & Schedule Work environment: Laboratory areas; team-based setting. Shift: Primarily second shift; must be flexible to work first or second shift as business needs vary. Schedule may vary from Monday Friday or Tuesday Saturday. Overtime is required based on business needs, including approximately one weekend per month. Additional Information On-site position; remote work is not available. Relocation assistance is not provided; candidates must already be local. No travel required. No work with toxins. Interview process: One interview round conducted via Microsoft Teams.