Quality control analyst jobs in Escondido, CA

Scientist, Protein Production and Characterization AlivaMab Biologics is a rapidly growing leader in the discovery of human antibody therapeutics, trusted by top-tier pharmaceutical and biotechnology companies to deliver panels of drug-quality human antibodies. We deliver on our partners' design goals, from simple to extraordinarily challenging, through collaborative access to our scientists' creativity and experience combined with proven technologies, including the AlivaMab Mouse suite of transgenic mice. Our organization is dedicated to creating a healthier world through partnerships that bring better medicines to patients faster, and we recognize our success starts with hiring people who share our passion for science. We are seeking a highly motivated and skilled Scientist to join our Protein Sciences team and contribute to both day-to-day operations and the advancement of Protein Science workflows. This position will focus on the design, optimization, and execution of transient transfection processes at various scales for antibody and protein production in mammalian expression systems. The successful candidate will leverage expertise in biophysical characterization and biochemical modification to evaluate key protein attributes. This position will report to the Associate Director of Protein Sciences and work closely with scientists in the Antibody Discovery, Antibody Engineering, Protein Sciences, and Project Management teams. The ideal candidate will drive innovation through process refinement, high-throughput automation, and growing proficiency of chemical conjugation techniques. This role offers the opportunity to work in a fast-paced, collaborative research environment, where creative solutions and a strong scientific approach are key to success. Responsibilities Responsibilities: Independently design, plan, and execute transient transfection workflows for antibody and protein production across various mammalian expression systems Develop, design, and optimize protein purification methods to enhance throughput, quality, and efficiency, as required Lead developability assessment studies by designing and conducting analytical experiments to evaluate protein stability, purity, and key biophysical characteristics Support production of complex construct design strategies (e.g VLPs, nanodiscs etc.), to enable immunization antibody discovery campaigns against challenging targets Drive implementation of automated high throughput processes to support protein production workflows using Bravo, and other robotic systems Maintain meticulous experimental records using electronic notebook (Benchling), and communicate results clearly through written reports and presentations to support project progression and scientific decision-making Contribute innovative ideas and collaborate effectively across teams to foster research excellence and ensure project success in a fast-paced environment Qualifications Qualifications: Ph.D. in Biochemistry, Chemistry, Molecular Biology, Protein Engineering, or a related field with a minimum of 2 years of industry experience or MS with minimum of 6 years of direct industry experience is required Proven hands-on experience with multiple mammalian expression platforms is required Proficiency with AKTA instrumentation, and a broad range of purification techniques, including affinity chromatography, ion exchange, HIC, and SEC, as well as standard protein QC methodologies is required Experience with therapeutic antibody developability assessment is highly desirable Strong analytical, troubleshooting, and communication skills with exceptional attention to detail Motivated self-starter with excellent organization, teamwork, and a passion for scientific innovation About AlivaMab Biologics AlivaMab Biologics sets its partners' antibody discovery programs on the fastest and most de-risked path through discovery and development. Trusted by top-tier pharmaceutical and biotechnology companies, AMB delivers drug-quality, fully human antibodies on exceptional timelines. AMB achieves its partners' design goals, from simple to extraordinarily challenging, through the generation and function-first screening of large, molecularly diverse panels of antibodies. AMB focuses on rapid and efficient delivery of antibodies, characterized for function, kinetics and developability, and engineering for alternative formats, including multi-specifics and CARs. The AMB team's experience and passion for antibody drug discovery and development combined with the use of trusted, proven technologies, including Ablexis' AlivaMab Mouse platforms, ensure the highest probability of success. The salary range for this position considers various factors, including skills, experience, training, certifications, and organizational needs. Note that this range does not reflect any geographic adjustments based on the location where the role will be based. At AlivaMab Biologics, it is uncommon for a new hire to start at or near the top of the salary range, as compensation is tailored to each individual's skills and breadth and depth of experience. The current estimated range is $98,500 - $140,000, plus a bonus target, benefits, and equity. AlivaMab Biologics provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to religion, race, creed, color, sex, sexual orientation, gender identification, alienage or citizenship status, national origin, age, marital status, pregnancy, disability, veteran or military status, predisposing genetic characteristics or any other characteristic protected by applicable federal, state or local law. #LI-DNI

Scientist, Protein Production and Characterization AlivaMab Biologics is a rapidly growing leader in the discovery of human antibody therapeutics, trusted by top-tier pharmaceutical and biotechnology companies to deliver panels of drug-quality human antibodies. We deliver on our partners' design goals, from simple to extraordinarily challenging, through collaborative access to our scientists' creativity and experience combined with proven technologies, including the AlivaMab Mouse suite of transgenic mice. Our organization is dedicated to creating a healthier world through partnerships that bring better medicines to patients faster, and we recognize our success starts with hiring people who share our passion for science. We are seeking a highly motivated and skilled Scientist to join our Protein Sciences team and contribute to both day-to-day operations and the advancement of Protein Science workflows. This position will focus on the design, optimization, and execution of transient transfection processes at various scales for antibody and protein production in mammalian expression systems. The successful candidate will leverage expertise in biophysical characterization and biochemical modification to evaluate key protein attributes. This position will report to the Associate Director of Protein Sciences and work closely with scientists in the Antibody Discovery, Antibody Engineering, Protein Sciences, and Project Management teams. The ideal candidate will drive innovation through process refinement, high-throughput automation, and growing proficiency of chemical conjugation techniques. This role offers the opportunity to work in a fast-paced, collaborative research environment, where creative solutions and a strong scientific approach are key to success. Responsibilities Responsibilities: * Independently design, plan, and execute transient transfection workflows for antibody and protein production across various mammalian expression systems * Develop, design, and optimize protein purification methods to enhance throughput, quality, and efficiency, as required * Lead developability assessment studies by designing and conducting analytical experiments to evaluate protein stability, purity, and key biophysical characteristics * Support production of complex construct design strategies (e.g VLPs, nanodiscs etc.), to enable immunization antibody discovery campaigns against challenging targets * Drive implementation of automated high throughput processes to support protein production workflows using Bravo, and other robotic systems * Maintain meticulous experimental records using electronic notebook (Benchling), and communicate results clearly through written reports and presentations to support project progression and scientific decision-making * Contribute innovative ideas and collaborate effectively across teams to foster research excellence and ensure project success in a fast-paced environment Qualifications Qualifications: * Ph.D. in Biochemistry, Chemistry, Molecular Biology, Protein Engineering, or a related field with a minimum of 2 years of industry experience or MS with minimum of 6 years of direct industry experience is required * Proven hands-on experience with multiple mammalian expression platforms is required * Proficiency with AKTA instrumentation, and a broad range of purification techniques, including affinity chromatography, ion exchange, HIC, and SEC, as well as standard protein QC methodologies is required * Experience with therapeutic antibody developability assessment is highly desirable * Strong analytical, troubleshooting, and communication skills with exceptional attention to detail * Motivated self-starter with excellent organization, teamwork, and a passion for scientific innovation About AlivaMab Biologics AlivaMab Biologics sets its partners' antibody discovery programs on the fastest and most de-risked path through discovery and development. Trusted by top-tier pharmaceutical and biotechnology companies, AMB delivers drug-quality, fully human antibodies on exceptional timelines. AMB achieves its partners' design goals, from simple to extraordinarily challenging, through the generation and function-first screening of large, molecularly diverse panels of antibodies. AMB focuses on rapid and efficient delivery of antibodies, characterized for function, kinetics and developability, and engineering for alternative formats, including multi-specifics and CARs. The AMB team's experience and passion for antibody drug discovery and development combined with the use of trusted, proven technologies, including Ablexis' AlivaMab Mouse platforms, ensure the highest probability of success. The salary range for this position considers various factors, including skills, experience, training, certifications, and organizational needs. Note that this range does not reflect any geographic adjustments based on the location where the role will be based. At AlivaMab Biologics, it is uncommon for a new hire to start at or near the top of the salary range, as compensation is tailored to each individual's skills and breadth and depth of experience. The current estimated range is $98,500 - $140,000, plus a bonus target, benefits, and equity. AlivaMab Biologics provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to religion, race, creed, color, sex, sexual orientation, gender identification, alienage or citizenship status, national origin, age, marital status, pregnancy, disability, veteran or military status, predisposing genetic characteristics or any other characteristic protected by applicable federal, state or local law. #LI-DNI

Work as part of a team that performs routine and non-routine incoming products using various analyzers and instruments to support release, characterization and stability testing of raw materials, production intermediates and final goods. Qualifications Education: •BS/MS in Biology/Molecular Biology, biochemistry, chemistry or related discipline •2 to 5 years of industry experience with Functional analysis QC of molecular-biology-based assays preferred, other QC, R&D or manufacturing experience will be considered. Additional Information All your information will be kept confidential according to EEO guidelines.

Scientist, Protein Production and Characterization AlivaMab Biologics is a rapidly growing leader in the discovery of human antibody therapeutics, trusted by top-tier pharmaceutical and biotechnology companies to deliver panels of drug-quality human antibodies. We deliver on our partners' design goals, from simple to extraordinarily challenging, through collaborative access to our scientists' creativity and experience combined with proven technologies, including the AlivaMab Mouse suite of transgenic mice. Our organization is dedicated to creating a healthier world through partnerships that bring better medicines to patients faster, and we recognize our success starts with hiring people who share our passion for science. We are seeking a highly motivated and skilled Scientist to join our Protein Sciences team and contribute to both day-to-day operations and the advancement of Protein Science workflows. This position will focus on the design, optimization, and execution of transient transfection processes at various scales for antibody and protein production in mammalian expression systems. The successful candidate will leverage expertise in biophysical characterization and biochemical modification to evaluate key protein attributes. This position will report to the Associate Director of Protein Sciences and work closely with scientists in the Antibody Discovery, Antibody Engineering, Protein Sciences, and Project Management teams. The ideal candidate will drive innovation through process refinement, high-throughput automation, and growing proficiency of chemical conjugation techniques. This role offers the opportunity to work in a fast-paced, collaborative research environment, where creative solutions and a strong scientific approach are key to success. Responsibilities Responsibilities: Independently design, plan, and execute transient transfection workflows for antibody and protein production across various mammalian expression systems Develop, design, and optimize protein purification methods to enhance throughput, quality, and efficiency, as required Lead developability assessment studies by designing and conducting analytical experiments to evaluate protein stability, purity, and key biophysical characteristics Support production of complex construct design strategies (e.g VLPs, nanodiscs etc.), to enable immunization antibody discovery campaigns against challenging targets Drive implementation of automated high throughput processes to support protein production workflows using Bravo, and other robotic systems Maintain meticulous experimental records using electronic notebook (Benchling), and communicate results clearly through written reports and presentations to support project progression and scientific decision-making Contribute innovative ideas and collaborate effectively across teams to foster research excellence and ensure project success in a fast-paced environment Qualifications Qualifications: Ph.D. in Biochemistry, Chemistry, Molecular Biology, Protein Engineering, or a related field with a minimum of 2 years of industry experience or MS with minimum of 6 years of direct industry experience is required Proven hands-on experience with multiple mammalian expression platforms is required Proficiency with AKTA instrumentation, and a broad range of purification techniques, including affinity chromatography, ion exchange, HIC, and SEC, as well as standard protein QC methodologies is required Experience with therapeutic antibody developability assessment is highly desirable Strong analytical, troubleshooting, and communication skills with exceptional attention to detail Motivated self-starter with excellent organization, teamwork, and a passion for scientific innovation About AlivaMab Biologics AlivaMab Biologics sets its partners' antibody discovery programs on the fastest and most de-risked path through discovery and development. Trusted by top-tier pharmaceutical and biotechnology companies, AMB delivers drug-quality, fully human antibodies on exceptional timelines. AMB achieves its partners' design goals, from simple to extraordinarily challenging, through the generation and function-first screening of large, molecularly diverse panels of antibodies. AMB focuses on rapid and efficient delivery of antibodies, characterized for function, kinetics and developability, and engineering for alternative formats, including multi-specifics and CARs. The AMB team's experience and passion for antibody drug discovery and development combined with the use of trusted, proven technologies, including Ablexis' AlivaMab Mouse platforms, ensure the highest probability of success. The salary range for this position considers various factors, including skills, experience, training, certifications, and organizational needs. Note that this range does not reflect any geographic adjustments based on the location where the role will be based. At AlivaMab Biologics, it is uncommon for a new hire to start at or near the top of the salary range, as compensation is tailored to each individual's skills and breadth and depth of experience. The current estimated range is $98,500 - $140,000, plus a bonus target, benefits, and equity. AlivaMab Biologics provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to religion, race, creed, color, sex, sexual orientation, gender identification, alienage or citizenship status, national origin, age, marital status, pregnancy, disability, veteran or military status, predisposing genetic characteristics or any other characteristic protected by applicable federal, state or local law. #LI-DNI

We are seeking a detail-oriented and highly responsible QC/SSHO to support a mechanical contract at Marine Corps Air Station (MCAS) Miramar. This individual will be responsible for overseeing quality control and site safety practices in accordance with U.S. Government, DoD, and California state regulations. A key aspect of the role includes documenting and uploading field observations (photos, statements, reports) into the Maximo Government database system. This is a mission-critical role that ensures safety, compliance, and accurate reporting on all aspects of the mechanical work performed. Key Responsibilities: Serve as the primary Quality Control and Safety point of contact on-site. Ensure compliance with all federal, state, and local safety and environmental regulations, as well as project-specific guidelines. Conduct daily safety inspections and QC audits to identify and mitigate potential hazards and quality issues. Document findings with photographs and written statements to be entered into Maximo in a timely and accurate manner. Coordinate and lead preparatory, initial, and follow-up QC meetings in accordance with the approved Quality Control Plan. Develop and submit activity hazard analyses (AHAs) and ensure their implementation in the field. Enforce all job site safety protocols and OSHA standards. Interface with government representatives, subcontractors, and field staff to maintain compliance with contract specifications. Maintain detailed site logs, inspection reports, and records in alignment with contract and Maximo requirements. Investigate incidents or near-misses, gather statements, and contribute to root cause analysis and corrective actions. Qualifications: Prior experience working as a QC Manager or SSHO on federal or DoD projects (NAVFAC or USACE experience preferred). Familiarity with mechanical systems and related inspection procedures. Working knowledge of Maximo or similar asset management platforms. OSHA 30-Hour Construction Safety Certification (required). EM 385-1-1 certification (preferred or required by contract). Strong verbal and written communication skills. Proficient in photo documentation and digital reporting processes. Ability to work independently, manage time effectively, and adhere to strict government protocols. U.S. Citizenship is required due to access requirements for military installations. Additional Requirements: Must be able to pass background checks and security clearance as required for access to MCAS Miramar. Must wear appropriate PPE and follow all site-specific safety procedures. Ability to climb ladders, navigate construction sites, and stand for extended periods. Must have a valid driver's license. Primary Place of Performance Southern California Compensation and Benefits Pay Range: $75,000 - $80,000 depending on experience Medical, Dental, Vision, Supplementary insurances, 401k match EQUAL OPPORTUNITY EMPLOYER…. Fortis Industries is an Equal Opportunity Employer. Prospective employees will receive consideration without discrimination because of race, color, religion, creed, gender, national origin, age, disability, marital or veteran status, sexual orientation, or any other legally protected status. We are committed to Equal Employment Opportunity and providing reasonable accommodation to applicants with physical and/or mental disabilities. Fortis Industries is an E-Verify employer. Applicants must receive favorable background and drug screen results and meet eligibility requirements for access to government computer systems and or facilities. Drug screens follow Federal guidelines.

Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in 1996, IRI has attracted, assembled and retained key employees who are experts in their fields. This has helped us expand into new sectors and steadily grow. Job Description Responsibilities: Trains and becomes proficient in all the required techniques, operation of relevant equipment and software packages associated with testing, data analysis, and data reporting. This may require working with human blood, human or mammalian cell culture and/or animals and animal tissues. Routine, accurate and timely completion of all assigned QC tests under supervision and according to standard protocols or operating procedures. Will prioritize daily workload and develop skills to work independently. Analyze data and report test results including completion of all required documentation and database entries as required by QC protocols or operating procedures. Calibrate and maintain equipment. Report problems to QC Supervisor or Manager. Maintain logs and required documentation as necessary. Prepare supplies and reagents, and assist with laboratory maintenance as needed. Promote a safe work environment. May provide recommendations on maintaining the safety of the work environment. Participate in Environmental, Health & Safety programs. Address corrective actions whenever a hazard is identified. Notify supervisor and Safety Officer(s) of all observed hazardous conditions or unsafe work practices. Keep abreast of the basic requirements for safety compliance in own area of work and complies with those requirements. Participate in assigned cross-training Perform other related duties and assignments as required. Qualifications BS degree, 1 year experience in a laboratory environment. The QC Temp is responsible for routine, accurate and timely testing of QC samples according to standard protocols and operating procedures. The QC Temp will prioritize daily workload and work somewhat independently. They will perform testing, report results, and complete all required documentation. Additional Information Thanks!! With Regards, Sasha Sharma Clinical Recruiter Integrated Resources, Inc IT REHAB CLINICAL NURSING Direct: 732-662-7964 | (W) 732-549-2030 x 219 Inc. 5000 - 2007-2015 (9 Years in a row)

About Us When you work at Chugach Government Solutions (CGS), you join a proud legacy of supporting missions while sustaining culture. The federal division of Chugach Alaska Corporation, CGS has been supporting critical missions as a government contractor for over 25 years. Our focus is to support facility maintenance, IT/technical services, construction and education. We are proud to have built, and continue to foster, an incredibly talented team spanning across the globe in hundreds of different fields - each team member proud to serve our country with first-class business services, while also making a difference for our Chugach shareholders. At CGS, empowering employees is a part of our core, and that focus is one of the ways we build and foster high-performing teams. We empower our employees through competitive compensation and benefits package, professional growth opportunities, truthful communication, and more! If you are looking for an opportunity to serve something bigger than yourself; if you want your day job to be one that creates meaningful value; if you are looking for an environment that highly values employees and respects individual differences - then Chugach Government Solutions may be the right fit for you! Job Overview Under the direction of the Task Order Manager, the Quality Control Inspector is responsible for conducting inspections to ensure compliance with contract requirements and Quality Control and Safety Plans. Pay Rate: $26.74/hourly Work Model: Onsite Responsibilities Essential Duties & Job Functions: * Review all site work to verify compliance in accordance with applicable plans and procedures. * Inspect and diagnose problems to determine corrective actions/repairs. * Inspect work in progress and finished work for discrepancies in accordance with the QC and applicable Safety Plans, and contract requirements.Complete necessary inspection reports and documentation required to support findings. * Assist in preparing Safety incident and hazard reports as required. * Maintains accurate administrative records. * Review all site work to verify compliance in accordance with applicable plans and procedures. * Respond to emergency site maintenance as required. * Ensures proper housekeeping practices are strictly observed. * Maintain open communications with personnel. * Performs other duties as assigned by the supervisor. * Other duties as assigned. Accountable For: * Tools and equipment within his or her possession. * Using PPE when required. * Timely completion and accuracy of all work. * Working closely and harmoniously with fellow workers. * Adherence to all Safety rules and regulations. Job Requirements Mandatory: * Working knowledge of Microsoft Programs, including but not limited to: Outlook, Word, PowerPoint, and Excel or equivalent software program. * Understanding of Government contracts, correspondence, reports, and records. * Knowledge of generally accepted standards of workmanship in custodial services. * Excellent communication skills, both oral and written. * Excellent organizational skills. * Mature judgment and ability to work with little or no supervision. * Ability to communicate ideas effectively with personnel at all levels. * United States Citizen. * High School Diploma or Equivalent. * Ability to pass pre-employment background check and drug screen. * Must be able to read, write, and speak English fluently. * Valid driver's license with excellent driving record (Must provide current driving record). * Ability to obtain access to U.S. Government Installations through the Defense Biometric Identification System (DBIDS). Preferred: * 2 yrs custodial experience. * Two-year degree in Safety, Industrial Hygiene, or a related field or broad experience in the same or similar areas. * Bilingual - Spanish Working Conditions: * Work is performed indoors and outdoors. Outdoor work is subject to temperature extremes and inclement weather conditions. * Work hours are subject to change, with overtime, weekend and/or holiday work as needed. * Subject to hazards that may cause personal bodily harm; diseases, cuts, bruises, burns, common cold, influenza, dust odors and elevated noise levels. * Tasks may be performed on uneven, inclined, hard and soft carpeted floors, cement structures and surfaces. * While performing duties of this job, the employee is occasionally required to stand and/or walk for long periods of time, sit, use of hands and fingers, handle, or feel objects, tools or controls, reach with hands and arms, climb stairs, climb ladders, balance, stoop, kneel, crouch or crawl, talk, hear, or smell. The employee must occasionally lift and/or move up to 35 pounds. Specific vision abilities required by the job include close vision. May be required to operate regular and specialized vehicles. Physical Requirements: * Must be able to lift to 50 lbs. * Must be able to climb stairs and ladders as required. * Must be able to load/unload materials, tools, and equipment. * Involves walking, bending, stooping, twisting, and reaching. Reasonable Accommodation: CGS will provide reasonable accommodations, according to applicable state and federal laws, to all qualified individuals with physical or mental disabilities. In compliance with the ADA Amendments Act (ADAAA), if you have a disability and would like to request an accommodation in order to apply for a position with Chugach Government Solutions or any if its subsidiaries, please email ******************. Equal Employment Opportunity: Chugach is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, gender, sexual orientation, gender identity or expression, age, pregnancy, disability, genetic factors, protected veteran status or other characteristics protected by law.

Shift hours 9-5: 30pm Interviews video, phone or in person in person Must haves on resume hands-on Flow Cytometry experience, data acquisition and analysis included The QC Associate I is responsible for routine, accurate and timely testing of QC samples according to standard protocols and operating procedures, such as flow cytometry related protocols. The QC Associate I will prioritize daily workload and work independently. They will participate in the review of data, report results, and complete all required documentation and database entries. QC Associate I will receive specific instructions and ongoing guidance regarding required tasks and expected results. JOB RESPONSIBILITIES Trains and becomes proficient in all the required techniques, operation of relevant equipment and software packages associated with testing, data analysis, and data reporting. This may require working with human blood, human or mammalian cell culture and/or animals and animal tissues. Routine, accurate and timely completion of all assigned QC tests under supervision and according to standard protocols or operating procedures. Will prioritize daily workload and develop skills to work independently. Analyze data and report test results including completion of all required documentation and database entries as required by QC protocols or operating procedures. Calibrate and maintain equipment. Report problems to QC Supervisor or Manager. Maintain logs and required documentation, as necessary. Prepare lab supplies, reagents, and assist with laboratory maintenance, as needed. Promote a safe work environment. May provide recommendations on maintaining the safety of the work environment. Participate in Environmental, Health & Safety programs. Address corrective actions whenever a hazard is identified. Notify supervisor and Safety Officer(s) of all observed hazardous conditions or unsafe work practices. Keep abreast of the basic requirements for safety compliance in own area of work and complies with those requirements. Participate in group or intra-department teams and projects as required. Participate in assigned cross-training. Perform other related duties and assignments, as required. EDUCATION AND EXPERIENCE: BS/BA in a related scientific discipline or some related college coursework with a minimum of 2 years related experience in a biotech lab environment. Experience in an industrial or research laboratory preferred. Flow Cytometry experience required Tissue Culture experience highly preferred. KNOWLEDGE AND SKILLS Basic computer skills: MS Excel & Word. Knowledge of general laboratory safety. Effective interpersonal, written and oral communication skills. Demonstrated ability to follow established policies/procedures, and ability to keep neat, accurate, and complete records and logs. Effective analytical and problem-solving skills.

Job DescriptionRare opportunity to learn and grow with our company! Liberty EnviroLab is currently seeking Full Time Experienced Laboratory Analysts specializing in wildfire, structure fire, asbestos, and mold analysis. Liberty EnviroLab is located in San Marcos in the northern San Diego County. Liberty offers a variety of analytical testing services to support environmental investigations focused on wildfire, structure fire, asbestos, mold (microbiology). Our management team has over 71 years of combined experience in particulate analysis and trace evidence examination. We believe in empowering our customers with accurate and defensible analytical results. Some Responsibilities Include: Safely perform analyses on samples according to Libertys Standard Operating Procedures (SOPs) using advanced instruments. Follow all laboratory QA/QC requirements Record data using computer software and programs. Maintain equipment according to manufacturer guidelines and company procedures. Perform other assigned duties, as requested by supervisor. Requirements: Associates or Bachelors Degree in a life science (biology, chemistry, environmental science, etc.) preferred. 1-2 years of Polarized light microscopy (PLM) experience required. 1 year of Phase contrast microscopy (PCM) experience required. Self-motivated, independent, and team oriented. Must be able to work in a fast-paced setting, multi-task, and prioritize assignments. Good communication, computer, typing, and organizational skills. Liberty EnviroLab offers full time benefits: medical, 401k, sick pay, paid time off, and holiday pay. Pay range for this position is $22.00-$29.00 per hour. The work schedule is flexible. Visit our website for more information about our company. ************************ Please submit your resume, or call us at ************ for assistance!

We're looking for people who put their innovation to work to advance our success - and their own. Join an organization that ensures a more secure world through connecting and protecting our customers with inventive electrical solutions. * DCC to conform to ISO system * Issue MRB to supplier and monitoring countermeasure * Update any daily records from QC operators. * Manage and control inspection for IQC, IPQC, OBA,OQC and equipment. * Provide quality monthly report to manager. * Cooperate with relate department for document cascade and control * Conduct to Internal & External Audit for ISO9001 and supplier audit. * Scrap control and management. * Manage and plan subordinators for inspection. WE HAVE: * A dynamic global reach with diverse operations around the world that will stretch your abilities, provide plentiful career opportunities, and allow you to make an impact every day * nVent is a leading global provider of electrical connection and protection solutions. We believe our inventive electrical solutions enable safer systems and ensure a more secure world. We design, manufacture, market, install and service high performance products and solutions that connect and protect some of the world's most sensitive equipment, buildings and critical processes. We offer a comprehensive range of systems protection and electrical connections solutions across industry-leading brands that are recognized globally for quality, reliability and innovation. * Our principal office is in London and our management office in the United States is in Minneapolis. Our robust portfolio of leading electrical product brands dates back more than 100 years and includes nVent CADDY, ERICO, HOFFMAN, ILSCO, SCHROFF and TRACHTE. Learn more at ************** * Commitment to strengthen communities where our employees live and work * We encourage and support the philanthropic activities of our employees worldwide * Through our nVent in Action matching program, we provide funds to nonprofit and educational organizations where our employees volunteer or donate money * Core values that shape our culture and drive us to deliver the best for our employees and our customers. We're known for being: * Innovative & adaptable * Dedicated to absolute integrity * Focused on the customer first * Respectful and team oriented * Optimistic and energizing * Accountable for performance * Benefits to support the lives of our employees At nVent, we connect and protect our customers with inventive electrical solutions. People are our most valuable asset. Inclusion and diversity means that we celebrate and encourage each other's authenticity because we understand that uniqueness sparks growth.

Quality Control Chemist Location: San Diego, CA | Employment Type: Full-Time Help ensure the quality behind life-changing peptide therapeutics. PolyPeptide Laboratories is seeking a Quality Control Chemist to join our dynamic analytical team. In this role, you'll perform essential testing that ensures the purity, safety, and consistency of our peptide products - directly supporting global customers and advancing breakthrough therapies. If you're detail-oriented, science-driven, and excited to grow in a fast-paced GMP environment, this role is for you. What You'll Be Doing * Perform analytical testing on raw materials, intermediates, in-process samples, and finished products * Work with key instruments including HPLC/UPLC, GC, MS, FTIR, Karl Fischer, elemental analysis, polarimetry, and more * Prepare samples and solutions following established methodologies and validated protocols * Calibrate lab equipment and perform basic troubleshooting * Document all testing in accordance with GMP and data-integrity requirements * Identify potential quality issues and support corrective actions * Contribute to SOP updates and improvements in QC workflows * Maintain a clean, organized, and audit-ready laboratory What You Bring Education & Experience * Bachelor's degree in Chemistry, Biochemistry, or closely related field * 1+ year of experience in a GMP pharmaceutical or biotechnology laboratory Technical Strengths * Hands-on experience with analytical instrumentation (HPLC/UPLC required; GC, MS, FTIR, KF, and others preferred) * Strong documentation skills and Microsoft Office proficiency Soft Skills * Exceptional attention to detail and strong technical writing ability * Ability to multitask and adapt to shifting priorities * Strong communication skills and the ability to work both independently and collaboratively Why PolyPeptide? At PolyPeptide, your precision powers progress. You'll join a collaborative, science-driven team that values expertise, integrity, and continuous improvement. Every measurement you make helps ensure the quality and safety of products that improve lives around the world. Ready to make an impact? Join us and help drive quality at the heart of peptide innovation. Salary: $26-$29/hr We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law.

Quality Control Chemist Location: San Diego, CA | Employment Type: Full-Time Help ensure the quality behind life-changing peptide therapeutics. PolyPeptide Laboratories is seeking a Quality Control Chemist to join our dynamic analytical team. In this role, you'll perform essential testing that ensures the purity, safety, and consistency of our peptide products - directly supporting global customers and advancing breakthrough therapies. If you're detail-oriented, science-driven, and excited to grow in a fast-paced GMP environment, this role is for you. What You'll Be Doing Perform analytical testing on raw materials, intermediates, in-process samples, and finished products Work with key instruments including HPLC/UPLC, GC, MS, FTIR, Karl Fischer, elemental analysis, polarimetry, and more Prepare samples and solutions following established methodologies and validated protocols Calibrate lab equipment and perform basic troubleshooting Document all testing in accordance with GMP and data-integrity requirements Identify potential quality issues and support corrective actions Contribute to SOP updates and improvements in QC workflows Maintain a clean, organized, and audit-ready laboratory What You Bring Education & Experience Bachelor's degree in Chemistry, Biochemistry, or closely related field 1+ year of experience in a GMP pharmaceutical or biotechnology laboratory Technical Strengths Hands-on experience with analytical instrumentation (HPLC/UPLC required; GC, MS, FTIR, KF, and others preferred) Strong documentation skills and Microsoft Office proficiency Soft Skills Exceptional attention to detail and strong technical writing ability Ability to multitask and adapt to shifting priorities Strong communication skills and the ability to work both independently and collaboratively Why PolyPeptide? At PolyPeptide, your precision powers progress. You'll join a collaborative, science-driven team that values expertise, integrity, and continuous improvement. Every measurement you make helps ensure the quality and safety of products that improve lives around the world. Ready to make an impact? Join us and help drive quality at the heart of peptide innovation. Salary: $26-$29/hr We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law.

Job Title: QC Inspector Join a leading medical manufacturing organization as a QC Inspector within our Machine Shop team. This role offers an opportunity to ensure the highest quality standards for precision components used in critical applications. You'll support machinists by performing detailed inspections and quality checks, contributing to the production of world-class medical devices. This is a first-shift position with competitive pay. Key Responsibilities: Assist machinists in machining operations, ensuring products meet all quality and safety standards Grind and prepare production tooling to specifications Conduct thorough inspections of all machined parts using precise measurement tools and blueprints Set up and edit CNC screw machines to produce consistent, high-quality components Perform initial and in-process inspections, verifying dimensions and tolerances Document inspection results accurately and maintain detailed quality records Follow standard operating procedures (SOPs) and adhere to regulatory requirements including cGMP and ISO standards Support continuous improvement initiatives to enhance inspection processes and product quality Perform additional duties as assigned by supervisor or manager Qualifications & Skills: Previous experience with cGMP and ISO standards is preferred Strong background in quality control inspection, with experience handling small parts and performing repetitive tasks Proficiency with measuring devices (calipers, micrometers, gauges) and interpreting blueprints Excellent attention to detail and organizational skills Ability to work independently with minimal supervision High school diploma or equivalent required Physical Requirements: Ability to sit, stand, walk, and reach frequently throughout the shift Regular use of hands and fingers to manipulate tools and inspect parts Ability to climb, balance, stoop, kneel, or crouch occasionally Lift and carry up to 10 lbs frequently and up to 25 lbs occasionally Close vision required for precision measuring and microscope work, as well as reading documents Distance vision required for any driving responsibilities Work environment is indoors, climate-controlled, with occasional exposure to outdoor weather conditions Work Environment & Schedule: Work shift: 6:00 AM - 2:30 PM Position offers growth opportunities within quality and manufacturing fields, with potential for skill development and career advancement

QCMI currently has an immediate need for a qualified Quality Inspector/CMM Programmer. Qualified individuals must have a strong technical background along with the desire to succeed personally as well as professionally by expanding their ability and knowledge at QCMI. Skills / Requirements: Must have previous experience as an Inspector in a machine shop. Previous experience as a machinist is a plus Must be proficient in all basic surface plate inspection methods and be able to work unsupervised. Able to build gages for operators and verify dimensions. Must have First Articles experience. Possesses knowledge of various types of metals including castings & forgings. Must be proficient in basic computer applications. Knowledge of lean manufacturing principals is a plus. Understands GD&T along with being proficient at reading & understanding blueprints. CMM Training Required. Must possess strong communication and writing skills in English. Familiar with 6Sigma methodologies and principals is a plus. Must be U.S. Person within the meaning of ITAR Should have a general understanding of ISO9001/AS9100 quality systems. Important Notes: We are looking for experienced Inspectors only. Candidates must have their own tools. This individual must have excellent communication skills and will be working with engineering, quality, and manufacturing departments to ensure QCMI meets customer deadlines and quality requirements. For consideration, all applicants must have previous experience as an Inspector. All candidates must possess the requirements above as well as dependability, strong work ethics, being a team player and willingness to work overtime when requested.

Job DescriptionQuality Control InspectorAre you passionate about ensuring the highest quality standards in the biotech industry? We are seeking a skilled and detail-oriented Quality Control Technician to join our reputable biotech diagnostic company. Location: CarlsbadPay Rate: $18 - $19.80/hr, contract Both 1st shift and 2nd shift available, Monday-Friday and weekends as needed Key Responsibilities: Perform routine and special inspections for visual, dimension, and functional assessments, ensuring adherence to inspection instructions. Document and report inspection findings, monitoring corrective actions for any identified issues. Execute product identification and traceability activities as required. Review, approve, and maintain Device History Records for all manufacturing functions, in compliance with relevant standards and regulations. Apply in-depth knowledge of QSRs/ISO and regulatory guidelines to daily tasks, ensuring quality standards are upheld. Monitor and comply with customer specifications and company quality assurance policies. Ensure proper calibration and maintenance of inspection equipment. Essential Functions: Conduct and document hourly inspections. Perform and document line clearance procedures. Carry out First Articles and Retention Samples, documenting and filing accordingly. Review, approve, and file documents for completeness and compliance. Work Environment:The work environment encompasses warehouse, laboratory, and manufacturing settings, where handling viral and bacterial hazards, potentially hazardous chemicals, and infectious bodily fluids and samples may occur. Flexible work hours may be required to meet project deadlines. Education, Skills & Experience: Minimum 6 months of Quality Control inspection experience required. Experience with Good Manufacturing Practice (GMP) Experience in a medical device high-volume manufacturing environment is strongly desired. Ability to read, interpret, and follow detailed procedures, instructions, and drawings. Solid understanding of QSRs/ISO standards. Demonstrated team-oriented interaction skills and professional behavior. Proficiency in word processing, data entry, and spreadsheet navigation. Familiarity with basic quality terms, definitions, and concepts. Understanding of traceability (product, material, and calibration). Basic math skills for determining appropriate sample sizes for inspection based on lot sizes. Problem-solving skills to identify processes and standards in need of improvement and initiate appropriate action. If you are driven by a commitment to excellence and have a passion for quality control in the biotech industry, we encourage you to apply. Join our dedicated team and make a significant impact on healthcare by maintaining the highest quality standards in our biotech diagnostic products.

GLAUKOS - QUALITY CONTROL INSPECTOR I - 1st SHIFT (SAN CLEMENTE, CA) How will you make an impact? The Quality Control Inspector I will be responsible for all aspects of inspection (receiving, in-process and final). In addition, this position will provide QSR support for other QA activities such as calibration, environmental monitoring, product testing, label control, etc. What will you do? Receiving Inspection * Receiving inspection of components following procedures, specifications and drawings. * Utilize a variety of standard metrology equipment, including: Optical comparator, height gauge, master height gauge, CMM, Vision Metrology System (VMS, e.g., Smartscope), calipers, micrometers, surface table, gauge blocks, pin gauges, dial indicators, durometer, measuring microscope, hardness testers, pull force testers, surface roughness testers, etc. * Read engineering drawings and interpret geometric dimensioning and tolerancing. * Review associated paperwork, complete inspection records using good documentation practices, and release components. * Program the Smartscope to run automatic routines for multiple part inspections. (Level 2 and higher) * Write clear and concise procedures for inspection of components, machined tubing, etc. (Level 2 and higher) * Carefully handle and process extremely small components without damaging them. In-Process Inspection * Perform Line Clearance for Operations activities * Inspect and release labeling * Review device history records for lot release. Ensure all quality records meet good documentation practices in accordance with internal procedures. * Perform inspections on components and assemblies in manufacturing Final Inspection * Review device history records for lot release. Ensure all quality records meet good documentation practices in accordance with internal procedures. * Perform final inspection on finished goods * Inspect finished goods for proper labels, packaging, tamper seals and product in accordance with procedures. * Coordinate final inspection activities with outside vendors, i,e, LAL, peel testing * Perform in-house peel testing on sealed packages * Maintain sample retain area Other Duties * Work with engineering in the design of high quality inspection / metrology fixtures. * Support equipment and process validation activities by inspecting process outputs * Conduct periodic compliance audits of manufacturing operations and procedures for cGMP compliance. * Ensures on a daily basis quality records and company practices are compliant with internal procedures and regulations. * Coordinate the monthly environmental monitoring of the cleanrooms. * Coordinate quarterly dose audits. How will you get here? * High School Diploma required. * 0-2 years industry experience. Knowledge, Skills, and Abilities * Medical device experience and working knowledge of QSR a must * Experience working in a clean room and/or performing in-process assembly and manufacturing verification inspections desirable * Attention to detail and accuracy a must * Must have excellent documentation skills * Team player, good written/oral communicator * Must be organized and able to coordinate activities with outside vendors #GKOSUS

Somacis, Inc. is a global leader in PCB manufacturing, serving Aerospace, Avionics, Military, Commercial, and Medical industries. With over 50 years of innovation and commitment to quality, we are a trusted partner in high-performance PCB solutions. Position Overview We are seeking a Chemical Lab Technician to support our Wet Lab Department by conducting chemical testing and analysis to ensure product quality and compliance. This role involves performing lab analyses, monitoring chemical processes, and collaborating with engineering teams to maintain production standards. Key Responsibilities Conduct chemical analyses using titrations, pH/ion meters, spectrophotometers, hydrometers, and other lab equipment. Collect and test chemical samples from process tanks to ensure compliance. Identify trends in analysis data and report findings to engineering. Handle acids and caustic chemicals safely. Generate chemical addition slips and document corrective actions. Maintain a clean and organized lab environment. Follow all safety protocols, including hazardous waste handling under EH&S guidelines. Communicate process improvements and safety concerns with supervisors and team members. Qualifications Basic understanding of chemistry lab procedures. Associate degree or higher in Chemistry (preferred). 1-2 years of experience in a chemical lab or wet process department (preferred). Strong attention to detail and adherence to procedures. Ability to stand for extended periods and lift up to 30 lbs. Proficiency in computer use and ability to read procedures and blueprints. Flexibility to work up to 9-hour shifts, 5 days a week, including weekends if needed. Physical Requirements Ability to work on a computer for extended periods. Fine motor skills for lab equipment and data entry. Bending at the head, neck, and waist as needed. Strong vision skills for microscope analysis. Benefits Medical, Dental, and Vision Insurance 401(k) Program Company-Sponsored Life & Long-Term Disability Insurance Voluntary Insurance Options: Life, Long-Term Disability, Short-Term Disability, AD&D, Accident, Hospital Indemnity, Critical Illness, and Legal Insurance Health Savings Account (HSA) and Flexible Spending Account (FSA) Options Paid Time Off (PTO) Program Employee Referral Program Education Reimbursement Program 14 Company Holidays Shift Differential Eligibility: Qualified applicants must hold U.S. Citizenship, Permanent, Asylee, or Refugee Status Note: Job descriptions aim to provide accurate overviews of roles without exhaustive detail. They serve as reference points for fair pay considerations. Somacis is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status, and will not be discriminated against on the basis of disability.

GLAUKOS - QUALITY CONTROL INSPECTOR I - 1st SHIFT (SAN CLEMENTE, CA) How will you make an impact? The Quality Control Inspector I will be responsible for all aspects of inspection (receiving, in-process and final). In addition, this position will provide QSR support for other QA activities such as calibration, environmental monitoring, product testing, label control, etc. What will you do? Receiving Inspection Receiving inspection of components following procedures, specifications and drawings. Utilize a variety of standard metrology equipment, including: Optical comparator, height gauge, master height gauge, CMM, Vision Metrology System (VMS, e.g., Smartscope), calipers, micrometers, surface table, gauge blocks, pin gauges, dial indicators, durometer, measuring microscope, hardness testers, pull force testers, surface roughness testers, etc. Read engineering drawings and interpret geometric dimensioning and tolerancing. Review associated paperwork, complete inspection records using good documentation practices, and release components. Program the Smartscope to run automatic routines for multiple part inspections. (Level 2 and higher) Write clear and concise procedures for inspection of components, machined tubing, etc. (Level 2 and higher) Carefully handle and process extremely small components without damaging them. In-Process Inspection Perform Line Clearance for Operations activities Inspect and release labeling Review device history records for lot release. Ensure all quality records meet good documentation practices in accordance with internal procedures. Perform inspections on components and assemblies in manufacturing Final Inspection Review device history records for lot release. Ensure all quality records meet good documentation practices in accordance with internal procedures. Perform final inspection on finished goods Inspect finished goods for proper labels, packaging, tamper seals and product in accordance with procedures. Coordinate final inspection activities with outside vendors, i,e, LAL, peel testing Perform in-house peel testing on sealed packages Maintain sample retain area Other Duties Work with engineering in the design of high quality inspection / metrology fixtures. Support equipment and process validation activities by inspecting process outputs Conduct periodic compliance audits of manufacturing operations and procedures for cGMP compliance. Ensures on a daily basis quality records and company practices are compliant with internal procedures and regulations. Coordinate the monthly environmental monitoring of the cleanrooms. Coordinate quarterly dose audits. How will you get here? High School Diploma required. 0-2 years industry experience. Knowledge, Skills, and Abilities Medical device experience and working knowledge of QSR a must Experience working in a clean room and/or performing in-process assembly and manufacturing verification inspections desirable Attention to detail and accuracy a must Must have excellent documentation skills Team player, good written/oral communicator Must be organized and able to coordinate activities with outside vendors #GKOSUS

At Devon, we will offer you a career full of energy and unmatched opportunities to solve today's greatest challenges. Innovation, creative problem-solving and positive change happen when people step out of their comfort zone and think differently. Our values, workplace practices, wellness programs, benefits and compensation are aimed at helping employees manage their unique personal life and care for their families so they can focus on contributing to the fullest. The Chemical Technologist, working under limited supervision, is responsible for leading production chemical support, corrosion strategies, risk assessment, failure analysis, and integrity management support to the production operations group. The role drives project prioritization and cost monitoring, and maintains regulatory, environmental, and safety compliance. The role directs monthly chemical review with vendors and Devon staff, leads failure review analysis for corrosion induced failures, and presents review results. The role leads cost/benefit analysis of individual chemicals, supports and facilitates field equipment installs and upgrades, conducts data analysis to enable equipment reliability improvement, repairs cathodic protection equipment, ensuring a cost effective approach to asset longevity. The role supports the vendor selection and qualification process, prioritizes, organizes, and completes basic assignments on time with some direction, frequently seeking guidance from experienced peers when faced with routine problems in chemical processes. * Leads production chemical support, corrosion strategies, risk assessment, failure analysis, and integrity management support to the production operations group, ensuring optimal performance and safety of production assets. * Drives project prioritization and cost monitoring, prepares recommendations to optimize chemical treating processes, and leads implementation of SOPs and technical documents. * Maintains regulatory, environmental, and safety compliance in conjunction with and through close coordination with the Operations Foreman, Superintendents, and Environmental Health and Safety Department. * Participates in monthly chemical review with vendors and Devon staff, leads failure review analysis for corrosion induced failures, and presents results of review reports during monthly chemical reviews. * Analyzes technical data to optimize chemical program with the goal to minimize chemical cost and asset failures, evaluates effectiveness of chemical treatment, improves process related to drilling, completions, and production, and analyzes data through SAP. * Leads cost/benefit analysis of individual chemicals along with each area's chemical program, educates lease operators on chemicals, injection rates, and chemical injection/storage equipment used in their area through training sessions. * Supports and facilitates field equipment installs and upgrades, reviews surface equipment failure database, conducts data analysis to enable equipment reliability improvement, and repairs cathodic protection equipment, ensuring a cost effective approach to asset longevity. * Implements modifications to routine tasks related to production chemical support, supports vendor selection and qualification process, and actively participates in proactive safety and continuous improvement activities, demonstrating a visible commitment to EHS. * Prioritizes, organizes, and completes basic assignments on time with some direction, frequently seeking guidance from experienced peers when faced with routine problems in chemical processes. * Possesses the right and obligation to stop work in unsafe conditions, contributing to a safe and secure working environment for all personnel. Education: * High School Diploma/General Education Diploma (GED)/Higher Secondary education and/or commensurate work experience is required. Associate's Degree in Engineering, Business Administration or any other related discipline is preferred. Experience: * 0-3 years of relevant experience with an Associate's Degree in Engineering, Business Administration or any other related discipline, otherwise 9+ years of relevant production operations experience, preferably in E&P Operations specializing in areas Chemical Treatment Processes, Equipment Maintenance, Process Optimization or a related field. Industry experience is preferred. Certifications: * Certified Chemical Technician (CCT) (preferred) Competencies: * Oral & Written Communication * Results Oriented * Active Learning * Digital Literacy * Business Acumen Skills: * Root Cause Analysis (RCA) * Corrosion Mitigation * Process Improvements * Failure Analysis * SAP ERP System * Risk Analysis * Data Analysis & Reporting * Equipment Maintenance Qualified applicants are considered without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, status as a protected veteran or other characteristics protected by law. For more information on Equal Employment Opportunity, please follow these links: EEO is the Law EEO is the Law Supplement Pay Transparency Provision