Quality Control Analyst jobs at Iovance Biotherapeutics

Agilent's Bioreagents business is a recognized leader in cancer diagnostics, delivering trusted answers that empower healthcare providers. We are seeking a driven and detail-oriented Quality Control Analyst with 4+ years of experience to join our team in supporting the full product lifecycle of Immunohistochemistry (IHC) products. Key Responsibilities Create, update, and maintain written procedures for the Quality Control laboratory to ensure compliance, clarity, and operational consistency. Perform analytical testing to support product release across all lifecycle stages: Incoming material inspection and titration In-process and final QC testing Real-time stability studies Manage material disposition and release decisions. Operate and maintain laboratory equipment; document results in compliance with quality standards. Collaborate effectively with QC management and manufacturing teams. Represent QC in cross-functional initiatives including: New Product Introduction (NPI) Efficiency programs Validations and stability studies Contribute to continuous improvement efforts aimed at cost reduction and performance enhancement. Train and mentor junior team members. Troubleshoot and resolve technical issues of varying complexity. Qualifications Bachelor's or master's degree in a relevant field; coursework in biochemistry, IHC, or related disciplines required. 4+ years of relevant experience or equivalent academic training, including hands-on testing and laboratory equipment operation. Hands-on experience with histology, microanatomy, and IHC techniques. Proficiency in Microsoft Office tools (Word, Excel, PowerPoint) and database systems. Familiarity with Change Control and Document Management systems (e.g., Agile). Experience with ERP systems such as SAP. Knowledge of GMP (Good Manufacturing Practices) and GDP (Good Documentation Practices). Strong organizational, problem-solving, and teamwork skills. Excellent written and verbal communication, including technical writing. Ability to manage multiple priorities in a fast-paced environment. Preferred Skills Experience working in GLP/ISO-compliant environments. Understanding of ISO 13485:2016 Quality Management System requirements. Additional Details This job has a full time weekly schedule. Applications for this job will be accepted until at least October 15, 2025 or until the job is no longer posted.The full-time equivalent pay range for this position is $42.43 - $66.30/hr plus eligibility for bonus, stock and benefits. Our pay ranges are determined by role, level, and location. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. During the hiring process, a recruiter can share more about the specific pay range for a preferred location. Pay and benefit information by country are available at: ************************************* Agilent Technologies, Inc. is an Equal Employment Opportunity and merit-based employer that values individuals of all backgrounds at all levels. All individuals, regardless of personal characteristics, are encouraged to apply. All qualified applicants will receive consideration for employment without regard to sex, pregnancy, race, religion or religious creed, color, gender, gender identity, gender expression, national origin, ancestry, physical or mental disability, medical condition, genetic information, marital status, registered domestic partner status, age, sexual orientation, military or veteran status, protected veteran status, or any other basis protected by federal, state, local law, ordinance, or regulation and will not be discriminated against on these bases. Agilent Technologies, Inc., is committed to creating and maintaining an inclusive in the workplace where everyone is welcome, and strives to support candidates with disabilities. If you have a disability and need assistance with any part of the application or interview process or have questions about workplace accessibility, please email job_******************* or contact ***************. For more information about equal employment opportunity protections, please visit *************************************** Required: 10% of the TimeShift: DayDuration: No End DateJob Function: Quality/Regulatory

Agilent's Bioreagents business is an industry leader for cancer diagnostics products that help provide trusted answers to customers. We are seeking an energetic and motivated Quality Control Analyst with at least 1 year of experience to join our team. This role focuses on quality control testing to support the full product lifecycle of Immunohistochemistry (IHC) products. Perform analytical testing to support product release across the entire lifecycle, including: Incoming material inspection and titrations In-process and final QC testing Real-time stability studies Support EQA studies Operate and maintain laboratory equipment and accurately document test results in compliance with quality standards Communicate effectively with the Quality Control management team and manufacturing partners. Participate in continuous improvement initiatives to reduce costs and improve site performance. Troubleshoot and resolve problems of varying scope and complexity. Qualifications Bachelor's or Master's degree in a relevant scientific discipline (or equivalent combination of education and experience). 1+ years of experience in a Quality Control or related laboratory role. Proficiency with office productivity tools (Word, Excel, PowerPoint, databases). Strong teamwork, problem-solving, and organizational skills. Effective verbal and written communication, including technical writing. Ability to manage multiple priorities in a fast-paced environment. Computer skills including the use of Microsoft office suite and understanding of ERP system mechanics. Preferred Skills Experience in GLP/ISO-compliant environments. Familiarity with GMP, GDP, and standard operating procedures. Knowledge of ISO 13485:2016 Quality Management System requirements. Hands-on experience with histology, microanatomy, and Immunohistochemistry techniques. Some experience operating laboratory instrumentation is preferred. Additional Details This job has a full time weekly schedule. Applications for this job will be accepted until at least October 15, 2025 or until the job is no longer posted.The full-time equivalent pay range for this position is $34.16 - $53.37/hr plus eligibility for bonus, stock and benefits. Our pay ranges are determined by role, level, and location. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. During the hiring process, a recruiter can share more about the specific pay range for a preferred location. Pay and benefit information by country are available at: ************************************* Agilent Technologies, Inc. is an Equal Employment Opportunity and merit-based employer that values individuals of all backgrounds at all levels. All individuals, regardless of personal characteristics, are encouraged to apply. All qualified applicants will receive consideration for employment without regard to sex, pregnancy, race, religion or religious creed, color, gender, gender identity, gender expression, national origin, ancestry, physical or mental disability, medical condition, genetic information, marital status, registered domestic partner status, age, sexual orientation, military or veteran status, protected veteran status, or any other basis protected by federal, state, local law, ordinance, or regulation and will not be discriminated against on these bases. Agilent Technologies, Inc., is committed to creating and maintaining an inclusive in the workplace where everyone is welcome, and strives to support candidates with disabilities. If you have a disability and need assistance with any part of the application or interview process or have questions about workplace accessibility, please email job_******************* or contact ***************. For more information about equal employment opportunity protections, please visit *************************************** Required: 10% of the TimeShift: DayDuration: No End DateJob Function: Quality/Regulatory

Quality Control Analyst III in Camarillo, CA Build your future at Curia, where our work has the power to save lives. The Quality Control Analyst III is responsible for supporting the manufacturing department and external customers. Routine functions include testing of raw materials, in-process, end product, and stability samples. Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life-saving treatments to patients. At Curia, we are on a mission to advance our customers' therapies from curiosity to cure and ultimately to improve patients' lives. We proudly offer * Generous benefit options (eligible first day of employment) * Paid training, vacation and holidays (vacation accrual begins on first day of employment) * Career advancement opportunities * Education reimbursement * 401K program with matching contributions * Learning platform * And more! Responsibilities * Perform complex testing and data evaluation, such as HPLC, ELISA, etc. * Troubleshoot equipment issues promptly and communicate resolutions to management * Participate in or assist with test method validations * Evaluate data for trends * Support and/or investigate OOS events by performing thorough root cause analyses, assessing potential product impact, and implementing appropriate CAPAs * Interact with outside departments including attending meetings, providing updates, etc. * Coordinate testing performed at outside testing labs, raw materials, etc. * Maintain a detailed and accurate recording of activities and results * Execute, author, and review SOPs, reports, protocols, investigations, change controls, and data summaries * Perform risk assessment as needed * Write/revise test methods, standard operating procedures, etc. * Provide training to others as needed. Attend internal and external training on related subjects, including both intra- and inter-departmental cross-training on new techniques and procedures * Support equipment upkeep * Prepare and order supplies, as necessary * Enter data into relevant data management systems and perform tracking and trending of data. Compile data and provide/present data summaries to management * Utilize a thorough understanding of regulatory and compliance guidelines for the pharmaceutical industry * Collaborate with cross-functional departments to coordinate testing, scheduling needs, and prioritization * Lead departmental projects and participate in cross-functional teams, including continuous improvement initiatives and new customer project teams * Lead the stability program, including management of test points, reporting of data, and investigations of out of specification or aberrant stability results Required * Bachelor's Degree in Chemistry or related field and 5+ years related work experience; OR * Master's Degree in Chemistry or related field and 3+ years related work experience; OR * PhD in Chemistry or related field and 1+ years related work experience * Experience working in cGMP or GLP pharmaceutical industry environment * Willing to work flexible hours (nights and weekends), as-needed (overtime eligible) Knowledge, skills and abilities * Excellent verbal and written communication skills, including the ability to effectively present information and respond to questions from groups of managers, clients, customers, and the general public * Ability to meet deadlines and work under pressure with limited supervision * Strong time management and organizational skills with the ability to multi-task and manage multiple projects independently * Ability to read, analyze, and interpret general business periodicals, professional journals, technical procedures, or governmental regulations * Ability to write reports, business correspondence, and procedures * Ability to apply advanced mathematical concepts such as exponents, logarithms, quadratic equations, and permutations * Ability to apply mathematical operations to such tasks as frequency distribution, determination of test reliability and validity, analysis of variance, correlation techniques, sampling theory, and factor analysis * Ability to define problems, collect data, establish facts, and draw valid conclusions * Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and handle several abstract and concrete variables * Proficient use of computer software, including Microsoft Office Suite and instrument manufacture-based systems * Knowledgeable in FDA GMPs (21 CFR, 211, 820, and/or 600); ISO 9001 and 13485 a plus Other Qualifications * Must pass a background check * Must pass a drug screen * May be required to pass Occupational Health Screening Pay Range: $85,000-$106,500/year Education, experience, location and tenure may be considered along with internal equity when job offers are extended. We do not accept unsolicited assistance from any headhunters or recruitment firms for any of our job openings. All resumes or profiles submitted by search firms to any employee at Curia, in any form without a valid, signed search agreement by an authorized signatory in place for the specific position, approved by Talent Acquisition, will be deemed the sole property of Curia. No fee will be paid in the event the candidate is hired by Curia because of the unsolicited referral. All interested applicants must apply online. Please be aware of scammers. Curia will only send offer letters and requests for sensitive personal information from a curiaglobal.com email address. Curia 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. Curia is an E-Verify employer. #LI-AC1

Quality Control Analyst II in Camarillo, CA Build your future at Curia, where our work has the power to save lives. The Quality Control Analyst II is responsible for supporting the manufacturing department and external customers. Routine functions include testing of raw materials, in-process, end product, and stability samples. Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life-saving treatments to patients. At Curia, we are on a mission to advance our customers' therapies from curiosity to cure and ultimately to improve patients' lives. We proudly offer * Generous benefit options (eligible first day of employment) * Paid training, vacation and holidays (vacation accrual begins on first day of employment) * Career advancement opportunities * Education reimbursement * 401K program with matching contributions * Learning platform * And more! Responsibilities * Perform complex testing and data evaluation, such as HPLC, ELISA, etc. * Troubleshoot equipment issues promptly and communicate resolutions to management * Participate in or assist with test method validations * Evaluate data for trends * Support and/or investigate OOS events by performing thorough root cause analyses, assessing potential product impact, and implementing appropriate CAPAs * Interact with outside departments including attending meetings, providing updates, etc. * Coordinate testing performed at outside testing labs, raw materials, etc. * Maintain a detailed and accurate recording of activities and results * Execute, author, and review SOPs, reports, protocols, investigations, change controls, and data summaries * Perform risk assessment as needed * Write/revise test methods, standard operating procedures, etc. * Provide training to others as needed. Attend internal and external training on related subjects, including both intra- and inter-departmental cross-training on new techniques and procedures * Support equipment upkeep * Prepare and order supplies, as necessary * Enter data into relevant data management systems and perform tracking and trending of data. Compile data and provide/present data summaries to management * Utilize a thorough understanding of regulatory and compliance guidelines for the pharmaceutical industry * Collaborate with cross-functional departments to coordinate testing, scheduling needs, and prioritization * Lead departmental projects and participate in cross-functional teams, including continuous improvement initiatives and new customer project teams * Lead the stability program, including management of test points, reporting of data, and investigations of out of specification or aberrant stability results Required * Bachelor's Degree in Chemistry or related field and 3+ years related work experience; OR * Master's Degree in Chemistry or related field and 1+ years related work experience; OR * Experience working in cGMP or GLP pharmaceutical industry environment * Willing to work flexible hours (nights and weekends), as-needed (overtime eligible) Knowledge, skills and abilities * Excellent verbal and written communication skills, including the ability to effectively present information and respond to questions from groups of managers, clients, customers, and the general public * Ability to meet deadlines and work under pressure with limited supervision * Strong time management and organizational skills with the ability to multi-task and manage multiple projects independently * Ability to read, analyze, and interpret general business periodicals, professional journals, technical procedures, or governmental regulations * Ability to write reports, business correspondence, and procedures * Ability to apply advanced mathematical concepts such as exponents, logarithms, quadratic equations, and permutations * Ability to apply mathematical operations to such tasks as frequency distribution, determination of test reliability and validity, analysis of variance, correlation techniques, sampling theory, and factor analysis * Ability to define problems, collect data, establish facts, and draw valid conclusions * Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and handle several abstract and concrete variables * Proficient use of computer software, including Microsoft Office Suite and instrument manufacture-based systems * Knowledgeable in FDA GMPs (21 CFR, 211, 820, and/or 600); ISO 9001 and 13485 a plus Other Qualifications * Must pass a background check * Must pass a drug screen * May be required to pass Occupational Health Screening Pay Range: $72,000-$89,800/year Education, experience, location and tenure may be considered along with internal equity when job offers are extended. We do not accept unsolicited assistance from any headhunters or recruitment firms for any of our job openings. All resumes or profiles submitted by search firms to any employee at Curia, in any form without a valid, signed search agreement by an authorized signatory in place for the specific position, approved by Talent Acquisition, will be deemed the sole property of Curia. No fee will be paid in the event the candidate is hired by Curia because of the unsolicited referral. All interested applicants must apply online. Please be aware of scammers. Curia will only send offer letters and requests for sensitive personal information from a curiaglobal.com email address. Curia 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. Curia is an E-Verify employer. #LI-AC1

Description Looking to join a passionate team dedicated to developing and manufacturing life-saving biopharmaceuticals? Avid Bioservices is a leading clinical and commercial biologics CDMO focused on creating innovative solutions to meet the needs of our clients and improve patient outcomes. Your Role: The Analyst, Quality Control will perform testing and sampling to support manufacturing, validation, process development and stability studies in a GMP environment. Perform and review routine assays for HPLC, ELISA/cell-based immunoassays, and/or electrophoresis (SDS-PAGE/IEF) with strict adherence to written analytical test procedures. Perform aseptic sampling, visual inspection, pH, conductivity, osmolality, and spectrophotometry. Review, revise and write test methods, standard operating procedures. In addition to performing QC testing, the Analyst may support validation projects, investigations, and method development projects. Other functions include but are not limited to writing study protocols and reports; training other analysts; working with other departments in developing, revising, and implementing QC procedures and policies. Knowledgeable of company cGMPs as well as industry regulations that apply to all job functions. Participate in regulatory inspections. Support continuous improvement initiatives. Other duties as assigned. Minimum Qualifications: Bachelor's degree in biology, biochemistry, chemistry or equivalent scientific field. A minimum of 2 years of relevant, hands-on experience working in a QC or analytical lab or equivalent combination of education/experience. Experience with analytical testing and equipment, writing reports/procedures/specifications, GMPs and regulatory audits are essential. Must be proficient with ELISA, Analytical Biochemistry or chemistry. Position Type/Expected Hours of Work: This role is a full-time position. Days and hours of work are Monday through Friday, 8:00a.m. to 5:00p.m. unless otherwise stated by Management. The employee must also, if instructed, have the ability to work overtime and/or weekends when necessary.Compensation: We offer competitive compensation packages for this role, including a base salary, performance-based bonuses, and comprehensive benefits such as health, dental, and vision insurance, 401(k) matching, and paid time off. The compensation range for this role is $26.73-$28.00 hourly depending on experience and qualifications. Additionally, we offer opportunities for career growth and development as well as a supportive and inclusive work environment. Who you are: You have a "bring it on!" team player approach and an unshakable positive attitude, always ready to tackle anything that comes your way. Your written and verbal skills are out of this world, and you communicate with clarity and confidence. You have exceptional multitasking skills and an unparalleled attention to detail that ensure the smooth running of everything. You are a master at building relationships, capable of establishing connections with anyone, be it team members, clients, vendors, or suppliers. Physical Demands & Work Environment: In this dynamic role, expect a blend of regular activities like sitting, standing, and walking, with occasional physically engaging tasks such as lifting objects up to 20 pounds. The work environment might expose you to electrical shocks, toxic chemicals, vibrations, or loud noise levels occasionally. However, reasonable accommodations are available to enable individuals with different abilities to perform effectively, ensuring a supportive and adaptable work setting. Your visual acuity, including close, distance, and color vision, will be essential in navigating through the diverse day-to-day demands of this position.

Looking to join a passionate team dedicated to developing and manufacturing life-saving biopharmaceuticals? Avid Bioservices is a leading clinical and commercial biologics CDMO focused on creating innovative solutions to meet the needs of our clients and improve patient outcomes. Your Role: The Analyst, Quality Control will perform testing and sampling to support manufacturing, validation, process development and stability studies in a GMP environment. * Perform and review routine assays for HPLC, ELISA/cell-based immunoassays, and/or electrophoresis (SDS-PAGE/IEF) with strict adherence to written analytical test procedures. * Perform aseptic sampling, visual inspection, pH, conductivity, osmolality, and spectrophotometry. * Review, revise and write test methods, standard operating procedures. In addition to performing QC testing, the Analyst may support validation projects, investigations, and method development projects. * Other functions include but are not limited to writing study protocols and reports; training other analysts; working with other departments in developing, revising, and implementing QC procedures and policies. * Knowledgeable of company cGMPs as well as industry regulations that apply to all job functions. * Participate in regulatory inspections. * Support continuous improvement initiatives. * Other duties as assigned. Minimum Qualifications: * Bachelor's degree in biology, biochemistry, chemistry or equivalent scientific field. * A minimum of 2 years of relevant, hands-on experience working in a QC or analytical lab or equivalent combination of education/experience. * Experience with analytical testing and equipment, writing reports/procedures/specifications, GMPs and regulatory audits are essential. * Must be proficient with ELISA, Analytical Biochemistry or chemistry. Position Type/Expected Hours of Work: This role is a full-time position. Days and hours of work are Monday through Friday, 8:00a.m. to 5:00p.m. unless otherwise stated by Management. The employee must also, if instructed, have the ability to work overtime and/or weekends when necessary. Compensation: We offer competitive compensation packages for this role, including a base salary, performance-based bonuses, and comprehensive benefits such as health, dental, and vision insurance, 401(k) matching, and paid time off. The compensation range for this role is $26.73-$28.00 hourly depending on experience and qualifications. Additionally, we offer opportunities for career growth and development as well as a supportive and inclusive work environment. Who you are: * You have a "bring it on!" team player approach and an unshakable positive attitude, always ready to tackle anything that comes your way. * Your written and verbal skills are out of this world, and you communicate with clarity and confidence. * You have exceptional multitasking skills and an unparalleled attention to detail that ensure the smooth running of everything. * You are a master at building relationships, capable of establishing connections with anyone, be it team members, clients, vendors, or suppliers. Physical Demands & Work Environment: In this dynamic role, expect a blend of regular activities like sitting, standing, and walking, with occasional physically engaging tasks such as lifting objects up to 20 pounds. The work environment might expose you to electrical shocks, toxic chemicals, vibrations, or loud noise levels occasionally. However, reasonable accommodations are available to enable individuals with different abilities to perform effectively, ensuring a supportive and adaptable work setting. Your visual acuity, including close, distance, and color vision, will be essential in navigating through the diverse day-to-day demands of this position.

Description Looking to join a passionate team dedicated to developing and manufacturing life-saving biopharmaceuticals? Avid Bioservices is a leading clinical and commercial biologics CDMO focused on creating innovative solutions to meet the needs of our clients and improve patient outcomes. Your Role: The Quality Control In-Process Analyst will perform testing and sampling to support manufacturing, validation, process development and stability studies in a GMP environment for the Quality Control In-Process team. Perform basic compendial test methods without supervision and with strict adherence to written protocols, analyze data and report results. Formulate buffers and reagents for the purpose of performing test methods. Write and revise test methods and procedures. Perform aseptic sampling, endotoxin, pH, conductivity, osmolality, A280 and endotoxin by LAL. Perform water testing and raw material sampling and testing. Perform QC testing for lot release, stability, development/validation projects, and investigations. Other functions include writing study protocols and reports. Work with other departments in developing, revising and implementing QC procedures and policies. Should be aware of company cGMPs as well as industry regulations that apply to all job functions. Perform sample pick up and sample locating without supervision and with strict adherence to written protocols. Other duties as assigned. Minimum Qualifications: BS degree in Biochemistry, Chemistry, Biology or a related field. 2 years of biotech industry experience working in a QC or analytical lab. Must have experience with analytical testing, writing reports, GMPs, and regulatory audits. Experience with most, if not all the methodologies listed above. Experience with basic maintenance and troubleshooting of analytical instrumentation is highly desirable. Position Type/Expected Hours of Work: This is a full-time position operating Sunday through Wednesday on a 4x10(4 days x 10 hours) schedule. Will have an adaptable schedule to accommodate operational and scheduling demands. Availability needed for overtime and weekend shifts as necessary. Compensation: We offer competitive compensation packages for this role, including a base salary, performance-based bonuses, and comprehensive benefits such as health, dental, and vision insurance, 401(k) matching, and paid time off. The compensation range for this role is $26.73 to $35.63 hourly, depending on experience and qualifications. Additionally, we offer opportunities for career growth and development as well as a supportive and inclusive work environment. Who you are: You have a "bring it on!" team player approach and an unshakable positive attitude, always ready to tackle anything that comes your way. Your written and verbal skills are out of this world, and you communicate with clarity and confidence. You have exceptional multitasking skills and an unparalleled attention to detail that ensure the smooth running of everything. You are a master at building relationships, capable of establishing connections with anyone, be it team members, clients, vendors, or suppliers. Physical Demands & Work Environment: In this dynamic role, expect a blend of regular activities like sitting, standing, and walking, with occasional physically engaging tasks such as lifting objects up to 20 pounds. The work environment might expose you to electrical shocks, toxic chemicals, vibrations, or loud noise levels occasionally. However, reasonable accommodations are available to enable individuals with different abilities to perform effectively, ensuring a supportive and adaptable work setting. Your visual acuity, including close, distance, and color vision, will be essential in navigating through the diverse day-to-day demands of this position.

Description Looking to join a passionate team dedicated to developing and manufacturing life-saving biopharmaceuticals? Avid Bioservices is a leading clinical and commercial biologics CDMO focused on creating innovative solutions to meet the needs of our clients and improve patient outcomes. Your Role: The Quality Control In-Process Analyst will perform testing and sampling to support manufacturing, validation, process development and stability studies in a GMP environment for the Quality Control In-Process team. Perform basic compendial test methods without supervision and with strict adherence to written protocols, analyze data and report results. Formulate buffers and reagents for the purpose of performing test methods. Write and revise test methods and procedures. Perform aseptic sampling, endotoxin, pH, conductivity, osmolality, A280 and endotoxin by LAL. Perform water testing and raw material sampling and testing. Perform QC testing for lot release, stability, development/validation projects, and investigations. Other functions include writing study protocols and reports. Work with other departments in developing, revising and implementing QC procedures and policies. Should be aware of company cGMPs as well as industry regulations that apply to all job functions. Perform sample pick up and sample locating without supervision and with strict adherence to written protocols. Other duties as assigned. Minimum Qualifications: BS degree in Biochemistry, Chemistry, Biology or a related field. 2 years of biotech industry experience working in a QC or analytical lab. Must have experience with analytical testing, writing reports, GMPs, and regulatory audits. Experience with most, if not all the methodologies listed above. Experience with basic maintenance and troubleshooting of analytical instrumentation is highly desirable. Position Type/Expected Hours of Work: This is a full-time position operating Wednesday to Saturday on a 4x10(4 days x 10 hours) schedule. Will have an adaptable schedule to accommodate operational and scheduling demands. Availability needed for overtime and weekend shifts as necessary. Compensation: We offer competitive compensation packages for this role, including a base salary, performance-based bonuses, and comprehensive benefits such as health, dental, and vision insurance, 401(k) matching, and paid time off. The compensation range for this role is $26.73 to $35.63 hourly, depending on experience and qualifications. Additionally, we offer opportunities for career growth and development as well as a supportive and inclusive work environment. Who you are: You have a "bring it on!" team player approach and an unshakable positive attitude, always ready to tackle anything that comes your way. Your written and verbal skills are out of this world, and you communicate with clarity and confidence. You have exceptional multitasking skills and an unparalleled attention to detail that ensure the smooth running of everything. You are a master at building relationships, capable of establishing connections with anyone, be it team members, clients, vendors, or suppliers. Physical Demands & Work Environment: In this dynamic role, expect a blend of regular activities like sitting, standing, and walking, with occasional physically engaging tasks such as lifting objects up to 20 pounds. The work environment might expose you to electrical shocks, toxic chemicals, vibrations, or loud noise levels occasionally. However, reasonable accommodations are available to enable individuals with different abilities to perform effectively, ensuring a supportive and adaptable work setting. Your visual acuity, including close, distance, and color vision, will be essential in navigating through the diverse day-to-day demands of this position.

Description Looking to join a passionate team dedicated to developing and manufacturing life-saving biopharmaceuticals? Avid Bioservices is a leading clinical and commercial biologics CDMO focused on creating innovative solutions to meet the needs of our clients and improve patient outcomes. Your Role: The Analyst (HPLC), Quality Control will perform testing and sampling to support manufacturing, validation, process development and stability studies in a GMP environment. This position requires a strong background in HPLC and supports/leads continuous improvement initiatives.Key Responsibilities: Perform and review routine assays for HPLC and CE (Capillary Electrophoresis) with strict adherence to written analytical test procedures. Perform aseptic sampling, visual inspection, gowning and working in clean room areas, 5S methodology. Review, revise and write test methods, standard operating procedures and perform trending analysis. In addition to performing QC testing, the Analyst may be designated as study lead for validation projects, investigations and method development projects. Other functions include, but are not limited to, writing study protocols and reports; training other analysts; working with other departments in developing, revising and implementing QC procedures and policies. Knowledgeable of company cGMPs as well as industry regulations that apply to all job functions. Participate in regulatory inspections to ensure laboratory is in compliance with current Good Manufacturing Practices. Demonstrate and provide evidence to FDA officials that the laboratory operations conform to code of federal regulation. Support continuous improvement initiatives by ensuring training relating to test methods, standard operating procedures, are up to date to comply with current good manufacturing practices. Utilize Instruments software to perform calculations to minimize errors and eliminate time allocation for manual calculations. Perform other duties as assigned. Minimum Qualifications: BS in chemistry or biology or related field plus 2-4 years industry experience in a QC or analytical lab, or equivalent combination of education/experience. Experience with analytical testing and equipment, writing reports/procedures/specifications, GMPs and regulatory audits are essential. Must have strong HPLC, Analytical Biochemistry and Chemistry experience. Must also have experience with most if not all of the following: protein characterization, electrophoresis, chromatography (normal phase, reverse phase, size exclusion, ion exchange, etc), aseptic techniques, assay and validation/qualification. Position Type/Expected Hours of Work:This role is a full-time position. Days and hours of work are Monday through Friday, 8:00 a.m. to 5 p.m. unless otherwise stated by Supervisor. The employee must also, if instructed, have the ability to work overtime and/or weekends when necessary. Compensation: We offer competitive compensation packages for this role, including a base salary, performance-based bonuses, and comprehensive benefits such as health, dental, and vision insurance, 401(k) matching, and paid time off. The compensation range for this role is $26.73 to $34.00 hourly depending on experience and qualifications. Additionally, we offer opportunities for career growth and development as well as a supportive and inclusive work environment. Who you are: You have a "bring it on!" team player approach and an unshakable positive attitude, always ready to tackle anything that comes your way. Your written and verbal skills are out of this world, and you communicate with clarity and confidence. You have exceptional multitasking skills and an unparalleled attention to detail that ensure the smooth running of everything. You are a master at building relationships, capable of establishing connections with anyone, be it team members, clients, vendors, or suppliers. Physical Demands & Work Environment: In this dynamic role, expect a blend of regular activities like sitting, standing, and walking, with occasional physically engaging tasks such as lifting objects up to 20 pounds. The work environment might expose you to electrical shocks, toxic chemicals, vibrations, or loud noise levels occasionally. However, reasonable accommodations are available to enable individuals with different abilities to perform effectively, ensuring a supportive and adaptable work setting. Your visual acuity, including close, distance, and color vision, will be essential in navigating through the diverse day-to-day demands of this position.

Looking to join a passionate team dedicated to developing and manufacturing life-saving biopharmaceuticals? Avid Bioservices is a leading clinical and commercial biologics CDMO focused on creating innovative solutions to meet the needs of our clients and improve patient outcomes. Your Role: The Analyst (HPLC), Quality Control will perform testing and sampling to support manufacturing, validation, process development and stability studies in a GMP environment. This position requires a strong background in HPLC and supports/leads continuous improvement initiatives. Key Responsibilities: * Perform and review routine assays for HPLC and CE (Capillary Electrophoresis) with strict adherence to written analytical test procedures. * Perform aseptic sampling, visual inspection, gowning and working in clean room areas, 5S methodology. * Review, revise and write test methods, standard operating procedures and perform trending analysis. * In addition to performing QC testing, the Analyst may be designated as study lead for validation projects, investigations and method development projects. * Other functions include, but are not limited to, writing study protocols and reports; training other analysts; working with other departments in developing, revising and implementing QC procedures and policies. * Knowledgeable of company cGMPs as well as industry regulations that apply to all job functions. * Participate in regulatory inspections to ensure laboratory is in compliance with current Good Manufacturing Practices. * Demonstrate and provide evidence to FDA officials that the laboratory operations conform to code of federal regulation. * Support continuous improvement initiatives by ensuring training relating to test methods, standard operating procedures, are up to date to comply with current good manufacturing practices. * Utilize Instruments software to perform calculations to minimize errors and eliminate time allocation for manual calculations. * Perform other duties as assigned. Minimum Qualifications: * BS in chemistry or biology or related field plus 2-4 years industry experience in a QC or analytical lab, or equivalent combination of education/experience. * Experience with analytical testing and equipment, writing reports/procedures/specifications, GMPs and regulatory audits are essential. * Must have strong HPLC, Analytical Biochemistry and Chemistry experience. * Must also have experience with most if not all of the following: protein characterization, electrophoresis, chromatography (normal phase, reverse phase, size exclusion, ion exchange, etc), aseptic techniques, assay and validation/qualification. Position Type/Expected Hours of Work: This role is a full-time position. Days and hours of work are Monday through Friday, 8:00 a.m. to 5 p.m. unless otherwise stated by Supervisor. The employee must also, if instructed, have the ability to work overtime and/or weekends when necessary. Compensation: We offer competitive compensation packages for this role, including a base salary, performance-based bonuses, and comprehensive benefits such as health, dental, and vision insurance, 401(k) matching, and paid time off. The compensation range for this role is $26.73 to $34.00 hourly depending on experience and qualifications. Additionally, we offer opportunities for career growth and development as well as a supportive and inclusive work environment. Who you are: * You have a "bring it on!" team player approach and an unshakable positive attitude, always ready to tackle anything that comes your way. * Your written and verbal skills are out of this world, and you communicate with clarity and confidence. * You have exceptional multitasking skills and an unparalleled attention to detail that ensure the smooth running of everything. * You are a master at building relationships, capable of establishing connections with anyone, be it team members, clients, vendors, or suppliers. Physical Demands & Work Environment: In this dynamic role, expect a blend of regular activities like sitting, standing, and walking, with occasional physically engaging tasks such as lifting objects up to 20 pounds. The work environment might expose you to electrical shocks, toxic chemicals, vibrations, or loud noise levels occasionally. However, reasonable accommodations are available to enable individuals with different abilities to perform effectively, ensuring a supportive and adaptable work setting. Your visual acuity, including close, distance, and color vision, will be essential in navigating through the diverse day-to-day demands of this position.

**Penn State Health** - **Hershey Medical Center** **Work Type:** Full Time **FTE:** 1.00 **Shift:** Day **Hours:** 8:00a - 4:30p **Recruiter Contact:** Denisse M. Rosado at ******************************** (MAILTO://********************************) **SUMMARY OF POSITION:** Responsible for the coordination, assessment, process improvement, and support for all quality assurance and performance improvement activities. Duties to include, but not limited to: data management, performance improvement, patient safety, and regulatory compliance. Responsible for assisting management with integrating program quality efforts across program components. **MINIMUM QUALIFICATION(S):** + Bachelor's degree **WHY PENN STATE HEALTH?** Penn State Health offers exceptional opportunities to learn and grow, exposure to a wide patient population, and the ability to provide individualized, innovative, and specialized care to patients in the community. **Penn State Health offers an exceptional benefits package including medical, dental and vision with no waiting period as well as a Total Rewards Program that highlights a few of the many additional offerings below:** + **_Be Well_** with Employee Wellness Programs, and Fitness Discounts (University Fitness Center, Peloton). + **_Be Balanced_** with Generous Paid Time Off, Personal Time, and Paid Parental Leave. + **_Be Secured_** with Retirement, Extended Illness Bank, Life Insurance, and Identity Theft Protection. + **_Be Rewarded_** with Competitive Pay, Tuition Reimbursement, and PAWS UP employee recognition program. + **_Be Supported_** by the HR Solution Center, Learning and Organizational Development and Virtual Benefits Orientation, Employee Exclusive Concierge Service for scheduling. **WHY PENN STATE HEALTH MILTON HERSHEY MEDICAL CENTER?** Penn State Hershey Medical Center is Central Pennsylvania's only Academic Medical Center, Level 1 Regional Adult and Pediatric Trauma Center, and Tertiary Care Provider. As a four-time Magnet-designated hospital, Hershey Medical Center values the hard work and dedication that our employees exhibit every day. Through our core values of Respect, Integrity, Teamwork, and Excellence, our employees are a team committed to compassionate care for our diverse patient population, our community and each other. As a valued team member, we promote continued professional development, specialty certification, continuing education, and career growth. **YOU TAKE CARE OF THEM. WE'LL TAKE CARE OF YOU. State-of-the-art equipment, endless learning, and a culture of excellence - that's Penn State Health. But what makes our healthcare award-winning? That's all you.** _This job posting is a general outline of duties performed and is not to be misconstrued as encompassing all duties performed within the position. Eligibility for shift differential pay based on the terms outlined in company policy or union contract._ _All individuals (including current employees) selected for a position will undergo a background check appropriate for the position's responsibilities._ _Penn State Health is an Equal Opportunity Employer and does not discriminate on the basis of any protected class including disability or veteran status. Penn State Health's policies and objectives are in direct compliance with all federal and state constitutional provisions, laws, regulations, guidelines, and executive orders that prohibit or outlaw discrimination._ **Union:** Non Bargained **Position** Quality Associate - Liver Transplant **Location** US:PA: Hershey | Quality | Full Time **Req ID** 85562

Job Description Chemistry Lab Analyst Why Ascend? Come work for a company that is transforming the industry! We are Ascend Clinical, LLC., one of the highest volume clinical laboratories in the United States. With the use of the most advanced tools and technology, we process millions of tests each month. For over 30 years, we have been delivering industry-leading service and excellence in testing. At Ascend, we are relentless about innovation and growing to pioneer the future of clinical and environmental laboratory testing. Ascend is unlike most companies, offering the discipline of a healthcare leader and the mentality of a tech startup. As a company that is on the leading edge, we are seeking individuals with a similar mindset who enjoy a dynamic, fast-paced environment. Job Summary The Chemistry Lab Analyst will perform moderate to high complexity testing on non-clinical specimens. Will operate and maintain highly complex instrumentations such as Inductively Coupled Plasma Mass Spectrometry (ICP-MS) and Ion Chromatography (IC), as well as demonstrate proficiency on routine environmental testing, instrument maintenance and troubleshooting in accordance with protocols established by Ascend Clinical. Perform a variety of standardized microbiological tests such as heterotrophic place counts and endotoxin detection assay. Processes specimens, performs test preparation, specimen verification and tracking, all related clerical functions and general clean-up tasks for routine as well as high complex tests. Reports, analyzes, and verifies environmental results, which are substantiated by the proper use of quality control systems. Must recognize problems, identify causes and determine alternative methods and solutions. Actively contributes to quality assurance activities and participates in proficiency testing. Responsibilities: Knows and complies with all Ascend Clinical policies and procedures: General Policies, Chemical Hazard, Illness and Injury Prevention Program, Quality Assurance Program and ELAP. Understands the hazards associated with failing to follow those procedures Performs high complexity testing of water analysis according to EPA, AAMI, and/or ELAP guidelines Proficient in setting up multiple laboratory instrumentations used for non-clinical specimens Instrument daily, weekly, and monthly maintenance Troubleshooting instruments Instrument validation Attends and completes advance training for department instrumentations Capable of assisting in sample processing and preparation in high complex test environments Actively participates in facility's Quality Assurance program Assists in orientation and training of new staff members, as directed by management Assumes responsibility for special projects, as directed by management Oversees completion of maintenance records and workstation/instrument supplies. Ensures that regular preventive maintenance by the manufacturer has been completed Qualifications: College degree, science related preferred or equivalent number of years of relevant job experience 2-4 years of experience Proficient in chemistry, math, medical terminology, knowledge of specimen preparation techniques, and principles of operation of common laboratory instruments Knowledge of analytical techniques and high complexity instrumentation such as ICP-MS and IC Ability to follow complicated instructions with accuracy and perform detailed tasks thoroughly and completely Compensation: $25-35/hr Compensation may vary for different individuals in the same role based on several factors, including but not limited to individual competencies, education/professional certifications, experience and performance in the role Benefits: As an Ascend Clinical employee, you will become part of a company that has received national recognition as a great place to work. We offer excellent full-time benefits including comprehensive medical coverage, life and disability insurance, 401(k) with company match, paid holidays and vacation, personal days, and dental and vision options. Ascend is an Equal Opportunity Employer - M/F/Disabled/Veteran Ascend Clinical, LLC is committed to promoting an equal employment opportunity workplace environment and is an equal opportunity employer. It is the policy of the company that all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, national origin, citizenship, pregnancy, genetic information (GINA), disability, military and/or veteran status, and/or any other status protected by applicable Federal, state, or local law. The company's policy is to recruit, hire, train, promote and administer all employment-related matters on the basis of an individual's qualifications, abilities and efforts without regard to protected status. Powered by JazzHR s3qDvPUViJ

Why Ascend? Come work for a company that is transforming the industry! We are Ascend Clinical, LLC., one of the highest volume clinical laboratories in the United States. With the use of the most advanced tools and technology, we process millions of tests each month. For over 30 years, we have been delivering industry-leading service and excellence in testing. At Ascend, we are relentless about innovation and growing to pioneer the future of clinical and environmental laboratory testing. Ascend is unlike most companies, offering the discipline of a healthcare leader and the mentality of a tech startup. As a company that is on the leading edge, we are seeking individuals with a similar mindset who enjoy a dynamic, fast-paced environment. Job Summary The Chemistry Lab Analyst will perform moderate to high complexity testing on non-clinical specimens. Will operate and maintain highly complex instrumentations such as Inductively Coupled Plasma Mass Spectrometry (ICP-MS) and Ion Chromatography (IC), as well as demonstrate proficiency on routine environmental testing, instrument maintenance and troubleshooting in accordance with protocols established by Ascend Clinical. Perform a variety of standardized microbiological tests such as heterotrophic place counts and endotoxin detection assay. Processes specimens, performs test preparation, specimen verification and tracking, all related clerical functions and general clean-up tasks for routine as well as high complex tests. Reports, analyzes, and verifies environmental results, which are substantiated by the proper use of quality control systems. Must recognize problems, identify causes and determine alternative methods and solutions. Actively contributes to quality assurance activities and participates in proficiency testing. Responsibilities: Knows and complies with all Ascend Clinical policies and procedures: General Policies, Chemical Hazard, Illness and Injury Prevention Program, Quality Assurance Program and ELAP. Understands the hazards associated with failing to follow those procedures Performs high complexity testing of water analysis according to EPA, AAMI, and/or ELAP guidelines Proficient in setting up multiple laboratory instrumentations used for non-clinical specimens Instrument daily, weekly, and monthly maintenance Troubleshooting instruments Instrument validation Attends and completes advance training for department instrumentations Capable of assisting in sample processing and preparation in high complex test environments Actively participates in facility's Quality Assurance program Assists in orientation and training of new staff members, as directed by management Assumes responsibility for special projects, as directed by management Oversees completion of maintenance records and workstation/instrument supplies. Ensures that regular preventive maintenance by the manufacturer has been completed Qualifications: College degree, science related preferred or equivalent number of years of relevant job experience 2-4 years of experience Proficient in chemistry, math, medical terminology, knowledge of specimen preparation techniques, and principles of operation of common laboratory instruments Knowledge of analytical techniques and high complexity instrumentation such as ICP-MS and IC Ability to follow complicated instructions with accuracy and perform detailed tasks thoroughly and completely Compensation: $25-35/hr Compensation may vary for different individuals in the same role based on several factors, including but not limited to individual competencies, education/professional certifications, experience and performance in the role Benefits: As an Ascend Clinical employee, you will become part of a company that has received national recognition as a great place to work. We offer excellent full-time benefits including comprehensive medical coverage, life and disability insurance, 401(k) with company match, paid holidays and vacation, personal days, and dental and vision options. Ascend is an Equal Opportunity Employer - M/F/Disabled/Veteran Ascend Clinical, LLC is committed to promoting an equal employment opportunity workplace environment and is an equal opportunity employer. It is the policy of the company that all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, national origin, citizenship, pregnancy, genetic information (GINA), disability, military and/or veteran status, and/or any other status protected by applicable Federal, state, or local law. The company's policy is to recruit, hire, train, promote and administer all employment-related matters on the basis of an individual's qualifications, abilities and efforts without regard to protected status.

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

MAIN JOB RESPONSIBILITIES / COMPETENCIES 1. Thorough knowledge and appropriate implementation of critical production functions such as Manufacture of Collamer Material 2. Assist in the Manufacture of In-Process materials (HEMA, Collagen Solution) as necessary 3. Maintain all equipment (including glassware) used for Collamer Material production 4. Completes required production documentation accurately. 5. Consistently meets quality and productivity targets. 6. Appropriately follows company policies, rules, and regulations. 7. Maintain work area environment in a clean and orderly manner. 8. Other duties as assigned. REQUIREMENTS EDUCATION & TRAINING * Minimum 4 yr Degree; or work experience EXPERIENCE * 2 years experience as a Formulation Technician I or Equivalent experience. * Experience with cleanroom environments preferred SKILLS * Ability to understand and implement general GMP concepts. * Ability to work in a clean/controlled environments. * Capable of learning and performing duties with minimum supervision. * Possess good communication, organizational and math skills. * Ability to read, write and speak English. * Ability to lift up to 25 pounds. * Ability to take direction from lead/supervisor and other management. * Ability to work with chemicals and utilize proper safety equipment. * Ability to follow detailed work instructions precisely and participate in process improvements. Pay range: $22 to 24/ per hour - Final compensation will depend on experience. STAAR Surgical is an Equal Opportunity/Affirmative Action employer and all qualified applicants will receive consideration without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran or disability status, or any other characteristic protected by law.

Certified Group is committed to delivering expert solutions and quality testing our customers can feel confident in - on time, every time - so the world can trust in what it consumes. As a leading North American provider of laboratory testing, regulatory consulting, and certification & audit services, Certified Group includes Food Safety Net Services (FSNS), FSNS Certification & Audit, Certified Laboratories, EAS Consulting Group, and Labstat International Inc. Certified Group provides analytical testing and regulatory guidance services in the food & beverage, dietary supplements & NHP, cosmetics, OTC, personal care, tobacco, nicotine, cannabis, and hemp industries. We have embarked on an important journey to unify and strengthen our culture by living these core values: Start with the Customer, Drive to Deliver, Commit to Safety and Quality, and Believe in the Team - including believing in you. We are currently looking for a Pathogen Lab Analyst to join our growing team! $1000 HIRING BONUS!!! Job Summary: Perform analytical and microbiological testing of food products, ingredients, and environmentals. The position performs the application and evaluation of approved microbiological techniques and methodologies. Essential Responsibilities: * Accurately perform and read test results and notify Laboratory Management of deviations * Prepare and analyze samples for indicator organisms, pathogens, and chemistries * Apply aseptic/microbiological techniques in daily workload * Report inventory and expendable supplies/materials needed for testing requirements * Provide routine preventive maintenance by daily cleaning, sanitizing, trash disposal, and equipment quality control * Assist in quality duties to by taking incubator temperatures, inoculating control organisms, running media controls, etc. * Pursue an assigned series of processes, procedures, or techniques in accordance with FSNS policies/procedures and customer requirements * Maintain a high degree of technical competence by reading scientific journals, attending professional workshops, and being aware of food industry issues and trends * Perform all activities in a neat, safe, hygienic, and efficient manner * Share information in an open and timely manner * Assisting with managing priorities and schedule such that individual goals as well as team goals are achieved with encouraged participation in the Food Safety Net Services Team * Responsible for the safety of oneself and others working within their area Supervision: * This job does has no supervisory responsibilities. Education & Experience: * Associate degree in Life Science or related field with two or more years of laboratory experience, preferred * Two or more years of experience in a commercial food-testing or analytical laboratory * Or equivalent combination of education and experience * Working knowledge of aseptic sampling technique, automated lab equipment, and acceptable methods and procedures * Familiarity with GLP, OSHA guidelines, FDA, BAM, APHA, ISO, and USP methods and procedures * Broad knowledge of concepts, practices, and procedures of a food testing laboratory * Ability to travel when necessary Physical Demands/Work Environment: * Dexterity of hands and fingers to operate a computer keyboard, mouse and to handle other communications/computer components * Potential exposure to odors, fumes, airborne particles, hazardous chemicals, and microbiological pathogens * Noise level varies from quiet to loud * Temperature varies from hot to cold * Interactive and fast-paced team oriented tasks * Overnight Travel is required at the discretion of management * Occasionally lift and/or move up to 25 pounds * Color vision and depth perception Benefits: * Progressive 401k Retirement Savings Plan * Employer Paid Short- Term and Long-Term Disability, and Life Insurance * Group Medical * Tuition Reimbursement * Flexible Spending Accounts * Dental * Paid Holidays and Time Off Certified Group values diversity in its workforce. The company is firmly committed to a policy of Equal Opportunity and will administer its policies in a manner that treats each employee and applicant for employment on the basis of merit. Certified Group will take affirmative action to seek out qualified applicants without regard to race, color, religion, sex, national origin, age, handicap, or veteran status.

Job Description The Quality Control Chemist is responsible for daily lab testing with the purpose of accepting or rejecting test samples based on pre-determined specifications. The successful candidate will be able to work quickly and safely and will assist the Quality Control Manager with other tasks, as needed. ESSENTIAL DUTIES AND RESPONSIBILITIES Include the following. Other duties may be assigned. • Performs laboratory tests including pH, fluoride, viscosity, specific gravity, color, and appearance. • Tests raw materials, bulk intermediates, finished products and stability samples for specific quality attributes. • Uses and maintains HPLC, GC, FTIR, and other instruments. • Assists in performing method validations. • Performs a variety of wet lab techniques including but not limited to: titrations, pH, ISE, etc. • Writes and revises SOPs and tests methods as needed. • Follows documented procedures: SOPs, test methods, transfer protocols. • Prepares reports and reviews data. • Follows lab safety procedures. • Performs other tasks, as assigned. SUPERVISORY RESPONSIBILITIES None QUALIFICATIONS To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. EDUCATION and/or EXPERIENCE Bachelors of Science in Chemistry. LANGUAGE SKILLS Able to read, analyze, and interpret general business periodicals, professional journals, technical procedures, or governmental regulations. MATHEMATICAL SKILLS Able to calculate figures and amounts such as proportions, percentages, area, circumference and volume. Able to apply concepts of basic algebra and geometry. REASONING ABILITY Able to apply common sense understanding to carry out instructions furnished in written, oral, or diagram form. Able to deal with problems involving several concrete variables in standardized situations. PHYSICAL DEMANDS The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Specific vision abilities required by this job include close vision and depth perception. WORK ENVIRONMENT The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

$10,000.00 SIGN-ON BONUS ELIGIBLE The Laboratory Technologist will demonstrate multiple analytical and judgment skills and knowledge of clinical laboratory science to provide accurate, timely results. The incumbent uses high complexity methods and instrumentation and will work independently in multiple areas of the laboratory. Essential Job Functions * Procure, prepare and process specimen using various approved techniques and procedures. * Perform phlebotomy in accordance with established procedures and in a manner consistent with customer service needs and expectations. * Receive specimens into the LIS, verifies orders, understands priorities and communicates all pertinent information. * Validate test orders, appropriateness of specimen and ensure required documentation is present. * Process and organize specimens using standard precautions, maintaining specimen integrity and identity. * Recognize, resolve and document specimen tracking and integrity issues. * Utilize specimen rejection and irretrievable specimen policies to document specimen issues. * Validate and research unusual reference test orders, arrange proper specimen collection, and ensure that documentation is complete and information effectively communicated. * Package specimens for transport according to regulations and established protocol. * Prepare appropriate quantity of reagents and consumables in accordance with section guidelines; maintains reagents to maximize stability and shelf-life. * Perform preventative and corrective maintenance; anticipate problem situations and take preventative action to avoid delay of patient care. * Maintain supplies at adequate levels to support operations, monitoring utilization and reporting unusual situations to supervisor. * Perform low, moderate and high complexity technical assays, evaluate and interpret results forming conclusions requiring a high level of judgment. * Determine and validate appropriate instrument settings and making adjustments as needed. * Demonstrate competency on all instrumentation and methods in assigned work areas. * Perform laboratory tests in assigned area, using established protocols and with an awareness of accuracy, method sensitivity, specificity, and turn-around-time and cost management. * Assess test methods for procedural validity and testing accuracy, re-evaluating patient data for validity when instrument or methodology malfunctions are suspected. * Perform and document all quality control, maintenance and variances. * Maintain an in-depth knowledge of the test methods and procedures in two or more laboratory sections, and show an understanding of the correlation of patient results to the overall clinical picture. * Identify, investigate and resolve questionable test orders and/or results through correlation of disease state/diagnosis and patient history. * Assess specimen integrity, validity and identification; recognize abnormal, unusual, or problem situations, and correlate patient laboratory results when specimens are suboptimal. * Correlate patient data with other clinical information to assess the possibility of inconsistent orders or results. * Participate in a quality management system to include quality control and assurance of laboratory testing, competency assessment and appropriate utilization of laboratory services. * Compose correlation studies, QC reports, and maintain monthly logs. * Evaluate quality control data to assist the supervisor in the assessment of accuracy, reproducibility and validity of methods. * Participate in section readiness to meet CAP, JCAHO, OSHA and DOH compliance. * Utilize HIS as needed for patient or test order information, and to process supply or work orders. * Utilize functions of LIS to accession, receive, result and monitor functions related to patient testing. * Participate in initial and monthly validation of LIS and instrument interfaces. * Evaluate laboratory data to assess the need for recollection of the specimen. * Correlate patient laboratory results to suspect pathological state, and recognizes the need for follow-up or reflex testing. * Redirect testing to appropriate backup or secondary test methods and seeks to resolve primary testing issues. * Interact with healthcare providers to interpret laboratory results within the framework of medical technology. * Answer inquiries from other healthcare providers concerning test appropriateness, quality, accuracy and procedural requirements. * Assist in the evaluation and development of new methods/instruments. * Recommend process improvements to workflow and assist in implementation of changes to improve operation. * Report and document critical values and read back verifications according to policy. * Adhere to laboratory and section specific Environmental Control Plan. * When appropriate, enter reflex testing codes into LIS to generate billing. * Retain records of instrument printouts and specimens according to policy. * Other duties as assigned. Competency and Experience [Knowledge, Skills and Abilities] Required Qualifications/Experience * Associate of Science or higher-level degree from an accredited institution in chemical, physical, biological or clinical laboratory science, or medical technology, OR, * Equivalent laboratory training and experience meeting the requirements defined by CLIA 88 for individuals performing high complexity testing. * Knowledge of Medical terminology and laboratory information system. * Functional skills in Microsoft Office applications, including Outlook. * Strong leadership ability, good organizational skills, independent and critical thinking skills, sound judgment, and knowledge of legal aspects and liability of nursing practice. * Strong ability to communicate complex and/or controversial topics and concepts to a wide and diverse audience. Preferred Qualifications/Experience * Prior experience within a clinical laboratory. License, Certification & Clearances * ASCP preferred. * Act 33 clearance with renewal. * Act 34 clearance with renewal. * Act 73 FBI Clearance with renewal. Position Type/Expected Hours of Work * Incumbent will be scheduled based on operational need (rotate shifts, standby, on-call, etc.). * Travel may be expected locally between System locations. Equal Employment Opportunity Independence Health and its affiliated companies are Equal Opportunity Employers. It is their policy to prohibit discrimination of any type and to afford equal employment opportunities to employees and applicants without regard to race, color, religion, sex, sexual orientation, national origin, age, marital status, disability, veteran status, or genetic information, or any other classification protected by law. Independence Health and its affiliated companies will comply with all applicable laws and regulations. Disclaimer This job description is not designed to contain a comprehensive listing of all activities, duties or responsibilities that are required of the employee. Moreover, duties, responsibilities and activities may change or new ones may be assigned at any time with or without notice. Work EnvironmentEffective March 2020 or during pandemic: goggles, face shield and mask are required according to CDC guidelines When lift requirement is in excess of 50#, lift assistance (2 person) and/or transfer device is required. Essential - Absolute Necessity. Marginal - Minimal Necessity. Constantly - 5.5 to 8 hours or more or 200 reps/shift. Frequently - 2.5 to 5.5 hours or more or 32-200 reps/shift. Occasionally - 0.25 to 2.5 hours or 2-32 reps/shift. Rarely - Less than 0.25 hours or less than 2 reps/shift. Physical Condition Essential Marginal Constantly Frequently Occasionally Rarely Never Extreme Heat X X Extreme Cold X X Heights X X Confined Spaces X X Extreme Noise(>85dB) X X Mechanical Hazards X X Use of Vibrating Tools X X Operates Vehicle X Operates Heavy Equipment X Use of Lifting/Transfer Devices X Rotates All Shifts X X 8 Hours Shifts X X 10-12 Hours Shifts X X On-Call X Overtime(+8/hrs/shift; 40/hrs/wk) X X Travel Between Sites X X Direct Patient Care X X Respirator Protective Equipment X X Eye Protection X X Head Protection (hard hat) X Hearing Protection X X Hand Protection X X Feet, Toe Protection X Body Protection X X Latex Exposure X X Solvent Exposure X X Paint (direct use) Exposure X Dust (sanding) Exposure X Ethylene Oxide Exposure X Cytotoxic (Chemo) Exposure X Blood/Body Fluid Exposure X X Chemicals (direct use) Exposure X X Mist Exposure X Wax Stripper (direct use) X Non-Ionizing Radiation Exposure X Ionizing Radiation Exposure X Laser Exposure X X Physical Demands When lift requirement is in excess of 50#, lift assistance (2 person) and/or transfer device is required. Essential - Absolute Necessity. Marginal - Minimal Necessity. Constantly - 5.5 to 8 hours or more or 200 reps/shift. Frequently - 2.5 to 5.5 hours or more or 32-200 reps/shift. Occasionally - 0.25 to 2.5 hours or 2-32 reps/shift. Rarely - Less than 0.25 hours or less than 2 reps/shift. Physical Condition Essential Marginal Constantly Frequently Occasionally Rarely Never Bending (Stooping) X X Sitting X X Walking X X Climbing Stairs X X Climbing Ladders X X Standing X X Kneeling X X Squatting (Crouching) X X Twisting/Turning X X Keyboard/Computer Operation X X Gross Grasp X X Fine Finger Manipulation X X Hand/Arm Coordination X X Pushing/Pulling(lbs. of force) X X Carry X X Transfer/Push/Pull Patients X Seeing Near w/Acuity X X Feeling (Sensation) X X Color Vision X X Hearing Clearly X X Pulling/Pushing Objects Overhead X X Reaching Above Shoulder Level X X Reaching Forward X X Lifting Floor to Knuckle X 25# Lifting Seat Pan to Knuckle X 10# Lifting Knuckle to Shoulder X 10# Lifting Shoulder to Overhead X 10# When lift requirement is in excess of 50#, lift assistance (2 person) and/or transfer device is required.

Join a Team That Makes a Difference! At Noble, the work you do matters. We manufacture innovative products that support the military, advance the medical field, and improve everyday life. Whether it's enhancing safety, enabling critical care, or solving real-world challenges, our solutions help people when it matters most. Be part of a purpose-driven team where your skills contribute to meaningful change. Noble Biomaterials, Inc is currently seeking a Chemical Lab Analyst for our 1st shift. The Chemical Lab Analyst performs laboratory testing on raw materials, in-process samples, and finished products to ensure quality and compliance. This role includes running various test methods, entering and verifying data, and maintaining lab equipment while following Good Documentation Practices (GDP) and Good Laboratory Practices (GLP). What You'll Get: Starting Pay: $18.00/hour Weekly Pay - Get Paid Every Thursday! Full Benefits Starting the 1st of the Month After Hire! Medical, Dental, Vision $2,000-$4,000 Health Reimbursement Account (HRA) An account that is funded by the company to cover a portion of the in-network deductible for you and your family. (debit card) Company-Paid Life, Short & Long-Term Disability FSA, Voluntary Insurance Options 401(k) + Company Match (after 6 months) 11 Paid Holidays + PTO What You'll Do: Perform routine and non-routine testing on raw materials, in-process samples, and finished goods Prepare and analyze samples using methods such as: Titration ASE extraction Atomic Absorption (AA) ICP-OES FTIR Conduct simulated at-home laundering on fabrics Record and interpret test results Enter and verify all testing data Maintain and troubleshoot basic lab equipment Assist with investigations and reporting when issues arise Communicate and collaborate with cross-functional teams Report out-of-specification or questionable results Perform other tasks as assigned by management Job Flexibility Employees in this position may be assigned to different work areas or job duties based on production demands. Applicants should be comfortable learning new tasks and adapting to changing priorities. The Skills You'll Need: Strong analytical and problem-solving skills High attention to detail and commitment to quality Reliable attendance and time management Team-oriented with strong communication skills Commitment to safety, ethics, and inclusive workplace practices Work in varied indoor conditions which may include heat, cold, dust, loud noise, etc., with the use of personal protective equipment (PPE) What We're Looking For: Associate degree in a related science field required 3-6 months of quality related experience in a manufacturing setting preferred. Proficiency with Excel, Word, and Outlook preferred Age 18+ with reliable transportation Ready to Join a Team That Invests in You? Apply today and take the next step in your manufacturing career with a company that values its employees and offers weekly pay and benefits that start right away! Equal Opportunity Employer/Veterans/Disabled