{"schemaVersion":"jobsearcher.job.v1","id":"3f7c026c0220619d8e303443","url":"https://jobsearcher.com/jobs/3f7c026c0220619d8e303443","canonicalUrl":"https://jobsearcher.com/jobs/3f7c026c0220619d8e303443","title":"Lab Technician – QC/Analytical Document Writer","description":"About the Job\nA rapidly growing specialty pharmaceutical company is seeking a motivated, detail-oriented Lab Technician – QC/Analytical Document Writer to support laboratory documentation activities at its Sacramento, California facility.\n\nThis position is responsible for preparing, revising, reviewing, and maintaining analytical and quality-control documentation in compliance with cGMP, FDA, ICH, and internal quality standards. The ideal candidate will have direct documentation experience within a GMP sterile-injectable or aseptic pharmaceutical environment, strong technical-writing skills, and excellent attention to detail.\n\nThis is a fully onsite position in Sacramento, California.\n\nResponsibilities\n\nPrepare, revise, review, and maintain analytical and quality documentation, including:\nTest methods and analytical procedures\nMethod-validation protocols and reports\nSpecifications and standard testing procedures\nSOPs, control sheets, and control worksheets\nChange controls, deviations, CAPAs, investigations, and related reports\nEnsure laboratory documentation complies with cGMP, FDA, ICH, data-integrity, and internal quality requirements.\nManage document-lifecycle activities, including version control, approval routing, issuance, archival, and traceability.\nCreate, route, and monitor documents through electronic approval workflows using TrackWise, eInfoTree, or comparable quality-document systems.\nEnter, review, and maintain analytical data and laboratory workflows in StarLIMS or a comparable LIMS.\nCollaborate with Quality Control, Quality Assurance, Analytical Development, Research and Development, and Regulatory Affairs during document preparation and review.\nSupport internal and external audits by retrieving and providing accurate, complete, and properly controlled records.\nIdentify documentation discrepancies and coordinate corrections with the appropriate laboratory and quality personnel.\nPerform additional documentation-related duties and special projects as assigned.\nRequired Qualifications\n\nHigh school diploma or GED.\nDirect experience working in a cGMP pharmaceutical environment.\nExperience within sterile-injectable, parenteral, or aseptic pharmaceutical manufacturing or laboratory operations.\nExperience preparing, revising, reviewing, or maintaining controlled laboratory, analytical, or quality documentation.\nWorking knowledge of GMP documentation practices, document control, version control, and data integrity.\nStrong proficiency with Microsoft Word, Excel, and Outlook.\nStrong attention to detail, organization, and proofreading skills.\nExcellent job-related written and verbal communication skills.\nAbility to manage multiple documents and priorities in a fast-paced, team-oriented environment.\nAbility to work fully onsite in Sacramento, California.\nPreferred Qualifications\n\nExperience preparing test methods, specifications, STPs, analytical procedures, or method-validation protocols and reports.\nExperience documenting deviations, investigations, CAPAs, or change controls.\nExperience with TrackWise, eInfoTree, StarLIMS, or comparable eQMS, EDMS, or LIMS platforms.\nExperience supporting pharmaceutical regulatory inspections or internal quality audits.\nFlexibility to support different shifts or occasional weekend work based on business needs.\nCompensation and Benefits\n\nPay range: $25–$27 per hour\nMedical, dental, and vision coverage\nPaid time off\n401(k)\nAdditional incentive-program eligibility may apply\nEmployment is contingent upon successful completion of the company’s pre-employment screening requirements.\n\n#IND-SPG\n\nEstimated Min Rate: $25/hr\nEstimated Max Rate: $27/hr\n\nWhat’s In It for You?\nWe welcome you to be a part of the largest and legendary global staffing companies to meet your career aspirations. Yoh’s network of client companies has been employing professionals like you for over 65 years in the U.S., UK and Canada. Join Yoh’s extensive talent community that will provide you with access to Yoh’s vast network of opportunities and gain access to this exclusive opportunity available to you. Benefit eligibility is in accordance with applicable laws and client requirements. Benefits include:\n\nMedical, Prescription, Dental & Vision Benefits (for employees working 20+ hours per week)\nHealth Savings Account (HSA) (for employees working 20+ hours per week)\nLife & Disability Insurance (for employees working 20+ hours per week)\nMetLife Voluntary Benefits\nEmployee Assistance Program (EAP)\n401K Retirement Savings Plan\nDirect Deposit & weekly epayroll\nReferral Bonus Programs\nCertification and training opportunities\nNote: Any pay ranges displayed are estimations. Actual pay is determined by an applicant's experience, technical expertise, and other qualifications as listed in the job description. All qualified applicants are welcome to apply.\n\nYoh, a Day & Zimmermann company, 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, disability, or status as a protected veteran.\n\nVisit https://www.yoh.com/applicants-with-disabilities to contact us if you are an individual with a disability and require accommodation in the application process.\n\nFor California applicants, qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. All of the material job duties described in this posting are job duties for which a criminal history may have a direct, adverse, and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.\n\nIt is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.\n\nBy applying and submitting your resume, you authorize Yoh to review and reformat your resume to meet Yoh’s hiring clients’ preferences. To learn more about Yoh’s privacy practices, please see our Candidate Privacy Notice: https://www.yoh.com/privacy-notice\nIND-SPG","company":"Yohaday","rawCompany":"yohaday","city":"Sacramento","state":"CA","isRemote":false,"isActive":false,"createdAt":"2026-07-21T12:13:23.709Z","occupations":[{"code":"19-4099.01","title":"Quality Control Analysts","slug":"quality-control-analysts"},{"code":"19-4031.00","title":"Chemical Technicians","slug":"chemical-technicians"},{"code":"11-3051.01","title":"Quality Control Systems Managers","slug":"quality-control-systems-managers"}],"industries":[{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"},{"code":"561410","title":"Document Preparation Services","slug":"document-preparation-services"},{"code":"541380","title":"Testing Laboratories and Services","slug":"testing-laboratories-and-services"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Lab Technician – QC/Analytical Document Writer","description":"About the Job\nA rapidly growing specialty pharmaceutical company is seeking a motivated, detail-oriented Lab Technician – QC/Analytical Document Writer to support laboratory documentation activities at its Sacramento, California facility.\n\nThis position is responsible for preparing, revising, reviewing, and maintaining analytical and quality-control documentation in compliance with cGMP, FDA, ICH, and internal quality standards. The ideal candidate will have direct documentation experience within a GMP sterile-injectable or aseptic pharmaceutical environment, strong technical-writing skills, and excellent attention to detail.\n\nThis is a fully onsite position in Sacramento, California.\n\nResponsibilities\n\nPrepare, revise, review, and maintain analytical and quality documentation, including:\nTest methods and analytical procedures\nMethod-validation protocols and reports\nSpecifications and standard testing procedures\nSOPs, control sheets, and control worksheets\nChange controls, deviations, CAPAs, investigations, and related reports\nEnsure laboratory documentation complies with cGMP, FDA, ICH, data-integrity, and internal quality requirements.\nManage document-lifecycle activities, including version control, approval routing, issuance, archival, and traceability.\nCreate, route, and monitor documents through electronic approval workflows using TrackWise, eInfoTree, or comparable quality-document systems.\nEnter, review, and maintain analytical data and laboratory workflows in StarLIMS or a comparable LIMS.\nCollaborate with Quality Control, Quality Assurance, Analytical Development, Research and Development, and Regulatory Affairs during document preparation and review.\nSupport internal and external audits by retrieving and providing accurate, complete, and properly controlled records.\nIdentify documentation discrepancies and coordinate corrections with the appropriate laboratory and quality personnel.\nPerform additional documentation-related duties and special projects as assigned.\nRequired Qualifications\n\nHigh school diploma or GED.\nDirect experience working in a cGMP pharmaceutical environment.\nExperience within sterile-injectable, parenteral, or aseptic pharmaceutical manufacturing or laboratory operations.\nExperience preparing, revising, reviewing, or maintaining controlled laboratory, analytical, or quality documentation.\nWorking knowledge of GMP documentation practices, document control, version control, and data integrity.\nStrong proficiency with Microsoft Word, Excel, and Outlook.\nStrong attention to detail, organization, and proofreading skills.\nExcellent job-related written and verbal communication skills.\nAbility to manage multiple documents and priorities in a fast-paced, team-oriented environment.\nAbility to work fully onsite in Sacramento, California.\nPreferred Qualifications\n\nExperience preparing test methods, specifications, STPs, analytical procedures, or method-validation protocols and reports.\nExperience documenting deviations, investigations, CAPAs, or change controls.\nExperience with TrackWise, eInfoTree, StarLIMS, or comparable eQMS, EDMS, or LIMS platforms.\nExperience supporting pharmaceutical regulatory inspections or internal quality audits.\nFlexibility to support different shifts or occasional weekend work based on business needs.\nCompensation and Benefits\n\nPay range: $25–$27 per hour\nMedical, dental, and vision coverage\nPaid time off\n401(k)\nAdditional incentive-program eligibility may apply\nEmployment is contingent upon successful completion of the company’s pre-employment screening requirements.\n\n#IND-SPG\n\nEstimated Min Rate: $25/hr\nEstimated Max Rate: $27/hr\n\nWhat’s In It for You?\nWe welcome you to be a part of the largest and legendary global staffing companies to meet your career aspirations. Yoh’s network of client companies has been employing professionals like you for over 65 years in the U.S., UK and Canada. Join Yoh’s extensive talent community that will provide you with access to Yoh’s vast network of opportunities and gain access to this exclusive opportunity available to you. Benefit eligibility is in accordance with applicable laws and client requirements. Benefits include:\n\nMedical, Prescription, Dental & Vision Benefits (for employees working 20+ hours per week)\nHealth Savings Account (HSA) (for employees working 20+ hours per week)\nLife & Disability Insurance (for employees working 20+ hours per week)\nMetLife Voluntary Benefits\nEmployee Assistance Program (EAP)\n401K Retirement Savings Plan\nDirect Deposit & weekly epayroll\nReferral Bonus Programs\nCertification and training opportunities\nNote: Any pay ranges displayed are estimations. Actual pay is determined by an applicant's experience, technical expertise, and other qualifications as listed in the job description. All qualified applicants are welcome to apply.\n\nYoh, a Day & Zimmermann company, 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, disability, or status as a protected veteran.\n\nVisit https://www.yoh.com/applicants-with-disabilities to contact us if you are an individual with a disability and require accommodation in the application process.\n\nFor California applicants, qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. All of the material job duties described in this posting are job duties for which a criminal history may have a direct, adverse, and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.\n\nIt is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.\n\nBy applying and submitting your resume, you authorize Yoh to review and reformat your resume to meet Yoh’s hiring clients’ preferences. To learn more about Yoh’s privacy practices, please see our Candidate Privacy Notice: https://www.yoh.com/privacy-notice\nIND-SPG","datePosted":"2026-07-21T12:13:23.709Z","dateModified":"2026-07-21T12:13:23.709Z","hiringOrganization":{"@type":"Organization","name":"Yohaday","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Sacramento","addressRegion":"CA","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"3f7c026c0220619d8e303443"},"url":"https://jobsearcher.com/jobs/3f7c026c0220619d8e303443"}}