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job summary: Paid Hourly- 27/hr M-F: 8:30am-5pm Direct Hire opportunity!! In this role you will conduct internal audits, inspections, and quality checks across production areas to ensure compliance with GMP, GDP, SOP, and 5S standards while managing non-conformances and supporting overall product quality. Required to have a minimum of 2 years of manufacturing experience, along with line clearance experience. Knowledge and experience with Microsoft Office and inspecting/auditing products!   location: Alameda, California job type: Permanent salary: $50,000 - 56,160 per year work hours: 8am to 4pm education: No Degree Required   responsibilities: Conduct internal audits of packaged "ready to close" units.Perform audits of work-in-progress (WIP) products on open work orders.Audit production processes and technician practices for compliance with GDP, GMP, and SOP standards.Inspect technician desks for line clearance and 5S, GMP, and GDP adherence.Audit manufacturing floor for compliance with 5S and GMP standards.Create and issue Non-Conformance Reports (NCRs) for identified issues.Maintain and update the QC Internal Audit Failure Log.Serve as quality contact for incoming inspections.Support technicians and leads with quality-related concerns on the production floor.Assist the buyer in managing and rejecting defective vendor materials. #LI-QM1   qualifications: Experience level: ExperiencedMinimum 2 years of experienceEducation: No Degree Required  skills: QualityManufacturing Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility). This posting is open for thirty (30) days. Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance. 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. We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance.

Exceptional opportunity for a skilled Maintenance Technician to earn top-tier pay while enjoying a compressed work schedule that provides three to four consecutive days off every week. We are searching for a highly self-motivated professional to maintain complex, high-volume production equipment. If you have the technical expertise and thrive with minimal oversight, we want to hear from you. The Offer: Pay & Schedule Pay Rate $35.00−$50.00 per hour (Based on Experience) ScheduleAlternative Work Schedule (AWS) - 12-hour shifts RotationAlternating 3-day and 4-day workweeks Shifts Available Day Shift: 6:00 AM - 6:00 PM OR Night Shift: 6:00 PM - 6:00 AM (Average 42 hours/week) BenefitsComprehensive health, dental, vision, and retirement planssalary: $72,000 - $100,000 per yearshift: Firstwork hours: 6 AM - 6 PMeducation: High SchoolResponsibilitiesResponsibilities:  Diagnose and restore all production equipment that is down or malfunctioning. Conduct installations and modifications of machinery according to work instructions. Execute and document comprehensive preventive maintenance (PM) schedules. Manage and track the use of spare parts and alert the inventory team to re-order needs. Evaluate equipment performance, develop maintenance procedures, and create detailed error logs (This is a critical function). Propose and implement process and tooling improvements to enhance efficiency. Install and integrate engineering upgrades to existing machinery. Collaborate with the equipment testing group to validate system functionality. Strictly adhere to Lockout/Tagout (LOTO) safety protocols. Qualifications:  A minimum of 5 years of hands-on maintenance experience in a manufacturing setting is highly preferred. strong mechanical aptitude including proficiency with pneumatics, vacuum systems, motor alignment, and various lifting apparatus like hoists. In-depth electrical knowledge (up to 480VAC) including experience with VFDs (Variable Frequency Drives), motor/encoder systems, and specialized high-temperature systems (up to 1200°C) is strongly valued. Proven expertise with PLC and automation systems is a must. Experience with Tool & Die methods, including precision measurement and adjustment techniques (e.g., laser alignment). Welding experience is a plus!  The essential functions of this role include:manual lifting up to 50lbsstanding for 12 hours at one timeworking up to 10 hrs of overtime per weekSkillsElectronic MaintenanceMechanical MaintenanceBlueprintsInspectingMigTigAutomationQualificationsYears of experience: 5 yearsExperience level: ExperiencedRandstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).This posting is open for thirty (30) days. Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance. 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. We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance.

job summary: SUMMARY The Technical Specialist, Quality Assurance Document Control, reporting to the Head of QA Document Control Novato, is responsible for supporting the management of all aspects related to documentation control processes for Quality Assurance and Quality Control and the management of documents in the Veeva Quality Management System. This role requires a working knowledge of Good Manufacturing Practices (GMP), FDA/EMA regulations and will involve collaboration with cross-functional teams to maintain commitment to quality and compliance.   location: Novato, California job type: Contract salary: $33.94 - 39.93 per hour work hours: 8 to 4 education: Associate   responsibilities: Support the development, implementation, maintenance and improvement of the document control system in accordance with FDA, EMA, and other regulatory agency requirements, ensuring that all quality documents are properly and efficiently managed and accessible.Support the maintenance of QADC hours for Logbooks, corrections, and archive access during business hours with additional hours as needed during audits and inspections.Ensure all quality documents are properly managed, accessible, and adhere to Good Documentation Practices (GDP).Support the management of the lifecycle of quality documents, including archiving and retrieval processes.Support the maintenance of multiple databases such as Logbook trackers, scanned logbooks, notebook trackers, and offsite storage.Support the management of the backlog of documents in the Veeva system, ensuring periodic review and timely lifecycle management of documents, including Documents to Effective (DtE) and Documents to Approval (DtA).Collaborate with cross-functional teams to ensure alignment on documentation practices and support quality initiatives.Ensure right the first time and compliance in all QA Document Control Activities.Ensure documents are returned promptly and maintain efficient flow of physical documents.Ensure audit readiness of QADC areas and act as a key point of contact for audits and inspections.Support the archival of documentation and ensure the QA Document Control room is always audit- ready.Support training team members as needed.Other duties as assigned.   qualifications: Experience: Minimum of 3 years within the biotechnology or pharmaceutical industry.Extensive knowledge of GMP, FDA, EMA, and other regulatory requirements.Proficient in Veeva EDMS. Education: BA/BS in life sciences or related fieldAdvance degree desirable but not required. Other: This role is hybrid and requires employee to be onsite three days/week. Onsite hours could be increased during FDA audits, Internal Audits or other special occasions. #LI-AO1   skills: Quality control, SOP, GMP (Good Manufacturing Practice), Food and Drug Administration (FDA) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility). This posting is open for thirty (30) days. Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance. 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. We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance.