Manufacturing technician jobs in Petaluma, CA - 211 jobs

Red Oak Technologies is a leading provider of comprehensive resourcing solutions across a variety of industries and sectors including IT, Marketing, Finance, Business Operations, Manufacturing and Engineering. Our client is an electronics manufacturer. They are looking for a Manufacturing Technician (Swing Shift) to join their team. This role is a CONTRACT position. Position will be ONSITE. Candidate must be able to commute onsite to San Francisco, CA. **Swing Shift - 2:00PM - 10:30PM - Monday through Friday - Some work on Saturday as needed** **Gated private parking lot available for contractors** **$30/hr - $35/hr** Position Requirements: Follow all Safety and Laser Safety procedures and requirements Be able to construct, test and calibrate engineering and production robotic and computer-controlled assembly systems using engineering prints, schematics, assembly instructions and engineering direction Knowledgeable in high precision measuring equipment, calibration, and detailed record generation Experienced and Proficient in the following: Mechanical hand and power tools Oscilloscopes, DMM, Signal Generators, Optics, Cameras Laser safety, lasers, laser pattern recognition, beam focus, and active alignment Auto dispense and cure of UV adhesive Multiple axis, vision assisted, computer controlled robotic assembly equipment in both a R/D and Volume Manufacturing environment Identification of “Root” Cause of Manufacturing, Quality and Yield issues Microsoft Office, Standard SPC and Flowcharts packages Pneumatic actuated Slides, Grippers, etc. Hex Pod Tables, Active Alignment Excellent reading, writing, and communication skills in English Minimum of 5 years industry experience, Lidar Sensor experience preferred but not required Be able to stand for long periods of time Lift and carry 35 lbs Red Oak Technologies is made up of people from a wide variety of backgrounds and lifestyles. We embrace diversity and invite applications from people of all walks of life. See what it's like to be at the top; connect with one of our recruiters and apply today. Red Oak Tech: Quality | Talent | Integrity Note: Compensation rates are based on years of experience and/or level of skills relevant to the opportunity.

The position will actively contribute to manufacturing projects at the site. As part of the Cell Culture/Upstream Manufacturing group, you will have opportunities to work on and take ownership of a wide-ranging set of projects for troubleshooting and investigations, system and workflow implementation, and tech transfers of processes into a GMP multi-product manufacturing facility. The role will support process monitoring, GMP readiness, and manufacturing activities. The scope of responsibilities may include but are not limited to document writing (SOPs, Equipment URSs, etc.), batch record testing and review, equipment validation execution support, and single-use assembly design. Responsibilities: Support upstream operations including but not limited to media prep; cell culture thaw, expansion, and cell banking; operation of single-use bioreactors, process monitoring, and harvest operations. Performs internal support activities such as maintenance of analytical equipment, stocking of consumables, discarding expired reagents, and material coordination. Maintains own training within compliance and trains other GMP associates upon completion of trainer qualification. Support in equipment troubleshooting, pilot scale material generation, non-GMP tox material generation and GMP Upstream activities. Author/review/approve technical documents such as tech transfer protocols and reports, experimental plans, production batch records, training materials, manufacturing SOPs, and regulatory filing documents per project needs. Documents work according to cGMP and cGDP. Adheres to established regulations and follows cGMP established by site. Maintain cleanroom standards, practices, and housekeeping according to SOPs. Recognize any minor issues from the equipment and any affiliated documentation and take appropriate corrective action within scope. Notify leads/managers of issues and discrepancies immediately. Assess impact of issues and non-conformities to products and projects as they pertain to product safety and efficacy or project milestones. Evaluate new technologies and innovations to improve operational efficiency or expand cell culture capabilities. Contributes to quality activities such as investigations and area walk-throughs and support authoring deviations, CAPA, change control. MSAT support, Material receipt, and inventory organization. Other duties as assigned to ensure appropriate compounding practices. Working Conditions: This position is required to work in a lab/office setting. The role requires walking, standing, stooping, kneeling, and crouching. The employee must occasionally lift and or move up to 20 pounds independently. Qualifications: BS in Engineering, Life Sciences, or related discipline with 1-2 years of relevant experience; AA degree with combination of industry experience and relevant degree; or combination of experience and relevant advanced degree, preferably in biopharma manufacturing role. Must have bioreactor operations experience. Basic understanding of mammalian cell culture performance is required. Experience with process monitoring software and equipment software (AVEVA/Wonderware) is a plus. Working knowledge of cGMP compliance as it pertains to procedures, processes, and manufacturing. Creative thinker that can identify better and more efficient methods to address issues and gaps. Demonstrate ability to work independently and on cross-functional teams. Ability to handle more than one task at a time, while maintaining attention to detail and working in a fast-paced environment. Strong analytical skills and attention to detail. Flexible mindset for a dynamic environment. Flexibility with work hours to meet business needs, including weekends and holidays, as needed.

A leading advertising technology company is seeking a Senior Machine Learning Engineer to design and implement large-scale ML systems in San Francisco. Candidates should have an M.S or Ph.D. in Computer Science with relevant industry experience, strong programming skills in Python or Java, and proficiency in ML algorithms. The salary range is $186,900 - $217,200, along with a performance bonus and comprehensive benefits package. This is a hybrid role requiring candidates to reside within 60 miles of San Francisco. #J-18808-Ljbffr

As a Sr. Distinguished Engineer at Capital One, you will be a part of a community of technical experts working to define the future of banking in the cloud.You will work alongside our talented team of developers, machine learning experts, product managers and people leaders. Our Distinguished Engineers are leading experts in their domains, helping devise practical and reusable solutions to complex problems. You will drive innovation at multiple levels, helping optimize business outcomes while driving towards strong technology solutions.At Capital One, we believe diversity of thought strengthens our ability to influence, collaborate and provide the most innovative solutions across organizational boundaries. You will promote a culture of engineering excellence, and strike the right balance between lending expertise and providing an inclusive environment where the ideas of others can be heard and championed. You will lead the way in creating next-generation talent for Capital One Tech, mentoring internal talent and actively recruiting to keep building our community.Distinguished Engineers are expected to lead through technical contribution. You will operate as a trusted advisor for our key technologies, platforms and capability domains, creating clear and concise communications, code samples, blog posts and other material to share knowledge both inside and outside the organization. You will specialize in a particular subject area, but your input and impact will be sought and expected throughout the organization.**About the Team:**When a customer's credit card or personal information is stolen, it is a defining and increasingly frequent moment in our customers' financial lives. According to Experian, in 2017 alone 14 million credit card numbers and 158 million social security numbers were exposed. Increasingly, this type of activity is carried out by sophisticated international criminal organizations, who are constantly innovating and using the latest technologies to commit these crimes.In the Fraud domain, we dream of building more intuitive, elegant products and experiences, leveraging AI & Gen AI, that change and have a positive impact on our customers' lives. We are looking for a Senior Distinguished Engineer to define, architect and drive the implementation of Fraud Products & Platforms powering dynamic, personalized experiences for customers and agents If you are ready to provide thought leadership and build engineering excellence across Capital One's engineering teams, come join us in our mission to change banking for good.**Key responsibilities:*** Articulate and evangelize a bold technical vision for your domain* Decompose complex problems into practical and operational solutions* Ensure the quality of technical design and implementation* Serve as an authoritative expert on non-functional system characteristics, such as performance, scalability and operability* Continue learning and injecting advanced technical knowledge into our community* Handle several projects simultaneously, balancing your time to maximize impact* Act as a role model and mentor within the tech community, helping to coach and strengthen the technical expertise and know-how of our engineering and product community**What you'll do:*** Define and drive technical strategy and roadmap for our systems and platforms that power Fraud defenses and Fraud & Disputes claims processing* Partner cross-functionally with client, cloud infrastructure, and machine learning platform teams to align on and co-develop technical solutions.* Architect and build highly secure & scalable systems that enable server-driven product experiences across devices, with exceptional reliability and availability.* Design high-throughput, low-latency services capable of handling millions of concurrent requests.* Design and implement API & federated BFF (Back-end for Front end) strategy for efficient data access (fetching, caching, request coalescing, etc.) between backend services and clients, with democratized data schema contribution.* Architect enhanced Observability and Monitoring frameworks to enable rapid issue detection, debugging and resolution, across the entire product system stack.* Provide organizational technical leadership to influence architecture, engineering standards, cross-team strategies, mentoring engineers and driving organization wide platform innovation.* Leverage proven leadership in driving platform strategy, fostering cross-functional collaboration, and influencing technical direction across the company## **Basic Qualifications*** Bachelor's Degree* At least 9 years of experience in software engineering* At least 9 years of experience designing distributed systems, backend architecture, and API platforms* At least 5 years of experience with public cloud technologies## **Preferred Qualifications:*** Master's Degree in Computer Science or a related field* 10+ years of professional experience coding in commonly used languages like Java, Python, Go, JavaScript, TypeScript, Swift,* 7+ years of experience in event-driven systems and architecting scalable, fault-tolerant, highly-available services* 7+ years of experience in building high-performance API platforms and federated BFF architectures (GraphQL, REST, API gateways, gRPC, caching, and streaming).* 7+ years of experience with cloud-native engineering (AWS, Azure, or GCP), containerization (Docker, Kubernetes) and automated deployment Capital One will consider sponsoring a new qualified applicant for employment authorization for this position.Capital One offers a comprehensive, competitive, and inclusive set of health, financial and other benefits that support your total well-being. Learn more at the . Eligibility varies based on full or part-time status, exempt or non-exempt status, and management level. #J-18808-Ljbffr

Primary Duties & Responsibilities * Communicate daily activities during shift turnover meetings. * Operate substrate cleaning equipment according to set parameter and established procedures. * Operate test equipment which include Cary measurement systems and Wafer-scan measurement systems. * Maintain suitable inventory of clean substrate for coating chamber production. * Maintain clean tooling using the glass beading machine for coating equipment requirements. * Maintain a customer first attitude and make sure all parts are produced according to specifications. * Foil/target changes are done according to given process parameters and check list are followed. * Maintain inventory control * Maintains various process charts. * Relevant IT and Quality procedures are understood and properly executed. * Responsible for maintaining a quality work environment. * Maintains a positive attitude and is cooperative in working with others. * Adapts readily to changes in work caused by new requirements and/or situations. * A high standard of ethics, professionalism, competency, and quality is established and maintained. * Role model for Quality, Customer Satisfaction, Employee Satisfaction and Business Results. Education & Experience * High School diploma or equivalent * Basic reading and math skills * 1 to 3 years manufacturing experience and/or advanced education or equivalent plus 1-2 years of coating manufacturing experience. * Experience with precision measurement methods and systems. * Ability to read and understand process procedures and work instructions. * Demonstrated ability to follow instructions and procedures closely while offering suggestions for continuous improvement. * Experience with networked PC based computer system (spreadsheets, Email, MRP systems). * Experience with problem analysis and resolution. * Demonstrated ability to achieve results independently or working with others. * Ability to recommend and implement improvements. * Excellent interpersonal and communication skills. * Experience with networked PC based computer systems. Skills * Strong interpersonal, teaming, and problem-solving skills. * Work effectively with other members of the team. * Able to work in a demanding production environment involving multi-tasking, forward thinking, strong attention to detail and quality. Responsible for high accuracy thin film coating deposition work. * Requires detailed observational and technical skills during cleaning, coating, and scanning stages of production to ensure proper performance of product. * Good manual dexterity. * Ability to handle multiple priorities involving external and internal priorities. * Ability to excel in a cross-organizational, cross cultural, global team environment. * Handle special assignments promptly and professionally. * Set a high standard of ethics, professionalism, leadership, and competency * Demonstrates and promotes the II-VI Worldwide values: Customer First; Honesty and Integrity, Open Communications, Teamwork, Continuous Improvement and Learning; Manage by the "Facts"; A Safe, Clean and Orderly Workplace. Working Conditions * Indoor controlled environment * Occasional exposure to noise, dust, heat, etc. Physical Requirements * Flow of work and type of duties involve constant normal mental and visual demand, along with manual coordination Safety Requirements * All employees are required to follow the site EHS procedures and Coherent Corp. Corporate EHS standards. Quality and Environmental Responsibilities * Depending on location, this position may be responsible for the execution and maintenance of the ISO 9000, 9001, 14001 and/or other applicable standards that may apply to the relevant roles and responsibilities within the Quality Management System and Environmental Management System. Culture Commitment Ensure adherence to company's values (ICARE) in all aspects of your position at Coherent Corp.: Integrity - Create an Environment of Trust Collaboration - Innovate Through the Sharing of Ideas Accountability - Own the Process and the Outcome Respect - Recognize the Value in Everyone Enthusiasm - Find a Sense of Purpose in Work Coherent Corp. is an equal opportunity/affirmative action employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law. If you need assistance or an accommodation due to a disability, you may contact us at ******************************.

Battery Manufacturing Technician - Front End Reports To: Senior Battery Engineer Coreshell's metallurgical Silicon anode technology delivers high capacity, fast-charging, and superior safety. Our low-cost liquid-phase nano-coating addresses critical electrode-surface degradation issues and enables batteries with a Silicon-dominant anode that have higher energy density, superior intrinsic thermal safety, and significantly lower cost/kWh compared to current LIBs. Our Si anode material is 50% the cost of graphite and 100% domestically sourced. We strive to transform the global automotive market by enabling low-cost and long-range EVs as a first step towards net-zero sustainability in the near future. Position: We are looking for a Battery Manufacturing Technician with battery production, manufacturing, and/or R&D lab experience to join the slurry production team on Coreshell's Pilot Line. The ideal candidate is detail-oriented and can take initiatives to troubleshoot problems. Flexibility to start the work day before 8am twice a week is preferred. Core Responsibilities: Mix 50L-scale slurries using Pilot Line scale machinery. Must be comfortable performing some manual tasks such as lifting weights no heavier than 25kg. Perform guided experiments to define optimal process parameters for cell performance and processing capabilities. Perform routine quality control tests using various material characterization tools. Clean mixing equipment and tools after slurry production runs in a timely manner. Manage inventory of manufacturing consumables. Maintain safe, tidy, and organized work areas. Follow and maintain standard operating procedures (SOPs). Required experience: Background in manufacturing work is required. Experience working in Li-ion battery fabrication and/or mixing processes is a plus. Previous experience in laboratory work. Familiarity with chemistry lab safety protocols. Required Qualifications: 2+ years of experience in manufacturing or battery industry OR a B.S. degree or equivalent in Chemistry, Materials Science, Engineering, or similarly relevant field. Location & Benefits: San Leandro, CA. Full-time. Hourly rate is $30-35 per hour with additional stock incentives dependent on experience. Dental, vision, healthcare and 401(k) benefits are included. Applications will be screened as received.

Job Title: Manufacturing Technician / Machinist Contract Duration: 12 months Pay Rate: $34-$40/hr on W2 Shift time: 07: 00 am - 15: 30 pm M-F - with overtime and weekend hours as needed Responsibilities: •Assist with transition from development to production •Manufacture, assemble, and test mechanical, according to written procedures and engineering models, drawings, specifications and written procedures •Interface with production leads, supervisors, manager and QA inspection to ensure timely customer delivery •Troubleshoot, diagnose, and correct discrepancies by modification, rework, repair, and/or maintenance. Perform root cause analysis and implement corrective actions for recurrence control •Setup and operate precision calibrated tools including but limited to, Lathe, gauges, etc. •Identify and implement continuous improvement projects for area safety and efficiency •Perform routine lathe, equipment maintenance and functions such as daily clean-up of work areas •Other duties as assigned or otherwise beneficial to achieving organizational success •Basic mathematics skills •High School diploma or GED •3-5 years direct experience in industrial manufacturing, integration, or other relevant field •Ability to work effectively with a strong work ethic and close attention to detail in a fast-paced dynamic team environment with rapidly changing roles and responsibilities •Ability to interpret engineering models, drawings, specifications, written work instruction •Hand dexterity required to assemble small mechanical components •Basic computer skills such as Windows, Microsoft Office, etc. •Strong verbal and written communication skills •Perform repetitive work including lifting of heavy items up to 44 lbs. •Work off-shift, extended hours overtime, and weekends if/when necessary •Must be a U.S. Citizen or national, U.S. Permanent resident (current Green Card holder), or lawfully admitted into the U.S. As a refugee or granted asylum. Desired •Industry certification, trade school training and/or degree in related field •Experienced in a team-based Lean Manufacturing environment •Experience with manual lathe machining •07: 00 -15: 30 with overtime and weekend hours as needed"

US Tech Solutions is a global staff augmentation firm providing a wide-range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit our website ************************ We are constantly on the lookout for professionals to fulfill the staffing needs of our clients, sets the correct expectation and thus becomes an accelerator in the mutual growth of the individual and the organization as well. Keeping the same intent in mind, we would like you to consider the job opening with US Tech Solutions that fits your expertise and skillset. Job Description Duties: Responsible for producing innovative biotherapeutic medicine by interfacing with highly automated production systems and controls in cGMP manufacturing environment, and maintain areas in high state of inspection preparedness. Operates production equipment for Cell Culture Purification that may include process monitoring, sampling, harvesting, purification, formulation and transfer. Performs media/buffer solution preparation operations. Maintains records and clean room environment to comply with regulatory requirements utilizing current Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOP). Essential Technician: Operate systems that clean and sterilize tanks and filtration systems. Prepare solutions for the production process. Review documentation and check all calculations (e.g. tickets, labels, equipment reading). Trouble shoot equipment and process problems. Comply with safety requirements, cGMP, SOP and manufacturing documentation. Use of automation to perform production operations. Provide support to Manufacturing to meet production demands. Operate automated systems for equipment operation. Assemble and prepare equipment for production. Exhibit detail oriented documentation skills Communicate effectively and ability to work in a team environment. Exhibit professional interpersonal skills. Work with coworkers and supervisor to effectively troubleshoot minor equipment and process issues. Follows established safety and environmental guidelines and procedures for all work performed. Immediately reports safety and environmental incidents including injuries, illnesses, near misses, and safety suggestions. Fosters a positive safety culture in which no one gets hurt. Job Matrix A good working knowledge of biopharm technology and processes. Trained and skilled in all operational procedures of at least one manufacturing department. Demonstrated ability to independently document and record information related to the process. Occasionally makes routine decisions based on experience. Identifies and suggests solutions to common basic problems. Recognizes non-routine problems, investigates and suggests potential solutions. Judgment is required in resolving problems and making routine recommendations. Ability to recognize deviation from accepted practices is required. Supplementary Responsibilities: Operate bioreactors, centrifuges, other harvest systems and protein purifications units. Operate and clean fixed tank and filtration systems Operate large scale column chromatography systems. Operate small-scale cell culture areas and systems by operating cleaning, set up, and maintaining 20L bioreactors; inoculating and maintaining spinner seed cultures using aseptic techniques, maintaining cell banks; and performing general seed lab operations. Perform Solution Preparation activities (media and buffer make-up) Clean, assemble, and sterilize equipment using glass washers and autoclaves. Perform automated CIP and SIP of fixed equipment. Qualifications Degree in Life Sciences or engineering and 1 year related experience Or Associate Degree and 3 year experience Or High school and 5 years' experience Biotech certificate from approved program Additional Information Sneha Shrivastava Sr Technical Recruiter 862 - 579 - 4236

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description: Purifies proteins in a regulated FDA licensed and ISO certified facility and performs cross-functional activities associated with downstream production runs in collaboration with Bulk Fill and QC testing groups. The role may include special projects such as process development and validation activities where scientific research principles are applied. Primary responsibilities: Purify recombinant proteins to ensure commercial product demands are met: 1. Works as part of the purification team to perform purification, filtration, and centrifugation operations according to standard operating procedures. 2. Executes laboratory operations including dispensing of chemicals, volumetric and gravimetric measurements, making accurate dilutions, and preparing solutions. 3. Performs SAP duties that include cycle counting, reservations, issuing to process orders, and charging of expiring raw materials. 4. Performs equipment preventative maintenance tasks, column packing, and column testing procedures. 5. Ability to multi-task and become proficient at purifying 14 different proteins and make conjugates. 6. Responsible for ordering raw materials and components, as required. 7. Maintains a safe and well-organized work environment and complies with safety procedures. Follow regulatory requirements: 1. Adheres to valid manufacturing procedures, manufacturing operations, and current good manufacturing practices (cGMP) and ISO requirements. Documentation: 1. Responsible for the completion and review of batch records and logbooks, which requires legible, clear, and concise data entry. 2. Completes all training documentation within a pre-defined timeframe. Analytical Testing: 1. Analyzes in-process samples generated from purification activities. 2. Operates lab equipment such as pH meters, balances, centrifuges, spectrophotometers, HPLC systems, and densitometers. Skills:Must have an understanding of protein purification processes. • Experience following and writing instructions. • Very good verbal and written communication skills. • Computer knowledge required with experience using MS Word and Excel. • Able to document work accurately and has excellent organizational skills. • Experience with preparation of reagents following instructions. • Delivers quality products and services on time to all customers. • Must be attentive to detail. • Effectively manages time. • Considers how all daily manufacturing activities impact product quality. • Monitor processes and products to identify opportunities for continuous improvement. • Able to lift and push up to 35 lbs. 1. Works well in a team environment to manufacture production lots. 2. Complies with cGMP and ISO requirements. 3. Maintains accurate documentation related to manufacturing processes. Education:BA/BS in the sciences (Biology, Engineering, or related field) or 2 years of relevant experience Languages:English Read Write Speak Additional Information Best Regards, Anuj Mehta ************

Who We Are BioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future of human health. Since our founding in 1997, we have applied our scientific expertise in understanding the underlying causes of genetic conditions to create transformative medicines, using a number of treatment modalities. Using our unparalleled expertise in genetics and molecular biology, we develop medicines for patients with significant unmet medical need. We enlist the best of the best - people with the right technical expertise and a relentless drive to solve real problems - and create an environment that empowers our teams to pursue bold, innovative science. With this distinctive approach to drug discovery, we've produced a diverse pipeline of commercial, clinical and preclinical candidates that have well-understood biology and provide an opportunity to be first-to-market or offer a substantial benefit over existing therapeutic options. About Technical Operations BioMarin's Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These engineers, technicians, scientists and support staff build and maintain BioMarin's cutting-edge manufacturing processes and sites, provide quality assurance and quality control to ensure we meet regulatory standards, and procure the needed goods and services to support manufacturing and coordinating the worldwide movement of our drugs to patients. CONTRACT ROLE-Sunday - Tuesday/Wednesday Shift from 6am - 7pm (Alternate every other Wednesday) Duties PROCESS KNOWLEDGE: Understanding of process theory and equipment operation. Ability to learn biopharmaceutical manufacturing processes including mammalian cell culture, depth filtration, tangential flow filtration, column chromatography, centrifugation, protein purification, and formulation of bulk drug substance. Support initiatives for process optimization. Identify and elevate processing issues and support solutions. Gain experience with automation systems (LIMS, MES, PI, etc.). TECHNICAL DOCUMENTATION: Provide feedback and/or suggested changes to operational procedures. Assist in the incorporation of new technologies, practices, and standards into procedures. Capable of writing and reviewing process documents. QUALITY AND COMPLIANCE: Understanding of cGMPs as related to Commercial Operations. Ability to utilize Quality systems (Deviations, CAPAs, Change Requests, Action/Alert Reports, etc.). BUSINESS: Ability to participate on projects and contribute to outcomes. Capability to learn and support new business systems (Track wise, ERP, etc.). Support trending of defined department metrics. WORK ENVIRONMENT/PHYSICAL DEMANDS * Consists of strenuous, repetitive work. The following list of physical movements may be used on a daily basis: bending, reaching, climbing stairs and ladders, kneeling and making numerous equipment connections using hands. * Independently have the ability to regularly lift, dispense, push and/or pull items with an average weight of 25 pounds. * May require work around loud equipment. • The use of personal protective equipment will be required. * Requires various shift based work and off hours. Skills * Strong communication skills-verbal and written * Ability to work in a team environment which includes good conflict resolution and collaboration * Displays good initiative to identify areas for improvement and implement solutions Education * Bachelor's degree in science related area or engineering * Associate's degree in science related area or Biotech certificate with 2+ years of experience in a biotech manufacturing environment or other regulated industry Note: This description is not intended to be all-inclusive, or a limitation of the duties of the position. It is intended to describe the general nature of the job that may include other duties as assumed or assigned. Equal Opportunity Employer/Veterans/Disabled 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. In the U.S, the salary range for this position is $ 15 to $ 30 per hour. The base pay actually offered will take into account internal equity, and may also vary depending on candidate's geographic region, job-related knowledge, skills, and experience amongst other factors. The salary range for this position is: $15 to $30. BioMarin considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans. For additional benefits information, visit:

The Manufacturing Technician is responsible for the production of therapeutic proteins (API) under cGMP conditions. The role involves executing process recipes, following written procedures (SOPs), and monitoring equipment and processes. Additionally, the technician will perform basic laboratory tasks, such as pH and conductivity testing, sampling, and routine sanitization to maintain facility and equipment standards. Training will be provided to ensure compliance with cGMP standards and demonstrate aseptic techniques in handling products and materials. Responsibilities * Set up, operate equipment, and monitor production processes, including clean-in-place (CIP) and steam-in-place (SIP) operations. * Report production in written and electronic documents in accordance with good manufacturing practice (GMPs) and good documentation procedures (GDPs). * Review documentation as appropriate. * Attain qualification for all assigned tasks and maintain an individual training plan. * Perform basic laboratory tasks, such as monitoring pH, conductivity, and testing product samples. * Perform material movements, transferring raw materials and chemicals into, out of, and across production areas. * Maintain facility and equipment through routine cleaning and sanitization, supporting 6S programs. * Engage in administrative tasks, including attending shift exchanges, meetings, sending/receiving emails, and participating in projects. Essential Skills * High School Diploma or Equivalent; AS/BS in a science-related discipline preferred. * 0-3 years of experience, with some prior experience in a manufacturing setting preferred. * Basic laboratory skills and familiarity with cGMP compliance. Additional Skills & Qualifications * Experience in a large, well-known company is advantageous. Work Environment The work environment is structured to support the production of therapeutic proteins under cGMP conditions. The facility emphasizes adherence to safety protocols, cleanliness, and efficiency. The role includes shift work, with routine cleaning and sanitization tasks as part of the 6S program to maintain a high standard of facility and equipment maintenance. Job Type & Location This is a Contract to Hire position based out of Vacaville, CA. Pay and Benefits The pay range for this position is $25.00 - $27.50/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Vacaville,CA. Application Deadline This position is anticipated to close on Jan 30, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Primary Duties & Responsibilities * Communicate daily activities during shift turnover meetings. * Operate substrate cleaning equipment according to set parameter and established procedures. * Operate test equipment which include Cary measurement systems and Wafer-scan measurement systems. * Maintain suitable inventory of clean substrate for coating chamber production. * Maintain clean tooling using the glass beading machine for coating equipment requirements. * Maintain a customer first attitude and make sure all parts are produced according to specifications. * Foil/target changes are done according to given process parameters and check list are followed. * Maintain inventory control * Maintains various process charts. * Relevant IT and Quality procedures are understood and properly executed. * Responsible for maintaining a quality work environment. * Maintains a positive attitude and is cooperative in working with others. * Adapts readily to changes in work caused by new requirements and/or situations. * A high standard of ethics, professionalism, competency, and quality is established and maintained. * Role model for Quality, Customer Satisfaction, Employee Satisfaction and Business Results. Education & Experience * High School diploma or equivalent * Basic reading and math skills * 1 to 3 years manufacturing experience and/or advanced education or equivalent plus 1-2 years of coating manufacturing experience. * Experience with precision measurement methods and systems. * Ability to read and understand process procedures and work instructions. * Demonstrated ability to follow instructions and procedures closely while offering suggestions for continuous improvement. * Experience with networked PC based computer system (spreadsheets, Email, MRP systems). * Experience with problem analysis and resolution. * Demonstrated ability to achieve results independently or working with others. * Ability to recommend and implement improvements. * Excellent interpersonal and communication skills. * Experience with networked PC based computer systems. Skills * Strong interpersonal, teaming, and problem-solving skills. * Work effectively with other members of the team. * Able to work in a demanding production environment involving multi-tasking, forward thinking, strong attention to detail and quality. Responsible for high accuracy thin film coating deposition work. * Requires detailed observational and technical skills during cleaning, coating, and scanning stages of production to ensure proper performance of product. * Good manual dexterity. * Ability to handle multiple priorities involving external and internal priorities. * Ability to excel in a cross-organizational, cross cultural, global team environment. * Handle special assignments promptly and professionally. * Set a high standard of ethics, professionalism, leadership, and competency * Demonstrates and promotes the II-VI Worldwide values: Customer First; Honesty and Integrity, Open Communications, Teamwork, Continuous Improvement and Learning; Manage by the "Facts"; A Safe, Clean and Orderly Workplace. Working Conditions * Indoor controlled environment * Occasional exposure to noise, dust, heat, etc. Physical Requirements * Flow of work and type of duties involve constant normal mental and visual demand, along with manual coordination Safety Requirements * All employees are required to follow the site EHS procedures and Coherent Corp. Corporate EHS standards. Quality and Environmental Responsibilities * Depending on location, this position may be responsible for the execution and maintenance of the ISO 9000, 9001, 14001 and/or other applicable standards that may apply to the relevant roles and responsibilities within the Quality Management System and Environmental Management System. Culture Commitment Ensure adherence to company's values (ICARE) in all aspects of your position at Coherent Corp.: Integrity - Create an Environment of Trust Collaboration - Innovate Through the Sharing of Ideas Accountability - Own the Process and the Outcome Respect - Recognize the Value in Everyone Enthusiasm - Find a Sense of Purpose in Work Coherent Corp. is an equal opportunity/affirmative action employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law. If you need assistance or an accommodation due to a disability, you may contact us at ******************************.

Primary Duties & Responsibilities Support manufacturing objectives and goals through various manufacturing techniques used in the Instrumentation processes. Responsibilities include performing daily operations, inspecting own work, following all safety and environmental guidelines, and producing work that demonstrates and promotes company values. Responsible for maintaining a quality work environment that follows company policies, practices, and guidelines. Education & Experience High School diploma or equivalent Basic reading and math skills Basic Microsoft Excel and Outlook 4-6 years manufacturing experience and/or advanced education or equivalent plus 3-5 years of experience. Experience with precision measurement methods and systems Ability to read and understand engineering drawings and process procedures Demonstrated ability to follow instructions and procedures closely while offering suggestions for continuous improvement Experience with networked PC based computer system Skills Able to work in a demanding production environment involving multi-tasking, forward thinking, strong attention to detail and quality. Requires detailed observational and technical skills to ensure proper performance of product. Good manual dexterity. Responsible for high accuracy and organization. Ability to work in a cross-cultural, team-based environment Good interpersonal and communication skills Handle special assignments promptly and professionally Set a high standard of ethics, professionalism, and competency Working Conditions On-Site Monday through Friday 6:00am to 2:30pm PST Safety Requirements All employees are required to follow the site EHS procedures and Coherent Corp. Corporate EHS standards. Quality and Environmental Responsibilities Depending on location, this position may be responsible for the execution and maintenance of the ISO 9000, 9001, 14001 and/or other applicable standards that may apply to the relevant roles and responsibilities within the Quality Management System and Environmental Management System. Culture Commitment Ensure adherence to company's values (ICARE) in all aspects of your position at Coherent Corp.: Integrity - Create an Environment of Trust Collaboration - Innovate Through the Sharing of Ideas Accountability - Own the Process and the Outcome Respect - Recognize the Value in Everyone Enthusiasm - Find a Sense of Purpose in Work Coherent Corp. is an equal opportunity/affirmative action employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law. If you need assistance or an accommodation due to a disability, you may contact us at ****************************** .

US Tech Solutions is a global staff augmentation firm providing a wide-range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit our website ************************ We are constantly on the lookout for professionals to fulfill the staffing needs of our clients, sets the correct expectation and thus becomes an accelerator in the mutual growth of the individual and the organization as well. Keeping the same intent in mind, we would like you to consider the job opening with US Tech Solutions that fits your expertise and skillset. Job Description Duties: Responsible for producing innovative biotherapeutic medicine by interfacing with highly automated production systems and controls in cGMP manufacturing environment, and maintain areas in high state of inspection preparedness. Operates production equipment for Cell Culture Purification that may include process monitoring, sampling, harvesting, purification, formulation and transfer. Performs media/buffer solution preparation operations. Maintains records and clean room environment to comply with regulatory requirements utilizing current Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOP). Essential Technician : Operate systems that clean and sterilize tanks and filtration systems. Prepare solutions for the production process. Review documentation and check all calculations (e.g. tickets, labels, equipment reading). Trouble shoot equipment and process problems. Comply with safety requirements, cGMP, SOP and manufacturing documentation. Use of automation to perform production operations. Provide support to Manufacturing to meet production demands. Operate automated systems for equipment operation. Assemble and prepare equipment for production. Exhibit detail oriented documentation skills Communicate effectively and ability to work in a team environment. Exhibit professional interpersonal skills. Work with coworkers and supervisor to effectively troubleshoot minor equipment and process issues. Follows established safety and environmental guidelines and procedures for all work performed. Immediately reports safety and environmental incidents including injuries, illnesses, near misses, and safety suggestions. Fosters a positive safety culture in which no one gets hurt. Job Matrix A good working knowledge of biopharm technology and processes. Trained and skilled in all operational procedures of at least one manufacturing department. Demonstrated ability to independently document and record information related to the process. Occasionally makes routine decisions based on experience. Identifies and suggests solutions to common basic problems. Recognizes non-routine problems, investigates and suggests potential solutions. Judgment is required in resolving problems and making routine recommendations. Ability to recognize deviation from accepted practices is required. Supplementary Responsibilities : Operate bioreactors, centrifuges, other harvest systems and protein purifications units. Operate and clean fixed tank and filtration systems Operate large scale column chromatography systems. Operate small-scale cell culture areas and systems by operating cleaning, set up, and maintaining 20L bioreactors; inoculating and maintaining spinner seed cultures using aseptic techniques, maintaining cell banks; and performing general seed lab operations. Perform Solution Preparation activities (media and buffer make-up) Clean, assemble, and sterilize equipment using glass washers and autoclaves. Perform automated CIP and SIP of fixed equipment. Qualifications Degree in Life Sciences or engineering and 1 year related experience Or Associate Degree and 3 year experience Or High school and 5 years' experience Biotech certificate from approved program Additional Information Sneha Shrivastava Sr Technical Recruiter 862 - 579 - 4236

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description: Purifies proteins in a regulated FDA licensed and ISO certified facility and performs cross-functional activities associated with downstream production runs in collaboration with Bulk Fill and QC testing groups. The role may include special projects such as process development and validation activities where scientific research principles are applied. Primary responsibilities: Purify recombinant proteins to ensure commercial product demands are met: 1. Works as part of the purification team to perform purification, filtration, and centrifugation operations according to standard operating procedures. 2. Executes laboratory operations including dispensing of chemicals, volumetric and gravimetric measurements, making accurate dilutions, and preparing solutions. 3. Performs SAP duties that include cycle counting, reservations, issuing to process orders, and charging of expiring raw materials. 4. Performs equipment preventative maintenance tasks, column packing, and column testing procedures. 5. Ability to multi-task and become proficient at purifying 14 different proteins and make conjugates. 6. Responsible for ordering raw materials and components, as required. 7. Maintains a safe and well-organized work environment and complies with safety procedures. Follow regulatory requirements: 1. Adheres to valid manufacturing procedures, manufacturing operations, and current good manufacturing practices (cGMP) and ISO requirements. Documentation: 1. Responsible for the completion and review of batch records and logbooks, which requires legible, clear, and concise data entry. 2. Completes all training documentation within a pre-defined timeframe. Analytical Testing: 1. Analyzes in-process samples generated from purification activities. 2. Operates lab equipment such as pH meters, balances, centrifuges, spectrophotometers, HPLC systems, and densitometers. Skills:Must have an understanding of protein purification processes. • Experience following and writing instructions. • Very good verbal and written communication skills. • Computer knowledge required with experience using MS Word and Excel. • Able to document work accurately and has excellent organizational skills. • Experience with preparation of reagents following instructions. • Delivers quality products and services on time to all customers. • Must be attentive to detail. • Effectively manages time. • Considers how all daily manufacturing activities impact product quality. • Monitor processes and products to identify opportunities for continuous improvement. • Able to lift and push up to 35 lbs. 1. Works well in a team environment to manufacture production lots. 2. Complies with cGMP and ISO requirements. 3. Maintains accurate documentation related to manufacturing processes. Education:BA/BS in the sciences (Biology, Engineering, or related field) or 2 years of relevant experience Languages:English Read Write Speak Additional Information Best Regards, Anuj Mehta ************

Who We Are BioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future of human health. Since our founding in 1997, we have applied our scientific expertise in understanding the underlying causes of genetic conditions to create transformative medicines, using a number of treatment modalities. Using our unparalleled expertise in genetics and molecular biology, we develop medicines for patients with significant unmet medical need. We enlist the best of the best - people with the right technical expertise and a relentless drive to solve real problems - and create an environment that empowers our teams to pursue bold, innovative science. With this distinctive approach to drug discovery, we've produced a diverse pipeline of commercial, clinical and preclinical candidates that have well-understood biology and provide an opportunity to be first-to-market or offer a substantial benefit over existing therapeutic options. About Technical Operations BioMarin's Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These engineers, technicians, scientists and support staff build and maintain BioMarin's cutting-edge manufacturing processes and sites, provide quality assurance and quality control to ensure we meet regulatory standards, and procure the needed goods and services to support manufacturing and coordinating the worldwide movement of our drugs to patients. CONTRACT *Shift schedule is Sundays to Tuesdays alternating Saturdays. Hours is 6pm to 7 am. * Duties PROCESS KNOWLEDGE: Understanding of process theory and equipment operation. Ability to learn biopharmaceutical manufacturing processes including mammalian cell culture, depth filtration, tangential flow filtration, column chromatography, centrifugation, protein purification, and formulation of bulk drug substance. Support initiatives for process optimization. Identify and elevate processing issues and support solutions. Gain experience with automation systems (LIMS, MES, PI, etc.). TECHNICAL DOCUMENTATION: Provide feedback and/or suggested changes to operational procedures. Assist in the incorporation of new technologies, practices, and standards into procedures. Capable of writing and reviewing process documents. QUALITY AND COMPLIANCE: Understanding of cGMPs as related to Commercial Operations. Ability to utilize Quality systems (Deviations, CAPAs, Change Requests, Action/Alert Reports, etc.). BUSINESS: Ability to participate on projects and contribute to outcomes. Capability to learn and support new business systems (Track wise, ERP, etc.). Support trending of defined department metrics. WORK ENVIRONMENT/PHYSICAL DEMANDS * Consists of strenuous, repetitive work. The following list of physical movements may be used on a daily basis: bending, reaching, climbing stairs and ladders, kneeling and making numerous equipment connections using hands. * Independently have the ability to regularly lift, dispense, push and/or pull items with an average weight of 25 pounds. * May require work around loud equipment. • The use of personal protective equipment will be required. * Requires various shift based work and off hours. Skills * Strong communication skills-verbal and written * Ability to work in a team environment which includes good conflict resolution and collaboration * Displays good initiative to identify areas for improvement and implement solutions Education * Bachelor's degree in science related area or engineering * Associate's degree in science related area or Biotech certificate with 2+ years of experience in a biotech manufacturing environment or other regulated industry Note: This description is not intended to be all-inclusive, or a limitation of the duties of the position. It is intended to describe the general nature of the job that may include other duties as assumed or assigned. Equal Opportunity Employer/Veterans/Disabled 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. In the U.S, the salary range for this position is $ 15 to $ 30 per hour. The base pay actually offered will take into account internal equity, and may also vary depending on candidate's geographic region, job-related knowledge, skills, and experience amongst other factors. The salary range for this position is: $15 to $30. BioMarin considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans. For additional benefits information, visit:

The Manufacturing Technician is responsible for the production of therapeutic proteins (API) under cGMP conditions. The role involves executing process recipes, following written procedures (SOPs), and monitoring equipment and processes. Additionally, the technician will perform basic laboratory tasks, such as pH and conductivity testing, sampling, and routine sanitization to maintain facility and equipment standards. Training will be provided to ensure compliance with cGMP standards and demonstrate aseptic techniques in handling products and materials. Responsibilities + Set up, operate equipment, and monitor production processes, including clean-in-place (CIP) and steam-in-place (SIP) operations. + Report production in written and electronic documents in accordance with good manufacturing practice (GMPs) and good documentation procedures (GDPs). + Review documentation as appropriate. + Attain qualification for all assigned tasks and maintain an individual training plan. + Perform basic laboratory tasks, such as monitoring pH, conductivity, and testing product samples. + Perform material movements, transferring raw materials and chemicals into, out of, and across production areas. + Maintain facility and equipment through routine cleaning and sanitization, supporting 6S programs. + Engage in administrative tasks, including attending shift exchanges, meetings, sending/receiving emails, and participating in projects. Essential Skills + High School Diploma or Equivalent; AS/BS in a science-related discipline preferred. + 0-3 years of experience, with some prior experience in a manufacturing setting preferred. + Basic laboratory skills and familiarity with cGMP compliance. Additional Skills & Qualifications + Experience in a large, well-known company is advantageous. Work Environment The work environment is structured to support the production of therapeutic proteins under cGMP conditions. The facility emphasizes adherence to safety protocols, cleanliness, and efficiency. The role includes shift work, with routine cleaning and sanitization tasks as part of the 6S program to maintain a high standard of facility and equipment maintenance. Job Type & Location This is a Contract to Hire position based out of Vacaville, CA. Pay and Benefits The pay range for this position is $25.00 - $27.50/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: - Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Vacaville,CA. Application Deadline This position is anticipated to close on Jan 30, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.

Primary Duties & Responsibilities Support manufacturing objectives and goals through various manufacturing techniques used in the optical dicing process. Responsibilities include performing daily operations, inspecting own work, following all safety and environmental guidelines and producing work that demonstrates and promotes company values. Responsible for maintaining a quality work environment that follows company polices, practices, and guidelines. Education & Experience High School diploma or equivalent Basic reading and math skills (add, subtract, multiply, divide) Desirable working experience in manufacturing environment Familiarity with operating automated equipment Ability to read and understand process procedures and inspection criteria Experience with networked PC based computer system (MS Office, spreadsheets, Email, and MRP systems) Skills Capable of applying basic math to product activities Familiarity with precision optics manufacturing Work in environment with open communication Perform tasks independently with minimal guidance from supervisor Ability to follow work priorities and multi-task when needed Good interpersonal and communication skills Set a high standard of ethics, professionalism, and competency Working Conditions Indoor controlled environment Long periods of standing / walking Physical Requirements Processes fine hand / eye motor skills Safety Requirements Company policy is followed regarding all safety, environmental and ergonomic requirements. Responsible for maintaining quality work environment housekeeping standards. Takes responsive action to correct any health or safety hazard found in work area. Initiates corrective measures within 24 hours of hazard identification. Quality and Environmental Responsibilities Follows all applicable work instructions related to the filter testing process Able to use all pertinent test apparatus and record data. Enter data into the appropriate data bases as needed Follows procedures as required, keep current on all process change notices. Depending on location, this position may be responsible for the execution and maintenance of the ISO 9000, 9001, 14001 and/or other applicable standards that may apply to the relevant roles and responsibilities within the Quality Management System and Environmental Management System. Culture Commitment Ensure adherence to company's values (ICARE) in all aspects of your position at Coherent Corp.: Integrity - Create an Environment of Trust Collaboration - Innovate Through the Sharing of Ideas Accountability - Own the Process and the Outcome Respect - Recognize the Value in Everyone Enthusiasm - Find a Sense of Purpose in Work Coherent Corp. is an equal opportunity/affirmative action employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law. If you need assistance or an accommodation due to a disability, you may contact us at ****************************** .

Who We Are BioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future of human health. Since our founding in 1997, we have applied our scientific expertise in understanding the underlying causes of genetic conditions to create transformative medicines, using a number of treatment modalities. Using our unparalleled expertise in genetics and molecular biology, we develop medicines for patients with significant unmet medical need. We enlist the best of the best - people with the right technical expertise and a relentless drive to solve real problems - and create an environment that empowers our teams to pursue bold, innovative science. With this distinctive approach to drug discovery, we've produced a diverse pipeline of commercial, clinical and preclinical candidates that have well-understood biology and provide an opportunity to be first-to-market or offer a substantial benefit over existing therapeutic options. From research and discovery to post-market clinical development, our WWRD engine involves all bench and clinical research and the associated groups that support those endeavors. Our teams work on developing first-in-class and best-in-class therapeutics that provide meaningful advances to patients who live with genetic diseases. These positions are for the 6pm to 7am shift from Wednesday to Saturday, with every other Saturday off. $28 hour Note: This description is not intended to be all-inclusive, or a limitation of the duties of the position. It is intended to describe the general nature of the job that may include other duties as assumed or assigned. Equal Opportunity Employer/Veterans/Disabled 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.