BIOTECH jobs in CA

Thousand Oaks, California

•

Today

Job Description: AgreeYa is a global Systems Integrator and is seeking an Project Manager to join our growing team. Key Responsibilities: Agile Delivery & Project Leadership Lead Agile ceremonies (planning, reviews, retrospectives, stand-ups) and ensure teams operate with strong discipline, transparency, and continuous improvement. Build and maintain detailed project plans, sprint schedules, work breakdown structures, and task assignments. Track progress against key milestones, escalating time

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Full-time

Depends on Experience

SAP Manufacturing & MES Integration Lead

Hybrid in Irvine, California

•

Today

Candidate must have deep functional knowledge of Manufacturing in SAP S4HANAAt least 10 years experience in SAP Manufacturing & MESExperience designing and developing integration between SAP & MESRollout of new Manufacturing Unit in SAP and MESDeep expertise in Pharma ManufacturingAt least two hands on upgrades in SAP S4HANAExcellent executive communication skills.Must have run Steering Committee meetings. Infant Selvin Senior Recruiter NexInfo infantselvin(dot) Thomas -at- nexinfo -dot- com

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Contract, Third Party

75 - 80

SAP Test Automation Delivery Lead

Remote or Hybrid in California

•

Today

Job Title: SAP QA Automation ( Tosca ) Lead Duration: 18 Months+ Location PST - 100% Remote Exp. Level: 10+ years Job Description Our client is looking for a TOSCA certified automation engineer who has experience to Lead automation strategy and delivery across SAP implementation projects, ensuring consistency and compliance (GxP, FDA). Client is looking for Pharma / BioTech domain in background. Key Responsibilities: Lead automation strategy and delivery across SAP implementation projects, ensu

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Full-time, Contract

BASED ON EXPERIENCE

Senior Engineer

Thousand Oaks, California

•

Today

Payrate: $42.00 - $44.00/hr. Summary: The position works in partnership with the maintenance, process development, project management, engineering technical authority, and manufacturing to develop project scope, schedule, budget and lead the implementation workstream. Responsibilities include working closely with Quality Assurance (QA) for GMP and Safety for safety compliance. The engineer will support the projects in defining strategies for systems verification and will work with the process de

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Contract

$42 - $44 hr

GXP / GMP Data Integration Engineer

Vacaville, California

•

Today

Senior Data Integration Engineer Location: Vacaville, CA Duration: - 6-12 Months+ Company: A leading organization in the Biotech, Pharma, or Healthcare IT sector. About the Role: We are seeking a highly skilled and analytical Senior Data Integration Engineer to play a pivotal role in architecting and delivering high-impact data solutions. This position is ideal for a professional who excels at bridging technical execution with strategic project leadership. You will be responsible for leading the

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Contract

Depends on Experience

Sr. Business Systems Analyst

Hybrid in South San Francisco, California

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15d ago

Local San Francisco Bay Area candidates only! Client is looking for candidates that can work onsite for 3 to 4 days a week. Direct W2 contractors only! No 3rd party agencies! No out of area candidates! We are not able to sponsor H1B Visa's Start date: November 12 month duration Global biotech company is looking for a Sr. Business Systems Analyst that will be responsible for taking requirements and doing discovery for a lab. This is a 2 year project. Skills required: 7 to 10 years experience as b

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Contract

$80 - $85

Regulatory Affairs Consultant

Remote

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7d ago

Position: Senior Manager, Regulatory Affairs Location: Remote We are seeking an experienced Senior Manager, Regulatory Affairs to support global regulatory activities and key submission deliverables for our growing biotech organization. This role is well-suited for someone who is hands-on, highly organized, and comfortable working in a lean, fast-paced environment.Key ResponsibilitiesSupport global regulatory strategy and execution for U.S. and ex-U.S. programs.Lead and coordinate IND/CTA subm

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Full-time

Depends on Experience

Veeva RIM BA (Documentation Specialist)- Foster City, CA(Hybrid)

Foster City, California

•

Today

Amtex Systems Inc is an information technology and talent solutions company offering talent and BI consulting to the companies in US for over 25 years. Our solutions are designed to fill resource gaps, by providing the right candidates who deliver value to the organization. Our propensity to nurture and build strong relationships with our clients helps us better understand their business demands and gives us the ability to provide services that are on time and rise above the rest. Job Title:

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Third Party, Contract

Engineer

Thousand Oaks, California

•

Today

Note: Onsite USTO - Will be onsite at least 2x/ week. Candidate must be within commutable distance and must be able to come on site 5 days a week if needed. Bippharm or Biotech experience and/or Equipment Validation experience within another industry. Position is split between lab and office. Job Details: Position involves support of senior staff in the initiation, design, and delivery of projects, particularly for container closure integrity testing (CCIT) related scope. Employ basic engine

Full-time

Computer System Validation (CSV) Engineer

Vacaville, California

•

Today

Computer System Validation Location: Vacaville CA (Onsite Role) Duration: - 6 -12 Months+ Job Requirements As a Computer System Validation (CSV) Engineer specializing in the pharmaceutical industry, you will ensure that computer-based systems such as Manufacturing Execution Systems (MES), process control software, and automation platforms comply with GxP, FDA 21 CFR Part 11, EU Annex 11, and other applicable regulations. Key Responsibilities: Develop, execute, and review validation deliverable

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Contract

Depends on Experience

Senior Medical Director Clinical Development

South San Francisco, California

•

Today

Job DescriptionSenior Medical Director, Clinical Development San Francisco Bay Area (On-site 3 4 days/week) Our client, a clinical-stage biotechnology company advancing next-generation GPCR-targeted therapeutics, is seeking a Senior Medical Director to lead strategy and execution across clinical development. This role will serve as the Clinical Development Lead for a key program, shaping trial design, guiding cross-functional alignment, and supporting regulatory interactions. Note: This opportu

Full-time

Compensation information provided in the description

AWS Infrastructure Qualification & Validation Specialist

California

•

Today

Job Description (JD): For a role focused on Infrastructure Qualification and Validation Documentation for AWS-tailored for regulated environments like pharma, biotech, or any GxP-compliant organization. We are seeking a skilled professional to lead and execute Infrastructure Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) documentation for AWS-hosted environments. This role is critical in ensuring our cloud infrastructure meets regulatory compliance standar

Full-time

Senior CQV Engineer

Thousand Oaks, California

•

Today

Job Summary : The Senior CQV Engineer will play a critical role in the successful startup and qualification of a new early-phase clinical biomanufacturing facility, encompassing cleanrooms, utilities, and a wide range of systems and equipment. This position is responsible for planning, executing, and documenting commissioning, qualification, and validation (CQV) activities to ensure all systems meet stringent regulatory and client-specific requirements Roles & Responsibilities: uthoring, editin

Full-time

GMP Shipping and Logistics Specialist

Santa Clarita, California

•

Today

Job Description: GMP Shipping and Logistics Specialist Overview Shipping and Logistics Specialist is responsible for coordinating and executing all domestic and international shipping activities for small molecule drug substances and drug product samples between our vendors, including Good Manufacturing Practice (GMP) samples. This role ensures strict adherence to all applicable regulatory requirements (e.g., FDA, EMA, IATA, DOT), maintaining product integrity and a full chain of custody/identi

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Contract

$75

CMC Project Management Consultant

Santa Clarita, California

•

Today

Job Description We are seeking an experienced CMC Project Manager to oversee and drive cross-functional development programs for small molecule therapeutics. This role will provide leadership and coordination across CMC, non-clinical, clinical, and regulatory functions, ensuring that programs are executed on time, within budget, and in compliance with global regulatory standards. The ideal candidate possesses broad expertise in drug development, strong organizational skills, and the ability to

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Contract

$150

Senior Validation Engineer

Thousand Oaks, California

•

Today

Job Description: This position is responsible for planning, executing, and documenting commissioning, qualification, and validation (CQV) activities to ensure all systems meet stringent regulatory and client-specific requirements. The Senior Validation Engineer will act as a subject matter expert, collaborating closely with cross-functional teams, including Manufacturing, Facilities, Quality Control and Quality Assurance to deliver robust validation strategies that enable compliant and efficient

Full-time

SAP Solution Architect [ OTC & Logistics & MM ]

Remote

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14d ago

Job Title: SAP Solution Architect OTC & Logistics & MM (Life Sciences) Location: Remote Experience Level: 15+ years in SAP Consulting Role Overview We are seeking an experienced SAP Solution Architect with deep expertise in Order-to-Cash (OTC) and Logistics Execution (LE) processes and secondary skills in Material Management (MM). The ideal candidate will have a strong understanding of end-to-end business processes, preferably within the Life Sciences industry, and a proven track record of deliv

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Contract

Depends on Experience

SDET

Remote

•

2d ago

Please note I have direct access to the Hiring Director on this position. Compensation: Base Salary + Bonus: 10% Position is 100% Remote This is an outstanding opportunity for a SDET to work on and test brand new mission critical bleeding edge products that actually save lives. We are the leading Global Biotech Company in our niche and are looking for a Sr. SDET due to company growth. We have been in business for 50+ years, are publicly traded, have 7+K global employees, have $5.2B in revenues (

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Full-time

$120,000 - $160,000

Clinical eTMF Consultant

Remote or Massachusetts

•

Today

Job Title: Clinical eTMF Consultant Department: Clinical Operations Position Summary: The Clinical eTMF Specialist is responsible for managing and maintaining the Electronic Trial Master File (eTMF) system to ensure compliance with regulatory requirements, internal quality standards, and study timelines. This role ensures that all clinical trial documentation is complete, accurate, and inspection-ready at all times. The eTMF Specialist serves as a key liaison between Clinical Operations, Qual

Contract, Third Party

DevOps Systems Engineer Consultant

Hybrid in San Diego, California

•

Yesterday

About The Role We are partnering with a groundbreaking biotech organization in its early clinical stages to identify a skilled and motivated DevOps Systems Engineer for a contract-to-hire opportunity. This role will play a pivotal part in maturing internal DevOps practices and supporting critical infrastructure as the company transitions from early-stage operations into a more regulated, GMP-compliant environment. The position is hybrid, with 3 days a week onsite in San Diego, and is ideal for s

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Contract

Depends on Experience

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BIOTECH jobs in California, USA