Plant Pathologist Salary at Voeks Inc BETA

Director, Pharmacovigilance Quality Hybrid Role - 3x per week in Redwood City, CA Key Responsibilities Oversee the development and implementation of pharmacovigilance (PV) quality and compliance programs to ensure adherence to global regulatory requirements. Lead internal and external audits, inspections, and quality assessments, identifying areas for improvement and ensuring corrective and preventive actions (CAPAs) are effectively implemented. Develop and maintain pharmacovigilance quality management systems (QMS), including policies, procedures, and training programs, to drive a culture of compliance and continuous improvement. Collaborate with cross-functional teams, including regulatory affairs, drug safety, and clinical operations, to align PV quality initiatives with broader organizational goals. Key Qualifications 10+ years of relevant industry experience, 5+ specifically in a PV leadership role Proven experience in audit and inspection management Experience supporting GVP QA f

Director, GCP QA Compliance Our biotech partner is a well-established, commercially successful clinical stage biotech that is seeking a Director of Clinical Quality Assurance to lead the CQA function and build/manage a team. This role will oversee CQA strategy across policies, SOPs, deviations, change control, CAPAs, and vendor audits. This is a great opportunity for a Clinical QA leader to help progress a robust pipeline of therapeutics across oncology, neurology, endocrinology, and more areas. This position will be 3 days onsite in Redwood City, CA. Responsibilities: Lead Clinical Quality Assurance as a manager to the CQA team supporting various therapeutic area programs in support of successful clinical studies Lead GCP audit strategy including audits of investigative sites, clinical vendors, internal department, TMF, and study documents Represent QA on clinical teams to provide compliance assessment and advice Manage clinical inspections by regulatory bodies across internal and ext

Director/Associate Director of Quality Control and Analytical Development (QC) We’re partnering with a leading cellular therapy organization that is seeking a highly motivated Director of Quality Control (QC) and Analytical Development with expertise in mAbs, ddPCR, flow cytometry, and cell-based assay methods. This role offers an exciting opportunity to lead quality initiatives supporting cellular therapies within a GMP environment. Key Responsibilities: Conduct GMP In-Process Control (IPC), lot release, and stability testing using ddPCR, flow cytometry, and cell-based methods. Lead method optimization, transfer, qualification, and validation for clinical drug product testing. Prepare detailed and organized reports and presentations describing analytical results. Facilitate cross-functional training and continuous improvement within the QC team. Develop and maintain Quality Control (QC) and Quality Management System (QMS) standards to align with internal and global regulatory requirem

⚡ Role: Principal Process Engineer 💼 Industry: Bioprocessing/Biotechnology 🌎 Location: San Francisco, CA 💰 Salary: Competitive (Based on Experience) ⚡ Principal Process Engineer A pioneering company at the forefront of bioprocess engineering is scaling its commercial operations, with an innovative approach to cell culture technology. With a state-of-the-art facility in San Francisco, CA, they are driving advancements in large-scale biomanufacturing. As they continue to evolve, they are seeking a Principal Process Engineer to lead the start-up, commissioning, troubleshooting, and optimization of new large-scale bioprocess equipment, including a 20,000L cell culture bioreactor, media preparation systems, CIP, and cell separation technologies. This highly hands-on role requires deep technical expertise across bioprocess instrumentation, pumps, valves, controls, and automation systems. This position will play a key role in supporting scale-up activities, driving process improvements, an

I’m working with a commercial-stage oncology biotech that’s making waves with its innovative approach to cancer treatment. They’re looking for a Director of Clinical Quality Assurance to join their growing team and take the lead on all things GCP. If you're passionate about quality, love rolling up your sleeves, and want to make a real impact in oncology drug development, this could be a great fit. Why this role stands out: Highly visible leadership opportunity in a fast-paced, mission-driven biotech On the cutting edge of oncology – multiple assets in development, including in immunotherapy Close-knit team with an emphasis on collaboration, transparency, and scientific rigor Great work-life balance with flexible hybrid setup (on-site 3 days/week) What you’ll be doing: Lead the development, implementation, and oversight of the GCP Quality System across clinical programs Act as the primary QA point of contact for clinical development and cross-functional teams Drive inspection readiness

Job Description Job Description We are seeking a Production Assembler to join our team! You will work on a production assembly line performing standardized work defined by work instructions. Responsibilities: Performing standardized work process and following defined work instructions and sequences at a defined pace, repetitively for an extended period of time, and rotating as required. Performs on-line inspections to ensure parts and assemblies meet production specifications and standards. Must be a self-starter capable of managing own activities as well as supporting team activities. Be able to use hand tools, screwdrivers, wrenches, torque drivers, and other small tools Ability to quickly come up to speed on novel assembly procedures and custom tooling or test methods Operate complex manufacturing equipment Escalating functional and process failures to the appropriate support groups and leaders Adhere to all safety policies and procedures Qualifications: Punctuality and a profession

Salary : $153,299.90 - $231,000.12 Annually Location : San Jose Job Type: Full-Time Job Number: 202500946 Department: Environmental Services Opening Date: 03/21/2025 Closing Date: 4/15/2025 11:59 PM Pacific Our diverse and inclusive workforce of more than 7,000 employees play a key role in the success of San Jos, the heart of the Silicon Valley. All City of San Jos employees work together as one team to make San Jos a vibrant, innovative, and desirable place to live and work. Visit to learn more about our One Team Leadership Values and Expectations, including quality and excellent customer service and here to learn more about San Jos. The City of San Jos is an equal opportunity employer. Applicants for all job openings will be considered without regard to age, race, color, religion, sex, national origin, sexual orientation, disability, veteran status or any other consideration made unlawful under any federal, state or local laws. The City of San Jos is committed to offering reasonable

Quality Control Associate Shift/Hours: Monday - Friday, First Shift 8:00 am-5:00 pm Pay Rate: $25-$30 per hour Location: San Jose, CA Experience: 6+ months of QCQA experience We are excited to share a new opportunity for a Quality Control Associate / QC - QA located in San Jose! This position is highly sought after and might not be available for long. Are you working, but looking to explore? Are you needing a new career opportunity? Give us a call at 408-298-6775 and/or apply directly to this posting for immediate consideration! Don't delay, apply today! Quality Control Associate Job Duties include: Approve incoming material by confirming specifications Document inspection results Complete company reports and logs Maintain a safe and healthy work environment Conduct various quality inspection tests & assessments Record quality results Quality Control Associate Preferred Skills include: Safety management experience Self-motivated and team-oriented Able to work with multiple departments