Lead Operator Salary at The Press Democrat BETA

Regional Director - Civil & Environmental - California Our client is seeking a dynamic Regional Director to lead operations across its California footprint, with a primary base in the Bay Area, Los Angeles or San Diego. This role is responsible for the strategic growth, profitability, and operational performance across multiple locations, comprising a talented staff of 50+ professionals. This is an opportunity for a forward-thinking leader to shape regional direction, drive cross-functional collaboration, and deepen impact across public and private sector markets. Key Focus Areas Strategic Business Leadership: Drive the development and execution of regional business plans aligned with California and Western U.S. growth objectives. P&L and Financial Oversight: Manage office-level performance including revenue, utilization, cash flow, and overhead—working in concert with broader regional metrics. Talent and Team Development: Inspire and lead multidisciplinary teams, building a culture of

*Remote* Director, GxP Quality Assurance Remote (West Coast working hours) Our client is a late-stage biologics company focused on treatments for autoimmune diseases and cancer. They are looking for a Director of GxP QA to lead the quality team and help build a scalable quality management system to support their clinical and future commercial efforts. Responsibilities Oversee and enhance GxP compliance across GMP, GCP, and GLP functions Lead development and implementation of the Quality Management System Manage quality processes: deviations, CAPAs, change control, audits, training, and documentation Support regulatory inspection readiness and ensure ongoing compliance Drive continuous improvement and risk-based decision-making across teams Partner cross-functionally on clinical development, tech transfer, and vendor oversight Requirements Bachelor’s or Master’s in a relevant science or engineering field 4–6+ years of QA/GxP experience in biotech, pharma, CRO, or CDMO settings Deep know

I'm partnering with a well-funded, pre-IPO biotech company in the Bay Area that’s developing cutting-edge therapies in a highly specialized space. As they prepare to scale their clinical programs, they’re looking to bring on a Director of Clinical GMP Quality to lead and evolve their quality systems through this critical phase of growth. This is a high-impact role offering visibility, influence, and the chance to shape quality strategy in a science-driven environment. If you’re looking for an opportunity to build, lead, and make your mark at a nimble and ambitious biotech—this could be a strong fit. What You'll Do: Lead Clinical GMP Quality activities including oversight of CMOs, QA batch review, and clinical material release Build and enhance quality systems in preparation for future growth and regulatory milestones Collaborate cross-functionally with Manufacturing, Regulatory, and Clinical teams to ensure compliance across early-stage programs Provide quality leadership during audits

We are partnered with a growing biotech organization that is seeking a Senior Manager of Upstream Manufacturing. This role is focused on leading cell culture manufacturing oversight across a network of CDMOs. They will represent the upstream function internally and externally. This is a great opportunity for someone who is interested in creating therapeutics for serious autoimmune and cancer indications, which are in clinical trials. The ideal candidate will work remotely, ideally be based on the West Coast, and travel to vendors as needed. Responsibilities: Provide technical oversight and guidance for upstream manufacturing to CDMO teams, fostering strong working relationships and supporting manufacturing operations Troubleshoot and evaluate manufacturing processes, parameters, and specifications to ensure product quality and consistency Manage internal quality systems including change controls, deviations, CAPAs, and review of batch records and trends (OOT/OOS) Author and review tech

Job Description: Senior Manager of Manufacturing Location: Santa Rosa, CA Company: NeilMed Company Overview NeilMed operates a global distribution network that requires our products to be manufactured in multiple languages. Our facilities produce dry powder and liquid products and assemble medical devices. With approximately 600 employees, we manufacture both sterile and non-sterile products. Our manufacturing company operates three shifts five days a week, with additional Saturday and Sunday shifts during peak demand periods. Our multilingual production staff communicate in English, Spanish, and several other languages. NeilMed consistently invests in advanced manufacturing equipment to enhance efficiency and prepare for growth without significant increases in manpower. Our clean and safe manufacturing facility produces close to one million cases for shipment each year. Summary of Responsibilities NeilMed is seeking a dynamic and experienced Senior Manager of Manufacturing to join our

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

⚡ 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

Vitality Bowls is a health minded, nutritionally conscious, energetic company, focused on the customer experience. Be a part of a fun, dynamic, growing team committed to bringing healthy food to the community! Originating in San Ramon, Vitality Bowls specializes in Aa bowls, fresh juice, smoothies, panini and salads. Vitality Bowls Shift Leader Job Description: Lead the team, making sure food is made accurately and taken to customers in a timely manner In charge of shifts and delegating tasks Show exemplary knowledge of the job and excellent customer service Deal with upset customers/problems with food in a polite way, making sure the customer is happy Accept deliveries, making sure that deliveries are complete and correct or that refunds are issued Communicate with managers/owners about the status of inventory; whether everything arrived on time and orders came complete and correct; whether any items in the store are running low Check daily petty cash and go to the bank for change if