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California, (TPMG) is one of the largest medical groups in the nation with over 10,000 physicians, 21 medical centers, numerous clinics throughout Northern and Central California and an 80-year tradition of providing quality medical care. Surrounded by a breathtaking landscape and shaded by towering Redwood trees, Kaiser Permanente’s Santa Rosa Medical Center is nestled between winding grapevines, rolling hills, mountains, and beaches nearby.

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The Permanente Medical Group, No. California, (TPMG) is one of the largest medical groups in the nation with over 10,000 physicians, 21 medical centers, numerous clinics throughout Northern and Central California and an 80-year tradition of providing quality medical care.TPMG is recruiting for a full-time Radiologist to join our team in beautiful Santa Rosa, California.Surrounded by a breathtaking landscape and shaded by towering Redwood trees, Kaiser Permanente’s Santa Rosa Medical Center is nestled between winding grapevines, rolling hills, mountains, and beaches nearby. Just 55 miles north of San Francisco and the fifth-largest city in the Bay Area, Santa Rosa boasts some of the most diverse and stunning scenery in the region. With its breathtaking surroundings, top-rated schools and welcoming communities, Santa Rosa is an excellent place to live, work, and play. It’s rich in culture, light on traffic and most importantly, full of opportunity. Especially with The Permanente Medical Group, Inc.SANTA ROSA/SONOMA COUNTY OFFERS: <ul><li>An opportunity to live and work in the same community - most of our physicians live in Sonoma County.</li><li>Ample opportunities to pursue your own health and wellness while working hard to encourage your patients to do the same.</li><li>Something for everyone: from the trails at Howarth Park and in Sebastopol to wide-open spaces to kayaking in Spring Lake or on the Russian River to a vibrant arts scene.</li><li>Farm to Table: summer nights at Coppola Winery with a live Salsa band to the first signs of Spring in Windsor to Hale’s Apple Farm in Sebastopol and jogging through the Fall colors in Healdsburg.</li><li>A taste of the Good Life and everything in between – redwood groves, coastal views, whale watching, and rolling farmland.</li><li>Easy access to San Francisco, Lake Tahoe, and San Jose.</li></ul>To learn more about Sonoma County, copy & paste this link into a browser: permanente.org/sonomaFull-time annual salary range is $514,139 - $530,040 plus additional potential incentives*. Reduced schedules with pro-rated compensation may be available. *Some incentive opportunities are estimates based on potential premium pay, approval requiredREQUIREMENTS: <ul><li>Board Certification or Eligibility</li><li>Must be eligible to obtain a CA medical license or be currently licensed to practice within CA </li></ul>A FEW REASONS TO CONSIDER A PRACTICE WITH TPMG:<ul><li>Work-life balance focused practice, including flexible schedules and unmatched practice support.</li><li>We can focus on providing excellent patient care without managing overhead and billing. No RVUs!</li><li>We are committed to cultivating and preserving an inclusive environment for all physicians and employees. We are an equal opportunity employer and VEVRAA Federal Contractor.</li><li>Multi-specialty collaboration with a mission-driven integrated health care delivery model.</li><li>We are Physician-led and develop our own leaders.</li><li>Professional development opportunities in teaching, research, mentorship, physician leadership, and community service.</li></ul>EXTRAORDINARY BENEFITS:<ul><li>Competitive compensation and benefits package, including comprehensive vision, medical, and dental</li><li>Interest Free Home Loan Program up to $250,000 (approval required)</li><li>Relocation Assistance up to $10,000 (approval required)</li><li>PSLF Eligible Employer</li><li>Paid holidays, sick leave, and education leave</li><li>Shareholder track</li><li>Three retirement plans, including a pension plan and 401(k)</li></ul>To learn about General Radiology and subspecialty opportunities, visit TPMG Physician Careers at: https://northerncalifornia.permanente.orgWe are an equal opportunity employer and VEVRAA Federal Contractor.

Kaiser Permanente - The Permanente Medical Group, Inc. -Northern California

Radiology Opportunity in Santa Rosa, CA | The Permanente Medical Group

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Education/Work Experience: Bachelor’s degree or equivalent preferably in an engineering, chemistry and/or biology or related field with 5+ years manufacturing production experience or 2-5 years of supervisory experience in a regulated environment, or equivalent combination of education and experience. Actual compensation will be provided in writing at the time of offer, if applicable, and is based on several factors we believe fairly and accurately impact compensation, including geographic location, experience, knowledge, skills, abilities, and other job permitted factors.

<div>The Production Supervisor II will supervise front-line employees in a chemical/reagent manufacturing or instrument assembly environment. You will plan and assign work to direct labor personnel, implement policies and procedures and recommend improvements in production methods, equipment, operating procedures and working conditions within established delivery, quality, compliance, safety, budget and cost standards.How You’ll Make An Impact: <ul><li> Hiring, training, coaching and managing a large production team of instrument assemblers and technicians </li><li> Responsible for meeting KMI’s such as production schedules, quality standards, production yield, scrap targets, safety metrics, budget etc. </li><li> Assignments are typically in the form of goals e.g. leading kaizen projects or Continuous Improvement (CI) and Safety programs. Drives lean implementation on the manufacturing lines. </li><li> Participates in Root Cause Analysis teams and supports with data analyses and presentation. </li><li> Solid understanding of change control, Identifies document updates and implements and executes training through Change request process </li><li> Supervises production assembly and packaging according to established processes, techniques and policies. </li><li> Schedules, assigns and manages the daily activities of a team. </li><li> Monitors employee performance and prepares and communicates performance reviews. </li><li> Coaches and trains personnel in their duties. </li><li> Assists in the development of documentation procedures. </li><li> Responsible for meeting key metrics such as production schedules, quality standards, production yields, cost targets and the like. </li><li> Monitors processes and makes adjustment to stay within schedule, budgets and established targets. </li><li> Participates in a variety of standing meetings. </li><li> Communicates priorities, performance results and objectives to team members. </li><li> Troubleshoots production issues and escalates as appropriate. </li><li> Participates on project teams as needed. </li><li> Interviews and selects personnel </li><li> Makes salary recommendations based upon individual performance </li></ul>Same as the previous level plus: <ul><li> Provides skilled technical and process guidance for resolution of production problems. </li><li> Develops objectives to meet production requirements, quality standards, control scrap, cost and budget targets. </li><li> Prepares operating procedures and standards that are reviewed by management. </li><li> Provides input and assists with the establishing of annual budgets. </li><li> Tracks expenses against budgets, and controls expenses. </li><li> Addresses customer concerns. </li><li> Work with employees on their development and career goals</li></ul>What You Bring: <ul><li> Education/Work Experience: Bachelor’s degree or equivalent preferably in an engineering, chemistry and/or biology or related field with 5+ years manufacturing production experience or 2-5 years of supervisory experience in a regulated environment, or equivalent combination of education and experience. </li><li> Strong Communication and interpersonal skills </li><li> Knowledge of regulatory requirements and Solid understanding of compliance standards and requirements, e.g., FDA, GMP, ISO, etc. </li><li> SAP experience is required with high level of proficiency with MS office and project management experience. </li><li> Experienced with the introduction of new products, process scale up and the transfer of products to other manufacturing locations with Lean manufacturing experience. </li><li> Full knowledge of assigned products. </li><li> Strong analytical, communication, and project management skills. </li><li> Knowledge of inventory management, demand flow technology, production processes and related technologies. </li><li> Relevant certifications or training a plus.</li></ul>Location: This position must be based in Hercules, California and requires the employee to be located within commuting distance of the office. Total Rewards Package: At Bio-Rad, we’re empowered by our purpose and recognize that our employees are as well. That’s why we offer a competitive and comprehensive Total Rewards Program that provides value, quality, and inclusivity while satisfying the diverse needs of our evolving workforce. Bio-Rad's robust offerings serve to enrich the overall health, wealth, and wellbeing of our employees and their families through the various stages of an employee’s work and life cycle. Benefits: We’re proud to offer a variety of options, including competitive medical plans for you and your family, free HSA funds, a new fertility offering with stipend, group life and disability,  paid parental leave, 401k plus profit sharing, an employee stock purchase program, a new upgraded and streamlined mental health platform, extensive learning and development opportunities, education benefits, student debt relief program, pet insurance, wellness challenges and support, paid time off, Employee Resource Groups (ERG’s), and more!  Compensation: The estimated base salary range for this position is $86,600 to $119,200 at the time of posting. Actual compensation will be provided in writing at the time of offer, if applicable, and is based on several factors we believe fairly and accurately impact compensation, including geographic location, experience, knowledge, skills, abilities, and other job permitted factors. This position is eligible for a variable annual bonus, which is dependent upon achievement of your individual objectives and Company performance.Who We Are: For 70 years, Bio-Rad has focused on advancing the discovery process and transforming the fields of science and healthcare. As one of the top five life science companies, we are a global leader in developing, manufacturing, and marketing a broad range of high-quality research and clinical diagnostic products. We help people everywhere live longer, healthier lives. Bio-Rad offers a unique employee experience with collaborative teams that span the globe. Here, you are supported by leadership to build your career and are empowered to drive change that makes an impact you can see.  EEO Statement: Bio-Rad is an Equal Employment Opportunity/Affirmative Action employer, and we welcome candidates of all backgrounds. Veterans, people with physical or mental disabilities, and people of all race, color, sex, sexual orientation, gender identity, religion, national origin and citizenship status are encouraged to apply. Agency Non-Solicitation: Bio-Rad does not accept agency resumes, unless the agency has been authorized by a Bio-Rad Recruiting Representative. Please do not submit resumes unless authorized to do so. Bio-Rad will not pay for any fees related to unsolicited resumes. Fraud Alert: Bio-Rad has received reports of individuals posing as Bio-Rad recruiters to obtain information, including personal and financial, from applicants. Beware of these fake "recruiters" and job scams. <a href="https://nam04.safelinks.protection.outlook.com/?url=https%3A%2F%2Fcareers.bio-rad.com%2Fonline-recruitment-fraud-alert&data=05%7C02%7Cralph_boquilon%40bio-rad.com%7C8d9650cd4e8f46d99f8c08dc4acbdd6c%7Cef0aebeb2af047a3b8ae5665f8a62d11%7C0%7C0%7C638467486669437441%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C0%7C%7C%7C&sdata=wjGJlszw7FfJBcWTjjq2gGZMbgtTzBbFV5I7P%2F9aW0o%3D&reserved=0" rel="nofollow noopener noreferrer" target="_blank">Click here</a> for more information on this scam and how to avoid it. #LI-KD2</div><div>Legal Entity: (USA_1000)Bio-Rad Laboratories, Inc.</div>

Bio-Rad Laboratories, Inc.

Production Supervisor II

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Supervise production personnel and activities to consistently meet customer requirements across commercial products, new product introductions, and clinical builds, ensuring every output supports high-quality patient outcomes. Lead the team in achieving production goals across Safety, Quality, Service, and Cost, fostering a results-driven environment that balances operational excellence with smart, forward-thinking decision-making.

Overview:
Join our high-impact Production team as the Production Supervisor at Endologix!  WHO WE ARE: Endologix LLC is a California-based global medical device company dedicated to improving patients’ lives through innovative therapies for the interventional treatment of vascular disease. Our therapeutic portfolio addresses clinically relevant unmet needs, spanning from abdominal aortic aneurysms to lower limb peripheral vascular disease. We are committed to delivering excellent clinical outcomes through precision in product design, advanced manufacturing, and comprehensive physician training—supported by industry-leading clinical evidence. At Endologix, we’re driven by purpose, innovation, and the opportunity to make a lasting impact in vascular health. What sets us apart is not just our technology, but our culture. At Endologix, we foster a forward-thinking, mission-driven environment where every team member plays a vital role in advancing patient care. Our core values guide how we operate. As for our people? We empower them with the tools, trust, and continuous learning they need to grow. If you’re passionate about making a meaningful difference in healthcare, you’ll find purpose and belonging here. Our Core Values are the guiding principles informing our choices and actions, because our customers and patients depend on us:<ul><li>Patient Outcomes Drive Us: We improve lives with every advancement we deliver.</li><li>Integrity Defines Us: We do what’s right, stay transparent, prioritize quality, and own our actions.</li><li>Innovation Advances Us: We stay curious, adaptable, and push boundaries.</li><li>Boldness Propels Us: We take smart risks and are unafraid in our pursuit of excellence.</li><li>Collaboration Unites Us: We partner across teams and with physicians to drive exceptional results.</li></ul>  ABOUT THE ROLE: The Production Supervisor is responsible for providing leadership to manufacturing personnel to produce high quality products for our customers. Responsibilities include direct management of production personnel, fulfillment of the production schedule, and ensuring quality compliance. Provide operations expertise to the supervision and support of manufacturing personnel to achieve New Product Development, Continuous Improvement, Quality, Compliance and Operational metrics. Supervise the activities of employees in the production area. Ensure that daily production schedules are met, manufacturing procedures are followed, and all production personnel are trained in those procedures. Ensure fair and equitable treatment of all employees by following company policies and department guidelines.

Responsibilities:
WHAT YOU'LL DO:<ul><li>Supervise production personnel and activities to consistently meet customer requirements across commercial products, new product introductions, and clinical builds, ensuring every output supports high-quality patient outcomes.</li><li>Lead the team in achieving production goals across Safety, Quality, Service, and Cost, fostering a results-driven environment that balances operational excellence with smart, forward-thinking decision-making.</li><li>Champion a culture of safety, accountability, and respect by promoting an injury-free work environment, maintaining high employee morale, and reinforcing adherence to standards and best practices.</li><li>Ensure full compliance with quality systems (FDA, GMP, QSR, ISO), product specifications, and company policies, upholding integrity through disciplined execution and transparent management of non-conformances and corrective actions.</li><li>Continuously challenge processes and team performance to deliver efficient, cost-effective solutions, encouraging innovation and calculated risk-taking to improve outcomes.</li><li>Establish clear performance expectations, drive accountability, and recognize contributions, fostering a collaborative team environment built on trust and shared success.</li><li>Administer and execute company policies and procedures consistently, ensuring alignment across individuals and team structures.</li><li>Track, analyze, and communicate key performance metrics, leveraging data-driven insights to guide decisions and drive continuous improvement.</li><li>Maintain timecards and attendance records, proactively planning for coverage needs and adapting to workforce fluctuations with agility.</li><li>Effectively manage shifting priorities and competing demands, demonstrating flexibility and resilience in a dynamic production environment.</li><li>Proactively identify and mitigate potential failure modes related to quality or business risks, reinforcing a culture of ownership and continuous improvement.</li><li>Recruit, develop, and retain top production talent, building a high-performing team equipped to meet evolving business and customer needs.</li><li>Assess and address training needs, ensuring employees are fully prepared and confident before undertaking responsibilities.</li><li>Drive lean manufacturing initiatives to enhance quality, improve productivity, reduce costs, and streamline cycle times, while empowering the team through education and engagement.</li><li>Forecast material, tool, and supply requirements, coordinating effectively to ensure seamless production flow and operational readiness.</li><li>Support ERP-related activities, including accurate entry of work order information as needed.</li><li>Monitor inventory levels and collaborate closely with Planning to ensure alignment and efficiency in daily operations.</li><li>Troubleshoot operational challenges with urgency and accountability, working cross-functionally to resolve issues and prevent recurrence.</li><li>Contribute to the development and implementation of new procedures and processes, supporting innovation and successful product introductions.</li><li>Create, review, and approve document change orders, ensuring accuracy, compliance, and alignment with production needs.</li><li>Conduct regular performance evaluations, providing constructive feedback and identifying development opportunities to support individual and team growth.</li><li>Operate effectively within a clean room environment, maintaining strict adherence to protocols and quality standards.</li><li>Perform other duties as assigned, demonstrating adaptability, ownership, and a commitment to team and organizational success.</li></ul>

Qualifications:
WHAT YOU'LL BRING: Education:<ul><li>High school diploma or equivalent.</li><li>Supervisor certification or AA preferred.</li></ul>Experience:<ul><li>1 year Manufacturing Supervisor experience (Medical Device preferred).</li><li>6+ years of related manufacturing experience in a leadership role (Internal Candidates).</li></ul> Skills/Compentencies:<ul><li>Experience working with manufacturing/ERP systems (QAD preferred).</li><li>Working knowledge of quality system requirements (QSR) and good manufacturing practices (GMP).</li><li>Experience working in a cleanroom environment and application of environmental procedures.</li><li>Experience with Microsoft Office or similar computer software.  </li></ul> WHAT WE OFFER: At Endologix, we know that great work starts with great people — and people do their best when they feel valued and supported. That’s why we offer competitive pay, solid benefits, career growth, a culture that genuinely cares, and the flexibility you need to thrive both at work and at home. But more than that, we offer purpose. You’ll be part of a team that’s making a real impact on patients’ lives. When you join us, you’re not just taking a job, you’re building a meaningful career with a team that’s invested in your success. The compensation package includes:<ul><li>Base salary of $100,000/yr-$112,500/yr</li><li>Discretionary bonus</li><li>Equity participation as approved by Board of Directors (4-year vesting schedule)</li><li>Comprehensive health, dental, and vision insurance plans</li><li>Flexible Health Savings Accounts (HSAs) and/or Flexible Spending Accounts (FSAs)</li><li>Generous paid time off (vacation, sick leave, holidays, and flexible time off that is available for Exempt employees)</li><li>401(k) retirement plan with company match</li></ul>Plus:<ul><li>Employee wellness initiatives, mental health resources, and Employee Assistance Program (EAP)</li><li>Employee recognition programs and awards</li><li>Commuter benefits or transportation stipends</li></ul> OUR COMMITMENT TO EQUAL OPPORTUNITY & VETERAN INCLUSION: Endologix LLC is an Equal Opportunity and Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status, or any other characteristic protected by applicable federal, state, or local law. As a federal contractor, Endologix LLC is committed to taking affirmative action to recruit, employ, and advance in employment qualified individuals with disabilities and protected veterans.

Endologix

Production Supervisor

[AW]-iCims

FULL_TIME

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Key ResponsibilitiesProduction Leadership: Direct daily activities, assign tasks based on skill level, and manage the shop floor schedule in coordination with Project Managers to meet strict deadlines. Technical Mastery: Expert-level proficiency in CNC programming (G-code), CAD/CAM software (Mastercam, Fusion 360), and reading blueprints/GD&T.

Blentech Corporation is seeking a seasoned Machine Shop Production Supervisor II  to lead our Santa Rosa machine shop operations. In this critical leadership role, you will bridge the gap between complex engineering designs and physical production, ensuring our custom food processing equipment meets the highest standards of quality, safety, and efficiency. We are looking for an expert who can mentor a diverse team while maintaining hands-on technical involvement in high-precision machining. Key Responsibilities<ul style="margin-bottom:11px"><li style="margin-bottom:11px">Production Leadership: Direct daily activities, assign tasks based on skill level, and manage the shop floor schedule in coordination with Project Managers to meet strict deadlines.</li><li style="margin-bottom:11px">Technical Oversight: Perform first-article inspections to ensure tight tolerances and surface finishes match CAD drawings. Provide "over-the-shoulder" guidance for complex setups on CNC mills, lathes, and manual machines.</li><li style="margin-bottom:11px">Process Improvement: Identify production bottlenecks and implement Lean Manufacturing principles or improved machining strategies to increase throughput.</li><li style="margin-bottom:11px">Safety & Maintenance: Enforce rigorous safety protocols (PPE, LOTO) in accordance with Cal/OSHA standards and oversee preventative maintenance (PM) schedules for all machinery.</li><li style="margin-bottom:11px">Team Development: Lead and train a team of 6+ machinists, conducting performance reviews and fostering a culture of continuous professional growth.</li><li style="margin-bottom:11px">Inventory Management: Manage the procurement of raw materials, specialized tooling, and inserts while maintaining an organized inventory.</li></ul>What you Bring to the Team<ul style="margin-bottom:11px"><li style="margin-bottom:11px">Experience: 15+ years of experience in CNC manufacturing and supervisory roles.</li><li style="margin-bottom:11px">Technical Mastery: Expert-level proficiency in CNC programming (G-code), CAD/CAM software (Mastercam, Fusion 360), and reading blueprints/GD&T.</li><li style="margin-bottom:11px">Materials Expertise: Deep understanding of machining stainless steel and food-grade alloys.</li><li style="margin-bottom:11px">Leadership Skills: Proven ability to resolve conflicts, manage priorities, and drive a high-performance culture.</li><li style="margin-bottom:11px">Communication: Effective verbal and written communication skills, including proficiency in Microsoft Office Suite and G-Suite.</li></ul>Physical Requirements & Environment<ul style="margin-bottom:11px"><li style="margin-bottom:11px">Ability to stand for long periods and walk/work in a workshop environment close to the manufacturing floor.</li><li style="margin-bottom:11px">Ability to occasionally lift and carry items up to 40 pounds.</li><li style="margin-bottom:11px">Visual acuity for close work, depth perception, and the ability to adjust focus.</li><li style="margin-bottom:11px">Tolerance for a work environment with moderate to loud noise levels.</li><li style="margin-bottom:11px">Flexibility for occasional weekend, evening work, or travel as required.</li></ul>Blentech Offers<ul><li>Paid Benefits: Medical, Dental, and Vision for the employee are 100% company-paid</li><li>Retirement: 401(k) with a 4% company match after 6 months</li><li>Growth: Career advancement opportunities and a supportive culture for professional development</li></ul> Compensation & Schedule (DOE)<ul><li>Pay Range: $35.44 - $51.00 per hour</li><li>Schedule: Full-Time, on-site in Santa Rosa, CA</li><li>PTO accrual and a boot allowance, and a collaborative professional culture</li></ul> Not open to Recruiters or International Candidates  Powered by JazzHR

Blentech Corporation

Machine Shop Production Supervisor II

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