New offer - be the first one to apply!
July 21, 2026
Manufacturing Process Lead (2nd/3rd Shift)
Mid
69,996 - 90,000 USD
Princeton, NJ
More than one million people in the United States today are fighting blood cancer. While a traditional allogeneic stem cell transplant has been the best hope for many, the transplant itself can prove fatal or lead to serious conditions, such as graft vs. host disease. Orca Bio is a late-stage biotechnology company redefining the transplant process by developing next-generation cell therapies with the goal of providing significantly better survival rates with dramatically fewer risks. With our purified, high-precision investigational cell therapies we hope to not only replace patients' blood and immune systems with healthy ones, but also restore their lives.
We are establishing manufacturing operations on the East Coast to ensure the consistent and reliable delivery of our high-precision cell therapy products. This site is essential to advancing our clinical pipeline and supporting future commercial availability of our life-saving therapies.
The Manufacturing Process Lead conducts cGMP manufacturing activities to produce clinical and commercial cell therapies and helps to optimize manufacturing processes. The Lead ensures adherence to quality standards, regulatory requirements, and aseptic production techniques. This position involves repeatedly executing manufacturing processes, cleaning and maintaining production equipment and workstations, and documenting production activities in a highly regulated environment. This position also entails on-shift oversight of production activities to ensure timely, efficient, and quality-driven execution of each day’s objectives.
Essential Duties & Key Responsibilities
- Oversee execution of routine manufacturing and occasional scientific protocols
- Develop and refine procedures for cell separation technologies, sterile connections, and aseptic techniques
- Serve as subject matter expert for cell therapy processes and new technology
- Provide verification for results and ensure detailed records are maintained
- Prepare, maintain, trouble-shoot, and operate instruments
- Plan the shift, including break management, shift pass downs, and process-appropriate decisions
- Supervise in-room operations and delegate individual tasks based on operator capacity
- Complete deviations
- Escalate issues appropriately
- Review and support continuous improvements of business processes, records, and SOPs
- Training and coaching employees
- Other duties as assigned
Minimum Qualifications
- Bachelor’s degree in a science-related field (Biology, Engineering, etc.) or related field required; Master’s degree preferred
- 2-3 years of experience in GMP Manufacturing, process sciences, or discovery
- Experience with aseptic techniques
- Familiarity with cell and/or gene therapy, including working with human cells, cell characterization methods, or cell separation techniques
- Direct or indirect people leadership preferred
- Flexibility to work outside standard business hours when needed to support site priorities, deadlines, or critical business needs
Shifts
- 2nd Shift: Monday - Friday, 4:00pm - 12:30am
- 3rd Shift: Monday - Friday, 12:00am - 8:30am
Physical Demands
- Must have visual acuity of 20/20 (corrected or uncorrected) and normal color vision to safely perform critical tasks such as visual inspection of materials, equipment, and labeling, including distinguishing color-coded components in a GMP environment
- Must be able to meet cleanroom gowning requirements, including wearing full gowning (face coverings, gloves, hoods, goggles) for extended periods as needed
- Use of cosmetics, jewelry, or facial piercings is not permitted in the cleanroom, and any skin conditions that cause shedding must be disclosed
Benefits
The anticipated annual salary range for this job is based on prior experience in the role or industry, education, location, internal equity, and other job-related factors as permitted by law. Full-time positions are eligible for pre-IPO equity, annual bonus, medical, dental, and vision benefits, PTO, 401(k), life and disability coverage, and parental leave benefits.
Company Culture
We are driven by a passion for science and compassion for patients. We act with urgency to ensure treatments are one day accessible to all who need them.
We live by our core values of passion, courage, and integrity. Excellence in our work means the chance to unlock a better quality of life for patients.
We innovate on a path that hasn’t been paved, embrace an entrepreneurial spirit, and take calculated risks to achieve our mission.
We maintain a start-up culture of camaraderie and leadership by example, regardless of title.
We’re proud to be an equal opportunity employer and recognize that celebrating differences creates stronger, lasting solutions that better serve our team, patients, and healthcare providers.
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The role collaborates across operations, quality, and production teams to improve throughput, audit readiness, and patient safety. 🗂️ Requirements: High school diploma or equivalent, Minimum 1 year pharmaceutical compounding experience, Sterile compounding experience, Vial filling experience, Aseptic technique experience, Controlled-environment production experience, Texas Board of Pharmacy Pharmacy Technician or Pharmacy Technician Trainee registration, Sterile/IV certification accredited by ACPE, Knowledge of cGMP standards, Knowledge of USP standards, Ability to maintain accurate compounding documentation, Ability to work in regulated pharmaceutical environments 📃 Skills: cGMP, USP, Aseptic, Compounding, Pharmacy, AI, Dashboards, Documentation, Compliance, Workflow, Production, Quality, Audit, VialFilling, Cleanroom 🏢 Description: POSITION SUMMARY The Sterile Compounding Lead drives safe, compliant, and scalable execution of sterile compounding operations that directly protect patients, strengthen production reliability, and support operational growth. This role owns shift-level workflow, aseptic discipline, documentation accuracy, technician readiness, and real-time issue escalation across a highly regulated 503A/503B environment. The Lead uses AI-enabled tools to improve scheduling insight, detect process variation, strengthen decision-making, and improve quality at scale while partnering across Pharmacy Operations, Quality, Training, and Production. RESPONSIBILITIES Sterile Operations - Lead sterile compounding activities with adherence to cGMP, SOPs, USP expectations, and aseptic technique. - Coordinate shift priorities, room readiness, staffing, and production handoffs to ensure CSPs are prepared accurately and on schedule. - Verify materials, equipment, documentation, and cleanroom conditions before compounding begins. - Use AI-supported dashboards, workflow signals, and trend analysis to identify bottlenecks and readiness gaps. Quality And Compliance - Reinforce frontline quality discipline through observation, coaching, and correction of nonconforming behaviors. - Maintain inspection-ready execution aligned with cGMP, USP, FDA, state board, and internal standards. - Ensure compounding records, equipment logs, cleaning documentation, and production entries are accurate and traceable. - Use AI-assisted review tools and analytics to reduce errors and improve documentation integrity. Team Leadership - Train and mentor technicians on aseptic discipline, procedural accuracy, safety expectations, and documentation standards. - Set expectations for shift execution, cleanroom conduct, documentation quality, and escalation discipline. - Deliver production schedules and act as point of contact in the absence of the supervisor. - Stay current on sterile compounding practices, regulatory expectations, and process updates. Cross Functional Execution - Partner with Quality, Training, Pharmacy Operations, Materials, and Production leaders to resolve operational constraints. - Escalate safety, quality, staffing, equipment, material, and process risks appropriately. - Lead continuous improvement initiatives that reduce defects and improve production flow. KNOWLEDGE AND SKILLS - Strong knowledge of sterile compounding operations, cGMP expectations, USP standards, aseptic technique, controlled environments, equipment use, and documentation requirements. - Ability to use AI-enabled dashboards, workflow signals, trend analysis, and digital tools to improve scheduling, quality visibility, training focus, and operational decisions. - Strong leadership, coaching, communication, and escalation skills. - Understanding of deviation prevention, audit readiness, batch documentation, pharmaceutical calculations, resource coordination, and continuous improvement. EXPERIENCE AND QUALIFICATIONS - High school diploma or equivalent required; bachelor's degree preferred. - Minimum of 1 year of pharmaceutical compounding experience required, including sterile compounding, vial filling, aseptic technique, and controlled-environment production activities. - Experience training or mentoring technicians in regulated environments preferred. - Experience with digital production systems, quality documentation platforms, workflow dashboards, AI-enabled tools, or data-driven performance management preferred. - Registration with the Texas Board of Pharmacy as a Pharmacy Technician or Pharmacy Technician Trainee required. - Sterile/IV certification accredited by the Accreditation Council for Pharmacy Education required. Key Competencies - Customer Focus - Strategic AI - Optimizes Work Processes - Collaborates - Resourcefulness - Manages Complexity - Ensures Accountability - Situational Adaptability - Communicates Effectively Values - People - Quality - Service - Innovation Employee Benefits, Health and Wellness Comprehensive benefits include medical, dental, and vision coverage, paid time off, 401(k) matching, wellness perks, IV therapy, and compounded medications. Physical Requirements The role requires frequent standing, walking, reaching, balancing, stooping, kneeling, crouching, crawling, and extended use of hands and computers in a production and office environment.
Technology

Peak Energy
Senior Director of Manufacturing
Senior
On-site
Burlingame, CA
233,004 - 275,004 USD/yr
🏢 Summary: Senior Director of Manufacturing responsible for leading end-to-end manufacturing strategy and execution for sodium-ion battery systems, scaling from pilot to giga-scale commercial production across multiple facilities. The role oversees manufacturing engineering, operations, process development, equipment, yield, and ramp readiness while driving cost, throughput, and quality performance. This position partners cross-functionally to build a scalable, high-performance production system supporting large-scale energy storage deployments. 🗂️ Requirements: 10+ years in battery, semiconductor, or high-volume precision manufacturing, Experience scaling from pilot to GWh-level or equivalent production, Proven leadership of manufacturing engineering teams (50+ people), Expertise in lean manufacturing, SPC, FMEA, Six Sigma, Experience in early-commercialization or growth-stage environments, BS or MS in Mechanical, Chemical, Electrical, or Industrial Engineering or equivalent experience, Ability to manage manufacturing KPIs (throughput, yield, OEE, cost per kWh, safety) 📃 Skills: Manufacturing, ProcessEngineering, Lean, SPC, FMEA, SixSigma, OEE, Automation, Quality, Equipment, Facilities, AI 🏢 Description: Role: Senior Director of Manufacturing Location: Burlingame, CA (with significant time at Sacramento, CA manufacturing facility) Department: Manufacturing Reports To: VP of Manufacturing Position Type: Full-time About the Role - Senior Director of Manufacturing The Senior Director of Manufacturing owns the end-to-end manufacturing strategy and execution for Peak's sodium-ion battery systems as we move from pilot through giga-scale commercial production. You will lead manufacturing engineering, manufacturing operations, process development, facilities, equipment, yield, and ramp readiness across the full BESS stack, spanning our Burlingame pilot operation and our Sacramento manufacturing facility. This role exists right now because Peak is in a critical operational phase. First commercial customer deliveries are imminent, multi-year supply contracts are landing, and the production system built over the next eighteen months will define cost structure, ramp velocity, and the ability to meet grid-scale demand through 2027 and beyond. You'll partner closely with engineering, supply chain, and the commercial team to bring product to market and stand up the production system that supports it. You'll inherit a strong technical bench and an ambitious roadmap, with autonomy to build the manufacturing organization needed for scale. What You'll Do (Responsibilities) - Lead the manufacturing engineering and process development organization through the ramp from pilot to giga-scale production - Define and execute the production ramp plan, including equipment specification, line layout, yield curves, and cost-down roadmap across Burlingame and Sacramento sites - Build and develop a manufacturing leadership bench spanning process engineering, equipment, quality, automation, and facilities - Partner with engineering to drive design-for-manufacturing into the product roadmap - Own manufacturing KPIs end-to-end: throughput, yield, OEE, cost per kWh, and safety performance - Drive process maturity from pilot-scale engineering handoffs into stable, repeatable, audit-ready production - Establish and manage relationships with equipment OEMs, automation partners, and consumables suppliers - Represent manufacturing in executive forums, board updates, and customer and investor due diligence What You'll Bring (Qualifications) - 10+ years in battery, semiconductor, or other high-volume precision manufacturing with progressive leadership scope - Direct experience scaling from pilot to GWh-level (or equivalent) production with documented yield, cost, and ramp outcomes - Demonstrated success building and leading manufacturing engineering organizations of 50+, including process, equipment, and quality functions - Hands-on fluency with lean manufacturing, SPC, FMEA, Six Sigma, and modern factory operating systems - Experience operating in early-commercialization environments - BS or MS in Mechanical, Chemical, Electrical, or Industrial Engineering, or equivalent practical experience - Strong commercial instincts regarding cost per kWh drivers and leverage points - Comfort with ambiguity and pace of a growth-stage, venture-backed company Preferred Qualifications - Direct lithium-ion or sodium-ion cell or pack manufacturing experience at commercial scale - Experience transitioning from prototype to commercial product - Familiarity with energy storage system integration and grid-connected operation - Comfort using modern AI tools in day-to-day workflow Compensation & Benefits The salary range for this role is $233,000-$275,000, with actual pay varying based on work location, experience, and skills. Competitive benefits package includes: - Flexible time off - Comprehensive medical, dental, and vision coverage - 401(k) plan - Equity opportunities - Additional work perks
Healthcare
New offer

TerrAscend
Integrated Pest Management Lead
Mid
Waterfall, PA
🏢 Summary: Full-time IPM Lead role supporting integrated pest management operations in a cannabis cultivation facility, including pest monitoring, crop protection application, team leadership, and cultivation support. The position requires knowledge of cannabis plant health, IPM practices, and compliance with safety and state regulations. Benefits include health coverage, PTO, retirement matching, and employee wellness programs. 🗂️ Requirements: High School Diploma or GED, Knowledge of Integrated Pest Management methods, Ability to identify cannabis pests and pathogens, Knowledge of cultivation practices such as cloning, transplanting, pruning, and watering, Ability to follow SOPs and state regulations, Private pesticide applicator license, Good documentation and organizational skills, Strong verbal and written communication skills, Ability to work weekends, holidays, and overtime, Must be at least 18 years old, Ability to pass comprehensive background check, Ability to lift and move up to 50 lbs, Ability to wear PPE and work with hazardous chemicals 📃 Skills: IPM, Cannabis, Pesticides, Scouting, Cultivation, Cloning, Pruning, Transplanting, Watering, Documentation, Inventory, Respirators, PPE, Sprayers, E-Verify 🏢 Description: At TerrAscend, we don’t just grow cannabis — we grow possibility. Whether it's cultivating top-tier flower, supporting patients with trusted therapies, or crafting premium products for adult use, we’re here to elevate lives. If you're ready to shape the future of cannabis with a team that believes in quality, care, and community — let’s grow together. Our next Full-Time IPM Lead will be responsible for carrying out tasks in a manner that follows the company’s Standard Operating Procedures to support the cultivation facilities Integrated Pest Management plan. The IPM Lead will also be expected to assist the Cultivation Associates with plant maintenance, and everyday cultivation tasks as needed. The Lead will be held accountable for the IPM team's effort and will be responsible for leading by example. Where you’ll be planted This position will be on-site at our Waterfall, PA facility. Responsibilities - Follow all SOPs, verbal directives, and policies when performing daily operational duties and fully comply with state regulations. - Acquire a proficient knowledge of plant diseases, insects, and fungi, as well as plant treatment options. - Follow detailed IPM plans and timelines for plant production from beginning to end of crop cycles (clone to harvest). - Perform routine monitoring, scouting, and documentation of plant population in all stages of plant development for problems revolving around insect pests, pathogens, viruses, etc. - Obtain a private pesticide applicator license. - Act as a Team Lead and lead by example for the rest of the Pest Management team. - Annually complete a respirator fit test with a certified physician if needed. - Apply crop protection agents under the direct supervision/direction of a certified pesticide applicator. - Document application of crop protection agents in accordance with regulations. - Lead and conduct training sessions on Integrated Pest Management strategies and practices. - Identify and execute preventative maintenance and elimination of pests and pathogens. - Maintain and clean PPE and pest management equipment. - Assist with cleaning rooms after harvest and preparing for room re-loads. - Perform cultivation tasks as assigned. - Sweep, mop, and assist with cleaning tasks daily. Requirements - High School Diploma or General Education Diploma (GED). - Knowledge of Integrated Pest Management methods and ability to identify cannabis pests and pathogens. - Knowledge of growing practices such as cloning, transplanting, pruning, training, and watering. - Ability to execute techniques accurately and consistently. - Good documentation, inventory, and organizational skills. - Ability to maintain a tight schedule and excellent attendance. - Strong verbal and written communication skills. - Basic weights and measurements skills and ability to operate a scale. - Flexibility to work weekends, holidays, and overtime. - Must be at least 18 years old. - Ability to pass a comprehensive background check. Benefits - Comprehensive health coverage including medical, dental, vision, and prescription plans. - Mental health and wellness support. - Flexible paid time off. - Employee Assistance Program. - Paid parental leave. - 401(k) with 4% company match and immediate vesting. - Pet insurance. - Employee discounts. - Recognition program. - Disability and life insurance. Environmental Factors This position requires working in an environment with high amounts of plant matter and pollen, varying temperatures, humidity, dust, and cleaning chemicals. Employees are required to wear protective gear and may perform repetitive movements. Physical Requirements - Able to push, pull, lift, or move a minimum of 50 lbs. - Capable of standing, kneeling, bending, squatting, sitting, and walking for extended periods. - Ability to use hands and fingers for handling and picking. - Ability to work with hazardous chemicals following strict safety guidelines. - Must wear PPE, close-toed non-slip shoes, and optional ear/eye protection. EEO Statement At TerrAscend, employees and applicants are evaluated based on their qualifications, skills, and ability to perform the duties and responsibilities of the position. TerrAscend is committed to equal employment opportunities and prohibits unlawful discrimination. Disclaimer This job description is not an employment agreement or contract. Management reserves the right to alter the description at any time without notice. This organization participates in E-Verify.
Technology

Peak Energy
Senior Director of Manufacturing
Senior
On-site
Sacramento, CA
233,004 - 275,004 USD/yr
🏢 Summary: Senior Director of Manufacturing role leading end-to-end manufacturing strategy and execution for sodium-ion battery systems, driving the ramp from pilot to giga-scale production across multiple facilities. The position owns manufacturing engineering, operations, process development, yield, cost, and ramp readiness while partnering cross-functionally to deliver commercial-scale energy storage systems. This is a high-impact leadership role focused on building scalable production systems and manufacturing teams in a fast-growing environment. 🗂️ Requirements: 10+ years in battery, semiconductor, or high-volume precision manufacturing, Experience scaling from pilot to GWh-level or equivalent production, Experience building and leading manufacturing engineering teams of 50+, Hands-on experience with lean manufacturing, Hands-on experience with SPC, Hands-on experience with FMEA, Hands-on experience with Six Sigma, BS or MS in Mechanical, Chemical, Electrical, or Industrial Engineering or equivalent experience, Experience in early-commercialization or growth-stage manufacturing environments 📃 Skills: Manufacturing, ProcessEngineering, Lean, SPC, FMEA, SixSigma, Automation, OEE, Battery, SodiumIon, LithiumIon, AI 🏢 Description: Role: Senior Director of Manufacturing Location: Burlingame, CA (with significant time at Sacramento, CA manufacturing facility) Department: Manufacturing Reports To: VP of Manufacturing Position Type: Full-time About the Role - Senior Director of Manufacturing The Senior Director of Manufacturing owns the end-to-end manufacturing strategy and execution for Peak's sodium-ion battery systems as we move from pilot through giga-scale commercial production. You will lead manufacturing engineering, manufacturing operations, process development, facilities, equipment, yield, and ramp readiness across the full BESS stack, spanning our Burlingame pilot operation and our Sacramento manufacturing facility. This role exists right now because Peak is in the most consequential operational moment of the company. First commercial customer deliveries are imminent, multi-year supply contracts are landing, and the production system we build over the next eighteen months will define our cost structure, our ramp velocity, and our ability to meet the grid-scale demand coming through 2027 and beyond. You'll partner closely with engineering, supply chain, and our commercial team to bring product to market and stand up the production system that supports it. You'll inherit a strong technical bench and an ambitious roadmap, and you'll have the autonomy to build the manufacturing organization the company needs. This role is for a builder. Someone who can move from in the weeds problem solving to board-level planning in the same day, and who wants to own outcomes and manage the process. What You'll Do (Responsibilities) - Lead the manufacturing engineering and process development organization through the ramp from pilot to giga-scale production - Define and execute the production ramp plan, including equipment specification, line layout, yield curves, and cost-down roadmap across our Burlingame and Sacramento sites - Build and develop a world-class manufacturing leadership bench spanning process engineering, equipment, quality, automation, and facilities - Partner with engineering to drive design-for-manufacturing into the product roadmap from day one - Own manufacturing KPIs end-to-end: throughput, yield, OEE, cost per kWh, and safety performance - Drive process maturity from pilot-scale engineering handoffs into stable, repeatable, audit-ready production for commercial customer shipments - Establish and manage strategic relationships with equipment OEMs, automation partners, and consumables suppliers - Represent manufacturing in executive forums, board updates, and customer and investor due diligence What You'll Bring (Qualifications) - 10+ years in battery, semiconductor, or other high-volume precision manufacturing, with progressive leadership scope - Direct experience scaling from pilot to GWh-level (or equivalent) production with documented yield, cost, and ramp outcomes - Demonstrated success building and leading manufacturing engineering organizations of 50+, including process, equipment, and quality functions - Hands-on fluency with lean manufacturing, SPC, FMEA, Six Sigma, and modern factory operating systems - Experience operating in early-commercialization environments where processes are still being developed - BS or MS in Mechanical, Chemical, Electrical, or Industrial Engineering, or equivalent practical experience - Strong commercial understanding of cost per kWh drivers - Comfort operating in a growth-stage, venture-backed company environment Preferred Qualifications - Direct lithium-ion or sodium-ion cell or pack manufacturing experience at a commercial-scale facility - Experience transitioning from prototype to commercial product - Familiarity with energy storage system integration and grid-connected operation - Comfort using modern AI tools in day-to-day workflow Compensation & Benefits The salary range for this role is $233,000-$275,000, with actual pay varying based on work location, experience, and skills. Competitive benefits package includes: - Flexible time off - Comprehensive medical, dental, and vision coverage - 401(k) plan - Equity opportunities - Additional work perks