Cure Hydration Promo Code Jobs in Usa

Job Description & Requirements Hospitalist
- Pediatric Hematology/Oncology StartDate: ASAP Pay Rate: $185000.00
- $230000.00 The rapidly expanding Hospitalist Medicine Program at the esteemed St.

Jude Children's Research Hospital in Memphis, TN, seeks a Pediatric Hematology-Oncology Hospitalist to join its team as a faculty member.

The Hospitalist Program is in a world-class medical environment, allowing for hands-on patient experiences covering a full range of hematologic and oncologic diagnoses.

Opportunity Highlights Be part of a highly acclaimed, leading children's research hospital Excellent work-life balance with flexible shifts throughout the month Nationally ranked as a Best Hospital (US News) Opportunities for teaching and clinical research Faculty and staff positions available, depending on experience and interest Join a Hospitalist Medicine Program with a large team of hem-onc-trained physicians and advanced practice providers Named a Glassdoor Best Place to Work (2022) Named a Top Place to Work in Healthcare by Becker's Healthcare (2023) Consistently ranked on Fortune Magazine's "100 Best Places to Work" This role is a wonderful opportunity to join a place unlike any other that is committed to advancement in cures and means of prevention of pediatric catastrophic diseases through research and treatment.

At St.

Jude Children's Research Hospital, no child is denied treatment based on a family's ability to pay.

For over 60 years, St.

Jude has been treating children with cancer and catastrophic illnesses while profoundly impacting children and their families seeking care in the United States and worldwide.

St.

Jude was founded on the ideals of equality and inclusion, and our mission inspires us to ensure our employees feel a sense of belonging, empowerment, and respect.

Community Information Memphis, TN, stands out among mid-sized cities for its low cost of living.

Rich in history, Memphis boasts a revitalized and historic downtown and a diverse, welcoming community with family-friendly activities.?Area Vibes gives Memphis A+ grades in Commute, Cost of Living, Housing, and Safety.

Memphis is a Best Place to Live and Retire (US News) Tennessee is a Best Place to Practice in 2023 (Medscape) Memphis is one of the 23 Best Places to Go in 2023 (Conde Nast Traveler) No state income tax?in Tennessee Home to a world-renowned music, theater, and arts scene Exciting sports events with an NBA team, multiple colleges, and professional USL soccer Mississippi Riverfront provides endless outdoor activities, including hiking, fishing, and boating Pleasurable year-round weather, beautiful parks, the Mississippi River, and plenty of lakes and trails Healthcare hub of the Midsouth with a growing local economy ? Facility Location With the Mississippi at her feet, music in her heart, and history on her mind, Memphis is Tennessees largest city and cultural center.

A blend of southern tradition and modern efficiency, this city knows how to showcase the old with the new.

The Home of the Blues and the Birthplace of Rock n Roll, Memphis offers career-enriching travel assignments at its highly respected facilities.

Job Benefits About the Company At AMN Healthcare, we strive to be recognized as the most trusted, innovative, and influential force in helping healthcare organizations provide quality patient care that continually evolves to make healthcare more human, more effective, and more achievable.

Pediatric Hospitalist, Hospitalist, Nicu, Picu, Pediatric Intensive Care, Pediatrician, Pediatrics, Pediatric Care, Child Care, Internal Medicine, Internal Care, Physician, Healthcare, Health Care, Patient Care, Hospital, Medical

Job Description & Requirements Gastroenterologist StartDate: ASAP Available Shifts: 4
- 4.5 days a week / 1:5 Call Pay Rate: $475000.00
- $575000.00 The Division of Gastroenterology and Hepatology at the nation's No.

1 hospital system seeks a gastroenterologist for a busy, comprehensive practice in La Crosse, WI.

The successful candidate will join eight other GIs providing consultative gastrointestinal services to a primary care patient base of 240,000.

Candidates must be board-certified or board-eligible in gastroenterology.

Opportunity Highlights Experience a blended clinical/consultative practice with research and teaching opportunities if desired Provide consultative gastrointestinal services to a primary care patient base of 240,000 Work in a state-of-the-art Endoscopy/ERCP/Fluoroscopy Unit in a 225-bed medical center, with HD Olympus endoscopic equipment, Givens capsule endoscopy, and single balloon and endoscopic ultrasound Excellent work-life balance with very light call Academic appointment Comprehensive practice includes 4 NPs who see patients in a self-contained GI clinic and hospital Collaborate with colleagues across the health system to cure, connect, and transform the way care is delivered in a multidisciplinary team-based environment Highly competitive salary and benefits, up to $100,000 appointment supplement, and comprehensive benefits Community Highlights Located along the banks of the Mississippi River, La Crosse is a charming community in southwest Wisconsin and a great place to live and work.

The area offers four seasons of recreational opportunities, such as biking, golf, snow skiing, and hiking 500-foot bluffs overlooking the Mississippi River.

Enjoy great arts, culture, shopping, and dining our city has all you need and more.

Livability named our city a Best Place to Live in the USA (2022) A low cost of living, affordable housing prices, and excellent public and private schools Plenty of opportunities to explore the outdoorsenjoy hiking, biking, camping, fishing, kayaking, and much more Four distinct seasons and breathtaking scenery Easy access to Rochester, Madison, and Minneapolis Medscape ranks Wisconsin a Best Place to Practice in 2022 Facility Location La Crosse is very definitely a college town, home to three universities (University of Wisconsin-Lacrosse, Viterbo University, and Western Technical College).

The La Crosse Center puts on a wide array of exciting events throughout the year, from conventions, to pageants, to sporting events.

Like any good college town, La Crosse possesses a vibrant night life, evidenced most strongly by Third Street, which is chock full of restaurants and bars.

The performing arts are well represented, and the La Crosse Community Theatre is nationally known.

In 2010, La Crosse was named one off "Most Secure Place to Live in the US".

Job Benefits About the Company At AMN Healthcare, we strive to be recognized as the most trusted, innovative, and influential force in helping healthcare organizations provide quality patient care that continually evolves to make healthcare more human, more effective, and more achievable.

Internal Medicine, Gastroenterologist, Gastroenterology, Digestive Track, Digestive, Gastrointestine, Physician, Healthcare, Health Care, Patient Care, Hospital, Medical, Doctor, Md

Job Description & Requirements Hospitalist
- Pediatric Hematology/Oncology StartDate: ASAP Pay Rate: $185000.00
- $230000.00 The rapidly expanding Hospitalist Medicine Program at the esteemed St.

Jude Children's Research Hospital in Memphis, TN, seeks a Pediatric Hematology-Oncology Hospitalist to join its team as a faculty member.

The Hospitalist Program is in a world-class medical environment, allowing for hands-on patient experiences covering a full range of hematologic and oncologic diagnoses.

Opportunity Highlights Be part of a highly acclaimed, leading children's research hospital Excellent work-life balance with flexible shifts throughout the month Nationally ranked as a Best Hospital (US News) Opportunities for teaching and clinical research Faculty and staff positions available, depending on experience and interest Join a Hospitalist Medicine Program with a large team of hem-onc-trained physicians and advanced practice providers Named a Glassdoor Best Place to Work (2022) Named a Top Place to Work in Healthcare by Becker's Healthcare (2023) Consistently ranked on Fortune Magazine's "100 Best Places to Work" This role is a wonderful opportunity to join a place unlike any other that is committed to advancement in cures and means of prevention of pediatric catastrophic diseases through research and treatment.

At St.

Jude Children's Research Hospital, no child is denied treatment based on a family's ability to pay.

For over 60 years, St.

Jude has been treating children with cancer and catastrophic illnesses while profoundly impacting children and their families seeking care in the United States and worldwide.

St.

Jude was founded on the ideals of equality and inclusion, and our mission inspires us to ensure our employees feel a sense of belonging, empowerment, and respect.

Community Information Memphis, TN, stands out among mid-sized cities for its low cost of living.

Rich in history, Memphis boasts a revitalized and historic downtown and a diverse, welcoming community with family-friendly activities.?Area Vibes gives Memphis A+ grades in Commute, Cost of Living, Housing, and Safety.

Memphis is a Best Place to Live and Retire (US News) Tennessee is a Best Place to Practice in 2023 (Medscape) Memphis is one of the 23 Best Places to Go in 2023 (Conde Nast Traveler) No state income tax?in Tennessee Home to a world-renowned music, theater, and arts scene Exciting sports events with an NBA team, multiple colleges, and professional USL soccer Mississippi Riverfront provides endless outdoor activities, including hiking, fishing, and boating Pleasurable year-round weather, beautiful parks, the Mississippi River, and plenty of lakes and trails Healthcare hub of the Midsouth with a growing local economy ? Facility Location With the Mississippi at her feet, music in her heart, and history on her mind, Memphis is Tennessees largest city and cultural center.

A blend of southern tradition and modern efficiency, this city knows how to showcase the old with the new.

The Home of the Blues and the Birthplace of Rock n Roll, Memphis offers career-enriching travel assignments at its highly respected facilities.

Job Benefits About the Company At AMN Healthcare, we strive to be recognized as the most trusted, innovative, and influential force in helping healthcare organizations provide quality patient care that continually evolves to make healthcare more human, more effective, and more achievable.

Pediatric Hospitalist, Hospitalist, Nicu, Picu, Pediatric Intensive Care, Pediatrician, Pediatrics, Pediatric Care, Child Care, Internal Medicine, Internal Care, Physician, Healthcare, Health Care, Patient Care, Hospital, Medical

Job Description & Requirements Gastroenterologist StartDate: ASAP Available Shifts: 4
- 4.5 days a week / 1:5 Call Pay Rate: $475000.00
- $575000.00 The Division of Gastroenterology and Hepatology at the nation's No.

1 hospital system seeks a gastroenterologist for a busy, comprehensive practice in La Crosse, WI.

The successful candidate will join eight other GIs providing consultative gastrointestinal services to a primary care patient base of 240,000.

Candidates must be board-certified or board-eligible in gastroenterology.

Opportunity Highlights Experience a blended clinical/consultative practice with research and teaching opportunities if desired Provide consultative gastrointestinal services to a primary care patient base of 240,000 Work in a state-of-the-art Endoscopy/ERCP/Fluoroscopy Unit in a 225-bed medical center, with HD Olympus endoscopic equipment, Givens capsule endoscopy, and single balloon and endoscopic ultrasound Excellent work-life balance with very light call Academic appointment Comprehensive practice includes 4 NPs who see patients in a self-contained GI clinic and hospital Collaborate with colleagues across the health system to cure, connect, and transform the way care is delivered in a multidisciplinary team-based environment Highly competitive salary and benefits, up to $100,000 appointment supplement, and comprehensive benefits Community Highlights Located along the banks of the Mississippi River, La Crosse is a charming community in southwest Wisconsin and a great place to live and work.

The area offers four seasons of recreational opportunities, such as biking, golf, snow skiing, and hiking 500-foot bluffs overlooking the Mississippi River.

Enjoy great arts, culture, shopping, and dining our city has all you need and more.

Livability named our city a Best Place to Live in the USA (2022) A low cost of living, affordable housing prices, and excellent public and private schools Plenty of opportunities to explore the outdoorsenjoy hiking, biking, camping, fishing, kayaking, and much more Four distinct seasons and breathtaking scenery Easy access to Rochester, Madison, and Minneapolis Medscape ranks Wisconsin a Best Place to Practice in 2022 Facility Location La Crosse is very definitely a college town, home to three universities (University of Wisconsin-Lacrosse, Viterbo University, and Western Technical College).

The La Crosse Center puts on a wide array of exciting events throughout the year, from conventions, to pageants, to sporting events.

Like any good college town, La Crosse possesses a vibrant night life, evidenced most strongly by Third Street, which is chock full of restaurants and bars.

The performing arts are well represented, and the La Crosse Community Theatre is nationally known.

In 2010, La Crosse was named one off "Most Secure Place to Live in the US".

Job Benefits About the Company At AMN Healthcare, we strive to be recognized as the most trusted, innovative, and influential force in helping healthcare organizations provide quality patient care that continually evolves to make healthcare more human, more effective, and more achievable.

Gastrointestinal Pathology, Gastrointestinal Pathologist, Gi Pathologist, Gi Pathology, Sugical Pathology, Pathology Lab, Pathology, Laboratory, Cytologic, Pathology

Job Title – Cell Therapy Technician I

Contract role

Location - Frederick MD

IMPORTANT: For the first 6-8 weeks of the assignment, all contractors are required to work Mon-Fri ( to complete New Hire Orientation and Manufacturing On-boarding Technical Training. After the training is successfully completed, the contractor is deployed onto the shift as needed by the dept leadership.

Role is full time 4/10 role but the roles and shifts can change with the needs of the dept. Shift times will be directed by the manager or dept leads.

6:00 am to 4:30 pm (Day Shift), Sun-Wed and Wed-Sat

3:00 pm to 1:30 am (Swing Shift), Sun-Wed and Wed-Sat

Job Description

Everyone at this facility is grounded by one common goal – curing cancer. Every single day, we seek to establish a direct line between that purpose and our day-to-day work. Would you like to join us in this mission?

We are seeking a highly motivated, Cell Therapy Technician to join our newly formed Cell Therapy Manufacturing team at our brand new, state of the art, commercial Cell Therapy facility in Frederick, Maryland.

The Cell Therapy Technician will perform and/or verify all tasks associated with the manufacture of commercial product following batch records and standard operating procedures (SOPs) to ensure safe and compliant operations as well as works as part of a team to execute GMP runs in close collaboration with Materials Management, Quality Control and Quality Assurance.

Are you passionate about making an impact on people’s lives? Would you be excited to work for a company leading the way in developing and producing unique, innovative immunotherapies? Do you have a background in cGMP manufacturing? If the answer is yes, we’d like to consider you!

Responsibilities (include but are not limited to):

To be considered for this role, you must meet the following basic criteria:

• Successfully troubleshoots processing and equipment issues while communicating said issues to management

• Completes required training assignments to maintain necessary technical skills and knowledge and to ensure compliance with cGMP requirements

• Routinely monitors, cleans, prepares and operates sophisticated automated cell processing, cell expansion and filling equipment in Grade B/C clean rooms. All required PPE and gowning for classified GMP manufacturing areas are provided by the company.

• Finds opportunities for improvement in manufacturing efficiencies and compliance while assisting with investigations/deviations and change controls

• Ability to wear a respirator during use of certain cleaning chemicals

Basic Qualifications:

1+ years related experience with High School Diploma

0+ years related experience with Associate’s Degree

This is a full-time, on-site role for a Large Format Additive Manufacturing Manager based in Merritt Island, FL. This position is responsible for owning and scaling Building Blocks’ large-format additive manufacturing capability from early application through fully integrated, production-ready use on live façade projects.

The role sits at the intersection of design, engineering, manufacturing, and project execution. The Additive Manufacturing Manager will lead the strategy, process development, and day-to-day operation of LFAM systems used to produce molds, tooling, and potentially end-use architectural components. Success in this role is defined by throughput, repeatability, quality, and reliability.

Responsibilities include defining and optimizing print processes and parameters, qualifying materials, commissioning and maintaining equipment, establishing QA/QC and safety standards, and integrating additive manufacturing directly into project workflows. The role also includes building and leading a high-performance team while driving continuous improvement in cycle time, cost, and output quality.

Close collaboration with design, engineering, tooling, and production teams is essential to ensure digital models translate into executable, production-grade print paths that meet real schedule and cost constraints.

Qualifications

• 8–12+ years of experience in advanced manufacturing, additive manufacturing, or industrial automation, with 3–5+ years in a leadership role
• Direct, hands-on experience with large-format additive manufacturing systems (robotic or gantry-based); concrete, cementitious, or composite materials strongly preferred
• Strong understanding of material behavior, process control, tolerancing, curing, and post-processing
• Proven ability to take emerging or LFAM technologies and turn them into reliable, repeatable production systems
• Experience establishing manufacturing standards, QA/QC criteria, safety protocols, and performance metrics
• Demonstrated leadership in building, training, and managing technical teams
• Strong problem-solving skills with a bias toward execution and accountability
• Bachelor’s degree in Engineering, Manufacturing, or a related technical field

Note to Recruitment Agencies: We love your enthusiasm, but we prefer to connect with our candidates directly. Building Blocks is not partnering with external agencies for this search, so please save the outreach, we’ve got this one covered. Any resumes submitted without a signed agreement in place will become the property of Building Blocks and no fees will be paid.

Building Blocks is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Accommodations: If you require reasonable accommodation in completing this application, interviewing, or otherwise participating in the employee selection process, please direct your inquiries to People Strategy Department - 321-338-7299.

Red Oak Technologies is a leading provider of comprehensive resourcing solutions across a variety of industries and sectors including IT, Marketing, Finance, Business Operations, Manufacturing and Engineering.

Our client is an electronics manufacturer. They are looking for a Manufacturing Technician (Swing Shift) to join their team. This role is a CONTRACT position. Position will be ONSITE. Candidate must be able to commute onsite to San Francisco, CA.

**Swing Shift – 2:00 PM – 10:30 PM – Monday through Friday – Some work on Saturday as needed**

**Gated private parking lot available for contractors**

**$30/hr - $35/hr**

Position Requirements:

• Follow all Safety and Laser Safety procedures and requirements
• Be able to construct, test and calibrate engineering and production robotic and computer-controlled assembly systems using engineering prints, schematics, assembly instructions and engineering direction
• Knowledgeable in high precision measuring equipment, calibration, and detailed record generation

Experienced and Proficient in the following:

• Mechanical hand and power tools
• Oscilloscopes, DMM, Signal Generators, Optics, Cameras
• Laser safety, lasers, laser pattern recognition, beam focus, and active alignment
• Auto dispense and cure of UV adhesive
• Multiple axis, vision assisted, computer controlled robotic assembly equipment in both a R/D and Volume Manufacturing environment
• Identification of “Root” Cause of Manufacturing, Quality and Yield issues
• Microsoft Office, Standard SPC and Flowcharts packages
• Pneumatic actuated Slides, Grippers, etc.
• Hex Pod Tables, Active Alignment
• Excellent reading, writing, and communication skills in English
• Minimum of 5 years industry experience, Lidar Sensor experience preferred but not required
• Be able to stand for long periods of time
• Lift and carry 35 lbs

Red Oak Technologies is made up of people from a wide variety of backgrounds and lifestyles. We embrace diversity and invite applications from people of all walks of life. See what it’s like to be at the top; connect with one of our recruiters and apply today.

Red Oak Tech: Quality | Talent | Integrity

Note: Compensation rates are based on years of experience and/or level of skills relevant to the opportunity.

About the Role:

We are hiring on behalf of a leading pre-stressed concrete manufacturer for a Pre-stressed Concrete Production Foreman to lead their production team in manufacturing high-quality pre-stressed concrete products, including beams, columns, and panels. This hands-on supervisory role is essential to ensuring safe, efficient, and precise operations that meet production schedules and quality standards. The Foreman serves as the key link between laborers, finishers, quality control, and management.

Key Responsibilities:

• Supervise and coordinate production crews involved in forming, reinforcing, pouring, tensioning, stressing, and finishing pre-stressed concrete products.
• Ensure production schedules and quality standards are consistently met.
• Mentor and manage yard employees, including laborers, finishers, and crew leaders.
• Assign tasks, monitor performance, and provide training as needed.
• Enforce safety protocols in compliance with OSHA standards.
• Conduct quality checks and coordinate with QC to resolve product defects or inconsistencies.
• Monitor use of raw materials, tools, and equipment; coordinate maintenance and repairs.
• Identify process improvements to increase efficiency and reduce waste.
• Maintain accurate records of production output, defects, and downtime.
• Prepare shift reports and communicate effectively with management.
• Manage inventory and ordering of supplies and materials, including take-offs for project production.

Skills & Qualifications:

• High school diploma or equivalent required.
• 3–5 years of experience in pre-stressed concrete production, with at least 1–2 years in a supervisory or lead role.
• Knowledge of pre-stressed concrete manufacturing processes; NPCA or PCI background preferred.
• Experience with beams, columns, panels, and other pre-stressed products.
• Strong understanding of concrete materials, mixing, curing, and pre-stressing methods.
• Ability to read and interpret blueprints, shop drawings, and tensioning charts.
• Strong leadership, communication, and problem-solving skills.
• Ability to work independently or with a team in a fast-paced environment.
• Familiarity with production tracking systems and basic computer skills preferred.
• Knowledge of OSHA and site safety regulations.

Physical Requirements:

• Constant use of hands, vision, and hearing.
• Occasional lifting up to 50 lbs, bending, twisting, kneeling, and climbing.
• Ability to meet job-specific physical qualifications.

Benefits:

• Health & wellness and ancillary benefits for full-time employees working a minimum of 30 hours per week.

Why Apply:

This is a great opportunity to take a leadership role in a high-quality pre-stressed concrete manufacturing environment. If you have hands-on experience with pre-stressed concrete processes, strong leadership skills, and a focus on safety and quality, this role could be an excellent fit.

Equal Opportunity Employer:

The client is an Equal Opportunity Employer and does not discriminate based on race, color, national origin, religion, sex, age, veteran status, genetic information, or any other legally protected class.

Legend Biotech is a global biotechnology company dedicated to treating, and one day curing, life-threatening diseases. Headquartered in Somerset, New Jersey, we are developing advanced cell therapies across a diverse array of technology platforms, including autologous and allogenic chimeric antigen receptor T-cell, T-cell receptor (TCR-T), and natural killer (NK) cell-based immunotherapy. From our three R&D sites around the world, we apply these innovative technologies to pursue the discovery of safe, efficacious and cutting-edge therapeutics for patients worldwide.

Legend Biotech entered into a global collaboration agreement with Janssen, one of the pharmaceutical companies of Johnson & Johnson, to jointly develop and commercialize ciltacabtagene autolecuel (cilta-cel). Our strategic partnership is designed to combine the strengths and expertise of both companies to advance the promise of an immunotherapy in the treatment of multiple myeloma.

Legend Biotech is seeking a Sr. QC Analyst as part of the Quality team based in Raritan, NJ.

Role Overview

The Sr. QC Analyst is an exempt level position with responsibilities for performing QC testing related to the manufacturing of cell therapy products for clinical trials and commercial operations in a controlled GMP environment.

Key Responsibilities

• Be responsible for the completion of QC testing related to the manufacturing of autologous CAR-T products for clinical trials and commercial operation in a controlled cGMP cleanroom environment.
• Ensure testing is completed in compliance with all applicable procedures, standards and GMP regulations.
• Conduct analytical testing of raw material/utility, in-process, or final product samples submitted to the QC laboratories.
• Perform peer review/approval of laboratory data.
• Utilize electronic systems (LIMS) for execution and documentation of testing.
• Create, review and approve relevant QC documents, SOP’s and WI’s.
• Perform tasks in a manner consistent with the safety policies, quality systems and cGMP requirements.
• Work in a collaborative team setting with quality counterparts that include Quality Assurance, Manufacturing Operations, and Analytical/Process Development.
• Job duties performed require routine exposure to and handling of biological materials and hazardous chemicals. 

Requirements

• Bachelor’s Degree in Science, Engineering or equivalent technical discipline is required.
• Minimum of 1 year relevant work experience, preferably within a biological and/or pharmaceutical industry is required.
• Experience in a Quality Control setting is preferred.
• Experience with processing samples in biosafety cabinets utilizing aseptic technique is strongly preferred.
• Knowledge of cGMP regulations and FDA/EU guidance related to manufacturing of cell-based products is strongly preferred.
• Knowledge of Good Tissue Practices is required.
• Knowledge of CAR-T QC test methods and related equipment is preferred.
• Excellent written and oral communication skill are required.
• Candidates must be able to accommodate shift schedule. Shifts include routine weekend and evening work as required by the manufacturing process.
• Candidates must be able to accommodate unplanned overtime (including nights and weekends) on little to no prior notice.
• The candidate must be highly organized and capable of working in a team environment with a positive attitude under some supervision.
• Comfortable with speaking and interacting with regulatory inspectors.
• This position may require occasional travel to partner sites in NJ or PA as business demands.
• This position may require up to 5% domestic or international travel as business demands.
• Takes responsibility for one's results and deliverables; sets and achieves goals to support organizational priorities.
• Takes initiative; willing to take unpopular positions/actions when necessary; courageous and assertive.
• Works effectively in the face of ambiguity, shifting priorities, and rapid change; maintains a positive outlook in difficult situations; a change agent.
• Identifies and focuses on activities of highest value and impact; makes informed decisions quickly.
• Results oriented; defines goals, metrics and actionable plans and manages work to deliver desired outcomes; has a sense of urgency.
• Considers resources, alternatives, constraints and desired outcomes to make effective decisions.
• Employs good project management principles to appropriately align time, resources, and budgets.
• Appreciates diverse perspectives and is actively inclusive of others' input and ideas; treats others with respect.
• Articulates ideas clearly and succinctly in a variety of settings and styles; can get messages across that have the desired effect.
• Leverages personal credibility and interpersonal skills to help others make better decisions and positively impact outcomes; able to develop/maintain effective working relationships internally and externally.
• Employs a global mindset in decision-making and errs on the side of over-communicating to create organizational transparency, trust and alignment.
• Takes initiative, actively shares knowledge, builds skills, promotes new ideas and embraces change.
• Generates new solutions to problems by challenging the status quo and conventional thinking. 
  
  

The base pay range below is what Legend Biotech USA Inc. reasonably expects to offer at the time of posting. Actual compensation may vary based on experience, skills, qualifications, and geographic location. The company reserves the right to modify this range as needed and in accordance with applicable laws.Other Types of Pay: Performance-based bonus and/or equity is available to employees in eligible roles.Benefits and Paid Time Off: Medical, dental, and vision insurance as well as a 401(k) retirement plan with a company match that vests fully on day one. We offer eight (8) weeks of paid parental leave after just three (3) months of employment, and a paid time off policy that includes vacation time, personal time, sick time, floating holidays, and eleven (11) company holidays. Additional voluntary benefits include flexible spending and health savings accounts, life and AD&D insurance, short- and long-term disability coverage, legal assistance, and supplemental plans such as pet, critical illness, accident, and hospital indemnity insurance. We also provide voluntary commuter benefits, family planning and care resources, well-being initiatives, and peer-to-peer recognition programs; demonstrating our ongoing commitment to building a culture where our people feel empowered, supported, and inspired to do their best work.

Pay Range (Base Pay): : $93,463 USD - $122,670 USD

Please note: These benefits are offered exclusively to permanent full-time employees. Contractors are not eligible for benefits through Legend Biotech.

EEO Statement

It is the policy of Legend Biotech to provide equal employment opportunities without regard to actual or perceived race, color, creed, religion, national origin, ancestry, citizenship status, age, sex or gender (including pregnancy, childbirth, related medical conditions and lactation), gender identity or gender expression (including transgender status), sexual orientation, marital status, military service and veteran status, disability, genetic information, or any other protected characteristic under applicable federal, state or local laws or ordinances.

Employment is at-will and may be terminated at any time with or without cause or notice by the employee or the company.

Location: Tarzana, CA

Duration: 90 days

Start Date: Apr 12, 2026

End Date: Jul 12, 2026

Contract Type: W2 through staffing supplier, Full-Time (40 hrs/week)

Pay: $25.20 per hour

Visa Sponsorship: Not provided

Interview Process:

30 minutes via MS Teams

At AstraZeneca's Oncology R&D division, we follow the science to explore and innovate. We are working towards treating, preventing, modifying, and even curing some of the world's most complex diseases. Here we have the potential to grow our pipeline and positively impact the lives of billions of patients around the world. We are committed to making a difference and have built our business around our passion for science. Now we are fusing data and technology with the latest scientific innovations to achieve the next wave of breakthroughs.

Position Summary:

We are seeking a Contractor to support our dynamic Manufacturing team in the production of TCR-T, CAR-T, and allogeneic cell therapy investigational products. This contract role is based in Tarzana, CA, with occasional travel to Santa Monica, CA as needed. The contractor will report to the Associate Director of Manufacturing, NGF70.

This role will ensure successful manufacture and release of cell therapy products by following established processes in full compliance with cGMP. This role also supports manufacturing operational readiness and the successful technology transfer of pipeline products using knowledge of cGMP regulations.

This is a 90 day contingent assignment, with the possibility of extension based on project needs, performance, and budget availability.

Compensation and employment terms will be managed through an approved staffing partner. This role is not eligible for company-sponsored benefits unless provided by the staffing agency.

Responsibilities:

• Using general application of principles, support activities to ensure GMP readiness for clinical manufacturing, including but not limited to equipment procurement, installation and qualification, facility qualification, and technology transfer.

• Perform operational tasks within a cleanroom environment in a manner consistent with safety policies, quality systems, and cGMP requirements.

• Assist in developing Standard Operating Procedures (SOPs) and other documents for manufacturing processes.

• Set up manufacturing areas and equipment, including complex automated cell processing equipment.

• Follow all cleaning and gowning procedures for the facility.

• Maintain appropriate inventories of material and supplies within the cleanroom areas to support manufacturing activities.

• Ensure all materials and equipment are identified and available in time for manufacturing activities.

• Support Process Development (PD) and Manufacturing Sciences & Technology (MSAT) to align manufacturing plans with product development plans.

• Ensure that all production operations are controlled and performed within cGMP regulatory guidelines.

• Provide verbal and written updates to Manufacturing leadership.

• Perform other responsibilities and project-based assignments as needed to support manufacturing operations.

Experience and Education:

• Minimum of five (5) years of experience with a High School Diploma or a BS/BA in a relevant science or engineering discipline.

• Understanding of cGMP process and knowledge of CMC regulatory framework for biologics.

• Knowledge of aseptic techniques for primary human cell cultures and GMP manufacturing and supporting tech transfer and GMP clinical/commercial manufacturing operations.

Additional Requirements:

• Knowledge of industry practices, cell therapy manufacturing experience preferred.

• Develop solutions to complex problems independently.

• Refer to established precedents and policies or use original thinking.

• Help determine goals of assignment.

• Plan schedules and arranges own activities.

• Work is reviewed upon completion for adequacy in meeting goals.

-CAR-T immunotherapy production operator/verifier/runner

-Deviation support

-Experience with operating cell therapy equipment such as NC-200 Nucleocounter Automated Cell Counter, Dynasellect, Cue, Welder, Sealer, Microscope, Sefia, Finia, Sepax, and ISO 5 aseptic operations

When we put unexpected teams in the same room, we fuel bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.