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Job Description SUMMARY Spectrum Staffing Services is seeking a QC Technician for a direct-hire opportunity in the Woodbridge area of New Jersey. This role performs quality testing of raw materials and formulas, supports laboratory operations and food safety activities, and assists with product investigations. RESPONSIBILITIES • Perform standard QC testing and sample incoming raw materials using established procedures, including GC and HPLC analysis., • Support analytical method development and provide technical support to Operations, R&D, suppliers and customers., • Perform laboratory equipment checks and calibrations while following GLP, GMP and safety standards., • Maintain laboratory supplies, raw materials, product retains, testing procedures, forms and lot records., • Investigate out-of-specification materials, deviations, rejections and internal or customer/vendor nonconformances., • Document material rejections and deviations to support root cause investigations and corrective actions., • Create, review and revise QC SOPs; support timely product approval, rework and rejection dispositions., • Assist with food safety responsibilities and interpret and report microbiological test results as needed. QUALIFICATIONS • BS in Food Science, Microbiology, Chemistry or a related science field., • 1–3 years of experience in a quality control laboratory or similar role., • Hands-on experience with both GC and HPLC, plus method development experience., • Food safety experience and a clear understanding of laboratory equipment., • Strong problem-solving, communication and interpersonal skills; proficiency in Word, Excel and Outlook., • Ability to stand for extended periods and lift up to 50 pounds. BENEFITS • Annual bonus eligibility of up to 10%, based on individual and company performance; paid in Q1., • Direct-hire opportunity with hands-on exposure to analytical testing, food safety and cross-functional laboratory support.\nCompany Description With over thirty-five years of Recruiting, Staffing and HR Consulting experience providing nationwide service to many of the largest organizations in the country, Spectrum has achieved a level of experience and expertise that benefits our clients, candidates and contractors. Through an in depth analysis of our client’s organization, we develop an understanding of the skills and experience required for the successful candidate or contractor. EXPERTISE: Our Staffing Consultants are specialists in Human Resources, Scientific/Medical Device, Engineering, Insurance and Business Operations placement. STAFFING OPTIONS: Spectrum offers a number of staffing options including, Direct Hire, Contract, Temp, Retained Search, Recruiting Process Outsourcing (RPO) and Pay-Rolling (Payroll Transfer). CANDIDATE COMMITMENT: Spectrum is committed to working with the top candidates and contractors in the country and developing a working relationship with them to secure the career opportunities that will match their skills, experience and personal aspirations. OPEN POSITIONS: To apply online for our career opportunities go to our job board. www.spectrumstaffingusa.com SPECIALTIES: Areas of specialization include: Human Resources, Scientific/Medical Device, Engineering, Insurance and Business Operations placement. With over thirty-five years of Recruiting, Staffing and HR Consulting experience providing nationwide service to many of the largest organizations in the country, Spectrum has achieved a level of experience and expertise that benefits our clients, candidates and contractors. Through an in depth analysis of our client’s organization, we develop an understanding of the skills and experience required for the successful candidate or contractor. \r\n\r\nEXPERTISE: \r\nOur Staffing Consultants are specialists in Human Resources, Scientific/Medical Device, Engineering, Insurance and Business Operations placement. \r\n\r\nSTAFFING OPTIONS: \r\nSpectrum offers a number of staffing options including, Direct Hire, Contract, Temp, Retained Search, Recruiting Process Outsourcing (RPO) and Pay-Rolling (Payroll Transfer).\r\n \r\nCANDIDATE COMMITMENT: \r\nSpectrum is committed to working with the top candidates and contractors in the country and developing a working relationship with them to secure the career opportunities that will match their skills, experience and personal aspirations.\r\n\r\nOPEN POSITIONS:\r\nTo apply online for our career opportunities go to our job board. www.spectrumstaffingusa.com\r\n\r\nSPECIALTIES: \r\nAreas of specialization include: Human Resources, Scientific/Medical Device, Engineering, Insurance and Business Operations placement.

Job Description Job Title: Microbiology Lab Technician Location: Elizabeth, New Jersey Type: Contract To Hire Compensation: $23.00 per hour Contractor Work Model: Onsite Hours: 6:00 AM – 2:30 PM (must be flexible to work additional or earlier hours when required) Responsibilities • Receive and prepare raw, in-process, and finished product samples for microbiological analysis., • Perform laboratory testing in compliance with established standards and regulations., • Maintain accurate and legible documentation following GLP guidelines., • Review test results against specifications; perform product holds and releases as needed., • Conduct bacterial identifications and maintain laboratory databases., • Perform equipment checks and safety monitoring., • Assist in maintaining the lab’s quality control system., • Sterilize microbiological waste and biohazards., • Adhere to GMP and safety standards; report any food safety or personnel safety concerns., • Participate actively in safety meetings and trainings., • Perform additional duties as assigned. Requirements, • Associate Degree (AA) or equivalent combination of education, training, and experience., • Preferred: BS Degree in Microbiology; graduates of Fortis Institute or Berdan Institute are encouraged to apply., • Experience in microbiological testing from an academic or lab setting., • Knowledge of GMPs, GLPs, and sanitation procedures is a plus., • Candidates must demonstrate genuine career interest and commitment., • Research the company prior to interview to understand the business. System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law. #M- #LI- Ref: #558-Scientific

Job Description Director of Quality | Dietary Supplement Manufacturing About the Role We're partnering with a growing supplement manufacturer that is looking for a Director of Quality to own its quality and compliance function. You'll set the strategy and stay close to daily execution, making sure every product that ships is safe, consistent, and fully compliant. You'll work closely with production, R&D, regulatory, procurement, and customers, and you'll be the face of quality during regulatory inspections and customer audits. This is an in-person position just outside of New Jersey What You'll Do • Build, maintain, and continuously strengthen the quality management system, ensuring alignment with FDA dietary supplement cGMP regulations (21 CFR Part 111), • Establish and enforce SOPs and quality policies across the organization, and train teams on quality expectations, • Own the supplier quality program, including approval of new vendors, on-site and remote audits, and ongoing performance monitoring, • Lead internal audit activity and keep the facility inspection-ready at all times, • Act as the lead quality contact for FDA inspections, third-party audits, and customer visits, • Approve incoming material documentation before use in production and release finished-product documentation to customers, • Review and sign off on analytical methods, test data, and specifications across raw, in-process, and finished materials, • Manage the stability and shelf-life program, • Lead investigations into deviations, out-of-specification results, and customer complaints, and drive corrective and preventive actions, • Run the retain sample program, including sensory evaluation of production lots, • Support customer-driven certification and qualification projects, • Partner with R&D, production, and regulatory teams so quality is built in from development through manufacturing, • Track and trend key quality metrics, such as complaints, deviations, and audit findings, to drive ongoing improvement What You Bring • Working knowledge of FDA regulations and cGMP, including 21 CFR Part 111, and sound quality system principles, • Hands-on experience with supplier qualification, auditing, and compliance, • Leadership presence and the ability to collaborate across departments, • Strong written communication, documentation, and problem-solving skills, • Comfort with Microsoft Office; experience with SharePoint or similar document-sharing platforms is a plus; ERP familiarity is helpful Background • Bachelor's degree in a scientific field such as chemistry, microbiology, or food science (or equivalent), • 5 to 10 years in quality management in the dietary supplement or nutraceutical industry, including exposure to laboratory operations Compensation: $140,000 - $165,000 If this sounds like the position you have been waiting for, please apply using the online application or the link below. All inquiries are strictly confidential. Our focus is to assist you in making your best next career move, and we will not use your information for any other purpose. Kalon Search is an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status. www.KalonSearch.com

Job DescriptionDescription: Position Summary The Microbiology Supervisor is responsible for overseeing day-to-day microbiology laboratory operations, supervising laboratory personnel, and ensuring microbiological testing and environmental monitoring activities are performed in compliance with cGMP requirements. This position supports product release, quality systems, laboratory investigations, and continuous improvement initiatives while maintaining a compliant and efficient laboratory operation. Essential Duties & Responsibilities • Coordinates microbiological testing, release of product, and testing for validation protocols., • Performs organism identification., • Performs technical review of batch filling records to ensure quality of aseptic processes., • Reads and interprets microbiological cultures and other related tests, including but not limited to environmental monitoring, sterility tests, growth promotion, and microbial limits tests., • May perform validation, technology transfer, and troubleshooting, and write policy procedures for quality initiatives., • Reviews and approves environmental monitoring data, laboratory equipment, and records. Prepares process and status reports, assigns and monitors document numbers, and reviews documents for accuracy and completeness., • Trains other Microbiologists on Department methods, processes, and procedures., • Works with other departments to accomplish Company goals or projects., • Performs other functions as required or assigned., • Complies with all company policies and standards.Requirements: Position Requirements and Qualifications: • Bachelor's degree in Biology, Microbiology, or related scientific discipline. 5+ years of microbiology laboratory experience in a cGMP environment. 2+ years of supervisory or leadership experience. Certification from professional organizations such as ASQ and ISPE is desired but not required., • Working knowledge of cGMP regulations (21 CFR Parts 210, 211, and applicable regulations)., • Working knowledge of Quality Systems including Deviations, CAPA, Change Control, and Validation/Qualification (IQ/OQ/PQ)., • Ability to read and interpret safety rules, operating instructions, technical procedures, and regulatory requirements., • Ability to prepare reports, documentation, and business correspondence., • Effective verbal communication and presentation skills. · Ability to interpret and apply written, verbal, schematic, and procedural instructions., • Strong organizational, analytical, and problem-solving skills., • Proficiency with Microsoft Office and applicable laboratory systems., • Strong organizational skills with the ability to prioritize multiple assignments and meet deadlines. Reporting and Work Environment • Typing, desk work, and plant auditing., • Must be able to read, write, and understand English., • Manufacturing clean rooms. Some brief and/or minimal exposure to hazardous chemicals may occur, requiring personal protective equipment., • Safety alertness is required due to working around hazardous equipment and conditions., • General work environment and physical demands as required to successfully perform the essential functions of this job., • Ability to work flexible hours as needed., • Ability to work under pressure and meet deadlines. This position description is not a complete list of all responsibilities, duties, or skills required for the job and is subject to review and change at any time, with or without notice, in accordance with the needs of the organization. Prolong Pharmaceuticals, LLC provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability, or genetics. In addition to federal law requirements, Prolong Pharmaceuticals, LLC complies with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.

Job DescriptionDescription: Position Summary Microbiologist reports to and takes direction from Microbiology Management. This individual works closely with Management on department strategy and work projects. Essential Duties & Responsibilities • Coordinates microbiological testing, release of product, and testing for validation protocols., • Performs organism identification., • Performs technical review of batch filling records to ensure quality of aseptic processes., • Reads and interprets microbiological cultures and other related tests, including but not limited to environmental monitoring, sterility tests, growth promotion, and microbial limits tests., • May perform validation, technology transfer, and troubleshooting, and write policy procedures for quality initiatives., • Reviews and approves environmental monitoring data, laboratory equipment, and records. Prepares process and status reports, assigns and monitors document numbers, and reviews documents for accuracy and completeness., • Performs other functions as required or assigned, • Complies with all company policies and standardsRequirements: Position Requirements and Qualifications Minimum Qualifications: A 4-year Bachelor's degree, preferably in a science or engineering discipline Experience: • Previous experience for Micro I (0 to 2 years or more), Micro II (2 to 5 years or more), and Micro III (5 plus years) in a cGMP biologics/biosimilars manufacturing laboratory environment is required., • Working knowledge of cGMP regulations (21 CFR210/211/820) is desired., • Working knowledge of Deviation, CAPA, Change Control, and Validation/Qualification (IQ/OQ/PQ) is desired., • Certification from professional organizations such as ASQ and ISPE is desired but not required. SPECIALIZED KNOWLEDGE AND SKILLS: • Other special projects and/or duties may be assigned by Management., • Trains other Microbiologists on Department methods, processes, and procedures., • Works with other departments to accomplish Company goals or projects., • Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals., • Ability to write routine reports and/or correspondence, • Ability to speak effectively before groups or employees of the organization., • Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form

Job Description Silver Lake Hospital of Newark, NJ is seeking to hire a full time Lab Medical Technologist I to perform and interpret automated and manual testing procedures. ABOUT SILVER LAKE HOSPITAL Silver Lake Hospital is a long-term acute care hospital with a reputation of providing patients with a place to heal before heading home. A long-term acute care hospital (LTACH) is an acute care specialty hospital that provides highly advanced and focused care for higher acuity patients who have not responded to short-term treatment in traditional general hospitals. The average length of stay in an LTACH is 25 days as compared to a 3-5 day average stay in a general hospital. Our safe and state of the art hospital is designed to admit and care for the most critically ill patients. POSITION SUMMARY This position is responsible for performing and interpreting automated and manual testing procedures on blood, urine, and other body specimens. This position does not involve direct patient care for a population of patients between the ages of 18 and older and does not require age specific experience, specialized training and/or expertise to serve this population. QUALIFICATIONS • BS Degree with a major in medical technology, chemistry, biology, or microbiology or a minimum of 90 credits. Foreign degrees require a Credential Equivalency Evaluation., • Up to 3 years of clinical lab experience required., • MT (ASCP) certification or eligible is desired., • Proficient in Microsoft Office., • Good close vision and color perception required and able to read the Jaeger Eye Chart. ARE YOU READY TO JOIN OUR TEAM? If you feel that you would be right for this position complete our initial 3-minute, mobile-friendly application. After this step, you will receive an invite to complete your full application. Thank you. Job Posted by ApplicantPro

Job Description About the company Deep Foods is one of the leading manufacturers of Indian foods. Since 1977, it has been tantalizing the taste buds of Indian food lovers. Using authentic recipes, Deep Foods offers delicious snacks, frozen meals, ice creams and other specialties. Position summary The FSVP/Regulatory Compliance Specialist supports and maintains the company’s Foreign Supplier Verification Program (FSVP) and import compliance activities for a diverse portfolio including RTE frozen foods, spices, snacks, ingredients, and finished goods. This role ensures imported foods meet FDA/FSMA requirements through supplier documentation management, verification activity tracking, risk-based assessments, and inspection-ready recordkeeping across multiple suppliers, products, and distribution locations. Department: Quality / Regulatory Reports to: Director of Quality/Regulatory Manager Location: Union, NJ Key responsibilities Standard Hours: 10:00 AM – 6:00 PM but flexible. This is not a remote position, and requires international travel to support supplier audits, facility visits, and verification activities. · Maintain FSVP files for each foreign supplier, ensuring completeness and inspection readiness. · Support the FSVP Qualified Individual (QI) by preparing documentation for hazard evaluations and supplier verification plans, and tracking completion to schedule. · Collect, review, and organize supplier compliance documents, verification activities, and file results in the FSVP system. · Support supplier approval/monitoring: maintain approved supplier list status, performance tracking, and escalation of issues. · Assist with import entry documentation coordination with customs brokers/forwarders: ensure required documents are available, consistent, and retrievable. · Initiate and document corrective actions for supplier nonconformances related to imported materials (e.g., import alerts, refusals), including follow-up and closure support. · Participate in inspection readiness: rapid retrieval of FSVP/import records for FDA inquiries/inspections; support responses and internal action tracking. · Work cross-functionally with QA, Procurement, Logistics, and Operations to align supplier compliance requirements with purchasing and receiving practices across distribution warehouses and the manufacturing facility. Qualifications Required · Bachelor’s degree in Food Science, Microbiology, Chemistry, Regulatory Affairs, or related (or equivalent experience). · 3–5 years in food industry QA/regulatory/supplier compliance, with exposure to imports and supplier verification. · Experience with RTE frozen foods, spices, and/or snacks. · Knowledge of FSMA/FSVP concepts. · Knowledge of relevant food safety legislation, GFSI audits, HACCP · Strong documentation control skills; comfortable with audits/inspection readiness. · Strong communication and follow-up skills with suppliers and internal teams. · FSVP Qualified Individual preferred. \nCompany Description Deep Foods is a major food manufacturer based that specializes in prepared Indian foods and frozen food products. Since 1977, we have been dedicated to delivering high-quality products through innovation and a commitment to excellence. Our mission is to bring authentic Indian cuisine to consumers nationwide while maintaining the highest standards of quality and safety. Deep Foods is a major food manufacturer based that specializes in prepared Indian foods and frozen food products. Since 1977, we have been dedicated to delivering high-quality products through innovation and a commitment to excellence. Our mission is to bring authentic Indian cuisine to consumers nationwide while maintaining the highest standards of quality and safety.

Job DescriptionRole Overview: The Quality Systems Supervisor will support the maintenance of the company's quality systems and food safety requirements, with a strong focus on BRCGS compliance, audit preparation, product quality, and sanitation operations. This individual will help ensure that required documentation is properly maintained and that production standards are consistently followed. The position works across Quality, Production, Maintenance, Sanitation, and Warehouse to support product safety and quality. The Quality Systems Supervisor will also oversee the Sanitation Department and supervise Quality Systems Technicians, requiring strong attention to detail, sound judgment, and the ability to work independently. Job Requirements: • Bachelor's degree in Food Science, Food Safety, Quality Assurance, Microbiology, or a related field preferred., • Knowledge of BRCGS standards, food safety requirements, and third-party audit preparation., • Familiarity with maintaining and organizing food safety and quality documentation., • Knowledge of production quality standards, including product color, shape, size, taste, and packaging., • Ability to coordinate with Production, Maintenance, Sanitation, and Warehouse to support product safety., • Experience or familiarity with sanitation operations, including sanitation chemicals and supplies., • Strong proficiency in Microsoft Excel and Outlook, along with internet research skills., • Bilingual English/Spanish required., • Excellent written and verbal communication skills., • Strong attention to detail and organizational skills., • Ability to work independently and as part of a team., • Demonstrated initiative, sound judgment, and the ability to make independent decisions., • Strong sense of urgency and commitment to maintaining quality and customer satisfaction. Personal Attributes / Skills: • Detail-oriented and highly organized., • Self-motivated and proactive., • Able to exercise sound judgment and make decisions independently., • Strong communicator with a collaborative approach., • Accountable and dependable., • Able to prioritize effectively in a fast-paced manufacturing environment., • Quality-focused with a strong sense of urgency., • Professional when working with employees across multiple departments., • Bilingual English/Spanish required. Key Responsibilities: • Support BRCGS Compliance: Assist with maintaining annual BRCGS requirements and ensuring the facility remains prepared for third-party audits., • Maintain Food Safety Documentation: Ensure supporting food safety documentation related to BRCGS standards is properly organized, maintained, and readily available., • Monitor Product Quality: Review production activities to ensure consistent product quality, including color, shape, size, taste, packaging, and other applicable standards., • Coordinate Product Safety: Work closely with Production, Maintenance, Sanitation, and Warehouse to support product safety throughout the manufacturing process., • Oversee Sanitation Operations: Supervise the Sanitation Department and ensure sanitation activities and requirements are properly supported., • Manage Sanitation Supplies: Monitor and order sanitation chemicals and supplies as needed., • Supervise Quality Systems Staff: Provide oversight to Quality Systems Technicians and support the effective execution of quality-related activities., • Support Audit Readiness: Assist with maintaining organized records and ensuring the facility is prepared for BRCGS and third-party audits., • Maintain Quality Standards: Help ensure production activities consistently meet established quality and food safety requirements., • Support Cross-Functional Communication: Coordinate quality and food safety matters with relevant departments and provide follow-up when issues arise., • Perform other job-related duties as assigned. GRIT Staffing & HR Solutions is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees and applicants. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status. If you require a reasonable accommodation during the application or interview process, please contact us at eoc@gritstaffinghr.com so we can assist you.

Job Title: QC Associate Scientist, Microbiology Location: Summit, NJ 07901 Assignment Duration: 06 months QC Associate Scientist, Microbiology - Wed-Sat 7:00 AM to 5:30 PM POSITION SUMMARY This position will work both independently and with the team to perform routine and non-routine microbiologica

R1607711 : Senior Specialist QC Microbiology Cell Therapy.

Medical Laboratory Scientist II - Perth Amboy, NJ, Rotating Schedule 7:00 AM to 3:30 PM.Quest Diagnostics is hiring a Medical Laboratory Scientist II in Perth Amboy, NJ.This role is a hospital-based position at Raritan Bay.Salary offers are based on a wide range of factors including relevant skills,

Requires an Associate Degree and lab testing experience. Microbiology Lab Technician needed for on-site contract-to-hire role. Responsibilities include sample preparation, laboratory testing, documentation, and maintaining lab quality control.

Eurofins Scientific is seeking a microbiology professional to lead environmental monitoring in a GMP setting in Rahway, NJ. You will perform cleanroom monitoring, EM sampling, and microbiology testing of utilities and finished products. The role requires 2+ years in pharma microbiology (MS) or 3+ ye

Physical Demands: General Office Environment.

The Quality Control Analyst is responsible for performing chemical, microbiological, and radiological testing of raw materials, intermediates, and finished radioligand pharmaceutical products.This role ensures compliance with GMP, FDA, and radiation safety regulations, supporting the release of high

MLS, Medical Laboratory Scientist, Medical Lab Scientist, Med Tech, Medical Technologist, CLS, Clinical Lab Scientist. Quest Diagnostics is hiring a Medical Laboratory Scientist II in Perth Amboy, NJ. Medical Laboratory Scientist II - Perth Amboy, NJ, Rotating Schedule 7:00 AM to 3:30 PM.

The Director, QC Microbiology is responsible for all operational aspects of the Quality Control Microbiology organization at the CAR T facility in support of stability programs, testing of raw materials, in-process controls, and final product samples, reading environment monitoring plates from routi

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CRA supports the day to day operations associated with the execution of clinical trials.He / she will monitor multiple clinical trial sites and studies.The primary objective and purpose of this position is to ensure the overall quality of clinical trials by monitoring study data and managing site ad

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Manage one or two multifamily projects from buyout to turnover.Own the budget, schedule, and monthly cost reporting.Lead subcontractor buyout, contracts, and change orders.Run OAC meetings and act as the main contact for the owner and design team.Work closely with the Superintendent on sequencing, l

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Founded in 1960, RW Dake Construction is an employee-owned specialty general contractor with 11 regional offices across New York, New Jersey, New England, Maryland, North Carolina, and Florida.For more than 65 years, RW Dake Construction has delivered the experience, quality, and safety our clients

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Founded in 1960, RW Dake Construction is an employee-owned specialty general contractor with 11 regional offices across New York, New Jersey, New England, Maryland, North Carolina, and Florida.For more than 65 years, RW Dake Construction has delivered the experience, quality, and safety our clients

Robert Half is looking for motivated Assistant Project Managers in the Commercial Construction space for our client in the Westfield, NJ area.This is an amazing opportunity to join a growing construction team and gain valuable project management experience in the commercial space.FANTASTIC benefits

Assistant Project Manager (Electrical Construction).South Plainfield, NJ (In-Person).McPhee Electric, a Phalcon Company is a high-performance electrical contractor known for delivering complex, fast-paced projects with precision, accountability, and strong field leadership.We don’t just manage pro

Accu Reference Medical Lab is a state-of-the-art medical testing laboratory that offers a comprehensive range of tests for the diagnosis, screening, and evaluation of diseases and health conditions.The laboratory is certified under the federal Clinical Laboratory Improvement Amendments (CLIA) and op

The Medical Assistant II provides clinical office support to physicians and surgeons and performs patient care and administrative duties necessary to deliver quality patient care.Mentors and assists less experienced staff members.Fulfills patient care responsibilities as assigned which may include:

Our client is an established renewable energy developer focused on advancing utility-scale solar and energy storage projects across key U.Backed by a global energy organization, the company combines financial strength with deep development expertise to deliver high-quality clean energy assets from e