QuVa Pharma jobs - 22 jobs

Our Production Technician I - Label Printing plays a vital role in ensuring the highest quality and safety standards of our pharmaceutical products. Once you complete our training, your responsibilities will include printing of labels for compounded sterile products (CSPs), bulk bags and non-sterile solutions in accordance with current Good Manufacturing Practices and Operating Procedures and communicates functions and duties necessary to operate the label printing equipment. Your attention to detail and adherence to precise procedures will guarantee that our medications meet the highest standards of safety, efficacy, and quality, providing patients with the best possible care and outcomes. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US. This is a full-time role for our 2nd Shift working Monday through Friday from 2:00 PM to 10:30 PM. This is a set, consistent schedule with minimum overtime requirements and based on site in our Bloomsbury, NJ location. This is a safety sensitive position that may be subject to random drug testing, in accordance with applicable laws. What the Production Technician I - Label Printing Does Each Day: Operates label printing/verification equipment to print product labels Safely transports label rolls from storage to printing area and back to printed label storage Performs Batch specific cleaning of room and equipment and fill out appropriate preventative maintenance forms and checklists Documents in a timely manner all tasks requiring written records Maintains a smooth flow of production and monitors equipment Escalates any equipment or process deviation Our Most Successful Production Technician I - Label Printing: Approach others in a tactful manner React well under pressure Follow through on commitments Carefully follows clear directions to ensure safety and accuracy Are detail-oriented and take careful notes Take initiative to identify problems and opportunities Minimum Requirements for this Role: A High School diploma or equivalent Able to successfully complete a background check Able and willing to walk, stoop, stand, bend, and lift up to 50 lbs. throughout each shift, with or without reasonable accommodation Familiarity with and comfortable using mobile devices such as smartphones, tablets, handhelds 18+ years of age Must be currently authorized to work in the United States on a full-time basis; Quva will not sponsor applicants for work visas Minimum of 1 year reliable and sustained performance as Production Technician (ILP, Post Compounding, Formulation, Warehouse) OR relevant work experience Label printing CAs as per Label Printing training curriculum Any of the Following Will Give You an Edge: College Degree with an emphasis in Chemistry, Biochemistry or equivalent Pharmaceutical experience Experience operating printing equipment, computer software & hardware Working knowledge of cGMPs and regulatory requirements as well as all applicable SOPs Benefits of Working at Quva: Set, full-time, consistent work schedule Comprehensive health and wellness benefits including medical, dental and vision 401k retirement program with company match 17 paid days off plus 8 paid holidays per year Occasional weekend and overtime opportunities with advance notice National, industry-leading high growth company with future career advancement opportunities The base compensation for this role is estimated to be within the range described below. The compensation offered may vary depending on relevant factors such as experience, skills, training, education, certifications, geographic location, and market conditions Range: $19.00-$23.00/hour + $2.50 shift differential for 2nd shift About Quva: Quva is a national, industry-leading provider of compounded injectable medicines and software solutions that help power the business of hospital and health-system pharmacy. Quva Pharma produces and distributes injectable medicines required by health care providers and critical to patient care. Quva BrightStream partners with health-systems to analyze large amounts of data and through AI and machine learning, develops software solutions that turns the data into insights that are used to better run their pharmacy operation. Quva's overall product and technology offerings help health-systems achieve greater value and deliver the highest-quality patient care. Quva is an equal opportunity employer and is committed to creating and maintaining a work environment that is free from all forms of discrimination and harassment. Quva's Equal Opportunity Policy prohibits harassment or discrimination due to age, ancestry, color, disability, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, race, religious creed, sex (including pregnancy, childbirth, breastfeeding, and any related medical conditions), sexual orientation, and any other characteristic or classification protected by applicable laws. All employment with Quva is “at will.” California Consumer Privacy Act (CCPA) Notice for Applicants and Employees

Our HR Generalist II plays a vital role within our organization. Once you complete our training, you will be responsible for providing broader Human Resources support with increasing autonomy. Your attention to detail and adherence to precise procedures will guarantee that our medications meet the highest standards of safety, efficacy, and quality, providing patients with the best possible care and outcomes. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US. What the Title Does Each Day: * Conducts onboarding activities including new-hire orientation * Maintains human resource information system records and compiles reports from the database; Maintain HRIS accuracy and compliance documentation * Provides frontline HR support to employees and managers * Supports the planning and execution of employee town halls * Lead and execute employee engagement initiatives * Assists with the administration of employee leave of absences * Partners with payroll/benefits to resolve escalated issues * Administers various human resource plans and procedures for all organization personnel; assists in the development and implementation of personnel policies and procedures * Participate in developing department goals, objectives and systems * Supports administration of the compensation program; monitors the performance evaluation program * Conducts exit interviews and report trends * Support employee relations investigations * Maintains compliance with federal, state and local employment and benefits laws and regulations * Supports and advises supervisors on employee relations issues * Facilitates performance management and goal-setting processes * Supports HR projects (policy updates, engagement initiatives, compliance audits) Our Most Successful HR Generalists: * Sense of urgency, accountability, and resourcefulness (e.g., work in changing environment) * Self-starter, independent learner * Communication: Promotes active listening with team members; Contributes appropriately to conversations; Strong verbal and written communication skills with the ability to work effectively with other departments within the organization and with people at all levels of the organization * Problem Solving: Understands how various issues affect each other and the outcome of projects; Improves upon existing approaches by seeking opportunities to creatively transform Minimum Requirements for this Role: * Education: BS, Human Resources or similar field * Experience- 2+ years direct experience * 18+ years of age * Able to successfully complete a drug and background check * Bachelor's degree in Human Resources or Business * 2-4 years' experience in Human Resources field * Knowledge of employment law and practices * Familiarity with recruiting systems and software * Experience supporting multiple professionals in a fast paced highly dynamic work environment * Advanced level of proficiency with Excel, Word, PowerPoint, and Outlook * May require local travel by car to other Quva locations * Must be currently authorized to work in the United States on a full-time basis; Quva is not able to sponsor applicants for work visas Any of the Following Will Give You an Edge: * SHRM-CP or SHRM-SCP certification or ability to obtain certification within 24 months of hire date Benefits of Working at Quva: * Set, full-time, consistent work schedule * Comprehensive health and wellness benefits including medical, dental and vision * 401k retirement program with company match * 17 paid days off plus 8 paid holidays per year * Occasional weekend and overtime opportunities with advance notice * National, industry-leading high growth company with future career advancement opportunities * The base compensation for this role is estimated to be within the range described below. The compensation offered may vary depending on relevant factors such as experience, skills, training, education, certifications, geographic location, and market conditions * Range: $65,023 - $89,407 Annually * This role is also eligible for an annual incentive bonus, subject to program terms and guidelines About Quva: Quva provides industry-leading health-system pharmacy services and solutions, including 503B sterile injectable outsourcing services and AI-based data software solutions that help power the business of pharmacy. Quva Pharma's multiple production facilities and industry-first dedicated remote distribution capabilities provide ready-to-administer sterile injectable medicines critical to patient care. Quva BrightStream partners with health systems to aggregate, normalize, and analyze large amounts of complex data across their sites of care, and through proprietary machine learning, transforms data into actionable insights supporting revenue optimization, script capture, inventory management, drug shortage control, and more. Quva's overall progressive and integrated platform helps health-systems transform pharmacy management to achieve greater value and deliver highest-quality patient care. Quva is an equal opportunity employer and is committed to creating and maintaining a work environment that is free from all forms of discrimination and harassment. Quva's Equal Opportunity Policy prohibits harassment or discrimination due to age, ancestry, color, disability, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, race, religious creed, sex (including pregnancy, childbirth, breastfeeding, and any related medical conditions), sexual orientation, and any other characteristic or classification protected by applicable laws. All employment with Quva is "at will." California Consumer Privacy Act (CCPA) Notice for Applicants and Employees

Our Warehouse Technician I - Picking plays a vital role in ensuring the highest quality and safety standards of our pharmaceutical products. Once you complete our training, your responsibilities will include completing the batch picking processes utilizing manual or automated technology. You will be integral in ensuring that batches are picked in support of production requirements and inventory is accurately transacted and maintained. Your attention to detail and adherence to precise procedures will guarantee that our medications meet the highest standards of safety, efficacy, and quality, providing patients with the best possible care and outcomes. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US. This is a full-time role for our 1st shift, working Monday through Friday from 6:00 AM to 2:30 PM. This is a set, consistent schedule with minimum overtime requirements and based on site in our Bloomsbury, NJ location. This is a safety sensitive position that may be subject to random drug testing, in accordance with applicable laws. Watch this Video to learn more. What Warehouse Technician I - Picking Does Each Day: * Picks starting materials and supplies according to the ERP generated picklist to support the batch manufacturing process * Transacts picked material utilizing an ERP system * Verifies picked material matches the picklist * Pulls from inventory items necessary to restock and restocks shelves * Rotates stock in accordance with First-Expired, First-out procedure * Checks for and pulls opened, damaged, expired and/or excess inventory and replaces unusable, damaged, or packaging, labels etc. * Handles defective, damaged and/or expired inventory in accordance with established departmental policy * Unloads trucks of materials and loads recycling material on trucks * Removes pallets, strapping and packing materials, and moves recycle materials to recycle area * Receives and puts away material in designated locations to support effective warehouse flow * Verifies bill of lading and packing Our Most Successful Warehouse Technicians I - Picking: * Are Highly detail oriented and organized * Follow procedures and clear instructions * Able to shift gears at a moment's notice Minimum Requirements for this Role: * A High School diploma or equivalent * Able to successfully complete a drug and background check * Able and willing to walk, stoop, stand, bend, and lift up to 50 lbs. throughout each shift, with or without reasonable accommodation * 18+ years of age * Familiarity with and comfortable using mobile devices such as smartphones, tablets, handhelds * Requires 1-2 years of experience in anyone, or combination of the following: Distribution, Warehousing, Shipping, Receiving, Logistics, Material handling, Customer Service, Inventory Control, or other comparable service line. * Competency assessment for Batch Picking * Completion of Material Handling Equipment training and understanding of inventory management and rotation * Must be currently authorized to work in the United States on a full-time basis; Quva will not sponsor applicants for work visas Any of the Following Will Give You an Edge: * Basic computer and data entry skills. * AS400 and INFOR or other ERP experience * Microsoft Office Suite. * Good communication and customer service skills. * Knowledge of discrete batch manufacturing in pharmaceutical or related field Benefits of Working at Quva: * Set, full-time, consistent work schedule * Comprehensive health and wellness benefits including medical, dental and vision * 401k retirement program with company match * 17 paid days off plus 8 paid holidays per year * Occasional weekend and overtime opportunities with advance notice * National, industry-leading high growth company with future career advancement opportunities * The base compensation for this role is estimated to be within the range described below. The compensation offered may vary depending on relevant factors such as experience, skills, training, education, certifications, geographic location, and market conditions * Range: $18.00-$21.00/hour About Quva: Quva is a national, industry-leading provider of compounded injectable medicines and software solutions that help power the business of hospital and health-system pharmacy. Quva Pharma produces and distributes injectable medicines required by health care providers and critical to patient care. Quva BrightStream partners with health-systems to analyze large amounts of data and through AI and machine learning, develops software solutions that turns the data into insights that are used to better run their pharmacy operation. Quva's overall product and technology offerings help health-systems achieve greater value and deliver the highest-quality patient care. Quva is an equal opportunity employer and is committed to creating and maintaining a work environment that is free from all forms of discrimination and harassment. Quva's Equal Opportunity Policy prohibits harassment or discrimination due to age, ancestry, color, disability, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, race, religious creed, sex (including pregnancy, childbirth, breastfeeding, and any related medical conditions), sexual orientation, and any other characteristic or classification protected by applicable laws. All employment with Quva is "at will." California Consumer Privacy Act (CCPA) Notice for Applicants and Employees

Our Production Maintenance Mechanic II plays a vital role in ensuring the highest quality and safety standards of our pharmaceutical products. Once you complete our training, your responsibilities will include performing maintenance, troubleshooting, and of cleanroom-critical production equipment, including automated inspection, labeling, and packaging equipment. This role requires demonstrated capability in aseptic gowning procedures and to maintain compliance with cGMP and 503B pharmaceutical regulatory standards. The position ensures all equipment is maintained in validated state, operates within defined parameters, and complies with site SOPs, FDA regulations, and applicable quality standards. Responsibilities include real time documentation in CMMS, adherence to aseptic practices, and sustaining a clean and complaint workspace to support sterile manufacturing operations. At Quva, you will be an essential part of a mission-driven organization dedicated to expanding critical access to quality, affordable medication and data insights while promoting a culture of innovation, collaboration, and continuous improvement. This is a full-time role for our 2nd shift, working Monday through Friday from 2:30 PM to 10:30 PM. This is a set, consistent schedule with minimum overtime requirements and based on site in our Bloomsbury, NJ location. What the Production Maintenance Mechanic II Does Each Day: * Performs and/or coordinates planned and demand maintenance activities on production and cleanroom equipment while following all applicable SOP's * Documents all maintenance work performed in site CMMS system * Ensures maintenance work orders are completed within the timeframe specified * Performs preventative maintenance on all production/manufacturing equipment following all applicable WI's/SOP's * Maintains site equipment list as well as calibration and preventative maintenance schedules * Maintains equipment spare parts list to ensure equipment reliability is always sustained * Maintain systems including mechanical, electrical and pneumatic controls * Troubleshoots and repairs faulty equipment parts * Coaches manufacturing personnel on technical aspects of production equipment * Recognizes priorities and acts, makes productive use of time * Coordinates work orders activities by communicating with the organization via email * Responds to issues after hours and during weekends * Operates in a safe manner utilizing applicable LOTO Procedures * Seeks opportunities to implement a culture of continuous process improvement as related to equipment, processes, and systems at the site * Performs general maintenance activities repair of electrical, mechanical, plumbing and hardware within the site. * Performs general maintenance activities including painting, wall patching, installation of fixtures in both production and office spaces * Assists in root cause analysis and corrective actions for equipment failures * Works in Clean Room Environments and obtains gowning certification Our Most Successful Production Maintenance Mechanic II: * Has a sense of urgency, accountability, and resourcefulness (e.g., work in changing environment) * Is a self-starter and independent learner * Promotes active listening with team members; Contributes appropriately to conversations; Strong verbal and written communication skills with the ability to work effectively with other departments within the organization and with people at all levels of the organization * Understands how various issues affect each other and the outcome of projects; Improves upon existing approaches by seeking opportunities to creatively transform Minimum Requirements for this Role: * High School Diploma or equivalent required * 5-7 years prior experience in Maintenance or Engineering field * 3 years Cleanroom experience/aseptic gowning procedures * 3 years experience in a cGMP/FDA regulated industry * Able to successfully complete a drug and background check * Must be currently authorized to work in the United States on a full-time basis; Quva will not sponsor applicants for work visas Any of the Following Will Give You an Edge: * Computerized Maintenance Management System (CMMS) principles * Experience working with PLC's, HMI's, Robotics, and SCADA systems * Equipment/Instrument Calibration principles * OSHA, Maintenance, or Electrical Certifications Benefits of Working at Quva: * Set, full-time, consistent work schedule * Comprehensive health and wellness benefits including medical, dental and vision * 401k retirement program with company match * 17 paid days off plus 8 paid holidays per year * Occasional weekend and overtime opportunities with advance notice * National, industry-leading high growth company with future career advancement opportunities * The base compensation for this role is estimated to be within the range described below. The compensation offered may vary depending on relevant factors such as experience, skills, training, education, certifications, geographic location, and market conditions * Range: $31.85 - $50.95 / Hour + $2.50 shift differential for 2nd shift About Quva: Quva is a national, industry-leading provider of compounded injectable medicines and software solutions that help power the business of hospital and health-system pharmacy. Quva Pharma produces and distributes injectable medicines required by health care providers and critical to patient care. Quva BrightStream partners with health-systems to analyze large amounts of data and through AI and machine learning, develops software solutions that turns the data into insights that are used to better run their pharmacy operation. Quva's overall product and technology offerings help health-systems achieve greater value and deliver the highest-quality patient care. Quva is an equal opportunity employer and is committed to creating and maintaining a work environment that is free from all forms of discrimination and harassment. Quva's Equal Opportunity Policy prohibits harassment or discrimination due to age, ancestry, color, disability, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, race, religious creed, sex (including pregnancy, childbirth, breastfeeding, and any related medical conditions), sexual orientation, and any other characteristic or classification protected by applicable laws. All employment with Quva is "at will." California Consumer Privacy Act (CCPA) Notice for Applicants and Employees

Our Automation Engineer supports, develops, and maintains automated systems used in pharmaceutical manufacturing. This role ensures that production equipment, control systems, and digital infrastructure operate reliably, efficiently, and in compliance with cGMP and regulatory standards. The engineer collaborates with cross‑functional teams to troubleshoot issues, implement improvements, and support new system installations or upgrades. Operates within legal and regulatory compliance, ensuring systems are maintained and operational within site and regulatory requirements. Capable of following procedures, documenting work as/when performed and maintaining a clean/organized workplace supporting site compliance and quality standards. Your attention to detail and adherence to precise procedures will guarantee that our medications meet the highest standards of safety, efficacy, and quality, providing patients with the best possible care and outcomes. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US. This is an onsite role in Bloomsbury, New Jersey; Monday - Friday 6 AM - 2:30 PM. What the Automation Engineer Does Each Day: * Provides technical skills and expertise to support operations, ensuring automated manufacturing equipment operates efficiently, including network configuration and integration principles, and the ability to work effectively with IT * Supports constant operations by trouble shooting machines, monitoring PLC issues, performing root cause analysis on complex issues, and executing improvements * Investigates automation incidents and problems to prevent recurrence including the development and implementation of corrective actions * Design and implementation of equipment and facilities related controls including PLC coding (Allen-Bradley/Siemens), HMI and SCADA systems * Evaluates automated and information technology systems, and develops strategies to optimize and ensure quality and stability of automation systems through future expansion, replacement, or upgrade * Efficient use of different software tools and computer applications including but not limited to Microsoft Office, PLC programming software, electrical schematic design software, HMI programming software, SCADA systems and industrial networks (Allen-Bradley/Siemens) * Effectively and accurately handles most technical questions and objections for assigned products * Maintains appropriate documentation for equipment and processes including change control, drawings, manuals, and validation * Streamlines workflows and develop automated laboratory processes and instrumentation systems, including collecting and documenting requirements, developing concepts, design, testing/validation, implementation, and training * Recognizes priorities and takes action; makes productive use of time * Understands and adheres to policies and procedures * Software validation, data integrity, GAMP 5 and 21 CFR part 11 experience * Operating and troubleshooting of Fanuc Robotics Our Most Successful Automation Engineer Has: * Experience in aseptic processing preferred * Experience with FDA, GMP, and ISO standards preferred * Must possess the ability to work effectively with all levels of organization * Demonstrated ability to build and maintain strong business and collaborative relationships, internally and externally * Must possess excellent interpersonal, communication, and writing skills, ability to analyze technical issues, define/solve problems, establish project plans, and draw valid conclusions * Ability to think analytically and systematically * Aseptic Operator Qualification and Process Simulation * Proficient in technical writing and current computer usage (Word, Excel, PowerPoint, etc.) * Good working knowledge of regulatory guidance as it pertains to APIs and injectable drug products Minimum Requirements for this Role: * Bachelor's degree in electrical engineering, Mechanical Engineering, or another related field, with 5+ years' experience in a manufacturing environment * Experience working with PLCs, HMIs, Robotics (Fanuc, Staubli), and SCADA systems, preferably Rockwell or Siemens platforms * Equipment/Instrument Calibration principles * Proven ability to adapt and manage effectively in fast paced, changing environment * 18+ years of age * Able to successfully complete a drug and background check * Must be currently authorized to work in the United States on a full-time basis; Quva is not able to sponsor applicants for work visas Benefits of Working at Quva: * Set, full-time, consistent work schedule * Comprehensive health and wellness benefits including medical, dental and vision * 401k retirement program with company match * 17 paid days off plus 8 paid holidays per year * Occasional weekend and overtime opportunities with advance notice * National, industry-leading high growth company with future career advancement opportunities * The base compensation for this role is estimated to be within the range described below. The compensation offered may vary depending on relevant factors such as experience, skills, training, education, certifications, geographic location, and market conditions * Range: $85,993 - $134,364 Annually About Quva: Quva provides industry-leading health-system pharmacy services and solutions, including 503B sterile injectable outsourcing services and AI-based data software solutions that help power the business of pharmacy. Quva Pharma's multiple production facilities and industry-first dedicated remote distribution capabilities provide ready-to-administer sterile injectable medicines critical to patient care. Quva BrightStream partners with health systems to aggregate, normalize, and analyze large amounts of complex data across their sites of care, and through proprietary machine learning, transforms data into actionable insights supporting revenue optimization, script capture, inventory management, drug shortage control, and more. Quva's overall progressive and integrated platform helps health-systems transform pharmacy management to achieve greater value and deliver highest-quality patient care. Quva is an equal opportunity employer and is committed to creating and maintaining a work environment that is free from all forms of discrimination and harassment. Quva's Equal Opportunity Policy prohibits harassment or discrimination due to age, ancestry, color, disability, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, race, religious creed, sex (including pregnancy, childbirth, breastfeeding, and any related medical conditions), sexual orientation, and any other characteristic or classification protected by applicable laws. All employment with Quva is "at will." California Consumer Privacy Act (CCPA) Notice for Applicants and Employees

Our Director, Quality Control Lab, plays a vital role within our organization. Once you complete our training, you will be responsible for day-to-day operations of the Quality Control testing laboratories supporting all Quva production sites. This position also coordinates, leads group activities, and develops and implements the department's short and long-term goals to assure compliance with cGMPs and agreement with Quva business initiatives. The Director, Quality Control Lab, manages and develops teams within the department to support Company activities. This role also serves as a technical expert for the site in the areas of chemistry, analytical methods, microbiology and test method transfer. At Quva, you will be an essential part of a mission-driven organization dedicated to expanding critical access to quality, affordable medication and data insights while promoting a culture of innovation, collaboration, and continuous improvement. Your attention to detail and adherence to precise procedures will guarantee that our medications meet the highest standards of safety, efficacy, and quality, providing patients with the best possible care and outcomes. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US. What the Director, Quality Control Lab Does Each Day: * Prepares resource analysis for the execution of projects; Prepares and manages the Department operational budget * Establishes and maintains effective cross functional relationships; Provides necessary support to other Departments * Provides leadership in the training program of laboratory staff; Evaluates subordinates through reviews and periodic discussions; Recommends future development objectives; Fosters teamwork, customer service and cross-functionality * Prepares/reviews/approves departmental documentation (i.e. SOPs, Analytical Method Transfer protocols) * Assures that departmental SOPs are followed and are compliant with current Good Manufacturing Practices (cGMP) and Company policies; Operates the laboratories in a safe and hazard-free manner * Leads the routine Quality Control release testing laboratories to ensure testing is completed on time in a compliant manner * Leads the corporate Stability laboratory to ensure products meet their BUD and with establishing BUD for new products * Applies fundamental knowledge of Analytical Chemistry and advanced technologies in analysis, interpretation and understanding of test results, for both qualitative and quantitative analyses * Provides expertise and assists in writing investigation reports for Laboratory investigation, Operations investigations, and Cross-functional investigations * Recommends or makes changes to tests, assays and specifications to ensure reliability, accuracy and their adequacy for the monitoring of product quality * Provides customer support as needed Our Most Successful Director, Quality Control Lab: * Has outstanding written and oral communication skills * Is excellent at organization of large volumes of data * Has experience in pharmaceutical manufacturing preferably sterile injectable * Manages multiple, parallel projects * Has Expert knowledge of regulatory requirements as they pertain to Human Drug Compounding and Pharmaceutical manufacturing Minimum Requirements for this Role: * A. /B.S. Degree in Chemistry, Biochemistry, Microbiology or related field with significant experience * Ten years of analytical chemical/microbiology laboratory and 5 years of management experience * Pharmaceutical laboratory experience in analytical methods development and validation area is expected * Able to successfully complete a drug and background check * Must be currently authorized to work in the United States on a full-time basis; Quva is not able to sponsor applicants for work visas Any of the Following Will Give You an Edge: * Has experience with manufacturing parenteral products * Has experience in QA/QC Benefits of Working at Quva: * Set, full-time, consistent work schedule * Comprehensive health and wellness benefits including medical, dental and vision * 401k retirement program with company match * 25 paid days off plus 8 paid holidays per year * Occasional weekend and overtime opportunities with advance notice * National, industry-leading high growth company with future career advancement opportunities About Quva: Quva provides industry-leading health-system pharmacy services and solutions, including 503B sterile injectable outsourcing services and AI-based data software solutions that help power the business of pharmacy. Quva Pharma's multiple production facilities and industry-first dedicated remote distribution capabilities provide ready-to-administer sterile injectable medicines critical to patient care. Quva BrightStream partners with health systems to aggregate, normalize, and analyze large amounts of complex data across their sites of care, and through proprietary machine learning, transforms data into actionable insights supporting revenue optimization, script capture, inventory management, drug shortage control, and more. Quva's overall progressive and integrated platform helps health-systems transform pharmacy management to achieve greater value and deliver highest-quality patient care. Quva is an equal opportunity employer and is committed to creating and maintaining a work environment that is free from all forms of discrimination and harassment. Quva's Equal Opportunity Policy prohibits harassment or discrimination due to age, ancestry, color, disability, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, race, religious creed, sex (including pregnancy, childbirth, breastfeeding, and any related medical conditions), sexual orientation, and any other characteristic or classification protected by applicable laws. All employment with Quva is "at will." California Consumer Privacy Act (CCPA) Notice for Applicants and Employees

Our Supervisor, Quality Assurance plays a vital role in ensuring the highest quality and safety standards of our pharmaceutical products. Once you complete our training, your responsibilities will include supervising all Quality Assurance (QA) aspects of compounding pharmaceuticals for compliance within the facility. This position operates within the legal and regulatory compliance, producing a quality product. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US. What the Supervisor, Quality Assurance Does Each Day: * Supervises Quality Assurance staff on assigned shift * Oversees failure and discrepancy investigations and documenting investigations on process deviations or equipment malfunctions * Develops and provides oversight to identification and implementation of appropriate corrective actions and preventive actions * Oversight of the environmental monitoring program including appropriate escalation of environmental and personnel monitoring results that exceed alert or action limits and interpreting results. * Responsible for timely and accurate disposition of finished product to assure each batch meets specification prior to release * Periodically review records to verify that quality standards for each drug product is met * Maintain compliance with FDA 503B and cGMP guidelines / state and federal laws * Responsible for maintaining QA records associated with internal and external testing * Responsible to maintain all testing equipment in compliance, calibration, and certification * Assists in developing policies and procedures related to QA * Promptly communicates with Operations regarding complaints, product issues/variance * Assists in maintaining compliant controlled substance documentation specifically associated with sample handling and reconciliation * Enforces applicable personnel policies and procedures Our Most Successful Supervisor, Quality Assurance: * Are detail-oriented with strong verbal and written communications skills * Express energy, show accountability, and multi-task * Fulfill expectations, establish sustainable relationships with team members, maintain effective and meaningful communication channels * Have good interpersonal skills and the ability to work effectively and efficiently in a team environment to accomplish goals Minimum Requirements for this Role: * A High School diploma or equivalent * Able to successfully complete a drug and background check * 1 year of supervisory or management experience required * 2 years' experience in Quality Assurance / cGMP / FDA regulated industry * Able and willing to walk, stoop, stand, bend, and lift up to 50 lbs. throughout each shift, with or without reasonable accommodation * Must be currently authorized to work in the United States on a full-time basis; Quva will not sponsor applicants for work visas Any of the Following Will Give You an Edge: * Bachelor's Degree in Life Science or other related field Benefits of Working at Quva: * Set, full-time, consistent work schedule * Comprehensive health and wellness benefits including medical, dental and vision * 401k retirement program with company match * 22 paid days off plus 8 paid holidays per year * Occasional weekend and overtime opportunities with advance notice * National, industry-leading high growth company with future career advancement opportunities * The base compensation for this role is estimated to be within the range described below. The compensation offered may vary depending on relevant factors such as experience, skills, training, education, certifications, geographic location, and market conditions * Range: $74,766 - $102,812 / Hour or Year About Quva: Quva provides industry-leading health-system pharmacy services and solutions, including 503B sterile injectable outsourcing services and AI-based data software solutions that help power the business of pharmacy. Quva Pharma's multiple production facilities and industry-first dedicated remote distribution capabilities provide ready-to-administer sterile injectable medicines critical to patient care. Quva BrightStream partners with health systems to aggregate, normalize, and analyze large amounts of complex data across their sites of care, and through proprietary machine learning, transforms data into actionable insights supporting revenue optimization, script capture, inventory management, drug shortage control, and more. Quva's overall progressive and integrated platform helps health-systems transform pharmacy management to achieve greater value and deliver highest-quality patient care. Quva is an equal opportunity employer and is committed to creating and maintaining a work environment that is free from all forms of discrimination and harassment. Quva's Equal Opportunity Policy prohibits harassment or discrimination due to age, ancestry, color, disability, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, race, religious creed, sex (including pregnancy, childbirth, breastfeeding, and any related medical conditions), sexual orientation, and any other characteristic or classification protected by applicable laws. All employment with Quva is "at will." California Consumer Privacy Act (CCPA) Notice for Applicants and Employees

Our Compounding Pharmacy Technician plays a vital role in ensuring the highest quality and safety standards of our pharmaceutical products. Once you complete our training, your responsibilities will include preparing sterile compounds according to work instructions in an aseptic, clean room environment. Your attention to detail and adherence to precise procedures will guarantee that our medications meet the highest standards of safety, efficacy, and quality, providing patients with the best possible care and outcomes. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US. This is a full-time role for our 2nd shift working Monday through Friday from 2:00 PM to 10:30 PM. This is a set, consistent schedule with minimum overtime requirements and based on site in our Bloomsbury, NJ location. This is a safety sensitive position that may be subject to random drug testing, in accordance with applicable laws. Watch this Video to learn more. What the Compounding Pharmacy Technician Does Each Day: * Compound sterile preparations accurately according to detailed instructions * Clean work area and cleanroom (typically wiping down surfaces with aseptic wipe and occasional mopping) * Keep accurate documentation for accountability and traceability of product following Good Documentation Practices (GDPs) * Comply with cGMPs and company International Organization for Standardization (ISO) standards upon key steps in the work Our Most Successful Compounding Pharmacy Technicians: * Have a strong attention to detail and carefully follows compounding protocols and all Standard Operating Procedures (SOPs) related to the job * Are proactive and demonstrate initiative when appropriate; uses their time wisely * Have a passion for connecting their work to a greater purpose Minimum Requirements for this Role: * A High School diploma or equivalent * Able to successfully complete a drug and background check * Able and willing to walk, stoop, stand, bend, and lift up to 50 lbs. throughout each shift, with or without reasonable accommodation * 18+ years of age * Able and willing to follow "garb and gown" requirements from head to toe in order to maintain a sterile, clean room environment. This includes: * Hand washing * Wearing hair net, shoe covers, facemask, sterile gown, and gloves, etc. * Stringent regulations concerning, for example, the carrying of cellphones, the wearing of jewelry and makeup, and the length / type of fingernails * Familiarity with and comfortable using mobile devices such as smartphones, tablets, handhelds * Must be currently authorized to work in the United States on a full-time basis; Quva is not able to sponsor applicants for work visas Any of the Following Will Give You an Edge: * Pharmacy Technician (CPhT) License * Certified in ACPE sterile products * Experience in pharmacy compounding * Knowledge of cGMP (Current Good Manufacturing Processes) * Knowledge of ISO 5/7 environment cleanroom gowning Benefits of Working at Quva: * A career path with defined steps for growth, offering regular opportunities to enhance skills, expand responsibilities, and increase earning potential * Set, full-time, consistent work schedule * Comprehensive health and wellness benefits including medical, dental and vision * 401k retirement program with company match * A minimum of 17 paid days off plus 8 paid holidays per year * Occasional weekend and overtime opportunities with advance notice * National, industry-leading high growth company with future career advancement opportunities * The base compensation for this role is estimated to be within the range described below. The compensation offered may vary depending on relevant factors such as experience, skills, training, education, certifications, geographic location, and market conditions * Salary Range: $22.00 - $24.00/hour + $2.50 shift differential for 2nd shift About Quva: Quva is a national, industry-leading provider of compounded injectable medicines and software solutions that help power the business of hospital and health-system pharmacy. Quva Pharma produces and distributes injectable medicines required by health care providers and critical to patient care. Quva BrightStream partners with health-systems to analyze large amounts of data and through AI and machine learning, develops software solutions that turns the data into insights that are used to better run their pharmacy operation. Quva's overall product and technology offerings help health-systems achieve greater value and deliver the highest-quality patient care. Quva is an equal opportunity employer and is committed to creating and maintaining a work environment that is free from all forms of discrimination and harassment. Quva's Equal Opportunity Policy prohibits harassment or discrimination due to age, ancestry, color, disability, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, race, religious creed, sex (including pregnancy, childbirth, breastfeeding, and any related medical conditions), sexual orientation, and any other characteristic or classification protected by applicable laws. All employment with Quva is "at will." California Consumer Privacy Act (CCPA) Notice for Applicants and Employees

The Technical Operations Trainer I is responsible for supporting the developing, implementing, and delivering of comprehensive training programs that ensure compliance with industry regulations, company standards, and best practices in production and quality assurance. The ideal candidate will possess a strong background in pharmaceutical manufacturing processes, equipment operation, and regulatory requirements, along with excellent communication and interpersonal skills. This role is critical in fostering a culture of continuous learning and operational excellence, ultimately contributing to the company's mission of delivering high-quality pharmaceutical products to market. The Technical Operations Trainer I will be instrumental in ensuring that employees are equipped with the necessary skills to meet production demands while adhering to safety and compliance standards. Responsibilities may include: * Assists in delivering hands-on training sessions and workshops under supervision * Supports the creation and updating of training materials, manuals, and presentations * Collaborates with production and quality teams to ensure training content aligns with SOPs and regulatoryrequirements * Learns to assess trainee competency through observations and feedback * Collaborates closely with cross-functional teams, including production, quality assurance, and regulatoryaffairs, to identify training needs, design curriculum, and create engaging training materials * Stays current with current industry trends, regulatory changes, and technological advancements tocontinuously improve training content and methodologies * Stay current with industry trends and best practices to enhance training programs * Responsible for evaluating training effectiveness * Collaborates with management and cross functional teams to assess training needs * Identifies training needs by evaluating employee skill gaps and organizational requirements * Assesses trainee progress and provide feedback, ensuring effective knowledge transfer * Prepares and maintains training records, reports, and documentation * Works with other teams and stakeholders to align training with organizational goals * Other duties as assigned Qualifications: * Legally authorized to work in the job posting country * High School Diploma required * 3-5 years of experience in pharmaceutical manufacturing or a related technical field, with a strong understanding of manufacturing processes and regulatory compliance. * 1-3 years of experience in a training, instructional design, or educational role, preferably within a pharmaceutical or biotechnology environment * Basic knowledge of GMP/cGMP compliance * Strong verbal and written communication skills * Proficient in LMS and other digital tools for training * Strong problem-solving skills * Salary range: $27.93- $40.50 To be considered: In order to be considered for this position you must complete the entire application process, which includes answering all prescreening questions and providing your eSignature on or before the requisition closing date. Candidates for regular U.S. positions must be a U.S. citizen or national, or an alien admitted as permanent resident, refugee, asylee or temporary resident under 8 U.S.C. 1160(a) or 1255(a)(1). Individuals with temporary visas such as E, F-1, H-1, H-2, L, B, J, or TN or who need sponsorship for work authorization now or in the future, are not eligible for hire. It is the policy of QuVa Pharma to afford equal opportunity for employment to all individuals regardless of race, color, age, national origin, physical or mental disability, history of disability, ancestry, citizenship status, political affiliation, religion, gender, transgender, gender identity, marital status, status as a parent, sexual orientation, veteran status, genetic information or other factors prohibited by law, and to prohibit harassment or retaliation based on any of these factors. California Consumer Privacy Act (CCPA) Notice for Applicants and Employees

Principal Engineering Investigator exists to ensure the accuracy, integrity, and timeliness of all technical investigations and CAPAs associated with sterile compounding and injectable manufacturing operations. This role is accountable for collaborating with the team that identifies true root causes, develops effective and implements sustainable corrective/preventive actions, and communicates results that withstand regulatory scrutiny. The role is pivotal in supporting continuous improvement initiatives that enhance and transform the quality, compliance, and operational efficiency while fostering a strong culture of accountability and excellence across Quva. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US. What the Principal Engineering Investigator Does Each Day: * Lead end-to-end analytical and manufacturing-related investigations, including out-of-specification (OOS), out-of-trend (OOT), analytical deviations, data anomalies, and lab incidents * Ensure investigations are scientifically sound, compliant, and completed within defined timelines, meeting all cGMP and regulatory expectations (FDA, EMA, USP /, and 503B guidance) * Apply structured problem-solving tools (e.g., 5 Whys, Fishbone Diagram, Fault Tree, FMEA, KT Analysis) to determine true root causes and recommend durable corrective and preventive actions * Collaborate cross-functionally with Manufacturing, Quality Assurance, Quality Control, Engineering, and Validation teams to collect data, review trends, and verify CAPA effectiveness * Review, approval, and/or author high-complexity investigation reports, technical assessments, and CAPA documentation to ensure technical accuracy and regulatory compliance * Identify and trend recurring issues, conducting periodic reviews to drive continuous improvement initiatives that enhance product quality and operational consistency * Perform thorough data review, analytical method assessments, equipment troubleshooting, and sample/laboratory workflow evaluation * Lead investigation, readiness, efforts and support internal and external audits, providing detailed summaries of investigation history, CAPA status, and site performance metrics * Collaborate with stakeholders to implement CAPAs, track progress, and verify effectiveness * Promote a culture of accountability and right-first-time documentation * Train others on Root Cause methodologies * Implement CAPA's with a mindset of driving the process with a Poke Yoke solution * The end state of the role is to reduce errors to the point where they can shift to more continuous improvement opportunities and release capacity and capture business opportunities as a result of their efforts * Prepare clear, concise, and defensible investigation reports that meet internal quality standards and FDA/EMA regulatory expectations * Support internal, customer, and regulatory inspections by presenting investigation logic, risk reasoning, and CAPA justification Our Most Successful Principal Engineering Investigator: * Has deep understanding of aseptic manufacturing processes and regulatory standards * Ability to mentor, coach, and develop high-performing technical staff * Applies sound judgment in resolving complex technical and quality issues * Has strong data analysis and trend evaluation capabilities. Ability to set data sets up to measure process capability, control charts for ongoing monitoring/effectiveness * Builds effective partnerships across cross-functional teams. Ability to work with the shop floor to engage in problem solving and also have executive presence to present to leadership * Champions a culture of compliance, integrity, and continuous improvement * Delivers clear, concise, and scientifically sound documentation and presentations Minimum Requirements for this Role: * Bachelor's degree in Pharmacy, Chemistry, Microbiology, Engineering, Life Sciences, or related discipline required * Minimum 5-7 years of experience in pharmaceutical or sterile injectable manufacturing * Demonstrated success managing investigations, CAPA programs, and technical documentation in a cGMP-regulated environment * KT Analysis certified * Strong working knowledge of sterile compounding, aseptic processing, cleanroom operations, and environmental control systems * Deep understanding of FDA and EMA inspection expectations, particularly regarding data integrity, documentation practices, and deviation management * Expertise in root cause analysis and problem-solving methodologies * Proficiency with electronic Quality Management Systems (eQMS) such as MasterControl, TrackWise, or Veeva * Strong technical writing and documentation review skills * Proficiency in Microsoft Office Suite and analytical tools (specifically Visio, Excel, Mini-Tab or JMP; Mind Manager or other brainstorming software preferred) * Ability to lead/facilitate Kaizan in problem solving Any of the Following Will Give You an Edge: * Lean or Six Sigma qualified. Experience with Lean Transformation is a plus, specifically McKinsey transformation * Experience supporting 503B outsourcing facilities, sterile injectables, or hospital compounding preferred Benefits of Working at Quva: * Set, full-time, consistent work schedule * Comprehensive health and wellness benefits including medical, dental and vision * 401k retirement program with company match * 17 paid days off plus 8 paid holidays per year * National, industry-leading high growth company with future career advancement opportunities * The base compensation for this role is estimated to be within the range described below. The compensation offered may vary depending on relevant factors such as experience, skills, training, education, certifications, geographic location, and market conditions * Range: $88,792 - $116,838 Annually About Quva: Quva provides industry-leading health-system pharmacy services and solutions, including 503B sterile injectable outsourcing services and AI-based data software solutions that help power the business of pharmacy. Quva Pharma's multiple production facilities and industry-first dedicated remote distribution capabilities provide ready-to-administer sterile injectable medicines critical to patient care. Quva BrightStream partners with health systems to aggregate, normalize, and analyze large amounts of complex data across their sites of care, and through proprietary machine learning, transforms data into actionable insights supporting revenue optimization, script capture, inventory management, drug shortage control, and more. Quva's overall progressive and integrated platform helps health-systems transform pharmacy management to achieve greater value and deliver highest-quality patient care. Quva is an equal opportunity employer and is committed to creating and maintaining a work environment that is free from all forms of discrimination and harassment. Quva's Equal Opportunity Policy prohibits harassment or discrimination due to age, ancestry, color, disability, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, race, religious creed, sex (including pregnancy, childbirth, breastfeeding, and any related medical conditions), sexual orientation, and any other characteristic or classification protected by applicable laws. All employment with Quva is "at will." California Consumer Privacy Act (CCPA) Notice for Applicants and Employees

Our Calibration Specialist plays a vital role within our organization. Once you complete our training, your responsibilities will include acting as the technical expert for all calibrated equipment at the Quva facility. The Calibration Specialist will provide direction and daily supervision of calibration staff. The role will also manage the working status of all calibrated equipment with minimal supervision. The Calibration Specialist coordinates routine and non-routine instrument calibrations to maintain the calibration schedule in support of cGMP manufacturing. Review calibrations completed in-house, and outside vendors/contractors completed calibration documents for accuracy, completeness, and compliance with applicable SOP's. Complete Qualification/Verification tasks for new Laboratory Equipment/Instruments per the Calibration Program Procedures and applicable site procedures. At Quva, you will be an essential part of a mission-driven organization dedicated to expanding critical access to quality, affordable medication and data insights while promoting a culture of innovation, collaboration, and continuous improvement. Your attention to detail and adherence to precise procedures will guarantee that our medications meet the highest standards of safety, efficacy, and quality, providing patients with the best possible care and outcomes. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US. What the Calibration Specialist Does Each Day: * Manages calibration and calibrated equipment maintenance, including execution of activities and/or scheduling with site operations and external vendors * Performs verification/qualifications, calibrations, maintenance of laboratory equipment/instruments to maintain a current qualified status * Continuously evaluates calibration and calibrated equipment maintenance against industry standards for continuous improvement * Manages the preventative maintenance program for all calibrated equipment * Develops standard operating procedures and work instructions for calibration activities * Works with site operations on out of service calibrated equipment priority, scheduling personal work and/or outsourcing in accordance with priority set by site operations management * Minimizes calibrated equipment downtime, tracks and reports metrics for calibrated equipment downtime, drives improvement, shares information and updates to facilities management * Sets up test equipment, collects measurements used to record various parameters (voltage, current, heat, flow, pressure, etc.) * Adjusts/repairs instruments to meet calibration tolerances * Coordinates instrument calibration and re-certification with outside standards laboratories, which includes inspections and documentation reviews on those instruments * Completes required documentation for calibration and certification activities * Serves as a technical resource on calibration issues and trains site operations and quality personnel on handling of calibrated equipment * Adheres to Good Documentation Practices Our Most Successful Calibration Specialist: * Has strong technical writing skills and verbal/written communication skills, including presentation skills * Utilizes analytical, critical thinking and structured root cause analysis techniques for problem solving * Has a sense of urgency, accountability, and resourcefulness (e.g., work in changing environment) * Is a self-starter and independent learner Minimum Requirements for this Role: * Associate's degree required * Minimum 3-years calibration experience in the pharmaceutical industry with proven problem-solving skills * Ability to deal with moderately complex processes and procedures * Must be able to demonstrate judgment and initiative in problem resolution * Must be able to work with minimal supervision * Good communication skills and detail oriented * 18+ years of age * Able to successfully complete a drug and background check * Must be currently authorized to work in the United States on a full-time basis; Quva is not able to sponsor applicants for work visas Any of the Following Will Give You an Edge: * Bachelor's Degree Benefits of Working at Quva: * Set, full-time, consistent work schedule * Comprehensive health and wellness benefits including medical, dental and vision * 401k retirement program with company match * 17 paid days off plus 8 paid holidays per year * Occasional weekend and overtime opportunities with advance notice * National, industry-leading high growth company with future career advancement opportunities * The base compensation for this role is estimated to be within the range described below. The compensation offered may vary depending on relevant factors such as experience, skills, training, education, certifications, geographic location, and market conditions * Range: $56,541- $77,744/ Year About Quva: Quva provides industry-leading health-system pharmacy services and solutions, including 503B sterile injectable outsourcing services and AI-based data software solutions that help power the business of pharmacy. Quva Pharma's multiple production facilities and industry-first dedicated remote distribution capabilities provide ready-to-administer sterile injectable medicines critical to patient care. Quva BrightStream partners with health systems to aggregate, normalize, and analyze large amounts of complex data across their sites of care, and through proprietary machine learning, transforms data into actionable insights supporting revenue optimization, script capture, inventory management, drug shortage control, and more. Quva's overall progressive and integrated platform helps health-systems transform pharmacy management to achieve greater value and deliver highest-quality patient care. Quva is an equal opportunity employer and is committed to creating and maintaining a work environment that is free from all forms of discrimination and harassment. Quva's Equal Opportunity Policy prohibits harassment or discrimination due to age, ancestry, color, disability, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, race, religious creed, sex (including pregnancy, childbirth, breastfeeding, and any related medical conditions), sexual orientation, and any other characteristic or classification protected by applicable laws. All employment with Quva is "at will." California Consumer Privacy Act (CCPA) Notice for Applicants and Employees

Our QC Laboratory Technician plays a vital role in ensuring the highest quality and safety standards of our pharmaceutical products. Once you complete our training, your responsibilities will include performing basic laboratory support functions related to the management of laboratory samples, materials, and testing supplies. Your attention to detail and adherence to precise procedures will guarantee that our medications meet the highest standards of safety, efficacy, and quality, providing patients with the best possible care and outcomes. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US. This is a full-time role working Monday through Friday from 8:00 AM to 4:30 PM. This is a set, consistent schedule with minimum overtime requirements and based on site in our Bloomsbury, NJ location. This is a safety sensitive position that may be subject to random drug testing, in accordance with applicable laws. What the QC Laboratory Technician Does Each Day: * Verifies information on incoming lab samples and enters sample information into the laboratory database * Place orders and stock laboratory supplies * Light housekeeping, including operation of glassware washer * Ensures all work is performed and documented in a timely manner and according to approved standard operating procedures and in general compliance with cGMPs Our Most Successful QC Laboratory Technicians: * Are accurate and well organized, with strong attention to detail * Express energy, show accountability, can multi-task and work in a fast-paced, quality-rich environment * Fulfill expectations, establish sustainable relationships with team members, maintain effective and meaningful communication channels * Have good interpersonal skills and work effectively and efficiently in a team environment to accomplish goals * Have strong verbal and written communications skills Minimum Requirements for this Role: * A High School diploma or equivalent * Able to successfully complete a drug and background check * Proficient in Microsoft Office, Word and Excel * Able and willing to walk, stoop, stand, bend, and lift up to 50 lbs. throughout each shift, with or without reasonable accommodation * Must be currently authorized to work in the United States on a full-time basis; Quva will not sponsor applicants for work visas Any of the Following Will Give You an Edge: * Bachelor's Degree in life science or related field * 1 to 2 years' experience in data entry/clerical, or related responsibilities Benefits of Working at Quva: * Set, full-time, consistent work schedule * Comprehensive health and wellness benefits including medical, dental and vision * 401k retirement program with company match * 17 paid days off plus 8 paid holidays per year * Occasional weekend and overtime opportunities with advance notice * National, industry-leading high growth company with future career advancement opportunities * Salary Range: $18.85-27.34/hour About Quva: Quva is a national, industry-leading provider of compounded injectable medicines and software solutions that help power the business of hospital and health-system pharmacy. Quva Pharma produces and distributes injectable medicines required by health care providers and critical to patient care. Quva BrightStream partners with health-systems to analyze large amounts of data and through AI and machine learning, develops software solutions that turns the data into insights that are used to better run their pharmacy operation. Quva's overall product and technology offerings help health-systems achieve greater value and deliver the highest-quality patient care. Quva is an equal opportunity employer and is committed to creating and maintaining a work environment that is free from all forms of discrimination and harassment. Quva's Equal Opportunity Policy prohibits harassment or discrimination due to age, ancestry, color, disability, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, race, religious creed, sex (including pregnancy, childbirth, breastfeeding, and any related medical conditions), sexual orientation, and any other characteristic or classification protected by applicable laws. All employment with Quva is "at will." California Consumer Privacy Act (CCPA) Notice for Applicants and Employees

Our Automation Engineer supports, develops, and maintains automated systems used in pharmaceutical manufacturing. This role ensures that production equipment, control systems, and digital infrastructure operate reliably, efficiently, and in compliance with cGMP and regulatory standards. The engineer collaborates with cross‑functional teams to troubleshoot issues, implement improvements, and support new system installations or upgrades. Operates within legal and regulatory compliance, ensuring systems are maintained and operational within site and regulatory requirements. Capable of following procedures, documenting work as/when performed and maintaining a clean/organized workplace supporting site compliance and quality standards. Your attention to detail and adherence to precise procedures will guarantee that our medications meet the highest standards of safety, efficacy, and quality, providing patients with the best possible care and outcomes. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US. This is an onsite role in Bloomsbury, New Jersey; Monday - Friday 2 PM - 10:30 PM. What the Automation Engineer Does Each Day: * Provides technical skills and expertise to support operations, ensuring automated manufacturing equipment operates efficiently, including network configuration and integration principles, and the ability to work effectively with IT * Supports constant operations by trouble shooting machines, monitoring PLC issues, performing root cause analysis on complex issues, and executing improvements * Investigates automation incidents and problems to prevent recurrence including the development and implementation of corrective actions * Design and implementation of equipment and facilities related controls including PLC coding (Allen-Bradley/Siemens), HMI and SCADA systems * Evaluates automated and information technology systems, and develops strategies to optimize and ensure quality and stability of automation systems through future expansion, replacement, or upgrade * Efficient use of different software tools and computer applications including but not limited to Microsoft Office, PLC programming software, electrical schematic design software, HMI programming software, SCADA systems and industrial networks (Allen-Bradley/Siemens) * Effectively and accurately handles most technical questions and objections for assigned products * Maintains appropriate documentation for equipment and processes including change control, drawings, manuals, and validation * Streamlines workflows and develop automated laboratory processes and instrumentation systems, including collecting and documenting requirements, developing concepts, design, testing/validation, implementation, and training * Recognizes priorities and takes action; makes productive use of time * Understands and adheres to policies and procedures * Software validation, data integrity, GAMP 5 and 21 CFR part 11 experience * Operating and troubleshooting of Fanuc Robotics Our Most Successful Automation Engineer Has: * Experience in aseptic processing preferred * Experience with FDA, GMP, and ISO standards preferred * Must possess the ability to work effectively with all levels of organization * Demonstrated ability to build and maintain strong business and collaborative relationships, internally and externally * Must possess excellent interpersonal, communication, and writing skills, ability to analyze technical issues, define/solve problems, establish project plans, and draw valid conclusions * Ability to think analytically and systematically * Aseptic Operator Qualification and Process Simulation * Proficient in technical writing and current computer usage (Word, Excel, PowerPoint, etc.) * Good working knowledge of regulatory guidance as it pertains to APIs and injectable drug products Minimum Requirements for this Role: * Bachelor's degree in electrical engineering, Mechanical Engineering, or another related field, with 5+ years' experience in a manufacturing environment * Experience working with PLCs, HMIs, Robotics (Fanuc, Staubli), and SCADA systems, preferably Rockwell or Siemens platforms * Equipment/Instrument Calibration principles * Proven ability to adapt and manage effectively in fast paced, changing environment * 18+ years of age * Able to successfully complete a drug and background check * Must be currently authorized to work in the United States on a full-time basis; Quva is not able to sponsor applicants for work visas Benefits of Working at Quva: * Set, full-time, consistent work schedule * Comprehensive health and wellness benefits including medical, dental and vision * 401k retirement program with company match * 17 paid days off plus 8 paid holidays per year * Occasional weekend and overtime opportunities with advance notice * National, industry-leading high growth company with future career advancement opportunities * The base compensation for this role is estimated to be within the range described below. The compensation offered may vary depending on relevant factors such as experience, skills, training, education, certifications, geographic location, and market conditions * Range: $85,993 - $134,364 Annually About Quva: Quva provides industry-leading health-system pharmacy services and solutions, including 503B sterile injectable outsourcing services and AI-based data software solutions that help power the business of pharmacy. Quva Pharma's multiple production facilities and industry-first dedicated remote distribution capabilities provide ready-to-administer sterile injectable medicines critical to patient care. Quva BrightStream partners with health systems to aggregate, normalize, and analyze large amounts of complex data across their sites of care, and through proprietary machine learning, transforms data into actionable insights supporting revenue optimization, script capture, inventory management, drug shortage control, and more. Quva's overall progressive and integrated platform helps health-systems transform pharmacy management to achieve greater value and deliver highest-quality patient care. Quva is an equal opportunity employer and is committed to creating and maintaining a work environment that is free from all forms of discrimination and harassment. Quva's Equal Opportunity Policy prohibits harassment or discrimination due to age, ancestry, color, disability, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, race, religious creed, sex (including pregnancy, childbirth, breastfeeding, and any related medical conditions), sexual orientation, and any other characteristic or classification protected by applicable laws. All employment with Quva is "at will." California Consumer Privacy Act (CCPA) Notice for Applicants and Employees

The Technical Operations Trainer I is responsible for supporting the developing, implementing, and delivering of comprehensive training programs that ensure compliance with industry regulations, company standards, and best practices in production and quality assurance. The ideal candidate will possess a strong background in pharmaceutical manufacturing processes, equipment operation, and regulatory requirements, along with excellent communication and interpersonal skills. This role is critical in fostering a culture of continuous learning and operational excellence, ultimately contributing to the company's mission of delivering high-quality pharmaceutical products to market. The Technical Operations Trainer I will be instrumental in ensuring that employees are equipped with the necessary skills to meet production demands while adhering to safety and compliance standards. Work hours: Monday- Friday 2PM- 10:30PM in our Bloomsbury, NJ location Responsibilities may include: * Assists in delivering hands-on training sessions and workshops under supervision * Supports the creation and updating of training materials, manuals, and presentations * Collaborates with production and quality teams to ensure training content aligns with SOPs and regulatory requirements * Learns to assess trainee competency through observations and feedback * Collaborates closely with cross-functional teams, including production, quality assurance, and regulatory affairs, to identify training needs, design curriculum, and create engaging training materials * Stays current with current industry trends, regulatory changes, and technological advancements to continuously improve training content and methodologies * Stay current with industry trends and best practices to enhance training programs * Responsible for evaluating training effectiveness * Collaborates with management and cross functional teams to assess training needs * Identifies training needs by evaluating employee skill gaps and organizational requirements * Assesses trainee progress and provide feedback, ensuring effective knowledge transfer * Prepares and maintains training records, reports, and documentation * Works with other teams and stakeholders to align training with organizational goals * Other duties as assigned Qualifications: * Legally authorized to work in the job posting country * High School Diploma required * 3-5 years of experience in pharmaceutical manufacturing or a related technical field, with a strong understanding of manufacturing processes and regulatory compliance. * 1-3 years of experience in a training, instructional design, or educational role, preferably within a pharmaceutical or biotechnology environment * Basic knowledge of GMP/cGMP compliance * Strong verbal and written communication skills * Proficient in LMS and other digital tools for training * Strong problem-solving skills * Salary Range: $27.93- $40.50 About Quva: Quva is a national, industry-leading provider of compounded injectable medicines and software solutions that help power the business of hospital and health-system pharmacy. Quva Pharma produces and distributes injectable medicines required by health care providers and critical to patient care. Quva BrightStream partners with health-systems to analyze large amounts of data and through AI and machine learning, develops software solutions that turns the data into insights that are used to better run their pharmacy operation. Quva's overall product and technology offerings help health-systems achieve greater value and deliver the highest-quality patient care. Quva is an equal opportunity employer and is committed to creating and maintaining a work environment that is free from all forms of discrimination and harassment. Quva's Equal Opportunity Policy prohibits harassment or discrimination due to age, ancestry, color, disability, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, race, religious creed, sex (including pregnancy, childbirth, breastfeeding, and any related medical conditions), sexual orientation, and any other characteristic or classification protected by applicable laws. All employment with Quva is "at will." California Consumer Privacy Act (CCPA) Notice for Applicants and Employees

Our Production Technician I - ILP plays a vital role within our organization. Once you complete our training, your responsibilities will include supporting execution of product visual inspection, labeling and packaging (ILP) operations at the Quva facility in accordance with established processes and procedures. At Quva, you will be an essential part of a mission-driven organization dedicated to expanding critical access to quality, affordable medication and data insights while promoting a culture of innovation, collaboration, and continuous improvement. Your attention to detail and adherence to precise procedures will guarantee that our medications meet the highest standards of safety, efficacy, and quality, providing patients with the best possible care and outcomes. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US. This is a full-time role for our 1st Shift, working Monday through Friday from 6:30 AM to 3:00 PM. This is a set, consistent schedule with minimum overtime requirements and based on site in our Bloomsbury, NJ location. This is a safety sensitive position that may be subject to random drug testing, in accordance with applicable laws. Watch this video to learn more What the ILP Technician Does Each Day: Assists preparation of inspection and packaging room materials supplies Conducts labeling and the processing of production materials as required Daily/ Bi-Weekly/Monthly cleaning of room and equipment and fills out appropriate preventative maintenance forms and checklists in accordance with SOP's Conduct and complete line and room clearances as per established procedures Completes necessary documents for accountability and traceability of products following Good Documentation Practices (GDPs); comply with cGMPs, and company ISO standards Complies with 503B guidelines; cGMPs, standard operating procedures and company policies Performs equipment calibration checks and troubleshoots production equipment as needed Completes documentation of activities in accordance with established procedures Immediately notifies production management of deviations to established processes or procedures Assists other areas as needed (cleaning; non-sterile filling; kitting and preparation operations, etc.) Primary, secondary, and tertiary labeling of products Secondary and final packaging of product Requires visual inspection of product Maintains inspection ready environment and supports internal / external audits Our Most Successful ILP Technicians: Promotes active listening with team members; Contributes appropriately to conversations; Strong verbal and written communication skills with the ability to work effectively with other departments within the organization and with people at all levels of the organization Understands how various issues affect each other and the outcome of projects; Improves upon existing approaches by seeking opportunities to creatively transform; mechanical aptitude a plus Effectively and productively engages with others and establishes trust, credibility, and confidence with others Listens to internal customers, ensures commitments are met, sets appropriate internal customer expectations Has working knowledge of cGMPs and regulatory requirements as well as all applicable SOPs Follows policies and procedures; completes administrative tasks correctly and on time Approaches others in a tactful manner; reacts well under pressure; treats others with respect and consideration regardless of their status or position; accepts responsibility for own actions; follows through on commitments Has strong attention to detail Is flexible and can adapt to support multiple production areas and shifts as needed Minimum Requirements for this Role: High school Diploma or GED from recognized institution or organization required Will be required to undergo a color perception exam and must be able to produce a passing test result Will be required to undergo a vision exam and must be able to produce 20/20 vision with or without correction Able to successfully complete a drug and background check 18+ years of age Must be currently authorized to work in the United States on a full-time basis; Quva will not sponsor applicants for work visas Any of the Following Will Give You an Edge: Pharmaceutical experience Benefits of Working at Quva: Set, full-time, consistent work schedule Comprehensive health and wellness benefits including medical, dental and vision 401k retirement program with company match 17 paid days off plus 8 paid holidays per year Occasional weekend and overtime opportunities with advance notice National, industry-leading high growth company with future career advancement opportunities The base compensation for this role is estimated to be within the range described below. The compensation offered may vary depending on relevant factors such as experience, skills, training, education, certifications, geographic location, and market conditions Range: $18.00 - $21.00Hr About Quva: Quva is a national, industry-leading provider of compounded injectable medicines and software solutions that help power the business of hospital and health-system pharmacy. Quva Pharma produces and distributes injectable medicines required by health care providers and critical to patient care. Quva BrightStream partners with health-systems to analyze large amounts of data and through AI and machine learning, develops software solutions that turns the data into insights that are used to better run their pharmacy operation. Quva's overall product and technology offerings help health-systems achieve greater value and deliver the highest-quality patient care. Quva is an equal opportunity employer and is committed to creating and maintaining a work environment that is free from all forms of discrimination and harassment. Quva's Equal Opportunity Policy prohibits harassment or discrimination due to age, ancestry, color, disability, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, race, religious creed, sex (including pregnancy, childbirth, breastfeeding, and any related medical conditions), sexual orientation, and any other characteristic or classification protected by applicable laws. All employment with Quva is “at will.” California Consumer Privacy Act (CCPA) Notice for Applicants and Employees

The Technical Operations Trainer I is responsible for supporting the developing, implementing, and delivering of comprehensive training programs that ensure compliance with industry regulations, company standards, and best practices in production and quality assurance. The ideal candidate will possess a strong background in pharmaceutical manufacturing processes, equipment operation, and regulatory requirements, along with excellent communication and interpersonal skills. This role is critical in fostering a culture of continuous learning and operational excellence, ultimately contributing to the company's mission of delivering high-quality pharmaceutical products to market. The Technical Operations Trainer I will be instrumental in ensuring that employees are equipped with the necessary skills to meet production demands while adhering to safety and compliance standards. Work hours: Monday- Friday 2PM- 10:30PM in our Bloomsbury, NJ location Responsibilities may include: Assists in delivering hands-on training sessions and workshops under supervision Supports the creation and updating of training materials, manuals, and presentations Collaborates with production and quality teams to ensure training content aligns with SOPs and regulatory requirements Learns to assess trainee competency through observations and feedback Collaborates closely with cross-functional teams, including production, quality assurance, and regulatory affairs, to identify training needs, design curriculum, and create engaging training materials Stays current with current industry trends, regulatory changes, and technological advancements to continuously improve training content and methodologies Stay current with industry trends and best practices to enhance training programs Responsible for evaluating training effectiveness Collaborates with management and cross functional teams to assess training needs Identifies training needs by evaluating employee skill gaps and organizational requirements Assesses trainee progress and provide feedback, ensuring effective knowledge transfer Prepares and maintains training records, reports, and documentation Works with other teams and stakeholders to align training with organizational goals Other duties as assigned Qualifications: Legally authorized to work in the job posting country High School Diploma required 3-5 years of experience in pharmaceutical manufacturing or a related technical field, with a strong understanding of manufacturing processes and regulatory compliance. 1-3 years of experience in a training, instructional design, or educational role, preferably within a pharmaceutical or biotechnology environment Basic knowledge of GMP/cGMP compliance Strong verbal and written communication skills Proficient in LMS and other digital tools for training Strong problem-solving skills Salary Range: $27.93- $40.50 About Quva: Quva is a national, industry-leading provider of compounded injectable medicines and software solutions that help power the business of hospital and health-system pharmacy. Quva Pharma produces and distributes injectable medicines required by health care providers and critical to patient care. Quva BrightStream partners with health-systems to analyze large amounts of data and through AI and machine learning, develops software solutions that turns the data into insights that are used to better run their pharmacy operation. Quva's overall product and technology offerings help health-systems achieve greater value and deliver the highest-quality patient care. Quva is an equal opportunity employer and is committed to creating and maintaining a work environment that is free from all forms of discrimination and harassment. Quva's Equal Opportunity Policy prohibits harassment or discrimination due to age, ancestry, color, disability, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, race, religious creed, sex (including pregnancy, childbirth, breastfeeding, and any related medical conditions), sexual orientation, and any other characteristic or classification protected by applicable laws. All employment with Quva is “at will.” California Consumer Privacy Act (CCPA) Notice for Applicants and Employees

Our Quality Assurance Technician plays a vital role in ensuring the highest quality and safety standards of our pharmaceutical products. Once you complete our training, your responsibilities will include performs basic QA functions related to verification of incoming materials, label checks, and oversight of support areas (i.e. prep and/or label printing) to ensure the manufacturing areas are set up for success. The on-the-floor quality team is responsible for making sure the process and documentation records are compliant with patient safety in mind, executing with efficiency always. Quality, safety, and on-time delivery is a must to be successful in this role! This is a full-time role for our 2nd shift, working Monday through Friday from 3:00 PM to 11:00 PM. This is a set, consistent schedule with minimum overtime requirements and based on site in our Bloomsbury, NJ location. This is a safety sensitive position that may be subject to random drug testing, in accordance with applicable laws. Watch this video to learn more. What the Quality Assurance Technician Does Each Day: * Ensure that all applicable US Regulatory requirements are being met within the procedures and practices * Quality review / verification of critical information related to the receipt of incoming goods or the distribution of finished goods for customer orders * Ensures compliance of incoming materials prior to use in Manufacturing Operations * Ensures verification of labels against batch record requirements complies with company standards * Ensures levels of cleanliness for components and equipment used in the manufacturing process meet the company standards Our Most Successful Quality Assurance Technicians: * Are detail-oriented with strong verbal and written communications skills * Express energy, show accountability, and multi-task * Fulfill expectations, establish sustainable relationships with team members, maintain effective and meaningful communication channels * Have good interpersonal skills and the ability to work effectively and efficiently in a team environment to accomplish goals Minimum Requirements for this Role: * A High School diploma or equivalent * Able to successfully complete a drug and background check * Able and willing to walk, stoop, stand, bend, and lift up to 50 lbs. throughout each shift, with or without reasonable accommodation * 18+ years of age * 20/20 vision (with or without corrective lenses) and the ability to successfully pass a color vision test * Familiarity with and comfortable using mobile devices such as smartphones, tablets, handhelds * Must be currently authorized to work in the United States on a full-time basis; QuVa will not sponsor applicants for work visas Any of the Following Will Give You an Edge: * 0 to 2 years' experience with FDA-regulated operations (cGMP processes) or Quality Assurance Benefits of Working at Quva: * Set, full-time, consistent work schedule * Comprehensive health and wellness benefits including medical, dental and vision * 401k retirement program with company match * 17 paid days off plus 8 paid holidays per year * Occasional weekend and overtime opportunities with advance notice * National, industry-leading high growth company with future career advancement opportunities * The base compensation for this role is estimated to be within the range described below. The compensation offered may vary depend on on relevant factors such as experience, skills, training, education, certifications, geographic location, and market conditions * Salary Range: $16.50 - $23.98 + $2.50 shift differential for 2nd shift About Quva: Quva is a national, industry-leading provider of compounded injectable medicines and software solutions that help power the business of hospital and health-system pharmacy. Quva Pharma produces and distributes injectable medicines required by health care providers and critical to patient care. Quva BrightStream partners with health-systems to analyze large amounts of data and through AI and machine learning, develops software solutions that turns the data into insights that are used to better run their pharmacy operation. Quva's overall product and technology offerings help health-systems achieve greater value and deliver the highest-quality patient care. Quva is an equal opportunity employer and is committed to creating and maintaining a work environment that is free from all forms of discrimination and harassment. Quva's Equal Opportunity Policy prohibits harassment or discrimination due to age, ancestry, color, disability, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, race, religious creed, sex (including pregnancy, childbirth, breastfeeding, and any related medical conditions), sexual orientation, and any other characteristic or classification protected by applicable laws. All employment with Quva is "at will." California Consumer Privacy Act (CCPA) Notice for Applicants and Employees

The Technical Operations Trainer I is responsible for supporting the developing, implementing, and delivering of comprehensive training programs that ensure compliance with industry regulations, company standards, and best practices in production and quality assurance. The ideal candidate will possess a strong background in pharmaceutical manufacturing processes, equipment operation, and regulatory requirements, along with excellent communication and interpersonal skills. This role is critical in fostering a culture of continuous learning and operational excellence, ultimately contributing to the company's mission of delivering high-quality pharmaceutical products to market. The Technical Operations Trainer I will be instrumental in ensuring that employees are equipped with the necessary skills to meet production demands while adhering to safety and compliance standards. Responsibilities may include: * Assists in delivering hands-on training sessions and workshops under supervision * Supports the creation and updating of training materials, manuals, and presentations * Collaborates with production and quality teams to ensure training content aligns with SOPs and regulatoryrequirements * Learns to assess trainee competency through observations and feedback * Collaborates closely with cross-functional teams, including production, quality assurance, and regulatoryaffairs, to identify training needs, design curriculum, and create engaging training materials * Stays current with current industry trends, regulatory changes, and technological advancements tocontinuously improve training content and methodologies * Stay current with industry trends and best practices to enhance training programs * Responsible for evaluating training effectiveness * Collaborates with management and cross functional teams to assess training needs * Identifies training needs by evaluating employee skill gaps and organizational requirements * Assesses trainee progress and provide feedback, ensuring effective knowledge transfer * Prepares and maintains training records, reports, and documentation * Works with other teams and stakeholders to align training with organizational goals * Other duties as assigned Qualifications: * Legally authorized to work in the job posting country * High School Diploma required * 3-5 years of experience in pharmaceutical manufacturing or a related technical field, with a strong understanding of manufacturing processes and regulatory compliance. * 1-3 years of experience in a training, instructional design, or educational role, preferably within a pharmaceutical or biotechnology environment * Basic knowledge of GMP/cGMP compliance * Strong verbal and written communication skills * Proficient in LMS and other digital tools for training * Strong problem-solving skills * Salary range: $27.93- $40.50 To be considered: In order to be considered for this position you must complete the entire application process, which includes answering all prescreening questions and providing your eSignature on or before the requisition closing date. Candidates for regular U.S. positions must be a U.S. citizen or national, or an alien admitted as permanent resident, refugee, asylee or temporary resident under 8 U.S.C. 1160(a) or 1255(a)(1). Individuals with temporary visas such as E, F-1, H-1, H-2, L, B, J, or TN or who need sponsorship for work authorization now or in the future, are not eligible for hire. It is the policy of QuVa Pharma to afford equal opportunity for employment to all individuals regardless of race, color, age, national origin, physical or mental disability, history of disability, ancestry, citizenship status, political affiliation, religion, gender, transgender, gender identity, marital status, status as a parent, sexual orientation, veteran status, genetic information or other factors prohibited by law, and to prohibit harassment or retaliation based on any of these factors. California Consumer Privacy Act (CCPA) Notice for Applicants and Employees

Our Quality Assurance Technician plays a vital role in ensuring the highest quality and safety standards of our pharmaceutical products. Once you complete our training, your responsibilities will include performs basic QA functions related to verification of incoming materials, label checks, and oversight of support areas (i.e. prep and/or label printing) to ensure the manufacturing areas are set up for success. The on-the-floor quality team is responsible for making sure the process and documentation records are compliant with patient safety in mind, executing with efficiency always. Quality, safety, and on-time delivery is a must to be successful in this role! This is a full-time role for our 1st shift, working Monday through Friday from 7:00 AM to 3:30 PM. This is a set, consistent schedule with minimum overtime requirements and based on site in our Bloomsbury, NJ location. This is a safety sensitive position that may be subject to random drug testing, in accordance with applicable laws. Watch this video to learn more. What the Quality Assurance Technician Does Each Day: * Ensure that all applicable US Regulatory requirements are being met within the procedures and practices * Quality review / verification of critical information related to the receipt of incoming goods or the distribution of finished goods for customer orders * Ensures compliance of incoming materials prior to use in Manufacturing Operations * Ensures verification of labels against batch record requirements complies with company standards * Ensures levels of cleanliness for components and equipment used in the manufacturing process meet the company standards Our Most Successful Quality Assurance Technicians: * Are detail-oriented with strong verbal and written communications skills * Express energy, show accountability, and multi-task * Fulfill expectations, establish sustainable relationships with team members, maintain effective and meaningful communication channels * Have good interpersonal skills and the ability to work effectively and efficiently in a team environment to accomplish goals Minimum Requirements for this Role: * A High School diploma or equivalent * Able to successfully complete a drug and background check * Able and willing to walk, stoop, stand, bend, and lift up to 50 lbs. throughout each shift, with or without reasonable accommodation * 18+ years of age * 20/20 vision (with or without corrective lenses) and the ability to successfully pass a color vision test * Familiarity with and comfortable using mobile devices such as smartphones, tablets, handhelds * Must be currently authorized to work in the United States on a full-time basis; QuVa will not sponsor applicants for work visas Any of the Following Will Give You an Edge: * 0 to 2 years' experience with FDA-regulated operations (cGMP processes) or Quality Assurance Benefits of Working at Quva: * Set, full-time, consistent work schedule * Comprehensive health and wellness benefits including medical, dental and vision * 401k retirement program with company match * 17 paid days off plus 8 paid holidays per year * Occasional weekend and overtime opportunities with advance notice * National, industry-leading high growth company with future career advancement opportunities * The base compensation for this role is estimated to be within the range described below. The compensation offered may vary depend on on relevant factors such as experience, skills, training, education, certifications, geographic location, and market conditions * Salary Range: $16.50 - $23.98 About Quva: Quva is a national, industry-leading provider of compounded injectable medicines and software solutions that help power the business of hospital and health-system pharmacy. Quva Pharma produces and distributes injectable medicines required by health care providers and critical to patient care. Quva BrightStream partners with health-systems to analyze large amounts of data and through AI and machine learning, develops software solutions that turns the data into insights that are used to better run their pharmacy operation. Quva's overall product and technology offerings help health-systems achieve greater value and deliver the highest-quality patient care. Quva is an equal opportunity employer and is committed to creating and maintaining a work environment that is free from all forms of discrimination and harassment. Quva's Equal Opportunity Policy prohibits harassment or discrimination due to age, ancestry, color, disability, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, race, religious creed, sex (including pregnancy, childbirth, breastfeeding, and any related medical conditions), sexual orientation, and any other characteristic or classification protected by applicable laws. All employment with Quva is "at will." California Consumer Privacy Act (CCPA) Notice for Applicants and Employees