Qureos Mentor

QuVa Pharma

<div>Quva Pharma is seeking a motivated and organized Warehouse Technician Intern to complete the inventory replenishment process utilizing manual or automated technology. You will be integral in ensuring that inventory is correctly stocked and labeled, protecting the integrity of sterile supplies. Our ideal candidate is highly organized, a master of prioritization and able to shift gears at a moment&rsquo;s notice. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US.

This internship runs through June 1 - July 31, 2026. Monday - Friday 8:00 AM - 4:00 PM at our Phoenix, Arizona Location.

What the Warehouse Technician Intern Does Each Day:
<ul>
<li>Follows established inventory re-order levels</li>
<li>Pulls from inventory items necessary to restock and restocks shelves, ensuring inventory is correctly labeled</li>
<li>Rotates stock in accordance with &quot;FIFE&quot; First-in, First-expired procedure. Notifies supervisor of any shortages of supplies</li>
<li>Checks for and pulls opened, damaged, expired and/or excess inventory and replaces unusable, damaged or dirty boxes/packaging, labels etc. Handles defective, damaged and/or expired inventory in accordance with established departmental policy</li>
<li>Assists in the preparation, packaging, shipment and complete documentation of supplies and/or equipment for vendor returns</li>
<li>Drive back-order improvements to support our service and sales business - Work closely with our supply and demand planners</li>
<li>Moves material within and from the various warehouse location based on inventory status, kitting requirements and production requirements</li>
<li>Supports customer order processing from pick list drop through to pick-up for transportation partner</li>
<li>Unloads trucks of materials and loads recycling material on trucks in a safe, timely and cost- effective manner</li>
<li>Removes pallets, strapping and packing materials, and moves recycle materials to recycle area</li>
<li>Receives and puts away material in designated locations to support effective warehouse flow</li>
<li>Completes accurately all required paperwork including manual entry on batch records and pick lists as well as ERP system transactions using good documentation practices aligned with CGMP and company policies and procedures</li>
</ul>
Our Most Successful Warehouse Technician Interns:
<ul>
<li>Are detail-oriented with strong verbal and written communications skills</li>
<li>Motivates others, shares knowledge, builds high performing team, shows respect towards others, gives constructive feedback</li>
<li>Display eagerness to learn and continuously improve, adapt quickly to change, and apply sound judgment</li>
<li>Foster team environment, invest in team members and peers by inclusion and listening, recognize employees effectively, demonstrate trust</li>
</ul>
Minimum Requirements for this Role:
<ul>
<li>Legally authorized to work in the job posting country</li>
<li>High school diploma or GED from recognized institution or organization required</li>
<li>Must be actively pursuing a bachelor's degree from an accredited institution, with an anticipated graduation date within the next two years</li>
<li>Must be in good standing with accredited institution where pursuing degree</li>
<li>Microsoft Word and Excel skills</li>
</ul>
Any of the Following Will Give You an Edge:
<ul>
<li>AS400 and INFOR or other ERP experience highly desired</li>
<li>Good communication and customer service skills</li>
<li>Knowledge of discrete batch manufacturing in pharmaceutical or related field preferred, but not necessary</li>
</ul>
Benefits of Working at Quva:
<ul>
<li>Set, full-time, consistent work schedule</li>
<li>National, industry-leading high growth company with future career advancement opportunities</li>
<li>Pay: $17.00/hour</li>
</ul>
About Quva: 
 
Quva Pharma is a national, industry-leading, FDA registered 503B outsourcing services company that provides hospitals with essential medications in ready-to-administer injectable formats that are critical for effective patient care. We are leading the way with unmatched expertise in current Good Manufacturing Practices and sterile pharmaceutical manufacturing, and the highest quality and safety standards so hospitals can more confidently and reliably focus on patient care nationwide. As a leader in sterile compounding, we continue to invest in automation and integrated technologies to improve our production processes, safety, consistency, and product quality. 
 
As part of our team, you'll experience being at the forefront of groundbreaking solutions, collaborating with brilliant minds, and making a tangible impact in healthcare delivery. 
 
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 &ldquo;at will.&rdquo;

California Consumer Privacy Act (CCPA) Notice for Applicants and Employees</div>

Warehouse Technician Intern

<div>Our Supervisor, Manufacturing Operations (Formulation) plays a vital role in ensuring the highest quality and safety standards of our pharmaceutical products. Once you complete our training, you will be responsible for daily coordination and working schedules of people and equipment in Formulation Operations. 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 6AM to 2:30PM. This is a set, consistent schedule 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 Supervisor, Manufacturing Operations (Formulation) Does Each Day:
<ul>
<li>Runs operation to meet or exceed delivery performance objectives for product or projects</li>
<li>Supervises staff in execution of daily work; assures operators comply with validated parameters and standard operating procedures, cGMP regulations and safety requirements; provides constructive operator feedback</li>
<li>Counsels, trains, &amp; develops technicians for efficient performance; creates an atmosphere of team effort &amp; open communication</li>
<li>Completes in-process checks &amp; verifications in alignment with Standard Operating Procedures</li>
<li>Reviews documentation such as batch records and logs to assure accurate recording of processes in conformance to policies and procedures and in compliance with Good Documentation Practices</li>
<li>Develops technician training programs &amp; assures operator training is conducted</li>
<li>Troubleshoots or resolves issues impeding daily/weekly deliverables; proactively demonstrates the ownership to achieve</li>
<li>Reviews operational performance and drives improvement opportunities</li>
<li>Initiates &amp; executes change control assignments in support of continuous improvement initiatives for equipment, documentation, or processes</li>
<li>Drives Quality Management System assignments (CAPA, Deviation, Change Control, GMP tasks) to on-time closure</li>
<li>Reports &amp; initiates production schedule changes, requests equipment and facility repairs, or modifications</li>
</ul>
Our Most Successful Supervisor, Manufacturing Operations (Formulation):
<ul>
<li>Meets productivity standards; Completes work in timely manner; Strives to increase productivity</li>
<li>Follows policies and procedures; completes administrative tasks correctly and on time</li>
<li>Prioritizes and plans work activities; Sets goals and objectives; Organizes or schedules other people and their tasks</li>
<li>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</li>
</ul>
Minimum Requirements for this Role:
<ul>
<li>High school Diploma or GED from recognized institution or organization required</li>
<li>2-3 years prior experience in cGMP / FDA regulated industry</li>
<li>1 year of supervisory or management experience required</li>
<li>Successful completion of certified in-house qualification programs</li>
<li>Experience training personnel on aseptic techniques and appropriate gowning techniques</li>
<li>Well versed in the compliance &amp; quality requirements of 503B pharmaceutical industry and CGMP's and have demonstrated strength in problem solving and resolution</li>
<li>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</li>
</ul>
Any of the Following Will Give You an Edge:
<ul><li>Bachelor&rsquo;s Degree in Life Science or another related field</li>
<li>Computer Skills</li>
<li>Training Software</li>
<li>Microsoft Suite</li>
<li>ERP software</li>
</ul>
Benefits of Working at Quva:
<ul>
<li>Set, full-time, consistent work schedule</li>
<li>Comprehensive health and wellness benefits including medical, dental and vision</li>
<li>401k retirement program with company match</li>
<li>22 paid days off plus 8 paid holidays per year</li>
<li>National, industry-leading high growth company with future career advancement opportunities</li>
<li>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</li>
<li>Range: $65,023- $89,047 Annually</li>
</ul>
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&rsquo;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&rsquo;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 &ldquo;at will.&rdquo;

California Consumer Privacy Act (CCPA) Notice for Applicants and Employees</div>

Supervisor, Manufacturing Operations (Formulation) 1st Shift

<div>We are looking for an HR Intern to perform various administrative tasks and support our HR department&rsquo;s daily activities. HR Intern responsibilities include updating our employee records with new hire information, auditing of data and changes, revising job descriptions, and updating organizational charts. If you&rsquo;re interested in kickstarting your career in HR and getting a closer look at how our company approaches payroll, compliance, benefits, compensation and employee development, we&rsquo;d like to meet you. Assist in organizing and coordinating our HR policies and procedures. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US. 
This is a role working Monday through Friday from 8:00 AM to 4:00 PM based on site in our Corporate - Sugar Land, TX location. Internship dates are June 1 - July 31, 2026.

What the Human Resources Intern Does Each Day:
<ul>
<li>Update our internal databases with new employee information, including contact details and employment forms</li>
<li>Revise job descriptions to match current staffing needs; ensure that job descriptions are organized and archived properly within our HR systems and shared drives</li>
<li>Update organizational chart and position seats</li>
<li>Assist with compliance documentation such as FMLA leave paperwork</li>
<li>File employee documentation in personnel folders</li>
<li>Help with audits on employee files; assist with corrections needed after the audit to stay in compliance</li>
<li>Address employee queries about benefits (like number of remaining vacation days)</li>
<li>Review and distribute company policies in digital formats or hard copies</li>
<li>Participate in organizing company events and careers days</li>
</ul>
Our Most Successful Human Resources Interns:
<ul>
<li>Are detail-oriented with strong verbal and written communications skills</li>
<li>Motivates others, shares knowledge, builds high performing team, shows respect towards others, gives constructive feedback</li>
<li>Display eagerness to learn and continuously improve, adapt quickly to change, and apply sound judgment</li>
<li>Foster team environment, invest in team members and peers by inclusion and listening, recognize employees effectively, demonstrate trust</li>
<li>Have excellent communication, are confidential, can critically evaluate, have relationship management skills</li>
</ul>
Minimum Requirements for this Role:
<ul>
<li>Experience as a Staff Assistant or similar junior HR role is a plus</li>
<li>Familiarity with HRIS databases</li>
<li>Experience with MS Office</li>
<li>Organizational skills</li>
<li>BS in Human Resources Management or similar field</li>
<li>Legally authorized to work in the job posting country</li>
<li>Microsoft Word and Excel skills</li>
</ul>
Benefits of Working at QuVa:
<ul>
<li>Set, full-time, consistent work schedule</li>
<li>National, industry-leading high growth company with future career advancement opportunities</li></ul> 


About QuVa: 
 
QuVa is a national, industry-leading provider of pharmacy services, including ready-to-administer sterile outsourcing and advanced AI-generated insights providing clarity for revenue capture and inventory management. QuVa Pharma delivers essential medications in injectable formats critical for effective patient care. LogicStream, a QuVa company, partners with health systems to aggregate, normalize, and analyze large amounts of complex data through AI and machine learning tools that generate actionable insights supporting revenue optimization, inventory management, and inventory-related workflows. Through QuVa&rsquo;s integrated solutions, health systems can transform pharmacy management to achieve greater value by operating more efficiently and effectively as they deliver high-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 &ldquo;at will.&rdquo;</div>

Human Resources Intern

<div>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 1st shift, working Wednesday to Saturday from 4:00 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 the Compounding Pharmacy Technician Does Each Day:
<ul>
<li>Compound sterile preparations accurately according to detailed instructions</li>
<li>Clean work area and cleanroom (typically wiping down surfaces with aseptic wipe and occasional mopping)</li>
<li>Keep accurate documentation for accountability and traceability of product following Good Documentation Practices (GDPs)</li>
<li>Comply with cGMPs and company International Organization for Standardization (ISO) standards upon key steps in the work</li>
</ul>
Our Most Successful Compounding Pharmacy Technicians:
<ul>
<li>Have a strong attention to detail and carefully follows compounding protocols and all Standard Operating Procedures (SOPs) related to the job</li>
<li>Are proactive and demonstrate initiative when appropriate; uses their time wisely</li>
Have a passion for connecting their work to a greater purpose 
<li>
 
 
</li></ul>Minimum Requirements for this Role:
<ul>
<li>A High School diploma or equivalent</li>
<li>Able to successfully complete a drug and background check</li>
<li>Able and willing to walk, stoop, stand, bend, and lift up to 50 lbs. throughout each shift, with or without reasonable accommodation</li>
<li>18+ years of age</li>
<li>Able and willing to follow &ldquo;garb and gown&rdquo; requirements from head to toe in order to maintain a sterile, clean room environment. This includes:
<ul><li>Hand washing</li>
<li>Wearing hair net, shoe covers, facemask, sterile gown, and gloves, etc.</li>
<li>Stringent regulations concerning, for example, the carrying of cellphones, the wearing of jewelry and makeup, and the length / type of fingernails</li>
</ul></li><li>Familiarity with and comfortable using mobile devices such as smartphones, tablets, handhelds</li>
<li>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</li>
</ul>
Any of the Following Will Give You an Edge:
<ul>
<li>Pharmacy Technician (CPhT) License</li>
<li>Certified in ACPE sterile products</li>
<li>Experience in pharmacy compounding</li>
<li>Knowledge of cGMP (Current Good Manufacturing Processes)</li>
<li>Knowledge of ISO 5/7 environment cleanroom gowning</li>
</ul>
Benefits of Working at Quva:
<ul>
<li>A career path with defined steps for growth, offering regular opportunities to enhance skills, expand responsibilities, and increase earning potential</li>
<li>Set, full-time, consistent work schedule</li>
<li>Comprehensive health and wellness benefits including medical, dental and vision</li>
<li>401k retirement program with company match</li>
<li>A minimum of 17 paid days off plus 8 paid holidays per year</li>
<li>Occasional weekend and overtime opportunities with advance notice</li>
<li>National, industry-leading high growth company with future career advancement opportunities</li>
<li>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</li>
<li>Salary Range: $22.00-$24.00/hour plus $1.00 shift differential</li>
</ul>
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&rsquo;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 &ldquo;at will.&rdquo;</div>

Compounding Pharmacy Technician I 1st Shift

<div>Our Accounting Intern plays a vital role within our organization. Once you complete our training, your responsibilities will include assisting with daily, monthly, and annual GL reconciliation and analysis in a growth capacity. This position will also include performing ad hoc projects for the department. 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 internship runs through June 1 - July 31, 2026. Monday - Friday 8:00 AM - 4:00 PM at our Sugar Land, TX Location.

 What the Accounting Intern Does Each Day:
<ul>
<li>Prepares consolidation of Financial Statements by assisting with the month, quarter and year-end close process</li>
<li>Prepares assigned monthly bank reconciliations and investigate discrepancies, including collaboration with accounts receivable and accounts payable clerks</li>
<li>Research cash application differences and voucher payable reconciliation differences</li>
<li>Performs consolidated financial close functions where responsibilities will include account reconciliations, preparation of journal entries, and other tasks to support the team</li>
<li>Creates ad-hoc reports and projects as requested</li>
</ul>
Our Most Successful Accounting Interns:
<ul>
<li>Have excellent written and verbal communication skills</li>
<li>Prioritize, handle and track multiple assignments</li>
<li>Collaborate in a team environment</li> 
</ul>
Minimum Requirements for this Role:
<ul>
<li>18+ years of age</li>
<li>Able to successfully complete a drug and background check</li>
<li>Currently pursuing a Bachelor&rsquo;s or Master&rsquo;s degree in Accounting (minimum of 12 hours of Accounting w/ GPA of 3.0 or higher)</li>
<li>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</li>
</ul>
Any of the Following Will Give You an Edge:
<ul>
<li>Strong knowledge of MS Office (Excel, Word, Outlook &amp; PowerPoint)</li>
<li>Basic understanding of accounting concepts</li>
</ul>
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&rsquo;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 &ldquo;at will.&rdquo;</div>

Accounting Intern

<div>Our Supervisor, Manufacturing Operations (Compounding) plays a vital role in ensuring the highest quality and safety standards of our pharmaceutical products. Once you complete our training, you will be responsible for daily coordination and working schedules of people and equipment in Compounding Operations. 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 2PM to 10:30PM. This is a set, consistent schedule 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 Supervisor, Manufacturing Operations (Compounding) Does Each Day:
<ul>
<li>Runs operation to meet or exceed delivery performance objectives for product or projects</li>
<li>Supervises staff in execution of daily work; assures operators comply with validated parameters and standard operating procedures, cGMP regulations and safety requirements; provides constructive operator feedback</li>
<li>Counsels, trains, &amp; develops technicians for efficient performance; creates an atmosphere of team effort &amp; open communication</li>
<li>Completes in-process checks &amp; verifications in alignment with Standard Operating Procedures</li>
<li>Reviews documentation such as batch records and logs to assure accurate recording of processes in conformance to policies and procedures and in compliance with Good Documentation Practices</li>
<li>Develops technician training programs &amp; assures operator training is conducted</li>
<li>Troubleshoots or resolves issues impeding daily/weekly deliverables; proactively demonstrates the ownership to achieve</li>
<li>Reviews operational performance and drives improvement opportunities</li>
<li>Initiates &amp; executes change control assignments in support of continuous improvement initiatives for equipment, documentation, or processes</li>
<li>Drives Quality Management System assignments (CAPA, Deviation, Change Control, GMP tasks) to on-time closure</li>
<li>Reports &amp; initiates production schedule changes, requests equipment and facility repairs, or modifications</li>
</ul>
Our Most Successful Supervisor, Manufacturing Operations (Compounding):
<ul>
<li>Meets productivity standards; Completes work in timely manner; Strives to increase productivity</li>
<li>Follows policies and procedures; completes administrative tasks correctly and on time</li>
<li>Prioritizes and plans work activities; Sets goals and objectives; Organizes or schedules other people and their tasks</li>
<li>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</li>
</ul>
Minimum Requirements for this Role:
<ul>
<li>High school Diploma or GED from recognized institution or organization required</li>
<li>2-3 years prior experience in cGMP / FDA regulated industry</li>
<li>1 year of supervisory or management experience required</li>
<li>Successful completion of certified in-house qualification programs</li>
<li>Experience training personnel on aseptic techniques and appropriate gowning techniques</li>
<li>Able and willing to walk, stoop, stand, bend, and lift up to 50 lbs. throughout each shift, with or without reasonable accommodation</li>
<li>Well versed in the compliance &amp; quality requirements of 503B pharmaceutical industry and CGMP's and have demonstrated strength in problem solving and resolution</li>
<li>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</li>
</ul>
Any of the Following Will Give You an Edge:
<ul><li>Bachelor&rsquo;s Degree in Life Science or another related field</li>
<li>Computer Skills</li>
<li>Training Software</li>
<li>Microsoft Suite</li>
<li>ERP software</li>
</ul>
Benefits of Working at Quva:
<ul>
<li>Set, full-time, consistent work schedule</li>
<li>Comprehensive health and wellness benefits including medical, dental and vision</li>
<li>401k retirement program with company match</li>
<li>22 paid days off plus 8 paid holidays per year</li>
<li>National, industry-leading high growth company with future career advancement opportunities</li>
<li>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</li>
<li>Range: $74, 766 - $102,812 Annually</li>
</ul>
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&rsquo;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&rsquo;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 &ldquo;at will.&rdquo;

California Consumer Privacy Act (CCPA) Notice for Applicants and Employees</div>

Supervisor, Manufacturing Operations (Compounding) 2nd Shift

Join QuVa Pharma and explore 6   exciting career opportunities. They're hiring for various roles with options for remote or on-site work. Apply today and become part of their innovative team.