Qureos Mentor

Medline Industries

<div>Job Summary
Our Medline Acute Care sales team serves as the main interface for various segments in the hospital such as OR, Cath Lab, ICU, Labor and Delivery, Emergency Department, Materials Management and C-suite. Our engagement with clinical and industry leaders allows us to deliver a robust product portfolio and patient-care solutions. We optimize care with quality hospital supplies and customized solutions which is why our customers continue to choose us as their trusted business partner - we make healthcare run better.
Job Description
Medline, a market leader in the advanced wound and skin care market, has an immediate opening in our Skin and Wound Care sales team based out of San Antonio, TX.
Responsibilities:
<ul><li>Calling on multiple clinical and non-clinical decision makers in Acute Care facilities within assigned territory
</li><li>Making sales presentations to multiple decision-makers
</li><li>Working with Medline sales force to grow targeted accounts
</li><li>Establishing and nurturing client relationships
</li><li>Developing strong relationships with key decision makers
</li><li>Maintaining existing business and presenting new products
</li><li>Acting as Product Specialist, collaborating with several sales reps
</li><li>Interacting with clinicians to communicate product choices, and conduct product evaluations, trials and in-services
</li><li>Providing timely reporting and analysis of business conditions within accounts
</li></ul>Required Experience:
<ul><li>Bachelor&rsquo;s degree and at least 2 years of quota-based sales experience demonstrating a background in cold calling, commission, full-cycle sales experience OR at least 5 years of quota-based sales experience demonstrating a background in cold calling, commissioned, full-cycle sales experience.
 </li><li>2 &ndash; 5 years medical sales, advanced wound care sales or successful business-to-business outside sales experience will also be considered.
</li><li>Comfortable working in a clinical setting
</li><li>Track record of demonstrable sales growth and quota attainment
</li><li>Ability and desire to learn and present multiple product lines
</li><li>Excellent communication and organizational skills
</li><li>Computer proficiency especially in MS Excel, Word, and Outlook
</li><li>Due to the nature of an outside sales representative position, the ability to drive a car, travel in that car 90% of each day, and interact with healthcare providers on site is required. 
</li></ul> 
The anticipated compensation for this position includes a base salary range of $70,000 to $80,000 with additional commission ranging between 5-12% net sales growth . This salary range is an estimate and the actual salary will vary based on applicant&rsquo;s location, education, experience, skills, and abilities. This role is bonus eligible. Medline will not pay less than the applicable minimum wage or salary threshold.
Our benefit package includes health insurance, life and disability, 401(k) contributions, paid time off, etc., for employees working 30 or more hours per week on average. For roles where employees work less than 30 hours per week, benefits include 401(k) contributions as well as access to the Employee Assistance Program, Employee Resource Groups and the Employee Service Corp.
We&rsquo;re dedicated to creating a Medline where everyone feels they belong and can grow their career. We strive to do this by seeking diversity in all forms, acting inclusively, and ensuring that people have tools and resources to perform at their best. Explore our Belonging page here .
Medline Industries, LP is an equal opportunity employer. Medline evaluates qualified individuals without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, age, disability, neurodivergence, protected veteran status, marital or family status, caregiver responsibilities, genetic information, or any other characteristic protected by applicable federal, state, or local laws.</div>

Skin Health Sales Representative

<div>Job Summary
Ensure the timely and accurate production of finished goods and the delivery of product to the customer. Maintain inventory integrity of components and finished items
Job Description
Responsibilities:
<ul><li>Oversee and coordinate product processing
</li><li>Monitor backorder reports and production scheduling and coordinate resources to ensure minimal backorders. Ensure overall quality of the items produced.
</li><li>Create inventory transfers and production orders to meet the established production schedules and service levels.
</li><li>Create all needed paperwork, the completion of all required functions and the electronic receipt of finished goods. Ensure compliance with all regulatory functions that apply.
</li><li>Ensure inventory integrity for components and finished product.
</li><li>Communicate with product divisions on backordered items and substitute items.
</li><li>Act as back-up on/for production equipment, material handling and warehouse.
</li><li>Develop and mentor staff through on-boarding, open communication, training and development opportunities and performance management processes; build and maintain employee morale and motivation; ensure the team is appropriately staffed with required competencies.
</li></ul>Required Experience:
<ul><li>High school diploma or equivalent.
</li></ul>Preferred Qualifications:
<ul><li>Previous SAP and Catalyst experience.
</li><li>At least 2 years previous production experience.
</li><li>Previous experience as a department lead or supervisor a plus.
</li><li>At least 1 year of experience managing people, including hiring, developing, motivating and directing people as they work.
</li></ul>Medline Industries, LP, and its subsidiaries, offer a competitive total rewards package, continuing education &amp; training, and tremendous potential with a growing worldwide organization.
The anticipated salary range for this position:
$73,000.00 - $110,000.00 Annual
The actual salary will vary based on applicant&rsquo;s location, education, experience, skills, and abilities. This role is bonus and/or incentive eligible. Medline will not pay less than the applicable minimum wage or salary threshold.
Our benefit package includes health insurance, life and disability, 401(k) contributions, paid time off, etc., for employees working 30 or more hours per week on average. For roles where employees work less than 30 hours per week, benefits include 401(k) contributions as well as access to the Employee Assistance Program, Employee Resource Groups and the Employee Service Corp.
We&rsquo;re dedicated to creating a Medline where everyone feels they belong and can grow their career. We strive to do this by seeking diversity in all forms, acting inclusively, and ensuring that people have tools and resources to perform at their best. Explore our Belonging page here .
Medline Industries, LP is an equal opportunity employer. Medline evaluates qualified individuals without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, age, disability, neurodivergence, protected veteran status, marital or family status, caregiver responsibilities, genetic information, or any other characteristic protected by applicable federal, state, or local laws.</div>

Production Supervisor - 2nd Shift

<div>Job Summary
This job involves ensuring efficient and safe production processes while minimizing downtime. The employee will support various production and warehouse activities, including repetitive line assembly tasks to mass-produce component trays, dressings, and labels for medical products. A key responsibility is sealing pouches on final packs using specialized machinery.
Job Description
The Pharmaceutical Production Technician is responsible for executing material staging and clean-in-place (CIP)/clean-out-of-place (COP) processes in a controlled ISO-classified cleanroom, ensuring contamination control, SOP/GMP compliance, accurate batch documentation, and consistent safe preparation of cloth, film, and solution contact components. Operators serve on the front line of aseptic behavior, environmental discipline, and product integrity, supporting compliant and efficient manufacturing operations.
MAJOR RESPONSIBILITIES
Cleanroom Conduct &amp; Gowning
<ul><li>Follow all cleanroom gowning requirements and adhere to gowning and material entry‑ protocols.
</li></ul><ul><li>Follow good aseptic practices when performing all tasks within ISO-certified environments.
</li></ul>Pre-Run Preparation
<ul><li>Complete all pre-run‑ checks, including:
<ul><li>Reconciliation of materials.
</li><li>Verifying process piping cleaning requirements for the upcoming batch.
</li><li>Confirming availability of cloth rolls, film, solution, and other materials.
</li></ul></li></ul>Material Staging
<ul><li>Stage cloth rolls, film, and other packaging materials per established procedures to minimize contamination risk.
</li><li>Maintain unidirectional flow of cloth, film, totes, and packaging components to prevent cross contamination.
</li></ul><ul><li>Manage raw materials to ensure expired or incorrect lots are not used.
</li></ul>CIP/COP Processes
<ul><li>Perform all cleaning activities related to process piping and components according to established procedures.
</li><li>Execute sanitization cleaning cycles for all raw materials entering cleanroom environments.
</li></ul><ul><li>Perform sanitization steps for all tools/equipment and execute proper changeover cleaning sequences.
</li></ul>Documentation &amp; Escalation
<ul><li>Real-time, accurate, and complete documentation on all forms and records.
</li><li>Follows Good Documentation Practices
</li><li>Immediately escalate deviations to the Supervisor or Quality.
</li></ul>Cleaning &amp; Responsibilities
<ul><li>Perform cleaning activities according to established procedures.
</li></ul><ul><li>Handle scrap per established procedure and ensure dedicated scrap receptacles never leave the cleanroom.
</li></ul>Safety &amp; Ergonomics
<ul><li>Follow all EHS procedures, including chemical handling requirements.
</li><li>Use proper ergonomic techniques when lifting and moving materials.
</li></ul>MINIMUM JOB REQUIREMENTS
Education
<ul><li>High school diploma or GED required
</li></ul>Work Experience
<ul><li>Prior manufacturing experience.
</li></ul>Knowledge / Skills / Abilities
<ul><li>Must be able to lift up to 50 lbs.
</li><li>Must be able to bend, twist, reach, push, lift for extended periods daily.
</li><li>Comfortable working in cleanroom and controlled environments while adhering to gowning, safety, and quality requirements.
</li><li>Other duties as assigned.
</li><li>Flexibility to work mandatory overtime based on business needs.
</li><li>Ability to speak, read, and write English with proficiency
</li></ul>PREFERRED JOB REQUIREMENTS
Work Experience
<ul><li>Experience in aseptic manufacturing experience in GMP and ISO-cleanroom environments.
</li></ul>Knowledge / Skills / Abilities
<ul><li>Strong working knowledge of GMP regulations, aseptic techniques, and biopharmaceutical manufacturing processes, with the ability to execute work in compliance with SOPs, batch records, and technical documentation.
</li><li>Proven ability to operate, monitor, troubleshoot, and maintain biopharmaceutical manufacturing equipment.
</li><li>Demonstrated attention to detail with the ability to accurately complete GMP documentation and support investigations and escalate issues.
</li></ul>Medline Industries, LP, and its subsidiaries, offer a competitive total rewards package, continuing education &amp; training, and tremendous potential with a growing worldwide organization.
The anticipated salary range for this position:
$20.25 - $29.25 Hourly
The actual salary will vary based on applicant&rsquo;s location, education, experience, skills, and abilities. Medline will not pay less than the applicable minimum wage or salary threshold.
Our benefit package includes health insurance, life and disability, 401(k) contributions, paid time off, etc., for employees working 30 or more hours per week on average. For roles where employees work less than 30 hours per week, benefits include 401(k) contributions as well as access to the Employee Assistance Program, Employee Resource Groups and the Employee Service Corp.
We&rsquo;re dedicated to creating a Medline where everyone feels they belong and can grow their career. We strive to do this by seeking diversity in all forms, acting inclusively, and ensuring that people have tools and resources to perform at their best. Explore our Belonging page here .
Medline Industries, LP is an equal opportunity employer. Medline evaluates qualified individuals without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, age, disability, neurodivergence, protected veteran status, marital or family status, caregiver responsibilities, genetic information, or any other characteristic protected by applicable federal, state, or local laws.</div>

Pharmaceutical Production Technician - 3rd Shift

<div>Job Summary
Responsible for performing advanced pharmaceutical drug manufacturing activities while providing day-to-day technical guidance and workflow coordination within regulated GMP environments. This role serves as a technical and operational resource on the production floor, supporting production flow, compliance, and continuous improvement without formal supervisory authority.
Job Description
MAJOR RESPONSIBILITIES
<ul><li>Acts as a technical and workflow lead by coordinating daily manufacturing tasks, prioritizing activities, and supporting efficient production flow without formal people management responsibility.
</li><li>Provides on-the-job guidance, mentoring, and training to manufacturing technicians and lower-level operators to ensure adherence to procedures, safety standards, and GMP requirements.
</li><li>Performs advanced, hands-on biopharmaceutical manufacturing activities, including media and buffer preparation, aseptic processing, equipment cleaning and sterilization, and any responsibilities to support production and schedule adherence.
</li><li>Sets up, operates, monitors, and adjusts bioprocessing equipment such as autoclaves, washer-sterilizers, filtration systems, fermenters, and fill-finish equipment.
</li><li>Prepares, cleans, assembles, and stages tanks, glassware, components, and systems for batch manufacturing operations in accordance with approved procedures.
</li><li>Monitors critical process parameters, production data, and outputs to ensure compliance with batch records, specifications, and quality standards.
</li><li>Identifies, documents, and escalates deviations, abnormal events, and process issues in accordance with quality systems and regulatory expectations.
</li><li>Maintains accurate and complete batch documentation, equipment logs, inventory records, and other GMP compliance documentation.
</li><li>Follows and reinforces standard operating procedures (SOPs), manufacturing instructions, and all applicable safety, quality, and regulatory guidelines.
</li><li>Collaborates with engineering, quality, and maintenance teams on troubleshooting, investigations, testing, and process optimization activities.
</li><li>Supports continuous improvement initiatives by providing technical input, identifying opportunities for efficiency or quality improvements, and assisting with implementation of approved changes.
</li></ul>MINIMUM JOB REQUIREMENTS
Education
<ul><li>High school diploma or GED required
</li></ul>Work Experience
<ul><li>2-3 years of manufacturing experience.
</li><li>Experience in aseptic manufacturing experience in GMP and ISO-cleanroom environments.
</li></ul>Knowledge / Skills / Abilities
<ul><li>Proven ability to operate, monitor, troubleshoot, and maintain biopharmaceutical manufacturing equipment.
</li><li>Demonstrated attention to detail with the ability to accurately complete GMP documentation and support investigations and escalate issues.
</li><li>Effective communication and interpersonal skills, including the ability to guide and collaborate with others.
</li><li>Comfortable working in cleanroom and controlled environments while adhering to gowning, safety, and quality requirements.
</li><li>Flexibility to work mandatory overtime based on business needs.
</li><li>Ability to speak, read, and write English with proficiency
</li></ul>PREFERRED JOB REQUIREMENTS
Education
<ul><li>Bachelor's degree in STEM field
</li></ul>Work Experience
<ul><li>2 years of hands-on experience in GMP-regulated pharmaceutical or biopharmaceutical manufacturing.
</li><li>Demonstrated experience performing advanced manufacturing operations such as aseptic processing, media/buffer preparation, and equipment operation
</li></ul>Knowledge / Skills / Abilities
<ul><li>Advanced knowledge of upstream and/or downstream bioprocessing operations
</li><li>Experience supporting audits, inspections, and regulatory interactions
</li><li>Familiarity with continuous improvement methodologies and operational excellence initiatives
</li><li>Strong problem-solving skills with the ability to work cross-functionally
</li></ul>Medline Industries, LP, and its subsidiaries, offer a competitive total rewards package, continuing education &amp; training, and tremendous potential with a growing worldwide organization.
The anticipated salary range for this position:
$28.75 - $41.75 Hourly
The actual salary will vary based on applicant&rsquo;s location, education, experience, skills, and abilities. Medline will not pay less than the applicable minimum wage or salary threshold.
Our benefit package includes health insurance, life and disability, 401(k) contributions, paid time off, etc., for employees working 30 or more hours per week on average. For roles where employees work less than 30 hours per week, benefits include 401(k) contributions as well as access to the Employee Assistance Program, Employee Resource Groups and the Employee Service Corp.
We&rsquo;re dedicated to creating a Medline where everyone feels they belong and can grow their career. We strive to do this by seeking diversity in all forms, acting inclusively, and ensuring that people have tools and resources to perform at their best. Explore our Belonging page here .
Medline Industries, LP is an equal opportunity employer. Medline evaluates qualified individuals without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, age, disability, neurodivergence, protected veteran status, marital or family status, caregiver responsibilities, genetic information, or any other characteristic protected by applicable federal, state, or local laws.</div>

Pharmaceutical Production Lead - 2nd Shift

<div>Job Summary
The Pharmaceutical Product Operator is responsible for executing cloth converting and/or packaging processes in a controlled ISO-classified cleanroom environment. This role ensures adherence to contamination control practices, SOP/GMP compliance, accurate batch documentation, and safe handling of cloth, film, and solution contact components. Operators serve on the front line of aseptic behavior, environmental discipline, and product integrity, supporting compliant and efficient manufacturing operations.
Job Description
MAJOR RESPONSIBILITIES
Cleanroom Conduct &amp; Gowning
<ul><li>Follow all cleanroom gowning requirements and adhere to gowning and material entry protocols.
</li></ul><ul><li>Follow good aseptic practices when performing all tasks within ISO-certified environments.
</li></ul>Pre-Run Preparation
<ul><li>Complete all pre-run checks, including:
</li></ul><ul><li>Line clearance procedures
</li><li>Verifying production parameter sheets and counter readings
</li><li>Checking machine cleanliness status
</li><li>Accurate documentation
</li></ul>Cloth Converting Operations
<ul><li>Load cloth rolls using approved cleanable dollies or carts, minimizing manual handling.
</li></ul><ul><li>Set up and operate unwind stations, tension controls, alignment systems, folding boards, and cutting mechanisms according to validated line parameters.
</li></ul><ul><li>Monitor dosing application (when applicable), including flow rate, nozzle alignment, and solution coverage.
</li></ul><ul><li>Continuously inspect the web path for defects (tears, fraying, or contamination) and adjust as needed.
</li></ul><ul><li>Perform required hourly inspections and document results.
</li></ul>OR
Packaging Line Operations
<ul><li>Load film rolls using approved cleanable carts or lifts, minimizing manual handling.
</li></ul><ul><li>Set up and maintain packaging parameters within validated specifications.
</li></ul><ul><li>Set up and verify date/lot coding equipment and inspection verification systems.
</li></ul><ul><li>Perform required hourly inspections and document results.
</li></ul>Documentation &amp; Escalation
<ul><li>Real-time, accurate, and complete documentation on all forms and records.
</li></ul><ul><li>Follows Good Documentation Practices
</li></ul><ul><li>Immediately escalate deviations to the Supervisor or Quality.
</li></ul>Cleaning &amp; Responsibilities
<ul><li>Perform cleaning activities according to established procedures.
</li></ul><ul><li>Assist with sanitization steps for all tools/equipment and execute proper changeover cleaning sequences.
</li></ul><ul><li>Handle scrap per established procedure and ensure scrap receptacles never leave the cleanroom.
</li></ul>Safety &amp; Ergonomics
<ul><li>Follow all EHS procedures, including chemical handling requirements.
</li></ul><ul><li>Use proper ergonomic techniques when lifting cloth rolls and moving materials.
</li></ul>MINIMUM JOB REQUIREMENTS
Education
<ul><li>High school diploma or GED required
</li></ul>Work Experience
<ul><li>Experience in aseptic manufacturing environment
</li></ul>Knowledge / Skills / Abilities
<ul><li>Effective communication and interpersonal skills, including the ability to guide and collaborate with others.
</li></ul><ul><li>Comfortable working in cleanroom and controlled environments while adhering to gowning, safety, and quality requirements.
</li></ul><ul><li>Other duties as assigned.
</li></ul><ul><li>Flexibility to work mandatory overtime based on business needs.
</li></ul><ul><li>Ability to speak, read, and write English with proficiency
</li></ul>PREFERRED JOB REQUIREMENTS
Work Experience
<ul><li>Hands-on experience in GMP-regulated pharmaceutical or biopharmaceutical manufacturing.
</li></ul>Knowledge / Skills / Abilities
<ul><li>Strong working knowledge of GMP regulations, aseptic techniques, and biopharmaceutical manufacturing processes, with the ability to execute work in compliance with SOPs, batch records, and technical documentation.
</li></ul><ul><li>Proven ability to operate, monitor, troubleshoot, and maintain biopharmaceutical manufacturing equipment.
</li></ul><ul><li>Demonstrated attention to detail with the ability to accurately complete GMP documentation and support investigations and escalate issues.
</li></ul><ul><li>Effective communication and interpersonal skills, including the ability to guide and collaborate with others.
</li></ul>Medline Industries, LP, and its subsidiaries, offer a competitive total rewards package, continuing education &amp; training, and tremendous potential with a growing worldwide organization.
The anticipated salary range for this position:
$21.75 - $31.50 Hourly
The actual salary will vary based on applicant&rsquo;s location, education, experience, skills, and abilities. Medline will not pay less than the applicable minimum wage or salary threshold.
Our benefit package includes health insurance, life and disability, 401(k) contributions, paid time off, etc., for employees working 30 or more hours per week on average. For roles where employees work less than 30 hours per week, benefits include 401(k) contributions as well as access to the Employee Assistance Program, Employee Resource Groups and the Employee Service Corp.
We&rsquo;re dedicated to creating a Medline where everyone feels they belong and can grow their career. We strive to do this by seeking diversity in all forms, acting inclusively, and ensuring that people have tools and resources to perform at their best. Explore our Belonging page here .
Medline Industries, LP is an equal opportunity employer. Medline evaluates qualified individuals without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, age, disability, neurodivergence, protected veteran status, marital or family status, caregiver responsibilities, genetic information, or any other characteristic protected by applicable federal, state, or local laws.</div>

Pharmaceutical Product Operator - 3rd Shift

<div>Job Summary
The Pharmaceutical Product Operator is responsible for executing cloth converting and/or packaging processes in a controlled ISO-classified cleanroom environment. This role ensures adherence to contamination control practices, SOP/GMP compliance, accurate batch documentation, and safe handling of cloth, film, and solution contact components. Operators serve on the front line of aseptic behavior, environmental discipline, and product integrity, supporting compliant and efficient manufacturing operations.
Job Description
MAJOR RESPONSIBILITIES
<div>Cleanroom Conduct &amp; Gowning
</div><div><ul><li>Follow all cleanroom gowning requirements and adhere to gowning and material entry protocols.
</li></ul></div><div><ul><li>Follow good aseptic practices when performing a ll tasks within ISO-certified environments .
</li></ul></div><div>Pre - Run Preparation
</div><div><ul><li>Complete all pre - run checks, including:
</li></ul></div><div><ul><li>Line clearance procedures
</li></ul></div><div><ul><li>Verifying production parameter sheets and counter readings
</li></ul></div><div><ul><li>Checking machine cleanliness status
</li></ul></div><div><ul><li>Accurate documentation
</li></ul></div><div>Cloth Converting Operations
</div><div><ul><li>Load cloth rolls using approved cleanable dollies or carts, minimizing manual handling.
</li></ul></div><div><ul><li>Set up and o perate unwind stations, tension controls, alignment systems, folding boards, and cutting mechanisms according to validated line parameters.
</li></ul></div><div><ul><li>Monitor dosing application (when applicable), including flow rate, nozzle alignment, and solution coverage.
</li></ul></div><div><ul><li>Continuously inspect the web path for defects (tears, fraying, or contamination) and adjust as needed.
</li></ul></div><div><ul><li>Perform required hourly inspections and document results. 
</li></ul></div><div>OR 
</div><div>Packaging Line Operations
</div><div><ul><li>Load film rolls using approved cleanable carts or lifts, minimizing manual handling.
</li></ul></div><div><ul><li>Set up and m aintain packaging parameters within validated specifications.
</li></ul></div><div><ul><li>Set up and verify date/lot coding equipment and inspection verification systems.
</li></ul></div><div><ul><li>Perform required hourly inspections and document results.
</li></ul></div><div>Documentation &amp; Escalation
</div><div><ul><li>Real-time , accurate , and complete documentation on all forms and records .
</li></ul></div><div><ul><li>Follows Good Documentation Practices
</li></ul></div><div><ul><li>Immediately escalate deviations to the Supervisor or Q uality .
</li></ul></div><div>Cleaning &amp; Responsibilities
</div><div><ul><li>Perform cleaning activities according to established procedures.
</li></ul></div><div><ul><li>Assist with sanitization steps for all tools/equipment and execute proper changeover cleaning sequences.
</li></ul></div><div><ul><li>Handle scrap per established procedure and ensure scrap receptacles never leave the cleanroom.
</li></ul></div><div>Safety &amp; Ergonomics
</div><div><ul><li>Follow all EHS procedures, including chemical handling requirements.
</li></ul></div><div><ul><li>Use proper ergonomic techniques when lifting cloth rolls and moving materials.
</li></ul></div>MINIMUM JOB REQUIREMENTS
Education
<ul><li>High school diploma or GED required
</li></ul>Work Experience
<ul><li>Experience in aseptic manufacturing environment
</li></ul>Knowledge / Skills / Abilities
<div><ul><li>Effective communication and interpersonal skills, including the ability to guide and collaborate with others.
</li></ul></div><div><ul><li>Comfortable working in cleanroom and controlled environments while adhering to gowning, safety, and quality requirements.
</li></ul></div><div><ul><li>Other duties as assigned.
</li></ul></div><div><ul><li>Flexibility to work mandatory overtime based on business needs.
</li></ul></div><div><ul><li>Ability to speak, read, and write English with proficiency
</li></ul></div>PREFERRED JOB REQUIREMENTS
Work Experience
<ul><li>Hands-on experience in GMP-regulated pharmaceutical or biopharmaceutical manufacturing.
</li></ul>Knowledge / Skills / Abilities
<div><ul><li>Strong working knowledge of GMP regulations, aseptic techniques, and biopharmaceutical manufacturing processes, with the ability to execute work in compliance with SOPs, batch records, and technical documentation.
</li></ul></div><div><ul><li>Proven ability to operate , monitor, troubleshoot, and maintain biopharmaceutical manufacturing equipment.
</li></ul></div><div><ul><li>Demonstrated attention to detail with the ability to accurately complete GMP documentation and support investigations and escalate issues.
</li></ul></div><div><ul><li>Effective communication and interpersonal skills, including the ability to guide and collaborate with others.
</li></ul></div>Medline Industries, LP, and its subsidiaries, offer a competitive total rewards package, continuing education &amp; training, and tremendous potential with a growing worldwide organization.
The anticipated salary range for this position:
$21.75 - $31.50 Hourly
The actual salary will vary based on applicant&rsquo;s location, education, experience, skills, and abilities. Medline will not pay less than the applicable minimum wage or salary threshold.
Our benefit package includes health insurance, life and disability, 401(k) contributions, paid time off, etc., for employees working 30 or more hours per week on average. For roles where employees work less than 30 hours per week, benefits include 401(k) contributions as well as access to the Employee Assistance Program, Employee Resource Groups and the Employee Service Corp.
We&rsquo;re dedicated to creating a Medline where everyone feels they belong and can grow their career. We strive to do this by seeking diversity in all forms, acting inclusively, and ensuring that people have tools and resources to perform at their best. Explore our Belonging page here .
Medline Industries, LP is an equal opportunity employer. Medline evaluates qualified individuals without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, age, disability, neurodivergence, protected veteran status, marital or family status, caregiver responsibilities, genetic information, or any other characteristic protected by applicable federal, state, or local laws.</div>

Pharmaceutical Product Operator - 1st Shift

<div>Job Summary
This job involves ensuring efficient and safe production processes while minimizing downtime. The employee will support various production and warehouse activities, including repetitive line assembly tasks to mass-produce component trays, dressings, and labels for medical products. A key responsibility is sealing pouches on final packs using specialized machinery.
Job Description
The Pharmaceutical Production Technician is responsible for executing material staging and clean-in-place (CIP)/clean-out-of-place (COP) processes in a controlled ISO-classified cleanroom, ensuring contamination control, SOP/GMP compliance, accurate batch documentation, and consistent safe preparation of cloth, film, and solution contact components. Operators serve on the front line of aseptic behavior, environmental discipline, and product integrity, supporting compliant and efficient manufacturing operations.
MAJOR RESPONSIBILITIES
Cleanroom Conduct &amp; Gowning
<ul><li>Follow all cleanroom gowning requirements and adhere to gowning and material entry‑ protocols.
</li></ul><ul><li>Follow good aseptic practices when performing all tasks within ISO-certified environments.
</li></ul>Pre-Run Preparation
<ul><li>Complete all pre-run‑ checks, including:
<ul><li>Reconciliation of materials.
</li><li>Verifying process piping cleaning requirements for the upcoming batch.
</li><li>Confirming availability of cloth rolls, film, solution, and other materials.
</li></ul></li></ul>Material Staging
<ul><li>Stage cloth rolls, film, and other packaging materials per established procedures to minimize contamination risk.
</li><li>Maintain unidirectional flow of cloth, film, totes, and packaging components to prevent cross contamination.
</li></ul><ul><li>Manage raw materials to ensure expired or incorrect lots are not used.
</li></ul>CIP/COP Processes
<ul><li>Perform all cleaning activities related to process piping and components according to established procedures.
</li><li>Execute sanitization cleaning cycles for all raw materials entering cleanroom environments.
</li></ul><ul><li>Perform sanitization steps for all tools/equipment and execute proper changeover cleaning sequences.
</li></ul>Documentation &amp; Escalation
<ul><li>Real-time, accurate, and complete documentation on all forms and records.
</li><li>Follows Good Documentation Practices
</li><li>Immediately escalate deviations to the Supervisor or Quality.
</li></ul>Cleaning &amp; Responsibilities
<ul><li>Perform cleaning activities according to established procedures.
</li></ul><ul><li>Handle scrap per established procedure and ensure dedicated scrap receptacles never leave the cleanroom.
</li></ul>Safety &amp; Ergonomics
<ul><li>Follow all EHS procedures, including chemical handling requirements.
</li><li>Use proper ergonomic techniques when lifting and moving materials.
</li></ul>MINIMUM JOB REQUIREMENTS
Education
<ul><li>High school diploma or GED required
</li></ul>Work Experience
<ul><li>Prior manufacturing experience.
</li></ul>Knowledge / Skills / Abilities
<ul><li>Must be able to lift up to 50 lbs.
</li></ul><ul><li>Must be able to bend, twist, reach, push, lift for extended periods daily.
</li><li>Comfortable working in cleanroom and controlled environments while adhering to gowning, safety, and quality requirements.
</li><li>Other duties as assigned.
</li><li>Flexibility to work mandatory overtime based on business needs.
</li><li>Ability to speak, read, and write English with proficiency
</li></ul>PREFERRED JOB REQUIREMENTS
Work Experience
<ul><li>Experience in aseptic manufacturing experience in GMP and ISO-cleanroom environments.
</li></ul>Knowledge / Skills / Abilities
<ul><li>Strong working knowledge of GMP regulations, aseptic techniques, and biopharmaceutical manufacturing processes, with the ability to execute work in compliance with SOPs, batch records, and technical documentation.
</li><li>Proven ability to operate, monitor, troubleshoot, and maintain biopharmaceutical manufacturing equipment.
</li><li>Demonstrated attention to detail with the ability to accurately complete GMP documentation and support investigations and escalate issues.
</li><li>Effective communication and interpersonal skills, including the ability to guide and collaborate with others.
</li></ul>Medline Industries, LP, and its subsidiaries, offer a competitive total rewards package, continuing education &amp; training, and tremendous potential with a growing worldwide organization.
The anticipated salary range for this position:
$20.25 - $29.25 Hourly
The actual salary will vary based on applicant&rsquo;s location, education, experience, skills, and abilities. Medline will not pay less than the applicable minimum wage or salary threshold.
Our benefit package includes health insurance, life and disability, 401(k) contributions, paid time off, etc., for employees working 30 or more hours per week on average. For roles where employees work less than 30 hours per week, benefits include 401(k) contributions as well as access to the Employee Assistance Program, Employee Resource Groups and the Employee Service Corp.
We&rsquo;re dedicated to creating a Medline where everyone feels they belong and can grow their career. We strive to do this by seeking diversity in all forms, acting inclusively, and ensuring that people have tools and resources to perform at their best. Explore our Belonging page here .
Medline Industries, LP is an equal opportunity employer. Medline evaluates qualified individuals without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, age, disability, neurodivergence, protected veteran status, marital or family status, caregiver responsibilities, genetic information, or any other characteristic protected by applicable federal, state, or local laws.</div>

Pharmaceutical Production Technician - 1st Shift

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