SurModics is a leading provider of surface modification technologies for the healthcare industry. With a history dating back to 1979, the company has been at the forefront of developing innovative solutions to enhance medical devices and improve patient outcomes. SurModics' cutting-edge technologies are used in a wide range of applications, from drug delivery systems to diagnostic assays, making a significant impact in the field of healthcare.

surmodics

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Ready to make a difference by utilizing your talents? Join a team driven by a mission to help patients, and a culture focused on developing medical device and diagnostic solutions.
Surmodics is pursuing highly differentiated medical devices that are designed to address unmet clinical needs and engineered to the most demanding requirements. This key growth strategy leverages the combination of the Company’s expertise in proprietary surface technologies, along with enhanced device design, development and manufacturing capabilities. The Company mission remains to improve the detection and treatment of disease.
Job Summary The Quality Associate 2 is responsible for quality assurance activities to support operations and product release, as well as contributing to the maintenance and improvement of the overall quality system to ensure compliance with Quality System Regulations (QSR), ISO and other applicable requirements.
Responsibilities&nbsp; Quality Assurance Support (20 - 50%) • &nbsp; &nbsp;Lead/participate in CAPAs/Nonconformances • &nbsp; &nbsp;Support Supplier Quality activities • &nbsp; &nbsp;Assist Quality Engineering in assigned tasks to support product and manufacturing operations • &nbsp; &nbsp;Support release of intermediates and final product for internal and external distribution • &nbsp; &nbsp;Assist in completion of customer-requested documentation (i.e. customer quality system surveys)&nbsp; • &nbsp; &nbsp;Participate in improvement and efficiency projects within Quality and cross-functionally&nbsp; • &nbsp; &nbsp;Oversee material/product retain management program
Quality Systems Support (50 - 80%) • &nbsp; &nbsp;Ensure quality procedures, processes and systems are standardized throughout the business and implemented consistently and correctly to ensure compliance to internal requirements and external regulations • &nbsp; &nbsp;Write and revise documents to ensure compliance to internal requirements and external regulations&nbsp; • &nbsp; &nbsp;Support internal audits of quality system processes, manufacturing areas and documentation, as assigned • &nbsp; &nbsp;Support Quality leadership in managing external audits (customer and Regulatory) • &nbsp; &nbsp;Develop and present training material for new or changing processes, as required, to ensure compliance to procedures/regulations • &nbsp; &nbsp;Serve as Quality Event (Nonconformances, CAPA, Complaint) Coordinator to assist in the completion and review of investigations/records for content, accuracy and completeness • &nbsp; &nbsp;Assist in developing and maintaining quality system metrics • &nbsp; &nbsp;Provide insight for statistical trends using quality system data and the creation of system solutions for quality system issues • &nbsp; &nbsp;Ensure all quality system documentation and record keeping activities are carried out and completed in compliance with established procedures and work instructions • &nbsp; &nbsp;Perform Document Administration activities within the eQMS software • &nbsp; &nbsp;Coordinate and archive quality records • &nbsp; &nbsp;Participate in improvement and efficiency projects within Quality and cross-functionally&nbsp;
Minimum Qualifications • &nbsp; &nbsp;Four-year technical degree with minimum two years of experience in medical device industry or minimum ten years of experience in Quality-related field in medical device industry • &nbsp; &nbsp;Proficient computer skills- Microsoft Word, Access and Excel • &nbsp; &nbsp;Excellent problem solving skills • &nbsp; &nbsp;Ability to read and follow detailed instructions • &nbsp; &nbsp;Ability to generate detailed instructions • &nbsp; &nbsp;Excellent written and verbal communication skills • &nbsp; &nbsp;Excellent interpersonal skills • &nbsp; &nbsp;Ability to prioritize activities relative to competing demands from multiple sources
Surmodics determines base pay by evaluating market data, internal equity, skills, abilities and level of experiences for each unique, potential employee.&nbsp;&nbsp;
Surmodics offers a competitive compensation and benefits package, including a bonus program, 401(k) with employer match, tuition reimbursement and student debt repayment program.
Surmodics is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.
&nbsp;<div class="content-pay-transparency"><div class="pay-input"><div class="title">Targeted Salary Range</div><div class="pay-range">$63,760&mdash;$95,698 USD</div></div></div>

Quality Associate 2

Ready to make a difference by utilizing your talents? Join a team driven by a mission to help patients, and a culture focused on developing medical device and diagnostic solutions.
Surmodics is pursuing highly differentiated medical devices that are designed to address unmet clinical needs and engineered to the most demanding requirements. This key growth strategy leverages the combination of the Company’s expertise in proprietary surface technologies, along with enhanced device design, development and manufacturing capabilities. The Company mission remains to improve the detection and treatment of disease.
Job Summary An individual in this role would be expected to manufacture products in accordance with supplied Standard Operating Procedures, adhering to Good Manufacturing Practices, in a clean, controlled environment. Maintaining accurate raw material inventories and adhering to the Quality Policy.
Responsibilities&nbsp; Production Chemistry (70%) • &nbsp; &nbsp;Manufacture product per SOP as directed by the production planner • &nbsp; &nbsp;Prepare and submit samples to the appropriate QC department • &nbsp; &nbsp;Ensure adherence to GMP guidelines for IVD manufacturing
Support Manufacturing (15%) • &nbsp; &nbsp;Transfer and issue consumed raw materials to batches via the MRP system • &nbsp; &nbsp;Maintain thorough, up-to-date production &amp; accounting forms&nbsp; • &nbsp; &nbsp;Review completed batch records for GMP/GDP compliance • &nbsp; &nbsp;Monitor inventory of raw materials
Efficient &amp; Organized Environment (15%) • &nbsp; &nbsp;Monitor inventory of general laboratory supplies • &nbsp; &nbsp;Maintains laboratory equipment and document maintenance activities • &nbsp; &nbsp;Oversee the routine housekeeping of the production area, cleaning process equipment, etc... • &nbsp; &nbsp;Keeping equipment on a preventative maintenance schedule
Minimum Qualifications • &nbsp; &nbsp;Bachelor’s degree in a laboratory technology field (i.e. Chemistry, Biology) or 2+ years of production experience as a high level Chemical Operator/Technician (or equivalent) • &nbsp; &nbsp;Organizational and documentation skills and basic problem solving ability • &nbsp; &nbsp;Good interpersonal skills and an ability to take work direction • &nbsp; &nbsp;Good written and verbal communication skills • &nbsp; &nbsp;Computer skills appropriate for work responsibilities
Surmodics determines base pay by evaluating market data, internal equity, skills, abilities and level of experiences for each unique, potential employee. &nbsp;
Surmodics offers a competitive compensation and benefits package, including a bonus program, 401(k) with employer match, tuition reimbursement and student debt repayment program.
Surmodics is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.<div class="content-pay-transparency"><div class="pay-input"><div class="title">Targeted Salary Range</div><div class="pay-range">$42,779&mdash;$59,914 USD</div></div></div>

Operator 1

Surmodics Services and Technologies, Inc. (SurmodicsST) is dedicated to delivering industry-leading expertise in the development, manufacturing, and application of coatings for medical devices. We are seeking a Human Resources Generalist to join our team!
The Human Resources Generalist develops and implements HR programs and initiatives that support business objectives, talent development, and employee engagement. This role partners with leaders and employees across the US, with a focus on leading recruitment efforts and serving as the primary HR site contact for the Horsham, PA office. The position balances strategic HR partnership with hands-on execution across talent acquisition, employee relations, performance management, and HR compliance.
<h3 style="text-align: left;">Key Responsibilities</h3>
Talent Acquisition &amp; Operational HR Services (60%) • &nbsp; &nbsp;Lead US recruitment efforts across the organization, partnering with hiring managers to define staffing needs, develop recruitment strategies, establish hiring priorities, and deliver effective hiring outcomes. • &nbsp; &nbsp;Manage the full-cycle recruitment process, including job postings, candidate sourcing, screening, interview coordination, candidate assessment, offer management, and onboarding partnership. • &nbsp; &nbsp;Build and maintain effective relationships with external recruiters, staffing partners, universities, and other talent sources to strengthen recruitment pipelines and support business growth. • &nbsp; &nbsp;Monitor recruitment metrics and prepare hiring activity reports to evaluate recruiting effectiveness, identify trends, and recommend process improvements. • &nbsp; &nbsp;Develop, launch, and manage a company-wide US internship program, including program design, stakeholder engagement, intern recruitment, university partnerships, onboarding, and ongoing program evaluation. • &nbsp; &nbsp;Partner with business leaders to identify meaningful internship opportunities, establish program objectives, and create a positive, development-focused experience for interns and participating teams. • &nbsp; &nbsp;Provide guidance and support to managers and employees on employee relations matters, performance concerns, workplace policies, and appropriate resolution strategies. • &nbsp; &nbsp;Lead or coordinate thorough, objective, and confidential employee investigations, documenting findings and recommending appropriate actions in partnership with relevant stakeholders. • &nbsp; &nbsp;Provide guidance, training, and interpretation of HR policies, procedures, and practices to promote consistency and effective application across the organization. • &nbsp; &nbsp;Serve as the primary HR site contact for the Horsham, PA office, supporting local employee needs, coordinating site-related HR activities, facilitating employee engagement initiatives, and promoting a positive and connected workplace experience. • &nbsp; &nbsp;Support site communications, employee events, office-related initiatives, and coordination with internal stakeholders to ensure the Horsham office remains aligned with broader organizational priorities.
Strategic HR Services (25%) • &nbsp; &nbsp;Partner with business leaders and functional stakeholders to develop and implement HR strategies and initiatives that support organizational priorities, strengthen company culture, and enhance employee engagement. • &nbsp; &nbsp;Facilitate organizational planning processes, including workforce planning, organizational structure assessments, and identification of talent needs and capability gaps. • &nbsp; &nbsp;Support talent management initiatives, including performance management, leadership development, succession planning, and employee development. • &nbsp; &nbsp;Contribute to the development and implementation of compensation strategies and programs that support business objectives and promote internal equity and external competitiveness. • &nbsp; &nbsp;Identify opportunities to improve HR processes, programs, and practices to enhance organizational effectiveness and the overall employee experience.
HR Administration and Compliance (15%) • &nbsp; &nbsp;Maintain current knowledge of applicable federal, state, and local employment laws and regulations and support compliance across the US. • &nbsp; &nbsp;Partner with Legal and other relevant stakeholders on employment-related matters, policy interpretation, investigations, and risk mitigation as needed. • &nbsp; &nbsp;Maintain accurate employee records, HR documentation, and HR information systems in accordance with company policies and applicable legal requirements. • &nbsp; &nbsp;Support the development, communication, implementation, and ongoing review of HR policies, procedures, and programs. • &nbsp; &nbsp;Maintain appropriate confidentiality and ensure the accurate handling of sensitive employee and organizational information. • &nbsp; &nbsp;Support HR reporting, documentation, and administrative processes to promote operational efficiency and data integrity.
<h3 style="text-align: left;">Qualifications</h3>
• &nbsp; &nbsp;3+ years of progressive HR experience, including experience supporting multiple business functions and managing a range of HR activities. • &nbsp; &nbsp;Bachelor’s degree in human resources, business administration, or a related field. • &nbsp; &nbsp;Demonstrated experience in recruitment and talent acquisition, including partnering with hiring managers and managing multiple open positions. • &nbsp; &nbsp;Experience developing, coordinating, or managing HR programs and initiatives; experience establishing an internship or early-career talent program is preferred. • &nbsp; &nbsp;Strong understanding of HR practices, employee relations, performance management, and applicable employment laws and regulations. • &nbsp; &nbsp;Excellent critical-thinking, analytical, problem-solving, and decision-making skills, with the ability to assess situations and recommend practical solutions. • &nbsp; &nbsp;Strong written, verbal, interpersonal, and relationship-building skills, with the ability to communicate effectively across all levels of an organization. • &nbsp; &nbsp;Demonstrated ability to manage competing priorities, independently develop project plans, and drive initiatives through successful execution. • &nbsp; &nbsp;Proficiency with Microsoft Office applications, including Excel, Word, and PowerPoint, and the ability to work effectively with HR information systems and recruiting technology. • &nbsp; &nbsp;Ability to handle confidential and sensitive matters with discretion, professionalism, and sound judgment. • &nbsp; &nbsp;A proactive, collaborative, and service-oriented approach, with the ability to build credibility and influence stakeholders across the organization.
SurmodicsST is an is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, gender, gender identity, sexual orientation, age, status as a protected veteran, status as a qualified individual with disability, or any other protected characteristic under law. SurmodicsST Human Resources leads recruitment and employment for SurmodicsST. Unsolicited resumes sent to SurmodicsST from recruiters do not constitute any type of relationship between the recruiter and SurmodicsST and do not obligate SurmodicsST to pay fees should we hire from those resumes. We ask those external recruiters and/or agencies not to contact or present candidates directly to our hiring managers or employees.
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HR Generalist

Surmodics is pursuing highly differentiated medical devices that are designed to address unmet clinical needs and engineered to the most demanding requirements. This key growth strategy leverages the combination of the Company’s expertise in proprietary surface technologies, along with enhanced device design, development and manufacturing capabilities. The Company mission remains to improve the detection and treatment of disease.
<h1>Job Summary</h1>
This position supports medical device coating services for Surmodics customers.&nbsp; The technician position will be responsible for the handling of medical devices and the coating of medical devices with Surmodics proprietary polymers.
Responsibilities
Manufacturing (% Varies) 
<ul>
<li style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Prepare and inspect materials for coating operations</li>
<li style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Perform Dip Coating operations and verification activities</li>
<li style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Perform Curing operations and verification activities</li>
</ul>
&nbsp;Manufacturing Support (% Varies)
<ul>
<li style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Measure dimensions of material to verify conformance to specifications</li>
<li style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Visually inspection materials to ensure quality of raw and finished medical device products</li>
<li style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Read procedures to determine product specifications or material requirements</li>
<li style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Record operational or production data in accordance with Good Documentation Practices to ensure quality</li>
<li style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Label or mark production or equipment with identifying information</li>
<li style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Train technicians on certified operations</li>
<li style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Reconciliation of batch records</li>
</ul>
Business Strategy (% Varies)&nbsp;
<ul>
<li style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Assist coating engineers with feasibility activities</li>
<li style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Review procedures and provide feedback on feasibility to be performed until commercial release requirements</li>
</ul>
<h1>Minimum Qualifications</h1>
<ul>
<li style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">High School Diploma or equivalent</li>
<li style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">2+ years Medical Device manufacturing experience</li>
<li style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Good Documentation Practices experience</li>
<li style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Research and Development production experience</li>
<li style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Intermediate computer skills</li>
<li style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Strong written and verbal communication skills</li>
<li style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Strong attention to detail</li>
<li style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Good interpersonal skills</li>
<li style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Ability to read and interpret documents</li>
</ul>
Surmodics determines base pay by evaluating market data, internal equity, skills, abilities and level of experiences for each unique, potential employee.&nbsp;&nbsp;
Surmodics offers a competitive compensation and benefits package, including a bonus program, 401(k) with employer match, tuition reimbursement and student debt repayment program.
Surmodics is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.<div class="content-pay-transparency"><div class="pay-input"><div class="title">Targeted Salary Range</div><div class="pay-range">$42,779&mdash;$59,914 USD</div></div></div>

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