instrumentation specialist

PM Group

<div>:
<div>
The <b>Instrumentation Startup Engineer</b> position is an exciting opportunity to join PM Group&rsquo;s quickly growing Outsourced Technical Services(OTS) team <b>at a site near Zebulon, NC</b>. Outsourced Technical Services (OTS) is an integral part of PM Group&rsquo;s ability to support clients across the complete project life cycle. We have over 50 years&rsquo; industry experience, strong technical knowledge and integrated resources. Clients look to us to provide experienced technical professionals that complement their project teams. Together we are sharing knowledge, learning, growing and continuing to be an integral part of supporting PM Group&rsquo;s ongoing expansion in the US.</div><div></div><div><br>
PM Group is seeking an experienced Instrumentation Startup Engineer to support the startup and operational readiness of a large-scale life sciences manufacturing facility. This field-based role will support commissioning, startup, troubleshooting, and turnover of instrumentation systems while working closely with engineering, automation, CQV, operations, and maintenance teams.</div><div></div><div><br>
PM Group is an employee owned, international project delivery firm with a team of 4,000+ people. We are world leaders in the pharma, food, biotech, medical technology and mission critical sectors. From our network of offices in Europe, Asia and the US, we work with the world's leading organizations. We are focused on growing a sustainable business centered on our people, our clients and trade partners.
</div>:
<ul><li>Support startup and commissioning of instrumentation systems.</li><li>
Participate in field troubleshooting and issue resolution.</li><li>
Perform system walkdowns and support punch list closure.</li><li>
Assist with loop checks and functional testing.</li><li>
Coordinate with Automation, Electrical, CQV, vendors, and Operations.</li><li>
Support operational readiness and system turnover activities.</li><li>
Assist with startup documentation and commissioning records.</li></ul>
:
<ul><li>Bachelor's degree in Engineering or related technical discipline preferred</li><li>
Experience supporting startup or commissioning activities within regulated manufacturing</li><li>
Strong troubleshooting and communication skills</li><li>
Ability to work full-time onsite</li></ul><p><b>
Preferred experience:
</b></p><ul><li>Pharmaceutical, biotechnology, or life sciences manufacturing</li><li>
Instrumentation field engineering</li><li>
Commissioning and startup support</li><li>
Smart instrumentation</li><li>
Pressure, flow, temperature, and level instrumentation</li><li>
Control valves</li><li>
Analytical instrumentation</li><li>
DeltaV or other DCS interfaces</li><li>
GMP manufacturing environments</li></ul><p>
All of your information is confidential according to EEO guidelines.</p><div><b>
Why PM Group?</b></div><div>
As an employee-owned company, we are inclusive, committed and driven. Corporate Responsibility and Sustainability are the heart of our new 2026 business strategy. Click here to read more in our <b>2025 Environmental, Social and Governance Report.</b></div><div></div><div><br>
Inclusion and Diversity are core to our culture and values. Wherever we work, we commit to a culture of mutual respect and belonging by building a truly inclusive workplace rich in diverse people, talents and ideas. Valuing the contributions of all our people and respecting individual differences will sustain our growth into the future.</div><div></div><div><br>
PM Group is committed to ensuring our hiring process is fair and accessible to all and will provide candidates with disabilities with reasonable accommodations required to participate in the recruitment process. If you require any assistance in this regard, please let us know.</div><div></div><div><b><br>
RECRUITMENT AGENCIES NEED NOT APPLY</b></div><div><b>
#LI-TF1</b></div></div>

Instrumentation Startup Engineer

MedPharm

<p></p><div><p><b>Job Purpose: </b>This position contributes to company success by providing calibration and instrumentation oversight for laboratory and facility equipment across MedPharm&rsquo;s Durham sites, including the Stirrup Creek GMP manufacturing facility and the Emperor Boulevard R&amp;D laboratories. The role executes scheduled calibrations and preventative / corrective maintenance in compliance with GMP regulations, internal procedures, and research laboratory requirements, ensuring equipment is maintained in a state of control and fitness for intended use across both regulated and non-GMP environments.</p><p></p><p><b>
Summary of Key Responsibilities:
</b></p><ul><li>Maintain and perform corrective, preventative maintenance calibrations on GMP and non-GMP equipment</li><li>
Performs maintenance, testing, troubleshooting, calibration, and repair of electrical circuits, components, analytical instruments, and pharmaceutical laboratory and manufacturing equipment</li><li>
Maintains all logs and required documentation</li><li>
Writes Out-Of-Tolerances (OOT&rsquo;s) and Deviations</li><li>
Disassembles and reassembles instruments and equipment, using hand tools, and inspects instruments and equipment for defects</li><li>
Entering and updating CMMS system information relevant to calibrations performed</li><li>
Provide recommendations for instrumentation / metrology spare parts and PM procedures</li><li>
Work closely with Validations and Stability Manager, Lab Operations, R&amp;D scientific teams (Emperor Boulevard, Manufacturing and Quality to ensure strict compliance with GMP guidelines, specifically to ensure to ensure instrumentation remains compliant and fit-for-purpose across both GMP and non-GMP operations</li><li>
Support calibration, maintenance, and troubleshooting of instrumentation across both GMP and R&amp;D environments, including bioanalytical, research biology, and in vitro testing at the Emperor Boulevard R&amp;D site</li><li>
Ensure instrumentation readiness, uptime, and compliance across two distinct operational environments: GMP-regulated manufacturing and non-GMP research laboratories</li><li>
Assist in the maintenance and review of calibration standards and vendor calibration documentation</li><li>
Work with contract service providers and support contractors executing calibration and metrology activities</li><li>
Provide support to other departments to troubleshoot, test, repair and optimize instruments, equipment and control systems</li><li>
Provide support for IQ/OQ and PQ of new systems throughout the facility</li></ul><p></p><p><b>
Required Qualifications and Skills:
</b></p><ul><li>B.S., in a scientific or engineering discipline, with 2-5 years of relevant GMP pharmaceutical experience, or an associate's degree in a relevant technical discipline with 5+ years of GMP pharmaceutical or equivalent</li><li>
Knowledge of current industry expectations of validation requirements for equipment validation and qualification</li><li>
Technical ability to problem solve and troubleshoot equipment systems in a pharmaceutical environment, including but not limited to: HPLCs, balances, pH meters, HVAC, chart recorders and stability chambers</li><li>
Flexibility to work outside of business hours, should issues arise</li><li>
Knowledge of Quality systems</li><li>
Speaks, writes, listens and presents information in a logical and articulate manner appropriate for the audience</li><li>
Able to multi-task productively, well organized, effectively applies time management processes and procedures</li><li>
Ability to recognize what needs to be done, taking action, and accomplishing results as the situation demands</li></ul><p></p><p><b>
Supervisory Responsibility:
</b></p><p>Direct Reports: None</p><p>
Indirect Reports: None</p><p></p><p><b>
Confidential Data: Yes</b></p><p><b>
Travel Requirements: </b>Limited local travel between Durham sites</p><p><b>
Work Environment</b><b>:</b> Climate controlled office and laboratory.</p><p><br>
All position requirements listed indicate the minimum level of knowledge, skills and/or experience necessary to perform the job proficiently. This position description is not to be construed as an exhaustive statement of duties, responsibilities or requirements. Employees will be required to perform any other job-related duties as requested by their supervisor, subject to reasonable accommodation.</p><p></p><p>
</p><p>hG9p34CXtP</p></div>

Metrologist

Louisiana State University

<div><div><div><div><div><div><div><div><h2 class="jobSectionHeader"><b>About Us:</b></h2></div></div></div></div></div></div></div><div><div><div><div><div><div><div><p>
At the forefront of medical discovery as it relates to understanding the causes of obesity, diabetes, cardiovascular disease, cancer and dementia, Pennington Biomedical Research Center is a campus of Louisiana State University and conducts basic, clinical and population research. The Center includes Basic Science, Clinical Research, and Population and Public Health, enabling both focused research and translational science. Research at Pennington Biomedical is supported broadly by multiple NIH Research Centers, and includes approximately 65 faculty and 20 postdoctoral fellows who comprise a network of 44 laboratories and 13 highly specialized core service facilities. Pennington Biomedical is located within state-of-the-art research facilities on a 222-acre campus in Baton Rouge, Louisiana.</p></div></div></div></div></div></div></div><p></p><h2 class="jobSectionHeader"><b>
All Job Postings will close at 12:01a.m. CST (1:01a.m. EST) on the specified Closing Date (if designated).</b></h2><p></p><h2 class="jobSectionHeader"><b>
If you close the browser or exit your application prior to submitting, the application progress will be saved as a draft. You will be able to access and complete the application through &ldquo;My Draft Applications&rdquo; located on your Candidate Home page.</b></h2><p></p><h2 class="jobSectionHeader"><b>
Job Posting Title:</b></h2>
Clinical Research Specialist 1, 2, or 3 - Mass Spectrometry<p><br>
</p><h2 class="jobSectionHeader"><b>Position Type:</b></h2>
Professional / Unclassified<p><br>
</p><h2 class="jobSectionHeader"><b>Department:</b></h2>
LSUPBRC Cores - Mass Spectonomy Stable Isotopes and Energy Expenditure (Valery Berrigan Hymel (00007182))<p><br>
</p><h2 class="jobSectionHeader"><b>Work Location:</b></h2>
LSU - Pennington Biomedical<p><br>
</p><h2 class="jobSectionHeader"><b>Pay Grade:</b></h2>
Professional<p><br>
</p><h2 class="jobSectionHeader"><b>Job Description:</b></h2><p>
Pennington Biomedical Research Center, a world-renowned academic research institute of Louisiana State University, is seeking a Clinical Research Specialist in the Stable Isotopes and Mass Spectrometry Laboratory.</p><p></p><p>
As part of a career progression group, this vacancy may be filled as a Clinical Research Specialist 1, 2, or 3 depending on the level of experience of the selected applicant.</p><p></p><p>
The Clinical Research Specialist will be responsible for operating and maintaining mass spectrometry instruments, developing and optimizing analytical methods, and preparing and processing biological samples. Key duties include data analysis, maintaining accurate records, and collaborating with interdisciplinary teams. The role also involves preparing supplies and specimens for shipping and contributing to various research projects. This position offers an exciting opportunity to work on cutting-edge research and make significant contributions to our scientific endeavors.</p><p></p><p><b><i>
Major Responsibilities</i></b></p><ul><li><p>
Operate, calibrate, and perform routine maintenance on mass spectrometry instruments and related laboratory equipment to ensure reliable operation.</p></li><li><p>
Prepare biological samples for mass spectrometry analysis by following established laboratory procedures for sample processing and quality control.</p></li><li><p>
Perform mass spectrometry analyses, review data for accuracy, and assist in interpreting and reporting research results.</p></li><li><p>
Help develop and improve laboratory methods and procedures to support research projects and ensure consistent, high-quality data.</p></li><li><p>
Maintain accurate laboratory records, including experimental procedures, instrument maintenance, and research data.</p></li><li><p>
Assist with the preparation of scientific reports, manuscripts, presentations, and grant materials.</p></li><li><p>
Prepare laboratory supplies, biological specimens, and research materials for shipping in accordance with laboratory and institutional procedures.</p></li><li><p>
Collaborate with investigators and research staff by providing technical support for studies involving stable isotopes and mass spectrometry.</p></li><li><p>
Maintain laboratory inventory, order supplies, and help ensure the laboratory remains organized, clean, and compliant with safety requirements.</p></li><li><p>
Perform other related duties as assigned in support of the laboratory's research programs.</p></li></ul><p></p><p><b><i>
Required Qualifications
</i></b></p><p><b><i>Clincial Research Specialist 1 - </i></b>Entry level with basic duties and responsibilities.</p><ul><li><p>
Bachelor&rsquo;s degree in Biology, Chemistry, Biochemistry, Biomedical Sciences, or a related scientific field.</p></li><li><p>
Exposure to laboratory research through academic coursework, laboratory classes, undergraduate research, or internships is preferred.</p></li><li><p>
Demonstrated proficiency in laboratory research methods, procedures, and analytical techniques.</p></li><li><p>
Ability to operate, maintain, and troubleshoot laboratory equipment while following established protocols.</p></li><li><p>
Ability to collaborate effectively with researchers, laboratory personnel, and interdisciplinary teams.</p></li><li><p>
Ability to organize, prioritize, and manage multiple research projects, experiments, and deadlines.</p></li><li><p>
Ability to learn new laboratory techniques, instrumentation, and research methodologies.</p></li></ul><p></p><p><b><i>
Clincial Research Specialist</i></b><b><i> </i></b><b>2</b> - Differs from Clinical Research Specialist 1 by working more independently and taking on greater responsibility.</p><ul><li><p>
Bachelor&rsquo;s degree in Biology, Chemistry, Biochemistry, Biomedical Sciences, or a related scientific field.</p></li><li><p>
Minimum of two (2) years of laboratory research experience in an academic, clinical, or relevant setting.</p></li><li><p>
Experience with biological sample preparation, laboratory instrumentation, data collection, and maintaining accurate research records.</p></li><li><p>
Ability to accurately collect, analyze, and maintain research data and laboratory records.</p></li><li><p>
Knowledge of quality control practices and the ability to ensure accuracy and reproducibility of laboratory results.</p></li></ul><p></p><p><b><i>
Clincial Research Specialist</i></b><b><i> 3 - </i></b>Differs from Clinical Research Specialist 2 by the presence of mentoring junior staff and contributing to protocol development.</p><ul><li><p>
Bachelor's degree in Biology, Chemistry, Biochemistry, Biomedical Sciences, or a related scientific field.</p></li><li><p>
Minimum of four (4) years of progressively responsible laboratory research experience.</p></li><li><p>
Demonstrated experience operating and maintaining laboratory instrumentation, analyzing research data, implementing laboratory procedures, and supporting multiple research projects.</p></li><li><p>
Experience training or mentoring laboratory personnel and assisting with laboratory operations is preferred.</p></li></ul><p></p><p><i>
Pennington Biomedical Research Center seeks to recruit a highly productive workforce with a broad range of backgrounds and perspectives and will provide equal employment opportunities to all employees and prospective employees. Employment decisions shall be based strictly on merit and without regard to religious or political beliefs, sex, race, or any other non-merit factor.</i></p><p><br>
</p><h2 class="jobSectionHeader"><b>Additional Job Description:</b></h2><p></p><h2 class="jobSectionHeader"><b>
Competencies:</b></h2>
None<p></p><h2 class="jobSectionHeader"><b>
Special Instructions:</b></h2>
Interested candidates should include a resume and a list of three (3) professional references to the online application. Professional references should be the name, title, company, and contact information from past employers. Professional references should include current or previous supervisors and/or coworkers. Personal references should not be considered for the reference check process. We will respect the request that we not contact a current employer. However, we will need to contact a prior supervisor if such a request is made.<br>
<br>
A letter of application/cover letter is recommended but not required. Official transcripts are required prior to hire and are not required at the time of application.<p><br>
</p><h2 class="jobSectionHeader"><b>Posting Date:</b></h2>
July 29, 2026<p><br>
</p><h2 class="jobSectionHeader"><b>Closing Date (Open Until Filled if No Date Specified):</b></h2>
August 12, 2026<p><br>
</p><h2 class="jobSectionHeader"><b>Additional Position Information:</b></h2><p>
Pennington Biomedical is located within state-of-the-art research facilities on a 222-acre campus in Baton Rouge, Louisiana. For more information, visit PBRC.</p><p>
Questions regarding career opportunities at Pennington Biomedical should be sent to hrm@pbrc.edu.</p><p><b>
Background Check - </b>An offer of employment is contingent on a satisfactory pre-employment background check.</p><div><div><div><div><div><div><div><p><b>
Benefits -</b> Pennington Biomedical Research Center offers outstanding benefits to eligible employees and their dependents including health, life, dental, and vision insurance; flexible spending accounts; retirement options; various leave options; paid holidays; wellness benefits; tuition exemption for qualified positions; training and development opportunities; employee discounts; and more!</p></div></div></div></div></div></div></div><div><div><div><div><div><div><div><p><br>
</p></div></div></div></div></div></div></div><div><div><div><div><div><div><div><p>Positions approved to work outside the State of Louisiana shall be employed through Louisiana State University&rsquo;s partner, nextSource Workforce Solutions, for Employer of Record Services including but not limited to employment, benefits, payroll, and tax compliance. Positions employed through Employer of Record Services will be offered benefits and retirement as applicable through their provider and will not be eligible for State of Louisiana benefits and retirement.</p></div></div></div></div></div></div></div><p><br>
</p><h2 class="jobSectionHeader"><b>Essential Position (Y/N):</b></h2><p><br>
</p><h2 class="jobSectionHeader"><b>Pennington Biomedical Research Center/LSU is an Equal Opportunity Employer.</b></h2><p><br>
</p><h2 class="jobSectionHeader"><b>Contact Information:</b></h2><p>
Questions or concerns can be directed to PBRC Human Resources at 225-763-2776 or hrm@pbrc.edu.</p></div>

Clinical Research Specialist 1, 2, or 3 - Mass Spectrometry

MENA HR Solutions LLC (IBD Group)

<div>
 <strong>
  Instrumentation &amp; Control (I&amp;C) Technician
  <br/>
  <br/>
 </strong>
 <strong>
  Location: Sur, Oman
  <br/>
  <br/>
  Industry: Power Generation
  <br/>
  <br/>
  Full-Time Position
  <br/>
  <br/>
 </strong>
 We are looking for an experienced Instrumentation &amp; Control (I&amp;C) Technician to join a leading power generation facility in Oman. The successful candidate will be responsible for maintaining, troubleshooting, calibrating, and optimizing instrumentation, control systems, PLCs, and DCS equipment to ensure safe, reliable, and efficient plant operations.
 <br/>
 <br/>
 <strong>
  Key Responsibilities
  <br/>
  <br/>
 </strong>
 Perform preventive and corrective maintenance on I&amp;C and DCS systems
 <br/>
 <br/>
 Troubleshoot instrumentation, PLC, and control system issues
 <br/>
 <br/>
 Support planned shutdowns and major maintenance activities
 <br/>
 <br/>
 Conduct calibration and testing of plant instrumentation
 <br/>
 <br/>
 Assist in maintaining maximum plant availability and reliability
 <br/>
 <br/>
 Ensure compliance with Health, Safety, Environmental, and Quality standards
 <br/>
 <br/>
 Maintain accurate maintenance records through CMMS
 <br/>
 <br/>
 Coordinate with operations and maintenance teams to resolve equipment issues
 <br/>
 <br/>
 <strong>
  Requirements
  <br/>
  <br/>
 </strong>
 Diploma in Instrumentation &amp; Control Engineering or related discipline
 <br/>
 <br/>
 Experience in power plants, preferably CCGT and Gas Turbine facilities
 <br/>
 <br/>
 Strong knowledge of DCS, PLC programming, instrumentation, and calibration
 <br/>
 <br/>
 Experience with computerized maintenance management systems (CMMS)
 <br/>
 <br/>
 Good troubleshooting, reporting, and communication skills
 <br/>
 <br/>
 Middle East experience is an advantage
 <br/>
 <br/>
 <strong>
  What We're Looking For
  <br/>
  <br/>
 </strong>
 Strong technical and problem-solving abilities
 <br/>
 <br/>
 Safety-conscious mindset
 <br/>
 <br/>
 Ability to work under pressure and during emergency situations
 <br/>
 <br/>
 Team player with excellent interpersonal skills
 <br/>
 <br/>
 Ability to work in a multicultural environment
</div>


Instrumentation and Control Technician

Autocontrol Process Instrumentation FZC

<p><i><b>Job Responsibilities</b></i></p><ul><li>Plan, execute, and manage instrumentation and control projects from start to finish.</li><li>Select and specify sensors, transmitters, controllers, and other automation devices.</li><li>Coordinate procurement, vendor communication, and technical evaluations.</li><li>Oversee installation, calibration, and commissioning of instruments.</li><li>Troubleshoot instrumentation issues and optimize system performance.</li><li>Prepare project schedules, reports, and technical documentation.</li><li>Ensure compliance with industry standards (ISA, IEC, ISO, ATEX, IECEx) and safety regulations.</li></ul><p><i><b>Requirements</b></i></p><ul><li>Background in Instrumentation / Mechanical / Electrical / Electronics Engineering.</li><li>Minimum 4 years of experience in process instrumentation or automation.</li><li>Strong knowledge of instrumentation, control systems, and project coordination.</li></ul><p>Apply Now</p><p>Send your CV to:</p><p>devika@autocontrolpi.com</p><p>Application Question(s):</p><ul><li>What is your notice period?</li><li>What is your current visa status?</li><li>What is your current monthly salary?</li></ul><p>Work Location: In person</p>

Project Engineer

PepsiCo

<div>
 <strong>
  Overview
  <br/>
  <br/>
 </strong>
 Responsible for regular maintenance &amp; trouble shooting of electrical &amp; instrumentation equipment and preventive maintenance of all types of electrical &amp; instrumentation equipment mainly for process and packaging equipment
 <br/>
 <br/>
 <strong>
  Responsibilities
  <br/>
  <br/>
 </strong>
 The required candidate would be responsible for maintenance &amp; troubleshooting of electrical &amp; instrumentation equipments, including, LT &amp; HT switchgear, Field panels, motors, PLCs, VFDs, MCC, panels and process instruments.
 <br/>
 <br/>
 <ul>
  <li>
   During annual maintenance or breakdowns, candidate would be responsible for troubleshooting and maintenance of all associated electrical &amp; instrumentation parts &amp; equipment&rsquo;s installed on the process and utilities equipment. And to coordinate with internal external stake holders where required for seamless execution.
  </li>
  <li>
   The candidate should be fully versed &amp; knowledgeable about all type of maintenance, having good trouble shooting techniques to minimize MTTR &amp; must be familiar with SAP / CMMS.
  </li>
  <li>
   He would also be responsible for developing/implementing the SOPs for the electrical &amp; instrumentation equipment&rsquo;s.
  </li>
  <li>
   Computer knowledge is essential.
  </li>
  <li>
   Flexibility and endurance in a challenging environment are the key for this job.
  </li>
  <li>
   To ensure maximum MTBF and minimum MTTR for process breakdowns.
  </li>
  <li>
   Ensure compliance of HSE rules and procedure as per PepsiCo safety policy
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Qualifications
  <br/>
  <br/>
 </strong>
 DAE Electrical with 5-7 years of experience OR B.Tech Electrical with 3-4 years of experience
</div>


Artisan E&I

Stryker

<div>
 <strong>
  Overview
  <br/>
  <br/>
 </strong>
 As a Clinical Specialist at Stryker, you will help improve orthopedic surgeries around the world and play a direct role in our mission of making healthcare better. In this role, you will build deep clinical and technical expertise across both robotic (Mako SmartRobotics&trade;) and manual orthopedic procedures. You will support surgeons in the operating room by assisting with pre-operative planning, case preparation, system setup, and real-time procedural workflows to ensure safe, accurate, and efficient outcomes.
 <br/>
 <br/>
 You will gain hands-on experience working with Mako technology&mdash;including CT-based planning, implant sizing, registration, and intra-operative support&mdash;while also developing strong competency in manual procedures, instrumentation, and OR protocols. Through shadowing experienced team members, supporting product demonstrations, and participating in labs and education programs, you will learn the systems, processes, and best practices that define world-class clinical support.
 <br/>
 <br/>
 This role requires adaptability, steady composure, and strong problem-solving in a fast-paced surgical environment. Because patients&rsquo; needs don&rsquo;t follow business hours, you will also participate in on-call coverage, including evenings, weekends, and holidays, to ensure uninterrupted support for urgent cases and time-sensitive customer needs.
 <br/>
 <br/>
 <strong>
  What You Will Do
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Gain competency in solo case coverage for manual and robotic procedures through hands-on training.
  </li>
  <li>
   Assist surgeons with pre-operative CT-based planning, implant sizing, and positioning using advanced software.
  </li>
  <li>
   Support full case preparation, including instrumentation checks, equipment setup, and OR readiness.
  </li>
  <li>
   Troubleshoot technical issues confidently and efficiently in the operating room.
  </li>
  <li>
   Learn and support workflow for daily account coordination, including inventory management and logistics.
  </li>
  <li>
   Shadow experienced teammates to understand territory dynamics and surgeon preferences.
  </li>
  <li>
   Participate in product demonstrations, cadaver labs, education programs, and customer training events.
  </li>
  <li>
   Build and maintain strong, trust-based relationships with surgeons, OR staff, and cross-functional partners.
  </li>
  <li>
   Manage administrative tasks related to accounts, system updates, and case documentation.
  </li>
  <li>
   Collaborate with sales partners to ensure seamless execution and a unified customer experience.
  </li>
  <li>
   Complete required trainings, competencies, and certifications.
  </li>
  <li>
   Provide on-call coverage during evenings, weekends, and holidays.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  What You Need
  <br/>
  <br/>
 </strong>
 Minimum Required:
 <br/>
 <br/>
 <ul>
  <li>
   Bachelor&rsquo;s degree
   <br/>
   <br/>
  </li>
 </ul>
 OR
 <br/>
 <br/>
 <ul>
  <li>
   Associate degree with 4 years of professional and/or related experience
   <br/>
   <br/>
  </li>
 </ul>
 OR
 <br/>
 <br/>
 <ul>
  <li>
   High school diploma with 6 years of professional and/or related experience
   <br/>
   <br/>
  </li>
 </ul>
 Preferred:
 <br/>
 <br/>
 <ul>
  <li>
   1 year of relevant work experience.
  </li>
  <li>
   Previous clinical experience (nursing, physical therapy, surgical technology, athletic training, personal training, medical scribing, etc.).
  </li>
  <li>
   Extracurricular involvement such as community service, leadership organizations, or athletic teams.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Additional Information
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   This position requires the handling of instruments that may have been contaminated by blood or bodily fluids. In compliance with Occupational Safety and Health Administration (OSHA) regulations, Stryker will provide a safe working environment for all employees.
  </li>
  <li>
   Ability to lift, push, pull, and carry up to 50 lbs.
  </li>
  <li>
   Ability to stand for extended periods.
  </li>
  <li>
   Ability to manage stressful OR situations with professionalism and focus
  </li>
  <li>
   Exerting up to 50 lbs of force occasionally and/or up to 20 lbs of force constantly to move objects.
  </li>
  <li>
   Must have a valid driver&rsquo;s license.
  </li>
  <li>
   Fluency in written and spoken English required.
   <br/>
   <br/>
  </li>
 </ul>
 $59,900 - $83,300 USD Annual
 <br/>
 <br/>
 Health benefits include: Medical and prescription drug insurance, dental insurance, vision insurance, critical illness insurance, accident insurance, hospital indemnity insurance, personalized healthcare support, wellbeing program and tobacco cessation program. Financial benefits include: Health Savings Account (HSA), Flexible Spending Accounts (FSAs), 401(k) plan, Employee Stock Purchase Plan (ESPP), basic life and AD&amp;D insurance, and short-term disability insurance. Stryker offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually. Depending on customer requirements employees and new hires in sales and field roles that require access to customer accounts as a function of the job may be required to obtain various vaccinations as an essential function of their role.
</div>


Clinical Specialist, Joint Replacement - Harrisburg, Pennsylvania

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