PSM Engineer II Position Available In Escambia, Florida

Job Description:

Bring more to life.

Are you ready to accelerate your potentialand make a real difference within life sciences, diagnostics andbiotechnology?

At Cytiva, one of 15+ operating companies, our worksaves lives-and we’re all united by a shared commitment to innovatefor tangible impact. -Working at Cytiva means being at theforefront of providing new solutions to transform human health. Ourincredible customers undertake life-saving activities ranging fromfundamental biological research to developing innovative vaccines,new medicines, and cell and gene therapies.

At Cytiva you will beable to continuously improve yourself and us – working onchallenges that truly matter with people that care for each other,our customers, and their patients. Take your next step to analtogether life-changing career.

Learn about the which makeseverything possible.

The PSM Engineer II is responsible foroptimizing manufacturing processes, managing projects, and ensuringthe efficient production of high-quality medical devices andproducts in a regulated environment. The ideal candidate will haveexperience in process engineering, project management, and a strongunderstanding of healthcare manufacturing and PSM standards.

Thisposition reports to the PSM Manager and is part of the PensacolaOperations and Safety teams located in Pensacola, FL and will be anon-site role.

What you will do: Manage cross-functional projects, ensuring that engineeringprojects are completed on time, within scope, and withinbudget. Analyze and troubleshoot manufacturing processes to identifyroot causes and implement corrective actions for continuousimprovement. Coordinate and collaborate with production teams, qualitycontrol, and other departments to ensure smooth operations. Develop and maintain process documentation, including standardoperating procedures (SOPs), process flows, and validationreports. Design, test, and implement new manufacturing processes,equipment, or systems to increase production capacity and improveprocess performance ensuring compliance with regulatoryrequirements (e.g., FDA, ISO, PSM) and contribute to audits andinspections as necessary.

Who you are: Bachelor’s degree in Engineering, Manufacturing, IndustrialEngineering, or a related field. Minimum of 3-5 years of experiencein a process engineering or project engineering role, preferably inhealthcare manufacturing or medical device production. 2+ years experience with regulatory standards and qualitysystems (e.g., FDA, ISO 13485, Good Manufacturing Practices -GMP). 2+ years experience with PSM/engineering projects with strongproject management skills in managing timelines, budgets, andresources for engineering projects. Strong analytical and problem-solving skills with the abilityto troubleshoot complex technical issues.

Travel, Motor VehicleRecord & Physical/Environment Requirements:

if applicable for role Must have a valid driver’s license with an acceptable drivingrecordIt would be a plus if you also possess previous experiencein: Translating technical jargon into clear, concise language for anon-technical audience. Working in Pharmaceuticals or Medical Device industry Experience with Veeva & Magic systemsCytiva, a Danaheroperating company, offers a broad array of comprehensive,competitive benefit programs that add value to our lives. Whetherit’s a health care program or paid time off, our programscontribute to life beyond the job. Check out our benefits at .Thesalary range range for this role is $65,000 – $95,000. This is therange that we in good faith believe is the range of possiblecompensation for this role at the time of this posting. This rangemay be modified in the future.

This job is also eligible forbonus/incentive pay.

We offer comprehensive package of benefitsincluding paid time off, medical/dental/vision insurance and 401(k)to eligible employees.

Note:

No amount of pay is considered to bewages or compensation until such amount is earned, vested, anddeterminable. The amount and availability of any bonus, commission,benefits, or any other form of compensation and benefits that areallocable to a particular employee remains in the Company’s solediscretion unless and until paid and may be modified at theCompany’s sole discretion, consistent with the law.#LI-SL21Join ourwinning team today. Together, we’ll accelerate the real-life impactof tomorrow’s science and technology. We partner with customersacross the globe to help them solve their most complex challenges,architecting solutions that bring the power of science to life.-For more information, visit . Danaher Corporation and all DanaherCompanies are committed to equal opportunity regardless of race,color, national origin, religion, sex, age, marital status,disability, veteran status, sexual orientation, gender identity, orother characteristics protected by law. We value diversity and theexistence of similarities and differences, both visible and not,found in our workforce, workplace and throughout the markets weserve. Our associates, customers and shareholders contribute uniqueand different perspectives as a result of these diverseattributes.

The EEO posters are available .We will ensure thatindividuals with disabilities are provided reasonable accommodationto participate in the job application or interview process, toperform crucial job functions, and to receive other benefits andprivileges of employment. Please contact us at to requestaccommodation.