Process Engineer 1
SHL Medical · Deerfield Beach, FL
- Level
- Engineer
- Team
- Process
- Experience asked
- 2+ years
- Industry
- Industrial
- Posted
- Recently
The role in 30 seconds
An engineer-level process role at SHL Medical (industrial) in Deerfield Beach, FL. In Biomedical Engineering/Mechanical Engineering or any relevant branch of study is preferred.
- They ask for
- 2+ years
- Tools it names
- Lean, Root cause, FMEA, CAPA, FDA / GMP, Validation (IQ/OQ/PQ)
Read from the posting. The full description is below.
From the plant jobs report · week of October 19, 2026
Process Engineer roles in Florida: typical posted base $60k–$123k.
Median of the low and high ends of 3 live postings that list pay, out of 14 process engineer openings in Florida, read from manufacturers' own careers sites.
Florida plant jobs report →Pay by team and state →What moves pay →
How this role compares
Against 13 other live process postings in Florida.
- Experience asked
- Less than usual (2+ vs 5+)
Similar roles usually ask 5+ years.
Skills these teams ask for most
- ✓ Lean 50%
- ✓ Root cause 50%
- ✓ New product launch 43%
- Tooling 43%
- Six Sigma 36%
- ✓ Validation (IQ/OQ/PQ) 29%
✓ = this posting asks for it too. % = share of similar postings that mention it.
Stands out: this posting asks for CAPA, Assembly lines, which few similar roles mention. If you have it, lead with it.
At a glance
Pulled from the posting text. If it's not listed here, the posting didn't say.
How to get in at this plant
Five moves over a week or two. The first one takes ten minutes.
- 1
Pick 2–3 people on the Process team at SHL Medical
Engineers who joined in the last year or two reply the most. Use the team search on this page to find them.
- 2
Send a short, curious note
One real question about their work. No favors yet. Each person gets a different note, written for this role.
- 3
Turn a reply into a short call
Questions worth asking about this team:
- What does a normal week look like on your team?
- Is the work mostly new product launches or sustaining existing lines?
- How much time do you spend on the floor versus at a desk?
- How did you land the job? What stood out in your interviews?
- 4
Apply with someone vouching for you
If the call went well, ask whether they’d pass your résumé to the hiring manager. Send your résumé link, apply that day, and let them know.
- 5
Bring proof to the interview
One page of before-and-after numbers from projects you led: scrap, OEE, cycle time, cost. Plant managers hire on results.
Full description from SHL MedicalAs posted on their careers site.ShowHide
Responsibilities
- ◆Support design transfer, specifically the final assembly, labeling, packaging, and serialization of products as they hand‑off from development to commercial launch.
- ◆Support the design, qualification, and implementation of new production equipment.
- ◆Draft and update Engineering Protocols (ENP) and Reports (ENR), Batch Records (BR), Bill of Materials (BOM), Technical Specifications (TS), Product Specifications (PS), Quality Work Instructions (QWI), Quality Operating Procedures (QOP), Quality Forms (QF), Templates (TEM), equipment design and qualification documentation (e.g., URS), pFMEAs, Change Controls, etc.
- ◆Draft documentation for computerized system validation (CSV) including Functional/Design Specifications, Design Qualification (DQ), Functional Risk Assessment (FRA),
Requirements
Traceability Matrix (RTM), etc.
- ✓Draft and execute Validation Project Plans (VPP), Validation Final Reports (VFR), and periodic reviews, as well as protocols and reports for Factory Acceptance Testing (FAT), Site Acceptance Testing (SAT), commissioning, Installation Operational Qualification (IOQ), Performance Qualification (PQ), and Process Validation (PV).
- ✓Document MS activities to support the MS Key Performance Indicators (KPI) tracking.
- ✓Perform troubleshooting and root cause analysis with a cross‑functional team to conduct investigations, Non‑conformance Reports (NCR), Corrective and Preventive Actions (CAPA), etc.
- ✓Serve as the second line of support after Manufacturing Engineering (ME) to Manufacturing (MFG).
- ✓Provide training on production equipment to ME and MFG personnel.
- ✓Identify opportunities for continuous improvement in MS and support the execution and implementation of LEAN projects.
- ✓Support and conduct customer complaint investigations.
- ✓Support or lead machine shop activities.
- ✓Comply with all quality, safety, and industry regulations.
Requirements
- ✓While performing the duties of this job, the employee is regularly required to use hands to handle or feel objects, tools, or controls; reach with hands and arms; stoop, kneel, or crouch.
- ✓Specific vision abilities required by this job include close vision, and the ability to adjust focus.
Show full description ↓Show less ↑
Process Engineer 1
Process Engineers are responsible for supporting the implementation of new process systems into manufacturing production while ensuring that all activities are completed and documented by SHL Pharma Quality System requirements. Serving as the voice of operations between the development site and manufacturing site, the Process Engineer will be responsible for supporting the design, development, testing, and evaluation of assembly, labeling, packaging, and serialization operations.
Execute Manufacturing Sciences (MS) Project activities under the guidance of MS Senior Process Engineers/MS Principal Process Engineers and MS Manager.
Job Overview
SHL Medical is the world‑leading solution provider in the design, development, and manufacturing of advanced drug delivery systems with more than 5000 employees worldwide. Our customers include top pharmaceutical and biotech companies from around the globe that require innovative devices such as auto‑injectors or pen injectors to effectively deliver their drugs. Headquartered in Switzerland since late 2018, with sites in Sweden, Taiwan, and the United States.
Main
Skills And Qualification
- •B.S. in Biomedical Engineering/Mechanical Engineering or any relevant branch of study is preferred.
- •0-2 years of experience within the medical device industry is preferred.
- •Familiarity with industry practices and guidelines including those outlined by the FDA and ISO is required.
- •Knowledge of Good Laboratory Practice (GLP), Good Manufacturing Practices (GMP), and Good Documentation Practices (GDP) is required.
- •Must have practical experience and a solid understanding of mechanical design principles, testing, and manufacturing processes.
- •Proficiency in Microsoft Excel and Microsoft Word is required.
- •Effective communication (written and verbal) and collaboration within cross‑functional teams are required.
Physical
We Offer
- •Competitive compensation package
- •Modern working environment with state‑of‑the‑art facilities and technologies
- •Challenging assignments in a fast‑growing and innovative industry
- •Position in a dynamic, international team of highly skilled professionals
- •Various opportunities for personal and professional development within a global organization
Seniority level
- •Associate
Employment type
- •Full‑time
Job function
- •Management and Manufacturing
Industries
- •Medical Device
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