Manufacturing Engineer at Fusion Life Sciences technologies LLC Raynham, MA
Fusion Life Sciences technologies LLC · Raynham, MA
- Level
- Engineer
- Team
- Manufacturing
- Experience asked
- 5+ years
- Industry
- Industrial
- Posted
- 8 days ago
The role in 30 seconds
An engineer-level manufacturing role at Fusion Life Sciences technologies LLC (industrial) in Raynham, MA. You'd own manufacturing process and equipment design from concept through process qualification and commercial release, and lead the full validation lifecycle — URS, risk assessments, FAT, SAT, IQ, OQ, and PQ — for new equipment and automation systems.
- They ask for
- 5+ years
- Tools it names
- Root cause, FDA / GMP, Validation (IQ/OQ/PQ), Automation
Read from the posting. The full description is below.
From the plant jobs report · week of October 19, 2026
Manufacturing Engineer roles in Massachusetts: typical posted base $100k–$145k.
Median of the low and high ends of 34 live postings that list pay, out of 62 manufacturing engineer openings in Massachusetts, read from manufacturers' own careers sites.
Massachusetts plant jobs report →Pay by team and state →What moves pay →
How this role compares
Against 61 other live manufacturing postings in Massachusetts.
- Base pay
- Not listed in this posting
- Experience asked
- Typical (5+ years)
Typical $95k–$134k, from 31 postings that list pay.
Similar roles usually ask 5+ years.
Skills these teams ask for most
- Tooling 55%
- Lean 53%
- ✓ Automation 45%
- ✓ Root cause 42%
- ✓ New product launch 39%
- Six Sigma 32%
✓ = this posting asks for it too. % = share of similar postings that mention it.
Stands out: this posting asks for FDA / GMP, 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 Manufacturing team at Fusion Life Sciences technologies LLC
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 Fusion Life Sciences technologies LLCAs posted on their careers site.ShowHide
requirements
and quality standards. What we're looking for
Required 5+ years of experience in manufacturing engineering within a regulated environment (medical device, pharmaceutical, or similar). Experience authoring and executing validation lifecycle documentation: URS, risk assessments, FAT, SAT, IQ, OQ, and PQ. Working knowledge of FDA regulations, ISO standards, and GMP requirements. Experience with change control, deviation investigations, and root cause analysis. Pay, benefits and schedule
$50–$55 per hour, on a 12-month contract. About Fusion Life Sciences Technologies LLC and apply
Fusion Life Sciences Technologies LLC is a staffing and workforce-solutions firm placing engineers and technical professionals with regulated life sciences, medical device, and pharmaceutical companies, with clients worldwide. Engineers are placed on a W2 basis, not as 1099 contractors, and Fusion's placements span manufacturing process setup, quality and compliance, regulatory affairs, and FDA remediation work governed by frameworks like 21 CFR Part 820, ISO, GAMP, and USP. This Manufacturing Engineer role is a client placement supporting a regulated medical device manufacturing site. If this sounds like a fit, apply through hireCNC and Fusion Life Sciences Technologies will follow up directly.
Show full description ↓Show less ↑
Updated October 1, 2026 At a glance Company: Fusion Life Sciences Technologies LLC Location: Raynham, MA 02767 Pay: $50 – $55 per hour Job Type: Contract (12 months) Experience: 5+ years Why this job is worth considering
This Manufacturing Engineer opening supports new product introductions, site capacity expansion, and transformational initiatives inside a regulated medical device manufacturing environment in Raynham, MA. You'd own manufacturing process and equipment design from concept through process qualification and commercial release, and lead the full validation lifecycle — URS, risk assessments, FAT, SAT, IQ, OQ, and PQ — for new equipment and automation systems. It's a cross-functional role: you'll work directly with internal stakeholders and outside suppliers to resolve technical issues and keep projects on track, with a direct hand in change control, deviation investigations, and continuous improvement. This is a 12-month contract paying $50–$55 per hour for someone with 5+ years in a regulated manufacturing setting. What you'll be doing
Develop and implement advanced manufacturing technologies supporting new product introductions, site capacity expansion, and transformational initiatives in a regulated medical device environment. Design manufacturing processes and equipment solutions for manufacturability, scalability, quality, and regulatory compliance from concept through process qualification and commercial release. Lead engineering activities and deliverables across cross-functional project plans, keeping scope, timelines, and business objectives aligned. Author, review, and execute validation lifecycle documentation, including URS, risk assessments, FAT, SAT, IQ, OQ, and PQ. Develop and maintain manufacturing procedures, work instructions, process specifications, and supporting documentation. Coordinate qualification and commissioning activities for manufacturing equipment, automation systems, utilities, and supporting software applications. Interface with internal stakeholders and external suppliers to resolve technical issues and drive successful project execution. Support change control, deviation investigations, root cause analysis, risk assessments, and continuous improvement initiatives. Review technical drawings, equipment designs, and vendor documentation for compliance with approved
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