Pharmaceutical Engineering Line Lead/Supervisor
Listed on 2026-09-12
-
Engineering
Manufacturing Engineer, Operations Management, Quality Engineering
Our client – a global and growing Bio Pharma CDMO company needs an Engineering Supervisor - Line Lead with Pharmaceutical Industry experience at their expanding plant in WA state, Excellent total comp.
up to $180K+ with excellent Benefits + Relocation Package
.
Job Title:
Pharmaceutical Engineering Line Lead / Supervisor
Overnight Travel: 10%
Location:
Spokane, WA
Relocation: YES – The client offers a generous package for relo assistance.
Compensation:
Salary range up to $165K+ Annual Bonus (10 %)
Full Benefits:
Medical, Vision, Dental,
15 days
’ vacation/Sick time,
10 - Holidays,
401k (match up to 4%).
Our client is a growing CDMO company in the Pharmaceutical Industry. They are a part of a global parent company with sites in many countries with around 1,300 people at this site in Spokane
, WA.
This is an integrated contract development and manufacturing organization (CDMO) offering specialized Aseptic Sterile manufacturing, filling and lyophilization of drug products in Vials.
Group InfoBe part of the Plant
Engineering group of around 60 technical people. This role will be responsible for the technical aspects of 1 of the 4 lines
This role will report to the Engineering Director.
Note 1The company recently completed their 3rd state-of-the-art Sterile Liquid compounding & Vial Filling line and are currently expanding again with a 4th line at this growing plant site.
Note 2The primary focus will be the technical and project engineering aspects of 1 complete filling line. This person will lead and supervise up to 3 Engineers.
Note 3Client will support transfer of existing H1B Visa for this permanent direct hire role, but will not sponsor for a new H1B visa.
Job SummaryThe Engineering Line Lead position provides leadership, manufacturing support and coordination of the engineering department for the CMO line specific projects.
This position ensures that contract projects, equipment functionality, compliance support, and capital expenditures are executed per Company management initiatives, compliance guidelines, the project management system, and the capital budget schedule.
It is the responsibility of this position to ensure line specific compliance of the CMO equipment and team with state, local, and federal regulations.
This position ensures operations and projects are carried out under adherence to GEPs and cGMPs.
Job Functions and Responsibilities in cGMP settings- Bachelors of Science in Engineering or related technical degree.
- 5+ years of Engineering Experience
- 3+ years of Bio Pharma industry
- 2+ years of Project Engineering/Management experience
- Some Leadership,
Supervisory experience over Jr. Engineers, Technicians. - Facility or Manufacturing Engineering Experience
- MS Office suite (Word, PowerPoint, Excel) experience
- BS in Mechanical, Chemical, Electrical, Manufacturing engineering
- Advanced degree or PE or PMP certification
- Experience with PM Software – MS Project
, Design software
- AutoCAD & ERP – SAP - Experience with Pharma sterile aseptic manufacturing, filling, Lyophilization
- Interfacing with OEM equipment vendors, Construction/consulting partners
Projects, Plant Project, engineering, Pharma, CDMO, manufacturing, plant, FDA, GMP, Sterile Aseptic liquid filling, Isolators, Clean rooms, Lyophilization, contract Manufacturing, Supervisor, Lead
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