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Live In Process Safety Engineer Jobs in Charleston, SC

Sr. Process Engineer

Charleston, SC · On-site

$97K - $125K/yr

Are you interested in joining our team? Job Summary The Sr. Process Engineer is accountable for driving results in a fast-paced environment by providing technical support for clinical and commercial ...

Sr. Process Engineer

North Charleston, SC · On-site

$99K - $128K/yr

Are you interested in joining our team? Job Summary The Sr. Process Engineer is accountable for driving results in a fast-paced environment by providing technical support for clinical and commercial ...

Manufacturing Process Engineer

Charleston, SC · On-site

$70K - $93K/yr

Whether in the areas of mobility solutions, consumer goods, industrial technology or energy and ... Lead projects to improve safety, quality, productivity, and cost. * Optimize cycle time, process ...

Manufacturing Process Engineer

Charleston, SC · On-site

$70K - $93K/yr

Whether in the areas of mobility solutions, consumer goods, industrial technology or energy and ... Lead projects to improve safety, quality, productivity, and cost. * Optimize cycle time, process ...

Manufacturing Process Engineer

Charleston, SC · On-site

$68K - $91K/yr

Whether in the areas of mobility solutions, consumer goods, industrial technology or energy and ... Lead projects to improve safety, quality, productivity, and cost. * Optimize cycle time, process ...

New

Manufacturing Process Engineer

Charleston, SC · On-site

$70K - $93K/yr

Whether in the areas of mobility solutions, consumer goods, industrial technology or energy and ... Lead projects to improve safety, quality, productivity, and cost. * Optimize cycle time, process ...

Legal Process Engineer FLSA STATUS : Exempt DEPARTMENT : Client Solutions Group SUPERVISOR ... Leveraging expertise in project management, process improvement, and data-driven insight, the LPE ...

Reliability Engineer

Moncks Corner, SC

$90K - $113K/yr

... PSM (Process Safety Management) and a strong safety-first mindset Hands-on experience with ... Lead projects and expand your expertise in reliability and capital execution Purpose-driven work:

Reliability Engineer

Moncks Corner, SC · On-site

$90K - $113K/yr

Experience with PSM (Process Safety Management) and a strong safety‑first mindset * Hands‑on ... Lead projects and expand your expertise in reliability and capital execution * Purpose‑driven ...

Showing results 21-40

Live In Process Safety Engineer information

See Charleston, SC salary details

$46.3K

$86.1K

$133.4K

How much do live in process safety engineer jobs pay per year?

As of Sep 14, 2026, the average yearly pay for live in process safety engineer in Charleston, SC is $86,112.00, according to ZipRecruiter salary data. Most workers in this role earn between $69,700.00 and $96,400.00 per year, depending on experience, location, and employer.

What is the difference between Live In Process Safety Engineer vs Process Safety Technician?

AspectLive In Process Safety EngineerProcess Safety Technician
CredentialsBachelor's degree in engineering or safety, certifications like CSP or APITechnical diploma or associate degree, safety certifications
Work EnvironmentDesigning safety protocols, overseeing safety systems, often on-site at industrial plantsMonitoring safety equipment, conducting inspections, supporting safety procedures
Employer & IndustryOil & gas, chemical plants, manufacturing facilitiesRefineries, chemical plants, industrial sites

The Live In Process Safety Engineer focuses on designing and managing safety systems, requiring higher-level engineering credentials. In contrast, the Process Safety Technician supports safety operations through inspections and equipment monitoring. Both roles are essential for maintaining safety standards in industrial environments, but they differ in responsibilities and qualifications.

How much does a live in process safety engineer make in the US?

A live-in process safety engineer in the US typically earns between $80,000 and $130,000 annually, depending on experience, location, and industry. Salaries may also include benefits such as housing allowances or relocation assistance, especially for roles requiring on-site presence and safety certifications.

What are the most commonly searched types of Process Safety Engineer jobs in Charleston, SC?

The most popular types of Process Safety Engineer jobs in Charleston, SC are:

What job categories do people searching Live In Process Safety Engineer jobs in Charleston, SC look for?

The top searched job categories for Live In Process Safety Engineer jobs in Charleston, SC are:

Infographic showing various Live In Process Safety Engineer job openings in Charleston, SC as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $86,112 per year, or $41.4 per hour.

Sr. Process Engineer

Charleston, SC • On-site

Alcami Corporation
Pharmaceutical and Medicine Manufacturing • 501 - 1,000 employees

$97K - $125K/yr

Other

Re-posted 5 days ago


Key responsibilities

  • Provides technical assistance for process tech transfer and validation efforts for manufacturing projects.

  • Writes Master Batch Records and monitors manufacturing processes during production runs to troubleshoot issues.

  • Authorizes manufacturing investigations, completes CAPA assignments, and composes process validation documentation.


Alcami rating

7.8

Company rating: 7.8 out of 10

Based on 9 frontline employees who took The Breakroom Quiz


Job description

At Alcami, we deliver reliable solutions that unlock the potential of transformative medicines from discovery to commercialization, through trusted partnership with our clients, recognized industry expertise and proven regulatory track record.

Are you interested in joining our team?

Job Summary

The Sr. Process Engineer is accountable for driving results in a fast-paced environment by providing technical support for clinical and commercial parenteral Drug Product manufacturing. The Sr. Process Engineer’s responsibilities include but are not limited to the following: performing tech transfers of new processes and technologies into the site, preparation of documentation to support process validation and batch manufacturing, troubleshooting manufacturing processes, completing process deviations and investigations, and coordinating lab studies with the formulation development lab. These functions will be executed following standard operating procedures and batch records in accordance with FDA and EU requirements and current Good Manufacturing Practices.

On-Site Expectations
  • 100% on-site position.
  • 1st Shift: Monday - Friday, 8:00am - 5:00pm.
Responsibilities
  • Provides technical assistance for process tech transfer and validation efforts for assigned manufacturing projects.
  • Writes Master Batch Records with a strong understanding of equipment, critical process parameters, in-process tests, etc.
  • Monitors manufacturing processes during production runs to assess any technical process issues and provides troubleshooting support as needed.
  • Author manufacturing investigations and complete CAPA assignments.
  • Composes process validation documentation, including CQA assessment, pFMEA risk assessment, and process validation protocols.
  • Identifies specific parameters, sampling, and tests used in the validation protocols of new and existing products.
  • Interact with clients during routinely scheduled project meetings.
  • Ensures timely completion and compliance with cGMP and all other relevant company training requirements.
  • Other duties as assigned.
Qualifications
  • Bachelor’s degree in Engineering, Pharmacy, or Chemistry.
  • 5 years of experience of technical support in a sterile pharmaceutical manufacturing environment.
  • Previous experience supporting tech transfer of parenteral Drug Products preferred.
Knowledge, Skills, and Abilities
  • Excellent verbal communication, written communication, documentation, negotiation, critical thinking, analytical, problem solving, detail orientation, organization and time management skills required.
  • Working knowledge of cGMP requirements related to sterile Drug Product manufacturing processes.
  • Working knowledge of EU regulations preferred.
  • Proficiency with Microsoft office (Word, Excel, Outlook) required.
  • Ability to interact with internal stakeholders and external customers.
Travel Expectations
  • Up to 5% domestic travel.
Physical Demands and Work Environment

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is required to frequently stand, walk, sit; talk or hear; use hands to finger, handle or feel. The employee is required some of the time to reach with hands and arms. The employee is required occasionally to climb or balance; and taste or smell. The employee must frequently lift and/or move up to 25 pounds. There is no special vision requirement for this job. The employee may occasionally work near moving mechanical parts; fumes or airborne particles; toxic or caustic chemicals.

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