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Process Technology Transfer Engineer Jobs (NOW HIRING)

Sr. Process Engineer

Charleston, SC · On-site

$99K - $128K/yr

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 ...

Sr. Process Engineer

Charleston, SC · On-site

$97K - $125K/yr

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 ...

Sr. Process Engineer

North Charleston, SC · On-site

$99K - $128K/yr

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 ...

Process Engineer III

Denver, CO · On-site

$85K - $119K/yr

The Process Engineer III serves as a senior technical resource within Manufacturing Science ... Lead complex process development, optimization, scale-up, technology transfer, new product ...

Process Engineer

Salisbury, MD · On-site

$80K - $1M/yr

Smiths Interconnect, a Molex company, is seeking a Process Engineer to a critical part in ... Experience supporting new product introduction and technology transfer initiatives. * Certification ...

Process Engineer III

Denver, CO · On-site

$85K - $119K/yr

The Process Engineer III serves as a senior technical resource within Manufacturing Science ... Lead complex process development, optimization, scale-up, technology transfer, new product ...

We are seeking an experienced Process Engineer to lead and support the successful transfer of ... Develop and execute technology transfer strategies to support clinical and commercial manufacturing ...

Senior Heat Transfer Engineer

Jupiter, FL

$102K - $140K/yr

At Florida Turbine Technologies (FTT), we're not just about cutting-edge products; we're about ... Document changes through a formal engineering change notification process. * Works on complex ...

Showing results 21-40

Process Technology Transfer Engineer information

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$49.5K

$92K

$142.5K

How much do process technology transfer engineer jobs pay per year?

As of Sep 11, 2026, the average yearly pay for process technology transfer engineer in the United States is $92,018.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,500.00 and $103,000.00 per year, depending on experience, location, and employer.

What cities are hiring for Process Technology Transfer Engineer jobs?

Cities with the most Process Technology Transfer Engineer job openings:

What states have the most Process Technology Transfer Engineer jobs?

States with the most job openings for Process Technology Transfer Engineer jobs include:

What are popular job titles related to Process Technology Transfer Engineer jobs?

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Infographic showing various Process Technology Transfer Engineer job openings in the United States as of June 2026, with employment types broken down into 1% As Needed, 38% Full Time, 51% Part Time, 2% Temporary, and 8% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $92,018 per year, or $44.2 per hour.

Sr. Process Engineer

Charleston, SC • On-site

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

$99K - $128K/yr

Full-time

Re-posted 2 days ago


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?


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.


  • 100% on-site position.
  • 1st Shift: Monday - Friday, 8:00am - 5:00pm.

  • 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.

  • 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.

  • 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.

  • Up to 5% domestic travel.

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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