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Full Time Cvd Process Engineer Jobs in Raleigh, NC

Sr Wastewater Process Engineer

Cary, NC · On-site

$96K - $124K/yr

Yes Full time/Part time : Full-Time Project Only Hire : No Visa Sponsorship Available: No Why Black ... Function in a lead wastewater process engineer role as a technical specialist in the areas of ...

Gopuff is seeking a Process Lead for our Operations team. Reporting to the Site Leader or Manager ... Medical/Dental/Vision Insurance (for full-time employees) * 401(k) Retirement Savings Plan * 25 ...

Gopuff is seeking a Process Lead for our Operations team. Reporting to the Site Leader or Manager, this role is a core part of the leadership team with the responsibility to ensure order accuracy and ...

Gopuff is seeking a Process Lead for our Operations team. Reporting to the Site Leader or Manager, this role is a core part of the leadership team with the responsibility to ensure order accuracy and ...

... process, refinery, and petrochemical markets. It is servicing the growth needs of the U.S. power ... All full-time employees are eligible for benefits on day one of employment! Purpose: To support and ...

... process, refinery, and petrochemical markets. It is servicing the growth needs of the U.S. power ... All full-time employees are eligible for benefits on day one of employment! Purpose: To support and ...

Quality Engineer

Oxford, NC · On-site

$70K - $75K/yr

Quality Engineer Job Type: Full-time (M-F, 7:30am - 4:30pm) Location: Oxford, NC 27565 Company ... Ensuring that workflows, processes, and products comply with safety regulations. * Creating Non ...

Quality Engineer

Oxford, NC · On-site

$70K/yr

Quality Engineer Job Type: Full-time (M-F, 7:30am - 4:30pm) Location: Oxford, NC 27565 Company ... Ensuring that workflows, processes, and products comply with safety regulations. * Creating Non ...

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Showing results 1-20

Full Time Cvd Process Engineer information

See Raleigh, NC salary details

$48.1K

$89.4K

$138.5K

How much do full time cvd process engineer jobs pay per year?

As of Jul 14, 2026, the average yearly pay for full time cvd process engineer in Raleigh, NC is $89,449.00, according to ZipRecruiter salary data. Most workers in this role earn between $72,400.00 and $100,100.00 per year, depending on experience, location, and employer.

What is the difference between Full Time Cvd Process Engineer vs Full Time PVD Process Engineer?

AspectFull Time Cvd Process EngineerFull Time PVD Process Engineer
CredentialsEngineering degree, certifications in chemical or process engineeringEngineering degree, certifications in materials or process engineering
Work EnvironmentCleanroom, semiconductor fabrication facilitiesVacuum chambers, thin film deposition labs
Industry UsageSemiconductor manufacturing, electronicsSemiconductor, optics, and coating industries
Job FocusChemical vapor deposition processes for thin filmsPhysical vapor deposition processes for coatings

Both roles involve process engineering in semiconductor fabrication but focus on different deposition techniques. Cvd Process Engineers specialize in chemical vapor deposition, while PVD Process Engineers focus on physical vapor deposition. Understanding these differences helps in choosing the right career path or job search focus.

Infographic showing various Full Time Cvd Process Engineer job openings in Raleigh, NC as of July 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $89,449 per year, or $43 per hour.
Sr. Process Engineer

Sr. Process Engineer

Alcami Corporation

Morrisville, NC • On-site

$97K - $125K/yr

Full-time

Posted 2 hours ago


Alcami rating

7.3

Company rating: 7.3 out of 10

Based on 5 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 engineering support for clinical and commercial parenteral Drug Product manufacturing. The Sr. Process Engineer's responsibilities include but are not limited to the following: evalutation 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 equipment troubleshooting and optimization.
  • Own change controls for new processes and process optimization initiatives.
  • Lead cycle and recipe development initiatives for new prcoesses.
  • 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.
  • Interact with clients for technical sterile fill finish expertise 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.

Employment Type: FULL_TIME

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