TN Visa Chemical Process Engineer Jobs
Chemical Process Engineer roles qualify for TN visa sponsorship under USMCA for Canadian and Mexican professionals with a degree in chemical engineering or a closely related field. Employers file the TN petition directly, with no lottery and no annual cap for Canadians. Mexican nationals are subject to a separate TN allocation.
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EQUAL OPPORTUNITY EMPLOYER
Corden Pharma provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. Corden Pharma embraces fair hiring practices. CordenPharma is a leading full-service contract development and manufacturing organization (CDMO) of active pharmaceutical ingredients (APIs), excipients, and pharmaceuticals Drug Products (DP) and packaging capabilities with > 2,600 employees across the world. Our services enable pharmaceutical and biotech companies to manufacture medicines with the ultimate goal of improving people’s lives.
Our network in Europe and the U.S. offers flexible and specialized solutions across five technology platforms: Peptides, Lipids, & Carbohydrates; Injectables; Highly Potent & Oncology; and Small Molecules. We strive for excellence in supporting this network and are committed to providing the highest quality products for the well-being of patients.
SUMMARY
Performs research and development activities for the purpose of transferring and designing/improving a process or technology. Provides process engineering support for manufacturing processes in assigned group or plant through developing and implementing continuous improvements. And through troubleshooting methods and equipment used in the production of bulk pharmaceutical intermediates and active pharmaceutical ingredients.
ESSENTIAL DUTIES AND RESPONSIBILITIES
Include the following. Other duties may be assigned.
- Provides day-to-day support to assigned processes, at times requiring attention outside of the normal work hours
- Evaluates new process fits into manufacturing with supervisory oversight, including consideration of safety, cost, equipment, chemistry, and unit operation technological needs
- With supervisory input, performs process development via process modeling or testing at lab scale, concentrating on key scale up parameters to scale up from kilo-scale to full production scale
- Participates in technology transfer from one manufacturing site to another; develops plans for successful tech transfers, and implements processes into pilot or commercial facilities, with supervisory oversight. Assembles technology transfer packages
- Implements process improvements and optimization that reduce costs; improve yields, cycle times or product quality; resolve or prevent environmental, health and safety impacts; reduce down time; improve process consistency; and improve process robustness
- Performs process troubleshooting to resolve operating or product problems; identifies and implements solutions to improve process robustness
- Supports manufacturing through compiling technical requirements for batch record generation; providing technical input on equipment setup requirements; providing process training for operators; providing technical support in production for processes in development; writing process validation protocols; providing technical input on deviations and investigations; and writing campaign summary reports. Ensures that documentation is consistent with the process filing
- Contributes to meeting Process Safety Management compliance by participating in Process Hazard Analysis reviews; and by providing mass and energy balances and other engineering data for the assigned process
- Strives to improve professional skills by participating in on-the-job training, attending guest lectures, being an active member of a professional organization, and attending formal training courses and conferences
LEADERSHIP & BUDGET RESPONSIBILITIES
As part of a cross functional team, this position is responsible and accountable for addressing process engineering requirements for assigned projects.
SAFETY & ENVIRONMENTAL RESPONSIBILITIES
Every individual is personally responsible for the safety and environmental aspects of his or her activities in the workplace. Each employee is expected to perform their job duties in a safe manner utilizing all their knowledge, training, ability, and experience.
QUALIFICATIONS
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
EDUCATION and/or EXPERIENCE
A BS in Chemical Engineering and 1 year experience in Process Engineering in a Pharmaceutical or Fine Chemicals Manufacturing environment.
LANGUAGE SKILLS
Ability to read, analyze, and interpret common scientific and technical journals, financial reports, and legal documents. Ability to respond to common inquiries or complaints from customers, regulatory agencies, or members of the business community. Ability to write speeches and articles for publication that conform to prescribed style and format. Ability to effectively present information to top management, public groups, and/or boards of directors.
MATHEMATICAL SKILLS
Ability to apply advanced mathematical concepts such as exponents, logarithms, quadratic equations, and permutations. Ability to apply mathematical operations to such tasks as frequency distribution, determination of test reliability and validity, analysis of variance, correlation techniques, sampling theory, and factor analysis.
REASONING ABILITY
Ability to define problems, collect data, establish facts, and draw valid conclusions. Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables.
CERTIFICATES, LICENSES, REGISTRATIONS
None.
PHYSICAL DEMANDS
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 frequently required to stand, sit, and talk or hear. The employee is occasionally required to walk; work with hands; reach above shoulder height; climb or balance; stoop, kneel, crouch, or crawl; and taste or smell. The employee must occasionally lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, distance vision, depth perception, and ability to adjust focus.
WORK ENVIRONMENT
The work environment characteristics described here are representative of those an employee encounters while performing 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 occasionally exposed to moving mechanical parts, fumes or airborne particles, low levels of toxic or caustic chemicals, outside weather conditions, and vibration. The noise level in the work environment is usually moderate.
CORE COMPETENCIES
These are the specific areas of knowledge, skill and ability that are important for successful job performance. They must be job related and consistent with business necessity.
- Expands knowledge of plant-scale unit operations, scale-up, and plant design considerations; builds on technical knowledge in chemical engineering and process improvement methodology
- Emerging knowledge of regulatory issues in pharmaceutical manufacturing including cGMPs, PSM, OSHA, and EPA requirements
- Develops computer skills, in the areas of: Microsoft Office Products – Word, Excel, PowerPoint; Batch +, statistical analysis programs, and chemical engineering simulation software
- Explores training opportunities in technical areas that will strengthen skills for current assignments; acquires training to use common tools that support job (for example, Batch Plus)
- Regularly applies basic science and engineering principles to assigned projects
- Participates in and understands the importance of regulatory compliance systems such as PHAs and incident reporting; completes assignments, i.e., action items, in a timely manner
- Conducts basic technical and economic evaluations
- Demonstrates problem analysis and troubleshooting skills, data compilation, and simple analysis; draws conclusions from data
- Demonstrates a trend toward working independently – and decreasing reliance on mentors and supervisors to guide work and daily activities
- Executes assigned, well-defined tasks and seeks assistance when appropriate; and begins to offer some input on assigned projects
- Follows established methods and procedures; generally, implements existing standards and technical solutions; or implements new ideas that were generated by others
- Displays initiative to drive ideas or issues that he/she supports, and follow through to completion
- Understands and applies the Corden values
- Familiar with manufacturing department’s activities and Corden’s business goals and strategy
- Learns basics of project economics and product line cost structure and is familiar with the product standards manual
- Demonstrates clear, concise writing skills, targeting detailed reports on specific subjects, often requiring review by more senior personnel
- Presentation skills are developed through frequent ‘short and to the point’ presentations; generally targeting technical staff, process team, and project groups
- Demonstrates willingness to work in teams and to contribute in technical, plant support and staff meetings
- Demonstrates emerging leadership skills, and influence over others in small groups and small projects; knows and uses key facility contacts required to make progress on projects
SALARY
Actual pay will be based on your skills and experience.
BENEFITS
- 401(k) matching - Corden Pharma will contribute 100% of the first 6% - 100% vested after 2 years of service
- Accident Plan
- Critical Illness Insurance
- Dental Insurance
- Disability Insurance
- Employee Assistance Program
- Flexible Spending Account
- Health Insurance PPO/HSA
- Hospital Indemnity Plan
- ID Theft Protection
- Life Insurance
- Paid Maternity/Paternity Leave
- Tuition Reimbursement
- Wellness Program
- Vacation – Three Weeks 1st Year
- Vision Insurance
This post will expire on May 22, 2026.

EQUAL OPPORTUNITY EMPLOYER
Corden Pharma provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. Corden Pharma embraces fair hiring practices. CordenPharma is a leading full-service contract development and manufacturing organization (CDMO) of active pharmaceutical ingredients (APIs), excipients, and pharmaceuticals Drug Products (DP) and packaging capabilities with > 2,600 employees across the world. Our services enable pharmaceutical and biotech companies to manufacture medicines with the ultimate goal of improving people’s lives.
Our network in Europe and the U.S. offers flexible and specialized solutions across five technology platforms: Peptides, Lipids, & Carbohydrates; Injectables; Highly Potent & Oncology; and Small Molecules. We strive for excellence in supporting this network and are committed to providing the highest quality products for the well-being of patients.
SUMMARY
Performs research and development activities for the purpose of transferring and designing/improving a process or technology. Provides process engineering support for manufacturing processes in assigned group or plant through developing and implementing continuous improvements. And through troubleshooting methods and equipment used in the production of bulk pharmaceutical intermediates and active pharmaceutical ingredients.
ESSENTIAL DUTIES AND RESPONSIBILITIES
Include the following. Other duties may be assigned.
- Provides day-to-day support to assigned processes, at times requiring attention outside of the normal work hours
- Evaluates new process fits into manufacturing with supervisory oversight, including consideration of safety, cost, equipment, chemistry, and unit operation technological needs
- With supervisory input, performs process development via process modeling or testing at lab scale, concentrating on key scale up parameters to scale up from kilo-scale to full production scale
- Participates in technology transfer from one manufacturing site to another; develops plans for successful tech transfers, and implements processes into pilot or commercial facilities, with supervisory oversight. Assembles technology transfer packages
- Implements process improvements and optimization that reduce costs; improve yields, cycle times or product quality; resolve or prevent environmental, health and safety impacts; reduce down time; improve process consistency; and improve process robustness
- Performs process troubleshooting to resolve operating or product problems; identifies and implements solutions to improve process robustness
- Supports manufacturing through compiling technical requirements for batch record generation; providing technical input on equipment setup requirements; providing process training for operators; providing technical support in production for processes in development; writing process validation protocols; providing technical input on deviations and investigations; and writing campaign summary reports. Ensures that documentation is consistent with the process filing
- Contributes to meeting Process Safety Management compliance by participating in Process Hazard Analysis reviews; and by providing mass and energy balances and other engineering data for the assigned process
- Strives to improve professional skills by participating in on-the-job training, attending guest lectures, being an active member of a professional organization, and attending formal training courses and conferences
LEADERSHIP & BUDGET RESPONSIBILITIES
As part of a cross functional team, this position is responsible and accountable for addressing process engineering requirements for assigned projects.
SAFETY & ENVIRONMENTAL RESPONSIBILITIES
Every individual is personally responsible for the safety and environmental aspects of his or her activities in the workplace. Each employee is expected to perform their job duties in a safe manner utilizing all their knowledge, training, ability, and experience.
QUALIFICATIONS
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
EDUCATION and/or EXPERIENCE
A BS in Chemical Engineering and 1 year experience in Process Engineering in a Pharmaceutical or Fine Chemicals Manufacturing environment.
LANGUAGE SKILLS
Ability to read, analyze, and interpret common scientific and technical journals, financial reports, and legal documents. Ability to respond to common inquiries or complaints from customers, regulatory agencies, or members of the business community. Ability to write speeches and articles for publication that conform to prescribed style and format. Ability to effectively present information to top management, public groups, and/or boards of directors.
MATHEMATICAL SKILLS
Ability to apply advanced mathematical concepts such as exponents, logarithms, quadratic equations, and permutations. Ability to apply mathematical operations to such tasks as frequency distribution, determination of test reliability and validity, analysis of variance, correlation techniques, sampling theory, and factor analysis.
REASONING ABILITY
Ability to define problems, collect data, establish facts, and draw valid conclusions. Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables.
CERTIFICATES, LICENSES, REGISTRATIONS
None.
PHYSICAL DEMANDS
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 frequently required to stand, sit, and talk or hear. The employee is occasionally required to walk; work with hands; reach above shoulder height; climb or balance; stoop, kneel, crouch, or crawl; and taste or smell. The employee must occasionally lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, distance vision, depth perception, and ability to adjust focus.
WORK ENVIRONMENT
The work environment characteristics described here are representative of those an employee encounters while performing 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 occasionally exposed to moving mechanical parts, fumes or airborne particles, low levels of toxic or caustic chemicals, outside weather conditions, and vibration. The noise level in the work environment is usually moderate.
CORE COMPETENCIES
These are the specific areas of knowledge, skill and ability that are important for successful job performance. They must be job related and consistent with business necessity.
- Expands knowledge of plant-scale unit operations, scale-up, and plant design considerations; builds on technical knowledge in chemical engineering and process improvement methodology
- Emerging knowledge of regulatory issues in pharmaceutical manufacturing including cGMPs, PSM, OSHA, and EPA requirements
- Develops computer skills, in the areas of: Microsoft Office Products – Word, Excel, PowerPoint; Batch +, statistical analysis programs, and chemical engineering simulation software
- Explores training opportunities in technical areas that will strengthen skills for current assignments; acquires training to use common tools that support job (for example, Batch Plus)
- Regularly applies basic science and engineering principles to assigned projects
- Participates in and understands the importance of regulatory compliance systems such as PHAs and incident reporting; completes assignments, i.e., action items, in a timely manner
- Conducts basic technical and economic evaluations
- Demonstrates problem analysis and troubleshooting skills, data compilation, and simple analysis; draws conclusions from data
- Demonstrates a trend toward working independently – and decreasing reliance on mentors and supervisors to guide work and daily activities
- Executes assigned, well-defined tasks and seeks assistance when appropriate; and begins to offer some input on assigned projects
- Follows established methods and procedures; generally, implements existing standards and technical solutions; or implements new ideas that were generated by others
- Displays initiative to drive ideas or issues that he/she supports, and follow through to completion
- Understands and applies the Corden values
- Familiar with manufacturing department’s activities and Corden’s business goals and strategy
- Learns basics of project economics and product line cost structure and is familiar with the product standards manual
- Demonstrates clear, concise writing skills, targeting detailed reports on specific subjects, often requiring review by more senior personnel
- Presentation skills are developed through frequent ‘short and to the point’ presentations; generally targeting technical staff, process team, and project groups
- Demonstrates willingness to work in teams and to contribute in technical, plant support and staff meetings
- Demonstrates emerging leadership skills, and influence over others in small groups and small projects; knows and uses key facility contacts required to make progress on projects
SALARY
Actual pay will be based on your skills and experience.
BENEFITS
- 401(k) matching - Corden Pharma will contribute 100% of the first 6% - 100% vested after 2 years of service
- Accident Plan
- Critical Illness Insurance
- Dental Insurance
- Disability Insurance
- Employee Assistance Program
- Flexible Spending Account
- Health Insurance PPO/HSA
- Hospital Indemnity Plan
- ID Theft Protection
- Life Insurance
- Paid Maternity/Paternity Leave
- Tuition Reimbursement
- Wellness Program
- Vacation – Three Weeks 1st Year
- Vision Insurance
This post will expire on May 22, 2026.
See all 296+ Chemical Process Engineer jobs
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Chemical Process Engineer roles.
Get Access To All JobsTips for Finding TN Visa Sponsorship as a Chemical Process Engineer
Align your credentials to USMCA's engineer category
TN status requires a degree in chemical engineering or a directly related discipline. A degree in chemistry or materials science may qualify if your job duties are clearly engineering-focused, so position your resume and credential documents around process design and optimization.
Target industries with recent visa sponsorship experience
Petrochemical, pharmaceutical, food processing, and semiconductor manufacturing employers have recent visa filing experience and often sponsor work visas for process engineers. Prioritize roles at manufacturers and refiners over consulting firms, which may have less established sponsorship infrastructure and could extend your hiring timeline.
Search TN-ready Chemical Process Engineer roles on Migrate Mate
Use Migrate Mate to filter Chemical Process Engineer jobs by employers with recent visa filings, indicating experience with work visa sponsorship. This cuts the time spent screening companies that may be unfamiliar with the TN visa process after you've already reached the offer stage.
Clarify the CBP entry method before accepting an offer
Canadian professionals can complete TN admission at the port of entry without a consular appointment. Mexican nationals need a visa stamp before entry. Confirm which pathway applies before your start date, since the timelines differ by several weeks.
Prepare a detailed support letter with process-specific duties
CBP officers assess whether your role qualifies as a specialty engineering position. Your employer's support letter should describe unit operations, process simulation tools, and regulatory compliance work rather than general project management tasks that could belong to any engineering discipline.
Understand how contract and staffing roles affect TN eligibility
TN status ties you to a specific employer of record. If you're placed through a staffing agency at a client site, the agency is your TN sponsor, not the end client. Verify that the agency has filed TN petitions before and can serve as the employer of record.
Chemical Process Engineer jobs are hiring across the US. Find yours.
Find Chemical Process Engineer JobsChemical Process Engineer TN Visa: Frequently Asked Questions
Does a Chemical Process Engineer role qualify for TN visa status?
Yes, chemical engineering is an explicitly listed profession under the USMCA TN category. Your degree must be in chemical engineering or a closely related field, and your job duties must reflect engineering work, such as process design, scale-up, or optimization. Roles that shift heavily toward general project management may face greater scrutiny at the port of entry or consulate.
How does TN compare to H-1B for Chemical Process Engineer positions?
TN has no annual lottery, no cap for Canadian nationals, and can be activated at the Canadian border or a preclearance airport without waiting for a consular appointment. H-1B requires winning a random lottery and waiting for an October 1 start date. For qualified Canadian and Mexican chemical engineers, TN is a faster and more predictable path to U.S. employment than H-1B.
Where can I find Chemical Process Engineer jobs that offer TN visa sponsorship?
Migrate Mate is built specifically for Canadian and Mexican professionals seeking TN-sponsored roles. You can filter by job title and sponsorship status to surface employers who have actively sponsored TN workers, rather than spending time applying to companies that are unfamiliar with the process or unwilling to file.
Can I switch employers while on TN status as a Chemical Process Engineer?
Yes, but your TN status is employer-specific. You cannot start working for a new employer until a new TN is approved or, for Canadians, until you've completed a new port-of-entry admission. A gap between your last day at the old employer and your first day at the new employer can create a status issue, so coordinate the timing carefully with both parties.
What documentation does my employer need to sponsor my TN visa for a Chemical Process Engineer role?
Your employer must provide a support letter that describes your specific engineering duties, your credentials, the duration of employment, and your compensation. You'll also need your degree certificate and transcripts. For Mexican nationals, the employer's letter accompanies your DS-160 application and is reviewed at the consulate. CBP may also request process engineering-specific evidence to confirm the role isn't a general management position.
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