STEM OPT Senior Control Engineer Jobs
Senior Control Engineer roles in automation, process control, and systems integration qualify for the STEM OPT 24-month extension if your degree falls under an eligible CIP code. Your employer must be enrolled in E-Verify, and you'll need a signed I-983 training plan before your extension begins.
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Get Access To All JobsINTRODUCTION
BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.
ROLE AND RESPONSIBILITIES
The QC Specialist is responsible for coordinating and completing assigned QC reviews, ensuring that clinical and regulatory documents undergo review, copyediting, data verification, and proofreading in a manner that conforms to domestic and/or international regulatory submission and internal document standards, while meeting project timelines. Clinical and regulatory documents include study reports, clinical study protocols or amendments, investigator’s brochures, and the clinical sections of INDs, NDAs, MAAs, and other regulatory submission documents. Other documents may include manuscripts, abstracts, posters, briefing documents, responses to health authorities, narratives, and any other documents authored or supported by Global Medical Writing that require a QC review.
This work can be done remotely or from any of BeOne’s global offices.
Essential Functions of the Job:
Document Review and Editing:
- Works effectively within the Global Medical Writing department to produce high-quality, scientifically accurate documents under strict timelines, and ensures consistency between related documents.
- Responsible for performing a quality check of clinical and regulatory documents before approval.
- Performs cross-referencing, fact-checking, and general quality assessments of documents.
- Proofreads documents for grammatical and formatting errors, hyperlink functionality, data source verification, and proper translation of data.
- Ensures compliance with Global Medical Writing conventions, processes, templates and applicable regulatory guidelines.
- Maintains strong attention to detail (ie, to consistency, grammar, syntax, and scientific accuracy) while performing technical edits.
Project and Process Management:
- Ability to prioritize tasks, work simultaneously on multiple projects, and complete high-quality QC reviews according to tight timelines and shifting priorities/demands.
- Adheres to QC timelines and communicates with Medical Writers to maintain awareness of expectations, milestones, and deliverables.
- Contributes to team direction and strategy discussions, with guidance from managers and mentors.
Influence and Training:
- Builds effective partnerships with all intradepartmental teams when collaborating on QC reviews and projects.
- Engages in trainings that will increase knowledge of medical writing, the types of documents in the scope of the Global Medical Writing team, medical terminology, and the development of drugs and biologics.
BASIC QUALIFICATIONS
- Demonstrated ability to communicate in clear, concise, and effective English (both written and verbal).
- Experience in conducting medical writing QC reviews of pharmaceutical industry regulatory documents (such as clinical study reports, protocols, and protocol amendments) or experience in technical editing in a related or similar industry; experience in reviewing clinical sections of INDs, MAAs, and NDAs is a plus.
- Familiarity with the general process of drug/biologics development as well as the key requirements for regulatory submissions as defined in FDA regulations and ICH guidelines is preferred.
SUPERVISORY RESPONSIBILITIES
Not applicable for this role.
OTHER QUALIFICATIONS
- Effective Communication: Explains own work clearly. Able to escalate questions/issues to appropriate stakeholders at an early stage, with guidance from manager/mentor. Takes part in discussions with different viewpoints, and be able to provide value-added inputs with guidance from manager/mentor.
- Embracing Change: Always seeking and open to new opportunities and changes. Copes well with change and new challenges with guidance from manager/mentor. Contributes to specific change activities.
- Creating Innovation: Demonstrates openness to innovation and applies new ways of working (eg, skills or techniques) in own work to improve time management, timeliness, and accuracy.
- Thinking Strategically: Understands key concepts (eg, strategic review, lean writing) related to own work with guidance from manager/mentor. Demonstrates awareness of company strategies and general events happening in the industry (eg, regulations, guidelines, and trends).
- Mentoring: Provides specific feedback to others within own team as requested. Solicits feedback and accepts and integrates changes from constructive criticism. Willingly shares own knowledge and experience to support others’ learning.
COMPUTER SKILLS:
- Technical expertise in Microsoft Word, Microsoft Outlook, Excel, PowerPoint, and Adobe Acrobat.
- Proficiency in navigating Microsoft Windows.
- Familiarity with SharePoint and Veeva Vault is a plus.
TRAVEL
Not applicable.
EDUCATION REQUIRED
BA/BS degree; Masters, PhD/PharmD, or other graduate-level degree is a plus.
At least 1 year of relevant industry experience as a QC editor/specialist, medical writer, or technical copyeditor.
COMPENSATION
- Salary Range: $74,600.00 - $99,600.00 annually
BeOne is committed to fair and equitable compensation practices. Actual compensation packages are determined by several factors that are unique to each candidate, including but not limited to job-related skills, depth of experience, certifications, relevant education or training, and specific work location. Packages may vary by location due to differences in the cost of labor. The recruiter can share more about the specific salary range for a preferred location during the hiring process. Please note that the listed range reflects the base salary or hourly range only. Non-Commercial roles are eligible to participate in the annual bonus plan, and Commercial roles are eligible to participate in an incentive compensation plan. All Company employees have the opportunity to own shares of BeOne Medicines Ltd. stock because all employees are eligible for discretionary equity awards and to voluntarily participate in the Employee Stock Purchase Plan. The Company has a comprehensive benefits package that includes Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off, and Wellness.
We are proud to be an equal opportunity employer. BeOne does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans’ Readjustment Assistance Act of 1974, Title I of the Americans with Disabilities Act of 1990, and any other applicable federal, state or local laws, applicants who require reasonable accommodation in the job application process may contact accommodationsus@beonemed.com.
INTRODUCTION
BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.
ROLE AND RESPONSIBILITIES
The QC Specialist is responsible for coordinating and completing assigned QC reviews, ensuring that clinical and regulatory documents undergo review, copyediting, data verification, and proofreading in a manner that conforms to domestic and/or international regulatory submission and internal document standards, while meeting project timelines. Clinical and regulatory documents include study reports, clinical study protocols or amendments, investigator’s brochures, and the clinical sections of INDs, NDAs, MAAs, and other regulatory submission documents. Other documents may include manuscripts, abstracts, posters, briefing documents, responses to health authorities, narratives, and any other documents authored or supported by Global Medical Writing that require a QC review.
This work can be done remotely or from any of BeOne’s global offices.
Essential Functions of the Job:
Document Review and Editing:
- Works effectively within the Global Medical Writing department to produce high-quality, scientifically accurate documents under strict timelines, and ensures consistency between related documents.
- Responsible for performing a quality check of clinical and regulatory documents before approval.
- Performs cross-referencing, fact-checking, and general quality assessments of documents.
- Proofreads documents for grammatical and formatting errors, hyperlink functionality, data source verification, and proper translation of data.
- Ensures compliance with Global Medical Writing conventions, processes, templates and applicable regulatory guidelines.
- Maintains strong attention to detail (ie, to consistency, grammar, syntax, and scientific accuracy) while performing technical edits.
Project and Process Management:
- Ability to prioritize tasks, work simultaneously on multiple projects, and complete high-quality QC reviews according to tight timelines and shifting priorities/demands.
- Adheres to QC timelines and communicates with Medical Writers to maintain awareness of expectations, milestones, and deliverables.
- Contributes to team direction and strategy discussions, with guidance from managers and mentors.
Influence and Training:
- Builds effective partnerships with all intradepartmental teams when collaborating on QC reviews and projects.
- Engages in trainings that will increase knowledge of medical writing, the types of documents in the scope of the Global Medical Writing team, medical terminology, and the development of drugs and biologics.
BASIC QUALIFICATIONS
- Demonstrated ability to communicate in clear, concise, and effective English (both written and verbal).
- Experience in conducting medical writing QC reviews of pharmaceutical industry regulatory documents (such as clinical study reports, protocols, and protocol amendments) or experience in technical editing in a related or similar industry; experience in reviewing clinical sections of INDs, MAAs, and NDAs is a plus.
- Familiarity with the general process of drug/biologics development as well as the key requirements for regulatory submissions as defined in FDA regulations and ICH guidelines is preferred.
SUPERVISORY RESPONSIBILITIES
Not applicable for this role.
OTHER QUALIFICATIONS
- Effective Communication: Explains own work clearly. Able to escalate questions/issues to appropriate stakeholders at an early stage, with guidance from manager/mentor. Takes part in discussions with different viewpoints, and be able to provide value-added inputs with guidance from manager/mentor.
- Embracing Change: Always seeking and open to new opportunities and changes. Copes well with change and new challenges with guidance from manager/mentor. Contributes to specific change activities.
- Creating Innovation: Demonstrates openness to innovation and applies new ways of working (eg, skills or techniques) in own work to improve time management, timeliness, and accuracy.
- Thinking Strategically: Understands key concepts (eg, strategic review, lean writing) related to own work with guidance from manager/mentor. Demonstrates awareness of company strategies and general events happening in the industry (eg, regulations, guidelines, and trends).
- Mentoring: Provides specific feedback to others within own team as requested. Solicits feedback and accepts and integrates changes from constructive criticism. Willingly shares own knowledge and experience to support others’ learning.
COMPUTER SKILLS:
- Technical expertise in Microsoft Word, Microsoft Outlook, Excel, PowerPoint, and Adobe Acrobat.
- Proficiency in navigating Microsoft Windows.
- Familiarity with SharePoint and Veeva Vault is a plus.
TRAVEL
Not applicable.
EDUCATION REQUIRED
BA/BS degree; Masters, PhD/PharmD, or other graduate-level degree is a plus.
At least 1 year of relevant industry experience as a QC editor/specialist, medical writer, or technical copyeditor.
COMPENSATION
- Salary Range: $74,600.00 - $99,600.00 annually
BeOne is committed to fair and equitable compensation practices. Actual compensation packages are determined by several factors that are unique to each candidate, including but not limited to job-related skills, depth of experience, certifications, relevant education or training, and specific work location. Packages may vary by location due to differences in the cost of labor. The recruiter can share more about the specific salary range for a preferred location during the hiring process. Please note that the listed range reflects the base salary or hourly range only. Non-Commercial roles are eligible to participate in the annual bonus plan, and Commercial roles are eligible to participate in an incentive compensation plan. All Company employees have the opportunity to own shares of BeOne Medicines Ltd. stock because all employees are eligible for discretionary equity awards and to voluntarily participate in the Employee Stock Purchase Plan. The Company has a comprehensive benefits package that includes Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off, and Wellness.
We are proud to be an equal opportunity employer. BeOne does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans’ Readjustment Assistance Act of 1974, Title I of the Americans with Disabilities Act of 1990, and any other applicable federal, state or local laws, applicants who require reasonable accommodation in the job application process may contact accommodationsus@beonemed.com.
See all 900+ STEM OPT Senior Control Engineer Jobs
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Get Access To All JobsTips for Finding STEM OPT Authorization as a Senior Control Engineer
Verify your CIP code before applying
Check that your degree's CIP code appears on the STEM Designated Degree Program List maintained by USCIS. Electrical engineering, mechanical engineering, and computer science codes commonly support Senior Control Engineer roles, but industrial technology codes vary by school and may not qualify.
Confirm E-Verify enrollment before accepting offers
Ask hiring managers directly whether the company is enrolled in E-Verify before you reach the offer stage. A company can be enthusiastic about hiring you but still be ineligible to employ STEM OPT workers if it hasn't completed E-Verify enrollment.
Build an I-983 training plan around control systems
Draft your I-983 before your start date, mapping your engineering degree learning outcomes to specific job duties like PLC programming, SCADA configuration, or closed-loop tuning. Generic descriptions get returned by DSOs; specificity tied to your coursework clears faster.
Target manufacturers with active DOL LCA filings
Use Migrate Mate to filter Senior Control Engineer roles by employers with verified DOL Labor Condition Application filing history. Companies that have filed LCAs for control or automation engineers have already navigated the E-Verify and prevailing-wage process.
Benchmark your offer against prevailing wage data
Run the job title and your target metro area through the OFLC Wage Search before evaluating offers. Employers sponsoring STEM OPT workers who later file for H-1B visa must meet DOL prevailing-wage thresholds, so an offer below Level I wages can create problems at the H-1B stage.
Use O*NET to align your resume with SOC codes
Senior Control Engineer maps to specific SOC codes in O*NET, which USCIS and DOL use to classify the role at H-1B petition time. Matching your resume's language to O*NET task descriptions for your target code strengthens continuity between your STEM OPT training plan and any future sponsorship petition.
Frequently Asked Questions
Does a Senior Control Engineer role qualify for the STEM OPT extension?
It depends on your degree, not just the job title. Your degree must appear on the STEM Designated Degree Program List and carry an eligible CIP code. Electrical, mechanical, and systems engineering degrees typically qualify. The role itself must also provide training directly related to that field of study, which you document in the I-983 training plan your employer signs.
What does the I-983 training plan need to include for a control engineering role?
The I-983 must connect your STEM degree's learning objectives to specific job duties you'll perform. For a Senior Control Engineer, that means describing how your coursework in control theory, instrumentation, or embedded systems applies to tasks like PLC logic development, process loop tuning, or HMI design. Vague descriptions tied to general engineering skills are frequently returned by DSOs for revision.
How do I confirm that a potential employer is enrolled in E-Verify?
Ask the recruiter or HR contact directly during the screening stage, before you invest time in technical interviews. E-Verify enrollment is required for any employer hiring STEM OPT workers, and not every company in automation or manufacturing has completed enrollment. You can also search the E-Verify employer search tool to check a company's enrollment status by name before applying.
What happens to my STEM OPT authorization if my H-1B is selected in the lottery but not yet effective?
If your employer files an H-1B petition before your STEM OPT expires and the petition is timely filed, the cap-gap provision extends your work authorization automatically until October 1, when the new fiscal year H-1B status takes effect. You can continue working as a Senior Control Engineer throughout that gap period without interruption, as long as you remain in the same qualifying role.
Where can I find Senior Control Engineer jobs at E-Verify enrolled companies?
Migrate Mate filters Senior Control Engineer listings by employers with verified E-Verify enrollment and DOL LCA filing history, so you're not applying to companies that can't legally employ STEM OPT workers. This saves time during the offer stage and helps you avoid discovering E-Verify gaps after you've already completed multiple interview rounds.