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Commission Pharmaceutical Biomedical Engineer Jobs

The Health Sensing Hardware team is looking for a highly-motivated optical engineer to work on the ... Additionally, this role might be eligible for discretionary bonuses or commission payments as well ...

We are seeking a Biomedical Engineering Specialist to: * Diagnose defective medical equipment and ... Commission and other accrediting agencies. * Assist with creating and conducting new device ...

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Commission Pharmaceutical Biomedical Engineer information

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$41K

$94.8K

$140K

How much do commission pharmaceutical biomedical engineer jobs pay per year?

As of Aug 14, 2026, the average yearly pay for commission pharmaceutical biomedical engineer in the United States is $94,807.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,500.00 and $116,000.00 per year, depending on experience, location, and employer.

What is the difference between Commission Pharmaceutical Biomedical Engineer vs Commission Biomedical Engineer?

AspectCommission Pharmaceutical Biomedical EngineerCommission Biomedical Engineer
CredentialsEngineering degree, biomedical or pharmaceutical certificationsEngineering degree, biomedical certifications
Work EnvironmentPharmaceutical manufacturing, hospitals, research labsHospitals, medical device companies, research labs
Employer & IndustryPharmaceutical companies, biotech firmsMedical device manufacturers, healthcare facilities
Search & Comparison IntentUnderstanding roles in pharmaceutical and biomedical fieldsGeneral biomedical engineering roles

The Commission Pharmaceutical Biomedical Engineer focuses on integrating pharmaceutical processes with biomedical engineering, often working in drug manufacturing and research. In contrast, the Commission Biomedical Engineer has a broader scope, working across various healthcare and medical device sectors. Both roles require similar credentials but differ mainly in industry focus and work environment.

What are the key skills and qualifications needed to thrive as a commission pharmaceutical biomedical engineer, and why are they important?

To excel as a Commission Pharmaceutical Biomedical Engineer, you need a solid background in biomedical engineering, pharmaceutical sciences, and regulatory compliance, often supported by a relevant degree and engineering licensure. Familiarity with validation protocols, GMP standards, CAD software, and laboratory instrumentation is typically required. Strong problem-solving skills, attention to detail, and effective communication are vital soft skills for this role. These competencies ensure safe, compliant, and innovative solutions in pharmaceutical manufacturing and biomedical device environments.

What is a commission pharmaceutical biomedical engineer?

A Commission Pharmaceutical Biomedical Engineer is a professional who specializes in designing, developing, and maintaining medical devices, equipment, and technologies used in pharmaceutical settings. They ensure that biomedical systems comply with regulatory standards and are safe for use in drug development and production. These engineers often work closely with scientists, regulatory authorities, and manufacturing teams to optimize processes and implement innovative solutions. The 'commission' aspect refers to their responsibility in overseeing the installation and validation of new equipment or systems before they are put into full operation.

What are the main challenges faced by a commission pharmaceutical biomedical engineer when collaborating with cross-functional teams during facility validation?

As a Commission Pharmaceutical Biomedical Engineer, you'll frequently work with multidisciplinary teams, including quality assurance, production, and regulatory specialists, to ensure new pharmaceutical facilities and equipment meet stringent validation standards. A key challenge is aligning diverse technical perspectives and requirements while maintaining compliance with industry regulations, such as Good Manufacturing Practice (GMP). Clear communication and strong project management skills are essential to coordinate timelines, address technical discrepancies, and document validation results comprehensively. This collaborative environment is rewarding but can be demanding, especially when managing multiple projects with tight deadlines.

What cities are hiring for Commission Pharmaceutical Biomedical Engineer jobs?

Cities with the most Commission Pharmaceutical Biomedical Engineer job openings:

What are the most commonly searched types of Pharmaceutical Biomedical Engineer jobs?

The most popular types of Pharmaceutical Biomedical Engineer jobs are:

What states have the most Commission Pharmaceutical Biomedical Engineer jobs?

States with the most job openings for Commission Pharmaceutical Biomedical Engineer jobs include:

Process & Cleaning Validation Specialist, Technical Services

Amneal Pharmaceuticals

Piscataway, NJ • On-site

$80K - $90K/yr

Full-time

Medical, Retirement

Re-posted 3 days ago


Amneal Pharmaceuticals rating

6.7

Company rating: 6.7 out of 10

Based on 12 frontline employees who took The Breakroom Quiz

74th of 86 rated pharmaceutical


Job description

Description:

Process Engineer reports to the Manager of Technical Services and plans, executes and functionally directs Process/Cleaning Validation/Study assignments and projects, which require sound pharmaceutical/engineering skills and independent judgment. Works as a team member, educates internal partners on the projects, monitors and executes. Maintains effective and cooperative relationships with all departments within and outside the organization. Managing the post approval projects.


Essential Functions:

  • Prepare validation protocols & reports for manufacturing process and cleaning process qualification, data analysisand prepare reports; execute the manufacturing process and cleaning process qualification/validation/study.
  • Managing the post approval projects. coordinating with cross functional Teams and ensuring the timely completion of projects.
  • Analyzes statistical data, products or functional specifications to determine conformance with standards andestablished quality requirements
  • Coordinate/oversee the development of new processes or troubleshoot existing ones
  • Assist in deviation/investigations to identify root causes and define corrective and/or preventative actions (CAPA) & assist in various audits


Additional Responsibilities:

  • Initiation of Change Controls and Planned Deviations when required

Education:

  • Bachelors Degree (BA/BS) Pharmaceutical/Biomedical Engineering - Required
  • Master Degree (MS/MA) Pharmaceutical/Biomedical Engineering - Preferred

Experience:

  • 2 years or more in Pharmaceutical/Manufacturing Industry

Skills:

  • Excellent verbal and written communication skills - Advanced
  • Proficiency in MS Word/Excel/ PowerPoint/MS project - Advanced

Specialized Knowledge:

  • Basic Analytical Knowledge desirable. In-depth knowledge of manufacturing equipment and processes for Solid Oral, Medical Device, Transdermal, Topical and Liquid Orals.

The base salary for this position ranges from $80,000 to $90,000 per year.   Amneal ranges reflect the Company's good faith estimate of base salary that Amneal reasonably believes that it will pay for said position at the time of the posting.  Individual compensation will ultimately be determined based on a variety of relevant factors, including but not limited to, qualifications, geographic location and other relevant skills.  At the heart of our Total Rewards commitment is a comprehensive, flexible and competitive benefits program for eligible positions that enables you to choose the plans and coverage that meet your personal needs. This includes above-market, diverse and robust health and insurance benefits to meet the varied needs of our employees as well as a significant 401(k) matching contribution to help our employees save for retirement.  We also promote employee well-being with programs that helps you enjoy your career alongside life's many other commitments and opportunities.


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