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Masters In Biomedical Science Jobs in West End, NC

Kymanox

(Contract) Senior Process Engineer

Sanford, NC · On-site

$130 - $180/hr

The ideal candidate will have an advanced degree (e.g., Master of Science, Master of Engineering) in a science-related field such as Biomedical Engineering, Mechanical Engineering, or Chemical ...

All JobsMasters In Biomedical Science JobsMasters In Biomedical Science Jobs in West End, NC

Masters In Biomedical Science information

See West End, NC salary details

$58K

$86.8K

$128.3K

How much do masters in biomedical science jobs pay per year?

As of Aug 24, 2026, the average yearly pay for masters in biomedical science in West End, NC is $86,752.00, according to ZipRecruiter salary data. Most workers in this role earn between $64,900.00 and $128,300.00 per year, depending on experience, location, and employer.

What can you do with a master's in biomedical science?

A Masters in Biomedical Science prepares graduates for a variety of careers in healthcare, research, pharmaceuticals, biotechnology, and academia. With this degree, you can work as a research scientist, laboratory manager, clinical trials coordinator, or pursue further studies such as a PhD or medical degree. Graduates also find roles in regulatory affairs, medical writing, and public health organizations. The degree provides specialized knowledge and technical skills that are highly valued in both industry and academic settings.

What are the key skills and qualifications needed to thrive with a master's in biomedical science?

A Master's in Biomedical Science requires a solid background in biology, laboratory research methods, and data analysis, usually supported by a relevant undergraduate degree. Familiarity with laboratory equipment, molecular biology techniques, and software such as SPSS or GraphPad Prism is common in this field. Critical thinking, attention to detail, and effective communication set professionals apart when interpreting results and presenting findings. These skills are crucial for conducting accurate research, advancing scientific knowledge, and contributing to healthcare innovations.

What types of career paths can a professional with a master's in biomedical science pursue within the healthcare and research sectors?

With a Master's in Biomedical Science, you can pursue a variety of roles such as research scientist, clinical laboratory technologist, regulatory affairs specialist, and medical science liaison. Many graduates work in hospitals, academic research labs, biotechnology firms, or pharmaceutical companies, often collaborating with clinicians, researchers, and regulatory professionals. The work environment is typically team-oriented and project-driven, offering opportunities to participate in cutting-edge research, support clinical trials, or ensure compliance with healthcare regulations. This degree also provides a strong foundation for further study, such as pursuing a PhD or professional healthcare degree.

What is the difference between Masters In Biomedical Science vs Medical Laboratory Technician?

AspectMasters In Biomedical ScienceMedical Laboratory Technician
Required CredentialsMaster's degree in biomedical science or related fieldAssociate's degree or post-secondary certificate in medical laboratory technology
Work EnvironmentResearch labs, universities, biotech companiesHospital labs, diagnostic labs, clinics
Employer & Industry UsageResearch institutions, academia, biotech firmsHealthcare facilities, hospitals, diagnostic centers

Masters In Biomedical Science typically involves advanced research and laboratory work in biomedical fields, often requiring a master's degree. Medical Laboratory Technicians focus on performing diagnostic tests in clinical settings with an associate's or certificate. Both roles are essential in healthcare and research, but they differ in education level, job responsibilities, and work environment.

Is a master's in biomedical science worth it?

A master's in biomedical science can enhance job prospects in research, healthcare, and biotech fields, often leading to roles such as laboratory technician, research associate, or clinical scientist. It provides specialized knowledge and skills that can improve employability and earning potential, especially when combined with relevant experience and certifications.

What cities near West End, NC are hiring for Masters In Biomedical Science jobs?

Cities near West End, NC with the most Masters In Biomedical Science job openings:

Masters In Biomedical Science jobs near you
Infographic showing various Masters In Biomedical Science job openings in West End, NC as of August 2026, with employment types broken down into 1% As Needed, 73% Full Time, 24% Part Time, and 2% Contract. Highlights an 74% Physical, 3% Hybrid, and 23% Remote job distribution, with an average salary of $86,752 per year, or $41.7 per hour.

(Contract) Principal Process Engineer

Kymanox

Sanford, NC • On-site

Contractor

Posted 12 days ago

Job description

Job Description:
Is Kymanox the right fit for you?
You want to make a difference and have an impact...
You enjoy having an influence in your day-to-day work...
You are motivated by working alongside a team filled with
subject matter experts who will help you learn and grow...
You wake up every day and do what you do
... because patients deserve better.
If this sounds like you, you've come to the right place.
The Principal Process Engineer will join our CMC & Pharmaceutical Sciences team and lead the design, development, and optimization of manufacturing processes for pharmaceutical products, including both drug substance and drug product processes for multiple modalities of drug products. . This role requires expertise in process engineering principles, regulatory compliance, quality assurance, and technical leadership. The successful candidate will drive process improvements while collaborating with cross-functional teams including Quality, Operations, and Regulatory Affairs. In addition to support from a direct, functional manager, work will also be done under the guidance of a senior Kymanox engineer and/or senior project manager.
100% onsite in Sanford.
Responsibilities:
  • Develop technical documentation for drug substance and drug product manufacturing across multiple product modalities (e.g., small molecule, biologics, gene therapies) including SOPs, CMC regulatory filings, manufacturing records, technical reports, process validation and technology transfer documents.
  • Design and develop manufacturing processes from concept through commercial implementation, utilizing industry best practices and regulatory guidelines (FDA, ICH, and other applicable standards).
  • Lead root cause analysis and implement continuous improvement initiatives to enhance process efficiency, reduce costs, and improve product quality and yield.
  • Create and maintain comprehensive process documentation including process flow diagrams, risk assessments, standard operating procedures (SOPs), batch records, and validation protocols.
  • Plan, execute, and oversee process validation studies (IQ/OQ/PQ) and technology transfer activities; ensure full regulatory compliance throughout the validation lifecycle.
  • Evaluate and select manufacturing equipment, conduct vendor assessments, and oversee equipment installation, qualification, and integration into production workflows.
  • Ensure all processes comply with cGMP, FDA regulations, and company quality systems; support regulatory submissions and maintain audit readiness.
  • Partner with Quality, Operations, Product Development, Regulatory Affairs, and Supply Chain teams to ensure seamless process execution and continuous improvement.
Educational Background:
  • The ideal candidate will have an advanced degree (e.g., Master of Science, Master of Engineering) in a science-related field such as Biomedical Engineering, Mechanical Engineering, or Chemical Engineering.
Experience:
  • 10+ years of experience in the pharmaceutical or combination products industry.
  • Demonstrated expertise in drug substance and drug product process development, process optimization, and continuous improvement methodologies.
  • Strong knowledge of cGMP regulations, FDA guidance documents, and quality systems
  • Excellent technical writing and documentation skills. Ability to independently support development of technical documentation such as SOPs, batch records, validation protocols, technical reports, and CMC-related content.
  • Strong problem-solving abilities with proven analytical thinking.
  • Effective communication and interpersonal skills with ability to work across departments
  • Experience with MS Office products (Outlook, Excel, PowerPoint, Word) strongly preferred.
Desired Aptitude and Skill Set:
  • Detail-oriented
  • Strong organizational skills and verbal/written communication skills
  • Highly motivated self-starter with a sense of ownership and willingness to learn
  • Thrive in a fast-paced, growing, and dynamic work environment
  • Ability to form partnerships with internal stakeholders
  • Seasoned soft skills (i.e., high EQ)
  • Technology savvy
Travel:
Up to 10% travel is possible for support at tradeshows, conferences, and related events. A passport is required for this job.
Employment Type: Contractor

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