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Biopharmaceutical Jobs in Raleigh, NC (NOW HIRING)

Manufacturing Assistant I

Durham, NC · On-site

$18.75 - $23.56/hr

KBI Biopharma is committed to providing a safe and healthy workplace. Any employee entering a KBI site located in the US must inform KBI Biopharma of their vaccination status and must submit their ...

KBI: US - Scientist I

Durham, NC · On-site

$86K - $115K/yr

At KBI Biopharma, we are advancing science and accelerating breakthroughs. As a global leader in biopharmaceutical development and manufacturing, we empower life science companies to bring new ...

New

Scientist I

Durham, NC · On-site

$84K - $115K/yr

KBI Biopharma is seeking a highly skilled and motivated Analytical Scientist to join our Analytical and Formulation Sciences (AFS) team in Durham, NC. This role is ideal for a PhD-level scientist ...

Scientist I

Durham, NC · On-site

$84K - $115K/yr

KBI Biopharma is seeking a highly skilled and motivated Analytical Scientist to join our Analytical and Formulation Sciences (AFS) team in Durham, NC. This role is ideal for a PhD-level scientist ...

Showing results 21-40

Biopharmaceutical information

See Raleigh, NC salary details

$32.4K

$97.8K

$144K

How much do biopharmaceutical jobs pay per year?

As of Aug 12, 2026, the average yearly pay for biopharmaceutical in Raleigh, NC is $97,824.00, according to ZipRecruiter salary data. Most workers in this role earn between $80,226.00 and $115,022.00 per year, depending on experience, location, and employer.

What is a biopharmaceutical?

Biopharmaceuticals are medical drugs produced using biotechnology, typically involving proteins (including antibodies), nucleic acids, or living cells as active ingredients, rather than being chemically synthesized. These products are used to treat a variety of diseases and conditions, such as cancer, autoimmune disorders, and genetic diseases. Common examples include monoclonal antibodies, vaccines, and recombinant proteins like insulin. Biopharmaceuticals often offer targeted therapies with improved efficacy and reduced side effects compared to traditional drugs. Their development and manufacturing require highly specialized techniques and strict regulatory oversight.

How to get into biopharmaceuticals?

To enter the biopharmaceutical industry, candidates typically need a relevant degree such as biology, chemistry, or biomedical engineering. Gaining experience through internships, entry-level positions, or certifications in Good Manufacturing Practices (GMP) and laboratory skills can improve job prospects. Strong analytical skills, attention to detail, and familiarity with laboratory equipment are also valuable.

What cross-functional collaborations can a biopharmaceutical professional expect, and how do they impact daily responsibilities?

Biopharmaceutical professionals frequently collaborate with teams across research, clinical development, regulatory affairs, manufacturing, and marketing. These collaborations are essential for advancing drug candidates from discovery through clinical trials and ultimately to market. On a daily basis, you might participate in interdisciplinary project meetings, contribute to regulatory documentation, and coordinate timelines to ensure product development milestones are met. Effective communication and teamwork are crucial, as the role often involves aligning scientific objectives with regulatory requirements and commercial strategies.

What key skills and qualifications are needed to thrive in a biopharmaceutical career?

To thrive in the biopharmaceutical industry, you need a strong background in life sciences, chemistry, or engineering, often with a relevant degree or advanced qualification. Familiarity with laboratory techniques, Good Manufacturing Practices (GMP), and regulatory compliance systems like FDA or EMA guidelines is typically required. Attention to detail, problem-solving abilities, and effective teamwork set standout professionals apart. These skills ensure safe, effective drug development and regulatory approval in a highly regulated and innovative environment.

What can you do with a biopharmaceutical degree?

A biopharmaceutical degree prepares individuals for roles in drug development, research, manufacturing, quality control, and regulatory affairs within the pharmaceutical and biotech industries. Graduates can work as research scientists, quality assurance specialists, clinical trial coordinators, or regulatory compliance officers, often utilizing laboratory skills and industry-specific certifications. The degree provides a foundation for careers focused on developing and ensuring the safety and efficacy of biopharmaceutical products.

What is the difference between Biopharmaceutical vs Pharmacist?

AspectBiopharmaceuticalPharmacist
Required CredentialsBiopharmaceutical degrees, biotech certificationsDoctor of Pharmacy (PharmD), state licensure
Work EnvironmentLaboratories, biotech companies, research facilitiesPharmacies, hospitals, healthcare settings
Industry UsageBiotech, pharmaceutical manufacturing, R&DHealthcare, retail pharmacy, clinical services

While both roles are integral to the pharmaceutical industry, biopharmaceutical professionals focus on developing and manufacturing biologic drugs in research and production settings. Pharmacists, on the other hand, primarily dispense medications and provide patient care in healthcare environments. Understanding these differences helps job seekers identify the right career path based on credentials, work environment, and industry focus.

What are the most commonly searched types of Biopharmaceutical jobs in Raleigh, NC? The most popular types of Biopharmaceutical jobs in Raleigh, NC are:
What are popular job titles related to Biopharmaceutical jobs in Raleigh, NC? For Biopharmaceutical jobs in Raleigh, NC, the most frequently searched job titles are:
What cities near Raleigh, NC are hiring for Biopharmaceutical jobs? Cities near Raleigh, NC with the most Biopharmaceutical job openings:
Infographic showing various Biopharmaceutical job openings in Raleigh, NC as of August 2026, with employment types broken down into 89% Full Time, 6% Part Time, 1% Temporary, and 4% Contract. Highlights an 85% Physical, 4% Hybrid, and 11% Remote job distribution, with an average salary of $97,824 per year, or $47 per hour.

QA Manufacturing Specialist II (Nights)

KBI Biopharma, Inc.

Durham, NC • On-site

Full-time

Re-posted 21 days ago


KBI Biopharma rating

6.5

Company rating: 6.5 out of 10

Based on 6 frontline employees who took The Breakroom Quiz


Job description

Please Note: This is a night shift opportunity that follows a 2-2-3 schedule

Job Summary

The QA Manufacturing Specialist II (Nights) is responsible for ensuring raw materials, products, processes, facilities, documentation, and systems conform to quality standards, internal procedures, systems, and governmental regulations.

This position will provide a broad range of quality oversight for activities that support bulk drug substance manufacturing. This position will be responsible for on the floor review of executed records (batch record section review, solution records, equipment records, and logbooks) supporting all aspects of cGMP operations. Client and regulatory audit/inspection support is also within job scope.

Job Responsibilities

  • Perform on-the-floor compliance review on executed records including batch records, equipment preparation records, and solution record and associated forms, in-process data, and logbooks.

  • Perform activities such as manufacturing walk-throughs, facility responses, label reconciliation, etc.

  • Support Manufacturing changeover process.

  • Work directly with manufacturing, the laboratory and other departments responsible for GMP activities to resolve deviations, CAPAs, and other compliance issues in a timely manner

  • Support client audits and regulatory inspections and client batch record review process.

  • Support QA Raw Material group with release of raw materials

  • Able to react to change productively and handle other essential tasks as assigned.

  • Review document revisions (SOPs, Forms, Solution Records, etc)

  • Supports training of other Quality department staff to perform quality duties as needed.

  • Support process improvement projects to include improving the lifecycle of batch record review cycle times and batch release dates.

Minimum Requirements

  • MQA Specialist II: BS/BA in scientific field and 5 years experience or MS/MA degree and 3 years' experience in a QA GMP regulated environment within Biopharmaceuticals or equivalent is required.

  • Knowledge of US and EU cGMP guidelines/regulations is desired.

  • Experience with electronic document management systems, SAP and Microsoft Office suite are preferred.

  • Demonstrated strong interpersonal skills, ability to work in a team environment, attention to details and excellent problem resolutions skills.

  • Knowledge of biopharmaceutical manufacturing including cell culture, protein purification, and single-use platform technology is preferred.

KBI Biopharma, Inc. is an EEO/AA employer and actively seeks to diversify its work force. Therefore, all qualified applicants, regardless of race, color, national origin, religion, gender, gender identity, sexual orientation, age, disability or veteran status, are strongly encouraged to apply.

I understand that neither the completion of this application nor any other part of my consideration for employment establishes any obligation for KBI Biopharma, Inc. to hire me. If I am hired, I understand that either KBI Biopharma, Inc. or I can terminate my employment at any time and for any reason, with or without cause and without prior notice. I understand that no representative of KBI Biopharma, Inc. has the authority to make any assurance to the contrary.

I attest with my signature below that I have given to KBI Biopharma, Inc. true and complete information on this application. No requested information has been concealed. I authorize KBI Biopharma, Inc. to contact references provided for employment reference checks. If any information I have provided is untrue, or if I have concealed material information, I understand that this will constitute cause for the denial of employment or immediate dismissal.


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