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Biopharmaceutical Manufacturing Associate Jobs in Roxboro, NC

MSD

Senior Technician Operations, 2nd Shift

Durham, NC · On-site

$63K - $100K/yr

Minimum Associates Degree in science or related field * Bioworks Certificate (working in an FDA or ... Biopharmaceutical Manufacturing, Biopharmaceutical Manufacturing, Business Process Management (BPM ...

KBI Biopharma, Inc.

Manufacturing Assistant

Durham, NC · On-site

$16.50 - $21.25/hr

At KBI Biopharma, we are advancing science and accelerating breakthroughs. As a global leader in ... High School Diploma or Associates Degree with 0+ years of experience. * Weekends, holidays ...

KBI Biopharma, Inc.

Manufacturing Assistant

Durham, NC · On-site

$16.50 - $21.25/hr

At KBI Biopharma, we are advancing science and accelerating breakthroughs. As a global leader in ... High School Diploma or Associates Degree with 0+ years of experience. * Weekends, holidays ...

KBI Biopharma, Inc.

Manufacturing Assistant I

Durham, NC · On-site

$18.75 - $23.56/hr

High School diploma or Associates Degree with 0+ years of experience. Bioworks certificate ... KBI Biopharma is committed to providing a safe and healthy workplace. Any employee entering a KBI ...

KBI Biopharma, Inc.

Manufacturing Assistant I

Durham, NC · On-site

$18.75 - $23.56/hr

High School diploma or Associates Degree with 0+ years of experience. Bioworks certificate ... KBI Biopharma is committed to providing a safe and healthy workplace. Any employee entering a KBI ...

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All JobsBiopharmaceutical Manufacturing Associate JobsBiopharmaceutical Manufacturing Associate Jobs in Roxboro, NC

Biopharmaceutical Manufacturing Associate information

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$16

$23

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How much do biopharmaceutical manufacturing associate jobs pay per hour?

As of Aug 21, 2026, the average hourly pay for biopharmaceutical manufacturing associate in Roxboro, NC is $23.86, according to ZipRecruiter salary data. Most workers in this role earn between $20.29 and $27.93 per hour, depending on experience, location, and employer.

What is a biopharmaceutical manufacturing associate?

As a biopharmaceutical manufacturing associate, your primary responsibilities are to prepare equipment and materials for the production of biopharmaceutical products. Your duties include moving the product, supplies, and inventory to support the manufacturing process and operating devices like autoclaves and washers. You monitor the production and operations, make adjustments to increase efficiency, and ensure that you are meeting all safety regulations. You work with downstream and upstream processes to control quality. You are also in charge of preparing reports and reviewing GMP documents to ensure compliance with laws and industry regulations.

What does a biopharmaceutical manufacturing associate do?

A Biopharmaceutical Manufacturing Associate is responsible for producing biopharmaceutical products such as vaccines, antibodies, or therapeutic proteins under strict regulatory guidelines. Their tasks typically include preparing equipment, monitoring production processes, maintaining sterile environments, and ensuring that all procedures adhere to Good Manufacturing Practices (GMP). They may also be involved in quality control, documentation, and troubleshooting equipment issues. This role is crucial for ensuring the safety, efficacy, and quality of biopharmaceutical products.

What are the key skills and qualifications needed to thrive as a biopharmaceutical manufacturing associate?

To thrive as a Biopharmaceutical Manufacturing Associate, you need a solid background in life sciences or engineering, with knowledge of GMP (Good Manufacturing Practices) and often a relevant bachelor’s degree or associate’s certification. Familiarity with bioprocessing equipment, automation systems like SCADA, and quality control tools is essential. Attention to detail, teamwork, and strong communication skills are crucial soft skills for this role. These competencies ensure the safe, accurate, and compliant production of high-quality biopharmaceutical products.

What are some common challenges faced by biopharmaceutical manufacturing associates, and how can they be addressed?

Biopharmaceutical Manufacturing Associates often encounter challenges such as maintaining strict adherence to Good Manufacturing Practices (GMP) and troubleshooting equipment malfunctions under tight production schedules. To address these challenges, associates are trained extensively on standard operating procedures and cross-functional communication to quickly resolve issues. Teamwork and attention to detail are essential, as the role frequently involves collaborating with quality assurance, engineering, and process development teams to ensure product safety and compliance. Continuous learning and proactive problem-solving are key to success in this dynamic environment.

What is the difference between Biopharmaceutical Manufacturing Associate vs Quality Control Technician?

AspectBiopharmaceutical Manufacturing AssociateQuality Control Technician
Primary RoleSupports production processes, prepares materials, and ensures manufacturing runs smoothlyPerforms testing and inspection of products to ensure quality standards
Required SkillsKnowledge of GMP, aseptic techniques, and manufacturing proceduresLaboratory skills, attention to detail, knowledge of testing methods
Work EnvironmentCleanrooms, manufacturing floors, production facilitiesLaboratories, testing labs, quality control areas
CertificationsGMP training, sometimes cGMP certificationLab safety, GMP, and quality assurance training

The Biopharmaceutical Manufacturing Associate focuses on supporting the production process in manufacturing environments, while the Quality Control Technician specializes in testing and verifying product quality. Both roles require GMP knowledge and work in regulated settings, but their daily tasks and skill sets differ significantly.

More about Biopharmaceutical Manufacturing Associate jobs

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The top searched job categories for Biopharmaceutical Manufacturing Associate jobs in Roxboro, NC are:

What cities near Roxboro, NC are hiring for Biopharmaceutical Manufacturing Associate jobs?

Cities near Roxboro, NC with the most Biopharmaceutical Manufacturing Associate job openings:

Biopharmaceutical Manufacturing Associate jobs near you
Infographic showing various Biopharmaceutical Manufacturing Associate job openings in Roxboro, NC as of August 2026, with employment types broken down into 1% As Needed, 68% Full Time, 26% Part Time, 1% Temporary, 3% Contract, and 1% Nights. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $49,626 per year, or $23.9 per hour.

Manufacturing Support Associate I/II

KBI Biopharma, Inc.

Durham, NC • On-site

Full-time

Posted 18 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

JOB SUMMARY
*Dayshift, 7am-7pm, 2-2-3 rotating schedule
The Manufacturing Support Associate I/II position is designed as an introduction to the environment of cGMP manufacturing. This position performs all routine/nonroutine cleanings of the GMP Facilities, manages Process Waste, and continuously supports the manufacturing operations. This position requires a 12-hour shift schedule. Aseptic and Gowning Qualifications are required for this position. Must be able to document and maintain records to comply with regulatory requirements, cGMP's, Policy Documents and SOPs.
JOB RESPONSIBILITIES
Responsibility of Time Performs and Maintains Manufacturing facilities by routine/nonroutine cleanings. Cleans, operates and maintains the Process Waste area. Ensures cleanliness of the area and discards waste materials within the area. Cleans drums and dollies as required. Prepare, build and complete processing assemblies (PAR) for production. Completes Facilities response forms and ensures communication to inform other departments requiring EM sampling if required. Stock general supplies in the manufacturing production areas. Handling and discarding of hazardous and nonhazardous waste.
JOB REQUIREMENTS
  • Manufacturing Support Associate Level I: High School Diploma or Associate Degree with 0+ years of experience.
  • Manufacturing Support Associate II: High School Diploma or Associate Degree with 2+ years of experience.

Language Ability
Ability to read and interpret English documents such as safety rules, standard operating procedures, and procedure manuals. Ability to write routine reports and correspondence. Ability to communicate with coworkers and supervisors.
Reasoning Ability
Ability to apply common sense understanding to carry out instructions furnished in written, oral, or diagram form. Ability to deal with problems involving several concrete variables in standardized situations.
Math Ability
Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals. Ability to compute ratio and percent.
Physical Demands
Must be able to stand, walk, wear steel toe shoes and have the ability to push, pull, squat, lift, reach and carry waste as needed, but not to exceed the Essential Physical functions of the job description.
Computer Skills
  • Word, Excel, E-mail
  • Equipment Use Computer, Telephone, Copy and Fax Machine

WORKING CONDITIONS:
Due to the use of Spor-Klenz, respirators (full faced and half faced respirators) are required for the job description, facial hair needs to be maintained short enough to ensure a good seal to properly wear the respirator.
The job requires working 12-hour shifts which may include working overnight. The job requires working within a cGMP manufacturing biotechnology facility which requires clean room operations. Clean room operations require donning clean room attire when entering clean room areas and maintaining good personal hygiene. While performing the duties of this job the employee regularly utilizes equipment and materials which include mechanical hazards, chemical hazards, electricity hazards, and tripping and falling hazards. The noise level in the environment is moderate to high.
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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