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Contract Manufacturing Jobs in Raleigh, NC (NOW HIRING)

Targan Inc

Manufacturing Quality Engineer II

Raleigh, NC · On-site

$72K - $93K/yr

Position Summary The Manufacturing / Quality Engineer is responsible for supporting and improving ... This document does not create an employment contract, implied or otherwise, other than an "at will ...

KBI Biopharma

ELN Administrator

Durham, NC · On-site

KBI Biopharma, Inc. (KBI) is a leading development and contract manufacturing organization serving the biopharmaceutical industry. We help Founded in 1996, the company is headquartered in Durham, USA ...

Air Clean Systems

Operations Manager

Creedmoor, NC · On-site

Manage financial costs of operations and look for cost effective solutions. * Assist in audits of potential contract manufacturing facilities and suppliers. * Aid in new product introduction from ...

AskBio

Process Engineer II

Durham, NC · On-site

The incumbent will onboard clinical programs into the MSAT laboratory, perform scale-up runs, and transfer programs to AskBio's contract manufacturing facility. Additionally, this position will be ...

SuCitta Stealth

Production Support Analyst

Cary, NC · On-site

Drives process improvement as it relates to contract manufacturing relationships, production execution, and the production/consumption posting process. Develops and maintains production records and ...

Capital Bank

Production Support Analyst

Cary, NC

Drives process improvement as it relates to contract manufacturing relationships, production execution, and the production/consumption posting process. Develops and maintains production records and ...

Capital Bank

Production Support Analyst

Cary, NC · On-site

... to contract manufacturing relationships, production execution, and the production/consumption posting process. • Develops and maintains production records and prepares management reports as ...

KBI Biopharma

IT Systems Specialist II

Durham, NC · On-site

KBI Biopharma, Inc. (KBI) is a leading development and contract manufacturing organization serving the biopharmaceutical industry. We help Founded in 1996, the company is headquartered in Durham, USA ...

Eaton

Contract Order Manager

Raleigh, NC · On-site

$69K - $101K/yr

Eaton's ES AMER ESS division is currently seeking a Contract Order Manager. This role is based out ... Eaton's Electrical Critical Power & Digital Infrastructure Division designs, manufactures, and ...

GRIFOLS, S.A.

Vice President, Quality

Clayton, NC · On-site

... contract manufacturers meet the desired quality attributes as verified in GT laboratories. • Responsible for the establishment of appropriate quality policies, standards, and practices for ...

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All JobsContract Manufacturing JobsContract Manufacturing Jobs in Raleigh, NC

Contract Manufacturing information

See Raleigh, NC salary details

$29.6K

$94.8K

$149.2K

How much do contract manufacturing jobs pay per year?

As of Jun 17, 2026, the average yearly pay for contract manufacturing in Raleigh, NC is $94,832.00, according to ZipRecruiter salary data. Most workers in this role earn between $75,800.00 and $117,100.00 per year, depending on experience, location, and employer.

What jobs pay $2000 a day?

In contract manufacturing, high-paying roles such as senior project managers, manufacturing directors, or specialized engineers can earn around $2,000 per day, especially with extensive experience, certifications, and leadership responsibilities. These roles often require advanced technical skills, industry knowledge, and sometimes long or flexible working hours.

What are the key skills and qualifications needed to thrive in the Contract Manufacturing position, and why are they important?

Excelling in contract manufacturing requires a solid understanding of production processes, supply chain management, and quality control, often backed by a degree in engineering, manufacturing, or business. Familiarity with ERP systems, manufacturing execution systems (MES), and ISO or GMP certifications is highly valued. Strong negotiation skills, attention to detail, and effective communication are essential soft skills. These competencies help ensure efficient production, seamless client collaboration, and adherence to quality and regulatory standards.

What is a contract manufacturing job description?

A contract manufacturing job involves producing goods on behalf of a client under a contractual agreement, often requiring skills in production processes, quality control, and adherence to specifications. Workers may operate machinery, monitor production lines, and ensure compliance with safety standards in a manufacturing environment.

How can I make 2000 a week working from home?

Contract manufacturing roles can offer high earning potential if you have specialized skills, equipment, or access to a network of clients. Achieving $2,000 weekly may require managing multiple projects, building a client base, and maintaining efficient production schedules, often involving technical knowledge and quality standards. Success depends on experience, industry demand, and your ability to scale operations remotely.

What is a Contract Manufacturing job?

A Contract Manufacturing job involves managing the production of goods through third-party manufacturers. Professionals in this role oversee vendor relationships, ensure quality control, negotiate contracts, and coordinate supply chain logistics. They work closely with suppliers to meet cost, production, and timeline requirements. This position is common in industries like pharmaceuticals, electronics, and consumer goods.

What does contract manufacturing do?

Contract manufacturing involves a company outsourcing the production of its goods to a third-party manufacturer. The contract manufacturer produces products according to the company's specifications, often handling tasks such as sourcing materials, assembly, and quality control, allowing the company to focus on design and marketing.

What types of companies or industries typically hire for contract manufacturing roles?

Contract manufacturing roles are in demand across a wide variety of industries, including pharmaceuticals, consumer goods, electronics, automotive, and food and beverage. Job seekers can expect to find opportunities with both specialized contract manufacturing organizations (CMOs) and large corporations that outsource aspects of their production processes. These positions often involve collaborating with diverse clients, managing production timelines, and ensuring adherence to high quality and regulatory standards. Working in this field can provide valuable exposure to multiple industries, offering strong potential for career advancement and skill development.

What are the most commonly searched types of Manufacturing jobs in Raleigh, NC? The most popular types of Manufacturing jobs in Raleigh, NC are:
What are popular job titles related to Contract Manufacturing jobs in Raleigh, NC? For Contract Manufacturing jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Contract Manufacturing jobs in Raleigh, NC look for? The top searched job categories for Contract Manufacturing jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Contract Manufacturing jobs? Cities near Raleigh, NC with the most Contract Manufacturing job openings:
Contract Manufacturing jobs near you
Infographic showing various Contract Manufacturing job openings in Raleigh, NC as of June 2026, with employment types broken down into 68% Full Time, 29% Part Time, and 3% Contract. Highlights an 79% Physical, 3% Hybrid, and 18% Remote job distribution, with an average salary of $94,832 per year, or $45.6 per hour.
KBI: US - QA Specialist II

KBI: US - QA Specialist II

KBI Biopharma, Inc.

Durham, NC • On-site

$55K - $86K/yr

Full-time

Posted 4 days ago

Job description

JOB SUMMARY
The Manufacturing Quality Assurance (MQA) Specialist is responsible for supporting the Manufacturing process and areas as part of a rapidly expanding GMP Contract Manufacturing Organization. MQA Specialists are expected to provide sound guidance to Manufacturing with respect to process, SISPQ of product, and risk. MQA Specialists share responsibility for the inspection readiness of the site. MQA Specialists are required to work on the cleanroom floor directly with the Manufacturing team to provide real time guidance and support. MQA Specialists are required to collaborate with Manufacturing and work on team initiatives. The MQA Specialist may also be responsible for coaching and mentoring as needed to foster a GMP compliant site. In addition to supporting Manufacturing, MQA Specialists are responsible for the execution of core activities, including but not limited to:
  • Executed Batch record review and approval
  • Logbook review and approval
  • Deviation Triage Record guidance and generation
  • Routine facility walkthroughs
  • Facility response for work compromising clean environment
  • SOP review
  • Bulk Fill Label reconciliation
  • Alarm response and acknowledgement
  • Support external client review and resolution of comments

JOB RESPONSIBILITIES
  • On the floor real time support of the Manufacturing process. This includes performance of compliance review of records (master batch records, executed batch records, and internal support records such as logbooks), aid in deviation determination/generation, general Quality guidance.
  • Works directly with manufacturing, the laboratory, and other departments responsible for GMP activities to support resolution of deviations and other compliance issues in a timely manner.
  • Support process improvement projects to include improving on the floor Quality activities, record review time, and batch release dates.
  • Performed Facility Walkthroughs including tracking and trending reoccurring observations.
  • Works directly with manufacturing, and other internal departments to support resolution of client comments in a timely manner in support of batch release activities.
  • Able to react to change productively and handle other essential tasks assigned.
  • Quality representation on interdepartmental meetings.

MQA Specialist role is dayshift, working 12 hours in duration 0700 - 1900 and operate on a 2, 2, 3 schedule to provide 24/7 site coverage.
Knowledge, Skills, Abilities
MQA Specialist I
- High School diploma or equivalent. Degree progression preferred.
- GMP / regulated industry / laboratory experience is required (approximate 1-3 years).
- Demonstrated ability to work in a team environment.
- Demonstrated ability to understand the manufacturing process.
- Ability to perform routine core MQA responsibilities.
- Review written procedures for accuracy and provide feedback as needed
MQA Specialist II
- Associate degree / Bachelor's degree strongly preferred or appropriate years of experience (approximate 4-6 years).
- Demonstrated ability to work in a team environment and strong communication skills within all levels of an organization.
- Demonstrated ability to represent Quality on interdepartmental meetings.
- Demonstrated knowledge of technical documents.
- Demonstrated ability to become qualified trainers.
- Ability to track and trend department metrics.
- Review written procedures for accuracy and provide feedback as needed
Salary: $55,000-$86,900
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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