Associate Manufacturing

Spectraforce Technologies; Holly Springs (NC); On-site; USD 24,796 - 44,083; Full time

Job summary

Spectraforce Technologies is seeking an Associate Manufacturing in Holly Springs, NC, to support the client’s cGMP drug substance operations. The initial schedule runs Monday–Thursday or Tuesday–Friday, 10-hour days, with a shift rotation implemented after startup.

This is an onsite position focused on manufacturing in a regulated environment. You will perform hands-on floor operations, maintain clean facilities, and follow SOPs/MPs/JHAs/CFR guidelines to ensure compliant production and accurate

Qualifications

• High school diploma / GED + 1 year of manufacturing and/or other regulated experience.
• Associate’s degree.
• High school/GED + 2 years work experience.
• Associate’s degree and 6 months work experience.
• Bachelor’s degree.

Responsibilities

• Compliance: Completes work in accordance with established cGMP procedures and policies (Standard Operating Procedures SOPs, Manufacturing Procedures MPs, Job Hazard Analysis JHAs, Code of Federal Regulations CFR) with strict adherence to safety and compliance.
• Ensure proper gowning and aseptic techniques are always followed.
• Perform hands‑on operation including set‑up, cleaning, sanitization, monitoring of equipment and assigned area.
• Buffer and Media preparation and transfer.
• Weigh and dispense materials to be used in the preparation of Buffers and Medias.
• Complete washroom activities: cleaning equipment, small to large scale, use in production activities.
• Run and monitor critical process per assigned procedures.
• Perform documentation for assigned function (i.e., equipment logs, EBRs).
• Maintain an organized, clean, and workable space.

Skills

Experience in regulated industry

GMP principles

Verbal and written communication

Microsoft Office

Education

High school diploma / GED

Associate’s degree

Bachelor’s degree

High school/GED + 2 years work experience

Associate’s degree and 6 months work experience

Tools

Microsoft Office

Job description

Associate Manufacturing

Duration: 11+ Months (Extension possible)

Location: Holly Springs, NC 27540

Work Arrangement: Fully Onsite

Ideal Candidate

• High school diploma / GED + 1 year of manufacturing and/or other regulated experience.

Job Description

In this vital role you will be an Associate Manufacturing in the manufacturing organization at the client's North Carolina (ANC). The initial schedule will be Monday-Thursday or Tuesday-Friday, 10 hour days. The schedule will transition to shifts (rotating 2-2-3, 12 hour shifts) upon completion of startup activities and as business needs dictate. You will be completing operations on the floor in Services area and are responsible for the manufacturing of cGMP (current Good Manufacturing Practices) drug substance.

With general direction, the Associate Manufacturing will support all floor operations in accordance with cGMP practices.

Responsibilities

• Compliance: Completes work in accordance with established cGMP procedures and policies (Standard Operating Procedures SOPs, Manufacturing Procedures MPs, Job Hazard Analysis JHAs, Code of Federal Regulations CFR) with strict adherence to safety and compliance.
• Ensure proper gowning and aseptic techniques are always followed.
• Perform hands‑on operation including set‑up, cleaning, sanitization, monitoring of equipment and assigned area.
• Buffer and Media preparation and transfer.
• Weigh and dispense materials to be used in the preparation of Buffers and Medias.
• Complete washroom activities: cleaning equipment, small to large scale, use in production activities.
• Run and monitor critical process per assigned procedures.
• Perform documentation for assigned function (i.e., equipment logs, EBRs).
• Maintain an organized, clean, and workable space.

Basic Qualifications

• High school diploma / GED + 1 year of manufacturing and/or other regulated experience.
• Associate’s degree.
• High school/GED + 2 years work experience.
• Associate’s degree and 6 months work experience.
• Bachelor’s degree.

Preferred Qualifications

• Team Player.
• Attention to detail.
• Ability to follow detailed work instructions (SOPs).
• Self Starter, Motivated, Curious (want to understand the why).

Must Have Skill Sets

• Experience in a regulated industry such as biotechnology or pharmaceutical.
• Basic understanding of GMP principles.
• Strong verbal and written communication skills.
• Proficient Microsoft Office skills.

Possible Extension

Yes