Job Title: Night Shift Associate ManufacturingJob Description
The Night Shift Associate Manufacturing plays a vital role in the on-site manufacturing organization, supporting the production of cGMP (current Good Manufacturing Practices) drug substance in a regulated environment. Working on a rotating night shift schedule, this position focuses on hands-on floor operations in the Services area, ensuring all activities comply with strict safety, quality, and regulatory standards.
Responsibilities
Complete all work in accordance with established cGMP procedures, Standard Operating Procedures (SOPs), Manufacturing Procedures (MPs), Job Hazard Analysis (JHAs), and applicable Code of Federal Regulations (CFR), maintaining strict adherence to safety and compliance requirements.
Follow proper gowning requirements and aseptic techniques at all times to support a controlled and compliant manufacturing environment.
Perform hands-on operations on the manufacturing floor, including equipment set-up, cleaning, sanitization, and routine monitoring of equipment and assigned areas.
Prepare and transfer buffers and media according to defined procedures, ensuring accurate measurements and adherence to quality standards.
Weigh and dispense materials used in the preparation of buffers and media with high attention to detail and documentation accuracy.
Complete washroom activities, including cleaning and handling equipment ranging from small to large scale that is used in production activities.
Run and monitor critical manufacturing processes according to assigned procedures, promptly identifying and reporting any deviations or issues.
Perform documentation activities for assigned functions, including maintaining equipment logs and completing electronic batch records (EBRs) in a timely and accurate manner.
Maintain an organized, clean, and workable space, supporting good housekeeping practices and readiness for inspections or audits.
Collaborate with team members to ensure smooth shift operations and effective handovers, communicating clearly about process status and any concerns.
Follow detailed work instructions and SOPs consistently, seeking clarification when needed to ensure correct execution of tasks.
Demonstrate curiosity and a desire to understand the underlying processes and rationale behind procedures, contributing to continuous improvement.
Essential Skills
High school diploma or GED with at least 1 year of manufacturing and/or other regulated industry experience, or equivalent combination of education and experience as outlined in qualifications.
Experience working in a cGMP or other regulated environment, with familiarity in following strict procedures and compliance requirements.
Ability to follow detailed work instructions, SOPs, and manufacturing procedures accurately and consistently.
Strong attention to detail in performing measurements, documentation, and equipment operations.
Capability to perform hands-on work, including equipment set-up, cleaning, sanitization, and monitoring in a manufacturing setting.
Basic understanding of buffer and media preparation, material weighing, and dispensing processes.
Ability to maintain accurate documentation, including equipment logs and electronic batch records (EBRs).
Reliability and readiness to work a rotating night shift schedule with 12-hour shifts.
Team-oriented mindset with the ability to collaborate effectively with colleagues in a fast-paced production environment.
Additional Skills & Qualifications
High school diploma or GED plus 2 years of work experience, or an associate degree with at least 6 months of work experience, or a bachelor's degree, as alternative qualification pathways.
BioWorks certificate or similar training in biomanufacturing or regulated production environments.
Approximately 1 year of GMP experience is preferred.
Associate or bachelor's degree in a relevant field is preferred.
Demonstrated ability to work as a team player, contributing positively to a collaborative work culture.
Self-starter mindset with motivation, curiosity, and a desire to understand the reasons behind processes and procedures.
Strong organizational skills with the ability to maintain a clean, orderly, and inspection-ready workspace.
Comfort working with manufacturing equipment at various scales, from small tools to large production systems.
Work Environment
This role is fully on-site in a regulated manufacturing facility, working in the Services area and other production spaces that operate under cGMP standards. The position follows a rotating 2-2-3 schedule of 12-hour night shifts, typically from 5:45 p.m. to 6:15 a.m., requiring comfort with extended hours and overnight work. The environment involves hands-on work with manufacturing equipment, buffer and media preparation, washroom activities, and routine cleaning and sanitization. Team members follow strict gowning requirements and aseptic techniques, with appropriate protective attire and compliance with safety procedures. The facility emphasizes organization, cleanliness, and adherence to documented processes, providing a structured setting where reliability, attention to detail, and teamwork are highly valued.
Job Type & Location
This is a Contract position based out of Holly Springs, NC.
Pay and Benefits
The pay range for this position is $25.00 - $28.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: - Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Holly Springs,NC.
Application Deadline
This position is anticipated to close on Aug 11, 2026.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.
San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.
Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.
