MCS Manufacturing Associate
About the role
The MCS Manufacturing Associate works fully onsite in a GMP-regulated manufacturing environment, focusing primarily on manual visual inspection and packaging of post-inspected units. This role supports critical production operations by following Standard Operating Procedures, operating key processing equipment, and using electronic manufacturing systems to help ensure product quality and schedule adherence.
Responsibilities
- Perform manufacturing activities under minimal supervision in accordance with Standard Operating Procedures (SOPs).
- Conduct manual visual inspection of units to ensure they meet established quality standards.
- Package post-inspected units accurately and in compliance with GMP and internal procedures.
- Understand key process parameters and identify process anomalies during operations.
- Operate critical processing equipment safely and consistently to support production.
- Aid in completing operations according to the manufacturing schedule and production priorities.
- Serve as a resource on the manufacturing floor for processing operations and related questions.
- Identify, communicate, and escalate problems or deviations observed during operations.
- Review, revise, and audit manufacturing and related documentation for accuracy and compliance.
- Perform computer-based operations using systems such as MES, EBR, MAXIMO, LIMS, and SAP.
- Recognize issues in electronic batch records and other systems and escalate them appropriately.
- Establish effective working relationships with colleagues outside the immediate area of expertise.
- Support a flexible shift structure, including potential early start times and weekend work, to meet production demands.
- Apply basic biology and physical principles as appropriate to manufacturing processes.
- Maintain strong organizational practices and complete assignments with a high degree of attention to detail.
- Communicate clearly in writing and verbally with peers, support functions, and leadership.
- Interpret and apply GMP regulations to daily manufacturing activities.
- Demonstrate routine discipline, reliability, consistent attendance, and adaptability to changing operational needs.
- Work collaboratively in a team-oriented and professional environment to achieve production goals.
Essential Skills
- Minimum of 1 year of experience in a GMP manufacturing environment.
- Ability to pass an eye exam, including color vision assessment, required for visual inspection tasks.
- Proficiency with computer systems and applications used in manufacturing operations.
- Experience using PAS-X Werum software for electronic batch records, including some understanding of editing and validation.
- Familiarity with MAXIMO, LIMS, and SAP, or the ability to learn these systems quickly.
- Working knowledge of GMP principles and the ability to interpret and apply applicable regulations.
- Experience with manual visual inspection of drug product or work in a GMP-regulated environment.
- Knowledge of manual visual inspection techniques or a strong understanding of related bioprocessing or drug product operations.
- Experience using PAS-X Werum software for electronic batch records, including some understanding of editing and validation.
- Familiarity with MAXIMO, LIMS, and SAP, or the ability to learn these systems quickly.
- Strong organizational skills with a high level of attention to detail in all tasks.
- Effective written and oral communication skills.
- Demonstrated reliability, routine discipline, and consistent attendance.
- Willingness and ability to support flexible shift structures, including early start times and possible weekend work.
- Ability to collaborate with colleagues outside the immediate area of expertise and build productive working relationships.
Additional Skills & Qualifications
- Experience with manual visual inspection of drug product or work in a GMP-regulated environment.
- Knowledge of manual visual inspection techniques or a strong understanding of related bioprocessing or drug product operations.
- Experience using PAS-X Werum software for electronic batch records, including some understanding of editing and validation.
- Familiarity with MAXIMO, LIMS, and SAP, or the ability to learn these systems quickly.
- Strong organizational skills with a high level of attention to detail in all tasks.
- Effective written and oral communication skills.
- Demonstrated reliability, routine discipline, and consistent attendance.
- Willingness and ability to support flexible shift structures, including early start times and possible weekend work.
- Ability to collaborate with colleagues outside the immediate area of expertise and build productive working relationships.
Work Environment
This position is fully onsite in a GMP-regulated manufacturing facility. The current primary shift is 6:00 a.m. to 3:00 p.m., with some training and specific processes requiring earlier start times of 4:00 a.m. or 5:00 a.m. The role may involve weekend work and offers the possibility of moving to swing or graveyard shifts, so flexibility with scheduling is important. Work is performed on the manufacturing floor and in related support areas, using critical processing equipment and computer-based systems such as MES, EBR, MAXIMO, LIMS, SAP, and potentially PAS-X Werum. The environment is process-driven and highly regulated, with a strong emphasis on documentation, quality, and safety. Team members follow established facility and GMP standards, including appropriate gowning and attire suitable for a clean, professional manufacturing setting.
Job Type & Location
This is a Contract position based out of Thousand Oaks, CA.
Pay And Benefits
The pay range for this position is $25.00 - $25.00/hr.
Requirements
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 Thousand Oaks, CA.
Application Deadline
This position is anticipated to close on Jul 13, 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.