Manufacturing Technician

TekWissen LLC

Vacaville, CA

JOB DETAILS
SALARY
$20–$27
SKILLS
Agriculture, Automation Systems, Biology, Biotech and Pharmaceutical, Business Solutions, Cell Cultures, Cleanroom, Column Chromatography, Communication Skills, Current Good Manufacturing Practice (cGMP), Customer Support/Service, Detail Oriented, Disease, Documentation, Driver's License, Email Software, Fermentation, Gene Therapy, Hazardous Materials/Substances, High School Diploma, Inventory Management, Maintain Compliance, Manufacturing, Manufacturing Equipment, Manufacturing Operations, Manufacturing Requirements, Manufacturing Systems, Material Science, Medical Products, Nutrition, OSHA, Operational Support, Personal Care, Physical Demands, Presentation/Verbal Skills, Process Management, Production Control, Production Schedule, Production Support, Production Systems, Regulations, Regulatory Compliance, Regulatory Requirements, Safety/Work Safety, Spreadsheets, Standard Operating Procedures (SOP), System Operations, Team Player, Time Management, Workforce Management
LOCATION
Vacaville, CA
POSTED
4 days ago

Overview:

TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients worldwide. Our client is a leading biotechnology company that combines technological insight with world-class manufacturing, scientific expertise, and process excellence and helps its customers deliver new and innovative medicines that help treat a wide range of diseases. Our client specializes in pharmaceutical ingredients, bioscience, biopharmaceuticals, custom manufacturing, biotechnology, life science ingredients, nutrition, microbial control, agriculture, materials science, personal care, and cell and gene therapy.

Job Title: Manufacturing Technician
Location: Vacaville, CA 95688
Duration: 12 Months
Job Type: Temporary Assignment
Work Type: Onsite
Shift: Wednesday, Thursday & Friday with alternating Saturdays -06:00 PM 07:00 AM (approx. 13-hour shifts)


Training Schedule: Please note that the training will be conducted on First Shift, Monday through Friday, from 8:00 AM to 5:00 PM. Upon successful completion of the training, employees will transition to the Night Shift for their regular work schedule.

Summary:

Responsible for producing innovative bio-therapeutic medicines by operating highly automated production systems and controls in a cGMP manufacturing environment. Maintains production areas in a constant state of inspection readiness while utilizing business systems for inventory and process management. Ensures compliance with regulatory requirements through accurate documentation, current Good Manufacturing Practices (cGMP), and Standard Operating Procedures (SOPs). Supports the routine production of mammalian cell culture products, with a primary focus on cleaning, sterilizing, and operating fixed vessel systems for media preparation, fermentation, and harvest operations. Performs seed train operations, component dispensing, hazardous material handling, buffer preparation, filtration, and column chromatography operations while adhering to established safety and environmental guidelines.

Responsibilities:

  • Operate systems used to clean and sterilize tanks and filtration systems.
  • Prepare materials required for manufacturing operations.
  • Maintain accurate production documentation, including tickets, labels, and equipment readings, to support Right-First-Time operations.
  • Escalate process issues to ensure timely resolution.
  • Comply with cGMP, SOPs, and manufacturing documentation requirements.
  • Operate automated production equipment and manufacturing systems.
  • Support manufacturing operations to meet production schedules and demands.
  • Assemble and prepare production equipment.
  • Communicate effectively within a team environment.
  • Work weekends, off-shifts, overtime, and other scheduled production hours as required.
  • Follow cleanroom gowning procedures and PPE requirements.
  • Handle hazardous materials and chemicals in accordance with OSHA guidelines.
  • Perform physical tasks including prolonged standing, walking, lifting, carrying, pushing, pulling, bending, reaching, twisting, and operating manufacturing equipment.
  • Utilize process automation systems, email, spreadsheets, and other computer applications.
  • Operate powered industrial trucks after meeting DOT physical requirements and maintaining a valid driver's license.

Required Skills:

  • High School Diploma or GED required.
  • Advanced college coursework, technical degree, or certification preferred.
  • Mechanical aptitude or hands-on mechanical experience.
  • Ability to work in a regulated, fast-paced cGMP manufacturing environment.
  • Knowledge of cGMP regulations, SOPs, and manufacturing compliance requirements.
  • Strong documentation and recordkeeping skills with attention to detail.
  • Ability to adapt to changing operational priorities while maintaining a strong work ethic.
  • Effective verbal communication and teamwork skills.
  • Flexibility to work weekends, off-shifts, and overtime.
  • Ability to meet the physical demands of the position, including prolonged standing, walking, lifting, carrying, pushing, pulling, stair climbing, and working in a cleanroom environment while wearing PPE.
  • Ability to operate powered industrial trucks after successfully completing the required DOT physical examination and maintaining a valid driver's license.

TekWissen Group is an equal opportunity/affirmative action employer (m/f/d/v) supporting workforce diversity.

About the Company

T

TekWissen LLC

WE THE TEKWISSEN PEOPLE

TekWissen offers you a broader portfolio of services, industry-leading solutions, and the meaningful innovations that give you greater flexibility and speed to respond to market dynamics, reduced costs and risk to improve enterprise performance, and increased productivity to enable growth.

To keep pace with global market demands, TekWissen keeps its finger on the pulse of change. Our organized approach to guiding a project from its inception to closure. Managing projects is becoming more and more important as we enter the digital era. To cope with the pace that this transition demands, a method is required to manage projects so they can yield quality work, while incorporating efficient use of time and resources.

Project involves identifying which quality standards are relevant to the project and determining how to satisfy them.

It is important to perform quality planning during the Planning Process and should be done alongside the other project planning processes because changes in the quality will likely require changes in the other planning processes, or the desired product quality may require a detailed risk analysis of an identified problem. It is important to remember that quality should be planned, designed, then built in, not added on after the fact.

Capabilities and accomplishments in one TekWissen business enhance the opportunity for success in the others. Put simply, TekWissen's unique combination of attributes promotes success.



COMPANY SIZE
100 to 499 employees
INDUSTRY
Computer/IT Services
FOUNDED
2009
WEBSITE
http://www.tekwissen.com/