Manufacturing Associate

TekWissen LLC

Indianapolis, IN

JOB DETAILS
SALARY
$15–$19
SKILLS
Biotech and Pharmaceutical, Clinical Research, Clinical Support, Clinical Trial, Corporate Compliance, Detail Oriented, Diversity, Food Production, Food and Beverage Industry, GMP (Good Manufacturing Practices), Healthcare, High School Diploma, Laboratory Equipment, Leading Edge Technology, Maintain Compliance, Manufacturing, Manufacturing Requirements, Product Development, Product Documentation, Purchasing/Procurement, Quality Metrics, Regulatory Compliance, Scientific Research, Team Player, Workforce Management
LOCATION
Indianapolis, IN
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. The job opportunity is for one of our clients specializing in biotechnology product development services. Our client is dedicated to supplying laboratory equipment, chemicals, supplies, and services essential in healthcare, scientific research, safety, and education. As the global leader in serving the field of science, our client boasts an annual revenue of around $40 billion with a mission to empower customers to make the world healthier, cleaner, and safer. Our client's global team is committed to delivering an unparalleled blend of cutting-edge technologies, convenient procurement options, and pharmaceutical services under their industry-leading brands.
Position: Manufacturing Associate
Location: Indianapolis, IN, 46221
Duration: 12 Months
Job Type: Temporary Assignment
Work Type: Onsite
Shift Timings: Monday to Thursday 02:45PM to 01:30 AM (Overtime is expected frequently on Friday's from 02:00PM - 08:00PM)
Summary
As a Packaging and Labeling Associate / Manufacturing Associate on the Indianapolis team, you will accurately assemble and label pharmaceutical clinical trial treatments and supplies while adhering to all regulatory manufacturing standards and procedures. This role ensures the safe and compliant preparation of clinical materials that support critical pharmaceutical research and production.
Responsibilities
  • Assemble and label pharmaceutical clinical trial treatments and supplies accurately.
  • Follow all regulatory manufacturing standards, procedures, and compliance requirements.
  • Support the safe and compliant preparation of clinical materials used in pharmaceutical research and production.
  • Perform manual and automated filling, packaging, and labeling of pharmaceutical products.
  • Count, verify, and prepare products to ensure inventory accuracy before and after production runs.
  • Complete required operational training and maintain compliance with company procedures and quality standards.
  • Follow GMP, safety, and manufacturing guidelines during all packaging activities.
Required Skills
  • High School Diploma or GED required.
  • Experience in pharmaceutical, biotechnology, manufacturing, or food and beverage industries preferred.
  • Familiarity with packaging processes and GMP (Good Manufacturing Practice) environments is highly desired.
  • Ability to read and interpret procedure manuals, training materials, batch records, and product documentation.
  • Strong attention to detail and accuracy.
  • Ability to follow detailed procedures and maintain compliance.
  • Team-oriented mindset with the ability to work safely, efficiently, and collaboratively.
TekWissen Group is an equal opportunity employer 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/