Highlights
Willingness to wear required cleanroom protective gear, including gloves, hairnets, beard nets, face coverings, and safety glasses, with no makeup or jewelry in designated areas. We are seeking a detail-oriented Manufacturing Operator / Manufacturing Process Associate to support the manufacturing, assembly, inspection, and packaging of medical bags and related components for the biotechnology industry in a controlled cleanroom environment.
Numbers & Facts
| Location | Millersburg, PA |
| Industry | Computer/IT Services |
| Salary | $15–$20.35 |
| Company Size | 100 to 499 employees |
| Year Founded | 2009 |
| Website | http://www.tekwissen.com/ |
Description
Overview:
TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to clients worldwide. The job opportunity below is with one of our clients specializing in biotechnology product development services. The client is dedicated to supplying laboratory equipment, chemicals, supplies, and services essential in healthcare, scientific research, safety, and education. As a global leader in serving the scientific community, the organization generates approximately $40 billion in annual revenue and is committed to making the world healthier, cleaner, and safer. Their global team delivers innovative technologies, convenient procurement solutions, and pharmaceutical services through industry-leading brands.
Job Title: Manufacturing Process Associate - 2nd Shift
Location: Millersburg PA 17061
Duration: 6 Months
Job Type: Temporary Assignment
Work Type: Onsite
Shift: Monday to Friday from 02:00 PM to 10:30 PM
Location: Millersburg PA 17061
Duration: 6 Months
Job Type: Temporary Assignment
Work Type: Onsite
Shift: Monday to Friday from 02:00 PM to 10:30 PM
Summary
We are seeking a detail-oriented Manufacturing Operator / Manufacturing Process Associate to support the manufacturing, assembly, inspection, and packaging of medical bags and related components for the biotechnology industry in a controlled cleanroom environment. The ideal candidate will perform manual assembly, material handling, equipment operation, quality inspections, and finished product packaging while following Standard Operating Procedures (SOPs), Work Instructions, blueprints, and established quality standards. This position requires strong attention to detail, accurate documentation, adherence to safety protocols, and the ability to work effectively in a fast-paced manufacturing environment.
Responsibilities:- Manufacture, assemble, and package medical bags and related biotechnology products in a cleanroom environment.
- Follow Standard Operating Procedures (SOPs), Work Instructions, blueprints, and established manufacturing practices.
- Perform manual assembly of tubing, connectors, and other components according to written instructions and technical drawings.
- Operate hand tools and manufacturing equipment safely and efficiently.
- Conduct visual inspections of in-process and finished products to ensure compliance with quality standards.
- Maintain accurate production records, inspection reports, and manufacturing documentation.
- Package and label finished products according to established specifications.
- Perform material handling and daily housekeeping activities to maintain a clean and organized work environment.
- Participate in Lean Manufacturing, Continuous Improvement, Practical Process Improvement (PPI), and 5S activities.
- Follow all cleanroom procedures, safety protocols, and Personal Protective Equipment (PPE) requirements.
- Collaborate with team members to meet production targets, quality standards, and operational deadlines.
Required Qualifications
- High School Diploma or equivalent experiecne required.
- 0 2 years of experience or training in manufacturing, production, laboratory operations, or a related environment.
- Experience in a cGMP-regulated or Lean Manufacturing environment preferred.
- Ability to read, understand, and follow SOPs, Work Instructions, blueprints, and technical drawings.
- Basic understanding of manufacturing, assembly, inspection, and packaging processes.
- Strong attention to detail with the ability to maintain accurate documentation.
- Good analytical, troubleshooting, and problem-solving skills.
- Effective verbal and written communication skills.
- Ability to follow complex procedures and work collaboratively in a team environment.
- Familiarity with cleanroom practices, PPE requirements, and workplace safety standards preferred.
- Ability to work in a fast-paced, temperature- and humidity-controlled cleanroom environment for up to 8 hours per day, with overtime as required.
- Willingness to wear required cleanroom protective gear, including gloves, hairnets, beard nets, face coverings, and safety glasses, with no makeup or jewelry in designated areas.
- Ability to stand, walk, bend, reach, stoop, grasp, and operate hand tools throughout the shift.
- Ability to occasionally lift and handle materials weighing up to 50 lbs without assistance.
- Commitment to following safety procedures, maintaining product quality, and meeting production schedules.
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About Company
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.