Job Description
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: Environmental Monitoring Technician
Location: Houston TX 77047
Duration: 6 Months
Job Type: Temporary Assignment
Work Type: Onsite
Location: Houston TX 77047
Duration: 6 Months
Job Type: Temporary Assignment
Work Type: Onsite
Shift: Monday to Friday from 07:00 PM to 07:30 AM - 12-hour rotating schedule: 2 days on, 2 days off, 3 days on, 3 days off.
Summary
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The Environmental Monitoring (EM) Core Technician is responsible for performing a variety of laboratory and production activities associated with the manufacturing of sterile biological pharmaceutical products. The role supports cGMP compliance, quality systems, and safe production practices while following established procedures and written guidelines. Most work is performed in a cleanroom environment requiring appropriate sterile gowning and personal protective equipment (PPE). The position also requires teamwork, effective communication, and the ability to support and guide team members.
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Responsibilities
- Perform laboratory and production tasks associated with the manufacturing of sterile biological pharmaceutical products.
- Follow all applicable safety policies, rules, regulations, and procedures.
- Ensure team members comply with established safety requirements.
- Maintain quality systems and support cGMP compliance throughout production activities.
- Ensure adherence to established processes, procedures, written instructions, and operational guidelines.
- Execute procedures according to written instructions and identify deviations from accepted practices.
- Work in a cleanroom environment while following required gowning and contamination-control procedures.
- Wear required cleanroom attire and PPE, including scrubs, hairnet, shoe covers, hood, gown, mask, boots, and two pairs of gloves.
- Collaborate with cross-functional departments to maintain safe, efficient, and compliant operations.
- Support a positive work environment through coaching, performance feedback, and collaboration.
- Communicate objectives clearly, monitor progress, and help manage competing priorities.
- Assist in coordinating resources and guiding team members to achieve production goals.
Required Skills
- High school diploma with intermediate laboratory experience in a cGMP clinical production environment, or a bachelor's degree with basic laboratory experience.
- Bachelor's degree in Life Sciences preferred.
- A minimum of 1 to 3 years of experience in Environmanet Monitoring is required.
- Basic understanding of cGMP requirements and quality systems in pharmaceutical production.
- Knowledge of laboratory safety policies and procedures.
- Ability to follow written procedures, work instructions, and established production guidelines.
- Ability to recognize and report deviations from approved procedures.
- Familiarity with cleanroom environments, sterile manufacturing practices, and required gowning procedures.
- Strong teamwork, communication, and interpersonal skills.
- Ability to motivate and support team members through coaching and constructive feedback.
- Organizational and time-management skills, including the ability to prioritize tasks and coordinate resources.
- Ability to work collaboratively across departments while maintaining quality, safety, and compliance standards.
Numbers & Facts
| Location | Houston, TX |
| Industry | Computer/IT Services |
| Salary | $20–$26.80 |
| Company Size | 100 to 499 employees |
| Year Founded | 2009 |
| Website | http://www.tekwissen.com/ |
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.Skills
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