TQ Constructors
CAREERS
TQ Constructors’ mission is to be the most preferred high-purity contractor in the U.S. Our four facilities are in Dayton, Kentucky, and Miamiville, Ohio; we serve large and small customers throughout the United States. Start your career in quality assurance, project management, or a different opening. See below for all our career opportunities.
HEADQUARTERS
Dayton, KY
FULL TIME
Project Manager
Location: Dayton, KY
Job Type: Full-Time, On-Site
As a Project Manager, you will be responsible for planning, executing, and closing projects related to the fabrication and installation of biopharmaceutical equipment. You will work closely with cross-functional teams, clients, and stakeholders to ensure that projects are delivered on time, within scope, and to the highest quality standards.
Key Responsibilities:
- Lead the planning and implementation of project objectives, timelines, and deliverables.
- Develop and manage project plans, including schedules, budgets, and resource allocation.
- Coordinate with engineering, fabrication, and quality assurance teams to ensure project alignment and adherence to specifications.
- Conduct regular project meetings to review progress, address issues, and update stakeholders.
- Monitor project performance and implement necessary adjustments to meet project goals.
- Identify and mitigate project risks, ensuring compliance with safety and quality standards.
- Maintain clear and open communication with clients, providing updates and addressing any concerns.
- Prepare and present project reports, documentation, and status updates to senior management and stakeholders.
- Foster a collaborative team environment, promoting best practices in project management and continuous improvement.
Qualifications:
- Bachelor’s degree, PMP certification preferred.
- Minimum of 3 years of project management experience, ideally in the biopharmaceutical or manufacturing sector.
- Strong understanding of biopharmaceutical equipment fabrication and installation processes.
- Excellent organizational, time management, and multitasking skills.
- Proven ability to lead cross-functional teams and manage stakeholder relationships.
- Proficient in project management software (e.g., MS Project, Primavera) and Microsoft Office Suite.
- Strong analytical and problem-solving abilities.
- Exceptional communication and interpersonal skills.
Benefits:
- Competitive salary and comprehensive benefits package.
- Opportunities for professional growth and development.
- Supportive and collaborative work environment.
How to Apply:
If you are a results-oriented leader with a passion for managing complex projects in the biopharmaceutical industry, we want to hear from you! Please submit your resume and a cover letter.
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About Us:
We specialize in the fabrication of high-purity systems for the biopharmaceutical industry. Our commitment to excellence drives us to deliver innovative solutions that meet the strict standards of our clients. We are looking for an experienced Project Manager to oversee our projects and ensure successful execution from inception to completion.
We is an equal-opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
PART TIME
Quality Assurance Specialist
Location: Dayton, KY
Job Type: Full-Time, On-Site
The Quality Assurance Specialist will ensure that all products meet industry standards and regulatory requirements. You will conduct inspections, audits, and assessments throughout the manufacturing process to maintain high-quality standards.
Key Responsibilities:
- Perform quality audits and inspections of materials, processes, and finished products.
- Document and investigate non-conformance reports and deviations.
- Collaborate with production teams to implement quality control measures.
- Review and approve batch records and quality documentation.
- Train staff on quality standards and practices.
Qualifications:
- Bachelor’s degree in Life Sciences or a related field.
- Minimum of [X] years of experience in quality assurance in the biopharmaceutical industry.
- Strong knowledge of regulatory standards (e.g., FDA, GMP).
- Excellent analytical and problem-solving skills.
Benefits:
- Competitive salary and comprehensive benefits package.
- Opportunities for professional growth and development.
- Supportive and collaborative work environment.
How to Apply:
If you are a results-oriented leader with a passion for managing complex projects in the biopharmaceutical industry, we want to hear from you! Please submit your resume and a cover letter.
—
About Us:
We specialize in the fabrication of high-purity systems for the biopharmaceutical industry. Our commitment to excellence drives us to deliver innovative solutions that meet the strict standards of our clients. We are looking for an experienced Project Manager to oversee our projects and ensure successful execution from inception to completion.
We is an equal-opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
DESIGN OFFICES & CLEAN LAB FACILITY #3
Miamiville, OH
FULL TIME
Validation Engineer
Location: Dayton, KY
Job Type: Full-Time, On-Site
The Validation Engineer will be responsible for ensuring that equipment and processes used in biopharmaceutical production are validated and compliant with regulatory standards.
Key Responsibilities:
- Develop and execute validation protocols for equipment and processes.
- Perform IQ, OQ, and PQ testing to ensure compliance.
- Collaborate with engineering and production teams to troubleshoot issues.
- Prepare and maintain validation documentation.
Qualifications:
- Bachelor’s degree in Engineering, Life Sciences, or a related field.
- Minimum of [X] years of experience in validation in the biopharmaceutical industry.
- Knowledge of FDA and EMA guidelines for validation.
Benefits:
- Competitive salary and comprehensive benefits package.
- Opportunities for professional growth and development.
- Supportive and collaborative work environment.
How to Apply:
If you are a results-oriented leader with a passion for managing complex projects in the biopharmaceutical industry, we want to hear from you! Please submit your resume and a cover letter.
—
About Us:
We specialize in the fabrication of high-purity systems for the biopharmaceutical industry. Our commitment to excellence drives us to deliver innovative solutions that meet the strict standards of our clients. We are looking for an experienced Project Manager to oversee our projects and ensure successful execution from inception to completion.
We is an equal-opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
PART TIME
Research Scientist
Location: Miamiville, OH
Job Type: Part-Time, On-Site
As a Research Scientist, you will contribute to the development of new biopharmaceutical products by conducting experiments and analyzing data.
Key Responsibilities:
- Design and execute experiments related to product development.
- Analyze and interpret experimental data to inform product strategies.
- Collaborate with team members to refine research methodologies.
- Prepare reports and presentations for stakeholders.
Qualifications:
- Ph.D. in Biology, Biochemistry, or a related field.
- Experience in drug development or biologics research preferred.
- Strong analytical skills and proficiency in statistical analysis software.
Benefits:
- Competitive salary and comprehensive benefits package.
- Opportunities for professional growth and development.
- Supportive and collaborative work environment.
How to Apply:
If you are a results-oriented leader with a passion for managing complex projects in the biopharmaceutical industry, we want to hear from you! Please submit your resume and a cover letter.
—
About Us
We specialize in the fabrication of high-purity systems for the biopharmaceutical industry. Our commitment to excellence drives us to deliver innovative solutions that meet the strict standards of our clients. We are looking for an experienced Project Manager to oversee our projects and ensure successful execution from inception to completion.
We is an equal-opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
APPLY NOW FOR CAREERS
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TQ CONSTRUCTORS
To message the TQ Constructors hiring team, please complete the form below. Tell us about yourself, your expertise, and why you’d be a good fit and want to start a career in one of our job openings. We’ll follow up if we’re going to move you to the next step for an interview.