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Biotech Project Management Jobs in Dallas, TX (NOW HIRING)

Manage and track RFIs, submittals, technical queries, design changes, drawing revisions, and ... biotechnology facilities, battery manufacturing plants, data centers, cleanrooms, advanced ...

IT Project Manager - Remote

Dallas, TX · On-site +1

$120K - $160K/yr

... biotechnology? At Beckman Coulter Diagnostics, one of Danaher's 15+ operating companies, our work ... Advanced Project Management Skills: Proficiency in project management methodologies (e.g., Agile ...

Research Project Mgr

Plano, TX · On-site

$66K - $85K/yr

Implements and executes management conclusions. * Prepares documents like brochures, case report ... Fosters relationships with academia, pharmaceutical, and biotechnology industries. Maintains ...

Research Project Mgr

Plano, TX

$66K - $85K/yr

Implements and executes management conclusions. * Prepares documents like brochures, case report ... Fosters relationships with academia, pharmaceutical, and biotechnology industries. Maintains ...

The ability to manage multiple tasks, prioritize effectively, and work independently while ... Ability to travel as required by the project. IQVIA is a leading global provider of clinical ...

CRA 1, IQVIA Biotech

Dallas, TX · On-site

$71K - $145K/yr

The ability to manage multiple tasks, prioritize effectively, and work independently while ... Ability to travel as required by the project. IQVIA is a leading global provider of clinical ...

CRA 1, IQVIA Biotech

Dallas, TX · On-site

$71K - $145K/yr

The ability to manage multiple tasks, prioritize effectively, and work independently while ... Ability to travel as required by the project. IQVIA is a leading global provider of clinical ...

CRA 1, IQVIA Biotech

Fort Worth, TX · On-site

$71K - $145K/yr

The ability to manage multiple tasks, prioritize effectively, and work independently while ... Ability to travel as required by the project. IQVIA is a leading global provider of clinical ...

Work closely with scientists, laboratory leadership, and project management teams to ensure client ... Strong network within biotech/pharma R&D or CMC organizations . * Proven ability to generate new ...

This position plays a key role in the clinical trial management process at Medpace. Incentives can ... biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the ...

This position plays a key role in the clinical trial management process at Medpace. Incentives can ... biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the ...

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Showing results 1-20

Biotech Project Management information

See Dallas, TX salary details

$38.1K

$101.6K

$160.3K

How much do biotech project management jobs pay per year?

As of Aug 21, 2026, the average yearly pay for biotech project management in Dallas, TX is $101,576.00, according to ZipRecruiter salary data. Most workers in this role earn between $77,700.00 and $121,700.00 per year, depending on experience, location, and employer.

What is a biotech project management?

A Biotech Project Management job involves overseeing and coordinating research, development, and commercialization projects in the biotechnology industry. Project managers in this field ensure that scientific, regulatory, and business objectives are met on time and within budget. They work closely with cross-functional teams, including scientists, regulatory experts, and business stakeholders, to drive project success. Strong organizational, problem-solving, and communication skills are essential for managing risks and ensuring compliance with industry regulations.

What are the key skills and qualifications needed to thrive in biotech project management?

To thrive in Biotech Project Management, you need a strong background in life sciences, experience in project planning and execution, and ideally a relevant degree (such as biology, biotechnology, or project management certification). Familiarity with project management software (like MS Project or Asana), regulatory compliance systems, and possibly certifications like PMP is often expected. Exceptional communication, leadership, problem-solving, and time management skills will help you stand out in this role. These competencies ensure projects remain on schedule, compliant, and collaborative in the fast-paced, highly regulated biotech industry.

What are the most common challenges faced by professionals in biotech project management?

Biotech Project Management professionals often juggle cross-disciplinary teams, tight timelines, and complex regulatory requirements, which can make prioritizing tasks a challenge. Navigating scientific uncertainties and adapting to project scope changes are daily realities given the fast pace of biotech innovation. Having strong organizational and people skills helps to manage competing priorities while keeping all stakeholders aligned. By mastering these challenges, professionals can significantly contribute to the timely advancement of vital scientific initiatives.

What are the most commonly searched types of Biotech Project Management jobs in Dallas, TX?

The most popular types of Biotech Project Management jobs in Dallas, TX are:

What are popular job titles related to Biotech Project Management jobs in Dallas, TX?

For Biotech Project Management jobs in Dallas, TX, the most frequently searched job titles are:

What job categories do people searching Biotech Project Management jobs in Dallas, TX look for?

The top searched job categories for Biotech Project Management jobs in Dallas, TX are:

What cities near Dallas, TX are hiring for Biotech Project Management jobs?

Cities near Dallas, TX with the most Biotech Project Management job openings:

Infographic showing various Biotech Project Management job openings in Dallas, TX as of August 2026, with employment types broken down into 90% Full Time, and 10% Part Time. Highlights an 90% In-person, and 10% Hybrid job distribution, with an average salary of $101,576 per year, or $48.8 per hour.

Engineering Operations & Project Lead

Pinnaql

Fort Worth, TX • On-site

Full-time

Posted 4 days ago


Job description

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking a talented, dedicated individual committed to work under the highest ethical standards for the following position:

  • Engineering Operations & Project Lead
Job Description

Reporting to the Engineering Manager, this role provides technical and project leadership across Engineering, Operations, Maintenance, Quality, Manufacturing, SHE/EHS, and Validation. The Engineering Operations & Project Lead will manage assigned capital and expense projects, coordinate engineering priorities and resources, resolve operational issues, and ensure work is completed safely, efficiently, and in compliance with GMP and company requirements. This position provides leadership and coordination without direct ownership of the Engineering department.

Please note, this is an onsite opportunity in Fort Worth, TX and does not offer relocation.

Key Responsibilities Project & Engineering Execution
  • Lead capital and expense projects from concept through commissioning, startup, and handover.
  • Develop project scopes, schedules, cost estimates, URS, budgets, and execution plans.
  • Manage contractors, vendors, and internal resources while tracking project progress, risks, costs, and deliverables.
  • Communicate project status, priorities, risks, and resource needs to stakeholders and site leadership.
  • Manage CAPEX activities in accordance with company policies and standards.
  • Collaborate with project managers, PMO, and senior engineers to improve project execution methods and maintain project profitability.
GMP, Quality & Validation
  • Support Change Controls, Deviations, CAPAs, and other project-related Quality Records.
  • Ensure engineering activities comply with GMP, safety, quality, and regulatory requirements.
  • Support equipment qualification and validation activities, including IQ/OQ/PQ.
  • Ensure new equipment is operationally ready at startup, including PM schedules, spare parts, SOPs, and required CMMS documentation.
  • Verify that vendors meet compliance requirements and are maintained on the approved vendor list.
Capital Planning & Asset Lifecycle
  • Support capital planning, project justification, and prioritization.
  • Coordinate equipment installations, upgrades, replacements, and obsolescence initiatives.
  • Ensure effective project turnover to Operations and Maintenance.
Operations & Cross-Functional Support
  • Coordinate day-to-day engineering priorities based on safety, compliance, production impact, reliability, and business needs.
  • Provide engineering support to Manufacturing, Packaging, and other site functions.
  • Partner closely with Operations, Quality, Validation, EHS/SHE, Maintenance, and other stakeholders.
  • Participate in and co-host project, PMO, and site meetings as needed.
  • Support training, knowledge transfer, and documentation for new equipment and systems.
Continuous Improvement & Reliability
  • Identify opportunities to improve safety, equipment reliability, efficiency, and cost.
  • Support Lean, TPM, automation, and digital manufacturing initiatives.
  • Promote engineering standards and best practices across the site.
  • Help reduce repeat issues, project-related downtime, and operational disruptions.
Skills & Experience
  • Strong technical knowledge of pharmaceutical manufacturing and/or packaging equipment and utilities in a GMP-regulated environment.
  • Demonstrated experience managing capital projects, equipment installations, contractors, and vendors.
  • Strong understanding of GMP requirements, Change Control, Deviations, CAPAs, and equipment qualification/validation (IQ/OQ/PQ).
  • Experience supporting pharmaceutical manufacturing or packaging operations.
  • Knowledge of pharmaceutical manufacturing processes, process development, and validation.
  • Exposure to automation, equipment installations, and validation activities.
  • Working knowledge of HVAC, utilities, and facility systems.
  • Strong project management, organizational, communication, problem-solving, and stakeholder-management skills.
  • Ability to lead individual projects while coordinating multiple cross-functional priorities.

Preferred: Experience with technical transfer of pharmaceutical products and production.

Qualifications
  • Bachelor's degree in Engineering or a related technical discipline.
  • Relevant professional certifications such as PMP, PgMP, Lean Six Sigma Black Belt, and/or CMRP are highy desirable.
Key Competencies

Project Management Problem Solving Commercial & Business Acumen Relationship Management Stakeholder Engagement Customer Service Results Focus Technical Knowledge

Key Performance Indicators

Success will be measured through:

  • Projects delivered safely, on schedule, and within budget, with a target of 90% on-time execution.
  • Contractor safety and compliance performance.
  • Effective project turnover and documentation completion.
  • Successful startup and performance of new equipment with 100% preventive maintenance readiness at handover.
  • Reduction in project-related downtime, disruptions, and repeat equipment issues.
  • Timely closure of Change Controls, Deviations, and CAPAs, with a target of 91%.
  • Project-related audit findings and compliance performance.
  • Continuous improvement initiatives and measurable cost savings or avoidance.
Success in This Role

The successful candidate will consistently:

  • Deliver engineering projects safely, on schedule, and within budget.
  • Effectively coordinate daily engineering priorities and resources.
  • Proactively identify and resolve engineering and operational issues.
  • Provide strong technical and project leadership across cross-functional teams.
  • Maintain compliance with GMP, safety, quality, and company requirements.
  • Improve equipment reliability, site performance, and operational efficiency.
  • Keep the Engineering Manager and site leadership informed of project status, risks, and resource needs.

At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.
Excited to build something meaningful together? We look forward to hearing from you.
Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.

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