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

Laekna LLC

Head of Business Development

Dallas, TX · Remote

... and project management skills with experience in partner management or portfolio management. · Deep understanding of pharmaceutical industry and cross-border collaboration with MNCs or biotech ...

ASTRO PAK

Process Engineer

Dallas, TX · On-site

Data Centers, Biotechnology, Pharmaceutical, Aerospace, Semiconductor, and other selected ... Strong project management, problem-solving, and leadership skills * Willingness to travel up to 50 ...

ASTRO PAK

Process Engineer

Dallas, TX · On-site

Data Centers, Biotechnology, Pharmaceutical, Aerospace, Semiconductor, and other selected ... Strong project management, problem-solving, and leadership skills * Willingness to travel up to 50 ...

ASTRO PAK

Process Engineer

Dallas, TX · On-site +1

... like aerospace, biotech, and beyond. This role reports directly to our Associate Director of ... Strong project management, problem-solving, and leadership skills * Willingness to travel up to 50 ...

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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 Sep 5, 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:

Biotech Project Management jobs near you
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.

Sourcing and Purchasing Manager

Mark Cuban Cost Plus Drug Company

Dallas, TX • On-site

$95K - $99K/yr

Full-time

Posted 5 days ago

Job description

JOB TITLE: Sourcing and Purchasing Manager 
DEPARTMENT: Operations
REPORTS TO: VP of Operations
EMPLOYEE STATUS:  Exempt
LOCATION: On-site Only 
WORK AVAILABLE: Full Time


SUMMARY

The Sourcing and Purchasing Manager leads cross‑functional, high‑impact initiatives that strengthen MCCPDC’s 503B supply chain resilience, operational readiness, and cost‑to‑serve efficiency. This role drives end‑to‑end project execution, spanning supplier optimization, material availability, risk mitigation, inventory strategy, and production‑supporting improvements.  
   
 This manager plays a critical role in ensuring material continuity, reducing shortages, improving throughput, and enabling scalability as MCCPDC expands its sterile manufacturing and distribution footprint. The position interfaces heavily with Procurement, Planning, Production, Engineering, Quality, Regulatory, Finance, and IT.

KEY RESPONSIBILITIES


Strategic Project Leadership

  • Lead medium‑ to large‑scale supply chain projects from initiation through completion using structured project management methodologies.
  • Own timelines, deliverables, risk registers, stakeholder communication, and executive‑level reporting.
  • Develop business cases, ROI models, and cost‑benefit analyses for proposed initiatives.
  • Translate operational pain points into actionable project charters with clear KPIs and success criteria.

Supplier & Material Strategy

  • Responsible for procurement to evaluate suppliers, diversify sources, assess risk, and support qualification activities.
  • Drive supplier‑related improvement projects (lead‑time reduction, MOQ optimization, contract alignment, cost reduction).
  • Collaborate with Quality on supplier assessments, nonconformance reductions, and corrective actions.

Production & Capacity Support

  • Analyze production demand, capacity constraints, material readiness, and changeover impacts; propose strategic solutions.
  • Collaborate with Production Managers to ensure upcoming campaigns have full material readiness.
  • Support tech transfers, new product introductions, and scale‑up initiatives with supply‑chain project leadership.

Compliance & 503B Operational Alignment

  • Ensure all supply chain projects align with cGMP, 503B outsourcing facility requirements, and MCCPDC’s internal QMS.
  • Work cross‑functionally during audits or regulatory reviews to provide supply‑chain evidence, data, and process maps.
  • Document project activities according to MCCPDC quality and document‑control standards.

Cross‑Functional Collaboration & Communication

  • Facilitate effective communication between Supply Chain, QA/QC, Production, Engineering, Finance, and leadership.
  • Build reporting dashboards and executive summaries showing KPIs, progress, risks, and mitigation plans.
  • Provide structured updates during tiered performance meetings and leadership reviews.


REQUIRED QUALIFICATIONS

· Bachelor’s degree in Supply Chain, Operations, Engineering, Business, or related field. 

· 3–7+ years of experience in supply chain, manufacturing, operations, or project management. 

· Experience in pharmaceutical, biotech, medical device, or other cGMP‑regulated environments. 

· Demonstrated success leading cross‑functional projects with measurable impact. 

· Strong analytical abilities: root‑cause analysis, data interpretation, and scenario modeling. 

· Proficiency with ERP/MRP systems and intermediate/advanced Excel or data tools. 

· Excellent communication, documentation, and stakeholder‑management skills.


PREFERRED EXPERIENCE

· Experience in 503B sterile compounding or commercial pharmaceutical production. 

· Certifications: PMP, Lean Six Sigma Green/Black Belt, APICS/ASCM (CSCP or CPIM). 

· Experience with quality investigations, deviations, CAPA, or supplier audits. 

· Familiarity with FDA 503B compliance and cGMP documentation practices.


CORE COMPETENCIES

· Strategic Thinking & Systems-Level Problem Solving 

· Project & Program Management 

· Data‑Driven Decision Making 

· Supplier & Stakeholder Management 

· Continuous Improvement & Operational Excellence 

· Strong Written and Verbal Communication 

· Bias for Action, Ownership, and Follow‑Through 
 

PERFORMANCE INDICATORS (KPI’s)

· Reduction in material shortages & supply disruptions 

· Improvement in lead times, supplier performance, and cost efficiencies 

· MRP accuracy and material‑readiness metrics 

· On‑time project completion rate 

· Improvement in operational throughput tied to supply‑chain projects 

· Internal customer satisfaction (Production, QA, Engineering) 

· Documentation and compliance accuracy

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