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Project Manager Biotech Jobs in Phoenix, AZ (NOW HIRING)

IQVIA

Senior Global Clinical Study Manager

Gilbert, AZ · On-site

IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of ... Partner with CRAs to optimize enrollment, data quality, and compliance Project & Stakeholder ...

IQVIA

Senior Global Clinical Study Manager

Phoenix, AZ · On-site

IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of ... Partner with CRAs to optimize enrollment, data quality, and compliance Project & Stakeholder ...

IQVIA

Senior Global Clinical Study Manager

Phoenix, AZ · On-site

IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of ... Partner with CRAs to optimize enrollment, data quality, and compliance Project & Stakeholder ...

IQVIA

Senior Global Clinical Study Manager

Gilbert, AZ · On-site

IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of ... Partner with CRAs to optimize enrollment, data quality, and compliance Project & Stakeholder ...

Inizio

District Manager

Phoenix, AZ · On-site

$109K - $202K/yr

This is your opportunity to join Inizio Engage, a top biotechnology company! Why You'll Love ... Communicate with key leadership regularly (written and verbal) to update on project performance ...

BMWC Constructors

Safety Specialist

Phoenix, AZ · On-site

This position regularly interacts with project managers, craft supervisors, and company operations ... biotechnology, and semiconductor. As one of the premier specialty construction companies in the ...

BMWC CONSTRUCTORS

Safety Specialist

Phoenix, AZ · On-site

This position regularly interacts with project managers, craft supervisors, and company operations ... biotechnology, and semiconductor. As one of the premier specialty construction companies in the ...

BMWC CONSTRUCTORS

Safety Specialist

Phoenix, AZ · On-site

This position regularly interacts with project managers, craft supervisors, and company operations ... biotechnology, and semiconductor. As one of the premier specialty construction companies in the ...

BMWC CONSTRUCTORS

Site Quality Inspector

Phoenix, AZ · On-site

This position regularly interacts with project managers, project engineers, site supervisors, and ... biotechnology, and semiconductor. As one of the premier specialty construction companies in the ...

BMWC Constructors

Site Quality Inspector

Phoenix, AZ · On-site

This position regularly interacts with project managers, project engineers, site supervisors, and ... biotechnology, and semiconductor. As one of the premier specialty construction companies in the ...

BMWC CONSTRUCTORS

Site Quality Inspector

Phoenix, AZ

This position regularly interacts with project managers, project engineers, site supervisors, and ... biotechnology, and semiconductor. As one of the premier specialty construction companies in the ...

Amgen

Strategic Sourcing Manager

Phoenix, AZ

$128K - $165K/yr

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Project Management Experience - able to lead teams that cut across geographic and functional ...

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Project Manager Biotech information

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How much do project manager biotech jobs pay per hour?

As of Aug 25, 2026, the average hourly pay for project manager biotech in Phoenix, AZ is $45.91, according to ZipRecruiter salary data. Most workers in this role earn between $39.86 and $50.38 per hour, depending on experience, location, and employer.

What does a project manager in biotech do?

A Project Manager in Biotech is responsible for planning, coordinating, and overseeing projects within biotechnology companies or research organizations. They work closely with scientists, regulatory teams, and other stakeholders to ensure that projects meet deadlines, stay within budget, and comply with industry regulations. Their tasks may include setting project timelines, managing resources, mitigating risks, and communicating progress to leadership. Project Managers play a crucial role in bringing new biotech products or research initiatives from conception to completion.

What are the key skills and qualifications needed to thrive as a project manager in biotech?

To thrive as a Project Manager in Biotech, you need a solid background in life sciences or engineering, experience in project management, and often a relevant degree such as a BSc or MSc, sometimes complemented by a PMP certification. Familiarity with project management software (such as MS Project or Jira), regulatory compliance systems, and budgeting tools is frequently required. Strong leadership, problem-solving, and effective communication skills set standout candidates apart by enabling them to coordinate cross-functional teams and manage complex timelines. These skills are essential to ensure that projects meet regulatory standards, stay on schedule, and achieve scientific and business goals.

How does a project manager in biotech typically collaborate with cross-functional teams to drive project success?

A Project Manager in the biotech sector routinely works with cross-functional teams that include scientists, regulatory experts, manufacturing staff, and quality assurance professionals. They coordinate meetings, align project timelines, and ensure clear communication of goals and milestones. Effective collaboration involves resolving conflicts, facilitating information flow among departments, and adapting plans as scientific or regulatory requirements evolve. This collaborative approach is essential for keeping projects on track, maintaining compliance, and achieving successful outcomes in a highly regulated and fast-paced industry.

What is the difference between Project Manager Biotech vs Clinical Project Manager?

AspectProject Manager BiotechClinical Project Manager
CredentialsBachelor's or Master's in Life Sciences, Project Management CertificationBachelor's or Master's in Life Sciences, Clinical Research Certification
Work EnvironmentBiotech companies, R&D labs, manufacturingClinical trial sites, hospitals, pharmaceutical companies
Industry UsageBiotech product development, research projectsClinical trial management, regulatory compliance
Common Search/ComparisonYesYes

The main difference between a Project Manager Biotech and a Clinical Project Manager lies in their focus areas. The Project Manager Biotech oversees research and development projects within biotech companies, focusing on product development and manufacturing. In contrast, the Clinical Project Manager specializes in managing clinical trials, ensuring regulatory compliance and patient safety. Both roles require strong project management skills and relevant certifications, but they operate in different phases of the biotech and pharmaceutical industry.

What are popular job titles related to Project Manager Biotech jobs in Phoenix, AZ?

For Project Manager Biotech jobs in Phoenix, AZ, the most frequently searched job titles are:

What job categories do people searching Project Manager Biotech jobs in Phoenix, AZ look for?

The top searched job categories for Project Manager Biotech jobs in Phoenix, AZ are:

What cities near Phoenix, AZ are hiring for Project Manager Biotech jobs?

Cities near Phoenix, AZ with the most Project Manager Biotech job openings:

Project Manager Biotech jobs near you
Infographic showing various Project Manager Biotech job openings in Phoenix, AZ as of August 2026, with employment types broken down into 90% Full Time, 9% Part Time, and 1% Contract. Highlights an 79% Physical, 3% Hybrid, and 18% Remote job distribution, with an average salary of $95,502 per year, or $45.9 per hour.

CSA Quality Manager, Phoenix, AZ - Semiconductor

Phoenix, AZ • On-site

World Wide Professional Solutions
Construction • 51 - 200 employees
Learn more about World Wide Professional Solutionsexternal

$82K - $110K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 28 days ago

Job description

WORLD WIDE PROFESSIONAL SOLUTIONS is a project solutions organization committed to implementing lean constructions, collaborative contracting, and execution approaches to enable breakthroughs in performance.
World Wide Professional Solutions is seeking a highly skilled, experienced, and motivated CSA Quality Manager (Civil, Structural, Architectural) to support a large scale semiconductor base build project in North Phoenix, Arizona.
This senior level role will be embedded with the owner side quality team and will focus on CSA oversight, field quality execution, turnover readiness, and commissioning support for active base build systems. The ideal candidate has deep experience operating in live semiconductor construction environments with strong knowledge of cleanroom construction, interstitial coordination, cleanroom wall systems, raised metal floor installations, and structural systems across base build scopes.
Candidates must demonstrate a proven track record of success in CSA quality, construction management, superintendent, or owner representative roles. The ideal candidate is technically strong, highly organized, field oriented, and able to communicate clearly with owners, general contractors, trade partners, inspectors, commissioning teams, and project leadership in a fast-paced construction environment.
The candidate's work history should reflect progressively increasing responsibility throughout their career. Direct semiconductor fab, cleanroom, advanced manufacturing, pharmaceutical, biotechnology, or mission critical construction experience is strongly preferred.
Key Responsibilities
  • Serve as the owner side CSA Quality Manager supporting civil, structural, and architectural oversight for semiconductor base build turnover execution.
  • Champion CSA safety and quality performance by setting clear expectations, leading by example, and holding contractors and trade partners accountable for safe, compliant, and high quality execution.
  • Provide field quality oversight for cleanroom construction, cleanroom wall systems, raised metal floors, interstitial spaces, structural systems, architectural finishes, and related CSA base build scopes.
  • Support turnover of Phase 2 base build systems by verifying field readiness, identifying open items, tracking punch list completion, and coordinating closeout requirements with construction, quality, and commissioning teams.
  • Review CSA work in progress for alignment with approved drawings, specifications, submittals, quality standards, inspection requirements, and owner expectations.
  • Coordinate with general contractors, subcontractors, design teams, commissioning teams, and owner representatives to resolve CSA quality issues that could impact turnover, room readiness, or commissioning readiness.
  • Perform field walks, inspections, deficiency tracking, and quality documentation review for CSA scope, with emphasis on cleanroom readiness, interstitial coordination, access, wall systems, floor systems, and structural completion.
  • Support construction turnover package development and review, including punch lists, inspection records, quality records, test documentation, redlines, closeout documentation, and system readiness deliverables.
  • Identify and escalate CSA construction defects, incomplete work, coordination gaps, and scope risks that may affect base build turnover, schedule, safety, or operational readiness.
  • Participate in project coordination meetings, quality walks, turnover meetings, commissioning readiness reviews, and field planning sessions as the CSA quality representative.
  • Work closely with design and construction teams to review constructability concerns, RFIs, submittals, change impacts, and field conditions related to CSA quality and turnover.
  • Maintain accurate and detailed records of field activities, deficiencies, corrective actions, progress status, quality observations, and turnover readiness by area, level, system, contractor, and activity.
  • Support compliance with project procedures, quality plans, inspection and test plans, safety requirements, and owner governance standards.
  • Provide practical field leadership in an active semiconductor construction environment where multiple trades, systems, access constraints, and turnover priorities must be coordinated simultaneously.
  • Contribute to CSA risk identification and mitigation, with particular focus on quality, cleanroom readiness, interstitial coordination, structural completion, turnover sequencing, and commissioning impact.

Knowledge and Skills Required
  • Minimum of 10 years of experience in CSA construction, field quality, construction management, superintendent, or owner representative roles supporting industrial, semiconductor, cleanroom, advanced manufacturing, pharmaceutical, biotechnology, or mission critical facilities.
  • Deep working knowledge of Civil, Structural, and Architectural construction principles, field execution practices, construction quality requirements, and applicable codes and standards.
  • Strong semiconductor or cleanroom construction experience, including familiarity with cleanroom wall systems, raised metal floor installations, interstitial spaces, architectural finishes, structural systems, access coordination, and base build turnover requirements.
  • Experience supporting turnover, quality, commissioning readiness, room readiness, closeout, punch list management, and field verification activities on complex construction projects.
  • Ability to read and interpret architectural drawings, structural drawings, civil drawings, specifications, submittals, RFIs, shop drawings, redlines, and construction quality documentation.
  • Strong understanding of CSA interfaces with MEP, process utilities, cleanroom systems, life safety, logistics, access, commissioning, and operational readiness requirements.
  • Proven ability to identify field quality issues, document deficiencies, drive corrective action, and communicate priorities clearly to contractors and project stakeholders.
  • Excellent verbal and written communication skills with the ability to interface effectively with owners, engineers, contractors, inspectors, commissioning teams, and project leadership.
  • Strong field presence and the ability to operate effectively in a fast paced active semiconductor construction environment with multiple contractors and overlapping priorities.
  • Working knowledge of project management and construction software used to manage documentation, schedule, quality, punch lists, turnover, and field progress.
  • Familiarity with OSHA requirements and construction safety practices applicable to large scale industrial construction sites.
  • Experience with temporary facilities, access constraints, logistics, phasing, and construction sequencing in active project environments is preferred.

Preferred Education and Experience
  • Bachelor's degree in construction management, Civil Engineering, Structural Engineering, Architecture, or a related field is preferred.
  • 10 or more years of relevant CSA construction, quality, superintendent, construction management, or owner representative experience.
  • Prior experience supporting semiconductor fab construction, cleanroom construction, base build turnover, advanced manufacturing, pharmaceutical, biotechnology, or mission critical facility projects is strongly preferred.
  • Prior owner side, EPCM, general contractor, cleanroom contractor, or specialty trade experience supporting CSA quality and turnover is preferred.

Role Environment
  • Senior level field-based role supporting a confidential semiconductor client.
  • Owner side quality team support with direct focus on CSA base build turnover execution.
  • Active construction environment with extensive coordination across CSA, MEP, cleanroom, commissioning, safety, and project controls stakeholders.
  • Primary focus areas include cleanroom readiness, interstitial coordination, cleanroom wall systems, raised metal floors, structural systems, architectural completion, punch list closure, and commissioning readiness.

Why Join WWPS
This is a full-time, direct employment opportunity with Worldwide Professional Solutions. We offer a comprehensive benefits package.
Benefits
  • Medical, dental, and vision insurance
  • Life insurance
  • Short-term and long-term disability coverage
  • 401(k) with company match
  • Paid holidays and paid time off

This is a full-time position for World Wide Professional Solutions. We offer excellent benefits including medical, dental, vision, life, short term disability, long term disability, and a company match retirement plan. All benefits begin the first of the month following your start date.
World Wide Professional Solutions provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.

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