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Biotech Manufacturing Jobs in Arizona (NOW HIRING)

Transfer Specialist - Reagent Manufacturing Operations Location : Oro Valley, AZ Work Model ... pharmaceutical, biotechnology, or medical devices industry. * Experience operating in a GMP ...

Transfer Specialist - Reagent Manufacturing Operations Location : Oro Valley, AZ Work Model ... pharmaceutical, biotechnology, or medical devices industry. * Experience operating in a GMP ...

Transfer Specialist - Reagent Manufacturing Operations Location : Oro Valley, AZ Work Model ... pharmaceutical, biotechnology, or medical devices industry. * Experience operating in a GMP ...

Pharmacist - Clinical

Chandler, AZ · On-site

$121K - $144K/yr

Complies with FDA mandates and self-imposed manufacturer restrictions. * Evaluates medication ... Dispenses pharmaceuticals including biotech drugs and other related items for patients with rare ...

Validation Engineer

Tucson, AZ · On-site

$39 - $42/hr

... with Manufacturing, Quality, Design Transfer Operations, and other departments to resolve ... We provide job opportunities within major pharmaceutical, biopharmaceutical, biotechnology, and ...

... manufacturing laboratory experimentation and other scientific activities to support Ventana ... We provide job opportunities within major pharmaceutical, biopharmaceutical, biotechnology, and ...

Showing results 21-40

Biotech Manufacturing information

See Arizona salary details

$11

$19

$31

How much do biotech manufacturing jobs pay per hour?

As of Aug 18, 2026, the average hourly pay for biotech manufacturing in Arizona is $19.42, according to ZipRecruiter salary data. Most workers in this role earn between $15.24 and $21.73 per hour, depending on experience, location, and employer.

What is biotech manufacturing?

Biotech manufacturing is the process of producing products using biological systems or living organisms, such as bacteria, yeast, or mammalian cells. This field is crucial for making pharmaceuticals, vaccines, enzymes, and other biological products on a large scale. Biotech manufacturing involves a combination of biology, chemistry, and engineering to ensure products are made efficiently, safely, and to high quality standards. It is a key part of the biotechnology industry and is vital for developing new medical treatments and therapies.

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

To excel in Biotech Manufacturing, a background in biology, chemistry, or engineering with knowledge of GMP (Good Manufacturing Practices) is typically required. Familiarity with bioprocessing equipment, laboratory information management systems (LIMS), and relevant certifications such as Six Sigma or ASQ is often expected. Attention to detail, problem-solving abilities, and strong teamwork skills help professionals stand out in this environment. These competencies are crucial for ensuring safe, efficient, and compliant production of biotechnological products.

What are some common challenges faced in biotech manufacturing, and how can new team members prepare for them?

In biotech manufacturing, common challenges include maintaining strict quality standards, adhering to complex regulatory requirements, and troubleshooting equipment or process issues. New team members can prepare by familiarizing themselves with Good Manufacturing Practices (GMP), developing strong attention to detail, and being proactive in learning about the latest industry protocols. Teamwork is essential, as much of the work involves cross-functional collaboration with quality assurance, engineering, and research departments to ensure smooth production and compliance.

What is the difference between Biotech Manufacturing vs Biotech Quality Control?

AspectBiotech ManufacturingBiotech Quality Control
CredentialsTypically requires a degree in biotech, biology, or chemistrySimilar credentials, often with additional certifications in quality assurance
Work EnvironmentProduction floors, laboratories, cleanroomsLaboratories, testing facilities, quality assurance labs
Employer & Industry UsageManufacturing plants, biotech companies, pharmaceutical firmsQuality assurance departments within biotech and pharma companies
Common Search & ComparisonBiotech Manufacturing vs Biotech Quality Control

Biotech Manufacturing focuses on producing biotech products, involving process development and production. Biotech Quality Control emphasizes testing and ensuring product quality, often working closely with manufacturing but with a focus on compliance and standards.

What are popular job titles related to Biotech Manufacturing jobs in Arizona?

For Biotech Manufacturing jobs in Arizona, the most frequently searched job titles are:

What cities in Arizona are hiring for Biotech Manufacturing jobs?

Cities in Arizona with the most Biotech Manufacturing job openings:

Infographic showing various Biotech Manufacturing job openings in Arizona as of August 2026, with employment types broken down into 89% Full Time, 5% Part Time, 2% Temporary, 2% Contract, and 2% Nights. Highlights an 94% Physical, 3% Hybrid, and 3% Remote job distribution, with an average salary of $40,389 per year, or $19.4 per hour.

CSA Quality Manager, Phoenix, AZ - Semiconductor

World Wide Professional Solutions

Phoenix, AZ

$82K - $110K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 21 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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