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Biotech Project Management Jobs in Iowa (NOW HIRING)

We unite precision breeding, advanced biotechnology trait choice, and digital platforms for ... Advanced project management capabilities to handle complex, overlapping activities with tight ...

We unite precision breeding, advanced biotechnology trait choice, and digital platforms for ... Advanced project management capabilities to handle complex, overlapping activities with tight ...

We unite precision breeding, advanced biotechnology trait choice, and digital platforms for ... Advanced project management capabilities to handle complex, overlapping activities with tight ...

Strategic Sourcing Manager

Des Moines, IA

$125K - $163K/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 ...

TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that ... The Project Engineering Piping/Mechanical Designer is responsible for completion of piping design ...

Lead large-scope projects with site and regional impact * Build and execute productivity plans ... BASIC QUALIFICATIONS - 3+ years of employee and performance management experience - Bachelor ...

... biotechnology? At Integrated DNA Technologies (IDT), one of Danaher's 15+ operating companies, our ... Strong analytical and project management skills. * Strong leadership and excellent in communication ...

Bachelor's degree in Reproductive Biology, Animal Science, Biological Sciences, Biotechnology ... Ability to work independently, manage multiple priorities, and organize work around project ...

Showing results 21-40

Biotech Project Management information

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 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 popular job titles related to Biotech Project Management jobs in Iowa? For Biotech Project Management jobs in Iowa, the most frequently searched job titles are:
Infographic showing various Biotech Project Management job openings in Iowa as of August 2026, with employment types broken down into 100% Full Time. Highlights an 92% In-person, and 8% Hybrid job distribution.

Senior Associate - Manufacturing Engineering

Elanco Animal Health Incorporated

Fort Dodge, IA • On-site

$101K - $138K/yr

Full-time

Posted 23 days ago


Elanco rating

7.8

Company rating: 7.8 out of 10

Based on 25 frontline employees who took The Breakroom Quiz

50th of 86 rated pharmaceutical


Job description

At Elanco (NYSE: ELAN) - it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets. At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose - all to Go Beyond for Animals, Customers, Society and Our People.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment. We believe that diversity is the driving force behind innovation, creativity, and overall business success. Here, you'll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals' lives better makes life better - join our team today!
Your Role: Lead Commissioning, Qualification & Validation (CQV) Engineer
As the Lead CQV Engineer, you will be part of the Engineering team responsible for leading the Commissioning, Qualification, and Validation (CQV) program for the Fort Dodge manufacturing site. In this role, you will provide technical leadership to ensure manufacturing equipment and systems are commissioned, qualified, and validated in compliance with GMP requirements while driving continuous improvement, standardization, and operational excellence across the site.
Your Responsibilities
  • Lead the site-wide Commissioning, Qualification, and Validation (CQV) program, ensuring compliance with Elanco standards and regulatory requirements.
  • Develop, maintain, and improve CQV business processes, including ownership of SOPs, templates, and qualification documentation.
  • Provide technical guidance and oversight for equipment commissioning, qualification, validation, and engineering projects while managing internal and external CQV resources.
  • Drive continuous improvement through Lean principles, process optimization, and collaboration with Engineering, Quality Assurance, and cross-functional teams.
  • Champion a strong safety culture by evaluating equipment and systems for potential safety risks and ensuring safe, compliant operations.

What You Need to Succeed (minimum qualifications)
  • Education: Bachelor's degree in engineering.
  • Experience: Minimum of 3 years of Commissioning, Qualification, and Validation (CQV) experience within the life sciences, pharmaceutical, biotechnology, or manufacturing industry.
  • Top 2 skills: Strong knowledge of GMP regulations, equipment commissioning, qualification and validation, combined with proven leadership and project management abilities.

What Will Give You a Competitive Edge (preferred qualifications)
  • Experience leading CQV programs for pharmaceutical, biologics, or vaccine manufacturing facilities.
  • Demonstrated success managing external contractors and cross-functional project teams.
  • Experience implementing Lean manufacturing and continuous improvement initiatives.
  • Strong understanding of regulatory compliance, risk management, and validation lifecycle principles.
  • Excellent communication skills with the ability to influence technical and non-technical stakeholders while driving project execution.

Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status
Elanco may use automated tools, including AI, to support parts of our recruitment process, such as reviewing applications against job-related criteria and/or transferrable skills. These tools help ensure a consistent, structured evaluation, but they do not make hiring decisions. All decisions involve a human reviewer. For more information on how we handle personal data, please see our Elanco Workforce Privacy Notice.

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