1

Project Manager Biotech Jobs in Rudd, IA (NOW HIRING)

Experience in regulated manufacturing (pharmaceutical, biotech, or chemical) strongly preferred. * Proven ability to lead multidisciplinary teams and manage multiple concurrent projects. * Strong ...

Experience in regulated manufacturing (pharmaceutical, biotech, or chemical) strongly preferred. * Proven ability to lead multidisciplinary teams and manage multiple concurrent projects. * Strong ...

Experience in regulated manufacturing (pharmaceutical, biotech, or chemical) strongly preferred. * Proven ability to lead multidisciplinary teams and manage multiple concurrent projects. * Strong ...

Project Manager Biotech information

See Rudd, IA salary details

$20

$44

$72

How much do project manager biotech jobs pay per hour?

As of Jun 8, 2026, the average hourly pay for project manager biotech in Rudd, IA is $44.04, according to ZipRecruiter salary data. Most workers in this role earn between $38.22 and $48.32 per hour, depending on experience, location, and employer.

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.

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 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, and why are they important?

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.
Automation Engineer Manager

Automation Engineer Manager

Cambrex

Charles City, IA • On-site

Full-time

Medical, Life, Retirement

Posted 9 days ago


Job description

Company Information

You Matter to Cambrex.

Cambrex is a leading global contract development and manufacturing organization (CDMO) that provides drug substance development and manufacturing across the entire drug lifecycle, as well as comprehensive analytical and IND enabling services. 

With over 40 years of experience and a team of 2,000 experts servicing global clients from North America and Europe, Cambrex offers a range of specialized drug substance technologies and capabilities, including continuous flow, controlled substances, liquid-phase peptide synthesis, solid-state science, material characterization, and highly potent APIs.

Your Work Matters.

At Cambrex, we strive to build a culture where all colleagues have the opportunity to:

  • engage in work that matters to our customers and the patients they serve
  • learn new skills and enjoy new experiences in an engaging and safe environment
  • strengthen connections with coworkers and the community

We're committed to attracting and nurturing a passionate team of valued professionals in our fast-paced and growing company.  We offer a competitive benefits package that includes healthcare, life insurance, planning for retirement, and more!

Your Future Matters.

Known for our customer-focused scientific and manufacturing excellence, as well as our strong commitment to quality and safety, we offer a range of career and growth opportunities across our global network of locations. Together with our customers, we aim to improve the quality of life for patients around the world. Start a career where You Matter by applying today!

Overview:

The Manager of Automation Engineering is a first-line technical leader responsible for overseeing the automation engineering team and ensuring reliable, efficient, and compliant operation of control systems across the site. This individual manages automation resources, develops team capability, and personally leads to high-impact automation projects or system upgrades. The role combines people leadership with hands-on engineering execution, driving continuous improvement in process automation, data systems, and manufacturing reliability. 

Responsibilities:
  • Leadership & People Management 

    • Directly supervise and mentor a team of automation engineers, technicians, and/or controls specialists. 
    • Set performance goals, conduct reviews, and support individual development and training plans. 
    • Allocate team resources across projects, maintenance support, and continuous improvement initiatives. 
    • Establish and enforce automation standards, engineering procedures, and best practices. 
    • Foster a culture of safety, accountability, collaboration, and innovation within the team. 

    Project Ownership 

    • Serve as project lead or subject matter expert on select automation projects, upgrades, and system integrations. 
    • Provide hands-on design, programming, configuration, and commissioning support for PLC, HMI, SCADA, and DCS systems. 
    • Ensure automation systems meet operational, reliability, cybersecurity, and regulatory requirements. 
    • Collaborate with cross-functional teams (engineering, operations, IT, maintenance, quality) to deliver integrated system solutions. 
    • Review and approve automation design packages, control narratives, and change control documentation. 

    Strategic and Continuous Improvement 

    • Lead the automation roadmap for the site - including system modernization, digital transformation, and process optimization initiatives. 
    • Identify opportunities for automation or advanced control to improve efficiency, reduce risk, and enhance product quality. 
    • Oversee vendor and integrator relationships, including scope of definition, project execution, and performance management. 
    • Ensure alignment with corporate IT/OT cybersecurity standards. 
    • Track and report automation of KPIs and reliability metrics. 

    Compliance & Documentation 

    • Ensure all automation work adheres to GMP, GAMP 5, OSHA, and other relevant regulatory standards. 
    • Oversee and approve documentation such as functional design specs (FDS), test protocols, and validation records. 
    • Maintain system lifecycle documentation and ensure changes are properly controlled and recorded. 

    Reports To 

    • Reports to: Director or Associate Director, Engineering / Capital Projects 
    • Direct Reports: 3-8 Automation Engineers and/or Controls Technicians 
    • Role Type: First-line people manager with active technical and project responsibilities. 
Qualifications / Skills:
  • Strong expertise in control system design, PLC/HMI programming (Allen-Bradley, Siemens, etc.), and network communications. 
  • Experience in regulated manufacturing (pharmaceutical, biotech, or chemical) strongly preferred. 
  • Proven ability to lead multidisciplinary teams and manage multiple concurrent projects. 
  • Strong communication, analytical, and stakeholder management skills. 
Education, Experience, and Licensing Requirements: (Text Only)  - Bachelor's degree in electrical, Chemical, Mechanical, or Automation Engineering (master's preferred).  - Minimum 7-10 years of engineering experience, with at least 2 years in a leadership or lead project role. Employment Type: FULL_TIME

Cambrex logo

About Cambrex

Sourced by ZipRecruiter

Industry

Pharmaceutical and medicine manufacturing

Company size

1,001 - 5,000 Employees

Headquarters location

East Rutherford, NJ, US

Year founded

1981

Social media