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 ...
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 ...
... projects or system upgrades. * Directly supervise and mentor a team of 3-8 Automation Engineers ... Experience in a regulated manufacturing environment (pharmaceutical, biotech, or chemical) strongly ...
... projects or system upgrades. * Directly supervise and mentor a team of 3-8 Automation Engineers ... Experience in a regulated manufacturing environment (pharmaceutical, biotech, or chemical) strongly ...
Fermentation Engineer
Osage, IA · On-site
$68K - $90K/yr
... VBC Management. The individual will have knowledge of fermentation science and biochemical ... Participate in new product development and realization projects * Track and trend yield and quality ...
Quick apply
Fermentation Engineer
Osage, IA · On-site
$68K - $90K/yr
... VBC Management. The individual will have knowledge of fermentation science and biochemical ... Participate in new product development and realization projects * Track and trend yield and quality ...
Sr. Fermentation Engineer
Osage, IA · On-site
$100K - $115K/yr
Support cost management activities including bill of materials and cost standard reviews. * Train ... Participate in capital projects, technology implementation, and cost-saving initiatives.
Quick apply
Sr. Fermentation Engineer
Osage, IA · On-site
$100K - $115K/yr
Support cost management activities including bill of materials and cost standard reviews. * Train ... Participate in capital projects, technology implementation, and cost-saving initiatives.
Project Manager Biotech information
See Rudd, IA salary details
$20.84 - $25.56
4% of jobs
$25.56 - $30.28
8% of jobs
$30.28 - $35.01
3% of jobs
$37.08 is the 25th percentile. Wages below this are outliers.
$35.01 - $39.73
21% of jobs
The median wage is $42.69 / hr.
$39.73 - $44.46
21% of jobs
$47.66 is the 75th percentile. Wages above this are outliers.
$44.46 - $49.18
25% of jobs
$49.18 - $53.91
13% of jobs
$53.91 - $58.63
2% of jobs
$58.63 - $63.36
1% of jobs
$63.36 - $68.08
1% of jobs
$68.08 - $72.81
0% of jobs
$20
$44
$72
How much do project manager biotech jobs pay per hour?
What is the difference between Project Manager Biotech vs Clinical Project Manager?
| Aspect | Project Manager Biotech | Clinical Project Manager |
|---|---|---|
| Credentials | Bachelor's or Master's in Life Sciences, Project Management Certification | Bachelor's or Master's in Life Sciences, Clinical Research Certification |
| Work Environment | Biotech companies, R&D labs, manufacturing | Clinical trial sites, hospitals, pharmaceutical companies |
| Industry Usage | Biotech product development, research projects | Clinical trial management, regulatory compliance |
| Common Search/Comparison | Yes | Yes |
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?
What does a Project Manager in Biotech do?
What are the key skills and qualifications needed to thrive as a Project Manager in Biotech, and why are they important?
Full-time
Medical, Life, Retirement
Posted 9 days ago
Job description
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.
- 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.
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