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Pharmaceutical Project Manager Jobs in Baton Rouge, LA

... project sales team to provide a coordinated effort to ensure customer satisfaction and completion ... From oil and gas to water and shipping, pharmaceuticals and food- these are the flows on which our ...

... project sales team to provide a coordinated effort to ensure customer satisfaction and completion ... From oil and gas to water and shipping, pharmaceuticals and food- these are the flows on which our ...

... project sales team to provide a coordinated effort to ensure customer satisfaction and completion ... From oil and gas to water and shipping, pharmaceuticals and food- these are the flows on which our ...

They are used in consumer goods in paper and packaging, food and pharmaceuticals, household and ... Has involvement with other special projects as assigned. Operational Excellence Manage the ...

They are used in consumer goods in paper and packaging, food and pharmaceuticals, household and ... Has involvement with other special projects as assigned. Operational Excellence Manage the ...

Plant Manager

Baton Rouge, LA · On-site

$125 - $150/hr

They are used in consumer goods in paper and packaging, food and pharmaceuticals, household and ... Has involvement with other special projects as assigned. Operational Excellence Manage the ...

MEP Inspector

Baton Rouge, LA · On-site

$80 - $100/hr

Identify potential quality issues and communicate them to project management. * Track deficiencies ... Pharmaceutical facilities * Power generation/distribution facilities * Large commercial buildings

MEP Inspector

Baton Rouge, LA · On-site

$22 - $29.25/hr

Identify potential quality issues and communicate them to project management. * Track deficiencies ... Pharmaceutical facilities * Power generation/distribution facilities * Large commercial buildings

Showing results 21-40

Pharmaceutical Project Manager information

See Baton Rouge, LA salary details

$43.2K

$100.8K

$162.8K

How much do pharmaceutical project manager jobs pay per year?

As of Sep 7, 2026, the average yearly pay for pharmaceutical project manager in Baton Rouge, LA is $100,850.00, according to ZipRecruiter salary data. Most workers in this role earn between $79,700.00 and $123,400.00 per year, depending on experience, location, and employer.

What is a pharmaceutical project manager?

A Pharmaceutical Project Manager oversees drug development projects from initiation to completion, ensuring they meet regulatory, budget, and timeline requirements. They coordinate cross-functional teams, including researchers, regulatory specialists, and manufacturing professionals, to bring pharmaceutical products to market. Their responsibilities include risk management, resource allocation, and stakeholder communication. Strong project management skills, industry knowledge, and attention to compliance are essential for success in this role.

What are the main challenges a pharmaceutical project manager faces during a drug development project?

Pharmaceutical Project Managers often encounter challenges such as navigating complex regulatory requirements, managing tight project timelines, and coordinating across multiple departments like clinical research, regulatory affairs, and manufacturing. Ensuring effective communication among diverse stakeholders and addressing unforeseen obstacles, such as changes in trial protocols or supply chain disruptions, are also common. Strong organizational and leadership skills are essential for adapting to evolving project demands and keeping teams aligned. By anticipating challenges and fostering collaboration, Pharmaceutical Project Managers help ensure successful project outcomes and regulatory approvals.

What are the key skills and qualifications needed to thrive as a pharmaceutical project manager, and why are they important?

A Pharmaceutical Project Manager needs a strong background in life sciences or pharmaceuticals, experience in project management, and often a relevant degree or certification such as PMP. Familiarity with tools like Microsoft Project, regulatory compliance systems (e.g., FDA or EMA guidelines), and document management platforms is crucial. Excellent communication, leadership, problem-solving, and organizational abilities set standout candidates apart. These skills are vital to effectively lead cross-functional teams, ensure regulatory compliance, and successfully deliver projects on time and within budget in a complex industry.

How much do pharmaceutical project managers make in the US?

Pharmaceutical project managers in the US typically earn between $90,000 and $130,000 annually, with salaries varying based on experience, location, and company size. Senior roles or those with specialized skills and certifications can earn higher compensation, often exceeding $150,000 per year.

How to become a pharmaceutical project manager?

To become a pharmaceutical project manager, candidates typically need a bachelor's degree in pharmacy, life sciences, or a related field, along with experience in pharmaceutical development or project coordination. Many roles require strong organizational, communication, and leadership skills, often supported by certifications such as PMP (Project Management Professional). Gaining industry-specific knowledge and experience with regulatory requirements can also enhance prospects in this field.

What are popular job titles related to Pharmaceutical Project Manager jobs in Baton Rouge, LA?

For Pharmaceutical Project Manager jobs in Baton Rouge, LA, the most frequently searched job titles are:

What cities near Baton Rouge, LA are hiring for Pharmaceutical Project Manager jobs?

Cities near Baton Rouge, LA with the most Pharmaceutical Project Manager job openings:

Infographic showing various Pharmaceutical Project Manager job openings in Baton Rouge, LA as of August 2026, with employment types broken down into 87% Full Time, 12% Part Time, and 1% Contract. Highlights an 83% Physical, 2% Hybrid, and 15% Remote job distribution, with an average salary of $90,752 per year, or $43.6 per hour.

Senior Manufacturing / Process Engineer

Therakos

Port Allen, LA

$99K - $129K/yr

Full-time

Re-posted 16 days ago


Job description

Job Title

Senior Manufacturing / Process Engineer

Requisition

JR000015860 Senior Manufacturing / Process Engineer (Open)

Location

Port Allen, LA

Additional Locations

Job Description Summary

This position provides technical leadership and hands-on engineering support for pharmaceutical manufacturing operations. Responsibilities include execution of capital projects, process / system engineering support / design, and general engineering support in a cGMP-regulated environment. The role combines project management, technical design, and process optimization, with opportunity to grow into broader engineering leadership responsibilities.
Position is cross functional and includes pharmaceutical drug (Ultra High Purity (UHP) compressed gas parental products), Device Engineering, Validation, Business Development, R&D / new product commercialization, Quality Assurance, Risk Management, Regulatory Affairs, HSE and Maintenance.
The position requires a self-starter with solid engineering expertise ranging from product/process conception through post commercialization activities and sustainment. The position will provide technical and project management support to include establishment of policies, SOPs, best practices, interdepartmental needs assessment and inclusion, team selection, project scoping, project tracking, leading status meetings, risk assessment, evaluating and reporting project progress, conflict resolution and post project reviews.

Job Description

Key Responsibilities:

  • Manage capital and improvement projects including scope, schedule, budget, and execution
  • Provide process engineering support including troubleshooting, root cause analysis, and continuous improvement
  • Develop and maintain engineering documentation (P&IDs, PFDs, electrical drawings, equipment files)
  • Support Manufacturing, Quality, Validation, R&D, and Business Development
  • Coordinate equipment modifications and installations including design and risk evaluation
  • Manage vendors, contractors, and engineering service providers
  • Perform field walkdowns and ensure documentation accuracy
  • Develop and maintain engineering standards, SOPs, and best practices
  • Support site capital planning and long-term engineering strategies
  • Other project activities that may be assigned by Management.

Minimum Requirements:

  • Bachelor's degree in engineering or relevant life sciences discipline.
  • 5+ years of engineering experience in manufacturing or regulated industries
  • Experience with capital projects and process engineering
  • Strong technical problem-solving and project execution skills
  • Ability to manage multiple priorities and deliver results
  • Demonstrated ability to lead and influence others to achieve outcomes.
  • Ability to effectively manage internal and external relationships and expectations.
  • Ability to effectively guide and lead teams to achieve desired results within timelines and budget commitments.

Preferred Qualifications

  • Thorough knowledge of the pharmaceutical drug commercialization process and team-based matrix management.
  • Experience with medical device manufacturing.
  • Experience in Ultra High Purity (UHP) industrial gas organizations.
  • Working knowledge of cGMPs, including hands-on experience with their interpretation and practical application.
  • Experience applying Risk Analysis Principles in validation or quality activities.
  • Proficiency with Microsoft applications (Word, PowerPoint, Excel, Outlook)
  • Skills that will contribute to success:
    • Experience working with high purity gases under high pressure and vacuum
    • Experience with development / support of automated systems and equipment
    • Expertise / experience working with Rockwell control solutions (RSLogix, Factory Talk, VFDs, etc)
    • Effective time management
    • Strong technical writing capabilities
    • Ability to lead or deliver presentations
    • Lean Manufacturing Training or experience

Relationship with Others/Scope of Position:

  • Develop and manage Vendors/Architectural & Engineering Firms/Consultant contract agreements and interactions ensuring capital project deliverables meet project design objectives & deliverables in compliance with cGMP requirements
  • Effectively communicate with individuals at all levels of responsibility within the various organizational levels within the facility and external.

Keenova offers employees a Total Rewards package which includes competitive pay and benefits. To learn more about our Total Rewards benefits please visit: Keenova Careers | Serve and Grow with Purpose | Keenova

Disclaimer: The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications. Management reserves the right to change or modify such duties as required.

At Keenova, we believe that no one should be alone in their pursuit of better health. This purpose drives us as we pair quality therapeutics with human support-showing up in big moments and small to help patients find comfort and confidence.

We bring deep expertise and resolve to every therapeutic area we serve, including immunology, urology,men's health, orthopedics, critical care, and pediatric endocrinology. We work with patients, care partners, and physicians to help them navigate healthcare system complexity and access therapies that make a meaningful difference.

We are Keenova-keen to solve, keen to serve. Learn more atwww.keenova.com.