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Pharmaceutical Manufacturing Manager Jobs (NOW HIRING)

Prior experience in nutraceutical or pharmaceutical manufacturing is highly preferred. * Strong ... Lead and manage the manufacturing department , ensuring smooth daily operations and alignment with ...

New

... pharmaceutical, glass, metals, and utilities industries. We also deliver equipment for use ... The Manufacturing Manager will be responsible for planning, coordinating, and monitoring the ...

... pharmaceutical, glass, metals, and utilities industries. We also deliver equipment for use ... The Manufacturing Manager will be responsible for planning, coordinating, and monitoring the ...

... pharmaceutical, glass, metals, and utilities industries. We also deliver equipment for use ... The Manufacturing Manager will be responsible for planning, coordinating, and monitoring the ...

Manufacturing Manager

Oak Ridge, TN · On-site

$90 - $130/hr

... pharmaceutical research. We are looking for individuals who thrive on making an impact and want the ... The Manufacturing Manager serves as the manufacturing leader, ensuring production objectives are ...

New

... pharmaceutical, or similarly regulated environments · Proven ability to lead manufacturing ... cost management, and industry best practices · Demonstrated ability to drive operational ...

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Pharmaceutical Manufacturing Manager information

See salary details

$39.5K

$99.2K

$148.5K

How much do pharmaceutical manufacturing manager jobs pay per year?

As of Aug 21, 2026, the average yearly pay for pharmaceutical manufacturing manager in the United States is $99,198.00, according to ZipRecruiter salary data. Most workers in this role earn between $77,500.00 and $118,500.00 per year, depending on experience, location, and employer.

What does a pharmaceutical manufacturing manager do?

A Pharmaceutical Manufacturing Manager oversees the production processes of pharmaceutical products, ensuring that operations comply with industry regulations and quality standards. They manage teams, coordinate manufacturing schedules, and work to optimize efficiency while maintaining product safety and efficacy. Additionally, they are responsible for implementing good manufacturing practices (GMP), troubleshooting production issues, and collaborating with quality control and regulatory departments. Their role is crucial in delivering safe and effective medications to the market.

What are the key skills and qualifications needed to thrive as a pharmaceutical manufacturing manager?

A Pharmaceutical Manufacturing Manager requires a solid background in pharmaceutical sciences, process engineering, and regulatory compliance, typically supported by a relevant degree and industry experience. Familiarity with Good Manufacturing Practices (GMP), quality management systems, and production planning software is essential. Strong leadership, problem-solving skills, and effective communication set outstanding managers apart in this role. These skills ensure consistent production quality, regulatory adherence, and efficient team coordination in a highly regulated environment.

What are some typical challenges faced by pharmaceutical manufacturing managers in ensuring regulatory compliance?

Pharmaceutical Manufacturing Managers often encounter challenges in maintaining strict adherence to Good Manufacturing Practices (GMP) and ever-evolving regulatory standards. These challenges include implementing process changes without disrupting production, conducting regular audits, and training staff on compliance protocols. Ensuring documentation accuracy and managing cross-functional communication between quality assurance, production, and regulatory affairs teams are also crucial. Staying updated with new regulations and swiftly addressing non-compliance issues are key aspects of the role.

What is the difference between Pharmaceutical Manufacturing Manager vs Pharmaceutical Production Supervisor?

AspectPharmaceutical Manufacturing ManagerPharmaceutical Production Supervisor
ResponsibilitiesOversees entire manufacturing processes, manages teams, ensures compliance, and develops production strategies.Supervises daily production activities, manages operators, and ensures production targets are met.
CredentialsBachelor's degree in pharmacy, chemistry, or related field; often with management experience.High school diploma or associate degree; relevant technical training or certifications.
Work EnvironmentOffice-based with plant visits; involved in planning and oversight.Factory floor; direct supervision of production staff.
Industry UsageCommonly used in larger manufacturing facilities and corporate settings.Found in production lines, manufacturing plants, and smaller facilities.

The Pharmaceutical Manufacturing Manager focuses on strategic oversight, compliance, and team management, while the Pharmaceutical Production Supervisor handles daily operations and direct supervision of production staff. Both roles are essential in pharmaceutical manufacturing but differ in scope and responsibilities.

What is the role of a pharmaceutical manufacturing manager in the pharmaceutical industry?

A pharmaceutical manufacturing manager oversees the production process of medications to ensure quality, safety, and compliance with regulatory standards. They coordinate staff, manage production schedules, implement quality control measures, and ensure adherence to Good Manufacturing Practices (GMP). This role often requires knowledge of manufacturing equipment, regulatory requirements, and strong leadership skills.
More about Pharmaceutical Manufacturing Manager jobs

What cities are hiring for Pharmaceutical Manufacturing Manager jobs?

Cities with the most Pharmaceutical Manufacturing Manager job openings:

What are the most commonly searched types of Pharmaceutical Manufacturing jobs?

The most popular types of Pharmaceutical Manufacturing jobs are:

What states have the most Pharmaceutical Manufacturing Manager jobs?

States with the most job openings for Pharmaceutical Manufacturing Manager jobs include:

Infographic showing various Pharmaceutical Manufacturing Manager job openings in the United States as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 81% Physical, 2% Hybrid, and 17% Remote job distribution, with an average salary of $99,198 per year, or $47.7 per hour.

Experienced Pharmaceutical Manufacturing Technician

Lonza

Bend, OR • On-site

Full-time

Re-posted 5 days ago


Lonza rating

8.3

Company rating: 8.3 out of 10

Based on 42 frontline employees who took The Breakroom Quiz

25th of 86 rated pharmaceutical


Job description

The actual location of this job is in Bend, Oregon (USA). Relocation assistance is available for eligible candidates and their families, if needed.
Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of.
Lonza Pharma & Biotech has an opening for an experienced Pharmaceutical Manufacturing Technician to join their Early Phase Clinical Manufacturing team. This role offers the outstanding opportunity to contribute to world-class pharmaceutical innovations, while working in a collaborative and inclusive environment. If you are ambitious and driven by the desire to make a meaningful impact, we want you to join our mission to improve lives.
What You Will Get:
  • Opportunity to contribute to the development and manufacture of innovative pharmaceutical products.
  • Hands-on experience supporting clinical manufacturing and product development activities across multiple scales.
  • Exposure to cross-functional teams, including manufacturing, engineering, quality, and technical operations.
  • Ownership of manufacturing process equipment and involvement in equipment lifecycle management.
  • Opportunities to develop technical expertise in pharmaceutical manufacturing processes and unit operations.
  • A collaborative environment that encourages continuous improvement, knowledge sharing, and professional growth.
  • Experience working within a regulated cGMP environment that emphasizes safety, quality, and compliance.

What You Will Do:
Manufacturing & Process Support
  • Support pharmaceutical product and process development through the manufacture of clinical trial materials.
  • Execute manufacturing activities in accordance with approved procedures and Good Documentation Practices (GDP).
  • Establish subject matter expertise in the assembly, operation, cleaning, and troubleshooting of process equipment.
  • Perform routine cleaning of manufacturing areas and support maintenance and calibration activities.
  • Participate in manufacturing technology transfers and provide technical feedback within areas of expertise.
  • Apply an ownership mindset to manufacturing equipment and production spaces.

Engineering Support & Technical Operations
  • Assist with equipment installation, startup, commissioning, qualification, and change control activities.
  • Support equipment qualification and process improvement initiatives.
  • Analyze and interpret process data to support project objectives and informed decision-making.
  • Drive continuous improvement initiatives related to manufacturing processes, equipment, and operational efficiency.

Documentation & Compliance
  • Prepare and maintain technical documentation, including:
    • Standard Operating Procedures (SOPs)
    • Work Instructions
    • Training Materials
    • Technical Reports
    • Memorandums
    • Technology Transfer Documentation
  • Support investigation activities, change controls, and quality system requirements.
  • Ensure all work is performed in compliance with cGMP regulations, site procedures, and safety requirements.
  • Clearly communicate technical findings and project outcomes to internal stakeholders and clients.

What We Are Looking For:
  • High School Diploma or equivalent with relevant industry experience; or bachelor's degree in chemical engineering, engineering, or a related scientific discipline.
  • Knowledge of pharmaceutical manufacturing process machinery and unit functions preferred.
  • Ability to develop technical expertise and serve as an equipment owner for specific process systems.
  • Experience working within a GMP-regulated environment preferred.
  • Strong attention to detail and commitment to documentation accuracy.
  • Ability to work effectively in a fast-paced, team-oriented environment.
  • Strong problem-solving, analytical, and organizational abilities.
  • Commitment to safety, quality, and continuous improvement principles.
  • Ability to learn new technologies, processes, and manufacturing techniques.
  • Ability to lift materials and equipment as required.
  • Comfortable working in a manufacturing environment requiring personal protective equipment (PPE).
  • Ability to safely work with and around hazardous chemicals while following established safety procedures.

Join us and be part of a team that drives outstanding pharmaceutical innovations and makes a significant difference in people's lives!
Every day, Lonza's products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.
People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.
Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.

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