1

Pharmaceutical Chemical Engineer Jobs (NOW HIRING)

As the Maintenance Manager, you'll lead the team that keeps our pharmaceutical chemical ... Partner with Engineering, EHS, Operations, Warehouse, and Quality on key decisions related to ...

As the Maintenance Manager, you'll lead the team that keeps our pharmaceutical chemical ... Partner with Engineering, EHS, Operations, Warehouse, and Quality on key decisions related to ...

... production packaging, chemical intermediates, pharmaceuticals, medical and agricultural ... Work with Project Engineering regarding capital project implementation including preparation of ...

Analytical Scientist

Ridgefield, CT · On-site

$94K - $103K/yr

Qualifications Academic Requirements: BS or MS in Chemistry, Chemical Engineering, Pharmaceutical Sciences, Materials Science, or a related discipline, with 2-5 years of relevant experience. Desired ...

Chemical Process Engineer Kelly ® Science & Clinical is seeking a Chemical Process Engineer for a contract position at a cutting-edge client in the pharmaceutical/API manufacturing industry in St ...

MS in Chemistry or related science with at least 10 years of pharmaceutical process development ... Chemical Engineering, Chemical Technology, Clinical Manufacturing, Collaborative Communications ...

Showing results 41-60

Pharmaceutical Chemical Engineer information

See salary details

$40K

$87.5K

$140K

How much do pharmaceutical chemical engineer jobs pay per year?

As of Aug 6, 2026, the average yearly pay for pharmaceutical chemical engineer in the United States is $87,487.00, according to ZipRecruiter salary data. Most workers in this role earn between $67,500.00 and $106,500.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a pharmaceutical chemical engineer?

A Pharmaceutical Chemical Engineer typically needs a degree in chemical engineering or a related field, a strong understanding of pharmaceutical manufacturing processes, and knowledge of regulatory standards like GMP. Familiarity with process simulation software, laboratory instrumentation, and certifications such as Six Sigma or Lean Manufacturing are commonly expected. Outstanding problem-solving, communication, and teamwork skills distinguish top performers in this field. These competencies are crucial for developing safe and efficient pharmaceutical production processes while complying with stringent quality and safety regulations.

What does a pharmaceutical chemical engineer do?

A typical workday for a Pharmaceutical Chemical Engineer often involves designing, developing, and optimizing processes for the production of pharmaceuticals, conducting risk assessments, and troubleshooting manufacturing issues. They collaborate closely with multidisciplinary teams including quality assurance, research scientists, and production staff to ensure that processes meet regulatory standards and project deadlines. Daily responsibilities may include data analysis, process validation, equipment calibration, and reporting findings to management. The role is dynamic and can alternate between office-based design work and hands-on activities in laboratories or production areas, depending on project needs.

Can you work in pharmaceuticals as a pharmaceutical chemical engineer?

Yes, pharmaceutical chemical engineers design and optimize processes for drug manufacturing, working in pharmaceutical companies or contract manufacturing organizations. They typically need a degree in chemical engineering, knowledge of Good Manufacturing Practices (GMP), and experience with process simulation and safety protocols.

How much do pharmaceutical chemical engineers make?

Pharmaceutical chemical engineers typically earn a median annual salary of around $80,000 to $110,000, depending on experience, education, and location. Entry-level positions may start lower, while experienced engineers or those in senior roles can earn higher salaries, especially with specialized skills or certifications in process design and quality control.

What is a pharmaceutical chemical engineer?

A Pharmaceutical Chemical Engineer designs, develops, and optimizes processes for manufacturing pharmaceuticals, ensuring efficiency, safety, and regulatory compliance. They work with chemical formulations, reaction processes, and quality control to produce medications at scale. Their role involves collaborating with chemists, biologists, and regulatory experts to meet industry standards. Additionally, they troubleshoot production issues and implement advancements to improve drug manufacturing processes.

More about Pharmaceutical Chemical Engineer jobs
What cities are hiring for Pharmaceutical Chemical Engineer jobs? Cities with the most Pharmaceutical Chemical Engineer job openings:
What are the most commonly searched types of Pharmaceutical Chemical Engineer jobs? The most popular types of Pharmaceutical Chemical Engineer jobs are:
What states have the most Pharmaceutical Chemical Engineer jobs? States with the most job openings for Pharmaceutical Chemical Engineer jobs include:
Infographic showing various Pharmaceutical Chemical Engineer job openings in the United States as of August 2026, with employment types broken down into 93% Full Time, 2% Part Time, and 5% Contract. Highlights an 87% Physical, 4% Hybrid, and 9% Remote job distribution, with an average salary of $87,487 per year, or $42.1 per hour.

Manager, Maintenance

AMRI

Springfield, MO • On-site

Full-time

Retirement

Re-posted 21 days ago


Job description

Manager, Maintenance in Springfield, MO

Build your future at Curia, where our work has the power to save lives 

Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life-saving treatments to patients. At Curia, we are on a mission to advance our customers' therapies from curiosity to cure and ultimately to improve patients' lives.

We proudly offer

  • Generous benefit options (eligible first day of employment) 
  • Paid training, vacation and holidays (vacation accrual begins on first day of employment)
  • Career advancement opportunities 
  • Education reimbursement
  • 401K program with matching contributions
  • Learning platform
  • And more! 

If you believe that a well-run facility is the foundation of everything else, this role is for you. At Curia, we operate from a simple truth: lives depend on the work we do. As the Maintenance Manager, you'll lead the team that keeps our pharmaceutical chemical manufacturing facility running safely, reliably, and in full compliance around the clock, every day of the year.

In this role, you'll oversee all maintenance and utilities functions at the site, driving equipment reliability, regulatory compliance, and operational efficiency through strategic planning, disciplined execution, and continuous improvement. You'll develop your team, manage complex priorities, and serve as a key site leader who embodies the Curia Way through accountability, urgency, and a commitment to excellence.

Essential Responsibilities

Maintenance Operations & Reliability

  • Provide accountable, day-to-day leadership of all maintenance and utilities functions for a 24/7 pharmaceutical chemical manufacturing facility.
  • Oversee all repair and maintenance activities for facility and equipment, ensuring site priorities of safety, cGMP compliance, and cost-effectiveness are consistently met.
  • Drive optimization of preventive and predictive maintenance programs to minimize unplanned downtime and reduce out-of-service time.
  • Implement systematic planning and scheduling processes that make effective use of human and financial resources.
  • Provide strategic direction for long-term equipment reliability and high uptimes, thinking beyond today's priorities to shape the facility's future.

Team Leadership & Development

  • Lead, motivate, and develop a team of multi-skilled maintenance technicians, supporting their growth, performance, and productivity.
  • Create a motivating work environment where skills development and career advancement are actively supported.
  • Measure performance and provide meaningful feedback through periodic reviews.
  • Ensure staff have appropriate documented training prior to assigning work.

Cross-Functional Collaboration & Planning

  • Partner with Engineering, EHS, Operations, Warehouse, and Quality on key decisions related to facility maintenance, repair, and related projects.
  • Develop and manage the departmental budget through disciplined cost estimation and control.
  • Develop and communicate clear goals and standards, ensuring all activities comply with DEA, FDA, EPA, OSHA, and other applicable regulations.
  • Escalate quality concerns to the Quality department, along with proposed compliant solutions.

Additional Duties

  • Support broader site and business needs as reasonably assigned.

Good Manufacturing & Documentation Practices

Quality is something we take pride in together. You'll perform your work in alignment with cGMP requirements and Curia's standards, which means:

  • Drive a quality first based culture for all work performed
  • Perform all documentation in compliance with ALCOA+ principles and site SOPs.
  • Adhere to applicable cGMP documents including SOPs, batch records, protocols, change controls, and controlled forms.
  • Keep all required cGMP training current for yourself and your team and escalate quality concerns along with proposed solutions to the Quality department.

Qualifications

We welcome candidates from a variety of backgrounds. Here's what we're looking for:

Required

  • Bachelor's degree in Engineering or related field
  • Minimum 5 years' relevant related work experience, plus 2 years in a team leadership role

Preferred

  • Pharmaceutical or regulated manufacturing environment strongly preferred 
  • Formal education and/or training in engineering or industrial technology; Bachelor's degree preferred.
  • Experience with predictive and preventive maintenance strategies and Computer Maintenance Management Systems (CMMS); SAP experience a plus.
  • Working knowledge of chemical manufacturing equipment including pumps, mixers, reactors, electrical systems, process control systems, and utility systems such as boilers, compressed air, and refrigeration.
  • Knowledge of safety regulations and FDA GMP requirements applicable to pharmaceutical chemical manufacturing.

Knowledge, Skills & Abilities

  • Strong leadership skills with a demonstrated track record of mentoring, developing, and inspiring multi-skilled teams.
  • Exceptional ability to engage technically and influence cross-functionally across a complex, regulated site.
  • Excellent communication and negotiation skills, with the ability to engage effectively with both technical and non-technical audiences.
  • Ability to read and interpret equipment manuals, mechanical blueprints, and P&IDs.
  • Demonstrated ability to recognize what needs to be done, take initiative, and drive results with urgency and integrity.
  • Proven ability to manage competing priorities and coordinate resources effectively.
  • Proficient in Microsoft Office Suite and CMMS platforms.
  • Strong organizational skills with the ability to manage multiple projects concurrently.

Other Qualifications

  • Must pass a background check
  • Must pass a drug screen
  • May be required to pass Occupational Health Screening

Physical Requirements

This role regularly requires standing, walking, talking, listening, and using hands to handle equipment, tools, and materials. The employee will frequently use hands and arms and communicate verbally and in writing. Occasional climbing, balancing, stooping, kneeling, and working in confined or elevated spaces may be required. The employee may occasionally lift and/or move up to 50 pounds. Specific vision abilities include close vision, distance vision, peripheral vision, color vision, depth perception and the ability to adjust focus.  Must be medically fit to wear a respirator.

Work Environment

This position operates on a sit with a regulated pharmaceutical chemical manufacturing environment.  While performing the duties of this job, the employee is regularly required to work in a normal office or maintenance shop environment.  The employee will be regularly exposed to fumes, airborne particles, low levels of toxic or caustic chemicals (Personal Protective Equipment required), wet or humid conditions, moving mechanical parts, high or precarious places, elevated noise levels, extreme heat, and risk of electrical shock. Outdoor work and exposure to varied weather conditions may also be required

Education, experience, location and tenure may be considered along with internal equity when job offers are extended.

We do not accept unsolicited assistance from any headhunters or recruitment firms for any of our job openings. All resumes or profiles submitted by search firms to any employee at Curia, in any form without a valid, signed search agreement by an authorized signatory in place for the specific position, approved by Talent Acquisition, will be deemed the sole property of Curia. No fee will be paid in the event the candidate is hired by Curia because of the unsolicited referral.

All interested applicants must apply online. Please be aware of scammers. Curia will only send offer letters and requests for sensitive personal information from a curiaglobal.com email address. Curia is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Curia is an E-Verify employer.