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Pharmaceutical Process Engineer Jobs in Ohio (NOW HIRING)

... processes. Job Knowledge Required: * B.S. Degree in Chemical, Mechanical, or Electrical engineering with 2+ years technical management experience in a related cGMP field, i.e., pharmaceutical or ...

Engineering Manager

Cincinnati, OH · On-site

$125K - $147K/yr

... processes. Job Knowledge Required: * B.S. Degree in Chemical, Mechanical, or Electrical engineering with 2+ years technical management experience in a related cGMP field, i.e., pharmaceutical or ...

Knowledge of pharmaceutical facility design, manufacturing operations, process support systems, and ... Consulting engineering experience supporting pharmaceutical or biotechnology clients strongly ...

Senior Mechanical Engineer

Toledo, OH · On-site

$102K - $135K/yr

Knowledge of pharmaceutical facility design, manufacturing operations, process support systems, and ... Consulting engineering experience supporting pharmaceutical or biotechnology clients strongly ...

Senior Mechanical Engineer

Toledo, OH · On-site

$150 - $160/hr

Knowledge of pharmaceutical facility design, manufacturing operations, process support systems, and ... Consulting engineering experience supporting pharmaceutical or biotechnology clients strongly ...

Senior Mechanical Engineer

Toledo, OH

$102K - $135K/yr

Knowledge of pharmaceutical facility design, manufacturing operations, process support systems, and ... Consulting engineering experience supporting pharmaceutical or biotechnology clients strongly ...

Showing results 41-60

Pharmaceutical Process Engineer information

See Ohio salary details

$29

$33

$37

How much do pharmaceutical process engineer jobs pay per hour?

As of Aug 11, 2026, the average hourly pay for pharmaceutical process engineer in Ohio is $33.51, according to ZipRecruiter salary data. Most workers in this role earn between $31.54 and $35.43 per hour, depending on experience, location, and employer.

What is the difference between Pharmaceutical Process Engineer vs Pharmaceutical Manufacturing Technician?

AspectPharmaceutical Process EngineerPharmaceutical Manufacturing Technician
Required CredentialsBachelor's degree in engineering, chemistry, or related field; often includes certifications in process validationHigh school diploma or associate degree; on-the-job training or technical certifications
Work EnvironmentDesign, optimize, and oversee manufacturing processes in labs or production facilitiesOperate equipment, monitor production lines, and ensure quality in manufacturing settings
Employer & Industry UsagePharmaceutical companies, biotech firms, contract manufacturing organizationsPharmaceutical manufacturing plants, biotech production facilities

The main difference is that Pharmaceutical Process Engineers focus on designing and improving manufacturing processes, requiring higher technical credentials, while Pharmaceutical Manufacturing Technicians handle day-to-day production tasks and equipment operation. Both roles are essential in pharmaceutical production but differ in responsibilities and qualifications.

What does a pharmaceutical process engineer do?

A pharmaceutical process engineer reviews the requirement to produce a pharmaceutical product and develops a process for manufacturing. In this career, your duties vary from employer to employer but usually include tasks such as providing technical specifications for machinery and equipment, working to estimate costs for production, and undertaking a negotiation for the procurement of necessary materials and ingredients. Your responsibilities as a process engineer may include providing analysis of the process to ensure efficiency, safety, and compliance with relevant regulations.

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

To thrive as a Pharmaceutical Process Engineer, you need a strong background in chemical or process engineering, pharmaceutical manufacturing, and regulatory compliance, typically supported by a relevant engineering degree. Familiarity with process simulation software (such as Aspen Plus), GMP standards, and quality management systems is essential. Attention to detail, problem-solving skills, and effective teamwork are crucial soft skills for optimizing processes and ensuring product quality. These competencies are vital for developing efficient, safe, and compliant pharmaceutical manufacturing processes that meet industry standards.

What are some common challenges faced by pharmaceutical process engineers when scaling up production from laboratory to manufacturing scale?

Pharmaceutical Process Engineers often encounter challenges when translating lab-scale processes to full-scale manufacturing, such as maintaining product quality, ensuring process consistency, and meeting strict regulatory requirements. Controlling variables like temperature, pressure, and mixing at a larger scale can introduce unforeseen issues that require innovative problem-solving. Collaboration with cross-functional teams—including quality assurance, validation, and production staff—is essential to address these challenges efficiently. Adaptability and attention to detail are crucial in ensuring a smooth and compliant scale-up process.

What does a pharmaceutical process engineer do?

A Pharmaceutical Process Engineer is responsible for designing, developing, and optimizing processes used in the manufacturing of pharmaceutical products. They ensure that production methods are efficient, safe, and compliant with regulatory standards. Their work involves troubleshooting process problems, implementing new technologies, and collaborating with other departments to improve product quality and production efficiency. They play a critical role in scaling up laboratory processes to full-scale manufacturing while maintaining product integrity and safety.
What are popular job titles related to Pharmaceutical Process Engineer jobs in Ohio? For Pharmaceutical Process Engineer jobs in Ohio, the most frequently searched job titles are:
What job categories do people searching Pharmaceutical Process Engineer jobs in Ohio look for? The top searched job categories for Pharmaceutical Process Engineer jobs in Ohio are:
What are popular job titles related to Pharmaceutical Process Engineer jobs in OH? For Pharmaceutical Process Engineer jobs in OH, the most frequently searched job titles are:
Infographic showing various Pharmaceutical Process Engineer job openings in Ohio as of August 2026, with employment types broken down into 84% Full Time, 3% Part Time, and 13% Contract. Highlights an 100% In-person job distribution, with an average salary of $69,695 per year, or $33.5 per hour.

Specialist II, Process Focus Team

Hikma Pharmaceuticals PLC

Columbus, OH

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 26 days ago


Hikma Pharmaceuticals rating

8.0

Company rating: 8.0 out of 10

Based on 30 frontline employees who took The Breakroom Quiz

43rd of 86 rated pharmaceutical


Job description

Job Title:      Specialist II, Process Focus Team

Location:      Columbus, OH

Job Type:     Full time

Req ID:         10914

 

About Us: 

As a developer, manufacturer, and supplier of essential medicines, Hikma Pharmaceuticals USA Inc. and its affiliates' mission is to bring Better Health. Within Reach. Every Day. for millions of patients around the world.  We are a trusted, reliable partner and dependable source of over 800 high-quality generic, specialty and branded pharmaceutical products that hospitals, physicians and pharmacists need to treat their patients across North America, the Middle East, North Africa and Europe.  Through our 32 manufacturing plants, eight R&D centers, and 9,500+ employees worldwide, we are always hard at work creating high-quality medicines and making them accessible to the people who need them.

Description:

We are committed to building a diverse and inclusive team and encourage applications from candidates of all backgrounds.  We are seeking a talented and motivated Specialist II, Process Focus Team to join our team.  

In this role, you will be responsible for the Process Focus Team will be actively involved in leading, coaching and mentoring activities (such as project teams, kaizen events, value stream mapping etc.) based on priorities.  Each project must be aligned with the Columbus Generics Site Strategy and support corporate LSP strategies.  These activities will be cross functional in nature. This person will be actively involved in identifying, leading and implementing process improvement projects. This person should meet the criteria for green belts certification in Six Sigma and demonstrate knowledge of lean manufacturing and process improvement

Key Responsibilities:

  • Regular and predictable onsite attendance and punctuality. 
  • Identify opportunities and implement strategic solutions aligned with Site Metrics, Business Objectives and Site Strategy. 
  • Lead and facilitate cross functional process improvement initiatives/teams. 
  • Facilitate the implementation/sustainability of cross functional improvements. 
  • Define/track performance for key KPI's.  Clearly quantify/communicate improvement targets/benefits, both theoretical and actual. 
  • Communicate identified opportunities, current project(s), implemented improvements and benefits. 

Qualifications:

We value the skills and experiences candidates bring to the table.  While we have listed some qualifications below, we encourage candidates to apply even if they do not meet all of them:

  • Bachelor's Degree in a technical or business-related discipline relating to process analysis/improvement and 1-3 years of work experience relating to process analysis/improvement or 6-8 years of experience in the pharmaceutical industry, process analysis/improvement or project management.
  • 1-3 years' experience in an industrial environment, preferably pharmaceutical, with demonstrated experience in technical, compliance, production or supply chain environments.
  • Demonstrated ability to: Define a problem. Determine Cost Analysis and Benefits Case. Identify and utilize resources to drive process improvements. Collect, statistically analyze and interpret data. Establish corrective and preventative actions. Implement improvements of medium to high complexity.
  • Demonstrated experience in project management (will consider experience within functional area).
  • Demonstrated ability to facilitate and/or be an active participant on teams.
  • A minimum of green belt Six Sigma certification. (To be attained during first year on the job).
  • Knowledge of lean Manufacturing and other techniques to implement process improvements.
  • Proficient in spreadsheet (report formatting, graphing, formula a calculation generation), database, presentation and project management tools.
  • Strong technical business writing and oral communication skills.

What We Offer*:

  • Annual performance bonus, commission, and share potential
  • Auto enrollment in a Hikma-sponsored 401(k) program at a pre-tax contribution rate of 4% of eligible pay.  Hikma will match 100% of the first 6% of eligible pay that you contribute
  • A generous paid time off (PTO) bank starting with 20 days (prorated based on hire date).  Additional days granted upon reaching work milestone anniversaries
  • 3 personal days (prorated based on hire date)
  • 11 company paid holidays
  • Comprehensive benefits including health, dental, vision, mental health, disability, life insurance, prescription drug coverage, and a variety of voluntary benefits
  • Employee discount program
  • Wellbeing rewards program
  • Safety and Quality is a top organizational priority
  • Career advancement and growth opportunities
  • Tuition reimbursement
  • Paid maternity and parental leave

*Eligibility requirements apply to some benefits and depend on the job classification, role, and length of employment.  Benefits are subject to change as well as specific plan or program terms.

Recruiters:

Please note that Hikma has a set roster of approved recruiters for specific roles agreed to in advance and does not accept unsolicited resumes or calls from third-party recruiters or employment agencies regarding open positions.  In the absence of a signed agreement and approval from Hikma's Human Resources department to submit resumes for a specific position, Hikma will not approve, nor will be under an obligation to make, any payment to such non-approved third-parties in the event a candidate they refer is hired by Hikma.

Equal Opportunity Employer:

Hikma Pharmaceuticals USA Inc. is an Equal Opportunity Employer.  Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status, or other characteristics protected by law.

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