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Pharma Chemical Engineer Jobs (NOW HIRING)

Stark Pharma Solutions Inc

Manufacturing Engineer

Orlando, FL · On-site

$68K - $87K/yr

Hi, My name is Sravani Dasari from Stark Pharma Solutions Inc. We are hiring talent for our client ... Chemical Engineering, Biomedical Engineering, Biotechnology, or a related engineering discipline ...

Stark Pharma Solutions Inc

Senior Process Engineer

Bend, OR · On-site

$109K - $141K/yr

Hi, My name is Karthik Mutyala, and I am a Recruitment Manager with Stark Pharma Solutions ... Required Qualifications * Bachelor's degree in Chemical Engineering, Mechanical Engineering ...

Stark Pharma Solutions Inc

CQV Engineer

Austin, TX · On-site

Hi, My name is Sravani Dasari from Stark Pharma Solutions Inc. We are hiring talent for our client ... Bachelor's degree in Mechanical Engineering, Chemical Engineering, Electrical Engineering ...

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Pharma Chemical Engineer information

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How much do pharma chemical engineer jobs pay per year?

As of Sep 13, 2026, the average yearly pay for pharma 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 cities are hiring for Pharma Chemical Engineer jobs?

Cities with the most Pharma Chemical Engineer job openings:

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Infographic showing various Pharma Chemical Engineer job openings in the United States as of August 2026, with employment types broken down into 94% Full Time, 2% Part Time, and 4% Contract. Highlights an 85% Physical, 5% Hybrid, and 10% Remote job distribution, with an average salary of $87,487 per year, or $42.1 per hour.

Manufacturing Process Engineer

Lexington, MA • On-site

Piramal Pharma Limited
See more jobs at Piramal Pharma Limitedexternal

$82K - $110K/yr

Full-time

Re-posted 17 days ago

Key responsibilities

  • Designs, project manages, and implements changes, improvements, new systems, and equipment in the manufacturing process.

  • Supports day-to-day production and maintenance activities, including troubleshooting and maintaining systems and equipment.

  • Develops and modifies SOPs, participates in deviation investigations, and manages technical documentation related to manufacturing systems.

Job description

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Division

Piramal Pharma Solutions

Piramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients through a globally integrated network of facilities in North America, Europe and Asia.

This enables us to offer a comprehensive range of services including Drug Discovery Solutions, Process & Pharmaceutical Development services, Clinical Trial Supplies, Commercial supply of APIs and Finished dosage forms. We also offer specialized services like development and manufacture of Highly Potent APIs and Antibody Drug Conjugation.

Our capability as an integrated service provider & experience with various technologies enables us to serve Innovator and Generic companies worldwide.

For more details, please visit : www.piramalpharmasolutions.com

Job Title

Manufacturing Process Engineer

Job Description

Business: Pharma Solutions Department: Facilities, Maintenance & Engineering Location: LexingtonJob DescriptionBusiness: Pharma Solutions Department: Facilities, Maintenance & Engineering Location: Lexington Job Overview Reporting to the Engineering Manager, the Manufacturing Process Engineer serves as subject-matter-expert and provides real-time, process engineering support to the manufacturing process. This position is responsible for design, project management, and implementation of new and existing systems, utilities and equipment, and ensures Quality, Compliance, and improved OTIF for all products produced at the manufacturing facility in Lexington, Kentucky. Reporting Structure This position reports to the Engineering Manager. Key Responsibilities: Designs and project manages changes, improvements, new systems and or equipment. Prepares Change Control Records (CCRs), Design Specifications, User Requirements Specifications, System Specifications, Design documents, Drawings, and Validation Documents for improvement, planned and corrective maintenance and system or process improvements Leads/assists in Continuous Improvement Projects, including identification of opportunities, researches literature and vendors, prepares and presents proposals, develops and executes projects, and closes projects, all following appropriate change control methodologies Represents Technical Subject Matter Expert (SME) in teams assembled to specify, install, troubleshoot and maintain systems, equipment and processes Supports day-to-day production and maintenance activities Provides training support as required. Develops and or modifies SOPs for the Processes and Equipment. Participates in deviation investigations to identify root causes and define corrective and preventive actions (CA/PA). Creates and maintains drawings and sketches. Manages Technical Publications Library to ensure the relevant manuals, specifications, design information for all of our facilities, utilities, equipment and products are on hand Primary/First Line responsibility for operation and maintenance of the Validated Systems to maintain production capability required. Primary/First Line responsibility for enhancements and upgrades of manufacturing related systems to maintain production capability. Qualifications: Bachelor's degree in Mechanical, Electrical, or Chemical Engineering Minimum 3-5 years of pharmaceutical manufacturing/maintenance experience required (parenteral/sterile filling experience preferred) Expertise in troubleshooting production equipment/systems Ability to work flexible schedule to support 24-hour operation (requires assignment on shift for 4 shift rotating days off schedule) PC literate with standard office application (Word, Excel, PowerPoint) competency Experience with maintenance and administration of both Windows-based and industrial (e.g., PLC) computer networks. Experience with Allen-Bradley ControlLogix and Siemens PLCs; experience with HMI software applications; experience with automating processes and equipment Knowledge and understanding of cGMPs including FDA, PMDA, and EU regulations; knowledge of cGMP validation requirements and techniques; experience with commissioning and validation protocol development and execution. Knowledge and experience in cGMP CA/PA, root-cause analysis, risk assessment and investigation tools and techniques.

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