ZipRecruiter

Log In

Cencora | Pharma solutions

64 Cencora Operations Jobs Hiring Near You

Stark Pharma Solutions Inc

Manufacturing Engineer

Mobile, AL · On-site

$72K - $93K/yr

Hi, My name is Sravani Dasari from Stark Pharma Solutions Inc. We are hiring talent for our client ... Participate in planning and optimizing production sequences for assembly operations. Balance ...

New

Piramal Pharma Limited

Process Engineer

Lexington, KY · On-site

Be the First to Apply Division Piramal Pharma Solutions Piramal Pharma Solutions is a contract ... Drafts experimental, development, and operational studies to expand expertise in parenteral ...

Piramal Pharma Limited

Process Engineer

Lexington, KY · On-site

Be the First to Apply Division Piramal Pharma Solutions Piramal Pharma Solutions is a contract ... operational studies to expand expertise in parenteral manufacturing. • Ensures that work is ...

previous pagenext page

Showing results 41-60

All JobsCencora Operations Jobs

Cencora | Pharma solutions Jobs Information

What is it like to work at Cencora?

Cencora is a company that values collaboration and innovation, fostering a dynamic work environment where employees can share ideas and work together to achieve common goals.

As a leading provider of specialty pharmaceuticals, Cencora operates with a patient-centric approach, focusing on developing and delivering high-quality treatments to improve patients' lives. The company's team structure is designed to promote open communication and cross-functional collaboration, with a flat organizational hierarchy that encourages employee growth and development.

Working at Cencora may appeal to candidates who are passionate about the pharmaceutical industry and want to be part of a company that prioritizes patient care and innovation, offering opportunities for professional growth and development in a dynamic and collaborative work environment.
What are the most popular job types at Cencora?
    What are the most popular jobs at Cencora?
    What are the most popular categories at Cencora?
    Infographic showing various Operations job openings at Cencora in the United States as of June 2026, with employment types broken down into 93% Full Time, and 7% Part Time. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution.

    Manufacturing Process Engineer

    Piramal Pharma Limited

    Lexington, KY • On-site

    $73K - $97K/yr

    Full-time

    Posted 6 days ago

    Job description

    Be the First to Apply
    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: 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.

    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.

    Bachelor's Degree - Mechanical Engineering

    Apply