Packaging Equipment Engineer III

Lake PharmaAlbuquerque, NM
41d

About The Position

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. The Packaging Equipment Engineer will be responsible for supporting daily packaging operations, ensuring optimal performance, reliability, and compliance of all packaging equipment within a GMP-regulated pharmaceutical manufacturing environment. This role will lead and support equipment optimization, troubleshoot technical issues, implement process improvements, and collaborate closely with cross-functional teams including Production, Maintenance, Quality, Validation, and Supply Chain. In addition, the candidate will provide technical mentorship to junior engineers and mechanics, reviews and approves engineering documentation, and collaborates with cross-functional teams to ensure compliance with GMP, safety, and regulatory requirements. By driving equipment performance and improvement initiatives, this role directly contributes to efficient, compliant, and safe pharmaceutical manufacturing operations.

Requirements

  • Bachelor's degree in Engineering or related field, Mechanical preferred.
  • Minimum of five (5) years' experience in packaging equipment within the manufacturing environment. Pharmaceutical, biotechnology, or medical device industry a plus.
  • Strong understanding of GMP, cGMP, and FDA regulations preferred.
  • Hands-on experience with packaging lines (vials, labeling, cartoning, serialization, etc.).
  • Proficiency in troubleshooting mechanical and automation systems (PLC, sensors, servos, HMIs).
  • Demonstrated experience managing equipment improvement or capital projects.
  • The ideal candidate should have the ability to read and interpret various documents, such as safety instructions, standard operating procedures, technical procedures, and governmental regulations in US English. Additionally, the person should possess strong written and verbal communication skills, along with effective presentation skills.
  • Proficient in executing arithmetic operations including addition, subtraction, multiplication, and division across various units of measurement, employing whole numbers, fractions, decimals, and percentages. Candidates must possess a strong grasp of algebraic and geometric principles.
  • Ability to define problems, collect data, establish facts, and draw valid conclusions. Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables.
  • The ideal candidate will possess a strong technical foundation and proven capability in effectively utilizing diverse software tools to streamline the organization's daily functions. Essential skills encompass adeptness in manufacturing and internet software, alongside proficiency in Microsoft Office tools including PowerPoint, Excel, Word, and Outlook.
  • Must pass a background check
  • Must pass a drug screen
  • May be required to pass Occupational Health Screening

Nice To Haves

  • Pharmaceutical, biotechnology, or medical device industry a plus.
  • Strong understanding of GMP, cGMP, and FDA regulations preferred.

Responsibilities

  • Provide technical support for daily packaging operations, ensuring minimal downtime and consistent product quality.
  • Lead equipment troubleshooting and root cause analysis to resolve mechanical, electrical, or automation issues.
  • Develop and execute optimization projects to improve line efficiency, reduce waste, and enhance equipment performance.
  • Collaborate with cross-functional teams (Production, Maintenance, Engineering, Validation, and Quality) to ensure smooth operation and compliance with cGMP standards.
  • Author and review equipment-related documentation, including SOPs, change controls, CAPAs, and technical reports.
  • Conduct root cause analyses for recurring or high-impact equipment issues and implement long-term corrective and preventive actions (CAPAs).
  • Support installation, qualification, and validation (IQ/OQ/PQ) of new or modified packaging equipment.
  • Identify opportunities for continuous improvement in packaging processes and equipment reliability.
  • Ensure compliance with all relevant regulatory and safety requirements (FDA, EMA, OSHA, etc.).
  • Manage and coordinate vendor support for equipment maintenance and upgrades.
  • Provide technical training to operators and maintenance personnel on equipment functionality and best practices.

Benefits

  • 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!

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What This Job Offers

Job Type

Full-time

Career Level

Mid Level

Industry

Chemical Manufacturing

Number of Employees

101-250 employees

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