Glaukos

Lead Manufacturing Technician - Pharma

Glaukos$75K — $95K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • 8-10 years of industry experience with a high school diploma
  • 6-8 years with an associate degree in science or engineering
  • 4-6 years with a bachelor's degree in science or engineering
  • Proven experience in the medical device, pharmaceutical, and/or biotechnology fields
  • Desirable experience in clean room maintenance following GDP, cGMPs, and QSR standards

Responsibilities

  • Manage operation and project schedules, adjusting resources as necessary
  • Supervise production technicians to enhance quality and output
  • Perform all Manufacturing Technician activities as needed
  • Ensure all documentation is accurate and compliant (cGMP, QSR, GDP)
  • Open and close jobs in Oracle system
  • Manage inventory requests and ensure accuracy in reconciliation
  • Revise documentation to maintain compliance and precision
  • Provide engineering feedback on Non-Standard Build Requests and validation builds

Benefits

  • Opportunity for career progression within a specialized industry
  • Hands-on work with compliance to high standards of manufacturing
  • Engagement in both production and management aspects of operations
  • Collaboration with engineering on innovative projects
  • Dynamic work environment focused on quality and efficiency
Full Job Description
Job Description

How will you make an impact?

The Lead Manufacturing Technician, based in San Clemente, CA will be responsible for the completion of the scheduled production and management of preventative maintenance. The Lead will ensure proper documentation (cGMP and GDP), open/close jobs in MRP system, and provide feedback and updates to Management and Engineering. This position will also prepare components, build assemblies, and bulk drug formulations. All activities will be performed with good documentation practices (GDP) in accordance with current good manufacturing practices (cGMPs) and quality system regulation (QSR) medical device good manufacturing practices (GMP) requirements.

Additional tasks will include performing the following:
  • Filing, capping, and crimping operations
  • Packaging and labeling operations
  • Sampling
  • Visual inspections
  • Documentation and data input into materials requirement planning (MRP), Batch Records (BRs), and Device History Record (DHR)
  • Track clean room, environmental chambers, and equipment preventive maintenance (PMs)

What will you do?
  • Manage the operation schedule, project schedule, and adjusts the schedule and resources accordingly
  • Supervise production technician(s) to optimize quality and output
  • Ability to perform all activities outlined for a Manufacturing Technician as needed
  • Verify all documentation is followed and completed accurately (cGMP, QSR, and GDP)
  • Manages Oracle to open and close jobs
  • Manages inventory requests and reconciliation for accuracy
  • Revise documentation to ensure accuracy and compliance
  • Communicate feedback to engineering on Non-Standard Build Requests, Validation builds, Clinical builds, etc.

How will you get here?

To be successful in this role, you will need to have the following:
  • Industry (medical device, pharmaceutical, and/or biotechnology) and educational experience.
  • 8 - 10 years' experience with high school diploma
  • 6 - 8 years' experience with associate degree in science or engineering
  • 4 - 6 years' experience with bachelor's degree in science or engineering
  • It is highly desirable to have experience working in and maintaining a clean room in accordance with GDP, cGMPs, and QSR standards.


#GKOSUS

About Glaukos

Glaukos Corporation is an ophthalmic medical technology and pharmaceutical company focused on novel therapies for the treatment of glaucoma, corneal disorders and retinal diseases. The company pioneered Micro-Invasive Glaucoma Surgery, or MIGS, to revolutionize the traditional glaucoma treatment and management paradigm. Glaukos launched the iStent, its first MIGS device, in the United States in 2012 and is leveraging its platform technology to build a comprehensive and proprietary portfolio of micro-scale injectable therapies designed to address the complete range of glaucoma disease states and progression. The company's second-generation MIGS device, the iStent inject, was approved by the FDA in June 2018. Glaukos is also developing a pipeline of innovative technologies in corneal health, including the recently acquired Microline surgical platform, as well as novel drug delivery technologies.
Learn more about Glaukos
Size
727 employees
Market Cap
$1.9 billion
Industry
Net Income
-$120.3 million
Founded
1998
5 Year Trend
+20.8%
Revenue
$224.9 million
NASDAQ

Similar Jobs

More Jobs at Glaukos

More Pharmaceuticals & Biotech Jobs

Find similar Lead Manufacturing Technician - Pharma jobs: