Purdue Pharma L.P. · 1 week ago
Packaging Maintenance Mechanic - Weekend Shift Friday -Sunday (6:00 AM - 6:30 PM)
Purdue Pharma L.P. is dedicated to developing and manufacturing medications to meet healthcare needs. The Packaging Maintenance Mechanic will be responsible for the setup, diagnosis, adjustment, and repair of pharmaceutical packaging equipment, ensuring high-quality production and minimal downtime.
BiotechnologyHealth CarePharmaceutical
Responsibilities
Ensure proper set-up and operation of oral solid dosage packaging such as but not limited to: descrambler, desiccant feeder, induction sealer, re-torquers, labelers, and outserter
Perform packaging equipment preventative maintenance as required
Ensure proper cleaning and assemble of the packaging equipment
Perform changeover of packaging equipment for different products including bottle size and format changes
Troubleshoot and correct mechanical issues as they occur
Ensure proper execution of batch records and standard operating procedures
Operate equipment as needed to ensure continuous operation of equipment
Function as Lead Technician (SME) in the production areas with a strong understanding of operating all equipment to achieve Overall Equipment Effectiveness (OEE)
Interpret and carry out detailed written or verbal instructions including work orders, blueprints, drawings and sketches related to the operation, maintenance, repair, or modification of packaging equipment control and power systems while exercising judgement and discretion in the most advantageous manner
Assist in the installation, modification, commissioning, and qualification/validation of equipment
Assist Pharmaceutical Technology with new product introductions and provide feedback of processing requirements
Provide technical leadership and process knowledge in the training of new operations personnel
Contact equipment/supply vendors as needed to resolve problems and ensure limited downtime due to mechanical issues
May provide support in the area of small project management in the definition of requirements for and procurement of small equipment
Function as subject matter expert (SME) in the production areas with a strong understanding of operating all equipment to achieve Overall Equipment Effectiveness (OEE)
Maintain strong presence on the floor to ensure that equipment problems are resolved in a timely manner with little downtime
Possess knowledge of working properties of common-stock materials, metallic and non-metallic
Disassemble equipment for repair, maintenance, modification, and/or training; reassemble the equipment, check for proper operation
Ensure compliance with cGMPs, OSHA, DEA, and any other regulatory guidelines and Company policies that may apply. Identify and report quality issues
Perform other related assignments and duties as required and assigned
Perform all functions according to current Good Manufacturing Practices (cGMP) and company Standard Operating Procedures (SOP)
Responsible for 'Downtime', 'Change Over Time', 'PM's' and 'Productivity' results
Qualification
Required
High School Diploma or equivalent
Minimum of five years of relevant pharmaceutical industry experience preferred or equivalent combination of education, demonstrated mechanical skill
Demonstrated advanced or expert level of mechanical knowledge, skills, and abilities supporting oral solid dose (OSD) pharmaceuticals Packaging and/or Packaging Serialization
Hands on maintenance, troubleshooting, repair and upgrade to packaging production equipment
Demonstrated ability to read and interpret documents such as safety policies, operating and maintenance instructions and procedure manuals, etc
Demonstrated ability to perform diverse and complex assignments in support of operations
Capability to perform basic/complex mathematical computations of addition, subtraction, multiplication, and division. Understanding of the Metric System of Measurement
Advanced knowledge of the functional/process area. The work calls for advanced comprehension of the area to solve unusual as well as common work problems, to be able to advise on technical matters, and to serve as a resource on the subject for others in the organization
Ensure compliance with cGMPs, OSHA, DEA, and any other regulatory guidelines and Company policies that may apply. Identify and report quality issues
Perform all functions according to current Good Manufacturing Practices (cGMP) and company Standard Operating Procedures (SOP)
Responsible for 'Downtime', 'Change Over Time', 'PM's' and 'Productivity' results
Preferred
Certification/Associate's/Bachelor's degree in Manufacturing, Engineering, or Technology related fields
Operational Excellence; Six Sigma Green Belt certified
Advanced Computerized Manufacturing
Controls (Programmable Logic Controls); Motors & Controls; Robotics
Maintenance, Installation, and Repair
Diagrams/Schematics
Root cause analysis/problem solving tools and techniques
Company
Purdue Pharma L.P.
Purdue and its subsidiaries develop, manufacture and market medications to meet the evolving needs of healthcare professionals, patients, and caregivers.
Funding
Current Stage
Late StageTotal Funding
$1.8MKey Investors
US Department of Energy
2018-05-29Grant· $1.8M
Leadership Team
Recent News
Hartford Business Journal
2025-11-19
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