Process Development Technician II
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Job Location:
Andover, KS - USA
Monthly Salary:
Not Disclosed
Posted on:
8 days ago
Vacancies:
1 Vacancy
Job Summary
Position Details:
Our client a world-leading Pharmaceutical Company in Andover MA is currently looking for an Manufacturing Technician to join their expanding team.
Job Title: Manufacturing Technician / Pharma Industry
Duration: 8 months contract extendable up to 48 months
Location: Andover MA
Our client a world-leading Pharmaceutical Company in Andover MA is currently looking for an Manufacturing Technician to join their expanding team.
Job Title: Manufacturing Technician / Pharma Industry
Duration: 8 months contract extendable up to 48 months
Location: Andover MA
Shift Schedule:
Rotating days 1st or 2nd shift
6:00 am-6:00 pm OR 2:00 pm-2:00 am
Rotating days 1st or 2nd shift
6:00 am-6:00 pm OR 2:00 pm-2:00 am
Note:
The client has the right-to-hire you as a permanent employee at any time during or after the end of the contract.
You may participate in the company group medical insurance plan
Job Description:
Role Summary
The Senior Process Technician drives the execution of Commercial Clinical and/or Development production according to Standard Operating Procedures and Production Schedule.
The Senior Process Technician will work on interdisciplinary self-directed teams to define and implement process improvements participate in process troubleshooting.
Schedule: Rotating days 1st or 2nd shift 6a-6p or 2p-2a
The Senior Process Technician drives the execution of Commercial Clinical and/or Development production according to Standard Operating Procedures and Production Schedule.
The Senior Process Technician will work on interdisciplinary self-directed teams to define and implement process improvements participate in process troubleshooting.
Schedule: Rotating days 1st or 2nd shift 6a-6p or 2p-2a
Role Responsibilities
Executes manufacturing operations on the production floor for buffer/media make-up tanks glass washers autoclaves bioreactors filtration equipment inoculum preparation chromatography skids and/or UF/DF skids with varying levels of automation.
Executes the execution of SOPs for unit operations including but not limited to CIPs SIPs Sanitization etc.
Implements the execution and issue resolution associated with process equipment commissioning qualification and validation.
Drives troubleshooting technical support/analysis and resolution of equipment automation and process issues on the manufacturing floor.
Drives for Right first time execution the timely review of daily documentation and executes data entry; Monitor Identify and/or Communicate process and compliance trends in real time.
Supports the assigned audit lead for walkthroughs/GMP100s and observation improvements.
View Role for controlled documentation; SOPs Manufacturing Batch/Formulation Records Forms etc.
Collaborates with the Subject Matter Expert for manufacturing operations in support of QTS investigations and CAPA implementations.
Responsible for remaining current and reviews curriculum for training programs in support of manufacturing processes.
Implements Lean Manufacturing Sustainability Operational Excellence initiatives; facilitate the drive towards continuous improvement in all manufacturing areas.
Collaborates with cross-functional manufacturing assets in support of manufacturing campaigns.
Collaborates in the escalation process through various levels of management when operations personnel safety equipment functionality product supply and/or quality compliance are at risk.
Ensures work requests are generated when issues arise with manufacturing equipment.
Proficient in enterprise systems to support manufacturing operations including but not limited to SAP LIMS AMPS PDOCS and/or QTS.
Operates production sustainability through the performance of inventory accuracy reconciliation and/or task prioritization to maintain metric adherence.
Executes manufacturing operations on the production floor for buffer/media make-up tanks glass washers autoclaves bioreactors filtration equipment inoculum preparation chromatography skids and/or UF/DF skids with varying levels of automation.
Executes the execution of SOPs for unit operations including but not limited to CIPs SIPs Sanitization etc.
Implements the execution and issue resolution associated with process equipment commissioning qualification and validation.
Drives troubleshooting technical support/analysis and resolution of equipment automation and process issues on the manufacturing floor.
Drives for Right first time execution the timely review of daily documentation and executes data entry; Monitor Identify and/or Communicate process and compliance trends in real time.
Supports the assigned audit lead for walkthroughs/GMP100s and observation improvements.
View Role for controlled documentation; SOPs Manufacturing Batch/Formulation Records Forms etc.
Collaborates with the Subject Matter Expert for manufacturing operations in support of QTS investigations and CAPA implementations.
Responsible for remaining current and reviews curriculum for training programs in support of manufacturing processes.
Implements Lean Manufacturing Sustainability Operational Excellence initiatives; facilitate the drive towards continuous improvement in all manufacturing areas.
Collaborates with cross-functional manufacturing assets in support of manufacturing campaigns.
Collaborates in the escalation process through various levels of management when operations personnel safety equipment functionality product supply and/or quality compliance are at risk.
Ensures work requests are generated when issues arise with manufacturing equipment.
Proficient in enterprise systems to support manufacturing operations including but not limited to SAP LIMS AMPS PDOCS and/or QTS.
Operates production sustainability through the performance of inventory accuracy reconciliation and/or task prioritization to maintain metric adherence.
