Aseptic Technician II
Job Location:
Job Location:
Pearl River, NY - USA
Monthly Salary:
Not Disclosed
Monthly Salary:
Posted on:
23 hours ago
Posted on:
Vacancies:
1 Vacancy
Vacancies:
Job Summary
Position Details:
Our client a world-leading Pharmaceutical Company in Pearl River NY is currently looking for an Manufacturing Technician to join their expanding team.
Our client a world-leading Pharmaceutical Company in Pearl River NY is currently looking for an Manufacturing Technician to join their expanding team.
Job Title: Manufacturing Technician / Pharma Industry
Duration: 09 months contract extendable up to 48 months
Location: Pearl River NY
Duration: 09 months contract extendable up to 48 months
Location: Pearl River NY
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
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:
What You Will Achieve:
The main function of an Aseptic Technician is to support the manufacturing of sterile pharmaceutical products by performing tasks in controlled environments using aseptic techniques.
A typical Aseptic Technician ensures product integrity and compliance with regulatory standards through meticulous attention to cleanliness documentation and process control.
You will have knowledge of process equipment and systems and manufacturing operations with the primary responsibility to execute process and equipment operation activities during manufacturing operations.
Due to your expertise in the manufacturing domain you may participate in training for operational qualifications and assist the Team Lead or other team members as needed.
The main function of an Aseptic Technician is to support the manufacturing of sterile pharmaceutical products by performing tasks in controlled environments using aseptic techniques.
A typical Aseptic Technician ensures product integrity and compliance with regulatory standards through meticulous attention to cleanliness documentation and process control.
You will have knowledge of process equipment and systems and manufacturing operations with the primary responsibility to execute process and equipment operation activities during manufacturing operations.
Due to your expertise in the manufacturing domain you may participate in training for operational qualifications and assist the Team Lead or other team members as needed.
You will conduct all activities in accordance with Company policies and standard operating procedures client Values and global regulatory guidelines environmental guidelines etc.
As an associate your focus on the job will contribute in achieving project tasks and goals.
Through your domain knowledge and commitment you will create a collaborative team environment for your colleagues.
It is your hard work and focus that will make Pfizer ready to achieve new milestones and help patients across the globe.
As an associate your focus on the job will contribute in achieving project tasks and goals.
Through your domain knowledge and commitment you will create a collaborative team environment for your colleagues.
It is your hard work and focus that will make Pfizer ready to achieve new milestones and help patients across the globe.
Role Responsibilities:
Execute production activities using knowledge of process equipment systems and manufacturing operations.
Participate in operational qualification training and assist the Team Lead as needed.
Ensure all activities comply with Company policies standard operating procedures Pfizer Values and global regulatory and environmental guidelines.
Work in a structured environment using established procedures.
Ensure work is regularly reviewed for technical judgment completeness and accuracy.
Assist in troubleshooting technology transfer and start-up activities. Applies established analytical tools to reduce cycle times and optimize production scheduling.
Oversee technical documentation for production and process approvals ensuring compliance with Current Good Manufacturing Practices and manage process activities by adhering to Standard Operating Procedures.
Assists production teams with batch paperwork and performs system transactions.
Monitors and communicates production metrics.
Ensures compliance with all government and company regulatory requirements.
Verifies batch reconciliation and investigates all discrepancies immediately. Prepares Manufacturing Discrepancy Reports as necessary and escalates issues requiring Management Investigation Reports (MIRs) regarding deviations in process tasks or equipment set-up and testing.
Execute production activities using knowledge of process equipment systems and manufacturing operations.
Participate in operational qualification training and assist the Team Lead as needed.
Ensure all activities comply with Company policies standard operating procedures Pfizer Values and global regulatory and environmental guidelines.
Work in a structured environment using established procedures.
Ensure work is regularly reviewed for technical judgment completeness and accuracy.
Assist in troubleshooting technology transfer and start-up activities. Applies established analytical tools to reduce cycle times and optimize production scheduling.
Oversee technical documentation for production and process approvals ensuring compliance with Current Good Manufacturing Practices and manage process activities by adhering to Standard Operating Procedures.
Assists production teams with batch paperwork and performs system transactions.
Monitors and communicates production metrics.
Ensures compliance with all government and company regulatory requirements.
Verifies batch reconciliation and investigates all discrepancies immediately. Prepares Manufacturing Discrepancy Reports as necessary and escalates issues requiring Management Investigation Reports (MIRs) regarding deviations in process tasks or equipment set-up and testing.
Partners with the Quality Technology and Operations personnel to investigate Manufacturing Incidents applying tools as CAPA to eliminate root cause in investigating.
Participates in continuous improvement initiatives applying tools like LEAN manufacturing and Six Sigma to improve quality cost safety and cycle time.
Able to handle routine problems independently. Works with cross-functional experts in solving problems.
Reviews updates and revises SOPs.
Participates in continuous improvement initiatives applying tools like LEAN manufacturing and Six Sigma to improve quality cost safety and cycle time.
Able to handle routine problems independently. Works with cross-functional experts in solving problems.
Reviews updates and revises SOPs.
Minimum Requirements:
BA/BS degree in a science/engineering field with any years of experience or Associates degree with 4 years of experience or high school diploma (or equivalent) with 6 years of relevant experience.
Knowledge of process equipment and manufacturing operations.
Ability to follow standard operating procedures and regulatory guidelines.
Basic understanding of Current Good Manufacturing Practices.
Strong organizational skills to manage project tasks and meet deadlines.
Technical documentation skills for production and process approvals.
BA/BS degree in a science/engineering field with any years of experience or Associates degree with 4 years of experience or high school diploma (or equivalent) with 6 years of relevant experience.
Knowledge of process equipment and manufacturing operations.
Ability to follow standard operating procedures and regulatory guidelines.
Basic understanding of Current Good Manufacturing Practices.
Strong organizational skills to manage project tasks and meet deadlines.
Technical documentation skills for production and process approvals.
Preferred Requirements:
Experience within the pharmaceutical industry.
Familiarity with Six Sigma or other operational excellence programs.
Proficiency in troubleshooting and technology transfer activities.
Strong analytical skills for process monitoring and data analysis.
Experience within the pharmaceutical industry.
Familiarity with Six Sigma or other operational excellence programs.
Proficiency in troubleshooting and technology transfer activities.
Strong analytical skills for process monitoring and data analysis.
