USA - Lab Technician - II - USD#26-15420
$24.00-$26.66 per hour
Pearl River, NY
Onsite
Job Description
In this role, you will:
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, Client 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 SOP's.
Here Is What You Need (Minimum Requirements):
BA/BS degree in a science/engineering field with any years of experience, or Associate's 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
Bonus Points If You Have (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
Excellent communication skills for presenting data in project team meetings
Strong problem-solving skills
EEO:
Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of - Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans
$24.00-$26.66 per hour
Pearl River, NY
Onsite
Job Description
In this role, you will:
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, Client 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 SOP's.
Here Is What You Need (Minimum Requirements):
BA/BS degree in a science/engineering field with any years of experience, or Associate's 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
Bonus Points If You Have (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
Excellent communication skills for presenting data in project team meetings
Strong problem-solving skills
EEO:
Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of - Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans
Job ID: 523483048
Originally Posted on: 6/3/2026
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