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Laboratory Technician Winston Staffing
Wayne, NJ6 days ago
- $20–$23 Per Hour
- Temporary
- Full-time
- Part-time
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Skills
- Analysis Skillsunmatched
- Antibodiesunmatched
- Biologyunmatched
- Biomedical Engineeringunmatched
- Biotech and Pharmaceuticalunmatched
- Chemical Engineeringunmatched
- Chemistryunmatched
- Communication Skillsunmatched
- Continuous Improvementunmatched
- Corporate Policiesunmatched
- Corrective and Preventative Action (CAPA) Systemsunmatched
- Cross-Functionalunmatched
- Current Good Manufacturing Practice (cGMP)unmatched
- Data Analysisunmatched
- Data Processingunmatched
- Discrepancy Reportunmatched
- Drug Manufacturingunmatched
- Drug Productsunmatched
- GMP (Good Manufacturing Practices)unmatched
- Government Regulationsunmatched
- High School Diplomaunmatched
- Identify Issuesunmatched
- Investigative Reportsunmatched
- Laboratoryunmatched
- Laboratory Techniquesunmatched
- Lean Manufacturingunmatched
- Lean Six Sigmaunmatched
- Maintain Complianceunmatched
- Manufacturingunmatched
- Manufacturing Operationsunmatched
- Manufacturing Systemsunmatched
- Manufacturing/Industrial Processesunmatched
- Metricsunmatched
- Oncologyunmatched
- Operational Supportunmatched
- Operations Processesunmatched
- Organizational Skillsunmatched
- Problem Solving Skillsunmatched
- Procedure Developmentunmatched
- Process Managementunmatched
- Process Manufacturingunmatched
- Process Validationunmatched
- Product/Service Launchunmatched
- Production Controlunmatched
- Production Scheduleunmatched
- Project/Program Managementunmatched
- Quality Managementunmatched
- Reconciliationunmatched
- Regulationsunmatched
- Regulatory Requirementsunmatched
- Root Cause Analysisunmatched
- Safety/Work Safetyunmatched
- Scientific Principlesunmatched
- Six Sigmaunmatched
- Standard Operating Procedures (SOP)unmatched
- Startupunmatched
- System Operationsunmatched
- Team Lead/Managerunmatched
- Team Playerunmatched
- Technical Operationsunmatched
- Technical Writingunmatched
- Time Managementunmatched
- Tool and Die Manufacturingunmatched
- Writing Skillsunmatched
Description
Job Title: Lab Technician - II
Location: Pearl River, NY
Duration: 6 months
Pay rate: $28/hr on w2
Work Environment & Schedule
On-site, 5 days per week
Standard hours: ~8:00 AM 4:30/5:00 PM
May require:
Early or late shifts (~6+ times/year)
Occasional weekend work (~2 times/year)
Work requires flexibility employees stay until work is complete
Hiring Manager Note:
Execute upstream manufacturing processes including:
Reports
SOPs
Batch records
Required Qualifications
Exposure to pharmaceutical or biotech manufacturing
Knowledge of GMP environments
Strong troubleshooting and analytical skills
Ideal Candidate Profile
What You Will Achieve
Here Is What You Need (Minimum Requirements):
Location: Pearl River, NY
Duration: 6 months
Pay rate: $28/hr on w2
Work Environment & Schedule
On-site, 5 days per week
Standard hours: ~8:00 AM 4:30/5:00 PM
May require:
Early or late shifts (~6+ times/year)
Occasional weekend work (~2 times/year)
Work requires flexibility employees stay until work is complete
Hiring Manager Note:
- We are seeking an entry-level to early-career Manufacturing Scientist/Engineer to support upstream operations within antibody-drug conjugate (Client) manufacturing in an oncology-focused pharmaceutical environment.
- This role combines hands-on manufacturing with process ownership, continuous improvement, and technical problem-solving.
Execute upstream manufacturing processes including:
- Fermentation
- Solvent-based recovery
- Multi-stage chemical synthesis
- Operate within a multi-step drug substance production process
- Prepare buffers and support in-house reagent production
- Own and execute assigned processes end-to-end (not shift hand-off based)
- Perform process monitoring, troubleshooting, and optimization
- Collaborate with engineering and cross-functional teams
- Involves use of specialized PPE and handling of cytotoxic materials under strict safety protocols
- Continuous improvement (CI) initiatives
- Process qualifications and validation
- Tech transfers and new product introductions
Reports
SOPs
Batch records
Required Qualifications
- Bachelor s degree in: Biology, Chemistry, Chemical Engineering, Biomedical Engineering, or related field
- Strong understanding of scientific principles and laboratory/manufacturing practices
- Ability to learn complex processes and equipment
Exposure to pharmaceutical or biotech manufacturing
Knowledge of GMP environments
Strong troubleshooting and analytical skills
Ideal Candidate Profile
- Entry-level or recent graduate (2-4 years' experience)
- Motivated to commit long-term (not short-term experience seekers)
- Comfortable with a non-routine, highly technical manufacturing environment
- Strong ownership mindset and adaptability
What You Will Achieve
- 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, *** 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 *** ready to achieve new milestones and help patients across the globe.
- 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, *** 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
- 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
Numbers & Facts
| Location | Pearl River, NY |
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