Clinical Lab Techician - Scien. Support

Novartis; East Hanover (NJ); On-site; USD 60,000 - 80,000; Full time

Job summary

A leading company in the pharmaceutical industry is seeking a Clinical Lab Technician - Scientific Support for their East Hanover, NJ site. This role involves supporting laboratory operations, managing sample testing, and ensuring compliance with SOPs. Ideal candidates will have a background in relevant sciences and experience in QC labs, with a focus on detail and communication.

Qualifications

• 0-5 years of experience in pharmaceutical, biologics, microbiology, sterile manufacturing, or medical device industries.
• Ability to identify and communicate errors in analytical procedures.
• Focus on customer satisfaction and responsiveness to internal and external requests.

Responsibilities

• Manage restocking PPE and other required materials in designated areas.
• Perform sample receipt of QC samples from the production unit.
• Conduct monthly review of laboratory logbooks and cleaning of laboratory and equipment.

Skills

Detail-oriented

Strong written and verbal communication skills

Organizational skills

Knowledge of GMP/GLP concepts

Education

AS/BA in cell biology, immunology, molecular biology, virology, biochemistry, microbiology, or related sciences

Job description

Join to apply for the Clinical Lab Technician - Scientific Support role at Novartis.

Summary
This position will be located at the East Hanover, NJ site and will not support remote work.
Please note that this role does not provide relocation assistance; only local candidates will be considered.
Under general supervision, perform supporting and administrative activities supporting Raw Materials, BioAnalytics, and Microbiology in the Analytical Operations department of TRD CGT East Hanover.

Key Responsibilities

1. Work on shifts covering daytime/evening and one or both weekend days, fixed according to business needs.
2. Manage restocking PPE and other required materials in designated areas.
3. Perform sample receipt of QC samples from the production unit.
4. Assist with sample management for cell and gene therapy modalities.
5. Manage shipment of samples in and out of the site.
6. Manage reagent and consumable inventory for assigned areas.
7. Prepare reagents and buffers required for testing.
8. Perform inspections and testing of raw materials.
9. Handle bulk gas receipt and testing.
10. Conduct monthly review of laboratory logbooks and cleaning of laboratory and equipment.
11. Ensure cleanliness of laboratory areas.
12. Perform all testing activities in compliance with SOPs and procedures.

Requirements

• Preferred AS/BA in cell biology, immunology, molecular biology, virology, biochemistry, microbiology, or related sciences.
• 0-5 years of experience in pharmaceutical, biologics, microbiology, sterile manufacturing, or medical device industries, ideally in QC labs.
• Knowledge of GMP/GLP concepts.
• Strong written and verbal communication skills.
• Detail-oriented with good organizational skills.
• Ability to identify and communicate errors in analytical procedures.
• Focus on customer satisfaction and responsiveness to internal and external requests.

Compensation & Benefits

The pay range at start is estimated between $25.19/hr and $46.83/hr. Note that salary ranges may fluctuate during 2025 due to market conditions, and final pay depends on experience, location, and other factors. The total package may include bonuses, stock units, and other benefits, including health and retirement plans. Details will be provided upon offer.

Note: No visa sponsorship or relocation support is provided for this role. Only apply if the location is accessible for you.

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