QC Laboratory Technician
NovartisAbout the role
Job Description Summary
The QC Laboratory Technician is responsible for supporting all QC Laboratory activities. The QC Laboratory Technician is encouraged to work independently on routine tasks and have conceptual understanding of all Quality Control functions and business areas. May need supervision/support to resolve some sophisticated issues. The QC Laboratory Technician will serve as technical specialist within job function. Thinks logically and acts decisively.
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Job Description
Location: This position is on-site in Morris Plains, NJ
Shift: Sunday - Wednesday PM Shift (3:00 PM to 1:30 AM) Please only apply if you are able to work these exact hours.
#LI-Onsite
This role is on-site 5 days a week and does not have the ability to work remotely.
Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you.
Major accountabilities:
Responsible for preparing, stocking/restocking working stations with consumables/reagents as needed.
Performing reagent inventory tasks and maintain stock and inventory ensuring seamless operations in the laboratory.
Support sample management activities such as sample inventory, destruction and shipping
Provide support for Laboratory Instrumentation: for setting up, performing daily calibrations of equipment, such as Flow cytometers and qPCRs
Maintenance of laboratory equipment: performing daily, weekly, monthly maintenance activities.
Acting as contemporaneous data verifier/reviewer for Analytical method steps.
Perform sample receiving and sample preparation activities and act as a sample runner for the laboratory.
Following standard operating procedures (SOPs), safety guidelines, and regulatory requirements to ensure a safe and compliant laboratory environment.
Working closely with other laboratory technicians and laboratory personnel to meet project goals and deadlines.
Any other task assigned by management.
Key performance indicators:
Timely delivery on commitments with and departmental KPIs.
Timely responses and solutions to training-related issues.
Efficient and flexible usage of the available resources.
Compliance to all relevant company policies and guidelines
Exhibiting core Novartis values and behaviors and fostering these within the team
Minimum Requirements:
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Education:
A minimum of an Associate degree in science or related field
Requirements:
A minimum of one (1) year related experience in medical device, biopharmaceutical, or pharmaceutical industry
Experience working in a laboratory.
Experience using micro pipettes and aseptic technique.
Good understanding of regulatory requirements, policies and guidelines
Working knowledge of Quality systems (i.e. ESOPs, etc.)
Experience in use of LIMS or similar systems.
Ability to lift up to 25 lbs.
Skills:
Knowledge and understanding of current Good Manufacturing Practices (cGMP) related to the QC laboratory and ability to identify gaps in processes or systems.
Proficient with using Microsoft Office applications (Outlook, Excel, Word, and PowerPoint) and lab management software system (LIMS)
Detail oriented and exceptional organizational skills.
Time management to manage multiple tasks and prioritize duties in fast paced environment.
Strong attention to detail in handling laboratory equipment, samples, and reagents.
Languages:
English.
Competency Profile:
Strong communication skills for interacting with a variety of collaborators and partner groups.
Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude
Must demonstrate flexibility in adjusting to changing priorities and schedules.
Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies.
Ability to function in a rapidly changing environment & handle multiple priorities.
Ability to collaborate cross functionally to drive operational and quality excellence.
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