QC Laboratory Technician

Davita Inc.; Morris Plains (NJ); On-site; USD 45,000 - 85,000; Full time

Job summary

A leading company in the pharmaceutical industry seeks a QC Laboratory Technician for their Morris Plains location. The role involves supporting various laboratory activities, ensuring compliance with quality and safety standards, and requires an associate's degree with relevant experience. The technician will work PM shifts, contributing to critical laboratory functions and collaborating with cross-functional teams to achieve project goals.

Benefits

Comprehensive benefits package including health, life, and disability benefits

401(k) with company contribution and match

Generous time off package including vacation and personal days

Performance-based cash incentive

Annual equity awards eligibility

Qualifications

• Minimum 1 year experience in medical device, biopharmaceutical, or pharmaceutical industry.
• Experience working in a laboratory with micro pipettes and aseptic techniques.
• Knowledge of cGMP and understanding FDA guidelines.

Responsibilities

• Prepare and maintain laboratory working stations with required consumables.
• Perform equipment calibration and maintenance of laboratory instrumentation.
• Support sample management activities including inventory and shipping.

Skills

Continued Learning

Dealing With Ambiguity

GMP Procedures

QA (Quality Assurance)

Quality Control (QC) Testing

Quality Standards

Self-Awareness

Technological Expertise

Education

Associate's degree in science or related field

Tools

Microsoft Office

LIMS systems

Job description

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.

Job Description

Shift: Sun-Wed PM (3:00pm-1:30am)

Number of positions available: 2

Location: Morris Plains, NJ
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:

• Deliver quality products and services on time to all customers, internal and external.

Ideal Background:

Education:

• Associate's degree in science or related field.

Languages:

• Fluent in English.

Experience:

• 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 techniques.
• Knowledge of cGMP and an understanding of the concepts of GLP, good clinical practices and FDA guidelines, applicable state and foreign regulations, and standards routinely used in the industry (i.e. ANSI, ISO, etc.).
• Knowledge of LIMS systems preferred.
• Working knowledge of Quality Systems (i.e. ESOPs, etc.)
• Proficient with using Microsoft Office applications (Outlook, Excel, Word, and PowerPoint)
• Ability to communicate clearly with a variety of individuals in various aspects of Novartis operations.
• Detail-oriented with expertise in problem solving and solid decision-making abilities.
• Strong interpersonal skills which include a professional demeanor when interacting with Novartis personnel.
• Strong attention to detail in handling laboratory equipment, samples, and reagents.
• Strong written and verbal communication skills are essential.

Why Novartis: Our purpose is to reimagine medicine to improve and extend people's lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture

The salary for this position is expected to range between $51,800 and $77,600 per year.

The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors.

Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards.

US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.

To learn more about the culture, rewards and benefits we offer our people click here.

You'll receive: You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook.

Handbook. https://www.novartis.com/careers/benefits-rewards

Join our Novartis Network:
If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here:
https://talentnetwork.novartis.com/network

EEO Statement:

The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status.

Accessibility and reasonable accommodations

The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to [e-mail] or call [phone] and let us know the nature of your request and your contact information. Please include the job requisition number in your message.

Salary Range

$45,300.00 - $84,100.00

Skills Desired

Continued Learning, Dealing With Ambiguity, Gmp Procedures, Qa (Quality Assurance), Quality Control (Qc) Testing, Quality Standards, Self-Awareness, Technological Expertise