Associate Scientist, QCA (Wed-Sat AM)

Novartis Farmacéutica; Morris Plains (NJ); On-site; USD 66,000 - 124,000; Full time

Job summary

An established industry player is seeking a dedicated Quality Control professional to join their team in Morris Plains. This role involves performing critical bio-analytical and microbial testing, ensuring compliance with quality standards, and contributing to various investigations. The ideal candidate will have a strong background in chemistry or microbiology, with experience in the pharmaceutical industry. Join a mission-driven organization that is committed to reimagining medicine and improving lives, while enjoying a competitive salary and a comprehensive benefits package.

Benefits

Sign-on bonus

Restricted stock units

Discretionary awards

Full range of medical benefits

Qualifications

• 0-5 years experience in pharmaceutical or related fields.
• Knowledge of cGMP and GLP concepts and FDA guidelines.

Responsibilities

• Perform Bio-Analytical and microbial testing.
• Maintain controls and reference standards for testing.
• Contribute to investigations and maintain GMP/GLP systems.

Skills

Bio-Analytical testing

Microbial testing

HPLC

GC

ELISA

qPCR

LabWare LIMS

Problem solving

Communication skills

Education

BA or MS in chemistry, biochemistry, microbiology

Tools

FTIR

UV/VIS

Polarimeter

Refractometer

Viscometer

Job description

Under general direction, perform testing and other activities in functions supporting the Quality Control department (Micro/EM, QC Bio-assay, and raw materials, as appropriate).

About the Role

Shifts Available: Wed-Sat AM 7:30am-6:00pm

Number of positions open: 1

Location: Morris Plains, NJ
Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you.

Key Responsibilities:

1. Perform Bio-Analytical testing such as Flow, ELISA, cell count, cell viability, qPCR as well as micro/EM testing such as environmental monitoring, gram stain, sterility, endotoxin, and mycoplasma.
2. Perform raw material testing such as HPLC, GC, FTIR, osmolarity, UV/VIS, polarimeter, refractometer, and viscometer.
3. Maintain controls and reference standards to support testing. Maintenance of Cell Lines and cell banks.
4. Review/approve data generated by other team members.
5. Perform method qualification/optimization of methods as per appropriate protocols.
6. Contribute to OOS/OOE investigations and deviation investigations.
7. Knowledge of LabWare LIMS and/or other QC data systems.
8. Maintain GMP/GLP quality systems and follow quality policies.

Role Requirements:

1. BA or MS in chemistry, biochemistry, microbiology, or other related science AND 0 - 5 years of experience in the pharmaceutical, biologics, microbiology, sterile manufacture, or medical device industry.
2. 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.).
3. Knowledge of microbiological and environmental monitoring, bioassay, and/or raw material test methods, as appropriate.
4. Knowledge of LIMS systems.
5. Ability to communicate clearly with a variety of individuals in various aspects of Novartis operations.
6. Detail-oriented with expertise in problem solving and solid decision-making abilities.
7. 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. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us!

The pay range for this position at commencement of employment is expected to be between $66,800 and $124,000/year; however, fluctuations in the job market may necessitate adjustments to pay ranges during this period. Further, final pay determinations will depend on various factors, including geographical location, experience level, knowledge, skills and abilities. The total compensation package for this position may also include other elements, including a sign-on bonus, restricted stock units, and discretionary awards in addition to a full range of medical, financial, and/or other benefits, dependent on the position offered.

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 & Reasonable Accommodations

The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If 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.