Project Engineer
Garonit Pharmaceutical
Project Engineer
Garonit Pharmaceutical
Global API manufacturer for pharmaceutical ingredients
Project Engineer
Location: Flanders, NJ
Garonit Pharmaceutical is seeking a Project Engineer to support capital projects at our growing Flanders, New Jersey facility. This role will focus on the construction, commissioning, and startup of new pharmaceutical manufacturing and laboratory spaces, working closely with contractors, vendors, and internal teams to ensure projects are completed safely, efficiently, and within established timelines.
Key Responsibilities
Qualifications
Compensation & Benefits
The anticipated salary range for this position is $100,000–$120,000 per year. Actual compensation will be determined based on factors such as experience, qualifications, skills, and other job-related considerations.
This position is also eligible for consideration for a discretionary year-end bonus, based on Company and individual performance. Any bonus is discretionary and is not guaranteed.
Garonit Pharmaceutical offers eligible employees a benefits package that includes medical, dental, and vision insurance; a 401(k) retirement plan with Company match; paid time off (PTO); paid holidays; and other benefits in accordance with applicable Company plans and policies.
About The Role
This is a full-time, onsite position based at our Flanders, New Jersey facility. The Project Engineer will work in an active construction and pharmaceutical manufacturing environment, with a strong focus on meeting critical construction and facility-readiness deadlines.
Equal Employment Opportunity
Garonit Pharmaceutical is an equal opportunity employer. We consider qualified applicants for employment without regard to race, color, religion, sex, pregnancy, national origin, age, disability, genetic information, veteran status, or any other characteristic protected by applicable federal, state, or local law.
Global API manufacturer for pharmaceutical ingredients
Garonit Pharmaceutical produces Active Pharmaceutical Ingredients, especially Chlorhexidine Gluconate, for global pharmaceutical customers. It uses a vertically integrated model from intermediates to finished dosage forms with cGMP/WHO-GMP facilities in the US and India and distribution warehouses in Europe. It plans a 200,000-square-foot New Windsor facility to become the world’s largest Chlorhexidine Gluconate producer, supported by New York state grants and including an R&D center for FDA-regulated products. With certifications from US FDA, EDQM, and PMDA, it competes on scale, end-to-end manufacturing, and global reach, aiming to supply large-scale, compliant Chlorhexidine Gluconate worldwide while expanding U.S. operations and developing FDA-regulated formulations.
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