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
- Execute and support CAPEX projects related to pharmaceutical facility construction, equipment installation, and commissioning.
- Support the construction and startup of GMP commercial manufacturing rooms, a Microbiology Laboratory, and a Quality Control (QC) Laboratory.
- Coordinate contractors, engineering partners, equipment vendors, and internal teams to ensure project milestones and deadlines are met.
- Monitor project schedules, budgets, deliverables, and construction progress and promptly communicate potential delays or risks.
- Review engineering drawings, facility layouts, equipment specifications, scopes of work, and related project documentation.
- Support equipment installation, startup, commissioning, qualification, and project turnover activities.
- Conduct project walkthroughs and coordinate onsite contractor and vendor activities.
- Ensure projects are completed in accordance with applicable cGMP, safety, engineering, regulatory, and Company requirements.
- Maintain project documentation and provide regular progress updates to management.
- Perform other related duties as assigned based on business and project needs.
Qualifications
- Bachelor’s degree in Engineering or a related technical discipline preferred.
- 2–3+ years of relevant engineering or project experience, preferably within the pharmaceutical, biotechnology, or life sciences industry.
- Experience supporting or completing CAPEX projects within a pharmaceutical or GMP-regulated facility strongly preferred.
- Experience with facility construction, equipment installation, commissioning, and startup activities.
- Experience working with contractors, engineering firms, and equipment vendors.
- Ability to read and interpret engineering drawings, layouts, equipment specifications, and technical documentation.
- Strong project coordination, organizational, communication, and problem-solving skills.
- Ability to manage multiple priorities and work effectively against strict project deadlines.
Compensation & Benefits
The anticipated salary range for this position is $95,000–$105,000 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.
Skills Required
- Bachelor's degree in Engineering or a related technical discipline
- 2-3+ years of relevant engineering or project experience
- Experience in the pharmaceutical, biotechnology, or life sciences industry
- Experience supporting or completing CAPEX projects within a pharmaceutical or GMP-regulated facility
- Experience with facility construction, equipment installation, commissioning, and startup activities
- Experience working with contractors, engineering firms, and equipment vendors
- Ability to read and interpret engineering drawings, layouts, equipment specifications, and technical documentation
- Strong project coordination, organizational, communication, and problem-solving skills
- Ability to manage multiple priorities and work effectively against strict project deadlines
What We Do
Garonit Pharmaceutical, a US-based multinational company owned by brothers Rohit and Nitin Garg, is making a global impact with its high-quality Active Pharmaceutical Ingredients (APIs). Headquartered in New Jersey, Garonit has expanded its reach to markets in the UK, Switzerland, Hong Kong, Brazil, and China. The company’s proactive and collaborative approach, along with a willingness to take risks, has earned it accreditations from top regulatory bodies like the FDA, EDQM, PMDA, and EPA. Garonit is known for its strong compliance standards, partnering with notable organizations such as Ernst & Young, SAP, and Citibank. This commitment to compliance has helped Garonit serve Fortune 500 companies and small-scale industries across North America, LATAM, and EMEA. Our state-of-the-art manufacturing plants in New Jersey, USA, and India are cGMP and US-FDA compliant. Additionally, we operate warehouses in Germany and the UK, ensuring efficient distribution worldwide. Beyond business, Garonit is dedicated to philanthropy. We partner with UNICEF, WHO, and The Red Cross to improve global health and welfare. Through our own Neelam Garg Foundation, we actively support girls’ education in underprivileged communities, aiming to make a positive impact on society.
Why Work With Us
Garonit Pharmaceutical, a US-based multinational owned by Rohit and Nitin Garg, excels in Active Pharmaceutical Ingredients (APIs). With headquarters in New Jersey and plants in the USA and India, it serves global markets like the UK, Switzerland, Hong Kong, Brazil, and China. Accredited by FDA, EDQM, PMDA, and EPA.







