R&D Operator

Position Summary 

Join our dynamic R&D team as an R&D Operator, where you'll play a key role in bringing new pharmaceutical products from concept to commercialization. In this hands-on role, you'll work closely with Scientists and Engineers to support formulation and process development, operate pilot-scale equipment, and contribute directly to innovations that impact lives. This is an excellent opportunity for someone who enjoys problem-solving, learning new technologies, and being deeply involved in early-stage development within a cGMP environment.

Job Type: Full-Time

Location: Hauppauge, NY 

Works Hours: Monday – Friday, 8:00AM – 4:30PM 

Pay Range: $ $25.00 per hour, depending on experience 

Start Date: ASAP

What makes this role exciting:

• Exposure to a variety of pharmaceutical manufacturing technologies
• Opportunities to learn directly from experienced Scientists and Engineers
• Hands-on involvement in pilot-scale production and product innovation
• Clear pathways for growth into Operations, Engineering, or Formulation roles
• A collaborative team environment where your work has visible impact

Why Join CPC?

At CPC, you'll be part of a team that has set the standard in pharmaceutical development and contract manufacturing since 1971, helping bring high-quality OTC, dietary supplement, and prescription products to market faster and safer than ever. We pride ourselves on quality as a core value, innovative problem-solving, and a collaborative culture where everyone plays a role in advancing formulation and manufacturing excellence. CPC offers an inclusive, respectful workplace with opportunities to grow your skills and career while working with cutting-edge technologies and serving leading global brands. With a commitment to employee success, competitive benefits, and a culture built on teamwork and integrity, CPC is a place where your contributions truly make an impact. 

Requirements

Responsibilities

In this role, you will:

• Be a key contributor to early product development, supporting the preparation, weighing, and dispensing of raw materials (active ingredients and excipients) according to formulation requirements.
• Set up, operate, and maintain specialized R&D equipment – including tablet presses, capsule filling machines, coaters, granulators, mills, and blenders – ensuring runs meet quality and safety standards.
• Execute trial and scale-up batches following protocols and Batch Manufacturing Records, helping translate lab concepts into scalable manufacturing processes.
• Collaborate closely with Formulation Scientists and Engineers to troubleshoot equipment or process issues and recommend process improvements.
• Maintain a clean, compliant, and inspection-ready lab environment, adhering to cGMP, GLP, and SOP requirements.
• Document all experimental data accurately and clearly, ensuring traceability and supporting regulatory expectations.
• Ensure readiness for daily operations by reporting on time in the appropriate PPE and contributing to a culture of safety and quality.

Education & Experience

• High school diploma or GED required; associate degree in a science or technical field preferred.
• Minimum 3 years of hands-on experience in pharmaceutical manufacturing (compression, encapsulation, granulation, blending, or coating).
• Prior experience operating pilot-scale or production-scale equipment.
• Experience working in a GMP or cGMP-regulated environment.
• Prior exposure to formulation development, R&D, or scale-up activities is a plus.
• Basic understanding of batch records, SOPs, and laboratory documentation practices.

Skills, Knowledge & Abilities

• Proficiency in operating equipment such as tablet presses, capsule filling machines, granulators, blenders, mills, and coaters.
• Understanding of raw material handling, weighing, dispensing, and GMP documentation.
• Ability to follow formulation sheets, batch records, and set-up sheets accurately.
• Basic troubleshooting skills for mechanical or process deviations.
• Familiarity with scale-up and pilot-batch operations preferred.
• Strong attention to detail and accuracy in documentation.
• Effective communicator; able to collaborate closely with scientists, engineers, and other operators.
• Bilingual English/Spanish preferred.
• Strong problem-solving mindset with initiative to improve processes.
• Ability to adapt quickly to changing priorities in an R&D environment.
• Commitment to quality, compliance, and continuous learning.