R&D Operator

CONTRACT PHARMACAL CORP•Town of Smithtown, NY

10d•$22 - $25•Onsite

About The Position

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. 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

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.
Basic understanding of batch records, SOPs, and laboratory documentation practices.
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.
Strong attention to detail and accuracy in documentation.
Effective communicator; able to collaborate closely with scientists, engineers, and other operators.
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.

Nice To Haves

Prior exposure to formulation development, R&D, or scale-up activities is a plus.
Familiarity with scale-up and pilot-batch operations preferred.
Bilingual English/Spanish preferred.

Responsibilities

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.

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