R&D Operator at CONTRACT PHARMACAL CORP

Town of Smithtown, New York, United States -

Full Time

Start Date

Immediate

Expiry Date

13 Mar, 26

Salary

25.0

Posted On

13 Dec, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Pharmaceutical Manufacturing, Equipment Operation, Formulation Development, Process Development, cGMP Compliance, Documentation Practices, Problem-Solving, Collaboration, Attention to Detail, Raw Material Handling, Batch Records, Troubleshooting, Scale-Up Operations, Communication, Initiative, Adaptability

Industry

Pharmaceutical Manufacturing

Description

Description 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: $22.00 - $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.

Responsibilities

The R&D Operator will support early product development by preparing and dispensing raw materials and operating specialized R&D equipment. They will also collaborate with scientists and engineers to troubleshoot issues and maintain compliance with quality standards.