Contract Pharmacal Corp
Join our dynamic R&D team as an
R&D Operator
in Hauppauge, NY. In this hands‑on role, you will work closely with scientists and engineers to support formulation and process development, operate pilot‑scale equipment, and contribute directly to innovations that impact lives.
Job Type:
Full‑Time Location:
Hauppauge, NY Work Hours:
Monday – Friday, 8:00 AM – 4:30 PM 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. We pride ourselves on quality, 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.
Responsibilities
Be a key contributor to early product development, supporting the preparation, weighing, and dispensing of raw materials 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.
Qualifications
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.
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.
#J-18808-Ljbffr
R&D Operator
in Hauppauge, NY. In this hands‑on role, you will work closely with scientists and engineers to support formulation and process development, operate pilot‑scale equipment, and contribute directly to innovations that impact lives.
Job Type:
Full‑Time Location:
Hauppauge, NY Work Hours:
Monday – Friday, 8:00 AM – 4:30 PM 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. We pride ourselves on quality, 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.
Responsibilities
Be a key contributor to early product development, supporting the preparation, weighing, and dispensing of raw materials 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.
Qualifications
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.
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.
#J-18808-Ljbffr