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R&D Technician - Oral Solid Dose (OSD) at Puretek Corporation

Los Angeles, California, United States -

Full Time

Start Date

Immediate

Expiry Date

03 Sep, 26

Salary

55000.0

Posted On

05 Jun, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Formulation Development, Oral Solid Dosage, cGMP, Process Optimization, Scale-up, Technology Transfer, Wet Granulation, Dry Granulation, Roller Compaction, Tablet Compression, Coating, Capsule Filling, Laboratory Documentation, Troubleshooting, Sample Preparation, Equipment Maintenance

Industry

Pharmaceutical Manufacturing

Description

Position Summary We are seeking an experienced R&D Technician to support the development of Oral Solid Dosage (OSD) pharmaceutical products. The successful candidate will assist formulation scientists with product development, process optimization, scale-up, and technology transfer while ensuring compliance with cGMP requirements. Key Responsibilities * Support formulation development of tablets, capsules, and other oral solid dosage forms. * Conduct laboratory and pilot-scale trials, including blending, granulation, compression, coating, and encapsulation. * Prepare, execute, and document experiments according to approved protocols. * Operate and maintain R&D and pilot-scale manufacturing equipment. * Assist in process optimization, scale-up, validation, and technology transfer activities. * Maintain accurate laboratory notebooks, batch records, and technical reports. * Coordinate sample preparation and testing with Analytical Development and Quality teams. * Follow cGMP, SOPs, and safety requirements at all times. Qualifications * Associate’s degree in Chemistry, Pharmaceutical Sciences, Chemical Engineering, or related field. * 1-2 years of experience in R&D, formulation development, or manufacturing. * Hands-on experience with OSD unit operations such as wet granulation, dry granulation, roller compaction, blending, tablet compression, coating, and capsule filling. (an advantage) * Knowledge of cGMP regulations and pharmaceutical documentation practices. * Strong troubleshooting, organizational, and communication skills

Responsibilities

Support the development and optimization of oral solid dosage pharmaceutical products through laboratory and pilot-scale trials. Execute experiments and maintain detailed technical documentation while ensuring compliance with cGMP standards.