PLS GMP Manufacturing Technician I

Pace® Analytical Services•Norristown, PA

63d•$26 - $30•Onsite

About The Position

This is a full-time, onsite, GMP Manufacturing Technician 1 (Solid Dose) position located in Norristown, PA, Monday through Friday, 7:30 a.m. - 4:00 p.m. Pace® Life Sciences delivers a comprehensive suite of contract CMC development, CTM manufacturing, regulatory compliance, consulting, and facility support services to the pharmaceutical, biopharmaceutical, and gene therapy industries. Operating across a network of CDMO sites, GMP analytical testing laboratories, and manufacturing support centers, we partner with clients to efficiently advance programs from early development through commercialization. Our experienced industry experts and continued investment in state-of-the-art facilities reflect our commitment to quality, speed, and reliability. United by a shared purpose, we bring meaningful value to patients, healthcare professionals, and health businesses worldwide by delivering services that support a safer, healthier future.

Requirements

1–2 years of GMP manufacturing experience, preferably in solid dose / small molecule production
Ability to lift 50 lbs.
Strong understanding of cGMP regulations
Strong understanding of Solid dose manufacturing processes and equipment
Strong understanding of Batch records, SOPs, and documentation practices
Familiarity with pharmaceutical manufacturing environments (oral solid dosage forms preferred)
Ability to operate and troubleshoot manufacturing equipment
Strong attention to detail and documentation accuracy
Mechanical aptitude and basic math skills
Willingness to learn new techniques
Effective communication and teamwork skills
Ability to follow detailed procedures in a regulated environment

Nice To Haves

Associate degree or technical certification in a science or engineering-related field preferred
OR High School diploma with relevant experience

Responsibilities

Perform dispensing, blending, granulation, compression, encapsulation, coating, and/or packaging of solid dose products
Execute GMP manufacturing activities in accordance with batch production records and SOPs
Document all manufacturing activities accurately in batch records and logbooks in compliance with GDP (Good Documentation Practices)
Operate and clean solid dose equipment such as: Blenders (V-blenders, bin blenders), Granulators (high shear/fluid bed), Tablet presses and encapsulators, Coating equipment, Sieves/mills and packaging lines
Adhere to all cGMP, FDA, and internal quality standards
Ensure all documentation is complete, accurate, and audit-ready
Identify and report deviations, and support investigations and CAPA activities
Assist in SOP development, revision, and continuous improvement initiatives
Perform equipment setup, changeover, and basic troubleshooting
Partner with Maintenance/Engineering on preventive maintenance and repairs
Ensure proper cleaning and line clearance to maintain compliance and prevent cross-contamination
Collaborate effectively within cross-functional teams including QA, QC, and Facilities
Contribute to process efficiency improvements and lean manufacturing initiatives