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PLS GMP Manufacturing Technician

Job in Norristown, Montgomery County, Pennsylvania, 19401, USA
Listing for: Pace
Full Time position
Listed on 2026-07-01
Job specializations:
  • Manufacturing / Production
    Pharmaceutical Manufacturing, Manufacturing & Industrial Operations
Salary/Wage Range or Industry Benchmark: 22 - 28 USD Hourly USD 22.00 28.00 HOUR
Job Description & How to Apply Below
Position: PLS GMP Manufacturing Technician I

GMP Manufacturing Technician (Solid Dose)

Shift: Monday through Friday, 7:30 a.m.

- 4:00 p.m.

Are you ready to work making the world a safer, healthier place? Join our mission to continuously move science forward; to innovate and advance all aspects of our business to improve the health and safety of our communities and lives.

This is a full-time, onsite, GMP Manufacturing Technician (Solid Dose) position located in Norristown, PA, Monday through Friday, 7:30 a.m.

- 4:00 p.m.

Compensation: $22.00 - $28.00 per hour

The salary for this position reflects a variety of factors. Compensation will be determined based on the candidate's geographic location, relevant experience, education, skills, and alignment with internal equity. Market conditions, budgetary considerations, and organizational compensation guidelines may also influence the final offer.

Position Summary

The GMP Manufacturing Technician is responsible for executing and supporting manufacturing, dispensing, and packaging operations for solid dose products (e.g., tablets, capsules, powders) in a current Good Manufacturing Practice (cGMP) environment.

This role ensures all activities are performed in compliance with batch records, SOPs, and regulatory requirements, while maintaining high standards of data integrity, quality, and safety. The technician will operate and maintain solid dose manufacturing equipment and collaborate cross-functionally with Quality, Engineering, and Facilities teams.

Key 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
GMP Compliance & Quality:
  • 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
Equipment & Facility Support:
  • 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
Team Support:
  • Collaborate effectively within cross-functional teams including QA, QC, and Facilities
  • Contribute to process efficiency improvements and lean manufacturing initiatives
Qualifications, Education & Experience
  • Associate degree or technical certification in a science or engineering-related field preferred
  • OR High School diploma with relevant experience
  • 1-2 years of GMP manufacturing experience, preferably in solid dose / small molecule production
Strong Understanding Of:
  • cGMP regulations
  • Solid dose manufacturing processes and equipment
  • Batch records, SOPs, and documentation practices
  • Familiarity with pharmaceutical manufacturing environments (oral solid dosage forms preferred)
Skills & Competencies
  • Ability to operate and troubleshoot manufacturing equipment
  • Strong attention to detail and documentation accuracy
  • Mechanical aptitude and basic math skills
  • Effective communication and teamwork skills
  • Ability to follow detailed procedures in a regulated environment

PHYSICAL/MENTAL REQUIREMENTS:
The physical demands described herein are representative of those that must be met by an employee to successfully perform the essential functions of the job. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.

Mobility to work in a lab and office setting, use standard office and lab equipment and stamina to sit for extended periods of time; exerting up to 20 pounds of force occasionally and/or up to 10 pounds of force frequently to lift, carry, push, pull or move objects; vision to read printed materials and computer screens;…

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