PLS GMP Manufacturing Technician I

LNN Pace Analytical Life Sciences, LLC; Norristown (Montgomery County); On-site; USD 74,677,000 - 85,962,000; Full time

Benefits offered by this job

Medical

Dental

Vision

401K retirement savings plan

Life insurance

Paid time off

Job summary

Pace® Life Sciences is seeking a GMP Manufacturing Technician I (Solid Dose) for our Norristown, PA site. The role supports dispensing, blending, granulation, compression, encapsulation, coating, and packaging of solid dose products in a cGMP environment.

You will ensure compliance with batch records, SOPs, and data integrity while collaborating with Quality, Engineering, and Facilities teams. The ideal candidate has an associate degree or equivalent, 1–2 years of GMP manufacturing experience,

Qualifications

• 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.
• Ability to lift 50 lbs.
• Strong understanding of: cGMP regulations, solid dose manufacturing processes and equipment, batch records and documentation practices.

Responsibilities

• Perform dispensing, blending, granulation, compression, encapsulation, coating, and/or packaging of solid dose products.
• Execute GMP manufacturing activities per batch production records and SOPs.
• Document manufacturing activities in batch records and logbooks per GDP.
• Operate and clean solid dose equipment and assist with preventive maintenance and line clearance to prevent cross-contamination.
• Collaborate with QA, QC, and Facilities to improve processes and support lean initiatives.

Skills

Operate and troubleshoot manufacturing

Attention to detail

Documentation accuracy

Teamwork

Willingness to learn

Education

Associate degree or technical certification in science/engineering

HS Diploma with relevant experience

Tools

Blenders

Granulators

Tablet presses

Encapsulators

Coating equipment

Sieves/mills

Job description

Shift: Monday through Friday, 7:30 AM - 4:00 PM 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 1 (Solid Dose) position located in Norristown, PA, Monday through Friday, 7:30 a.m. - 4:00 p.m. Compensation: $26.00 - $30.00 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.

Make an Impact. Build a Career. 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.

Summary The GMP Manufacturing Technician I 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
• Ability to lift 50 lbs.
• 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
• Willingness to learn new techniques
• 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 50 pounds of force frequently to lift, carry, push, pull or move objects; vision to read printed materials and computer screens; and hearing and speech to communicate in person or over the telephone.

WORKING ENVIRONMENT

Work is performed in a lab and office setting. Work is subject to chemicals, fumes, gases, noxious odors, and related items in a lab and sample setting.

Find Your Place at Pace - We need you - your curiosity, your talents, and your drive - to help us advance this important work.

Benefits

• competitive salaries
• medical
• dental
• vision
• 401K retirement savings plan (100% vested immediately in the employer match)
• life
• disability and voluntary benefits
• paid time off for holiday, sick and vacation days
• HSA
• wellness program
• flexible spending accounts
• tuition reimbursement
• Employee Assistance program
• parental leave
• optional legal coverage and ID theft

Equal Opportunity Employer

Pace® provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, creed, color, religion, genetics, protected veteran status, national origin, sex, age, disability, marital status, sexual orientation, gender identity or expression, citizenship, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.

Pace® makes the world a safer, healthier place. We partner with clients to provide the service, science, and laboratory data needed to make critical decisions that benefit us all. Through a nationwide laboratory network, Pace® advances the science of businesses, industries, consulting firms, government agencies, and others. More at PACELABS.com.