This job is closed
Applications are no longer available for this announcement. Explore current related opportunities below.
Job description
GMP Manufacturing Technician 1 (Solid Dose)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 hourThe 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.SummaryThe 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 productsExecute GMP manufacturing activities in accordance with batch production records and SOPsDocument 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 encapsulatorsCoating equipmentSieves/mills and packaging linesGMP Compliance & Quality:Adhere to all cGMP, FDA, and internal quality standardsEnsure all documentation is complete, accurate, and audit-readyIdentify and report deviations, and support investigations and CAPA activitiesAssist in SOP development, revision, and continuous improvement initiativesEquipment & Facility Support:Perform equipment setup, changeover, and basic troubleshootingPartner with Maintenance/Engineering on preventive maintenance and repairsEnsure proper cleaning and line clearance to maintain compliance and prevent cross-contaminationTeam Support:Collaborate effectively within cross-functional teams including QA, QC, and FacilitiesContribute to process efficiency improvements and lean manufacturing initiativesQualifications, Education & ExperienceAssociate degree or technical certification in a science or engineering-related field preferredOR High School diploma with relevant experience1–2 years of GMP manufacturing experience, preferably in solid dose / small molecule productionStrong understanding of:cGMP regulationsSolid dose manufacturing processes and equipmentBatch records, SOPs, and documentation practicesFamiliarity with pharmaceutical manufacturing environments (oral solid dosage forms preferred)Skills & CompetenciesAbility to operate and troubleshoot manufacturing equipmentStrong attention to detail and documentation accuracyMechanical aptitude and basic math skillsEffective communication and teamwork skillsAbility to follow detailed procedures in a regulated environmentPHYSICAL/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.BenefitsWhen you join Pace®, you commit to work that makes a positive impact on our communities and our world. We commit to supporting you with benefits and perks that make a positive impact on your life. Full-time roles are eligible for our comprehensive benefits program which includes 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 EmployerPace® 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.
Worksite address
norristown, PA, 19401, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.