Manufacturing Operator

Staffing Resource Group, Inc; Quakertown (Bucks County); On-site; USD 26,000 - 34,000; Part time

Job summary

Staffing Resource Group, Inc. in Quakertown, PA is seeking a Manufacturing Operator for night shift in a pharmaceutical manufacturing environment. You will operate processing systems, follow CSBP, ensure compliance with cGMP, and maintain cleanroom practices.

Requirements include a high school diploma or equivalent, 2+ years manufacturing experience (pharma/FDA-regulated preferred), and familiarity with SOPs. Micronization experience and forklift operation are a plus.

Qualifications

• High School Diploma or equivalent required; associate degree a plus.
• 2+ years manufacturing experience; pharma or FDA-regulated preferred.
• Experience with micronization or particle size reduction is a plus.
• Familiarity with cGMP, SOPs, and cleanroom/controlled environment operations.

Responsibilities

• Operate assigned processing system to meet CSBP requirements.
• Read and follow Customer Standard Batch Procedures (CSBP).
• Maintain a clean and orderly processing system; report unsafe conditions.

Skills

Micronization

cGMP SOPs

Attention to detail

Safety practices

Education

High School Diploma or equivalent

Associate degree in life sciences/manufacturing

Tools

Forklift operation

Job description

Manufacturing Operator - Night ShiftLocation: Quakertown, PAIndustry: Pharmaceutical ManufacturingHours: 5PM-5AM Monday-ThursdayPay: $22 per hourEmployment Type: Contract-to-HireOverviewJoin a trusted pharmaceutical manufacturer with over 30 years of expertise supporting leading biotech and pharma innovators. Our 100,000+ sq. ft. facility specializes in advanced particle engineering technologies that enhance solubility and bioavailability, enabling the development of life-changing therapies from early discovery through commercial launch.As a Manufacturing Operator, you will play a key role in delivering safe, compliant, and high-quality products within an FDA-regulated, cGMP-compliant environment. You will operate specialized equipment, ensure strict adherence to manufacturing protocols, and contribute to processes that directly impact patient health worldwide.Job Responsibilities:Operate assigned processing system to meet all requirements of the CSBP. Read and comprehend the Customer Standard Batch Procedure (CSBP) applicable to an assigned processing system. Advise management if any requirement of the CSBP is in conflict with actual operating conditions in the processing system. Operate basic suites with minimal supervisionObserve and monitor general conditions in an assigned processing system, reporting on and correcting unsafe conditions.Understands and follows all safety protocols.Maintain an assigned processing system in a clean and orderly condition, removing all unnecessary tools, supplies, waste, etc.Perform equipment cleaning activities as instructed by manager, following standard operating procedures.Label as instructed, finished product containers and sample containers.Conduct equipment inspections, recording data on forms provided.Maintain accurate production and environmental records, recording data on the forms provided.Inspect raw material, as instructed by Manager and record required label information and observation details, prior to discharging raw material into the raw material bins.Place pallets of finished product in the warehouse area designated by manager.Adhere to PPE requirements outlined in Microsize SOPs, which includes wearing a respirator system within production suites.Assist managers, as instructed, in any other activity that may be required for the efficient and safe functioning of the facility.QualificationsHigh School Diploma or equivalent (Associate s or technical degree in life sciences/manufacturing a plus)2+ years of experience in a manufacturing environment; pharmaceutical or FDA-regulated experience strongly preferredExperience with Micronization or particle size reduction processes preferredFamiliarity with cGMP, SOPs, and cleanroom/controlled environment operationsMechanical aptitude; forklift operation experience a plusStrong attention to detail, documentation accuracy, and safety practicesAbility to lift/move materials frequently and perform physically demanding tasks throughout the shiftWhy Join UsGain hands-on experience with cutting-edge pharmaceutical technologiesWork in a facility trusted by top pharmaceutical and biotech companies worldwideBuild a long-term career in a growing, specialized sector of the pharmaceutical industryJoin a collaborative team where safety, quality, and continuous improvement come firstKeywords: Manufacturing Operator, pharmaceutical manufacturing, FDA-regulated environment, cGMP, Micronization, GMP compliance, SOPs, batch records, cleanroom, controlled environment, equipment operation, equipment cleaning, preventative maintenance, equipment inspection, raw material inspection, product labelingSRG4 offers flexible staffing solutions with a national presence. We provide contract, contract-to-hire, direct hire and executive search services. SRG4 utilizes an innovative approach to identify and qualify talent that is unique to the Staffing industry, featuring a cutting-edge platform that allows us to rapidly and precisely match professionals to client requirements. We have a proprietary database of over one million candidates and maintain continuous contact with our qualified talent.EOE/ADAIND123