Manager, QA Compliance
$19 - $30 per hourUS Pharma Lab
If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process. Operator, Blending / Granulation Manufacturing Full Time North Brunswick, NJ, US Salary Range: $19.00 To $30.00 Hourly Job Description Date 06/2025 Location 1300 Airport Road, North Brunswick NJ Title Operator, Granulation/ Blending Department Standard Manufacturing FLSA (Exempt or Non-Exempt Non-Exempt Role Overview The Granulation/Blending Operator is responsible for the operation and set up of granulators, drying oven, blenders, screening equipment etc. in accordance with company standard operating procedures. The position includes set up, operation, cleaning, and preventative maintenance of all related equipment. The Operator is accountable for overall performance including safety, quality, shrink, attainment, and production efficiency. Operators must be capable of operating multiple like machines at one time and learning to operate a variety of equipment within the manufacturing area. Areas of Responsibility Follow batch records, SOP’s, and cGMP's guidelines to ensure product specifications and tolerances are met. Ensures full compliance with Company policies, procedures, GMP’s, Ethical Business Practice, and SOP’s at all times. Ensures documentation such as operation logs, batch records, etc. are fully completed, signed and in compliance with company standards and regulatory requirements. Ensures that product meets applicable quality standards. This includes inspection for quality during operation and performing all required sampling and testing. Complete all labeling and inventory movements to ensure accurate inventory control. Dismantle and clean any accessories and equipment while also maintaining a clean work area. Train in the operation, cleaning and set-up of the following pieces of equipment as well as new equipment: Rapid Mixer Granulator: 100L & 600L and planetary mixer Tray Drying Ovens Double cone/V- blenders: 6cu. ft. to 150 cu. ft. Screening/ sieving equipment Fill in appropriate logbooks for equipment and rooms. Perform all material handling of products and components. Correctly document all steps on batch record. Participate in any investigation for a deviation involving a batch record. Maintain proper gowning and hygiene to ensure integrity of the product as per company policies. Works extended hours and occasional weekend overtime. Other duties as assigned. Other Responsibilities Including Safety: N/A Requirements Education & Qualification Level 1 Pay Rate $19.00 - $22.00 High school graduate or GED equivalent 3+ years Granulating/Blending Operator experience Minimum of one (1) year work experience in nutritionals, supplements, food, or pharmaceutical manufacturing industries Must be proficient in proper setup and operation of blenders. Level 2 Pay Rate $21.00 - $24.00 High school graduate or GED equivalent 3+ years Granulating/Blending Operator experience Minimum of one (1) year work experience in nutritionals, supplements, food, or pharmaceutical manufacturing industries 1 years of experience Operates 5 machines (blending, milling, sifting, tray dryer and granulation). A clear understanding of the principal functions of the blending /granulation department. Certified forklift operator. Completes batch card independently, follow SOP’s and GMP’s strictly Level 3 Pay Rate $23.00 - $31.00 High school graduate or GED equivalent 3+ years of experience Operate all machines. Must be highly skilled in the proper set up an operation of blenders and granulators. Applies cGMP’s & completes batch card instructions accurately - able to train all activities in blending & granulation department. Certifications, Licenses, Credentials N/A Skills & Ability Demonstrates ability to work in a team and assist others. Able to follow written instructions precisely and perform basic math calculations as required. Understands and is knowledgeable of cGMP, OSHA standards etc. Mechanically inclined to understand the inner workings of equipment. Demonstrates the ability to read and write basic English in order to be able to understand the industry regulated instruction sheets. Physical Requirements (lifting, etc.) Ability to lift up to 50 lbs.; occasionally lift and move up to 75 pounds. Must stand and walk on the production floor for a minimum of 6 hours per shift. Uses hands to finger, handle, feel, or operate objects or controls, lifting to waist height and/or above shoulder height, frequent bending from the waist, or squatting, walking short distances. Occasionally works from a rolling ladder or step stool, must be to lean over equipment as well as kneeling on the floor to clean under the equipment. Must be able to wear all PPE including a lab coat, face mask, booties, gloves, safety glasses/goggles, and respirators. Work Environment (Office, Warehouse, temperature extremes, etc.) Work is regularly performed inside a manufacturing environment where temperatures can be moderate, exposure to dust, odors, noise, and fumes. The noise level is usually moderate. Employees can be exposed daily to chemicals and cleaning agents. The above statements are intended to describe the general nature and level of work being performed by people assigned to this job. They are not intended to be an exhaustive list of all the job responsibilities, duties, skill, or working conditions. In addition, this document does not create an employment contract, implied or otherwise, other than an "at will" relationship. USPL is proud to be an Equal Opportunity Employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy), sexual orientation, gender identity or expression, national origin, age, genetic information, disability, protected veteran status, or any other characteristic protected by applicable local, state, or federal law. Benefits And Compensation: From health and wellness benefit options including: medical, dental, vision, short and long term disability, basic life insurance, supplemental life insurance, AD&D insurance. matched 401(k) savings plan. premium pay such as overtime, shift differential, holiday pay, sick time, etc. Newly hired employees receive up to 10 days of vacation the first year, which grows to 12 days starting the second year of employment. #J-18808-Ljbffr
$90k - $105k
...application due to a disability, contact this employer to ask for an accommodation or an alternative application process. Manager, QA Compliance Quality Assurance & Regulatory Full Time North Brunswick, NJ, US 2 days ago Requisition ID: 1625 Salary Range: $90,000.00...SuggestedFull timeContract workTemporary workWork experience placementWork at officeLocal areaShift work- ...Keenova seeks a Senior Manager, Quality Assurance to lead quality operations and systems... ...NJ and Rye, NY facilities, ensuring cGMP compliance and FDA-aligned quality practices. You will... ...initiatives. The role requires 8+ years in QA, 3–5 years of people leadership, and...Suggested
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$111k - $135.5k
...packaging records, certificates of analysis/compliance and all related supporting documentation... ...from a Global Quality perspective.QA SME for manufacturing (Sterile & OSD), environmental... ...Reader, TrackWise, LMS (Learning Management System) etc.Knowledge of project...SuggestedFlexible hours- ...Supervisor, Quality Assurance to schedule and coordinate daily QA priorities for raw materials, in-process testing, and packaging... ...and supervise QA inspectors and auditors to ensure SOP and cGMP compliance, while supporting CAPA activities and investigations. You will monitor...
- ...Job Description As the Quality Assurance Manager, your responsibility is to ensure that... ...batch records, printed components, artwork compliance, and expiration dating configurations.... ...Lead, mentor, and scale a high-performing QA organization (including Senior QA specialists...
$137k - $167.5k
POSITION SUMMARYThe Senior Regulatory Compliance Manager is responsible for providing independent quality assurance assessment of global regulatory compliance activities supporting clinical development programs, labelling compliance for investigational products (IP) assets...Local areaFlexible hours$140k - $160k
...STATUS: Full-Time REPORTS TO: Production General Manager FLSA: Exempt SUPERVISORY RESPONSIBILITIES: QC/QA Supervisors and four QC Technicians.... ...all Quality Department activities are conducted in compliance with applicable company environmental health and...Full timeTemporary workWork at officeFlexible hours- 100% onsite Job Title: Quality Manager, Clinical Supply Chain Quality Job Description... ...role is to ensure quality oversight and compliance with GMPs and GDPs (Good Distribution Practices... ...GDP function. Experience within a QA role is an asset. Broad experience in...Work at office
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- ...Bristol Myers Squibb is seeking a Director for Management Review Strategy & Insights in New Brunswick, NJ. You will own the strategy and governance... ...-driven decision making and regulatory alignment across global QA functions. You will lead enterprise-level meetings, develop...
$122k - $212.75k
...Senior Manager, Health Care Compliance OfficerWe are searching for the best talent for a Senior Manager, Health Care Compliance Officer to be located in Jacksonville, FL; Irvine, CA; Danvers, MA; Raritan, NJ; or New Brunswick, NJ.Purpose: This role provides strategic leadership...Local areaImmediate startWorldwide$100k - $180k
...is seeking an Associate Director for Quality Assurance in Cranbury, NJ. This role focuses on establishing and improving Quality Management Systems supporting GMP clinical manufacturing. Successful candidates will have extensive experience in the pharmaceutical industry...$149k - $155k
Tavant Technologies Inc. is seeking an Associate Director of Quality Assurance in East Brunswick, NJ. The role requires leading QA efforts, managing test teams, and ensuring product quality throughout development. The ideal candidate will have at least five years'...$200k
...Director of Quality Assurance to lead our QA strategy, processes, and team. This role is... ...ensures product quality, reliability, and compliance across all releases. You will partner closely with engineering, product management, and operations to embed quality into every...Immediate start$80 - $88 per hour
...Rate: $80 - $88/Hour Duties: A Senior Program Manager Tech is part of a key team of Technology professionals... ...risk, and complexity. As part of the Governance, Risk, and Compliance organization, this Senior Program Manager Tech will support our...Work experience placement$120k - $160k
...matching, and excellent health benefits.Position SummaryThe Manager, IT - GxP Systems & Compliance, is responsible for ensuring reliable, complaint, and... ...remediation of operational risks in partnership with IT, QA, Validation, Manufacturing, QC, and Automation teams.ResponsibilitiesProvide...Full timeTemporary workWork at officeLocal areaShift work- ...Guerbet is seeking a qualified QA Manager in Princeton, NJ to strengthen our quality management system. You will develop, review, and revise SOPs, ensuring compliance with FDA CFRs, ISO standards, and regulatory requirements for our medical devices and pharmaceutical products...
- ...Director of Compliance & Validation, Life Sciences Location: East Brunswick, New Jersey Who You’ll Work With You will join our East Brunswick... ...responsibility in validation/quality service and project management of life sciences, biotech or other FDA regulated projects....Work at office
$110k - $150k
...office for Catalent. The facility is located approximately 45 minutes from Newark Liberty airport. Position Summary The Manager, Global Trade Compliance supports the development, implementation, and continuous improvement of the organization’s global trade compliance...Work at officeLocal area- ...and highly collaborative Quality Assurance Manager to support and strengthen our Quality Management System and ensure continued compliance across our pharmaceutical and medical... ...The ideal candidate brings strong technical QA expertise, sound judgment, and the ability...For contractorsLocal area
$138k - $172.1k
...days per week onsite and may be based in either our San Diego, CA or Princeton, NJ office Position Summary The Sr. Manager, Quality Assurance Compliance will play a key role in supporting Acadia’s growing portfolio by leading internal and external GMP audit activities...Contract workWork at officeLocal areaRemote workNight shift3 days per week- ...Brunswick, NJ is looking for a Director of Regulatory Affairs. This full-time position involves leading regulatory strategy and compliance for generic veterinary products and acting as the primary liaison with regulatory agencies. Candidates should have significant experience...Full time
- ...Verizon in New Jersey is seeking a Senior Manager of QA Test Automation to lead and transform our web and service automation testing frameworks, integrating AI solutions into our testing ecosystem. You will drive strategic execution and optimization of automation and AI...
- ...WHAT WE ARE LOOKING FOR Guerbet is looking for a qualified, dynamic QA Manager to enhance our quality management system through comprehensive SOP development, review, and revision, ensuring compliance with FDA regulations including CFR (Code of Federal Regulations), ISO...For contractorsLocal area
- Guerbet is looking for a qualified, dynamic QA Manager to enhance our quality management system through comprehensive SOP development, review, and revision, ensuring compliance with FDA regulations including CFR (Code of Federal Regulations), ISO standards, industry best...For contractorsLocal area
$140k - $165k
...certificate programs and our investment in resources that enable self-paced learning. Role Overview The Senior Manager, Enterprise Compliance (Americas) serves as a key partner in advancing the Americas Compliance program through governance, program management,...Casual workWork at officeLocal areaImmediate startRemote workWorldwideFlexible hoursWeekend work2 days per week- Tris Pharma, Inc. in Monmouth Junction, NJ is seeking an Associate Director or Director, Advertising & Promotions to join the Regulatory Affairs team. The role provides senior regulatory oversight for review and approval of promotional materials to ensure FDA-compliant ...
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