1 Manufacturing Associate Job in New Brunswick, NJ
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ProStaff Solutions Inc is Hiring a Manufacturing Associate Near New Brunswick, NJ
Are you looking to be a part of a premier pharmaceutical company? One of our largest clients is currently seeking a Manufacturing Associate to join their New Brunswick, New Jersey team. Our client is one of the leading pharmaceutical companies specializing in developing and manufacturing of solid dosage products. If you believe you are qualified, we would be excited to connect and discuss this opportunity in more detail.
Please visit us at https://www.prostaffworkforce.com/ to explore all opportunities.ContractPay Rate: DoEJob Summary:Support Quality activities at Contract Manufacturing Organizations (CMO) by providing timely and effective quality oversight. Accomplish quality objectives by planning and evaluating project activities. Support may include operations and validation.Area of Responsibility:· Review of manufacturing and packaging records· Review certificate of analysis and Certificate of compliance· Ensure the release packages are ready prior to batch disposition· Review of QMS records submitted by CMO and monitoring (e.g. change controls/deviations, quality agreements but not limited to)· Manage and oversee complaint, change control, and variation-filing modules for CMO activity.· Actively participate in day to day meetings· Participate in the qualification process and support assigned CMO aligned with the companys Quality Management Systems and provide reports as required.· Implement, report and monitor CMO Quality Metrics and ensure identification and implementation of improvements needed through routine CMO business review.· Implement and maintain Regional CMO data in the Global CMO database.· Ensure the Quality Assurance Agreements which are created and maintained according to requirements, are regularly reviewed and followed.· Conduct review and approve batch release documentation.· Support significant quality issues associated with Drug Products or Medical Devices originating from assigned CMO (complaints, deviations, recalls, counterfeits and product tampering, stability failures, etc.) appropriately and in a timely fashion.· Maintain annual auditing program, participate in technical visits and/or audits, manage action plans and follow up on agreed upon CAPAs.· Manage and oversee complaint module.Travel estimate: Up to 10%Requirements:· Minimum of a Bachelor’s degree in a scientific discipline; MS preferred.· Certified Quality Auditor (e.g. ASQ) certification preferred.· Minimum of five (05) years of related experience in a cGMP environment, preferably in a project management capacity for pharmaceutical or biotechnology industries.
• Experience in drug product sterile pharmaceutical/biologics manufacturing and QC is an asset.· Expert skills related to investigations (e.g. Lean Six Sigma) Quality Agreements, and CMO management.· Ability to identify key priorities necessary for and be able to author/implement global policies and procedures.· Strong understanding of technical pharmaceutical processes as well as risk assessment and risk management fundamentals/tools.· Strong knowledge of cGMP, QA/QC and regulatory compliance (US, EU and other regulatory requirements).· Strong interpersonal and communication, both written and verbal, skills.· Good negotiation and influencing skills.· Operational knowledge of pharmaceutical processing and packaging operations.· Task oriented team plan who is able to manage multiple complex priorities and work in a cross-cultural working environment.About ProStaffworkforce SolutionsWe are a fast growing and successful agency that treats all its clients and candidates with a personal touch. ProStaffworkforce Solutions is a group of industry experts—many hailing from larger agencies—who know their business well and enjoy working in a more hands-on and flexible environment, with attention to detail. Our mission is to match quality people with quality jobs and quality companies to maximize productivity and profitability. We develop long-term relationships and provide a level of customer service and expertise that instill confidence and trust in our client companies and candidates. Our Values• Integrity • Commitment• Quality• DiversityBenefits for eligible employees• Direct deposit• Weekly pay • Medical benefits • 401(k) Plan #IND1
Job Summary
Full Time
Business Services
09/11/2022
12/05/2022
prostaffnj.com
LAURENCE HARBOR, NJ
<25
Private
<$5M
Business Services
Related Companies
The job skills required for Manufacturing Associate include Packaging, Commitment, Biotechnology, Integrity, Project Management, Customer Service, etc. Having related job skills and expertise will give you an advantage when applying to be a Manufacturing Associate. That makes you unique and can impact how much salary you can get paid. Below are job openings related to skills required by Manufacturing Associate. Select any job title you are interested in and start to search job requirements.
The following is the career advancement route for Manufacturing Associate positions, which can be used as a reference in future career path planning. As a Manufacturing Associate, it can be promoted into senior positions as an Industrial Engineer IV that are expected to handle more key tasks, people in this role will get a higher salary paid than an ordinary Manufacturing Associate. You can explore the career advancement for a Manufacturing Associate below and select your interested title to get hiring information.
If you are interested in becoming a Manufacturing Associate, you need to understand the job requirements and the detailed related responsibilities. Of course, a good educational background and an applicable major will also help in job hunting. Below are some tips on how to become a Manufacturing Associate for your reference.
Step 1: Understand the job description and responsibilities of an Accountant.
Quotes from people on Manufacturing Associate job description and responsibilities
Manufacturing associates typically have varied duties and responsibilities like plans and designs manufacturing processes for a production facility .
12/16/2021: Middlesex, NJ
Maintained batch records and logbooks to comply with regulatory requirements, manufacturing practices and aseptic processing of commercial products using Procedures.
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Worked from Engineering Drawings and Bills of Material to develop manufacturing methodology for circuit board production.
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Maintain good Documentation practices (GDP) and good manufacturing practices (GMP) throughout production.
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Maintain production procedures to maintain high standard of manufacturing operations, product quality, reliability, and safety.
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Step 2: Knowing the best tips for becoming an Accountant can help you explore the needs of the position and prepare for the job-related knowledge well ahead of time.
Career tips from people on Manufacturing Associate jobs
Manufacturing Associates who do attend college, typically earn either a Bachelors degree or a Business degree.
02/08/2022: Orlando, FL
The physical and mental demands for manufacturing associate is hard but needed to perform the essential functions of this job.
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This position requires good knowledge and experience with cell culture, bioreactors, and good knowledge and skills related to manufacturing of bio-products.
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Some popular Manufacturing Associate hard skills are Good Manufacturing Practice (GMP), Aseptic Technique, Standard Operating Procedure (SOP), Aseptic Processing, Biotechnology, Cell Culture, cGMP manufacturing and Manufacturing.
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Manufacturing companies offer a wide variety of manufacturing associate jobs and the skills or experience required differ greatly.
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Step 3: View the best colleges and universities for Manufacturing Associate.
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