Plant Manager Jobs in New Jersey

Job Title: Site Plant Manager FDA Sterile Company: Location: Princeton, NJ Description: SUMMARY DESCRIPTIONThe Plant Manager is responsible for directing the overall plant operations to obtain optimum efficiency and maximize profits. Responsibilities include administration, engineering, manufacturing, quality, purchasing and planning, process development, finance, facilities and EH&S. The incumbent is accountable to the Senior Director of Operations for the achieving profit/loss goals and the attainment of current and long-term objectives. SUPERVISION RECEIVEDUnder direct supervision of Senior Director of OperationsSUPERVISION EXERCISEDDirect supervision of plant functional managers. Indirect supervision of finance manager.ESSENTIAL DUTIES AND RESPONSIBILITIESTo perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Responsible for all manufacturing operations. Provides guidance and leadership to all plant personnel. Supervises, motivates and directs employees to obtain optimal productivity. Ensures effective staffing, training, development of the organization as well as develops succession plans for future growth and stability. Responds to production problems and pursues / implements remedies to such problems. Develops, manages and tracks operational metrics for the plant. Responsible for overseeing Quality Assurance and Quality Control to ensure compliance. Ensures adherence and compliance with all company policies, procedures and practices of all plant personnel. Ensures a high level of customer satisfaction. Participates on due diligence teams to evaluate potential acquisitions, when requested. Responsible for maintaining appropriate inventory levels of finished goods, work in process and raw materials. Acts as Operations liaison with our OEM customers. Ensures new product introductions are supported and executed to the established project plans. Assumes responsibility for costs, cost saving initiatives, methods, and budgets. Works with Corporate departments to ensure compliance with established policies and procedures. Provides short and long term objectives for the plant and executes to those objectives. Promotes constant and effective communication channels at all levels to maintain a stable and productive work climate. Performs other duties and responsibilities as required.DESIRED MINIMUM QUALIFICATIONSThe requirements listed below are representative of the knowledge, skill, and/or ability required for this position. Bachelors Degree required. MBA preferred 10 to 15 years of general management experience in the medical device industry. Effective written and verbal communication skills, interpersonal skills, and demonstrated ability to interface with production and supervisory personnel. Ability to work in a Total Quality Management/Continuous Improvement environment. Knowledgeable in the following areas: Lean Manufacturing and Six Sigma Enterprise Resource Planning (ERP) and Materials Requirement Planning (MRP) Statistical Process Control/Defect tracking Project management Food and Drug Administration (FDA), International Standards Organization (IS), and other nations regulatory requirements Must be computer literate and proficient with MS Office software.

Job Title: Process Engineer/Chem Plant Supervisor Company: Chemtura Corporation Location: East Hanover, NJ Description: Company: Chemtura Corporation Job Title: Process Engineer/Chem Plant Supervisor Jobid: chemtura-1466 Job Location: East Hanover, NJ, 07936, USA Description: Process Engineer/Chem Plant Supervisor Job Code :1466 Division :Performance Products - Petroleum Additives Location :East Hanover NJ US 07936 Job Type :Full Time Career Level :Manager (Manager/Supervisor of Staff) Education :Bachelor's Degree Category :Manufacturing Job Description : We are currently seeking an enthusiastic, motivated and talented individual for the position of Process Engineer/Chem Plant Supervisor in our East Hanover site. Day-to-day supervision and process improvement of the Chemical plant unit at the East Hanover site. Job Requirements : Primary Responsibilities: * Ensure daily production requirements are carried out in a safe and efficient manner. * Analyze, modify and upgrade existing processes and procedures. * Assess safety and potential environmental impact of operating units. * Continually improve safety, efficiency and output of operating units. * Ensure processes operate at optimum level in regards to quality and output. * Observe, measure, collect, and analyze process data. * General supervision; training and development of subordinates Required Skills or Abilities: * Project/Process engineering experience in a batch manufacturing environment. * Supervisory experience in a diverse manufacturing environment. * Strong time management and prioritization skills. * Strong leadership, communication, and interpersonal skills * Software: Microsoft Office; Access; SAP; etc. * Working knowledge of OSHA-PSM; MOC; ISO; LEAN; HPWT’s

Job Title: Manufacturing Supervisor - Cell Company: Dendreon Corporation Location: New Brunswick, NJ Description: Manufacturing Supervisor - Cell Processing - Alternate ShiftJob Type: Full-Time 1:30 a.m. - 11:30 a.m.Location: Morris Plains, NJJob Description:Dendreon is seeking a top-notch Manufacturing Supervisor to oversee the New Jersey manufacturing operations of the Cell Processing Associates. This is an alternate shift working from 1:30 am - 11:30 am and is eligibile for shift differential. The successful candidate will provide daily supervision of manufacturing operations, and have the opportunity to be on the front lines of manufacturing a first-in-class cancer treatment!General Summary:* Provides daily supervision of manufacturing operations, including the development, planning, implementation and maintenance of manufacturing methods, processes and operations for new or existing products and technologies.* May be responsible for one or more of the following:* Prepares documentation, reports and standard operating procedures.* Formulates and recommends manufacturing policies, procedures and programs.* Assists with manufacturing investigations and audits.* Works closely with Quality groups to ensure strict compliance with cGMP guidelines at all times.* Makes recommendations for corrective action necessary to ensure conformity with quality specifications.* Ensures finished products conform to company standards and satisfy GMP regulations.* Through the efforts of other employees, vendors and contractors, ensures department timelines are met.Job Requirements:* Bachelor's degree in a scientific discipline or equivalent.* Typically 5 years of experience years related experience in cGMP/FDA regulated industry.* Typically 2 years leadership experience.* Knowledge of cGMP/ICH/FDA regulations.* Proficient in MS Office applications.Working Conditions and Physical Requirements:* Ability to gown aseptically for work in Clean Room environments.* Handling of biologic materials.* Required to work alternate shift.* Extensive use of laboratory equipment, chemicals and biological materials.* Ability to lift 50lbs unassisted.* Some travel may be required.The preceding job description has been designated to indicate the general nature and level of work performed by employees within this classification. Additional and incidental duties related to the primary duties may be required for company business needs from time to time.

Job Title: Plant Manager Company: Cintas Location: New Brunswick, NJ Description: Title: Plant ManagerLocation: NJ-PiscatawayCintas is the leader in corporate identity uniform programs, helping companies of all sizes consistently present a clean, crisp, professional look. We also have specialized flame resistant garments and garments for cleanroom environments. In addition to offering the largest variety of uniform colors and styles in the industry, our Facility Services group helps our customers keep their businesses looking clean and professional with floor mats, restroom supplies, mops, and shop towels. Our floor mats, which can be customized with corporate logos, check dirt at the door while reducing slips, falls and housekeeping costs. We handle all of the details so our customers don't have to.Cintas is currently looking for a Plant Manager to lead a team of Production partners, including Supervisors, as well as manage all aspects of a fast-paced, industrial (possibly multi-shift) laundry plant. Daily duties include monitoring a budget, safety, production flow, material costs, wastewater management, and departmental profit and loss. Additional responsibilities include motivating, training and directing Production Supervisors as well as entry-level production workers. This is a high-level management position, with key management responsibility and accountability for the bottom line results.* A high school diploma or GED* A four year college degree or equivalent work experience* The ability to handle physical requirements, including but not limited to, repeated bending, stretching, twisting, and lifting* 3-5 years Production supervisory experience, preferred* P&L and budget experience, preferred* Availability to start within two weeks after offer made/accepted, preferred Our Plant Manager partners enjoy:* Competitive Pay* 401(k)/Profit sharing/ESOP* Medical, Dental and Vision Insurance Package* Disability and Life Insurance Package* Paid Vacation and Holidays* Career Advancement OpportunitiesCintas Corporation is an EEO/Affirmative Action Employer M/F/D/V

Job Title: Director of Manufacturing and Supply Chain Management - Company: CyberCoders Location: Morristown, NJ Description: Director of Manufacturing and Supply Chain Management - Global Process - Distribution - PackagingIf you are a Director,Associate Director, Sr Director of Manufacturing and Supply Chain Management, with a PhD, and 10-15 years of experience, 7 in Pharma industrial operations, please read on!What you need for this position:-PhD or equivalent in Chemistry, Biology, Biochemistry, Pharmaceutical Science, Pharmaceutical, or Chemical Engineering-10-15 years experience and 7 years in the Pharma industry specifically working in development/industrial operations-Material management and forecast planning-Expert understanding of: Formulation/drug product process developmentand scale-up; packaging, technology transfer, cGMP's, ICH guidelines; and CMC content of Regulatory Submissions-Experience in the implementation of quality systems in development and commercial operations. -Working knowledge of cGMP'sWhat you'll be doing:-Directing the manufacturing, packaging and distribution aspects for global supply chain process for development programs, clinical supplies, and commercial manufacturing activities for biological and small molecule projects at contract research or manufacturing facilities. Responsible for the drug process development, the CMC section of regulatory documents relating to both.What's in it for you:-Excellent compensation package, stock options and bonus structure-Opportunity to work on drugs for disorders with high unmet medical needs-Growth opportunity and a highly visible position within the organizationSo, if you are a Director, Associate Director, Sr Director of Manufacturing and Supply Chain Management, with a PhD, and 10-15 years of experience, 7 in Pharma industrial operations,, please apply today!Must be authorized to work in the United States on a full-time basis for any employer.

Job Title: Manufacturing Supervisor I - Converting* Company: Agfa Corporation Location: Branchburg, NJ Description: .desc Manufacturing Supervisor I - Converting* Overview: Supervises, oversees training, and assigns work to a group of employees in a manufacturing environment to insure production schedules are met in a timely fashion while maintaining product quality and employee safety. Capable of working a Day or Night shift as assigned Responsibilities: Responsible for adherence to cost standards, yields, and labor utilization standards. Actively involved in recommending improvements to processes/ products and work methods. Conducts employee performance appraisals and develops performance improvement programs where individual performance is less than quality. Responsible for proper maintenance of tools and equipment and the cleanliness of department/ area. Qualifications: BS Degree in a technical or business related discipline or equivalent. Minimum of 5 years in manufacturing with at least 3 years in a supervisory or leadership role.Demonstrated ability to rapidly learn and apply technical aspects of the positions area/ processStrong leadership skills required to lead production teams, manage processes and implement new conceptsExcellent skills needed in planning/ organizing work assignmentStrong interpersonal skills needed to interact and coach a diverse group of peopleBe able to read/write and verbally communicate in English Agfa Corporation is an equal opportunity employer

Job Title: Food Manufacturing Operations Manager Company: The Judge Group Location: Paterson, NJ Description: The Judge Grup is looking for an Operations Manager for a food manufacturer in the Paterson, NJ area. Strong management experience within  food processing, 5-10 years of experience,  and an engineering degree is preferred. The company is not looking to offer relocation but will consider some assistance for the right candidate. A BS/BA and food processing experience is required. Please send resumes to Adam Candela at Register to View

Job Title: Plant Manager, biosolids to fertilizer Company: VitAG Corp. Location: Kearny, NJ Description: PLANT MANAGER VitAg Corp. is seeking candidates for an immediate opening for Plant Manager of its state of the art biosolids-to fertilizer manufacturing facility in the Newark, NJ area. Candidates must have 5 yrs chemical mfg plant experience and 3 yrs supervisory exp. Excellent compensation and benefits package. Send resume to Register to View Reference Code Register to View

Job Title: OSD Clinical Manufacturing Supervisor Company: Bristol-Myers Squibb Location: New Brunswick, NJ Description: Employer Information About Bristol-Myers Squibb Bristol-Myers Squibb Mission: To discover, develop and deliver innovative medicines that help patients prevail over serious diseases. View all our jobs Job The candidate will be responsible for the following operationally based activities: • Establish plans for managing workload with efficient resource utilization and within designated timeframes. • Effectively supervise technicians to ensure product is made in accordance with pertinent specifications and cGMP requirements. • Generate and review SOPs and IQ/OQ documentation. • Coordinate activities with other departments to ensure timely release of products. • Interface with Biopharmaceutics R&D to ensure proper technical transfer and scale-up of formulae and processes into Clinical Manufacturing and out to commercial manufacturing. The candidate will work on a variety of processes, including the use of state of the art containment and PAT technology. He/She will supervise in a complex and dynamic organization, working in concert with other members of Clinical Supply Manufacturing to coordinate equipment and manpower requirements. The candidate will participate in the development of procedures and guidelines leading to a clear vision, with short- and long-term goals, for clinical manufacturing planning and management, in alignment of the business goals of Clinical Supply Operations. Additionally, this position will participate in high performing teams which develop strategies for incorporating new technology, improving regulatory compliance, and improving technology transfer within the Bristol-Myers Squibb research and development organization. NOTE: This position resides on the second (night) shift.

Job Title: Manufacturing Supervisor I - Con Company: AGFA Healthcare Corporation Location: New Brunswick, NJ Description: Manufacturing Supervisor I - Converting*Job ID: 2010-3497# Openings: 1Location: US-NJ-BranchburgPosted Date: 1/12/2010Category: Manufacturing & ProductionCommission Eligible: ..Shift: ..Hours: ..More information about this job:Overview:Supervises, oversees training, and assigns work to a group of employees in a manufacturing environment to insure production schedules are met in a timely fashion while maintaining product quality and employee safety.Capable of working a Day or Night shift as assignedResponsibilities:Responsible for adherence to cost standards, yields, and labor utilization standards. Actively involved in recommending improvements to processes/ products and work methods. Conducts employee performance appraisals and develops performance improvement programs where individual performance is less than quality. Responsible for proper maintenance of tools and equipment and the cleanliness of department/ area.Qualifications:BS Degree in a technical or business related discipline or equivalent. Minimum of 5 years in manufacturing with at least 3 years in a supervisory or leadership role.Demonstrated ability to rapidly learn and apply technical aspects of the positions area/ process*Strong leadership skills required to lead production teams, manage processes and implement new concepts*Excellent skills needed in planning/ organizing work assignment*Strong interpersonal skills needed to interact and coach a diverse group of people*Be able to read/write and verbally communicate in EnglishAgfa Corporation is an equal opportunity employer