General Manager Jobs in New Jersey

Job Title: Director of Manufacturing and Supply Chain Management - Global Process - Distribution - Packaging Company: CyberCoders Location: Morristown, NJ Description: Director of Manufacturing and Supply Chain Management - Global Process - Distribution - Packaging .body .body h4 .body .section tr.oddRow a, a:link, a:visited Director of Manufacturing and Supply Chain Management - Global Process - Distribution - Packaging near Morristown, NJ This job is open as of 2/20/2010. Apply Now! Not a fit for this job? Search other Director of Manufacturing and Supply Chain Management jobs! Are you an employer? Visit us for more info! Email this job to a friend - $1000 Location Morristown, NJ; Plainfield, NJ Salary $100,000 - $175,000 Education PhD Category Supply Chain Experience Required At least 2 Years Short Description Director of Manufacturing and Supply Chain Management - Global Process - Distribution - Packaging Required Skills Manufacturing, Supply chain, global supply chain, commercial manufacturing, Pharmaceutical, biotech, industrial operations, supply chain management, small molecules, packaging Recruiter Erin Beagle Date Updated 2/20/2010 Skills Required Manufacturing, Supply chain, global supply chain, commercial manufacturing, Pharmaceutical, biotech, industrial operations, supply chain management, small molecules, packaging Job 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. Are you a fit for this position? Please Click Here to Apply! (your information will be kept strictly confidential!) Not a fit for this position? Click Here to Search Other CyberCoders Jobs! Looking forward to receiving your resume through our website and going over the position with you. Clicking apply is the best way to apply, or you may also: Email your resume in Word to: Register to View **Please do NOT change the email subject line in any way. You must keep the JobID: CC HotJobAp : EB-ManuSupplyMgmt -- in the email subject line for your application to be considered.*** Erin Beagle - Executive Recruiter - CyberCoders Other Jobs

Job Title: DNA Manufacturing Supervisor Company: Cancer Genetics Inc. Location: Rutherford, NJ Description: Cancer Genetics, Inc. (CGI) is a rapidly expanding diagnostic, genomics research, and DNA diagnostics probe company, and a pioneer in developing disease specific CGH Arrays for cancer.  We are dedicated to the mission of providing genomic solutions to the clinical, biopharmaceutical, and research communities.   Job Title:  DNA Manufacturing Supervisor Job Location:  201 Route 17 North, 2nd Floor, Rutherford, NJ  07070 Salary: Based on experience  Essential Functions and Duties The employee is responsible for the overall technical planning, delivery and QC validation of BAC and plasmid DNA for use by manufacturing, research and development and contract agreements of the company. The employee will be responsible for managing the DNA production and performance of analytical validations during the manufacture of DNA-FISH probes according to predefined protocols while maintaining accurate document control.      In consultation with the product development and research project leaders, the employee is expected to carry out independent research projects at the bench showing comprehensive documentation, compilation and organization of the data.  He/she is expected to collaborate with the production leader to analyze the results, to identify possible methodological problems, and to assist in solving technical issues. This position will participate in group meetings for experimental planning and reviews Experience or training in molecular biology and DNA FISH probe design, production and QC, is required.  RequirementsMasters degree in molecular biology or related filed is required. Demonstrated supervisory experience is necessary. Budgetary responsibility is a plus. 5-10 years of experience in molecular biology techniques involving  BAC and plasmid design and construction, DNA purification and characterization, and DNA modification is required.Excellent critical thinking skills and attention to detail are requiredAbility to maintain laboratory records in an orderly and comprehensive mannerMust be able to communicate and supervise technical staff effectivelyKnowledge, Skills and Abilities Strong verbal and written communication skills.Strong project management skills.Strong analytical and problem solving abilities.NOTE: This job profile describes the duties and requirements of the position.  Requirements stated are representative of minimum levels of knowledge, skills and/or abilities required to successfully perform the job.  This position requires at least 40 hours a week and may occasionally require additional time evenings and weekends to meet deadlines or solve unexpected problems. The employee may be asked to perform other job-related duties as required.EOE

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: OSD CLINICAL MANUFACTURING SUPERVISOR Company: Bristol-Myers Squibb Location: Princeton, NJ Description: 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.A B.E./B.S. in Engineering or in a related science field. Experience in pharmaceutical manufacturing and/or formulation with 5 - 7 years experience with pharmaceutical processes, solid dosage dose manufacturing and/or product or process development is essential. Detailed knowledge of pharmaceutical solid dose manufacturing equipment is required along with the capability to plan and execute projects. The successful candidate will have the ability to lead and motivate others, the capability to solve process related problems and the command of effective communication skills. A complete understanding of regulatory and cGMP requirements and their application to clinical manufacturing are required.

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: Process Engineer/PUD Plant Supervisor Company: Chemtura Corporation Location: Perth Amboy, NJ Description: Company: Chemtura Corporation Job Title: Process Engineer/PUD Plant Supervisor Jobid: chemtura-1463 Job Location: Perth Amboy, NJ, 08861, USA Description: Process Engineer/PUD Plant Supervisor Job Code :1463 Division :Performance Products - Urethanes Location :Perth Amboy NJ US 08861 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/PUD Plant Supervisor for day-to-day supervision and process improvement of the PUD plant unit at our Perth Amboy, NJ 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: Plant Operations Manager I - Moonachie, NJ Company: Sara Lee Location: Newark, NJ Description: Position Summary: Responsible for coaching, teaching and mentoring supervisory personnel on a daily basis. Ensures all GMP and safety programs are enforced and maintained. Demonstrate dependability and promote teamwork as well as a professional demeanor. Interfaces with supervisory staff on a daily basis to ensure operational readiness. Demonstrate dependability, flexibility and promote teamwork as well as a professional demeanor Essential Duties & Responsibilities: Bachelor's degree or equivalent education/experience7-10 years of Supervisory experience with managerial experience in a consumer product environment, coffee manufacturing experience preferredStrong verbal and written communication skills requiredAbility to communicate with personnel at all levelsRequires extended time on the floor during production hours We make it our mission at Sara Lee to "Simply delight you...every day." Our brands make up one of the world's best-loved portfolios of innovative food, beverage, household, and body care products. Our leading, trusted brands include Ambi Pur, Ball Park, Douwe Egberts, Hillshire Farm, Jimmy Dean, Kiwi, Sanex, Sara Lee, and Senseo. Collectively, these brands generate nearly $13 billion in annual net sales as they delight millions of consumers every day in approximately 200 countries around the world. The global Sara Lee team consists of 41,000 employees At Sara Lee, we believe that careers are as unique as individuals. That's why we offer employment opportunities that give you ownership of your career. With the resources of a global corporation and direct responsibility to make it happen, you can be confident that you'll always be able to perform your best and be recognized for it. At Sara Lee, the difference is you The Sara Lee compensation program is designed to provide you with comprehensive, flexible benefits that enable you to select those features that best fit your needs. Our benefits include, but are not limited to: medical, prescription drug, dental, vision, life, short and long term disability, retirement plans, and tuition reimbursement. An Equal Opportunity / Affirmative Action 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 Company: Cintas Corporation Location: Piscataway, NJ Description: Cintas 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.

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.