WuXi Biologics USA LLC

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• Biocon

  

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  Job Purpose Responsible for the execution of all aspects of solid-dosage manufacturing which includes, but is not limited to, the dispensing, granulation, sifting, milling, drying, encapsulation, coating, compression, and cleaning related activities. Must be able to interact daily with all site support personnel as required. Must be able to complete all required batch record documentation in a thorough, accurate, and legible manner in English. Must be capable of reading and understanding all documented Standard Operating Procedures in English plus demonstrate competency through action and written evaluation. Essential Duties and Responsibilities include the following. Other duties may be assigned: • Assist Production Management with all scheduled and requested activities in an efficient and smooth operation., • Ensure all scheduled commercial and non-commercial manufacturing activities are completed on time., • Become proficient in the setup, operation, and cleaning of all cGMP equipment used during production operations., • Participate in all Quality Investigations as required., • Adhere to all approved Standard Operating Procedures, Batch Records, and Safety Procedures as written when performing all daily activities., • Ensure the cGMP area is cleaned and maintained following all SOP’s and good housekeeping practices., • Must use required PPE during cGMP activities as specified in the Batch Records and Safety Data Sheets. To perform this job successfully, an individual should have: • Familiarity with working in a regulated pharmaceutical solid dosage facility., • Ability to read and write documents written in English., • Excellent written communication skills., • Familiarity with various cGMP solid dosage Pharmaceutical manufacturing equipment. Able to setup, operate clean, and troubleshoot the solid dosage Pharmaceutical manufacturing equipment being used., • Able to work with minimal supervision., • Able to stand on feet throughout an eight-hour work day., • Able to lift up to 30 Ibs (14 Kgs) without assistance., • Maintain personal hygiene habits consistent with working in a cGMP environment, • Be capable of wearing all required PPE; including partial and full facepieces based on OSHA guidelines. Education : High School Diploma or GED Equivalent. Bachelor’s degree in Physical Sciences or Pharmaceutical life science related field of study. Years of related experience 2-8 years related experience in cGMP production operation activities. Must have Valid work permit.

• I AM Acquisition LLC [159004]

  

  Production Supervisor

  14 days ago

  Cranbury

  Job DescriptionDescription: Title: Production Supervisor Location: Cranbury, NJ Shift(s): N/A Internal/External posting: External AI Applicant Screening used: No Salary Range: $75,000 - $90,000 (DOE) Contract Packaging and Manufacturing Company has an immediate need for a Production Supervisor. The Production Supervisor is required to support the growth of a National Packaging Company. The candidate selected for this position must have an entrepreneurial spirit and must have experience with all operational functions within a high-volume production facility including extensive production floor management and direct contact with our customers. At least 5 years’ experience in a similar role is required. The Production Supervisor will be responsible for: safety, maintaining the production workflow, as well as the production line set-up and labor utilization. Also, they must also drive Continuous Improvement, control labor costs during each shift, and display strong communication skills. Strong leadership skills and communication skills are critical to the success of the position. This individual will have the unique opportunity to leverage their skills, technical expertise, and business acumen while working with a company that lives their culture every day - Miss Nothing, Question Everything and Innovate Daily. If you have a passion for developing and scoping value-driven services that lead to successful customer projects - then we are looking for you! REPORTS TO: Production Manager • Accomplishes project results by communicating job expectations; planning, monitoring, and appraising job results; coaching, counseling, and disciplining employees; initiating, coordinating, and enforcing systems, policies, and procedures., • Maintains staff by recruiting, selecting, orienting, and training employees; developing personal growth opportunities., • Maintains work flow by monitoring steps of the process; setting processing variables; observing control points and equipment; monitoring personnel and resources; studying methods; implementing cost reductions; developing reporting procedures and systems; facilitating corrections to malfunctions within process control points; initiating and fostering a spirit of cooperation within and between departments., • Completes production plan by scheduling and assigning personnel; accomplishing work results; establishing priorities; monitoring progress; revising schedules; resolving problems; reporting results of the processing flow on shift production summaries., • Maintains quality service by establishing and enforcing organization standards., • Ensures operation of equipment by calling for repairs; evaluating new equipment and techniques., • Provides information by compiling, initiating, sorting, and analyzing production performance records and data; answering questions and responding to requests., • Creates and revises systems and procedures by analyzing operating practices, record-keeping systems, forms of control, and budgetary and personnel requirements; implementing change., • Maintains safe and clean work environment by educating and directing personnel on the use of all control points, equipment, and resources; maintaining compliance with established policies and procedures., • Resolves personnel problems by analyzing data; investigating issues; identifying solutions; recommending action., • A 4-year BA or BS degree or equivalent work experience., • 5+ years of Supervision with Production position, • Provide leadership to full time and temporary staffing., • Previous experience managing processes and process improvements, • Previous experience in production planning, • Ability to communicate clearly and effectively in all situations with strong interpersonal skills., • Strong reasoning, analytical, budget, and problem-solving skills., • Ability to interpret and understand policies and procedures and relate them to others., • Working knowledge of Windows, Microsoft Office, Word and Excel along with WMS experience., • Previous experience managing diverse teams of 100+ Associates., • Available to support multiple shifts as required., • The physical demands described here represent those that an employee must meet to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions., • Lifting of up to 50 lbs., • Adhere to company safety policies and procedures, • Wear required PPE (personal protective equipment) where needed While the work environment characteristics described here represent those an employee encounters while performing the essential functions of this job, they are in no way all-inclusive. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. • While performing the duties of this job, the employee regularly works on equipment on the production floor, • The employee often works at a desk or on other equipment., • The noise level in the work environment is typically minimal.

• YO IT CONSULTING

  

  Production Operator - Pharmaceutical Solid Dosage

  16 days ago

  Cranbury

  Job Description Location: Cranbury Shift: Second Shift Employment Type: Full-Time Mandatory Requirement: • Minimum 3 years of current relevant experience as a production operator, • -Familiarity with working in a regulated pharmaceutical solid dosage facility (SOLID - TABLETS), • -performing tasks like dispensing, granulation, sifting, milling, drying, encapsulation, coating, compression, and cleaning activities, • -Proficiency in setup, operation, and cleaning of all cGMP production equipment, combined with strict adherence to Standard Operating, • Procedures (SOPs), Batch Records, safety procedures, and good housekeeping practices, ensuring efficient, compliant, and safe manufacturing operations, • -Ability to read and write documents written in English., • Familiarity with various cGMP solid dosage Pharmaceutical manufacturing equipment., • Able to work with minimal supervision., • Able to stand on feet throughout an eight-hour work day., • Maintain personal hygiene habits consistent with working in a cGMP environment, • Be capable of wearing all required PPE; including partial and full facepieces based on OSHA guidelines. Essential Duties and Responsibilities include the following. Other duties may be assigned: • Assist Production Management with all scheduled and requested activities in an efficient and smooth operation., • Ensure all scheduled commercial and non-commercial manufacturing activities are completed on time., • Become proficient in the setup, operation, and cleaning of all cGMP equipment used during production operations., • Participate in all Quality Investigations as required., • Adhere to all approved Standard Operating Procedures, Batch Records, and Safety Procedures as written when performing all daily activities., • Ensure the cGMP area is cleaned and maintained following all SOPs and good housekeeping practices., • Familiarity with working in a regulated pharmaceutical solid dosage facility., • Ability to read and write documents written in English., • Excellent written communication skills., • Familiarity with various cGMP solid dosage Pharmaceutical manufacturing equipment. Able to set up, operat,e clean, and troubleshoot the solid dosage Pharmaceutical manufacturing equipment being used., • Able to work with minimal supervision., • Able to stand on feet throughout an eight-hour workday., • Able to lift up to 30 Ibs (14 Kgs) without assistance., • Maintain personal hygiene habits consistent with working in a cGMP environment

• YO IT CONSULTING

  

  Production Operator

  28 days ago

  Cranbury

  Job DescriptionLocationCranburyJob Purpose Responsible for the execution of all aspects of solid-dosage manufacturing which includes, but is not limited to, the dispensing, granulation, sifting, milling, drying, encapsulation, coating, compression, and cleaning related activities. Must be able to interact daily with all site support personnel as required. Must be able to complete all required batch record documentation in a thorough, accurate, and legible manner in English. Must be capable of reading and understanding all documented Standard Operating Procedures in English plus demonstrate competency through action and written evaluation. Essential Duties and Responsibilities Assist Production Management with all scheduled and requested activities in an efficient and smooth operation. Ensure all scheduled commercial and non-commercial manufacturing activities are completed on time. Become proficient in the setup, operation, and cleaning of all cGMP equipment used during production operations. Participate in all Quality Investigations as required. Adhere to all approved Standard Operating Procedures, Batch Records, and Safety Procedures as written when performing all daily activities. Ensure the cGMP area is cleaned and maintained following all SOPs and good housekeeping practices. Must use required PPE during cGMP activities as specified in the Batch Records and Safety Data Sheets. Requirements to Perform the Job Successfully Familiarity with working in a regulated pharmaceutical solid dosage facility. Ability to read and write documents written in English. Excellent written communication skills. Familiarity with various cGMP solid dosage pharmaceutical manufacturing equipment. Able to setup, operate, clean, and troubleshoot the solid dosage pharmaceutical manufacturing equipment being used. Able to work with minimal supervision. Able to stand on feet throughout an eight-hour workday. Able to lift up to 30 lbs (14 kgs) without assistance. Maintain personal hygiene habits consistent with working in a cGMP environment. Be capable of wearing all required PPE, including partial and full facepieces based on OSHA guidelines. Education High School Diploma or GED Equivalent. Bachelors degree in Physical Sciences or Pharmaceutical Life Sciencerelated field of study.

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