- Aequor (Golden Valley, MN)
- …Pilot Plant Technician (2nd shift) - Cereal, Meals & Baking, Snacks, Morning Foods , and Pet LOCATION: Golden Valley, MN - onsite SHIFT/SCHEDULE: 2nd shift (2:00pm ... to the table with a shared passion for making food the world loves, to solve problems and shape...ground-breaking R&D work for various platforms including Snacks, Morning Foods , Meals and Baking, Pet and Cereal. The Pilot… more
- Exela Pharma Sciences, LLC (Lenoir, NC)
- …our manufacturing operations. The ideal candidate will have a strong background in Food & Beverage or Automotive production, leadership skills, and a commitment to ... years of experience in plant management or similar roles within the food and beverage industry, automotive industry, or similar rigorous production. Strong… more
- Aequor (Golden Valley, MN)
- …ALLERGEN STATEMENT: This position involves potential exposure and contact with common food , environmental and chemical allergens. SCHEDULE: Working 40 hours per week ... Ability to use multiple computer systems (LIMS, Microsoft Office) Broad knowledge of food testing services Skills & Abilities Strong attention to detail Fast learner… more
- Aequor (Cincinnati, OH)
- …in a manufacturing environment within pharmaceutical, nutraceutical or food processing industries.Skills/Knowledge/Abilities: Ability to receive instruction and ... follow directions. Ability to interact positively with co-workers and management. Ability to communicate effectively with written and oral communication skills. Ability to follow company policies and procedures. Ability to follow cGMP and other regulatory… more
- Merck & Co. (Rahway, NJ)
- …collectively to make a positive difference in animal care and the world's food supply and have a deep sense of responsibility towards our customers, consumers, ... animals, society, and our planet.Through our commitment, we offer veterinarians, farmers, pet owners and governments one of the widest ranges of veterinary pharmaceuticals, vaccines and health management solutions and services as well as an extensive suite of… more
- Exela Pharma Sciences, LLC (Lenoir, NC)
- …required. Pharmaceutical or other highly regulated industry (medical device, food , etc.) highly preferred. Sterile drug product manufacturing experience ... Areas of responsibility include capital projects, manufacturing and facilities equipment installation, troubleshooting, modification and maintenance, utilities, preventive maintenance program, contractors, equipment reliability, engineering document and… more
- Tris Pharma (Monmouth Junction, NJ)
- …roadblocks Ensures compliance with all current Good Manufacturing Practices (cGMP), Food and Drug Administration (FDA), Drug Enforcement Administration (DEA), and ... Occupational Health and Safety Administration (OSHA) regulations, as well as all applicable company compliance guidelines, standards and objectives; Ensures all systems and services are in compliance with GxP, FDA, Data Privacy regulation, guidelines and… more
- Exela Pharma Sciences, LLC (Lenoir, NC)
- …procedures, corporate policies, and the regulatory requirements of the US Food and Drug Administration. Job Responsibilities:Comply with garbing and behavior ... requirements that align to established cGMP practices for pharmaceutical finishing activitiesFollow Standard Operating Procedures (SOPs), batch records, current Good Manufacturing Practices (cGMP), including Data Integrity and Good Documentation Practices… more
- Twist BioScience (South San Francisco, CA)
- …response Maintain professional appearance of building lobby, reception area, and food service area Perform set-ups and teardowns of multi-purpose, conference, and ... training rooms as directed by manager May manage company parking or parking permit system for the building lots Additional responsibilities, duties and projects as assigned by department head Follow regulatory and ISO 13485 requirementsWhat You'll Bring to the… more
- Exela Pharma Sciences, LLC (Lenoir, NC)
- …procedures, corporate policies, and the regulatory requirements of the US Food and Drug Administration. Job Responsibilities:Enforce/Maintain clean room protocols by ... complying with garbing and behavior requirements that align to established cGMP practices and techniques Enforce/follow Standard Operating Procedures (SOPs), batch records, current Good Manufacturing Practices (cGMP), including Data Integrity and Good… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Good Clinical Practices (GCPs), appropriate Standard Operating Procedures (SOPs), Food and Drug Administration (FDA) regulations/EU Directive, and International ... Conference on Harmonization (ICH) guidelines. Key focus is on providing clinical trial management support to study teams and tracking CRO and other vendor performance against project goals and milestones to monitor and ensure compliance with Daiichi Sankyo… more
- Merck & Co. (Rahway, NJ)
- …(PBPK) models to facilitate decisions in areas including formulation development, food effect evaluation, in vitro-in vivo correlations and dissolution specification ... settingStrong knowledge of formulation development of small moleculesRelevant experience in pharmaceutical development with exposure to all stages and aspects of development (pre-clinical, clinical, and commercial)Strong influencing and communication skills… more
- Exela Pharma Sciences, LLC (Lenoir, NC)
- …corporate policies and the regulatory requirements of the US Food and Drug Administration.Experience RequirementsKnowledge and experience with FDA ... regulations.Self-motivated with demonstrated ability to work effectively with people from multiple departments, ensure deadlines are met, and manage multiple and changing priorities.Excellent communication, collaboration, teamwork, and interpersonal… more
- Exela Pharma Sciences, LLC (Lenoir, NC)
- …corporate policies, and the regulatory requirements of the US Food and Drug Administration.Job Responsibilities:Draft and review technical documents supporting ... raw material and/or drug product release and stability with some supervisionPerform calibrations and calibration verificationCompile data to support trending analysisPerform analytical testing of samples supporting incoming raw materials, in-process… more
- Exela Pharma Sciences, LLC (Lenoir, NC)
- …local procedures, corporate policies, and the regulatory requirements of the US Food and Drug Administration. The individual will be responsible for implementing ... policies and procedures that improve safety and productivity of his/her group.Job ResponsibilitiesWrite and Implement Standard Operating Procedures according to cGMP and cGLP.Assist in validation of new test methods for raw material, in-process, and finished… more
- Exela Pharma Sciences, LLC (Lenoir, NC)
- …corporate policies, and the regulatory requirements of the US Food and Drug Administration.Job Responsibilities:Perform analytical testing of samples supporting ... incoming raw materials, in-process production, drug product and stability samples with some supervisionUtilize analytical instrumentation such as FTIR, HPLC, GC, AA, wet chemistry techniques, UV/VIS, KF, and Polarimeter, etcPerform instrument troubleshooting… more
- Tris Pharma (Monmouth Junction, NJ)
- …of regulatory and industry standards related to Medical Affairs role including Food and Drug Administration (FDA), Office of Inspector General (OIG), Pharmaceutical ... Researchers and Manufactures of America (PhRMA), etc.)Expertise in pharmaceutical compliance laws, regulations and guidelines related scientific communications, as well as industry best practices related to MSL activitiesExperience leading Medical Affairs… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …meeting deliverables including ensuring all final arrangements are in place, including food and beverage menus, audio visual requirements, room arrangements and any ... meeting requirement expected of the facility Oversee the work activities of the conference room management team and strategically manage events and programs ensuring those are aligned with the client's business needs, goals, and objectives Lead departmental… more
- Merck & Co. (South San Francisco, CA)
- …of the following areas: enteroendocrine biology, peripheral and central control of food intake and energy expenditure, and adipose or muscle biology, and ... neurobiologyProficiency in both in vitro and in vivo techniques, with extensive bench experienceAbility to work productively and independently, design appropriately controlled experiments, interpret data and present results to audiences with diverse scientific… more
- Exela Pharma Sciences, LLC (Lenoir, NC)
- …local procedures, corporate policies, and the regulatory requirements of the US Food and Drug Administration. Job Responsibilities: Comply with garbing and behavior ... requirements that align to established cGMP practices for pharmaceutical finishing activitiesFollow/enforce Standard Operating Procedures (SOPs), batch records, current Good Manufacturing Practices (cGMP), including Data Integrity and Good Documentation… more
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