Home   Science and Research Jobs
  • Valid City, State or Zip Code: Middletown
    Job Type : Contract
    Date: Monday, 25 October 2021
    Document Control Administrator
    Middletown, VA

    Do you have experience generating product labels? Does your experience include scientific terminology, medical or pharmaceutical manufacturing processes or GMP? In this role you will:

    * Manage and track all IVDR project labeling tasks, provide status and work with internal Subject Matter Experts (SMEs) to make required changes before implementation due date.
    * Create, prepare artwork for labels/inserts and newly created documents for company or OEM-branded products.
    * Assist with the formatting of Product Master Records (PMRs) to align with the new template in Master Control.
    * Control of the documents that include Product Master Records, Batch Records, Forms and SOPs as required by GMP including trial documents.
    * Creates production and testing documentation, new and revised, in accordance with GMP/QSR requirements.
    * Initiates and coordinates Change Orders.
    * Controls and maintains Departmental Databases for PMR and specification changes.
    * Assists in updating and maintaining plant system databases (including but not limited to: MRP, Master Control, Bartender & InDesign).
    * Proofreads corrections made to documents.
    * Maintains complete and accurate files of documents under the change control of the Documentation Department as required by GMP.
    * Update and maintain template library via Master Control.
    * Collate data from various departments and enter metric monitoring system for the site. Construct and disseminate KPI reports.
    * Writes Standard Operating Procedures (SOPs), Work Instructions (WI), Training Summary Forms (TSFs), and Change Orders (Cos).

    Interested? Well qualified candidates will bring:
    * High School Degree/College degree preferred
    * 2+ years relevant experience required in product label generation.
    * Knowledge of scientific terminology, medical or pharmaceutical manufacturing processes and GMP desirable.
    * Knowledge of in vitro diagnostic processes highly desired
    * Intermediate to advanced word-processing skills; spreadsheet and database skills a plus (Microsoft Office preferred)
    * Proficiency in documentation best practices, typing, proofreading and editing required
    * Ability to interact with and provide training to all levels of staff, internal & external customers
    * Strong oral and written communication skills.
    * Excellent organization skills and ability to manage multiple requests/projects, along with rapidly changing priorities

    Apply today to learn more about this excellent long-term Contract opportunity that pays up to $28/hr.
  • Valid City, State or Zip Code: Wanamingo
    Job Type : Temporary
    Date: Thursday, 21 October 2021
    Lab Technician

    Interested in finding way to take a world class manufacturing operation to the next level? Manpower is now hiring entry level Lab Technicians for our client in Wanamingo, MN.

    What's in it for you?
    ● Monday-Thursday: 4p-2a
    ● $22.64 per hour
    ● Temp to Hire opportunity
    ● Clean and safe working environment
    ● Weekly paycheck

    What is the job?
    ● This role provides you the opportunity to work in a fast paced factory, helping deliver the highest quality standards to improve the overall company.
    ● Actively finding areas for improvement in food/beverage formulas
    ● Ensure that customers are depending on the company for the best products

    What do you bring to the job?
    ● Experience and love of working a in fast paced environment
    ● Background in manufacturing or quality
    ● Understands the importants of quality controls, tech manuals and processes
    ● Detail oriented, organized, and willing to help others
    ● Collaborative, supportive and strives for improvement

    What are the requirements for the position?
    * Background/Drug Screening

    Why work with Manpower?
    ● Free training to upgrade your skills
    ● 24 - 7 Manpower customer care support
    ● Weekly pay deposited right to your account

    So, are you interested? Know someone who might be? Connect with us right away for the opportunity for a solid career. Help friends and family find a job!

    Manpower
    2746 Superior Dr. NW
    Rochester, MN 55901
    507-285-0710

    ManpowerGroup recognizes the importance of providing an accessible and barrier-free environment. We are committed to creating a welcoming, fair and inclusive environment by offering equal opportunity to access our services. At ManpowerGroup, we are committed to providing accommodations, and will work with you to meet your needs.
  • Valid City, State or Zip Code: Evansville
    Job Type : Temporary
    Date: Thursday, 21 October 2021
    We are currently recruiting for 2 Lab Technicians. These roles will work in a Quality control lab working an off shift within a major company on Evansville's west side. If you have the following experience, go to www.manpower.com and apply, then call 812.429.7321 to discuss next steps.

    Job Responsibilities Include:
    Laboratory Technician: Collect, prepare and analyze routine quantitative samples of raw materials, finished products and premixes. Perform chemical quality control tests of minerals and other nutrients following established methods and utilizing accepted laboratory techniques. Operate laboratory instruments. Perform duties required in the routine maintenance of a safe and appropriate laboratory environment which is compliant with company and regulatory standards. Maintain current, complete, legible notebooks and laboratory records in compliance with good scientific and regulatory practices. Work in a laboratory environment using teamwork and interpersonal skills to accomplish goals.

    Job Requirements/Education:
    Bachelor's degree in a natural science (chemistry, biology, food science, etc.) preferred. Non-degreed candidates with equivalent skill and experience will also be considered. Demonstrates attention to detail and the ability to prioritize and manage multiple tasks simultaneously. Demonstrates ability to work both independently and as part of a team. Experience using Microsoft based computer applications a must. Familiarity with ion chromatography, ICP, mass spectrometry detection and laboratory information management computer systems a plus. Demonstrates effective verbal and written communication skills. Demonstrates the ability to achieve results while operating within company policies and procedures.

    Additional Information:
    This position requires the individual to work with chemical or physical agents which may pose health or safety hazards if improperly handled.

    www.manpower.com
  • Valid City, State or Zip Code: Frederick
    Job Type : Contract
    Date: Thursday, 21 October 2021
    Warehouse Material Handlers - Up to $19.55 an Hour
    Frederick, MD - 1st, 2nd, and 3rd shifts available!
    Are you looking for a position that will allow you to put your warehouse experience to use? Are you interested in starting a new career in a warehouse setting? This could be the position for you!
    About this job:
    * Our client is looking for reliable individuals for these important warehouse roles
    * In this position you would be preparing inventory for shipment; providing shipping, receiving, storage, and order fulfillment services for finished goods, inventory, materials, supplies, parts, and equipment
    * Safely work in a warehouse setting in various temperatures including room temperature, cold room, and freezer room (Protective garment provided when needed)
    * Safely operate material handling equipment
    * Temporary position with potential to become permanent position
    Ideal candidates are those who:
    * Are reliable and have great attendance in their previous work history
    * Are comfortable working with various material handling equipment
    * Can lift, push, or pull 25lbs routinely
    * Are eager to work with a bio-science, drug free warehouse in Frederick, MD.
    Apply TODAY!!
  • Valid City, State or Zip Code: Lexington
    Job Type : Contract
    Date: Wednesday, 20 October 2021
    Do you want to be part of a global, purpose-led company in Health, Nutrition & Bioscience, applying science to improve the health of people, animals and the planet? Then we have an opportunity for you!

    As a Lab Technician you will create brighter lives for all. You will be responsible for fermentor preparation, assembly, medium preparation, fermentation monitoring, sampling and sample processing.

    Fermentation Responsibilities:

    * Clean, setup, maintain and operate bench-scale fermentors

    * Fermentor sampling and data logging

    * Prepare media and stock solutions in support of fermentation experiments

    * Monitoring fermentation process, report deviations and observations to senior team members

    * Performs other laboratory housekeeping tasks as assigned

    Analytics Responsibilities:

    * Prepare fermentation samples to transfer to analytics team

    * Communicate with team members for schedule of sampling and sample processing

    * Prepare reagents for sample processing

    Qualifications/Experience:

    * B.S. or Associate's degree in Biology or Chemistry, previous work experience in Biotechnology highly desirable

    * Experience using standard lab equipment such as pH meter etc.

    * Understanding of biology and microbiology techniques preferred

    * Display strong attention to detail, and strictly follow all safety and lab regulations

    * Must be able to lift 50 pounds of weight

    * The ability to work independently and to effectively prioritize multiple work activities with varying deadlines

    * A familiarity with common chemistry laboratory equipment such as pipettes, volumetric glassware and working in a chemical hood.

    * Experience in multi-step sample preparation procedures

    * Experience in following written protocols, without deviation, to ensure reproducibility of data

    * Demonstrates proficiency in the use of basic computer skills including MS Office platforms such as Excel, Word, and PowerPoint
  • Valid City, State or Zip Code: Rockville
    Job Type : Contract
    Date: Wednesday, 20 October 2021
    Our client is looking for a Manufacturing Technician in life sciences with assembly experience
    WHAT'S THE JOB:
    Techs will need to work in a cleanroom environment and will be required to wear PPE which are provided by the company (scrub top, scrub pants, lab coat, safety shoes, ear plugs, gloves, hair cover, face/beard cover, and safety glasses (surgical face mask if not fully vaccinated) * High school (or equivalent) diploma is required. * At least 1 year of work experience working in a team-based organization. * Good communications skills. Ability to read, write and interpret written and/or verbal instructions (English) *

    WHAT'S THE RESPONSIBILITIES:
    The Manufacturing Technician I will execute entry level production duties with supervision in the manufacturing of custom products used in cell and gene therapy clinical trials, critical applications in final fill assemblies, and molded components in ISO 7 and ISO 8 cleanrooms. * Ability to perform entry level work station activities * Follow SOPS/Work Instructions/drawings with guidance. * Demonstrate basic problem identification and able to escalate accordingly.

    WHAT'S IN IT FOR YOU:
    Possible perm opportunity
    Manpower benefits - Medical - dental - 401K - vision - Paid sick leave- Earned holidays - free access to Manpower training.
    FOR IMMEDIATE CONSIDERATION KINDLY SEND RESUME
  • Valid City, State or Zip Code: Alachua
    Job Type : Contract
    Date: Wednesday, 20 October 2021
    Are you looking for an office or clerical position?
    Are you self motivated and able to prioritize your workload with a high level of attention to detail?

    Manpower is currently looking for a File Clerk for a large, established company in Alachua!

    Hours are Monday - Friday 8am to 5pm

    Pay is $14-16 depending on experience.
  • Valid City, State or Zip Code: Charleston
    Job Type : Temporary
    Date: Monday, 18 October 2021
    Temperature Greeter
    Ae you exploring new and exciting career opportunities? Manpower in is excited to share that we are NOW HIRING multiple Temperature Screening Greeters to join our growing Healthcare COVID-19 Response Team. This is a full-time opportunity with multiple shifts available. Qualified candidates enjoy working with others and making a difference! Temperature Screening Greeters will screen all incoming visitors, guests and employees to promote safety guidelines and answer visitors' questions.
    Manpower is an excellent company to grow your career and get your foot in the door at potentially hundreds of regional companies across the Tri-State. With a 5-star rating on Facebook, Manpower is confident we offer a great work experience for job seekers.
    Responsibilities:
    * Visibly review, note and process all guests, visitors and employees for cold, flu and respiratory symptoms before entering the facility.
    * Check temperature of all visitors and employees using a no-contact thermometer
    * Record all results of each visitor and employee who are not permitted on property and submit to Human Resources and Safety representatives.
    * Submit reports and data insights
    * Comply with all designated safety policies and procedures to include wearing company provided and required PPE in the work area.
    * Assisting visitors with instructions and directions to navigate the facility and comply with the facilities regulations.
    * Other duties as assigned
    * Shifts: Multiple Shifts Available
    Requirements:
    * Strong interpersonal, communication and customer service skills.
    * Must enjoy working with people and solving problems
    * Must be able to stand or sit for extended periods of time
    * Must be able to pass pre-employment screenings: background check and drug screen
    * Professional appearance and attitude.
    Who Is Manpower?
    Locally owned, but globally connected, Manpower is a full-service staffing and recruiting company. Manpower connects qualified candidates with great regional employment opportunities throughout the Tri-State and beyond.
    Manpower is an EEO/AA/ADA/Veterans employer
    Questions or want to speak with a Recruiter? Text/Call Manpower at [304.346.9617]
  • Valid City, State or Zip Code: Columbus - Franklin
    Job Type : Contract
    Date: Wednesday, 13 October 2021
    Lab Technician Needed - FANTASTIC company to work for! - $19 - 25 /hour

    Looking for someone with lab tech experience!!! Manpower recently partnered with a client in Columbus who is looking for someone who has worked with SOPs. This is a FANTASTIC company to work for with excellent benefits! Company has a very upbeat, positive, employee focused culture. This is a temp to perm opportunity that could easily turn into a long-term career! Stop your search and apply today!

    What's in it for you?
    * Monday through Friday - NO OT
    * 7am-3pm or 8am-4pm available
    * Clean and safe work environment
    * Fully PAID - on the job training
    * Full time Hours
    * Competitive wages - $19 - 25/hr - depending on experience
    * Employee focused culture
    * Supportive management team with career growth opportunities
    * Your own work area, but still team focused

    What's the job?
    * Understand and follow batch recipes with high accuracy for weights and measurements
    * Perform standard testing procedures including prep of materials
    * Accurately document work in lab notebooks both physical and electronic
    * Follows all lab safety requirements

    What do you bring?
    * Strong work ethic
    * Highly motivated
    * Strong problem solving
    * Strong attention to detail and quality control
    * Excellent verbal and written communication skills
    * 0-3 years of experience in Chemistry or Coatings industry
    * Must have basic Microsoft Excel, Word and Powerpoint
    * Must have an Associates Degree or Technical Certification
    Why Manpower?
    * Voted #1 best places to work by Glassdoor 2020
    * Weekly pay with direct deposit
    * Free upskill training programs available
    * Paid referral program

    Interested?
    Stop your job search and apply today! A recruiter will be in touch within 24 hours.

    Share this job with friends and family and earn dollars with every successful hire.

    ManpowerGroup recognizes the importance of providing an accessible and barrier-free environment. We are committed to creating a welcoming, fair and inclusive environment by offering equal opportunity to access our services. At ManpowerGroup, we are committed to providing accommodations, and will work with you to meet your needs.
  • Valid City, State or Zip Code: Phoenix
    Job Type : Permanent
    Date: Wednesday, 13 October 2021
    GREAT OPPORTUNITY!! FANTASTIC COMPANY!! PERMANENT POSITION
    paying $19.00 to $28.00 hourly

    Why You'll Love Working With Us

    12 hour shifts with every other weekend off
    All expenses paid during Training
    Permanent position with a Great Company in Goodyear, AZ

    What Will You Be Doing

    Learn and become familiar with manufacturing/engineering process and stay informed of any changes in procedures.
    * Conduct wafer inspection, complete necessary reworks and/or assisting in handling of abnormal events that occur.
    * Conduct wafer test piece preparation, including operating preliminary work and wafer dicing.
    * Assist in executing experimental plans and in subsequent data collection and analysis.
    * Review Statistical Process Control (SPC) charts for tool stability monitoring, and take necessary actions to bring the process conditions back to baseline per operating instructions and procedures.

    What You Bring to the Job

    High School Graduate or GED
    Positive attitude
    Willingness to learn

    Interested?

    Select APPLY NOW and a Recruiter will reach out within 24 hours

    Share this job with friends and family and earn dollars with every successful hire.

    ManpowerGroup recognizes the importance of providing an accessible and barrier-free environment. We are committed to creating a welcoming, fair and inclusive environment by offering equal opportunity to access our services. At ManpowerGroup we are committed to providing accommodations and will work with you to meet your needs.
  • Valid City, State or Zip Code: Laval
    Job Type : Permanent
    Date: Monday, 11 October 2021
    Un laboratoire de recherche contractuel et chef de file de services personnalisés pour les études cliniques et précliniques, embauche un gestionnaire de projets recherche et développement.
    Ce que nous offrons :
    *Entreprise très stable
    *Régime d'épargne -Retraite
    *Assurance collective 50% employeur 50% employé
    *Assurance dentaire
    En quoi consiste le poste?
    *Comprendre l'objectif de chacun des projets scientifiques sous sa responsabilité;
    * Analyser, définir et implanter une stratégie visant à l'atteinte de l'objectif pour chacun des projets qui lui sont confiés;
    * Coordonner l'ensemble des différentes étapes et activités des projets scientifiques qui lui sont confiés en collaboration avec l'équipe assignée au projet incluant, l'assignation des activités auprès des différentes unités, la mise en place d'un processus de suivi;
    * Développer un plan de travail et des outils de gestion de projet qui permettront à tous les membres de l'équipe travaillant sur l'étude à suivre de façon efficace le développement de l'étude ainsi que les résultats anticipés.
    * Coordonner et réaliser divers analyses ou travaux à caractère technique de recherche de laboratoire au niveau de l'unité;
    * Préparer, rédiger et analyser les différents protocoles, rapports et MON qui lui sont confiés tout au long du projet et s'assurer du respect et de la conformité des standards de qualité de l'entreprise;
    * Coordonner les réunions et activités liées aux projets scientifiques sous sa responsabilité. Préparer les notes de service et les documents connexes afin d'optimiser la communication et d'assurer la coordination et l'intégration des ressources impliquées. Établir et tenir à jour des dossiers, des comptes-rendus, des fichiers et des budgets reliés à ces projets.
    * Fournir un support dans le design d'expérience et la résolution de problèmes pour toutes nouvelles méthodes de développement R&D ainsi qu'un support scientifique et technique pour l'équipe de soutien en R&D.
    * Interagir avec les clients internes et externes dans la gestion et l'évaluation des projets scientifiques en R&D.
    * Fournir un leadership scientifique et technique pour la gestion et l'évaluation des projets en R&D.
    * Répondre aux questions et demande d'information de la clientèle et s'assurer de rediriger ces demandes au sein de l'entreprise.
    * Compléter les projets assignés tout en respectant la règlementation BPL.
    * Agir en tant que Directeur d'étude ou Principal Investigateur et adhère aux rôles et responsabilités tel que requis par la PON sur les études BPL.
    * Fournir un support à la préparation de soumissions.
    Qualifications et Exigences :
    *Un Ph. D. en immunologie, virologie, biologie cellulaire, biologie moléculaire ou biochimie.
    * Une expérience de 1 à 2 années en gestion de projet en recherche dans l'industrie biopharmaceutique ou une société de recherche clinique à contrat (CRO).
    * Expériences en immunologie (Cytométrie, Méthodes ELISA, méthodes cellulaires), en virologie ou dans le domaine connexe aux vaccins et en biologie moléculaire (qPCR et RT-PCR) constituent un atout.
    * Excellente connaissance des normes réglementaires GLP (Good Laboratory Practices).
    * Parfaitement bilingue en français et anglais
    * Maturité, éthique professionnelle et sens développé du service à la clientèle.
    CNESST permit: AP-2000535 // permis CNESST: AP-2000535.
  • Valid City, State or Zip Code: Ada
    Job Type : Contract
    Date: Monday, 11 October 2021
    Looking for a Lab Technician who will be under general supervision, does technical work in the Packaging Science Laboratory, through Manpower.

    Primary Job Responsibilities:

    Plans, organizes and executes a variety of laboratory tests using the more advanced types of equipment, on primary package containers, secondary package materials and other packaging materials. You will be receiving only general instruction and limited supervision; including receiving test materials from engineers, execution of tests including comprehensive periodic evaluations, detailed accurate recording of data and observations, and preparation of detailed reports.

    Responsible for areas of the Packaging Science Laboratory; including test material inventory control, sample package materials inventory and control, test equipment maintenance/calibration and laboratory supplies procurement and inventory control.

    Researches publications and drafts new or modifies existing, test procedures as required; drafts laboratory test equipment/apparatus standard operating procedures.

    Preferred Experience:
    Past lab work experience
    Proven ability to work in a team environment
    Familiarity with Microsoft Excel, Word, PowerPoint, Adobe
    Experience with transportation testing is ideal but not required
  • Valid City, State or Zip Code: Hawthorn Woods
    Job Type : Contract
    Date: Wednesday, 06 October 2021
    Do you want to be part of a team where you'll do important work and your work will have a real-world impact? Do you want to be supported in achieving your career goals? Then we have an opportunity for you!

    As a Medical Device Labeling Specialist you will lead small scale medical device labeling projects to support R&D initiatives, quality/compliance initiatives, and market expansion.

    Primary Responsibilities:

    * Lead small scale medical device labeling projects to support R&D initiatives, quality / compliance initiatives, and market expansion.
    * Participate in cross-functional team meetings to define label requirements.
    * Support Fresenius Kabi production facilities with implementation of labeling changes.
    * Process design change control documentation in the electronic change management system, and process label change orders in the electronic document management system for updates to labeling and related specifications.
    * Revise product specifications and Bill of Materials to implement label changes.
    * Support and lead label changes as required by the new European MDR Regulation, complete Change Control documentation and work with the manufacturing facilities to implement the new labels.

    Qualifications/Skills:

    * Detail-oriented, process-oriented thinker with experience on cross-functional teams.
    * Bachelor's degree required; concentration in engineering or packaging technology preferred.
    * Medical device background and/or experience with electronic document management systems and/or label/material specifications preferred.
    * Proficiency with standard Microsoft desktop applications and Adobe Acrobat required.
    * Bar code / UDI experience is helpful.
    * Knowledge of country-specific regulatory requirements not required.

    Mon - Friday 8am to 5pm CST - flexible 8 hour shift
  • Valid City, State or Zip Code: West Hills
    Job Type : Contract
    Date: Tuesday, 05 October 2021
    Are you experienced in Production/Manufacturing Lab work? Are you passionate about working in a fast- paced environment? Do you desire a position which will allow you to work full time and receive a full 40 hours a week? Do you have experience working in clean lab room environment? If you answered YES! to these questions Manpower would like to speak to you about our Production Lab Operator in West Hills, Ca.

    What's in it for you?

    Full time hours.
    1st Shift--Monday-Friday with regular OT and some weekends
    8am- 5pm
    Weekly pay (Every Friday).
    True Temp to Hire opportunity
    Competitive pay starting at $19-22an hour
    Free College Tuition Program

    What you'll be doing:

    Read, understand, and implement written SOPs
    Perform manufacturing/ production tasks as scheduled
    Handle and work with biological and chemical reagents
    Work with laboratory equipment including but not limited to: UV Spectrophotometer, Thermal Cycler, qPCR, robotic systems, centrifuges, multichannel pipettes
    Work in a clean room laboratory environment with adherence to CGMP guidelines
    Review data and recognize and report data inconsistencies
    Ability to climb, stoop, kneel, reach, push, pull, grasp, and perform repetitive motions
    Regularly stand, walk, and sit for extended periods of time
    Abide by all company safety and hygiene regulations

    Who were looking for:

    Bachelor's degree in a technical or scientific field or equivalent
    Ability to write basic SOPs and other common production documents
    Ability to perform basic laboratory calculations
    Good working knowledge of Microsoft Word, Excel, and Power Point
    Able to work critical and shifting timelines while demonstrating a 'can do' attitude
    Ability to work overtime and nonstandard work schedules as required to meet production schedule
    Respect for rules relating to safety of the employee and his/her colleagues
    Must work overtime and weekends as needed.
    A demonstrated ability to follow instructions regarding the operation of machinery
    The willingness and ability to follow company policies prohibiting harassment and discrimination of any kind
    A mature temperament that does not require constant supervision.

    Stop your job search and apply today. We love referrals so please share our job with friends and family.

    We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance
  • Valid City, State or Zip Code: Plymouth
    Job Type : Permanent
    Date: Monday, 04 October 2021
    Sr. Regulatory & Clinical Affairs Specialist | Direct Hire | $107-$129k Salary | Plymouth, MN

    This position is responsible for preparing and coordinating regulatory submissions in accordance with policies and procedures on a world-wide basis. This position works closely with product development teams to develop and provide timely and accurate regulatory requirements, submission strategies and guidance for new products and product modifications. This position works closely with regulatory authorities to assure that products comply with regulatory requirements and are approved in a timely manner; this position also liaisons with third-party, external clinical experts for strategic clinical feedback.

    Essential Job Functions:



    * Serve as the senior most shared regulatory resource subject matter expert across Nonin's product portfolios.
    * Prepare and maintain U.S. regulatory submissions for product approval and/or marketing clearance.
    * Prepare and maintain international product submissions to meet registration, licensing, certification and approval requirements.
    * Monitor international regulatory changes and communicate appropriate information and actions throughout the company.
    * Identify, understand and apply worldwide regulatory laws and regulations to our business.
    * Evaluate changes to product design and labeling and maintain a documented regulatory history of compliance for the life of our products.
    * Establish /maintain policies and procedures that detail the conduct of regulatory activities at Nonin Medical Inc.
    * Assist in the development of the regulatory budget.
    * Meet defined goals and objectives through own initiatives, activities and available resources with minimum of supervision.
    * Develop global regulatory strategies for Nonin product(s), product families, product claims, and competitive positions.
    * Develop and communicate regulatory requirements to product development teams and work closely with the team(s) to assure compliance with and understanding of all regulatory strategies.
    * Perform reviews of labels, labeling, literature, and web site for accuracy, consistency, and regulatory compliance.
    * Initiate and/or participate in the review and development of new legislation and/or regulations and assist in the preparation of comments for submission into the promulgation process.
    * Provide regulatory support for product complaints and worldwide adverse event reporting requirements.
    * Serve as the liaison between Nonin and third-party CROs or MROs, as needed.
    * Mentorship and coaching of junior team members.

    Minimum Qualifications:

    Required Education & Experience:



    * Bachelor's in engineering, biological sciences, medical or related and minimum 5-10 years' experience in preparing and executing regulatory submissions on a world-wide basis or equivalent combination of education and experience.

    Preferred Qualifications:



    * Experience in and knowledge of international registration, licensing and regulatory affairs.
  • Valid City, State or Zip Code: Temple City
    Job Type : Contract
    Date: Wednesday, 29 September 2021
    Are you experienced in Inventory Control? Are you passionate about working in a fast- paced environment? Do you desire a position which will allow you to work full time and receive a full 40 hours? If you answered YES to these questions Manpower would like to speak to you about our Inventory Control Specialist position in Temple City, Ca.

    What's in it for you?

    Monday - Friday (Possible Overtime and Weekends)
    Full Time Hours
    1st Shift 8:30am-5pm
    $20-22/Per Hour (Weekly Pay)
    True Temp to Hire opportunity
    College Tuition Program

    What you'll be doing:

    Verify inventory computations by comparing them to physical counts of stock, and investigate discrepancies or adjust errors.
    Issue or distribute materials, products, parts, and supplies to customers or coworkers, based on information from incoming requisitions.
    Provide assistance or direction to other stockroom, or warehouse workers.
    Prepare and maintain records and reports of inventories, price lists, shortages, shipments, expenditures, and goods used or issued.
    Determine proper storage methods, identification, and stock location, based on turnover, environmental factors, and physical capabilities of facilities.
    Dispose of damaged or defective items, or return them to vendors.
    Compile, review, and maintain data from contracts, purchase orders, requisitions, and other documents to assess supply needs.
    Prepare products, supplies, equipment, or other items for use by adjusting, repairing or assembling them, as necessary.
    Clean and maintain supplies, tools, equipment, and storage areas to ensure compliance with safety regulations.
    Recommend disposal of excess, defective, or obsolete stock.
    Determine sequence and release of back orders according to stock availability.
    Confer with engineering and purchasing personnel and vendors regarding stock procurement and availability.
    Purchase new or additional stock, or prepare documents that provide for such purchases.
    Keep records on the use or damage of stock or stock-handling equipment.
    Advise retail customers or internal users on the appropriateness of parts, supplies, or materials requested.

    Who were looking for:

    4+ years of Inventory Required
    Comfortable working in cold environments
    Data entry and ERP/WMS Experience Required
    Someone with great attendance and perfect punctuality.
    Detail-oriented and organized with an ability to work independently
    Able to lift to 50 pounds
    Someone with a "Yes, can do!" Attitude.
    Able to pass a Background Check and Drug Screen.
    Comfortable Undergoing Covid Screenings.

    We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance

    We love referrals so please share our job with friends and family.
  • Valid City, State or Zip Code: Scarborough
    Job Type : Contract
    Date: Tuesday, 28 September 2021
    Lab Technician Job in Scarborough, Maine

    ⏰ Schedule: 4:45a-5:15p 📆 Assignment Length: Long-Term Temp

    Do you have an associate degree in Chemistry or a related life science field? Do you have proficiency with computers? Are you looking for a steady, long-term job with a great company? We are now hiring a Lab Technician for a client in Scarborough. Apply today!

    ☑️ Perks:
    * Great pay rate!
    * Exciting work with an innovative company
    * Access to health, dental, and vision benefits
    * Maine earned paid leave

    ☑️ Duties:
    * Ensure all documentation is filled according to operating procedures
    * Maintain quality systems and proper GMP/GLP
    * Conduct chemical and laboratory tests
    * Set up laboratory equipment and instrumentation required for tests

    ☑️ Requirements:
    * Associates Degree in Chemistry, Life Science, or a related field
    * Ability to perform basic mathematical functions
    * General knowledge of computer applications
    * Able to communicate effectively through written and verbal correspondence

    We've made it easy to apply for this Lab Technician job in Scarborough, Maine. Simply contact us by choosing an option below.

    ✔️ Apply Now: see below
    📱 Text: 'LAB' to 207.806.5398
    📞 Call: 207.774.8258
    📧 Email: [email protected]
  • Valid City, State or Zip Code: West Hills
    Job Type : Contract
    Date: Monday, 27 September 2021
    Are you experienced in Data Entry and Warehouse work? Are you passionate about working in a fast- paced environment? Do you desire a position which will allow you to work full time and receive a full 40 hours a week? Do you have experience working in clean lab room environment? If you answered YES! to these questions Manpower would like to speak to you about our Document Control Warehouse Coordinator position in West Hills, Ca.

    What's in it for you?

    Full time hours.
    1st Shift--Monday-Friday with regular OT and some weekends
    8am- 5pm
    Weekly pay (Every Friday).
    True Temp to Hire opportunity
    Competitive pay starting at $15-17 an hour
    Free College Tuition Program

    What you'll be doing:

    Ensure safe and efficient handling and processing of controlled documents and document control related activities in accordance with documented standard operating procedures.
    Responsible for the routine maintenance of active and archived controlled documents and records in accordance with department SOPs.
    Responsible for proficient initiation/coordination of Collaboration Tasks and Releasing of assigned document(s) within Master Control in a timely manner
    Ensure new/revised software analysis files are disposition according to defined document specifications and plans.
    Coordinate the translation of all required documents.
    Manage and maintain off-site storage, document retention and retrieval of documents per department SOP.
    Assist with printing document copies for packaging/shipping as needed.
    Assist with reviews and edits to SOPs as needed.
    Assist with audits in retrieving documents and supplying them to the audit team in a timely/urgent manner
    Support QA department with all other misc. administrative tasks as needed.
    Maintain accurate account of electronic and hard copy records for all applicable QS documentation.
    Provide assistance with editing, formatting and final drafting of SOPs as requested and approved by supervisor.
    Records retention, storage and retrieval.
    Regularly stand, walk, and sit for extended periods of time
    Abide by all company safety and hygiene regulations

    Who were looking for:

    A high school diploma minimum. Some college is desirable. 2-5 years related work experience Prior work with documentation in a GMP manufacturing environment preferred.
    Proficient in Microsoft office, including MS Word, Excel. Knowledge of GMP document control regulations a plus
    Follow instructions, organizational, written and verbal communication skills important. Attention to detail important.
    This position will operate a computer terminal on a daily basis. Occasional lifting of equipment of up to 35 pounds.
    Able to work critical and shifting timelines while demonstrating a 'can do' attitude
    Ability to work overtime and nonstandard work schedules as required to meet production schedule
    Respect for rules relating to safety of the employee and his/her colleagues
    Must work overtime and weekends as needed.
    The willingness and ability to follow company policies prohibiting harassment and discrimination of any kind
    A mature temperament that does not require constant supervision.

    Stop your job search and apply today. We love referrals so please share our job with friends and family.

    We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance