Home  Science and Research Jobs
  • Location: Vista
    Job Type : Permanent
    Date: Friday, 17 February 2017
    Job Title: Quality Assurance Technician Location: Vista 92085 Schedule: Mon-Fri 8am-5pm Duration: Direct Hire Pay: DOE Job Summary: The Quality Assurance Technician is responsible for QA laboratory testing, systems and database development, raw materials and finished goods evaluation, SOP writing, root cause investigation support, and product and process innovation. The QA Technician participates as an active Operations Services & Innovation team member, providing technical support to ongoing team-wide efforts and company special projects as needed.
  • Location: Rohnert Park
    Job Type : Permanent
    Date: Monday, 13 February 2017
    Are you a Senior Mechanical Inspector looking for a new opportunity? Visualize this: every day, you play a role in creating products that are the best they can be. Every week, you receive a paycheck that reflects your commitment to doing quality work. You also can depend on a full benefits package. You're working in an industry that is in high demand, with opportunities for change and growth. If that's your vision, Manpower has work for you. You offer your unique skills and experiences. And Manpower offers something unique for you. We're the place for talented individuals who want to do things differently, get ahead and establish a lifelong career.

    For the Senior Mechanical Inspector position, You'll have the opportunity to:

    * Work closely with the Quality Manager, conduct inspections, non-conforming material process and first article process and programmer and operator of measuring machine.
    * Maintains files, records and other documents that apply to laboratory records, modify First Article and inspection test plans.
    * Prepare inspection procedures and determine appropriate inspection points.
    * Inspect, measure, and test diverse parts for in-process testing and outsourcing procedures: Uses calipers, comparator, gages, centrifuge, manual pipettes, thermal cycler, vacuum leak tester, vision system (vertex), etc to perform required tests. Enters results into database. Use unipoint and agile to locate PQRs and forms.
    * Assist in internal auditing procedures, ISO - AS9100c and GMP requirements.
    * Must have experience with CMM operation and experience with Zeiss Contura is a plus.
    * Completes and maintains appropriate documentation to support testing procedures.
    * Applies analysis to collected database, implement action plan with assistance.
    * Identify non-conformances during daily testing and reports them
    * Work in combination with Quality Control management to maintain quality day to day.
    * Conduct test, operate testing equipment, enter result in to computer software programs
    * Complete documentation needed to support testing procedures
    * Monitor testing procedures to ensure that all tests are performed according to established specifications, standard test methods or protocols.
    * Performs receiving inspection of machined parts, plated parts and miscellaneous purchased parts.
    * May inspect in-process and/or finished production assemblies and subassemblies for conformance to product specifications and/or quality assurance standards
    * Calibrate, validate, and maintain equipment
    * Qualified candidate will possess excellent communication skills, attention to detail, as well as the ability to work well autonomously or as a part of a team. You are a problem solver. Driven.
    * Must pass the pre-employment requirements and salary is DOE: up to $60K

    Apply with Manpower, log on to www.manpower.com and call our office at 707-576-7855.
  • Location: San Diego
    Job Type : Temporary
    Date: Friday, 10 February 2017
    Job Title: Associate Scientist Location: Sorrento Valley 92121 Schedule: Monday-Friday 8am-5pm Duration: Temp 6 months+ Pay: $30-$33/hr. Description: You will perform a variety of biochemical and molecular assays that involve nucleic acid research. You will design, execute, and report experimental data to the team.
  • Location: Shelton
    Job Type : Temporary
    Date: Friday, 10 February 2017
    Major consumer products manufacturer located in Trumbull CT has multiple temporary full-time openings for degreed and experienced individuals to work as a Lab Technician in their Research and Development facility. These positions are diverse and duties will vary depending on the laboratory environment. The successful candidate for these temporary full-time positions will have a degree in Science-(chemistry; biology, micro-biology; bio-chemistry, chemical engineering; and others may qualify) and have 1-3 years' experience in lab procedures and possess a commitment to safe lab practices. Detail-oriented individuals with the ability to multi-task are urged to apply. Great communication skills and proficiency in English required. Microsoft Excel, Word, and PowerPoint proficiency required. Duties and responsibilities include: following Standard Operating Procedures(SOPs), maintaining laboratory notebook, managing the laboratory inventory of raw materials, filling, labeling and shipping prototype samples for consumer testing, maintaining a clean and safe laboratory work area while adhering to safety protocols. Must be able to be on your feet for a significant portion of the day. Must be able to occasionally lift up to 35lbs.
  • Location: San Diego
    Job Type : Temporary
    Date: Friday, 10 February 2017
    Job Title: Research Associate II Location: Sorrento Valley 92121 Schedule: Monday-Friday 8am-5pm Duration: 9+ months (potential temp to hire Pay: $23-$25/hr. Description: As a Research Associate in Consumables Product Development you will work in a dynamic, team-oriented environment to develop and build consumables in support of product development programs.
  • Location: Lansing
    Job Type : Contract
    Date: Wednesday, 08 February 2017
    Lateral Flow Chemist being added for Scientific manufacturing client company for indefinite contract position. This is for the first shift and will be an hourly pay position. Will be responsible for formulating reagents and preparing components used in the assembly of diagnostic products. Other duties would include testing and documenting results and following ISO and GMP guidelines.
    College education/degree in Protein Chemistry, Chemistry, Biochemistry or related Life Science field and one year related lab work experience or college coursework lab experience. Should have basic math skills, Microsoft Office Suite experience and ability to work and communicate in a team.
    If qualified and interested in this indefinite contract position, please email resume and professional reference list to: carrie.cervantes@manpower.com.
  • Location: Westbrook
    Job Type : Temporary
    Date: Wednesday, 08 February 2017
    Chemistry Lab Technician, $16/hour!
    Now seeking a mechanically inclined Chemistry Lab Technician! If you're looking to put your scientific knowledge to use in a stable, long term position at a well-established company, then this may be the opportunity for you!

    What's in it for you?
    * Full time, long term position
    * 8am-5pm Monday-Friday schedule
    * $16/hour and a weekly paycheck
    * $0.50 raise after 6 months, $1 after a year, plus a bonus during the year!

    What will you be doing?
    * Preparing and testing lab coatings
    * Operating complex and valuable bench size testing, lab, and pilot equipment
    * Running the pilot line
    * Performing basic mechanical change-over and maintenance tasks
    * Performing safety checks

    What will you bring to the job?
    * Prior chemistry lab experience
    * A strong mechanical and mathematical aptitude
    * Excellent attention to detail
    * A degree in chemistry or a related scientific/mathematic discipline (preferred)

    Let's try to put an end to your job search by applying today. Contact a team member today by applying online or calling 774-8258.
    You can also find all of our open positions by visiting www.ManpowerMaine.com. We look forward to working with you!
    We love referrals, so please share our job with friends and family!
  • Location: Lethbridge
    Job Type : Contract
    Date: Wednesday, 08 February 2017
    Lab Research Assistant

    With over 55 years of experience in the Alberta marketplace, Manpower specializes in matching great talent with great companies. In tandem with our client, a leading agriculture company, Manpower is seeking a Lab Research Assistant, to fulfill a long-term contract in Lethbridge, Alberta.

    In this role, as a Lab Research Assistant, your responsibilities will include:
    * Participating in projects seeded in growth room facilities; filling pots, seeding, maintenance of canola plants, cross pollinating, self-pollinating, harvest and threshing
    * Maintaining and organizing growth room records
    * Applying automated process improvements to daily tasks
    * Preparing seed samples and sampling plant material for marker projects
    * Preparing seed samples for summer nurseries
    * Harvesting and threshing bagged plants
    * Following safety rules and Standard Operating Procedures
    * Working occasionally in the summer nursery field to help with planting / bagging / harvest
    * Other duties as assigned

    To be successful in this role, as a Lab Research Assistant, you will have:
    * Degree or diploma in Agricultural Science or related field
    * Field or growth room research experience
    * Pesticide Sprayer Training and Application of pesticides required; training will be provided and paid for
    * Ability to work under diverse environmental conditions in the growth room and in the field; heat, cold, wind and/or dust
    * Intermediate computer skills; MS Word, Excel; ability to learn company specific software systems
    * Valid Alberta Driver's License and clean driving record; minimum of 2 years driving experience
    * Ability to work independently or as part of a team
    * High attention to detail and accuracy
    * Ability to focus/concentrate for sustained periods of time
    * Excellent organizational skills and ability to multi-task and prioritize
    * Flexible attitude and ability and drive to learn new procedures

    Please apply online and / or create and manage your profile at www.manpower.ca. Alternatively, you can email us at calgary.ab@manpower.com or contact us at 403.269.6936 and ask for our Office Team.

    Manpower would like to thank all applicants for their interest; however, due to the number of individuals applying to positions at Manpower, only successful applicants will be contacted. All other resumes will be retained for future opportunities.

    To learn more about the changing world of work, please visit our website at www.manpowerab.com, follow us on Twitter @ManpowerAB, and like Manpower Alberta on Facebook.
  • Location: Lincoln - Lancaster County
    Job Type : Contract
    Date: Wednesday, 08 February 2017
    Lab Tech - Visualize this. You work at a place that recognizes and values your contributions. Your work challenges you and keeps you interested every day. And it provides compensation worthy of your expertise and hard work. If that's your vision but not your current reality, you need a career change. Manpower has the ideal opportunity for you.

    You're precision-oriented, intuitive and a stickler for doing it right. Research is your passion. Laboratory work your expertise. You're a critical thinker who is adept at using logic and reasoning to identify the strengths and weaknesses of alternative solutions. You understand the value of working as a team, yet you function strongly on your own. If this describes you, it's time to talk to Manpower.

    In this Lab Tech position, you'll have the opportunity to:
    * Perform laboratory testing and services to support customer data generation including the sequenom, microsatellite, veterinary diagnostics and sequencing
    * Conduct entire spectrum of sequencing data generation from sample management and processing
    * RNA/DNA extraction
    * Sample preparation for analysis and sequencing
    * Operate highly throughput instrumentation
    * Generate and analyze data from a variety of laboratory techniques and analytical instrumentation
    * Maintain laboratory notebooks, archives, and sample specimen repository, as applicable
    Are you interested? The ideal Lab Tech candidate will possess:
    * Proficiency in providing input to the best ways to maximize laboratory efficiency
    * Bachelor's degree from four year college or university (chemistry, microbiology, biochemistry, immunology, animal science) OR 1-2 years related training/experience
    * The ability to be reliable and on time
    * The ability to pass a background check and drug screen
    You can see it. More challenging work. A more interesting work environment. The opportunity to use your finely honed skills to make a real difference. And to collect pay that reflects your talent and expertise. If this is what you see for yourself, you need to talk to Manpower.

    Besides gaining valuable experience with some of the most reputable organizations in the market, you'll gain access to Manpower comprehensive benefits package.

    Manpower reach and resources bring you career options you couldn't find on your own. We're experts at placing each of our candidates into his/her "dream job" - one perfectly matched to skills, ambition and lifestyle.
  • Location: Hackensack
    Job Type : Contract
    Date: Wednesday, 08 February 2017
    Job Description
    Position Summary:
    To work with the Specification staff, interface with R&D, Supply Chain, and Global personnel in a manner as to support Specification Management and MET (Material Expert Team) to deliver quality ingredient specifications.

    Position Responsibilities (Expected Work):
    The Ingredient Specification Temp is generally expected to be responsible for the following work activities:
    - Works independently to support the SMT and MET team in the execution of updates and creation of quality ingredient specifications.
    - Perform various data entry tasks, and data pulls from R&D Information Systems.
    - Actively participate with other team members working in R&D SMT Systems for complex R&D and MET initiatives involving specification systems.
    - Develop reports and spreadsheets to communicate new ingredient specifications.
    - Communicate effectively to members of immediate team, other corporate functional groups and Unilever plants & 3PM sites.

    Challenges:
    - Meeting critical deadlines by maintaining order and structure in a multi-tasked work flow.
    - Maintaining active communications with Global METs, Regional METs, and other SMT team members in a manner that supports work flow and deadlines.
    - Learning new concepts quickly with minimal instruction and with a "take charge" approach.

    Position Requirements:
    - BS in science: Food Science, Biology, Chemistry, Nutrition degrees preferred.
    - Must have strong organizational skills and able to work well in a fast paced corporate environment, independently and as part of a team.
    - Multi-tasking of responsibilities is key to the success of this position.
    - Strong working relationships in a team environment is a must.
    - Ability to prioritize workload to meet strict project deadlines.
    - Strong written and verbal communication skills are a must.
    - Maintain confidential information.
    - Must have basic knowledge of Microsoft Office (must be able to create and maintain spreadsheets in MS Excel)
    - Raw Material experience a plus.
    - Foods experience a plus.
    Knowledge of SAP and/or other manufacturing systems
  • Location: Lincoln - Lancaster County
    Job Type : Contract
    Date: Tuesday, 07 February 2017
    The ideal candidate has strong attention to detail, strong work ethic, and good time management skills. Flexibility with schedule, good communication skills, and key emphasis on quality are required. Strong preference towards individuals with Microsoft Office experience and the ability to multi-task.

    Within a lab environment, the responsibilities include sample tracking, lab maintenance, data entry, and inventory assistance. Contribute to established protocols with suggestions to improve current processes.

    Education and/or Experience:

    High School Diploma or Equivalent; some additional higher education or concurrent pursuit of a Bachelor's degree is beneficial. Previous laboratory experience is preferred but not required. Must have previous office experience & be willing to submit to a background check and drug screen.
  • Location: Des Moines
    Job Type : Permanent
    Date: Tuesday, 07 February 2017
    •Responsible for all aspects of customer service from the FSS group, including scheduling, responsiveness, feedback and communications, oversee overall management, planning, systems, and controls of customer audit programs. •Responsible for the processing and upkeep of CB documentation, qualifications and general personnel requirements. •Interfacing with sister business divisions (China, France, New Zealand, Chile). •Support Business Development Manager with strategic development of new and existing schemes. •Responsible for the monitoring and achievement of all scheme owners KPIs, adherence and compliance to all scheme owner KPIs, in addition to internal KPIs. •Responsible for the auditor utilization and output for all FSS activities. •Responsible for the monitoring of monthly revenue and cost considerations including DSO invoicing, profit and loss statements and cost control initiatives. Participation in the budget process under the direction of the Business Unit Manager. •Ensure execution of the quality management system for all FSS functions. •Lead all technology, support and administration services (IT, finance, HR, etc.) to maximize output. •Development of unaccredited audit programs and operations strategy. •Assist with marketing initiatives with sales and marketing team. •Review financial statements, sales or activity reports or other performance data to measure productivity or goal achievement or to identify areas needing cost reduction or program improvement. •Direct and coordinate activities of business concerned with the production, pricing, or distribution of products. •Direct administrative activities related to providing services. •Monitor suppliers/auditors to ensure that they efficiently and effectively provide needed services within budgetary limits. •Applies good practices in all areas of responsibility, as appropriate. •Demonstrates and promotes the company vision. •Regular attendance and punctuality. •Conducts all activities in a safe an efficient manner. •Advise on complex issues and make business decisions. •Lead and participate in staff meetings. •Develop and conduct presentations for customers, potential customers, and industry. •Maintain confidentiality and impartiality in all aspects of work and adhere to all procedures established by the company and it’s auditing clients. •Other duties as assigned.
  • Location: Palatine
    Job Type : Permanent
    Date: Friday, 03 February 2017
    The QA Manager position requires applying judgment within generally defined practices and policies for obtaining solutions in relation to a diverse scope of problems where analysis of data and/or systems requires evaluation.Individual is an integral team member to provide assurance that all systems, processes, procedures as well as products produced in the facility are in compliance with the applicable medical device regulations and company policies.

    Specific primary efforts will be directed towards the following:
    * CAPA system
    * Training program
    * Deviations/Nonconformances
    * Device History Record review and product release
    * Change Management
    * Supplier Management
    * Design Control
    * Validations/Qualifications
    * Training
    * Customer and Regulatory Audits

    Responsibilities:

    Management and Oversight of the Core Quality Systems - Actively manage the necessary processes and functions within the required system in regards to cGMP compliance for medical devices, 21 CFR Part 820 (Quality Systems Regulation):
    * CAPA System
    * Change Management/Document Control System
    * Customer Complaint System
    * Deviations/Nonconformances
    * Device History Record review and Product Release
    * Quality/Regulatory record and retain management
    * Management reviews of Quality System- monthly and quarterly

    Supplier Management
    Review and approve associated documentation in relation to the quality status of our material and component suppliers. Manage the electronic database reflecting current status of the vendors. Coordinate the functions of the Material Review Board and the accompanying CAPA reports (nonconforming material/corrective actions) to the status of the supplier list.

    Audits/Inspections
    Manage customer and regulatory (FDA) audits/inspections. Actively schedule and conduct internal audits
    of our Quality Systems in regards to cGMP. Perform audit follow up/verification for completing commitments to audit responses. Track and trend all audits and associated observations/corrective
    actions.

    Training
    Conduct the training of personnel in cGMP concepts for medical devices as deemed necessary and applicable by the Director of QA/Regulatory. Manage the maintenance of training records in addition to the required tracking and trending requirements.

    Design Control
    Oversee Design Control Activities from a quality perspective as deemed necessary and applicable by the
    Director of QA/Regulatory.

    Regulatory
    Manage the following regulatory records:
    * FDA site registration
    * Annual Reports
    * UDI Labeling database and requirements

    Direct Reports
    Manage the activities and functions of the Quality Assurance Specialist.

    Position Requirements/Experience:
    * Minimum of a BS degree in a scientific or engineering field.
    * 8-12 years direct experience in medical device/biotechnology arena.
    * Effective personnel and project management skills are essential.
    * Candidate must possess excellent communication, organizational/prioritization and observational skills, as well as strong interpersonal and team orientation.
    * Working knowledge of the cGMP and QSR regulations for Class II and III IVD medical devices.
    * PC skills required, i.e. proficiency with Microsoft Word, Excel and database management software.
    * A history of managing direct reports.

    Interested applicants should apply directly, or email resume to Krystal.Grady@manpower.com
  • Location: Palatine
    Job Type : Permanent
    Date: Friday, 03 February 2017
    The Quality Assurance Specialist position requires applying judgment within generally defined practices and policies for obtaining solutions in relation to a diverse scope of problems where analysis of data and/or systems requires evaluation. Individual is an integral team member to provide assurance that all systems, processes, procedures as well as products produced in the facility are in compliance with the applicable medical device regulations and company policies.

    Responsibilities:

    Administration of the Core Quality Systems - Actively perform the necessary processes and functions within the required system in regards to cGMP compliance for medical devices, 21 CFR Part 820 (Quality Systems Regulation):
    * Change Management/Document Control System
    * Product Release-performing QC release of manufactured kits
    * Assist in complaint investigations and maintaining complaint records
    * Quality/Regulatory record and retain management

    Supplier Management
    Create the necessary quality documentation in relation to our material and component suppliers or as directed by the Quality Manager. Maintain the electronic database reflecting current status of the vendors.

    Audits/Inspections
    Assist with customer and regulatory (FDA) audits/inspections. Assist with scheduling and conducting internal audits of our Quality Systems in regards to cGMP. Track and trend all audits and associated observations/corrective actions.

    Training
    Maintain training records in addition to the required tracking and trending requirements.

    Position Requirements/Experience:

    * Minimum of a BS degree in a scientific or engineering field.
    * 5-8 years direct experience in medical device/biotechnology arena.
    * Candidate must possess excellent communication, organizational/prioritization and observational skills, as well as strong interpersonal and team orientation.
    * Working knowledge of the cGMP and QSR regulations for Class II and III IVD medical devices. Specifically in regards to:
    ¾ Quality Control as pertaining to release of finished product, ¾ Processing change controls through the Change Management process.
    * PC skills required, i.e. proficiency with Microsoft Word, Excel and database management software.

    Interested applicants should apply directly, or email resume to Krystal.Grady@manpower.com
  • Location: Frederick
    Job Type : Temporary
    Date: Thursday, 02 February 2017
    Attention! Manpower is currently accepting applications for a logistics manager.

    Candidates should have 3 years prior experience in working with shipping and receiving. A successful candidate will also be accustomed to working in a cold environment with experience in working with liquid nitrogen. Forklift and cryogenic storage experience is also a plus.

    This temporary position will last for three weeks and will pay $19 an hour.

    Apply today!
  • Location: Muscatine
    Job Type : Contract
    Date: Wednesday, 01 February 2017
    Performs laboratory technical tasks. Responsible for the care and maintenance of laboratory equipment. Will be required to offer assistance in the operation of the equipment and the gathering of data. Assists with receipt and inspection of raw materials, ordering and stocking. . Requires an Associate's Degree or its equivalent and 0-3 years of related experience. Has knowledge of commonly-used concepts, practices, and procedures within a particular field. Relies on instructions and pre-established guidelines to perform the functions of the job. Works under immediate supervision. Typically reports to a supervisor.

    Job Summary: This is a Laboratory position that supports production units in a chemical manufacturing facility.

    Scope / Specific Responsibilities of the Position:
    * Performs analyses of raw materials, packaging materials, bulk, intermediate, and finished products
    * Determines conformance to accepted specifications for a particular chemical or physical property
    * Monitors and verifies quality in accordance with statistical process or other control procedures
    * Performs troubleshooting and calibration of instruments
    * Prepare reagents, solutions, and standards. Maintain instruments, and apparatus according to established procedures to support testing activities of the unit
    * Interpret results based on trends, specification limits, and comparison data
    * Ability to conduct lab analyses and communicate with customers in a professional environment

    Specialized Skills:
    * Troubleshooting and maintenance of laboratory equipment
    * Identifying optimization opportunities
    * Work with chemists on special projects
    * Effective communication with production areas
    * Identification of data trends through analysis
    * Attention to detail

    Experience
    0 to 3 years in a laboratory setting preferred.

    Competencies/Skills
    Proficient in Windows-based programs (Word, Excel, PowerPoint, Access, and Outlook)
    Excellent oral and written communication skills
    Works well in a team environment

    Ideal Candidate Will Also Possess:
    Chromatography, LIMS and CDS experience
    Experience with GC, LC, IC, and Mass Spec instrumentation
    Ability to interpret, modify, and integrate chromatograms

    Description of Specific Work Conditions and Physical Requirements:

    Rotating shift work is required, as the Lab is staffed continuously 24 hours per day, 7 days per week. This role is in a laboratory environment within a chemical manufacturing facility, and includes working around agricultural chemicals and laboratory equipment. This position requires the ability to stand, sit, and walk between various laboratory stations and equipment.

    1.ROTATING SHIFT INFORMATION-
    We run what is called a four week flex schedule. Shifts change every week in the following order:

    Nights (11pm-7am)
    Flex Week (2 days in during the week covering vacations then 12 hours on Saturday and Sunday)
    Evenings (3pm - 11pm)
    Days (7am - 3pm)
  • Location: South Burlington
    Job Type : Contract
    Date: Tuesday, 31 January 2017
    Manpower is currently looking for a Chemistry Lab Technician for the Quality department at company in Georgia, VT that manufactures baby formula and other nutritional products. This position will be mostly bench chemistry and an ideal candidate would have a bachelor's degree in a life science and understanding of cGMP is preferred. They will work with Analytical instrumentation, primarily NMR Fat Analyzer, Nitrogen Analyzer, NIRSpectroscopy, and HPLC (High Pressure Liquid Chromatography). Some of the assistance needed includes, but not limited to:
    * Preparation of analytical standards. Accurately identify, weigh, and dilute stock standard materials for calibration purposes
    * Weighing of samples. Accurately identify and weigh sample materials for processing through analytical methods
    * General sample manipulations, to include: quantitative sample dilution, addition of analytical reagents, processing of samples through incubators, shakers, centrifuges, evaporators, etc.
    * Extraction of sample solutions, to include liquid-liquid and solid-phase techniques
    * Quantitative transfer of sample extracts between vessels
    * Instrument configuration and routine operation
    * Preparation of general laboratory reagents (buffers, mobile phases, etc.)
    * General cleaning of materials after analysis
    * Other duties as assigned.

    Hours:
    This position is on 2nd shift, 4 PM-12:30 AM (Friday-Tuesday).

    Pay:
    Pay begins at $17/hr, but is based on experience.

    Qualified candidates will be able to clear a 7 year background check and hold a Bachelor's degree, preferably in a life science.
  • Location: Lawrence
    Job Type : Contract
    Date: Tuesday, 31 January 2017
    Do you enjoy working in a lab environment? Manpower is currently recruiting for a lab tech position. Prefer candidates who possess a BS in Biology or related Science as well as experience with automated fermentation equipment and understanding of aseptic process in daily activities.

    You will be supporting the Lead Lab Tech in the preparation and operation of fermenters - both small and large scale. This is a great opportunity for the right person. Interested? Contact Manpower in Lawrence, KS today!
  • Location: Lansing
    Job Type : Contract
    Date: Monday, 30 January 2017
    Manufacturing Scientific Formulator being added to manufacturing Scientific client site for contract to eventual perm position. The shift for this position is Saturday-Monday, 7pm-7:30am.
    Will be responsible for bulk formulation, manufacturing, sterilization and dispensing of liquid media and ancillary products in Manufacturing. Will assemble and package diagnostic test kits used in the food safety industry according to Standard Operating Procedures ensuring accuracy and quality throughout the process.
    Ideal candidate will hold minimum Associates degree in Biochemistry, Chemistry, Microbiology, Food Science or other related Life Sciences. Perfect position for a student who takes classes during the day to get real work life experience on the job; excellent resume builder with a long term company!
    Should have great language and mathematical skills and good problem solving, planning/organizing skills and a passion for quality in a teamwork environment. If qualified and interested, please email resume and professional reference list to: carrie.cervantes@manpower.com.