Home  Pharmaceuticals Jobs
  • Location: West Palm Beach , Boca Raton , Delray Beach , Riviera Beach
    Job Type : Contract
    Date: Thursday, 23 March 2017
    We are currently seeking a Licensed Pharmacy Technician with a flexible schedule to join our team. Technicians would be responsible for completing the authorization process of pending prescription orders from Veterinarian Offices or Clinics. Prescriptions would come through via fax, mail, or phone calls.
  • Location: Allentown
    Job Type : Contract
    Date: Thursday, 23 March 2017
    Packaging Operators* Responsible for packaging of finished drug products on the company's packaging equipment, following approved Standard Operating Procedures (SOP's) and Current Good Manufacturing Practices (cGMP's).
    * Responsible for the operation, maintenance and cleaning of various packaging equipment, following approved following approved Standard Operating Procedures (SOP's) and Current Good Manufacturing Practices (cGMP's).
    * Maintain equipment logs.
    * Maintain the tooling in a clean and operational manner.
    * Assist in other production and packaging functions, when available.
    * Perform cross-functional tasks in other production departments, as needed, and as directed by senior managers.
    * May be responsible for access to the DEA controlled substances storage areas.

    Pack or package by hand a wide variety of products and materials.
  • Location: Chantilly
    Job Type : Temporary
    Date: Wednesday, 22 March 2017
    Manpower is seeking TOP TALENT for an experienced Laboratory Cleaning Technician. This position is located in Chantilly, VA. The responsibilities of this position would be to provide laboratory glassware washing and sterilization services; sweeping and mopping of lab floors, removal of trash, cleaning and dusting equipment, and general housekeeping duties. Work a Monday through Friday schedule, with a pay rate of $13 hourly. Position requires a drug and criminal background check. Please submit your resume for immediate consideration.
    Local candidates please.
  • Location: Sioux City
    Job Type : Contract
    Date: Tuesday, 21 March 2017
    Manpower is currently recruiting for a PROCESS OPERATOR 1 in Sioux City, IA!!. This is an excellent Temp - Perm opportunity you don't want to miss out on! Salary is $15.50/hour + night differential.

    Job Responsibilities include but are not limited to:
    -Learns, understands and applies Good Manufacturing Practices (GMP)
    -Learns to safely work with acids, caustics, proteolytic enzymes and solvents
    -Operates and cleans paunch drying system
    -Is trained and demonstrates the capability to perate fork trucks safely and efficiently
    -Completes written records of cleaning logs, MI's and other pertinent records as work is preformed
    -Drains I-tanks and cleans and preserves the loaded ion-exchange resin according to current MI's
    -Learns to perform various calculations and metric conversions
    -Specifically trains to unloand and clean tankers and activate raw material.

    Job Requirements:
    -Verifiable High School Diploma/GED
    -6 months experience in a manufacturing setting
    -Ability to Lift up to 50lbs consistently in a fast paced environment
    -Ability to pass a pre employment assessment

    If this is the opportunity you've been waiting for call Manpower today @ 605 361 1560!
  • Location: Fairmont
    Job Type : Contract
    Date: Tuesday, 21 March 2017
    Manpower is currently recruiting for a Lab Tech II Assistant Position in Wothington, MN. This position is a TEMPORARY position lasting from April 2017 - April 2018 with potential hire after that time.
    Monday -Friday DAY SHIFT hours
    Salary: $14.00 - $15.00/hr DOE
    Formal education with a minimum AS Degree in a technical scientific discipline is preferred with 1-3 years of experience in a biologic laboratory setting.
    Ability to perform high end quality work.
    Ability to work successfully in a team-oriented environment.
    Ability to effectively follow procedural guidelines.
    Strong computer skills with excellent communication and writing skills desired
    Ability to troubleshoot assay issues with a solid scientific foundation.
    Ability to assume additional technical responsibilities and complete them successfully with very little initial guidance and minimum supervision

    Quality Control Laboratory Assistant Position Description:
    This position will work, under minimal supervision, in the Quality Control Testing Team.
    Responsibilities will include the following:
    Under general supervision, this position assists professional laboratory personnel by performing routine biological testing to evaluate the purity of animal vaccines in accordance with 9 CFR and local procedural guidelines (to a lesser extent, efficacy and potency testing).
    Provides data for testing trend analysis.
    Provides test data for the investigation of testing issues and Out of Specification (OOS) test results. Laboratory cleaning, restocking testing supplies test media preparation.
    Instrument and test calibrations.
    Laboratory record completion and project notebook maintenance.
    Reviews internal documents against regulatory requirements for accuracy and compliance.
    The equipment used includes but is not limited to: microscopes, centrifuges, pipettes, pipettes aids, syringes, laminar flow hoods, balances, autoclaves, incubators, freezers, coolers, liquid nitrogen, flow cytometry etc.

    This position will require working in a "clean room environment" and wearing scrubs and other cleanroom attire on a daily basis.

    -Minimum of AS Degree
    -MUST be able to pass a drug screen & background check
    -MUST have excellent written & oral communication skills
    -MUST have exceptional organizational skills and be very detail oriented
    -MUST have excellent computer skills

    If this sounds like the opportunity you've been waiting for contact Manpower @ 605 361 1560 TODAY!!
  • Location: Kingston
    Job Type : Permanent
    Date: Friday, 10 March 2017
    Cleaning Validation Specialist / Engineer

    Fortune 500 company and leader in the pharmaceutical manufacturing industry is seeking a Cleaning Validation Specialsit / Engineer for their Eastern Ontario facility.

    This is an excellent opportunity to work for a top-notch employer that values the development and growth of their employees.

    * Relocation package (cost of living and housing market significantly less in this part of beautiful eastern ontario)
    * First-rate training and the opportunity to work with state of the art equipment
    * Opportunity to enhance your skills and grow your career with an industry leader
    * Excellent salary and benefits package
    * Strong leadership and supportive team-oriented work environment

    This position will focus primarily on equipment and facility qualifications but will have significant overlap and interaction with process validation initiatives. As a key member of the validation team within Engineering - Technical Services, this role acts as subject matter expert and technical resource to Operations and the larger organization. The individual will design, write and execute cleaning (validation, qualification, verification) studies for production and facility equipment that impacts the quality of GMP-regulated products.
    The Cleaning Validation Specialist will provide data analysis and recommendations for operational process improvements that simultaneously improve the quality of manufactured products and processing efficiency. This is a central role with a broad base of internal and external customers including Operations, Technical Services, and Quality Systems. The Validation group plays a central role in program execution and has frequent interaction with external customer peer groups (Engineering, Operations, and Quality).

    Bachelor of Science/ Engineering or equivalent, with 5+ years of experience in the Pharmaceutical or Health Care industry
    Demonstrated high level of knowledge, skill, or expertise in validation concepts, with experience using statistical tools for evaluation of process capability and control.
    Proven organizational, time management, and project management skills-
    PMP designation or equivalent is a highly desired asset
    Ability to analyze systems and processes and recommend process improvements.
    Excellent problem solving and troubleshooting abilities.
    Knowledge of root cause analysis (RCA) tools and methods.
    Excellent oral and written communication skills.
    Strong interpersonal skills.
    Strong judgment, decision making and trouble shooting skills Demonstrated ability to work effectively as a team member with employees at all levels of the organization.

    If you are interested in hearing more about this opportunity, please send your resume to JAN.GIORDANO@MANPOWER.COM Thank you!

    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.
  • Location: Albuquerque
    Job Type : Permanent
    Date: Wednesday, 08 March 2017
    Quality Assurance Engineer - 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.

    We are currently recruiting for a Quality Assurance Engineer to work at a great company located in Belen, NM. This is a permanent opportunity. For immediate consideration for this opportunity, please call 505-998-6200 or apply directly at www.manpower-nm.com.
  • Location: Rockford
    Job Type : Permanent
    Date: Tuesday, 07 March 2017
    Manpower is looking for multiple Project Managers for a client in Rockford.
    DIRECT HIRE $60,000-$70,000 Salary range, based on experience/interview

    Manages designated customer projects to ensure that goals and objectives are accomplished within prescribed time frame and budget while adhering to applicable regulations and protocol requirements. Lead and play an integral part in individual project success and provide PCI a competitive advantage in long-term customer management.

    3-5 years experience in similar position and/or Bachelors Degree

    PMs with concurrent project experience is ideal, excellent planning & forecasting, and stellar customer facing ability is a must.

    Please apply with your resume. A representative from Manpower will contact you for next steps if you meet the requirements.
  • Location: Albuquerque
    Job Type : Permanent
    Date: Tuesday, 07 March 2017
    Quality Technician - 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.

    We are currently recruiting for a Quality Technician to work at a great company located in Belen, NM. This is a direct hire opportunity. For immediate consideration for this opportunity, please call 505-998-6200 or apply directly at www.manpower-nm.com.
  • Location: Fort Collins
    Job Type : Permanent
    Date: Sunday, 05 March 2017
    Are you looking for a great career opportunity? With your stable work history, you could be looking at a new career in pharmaceutical manufacturing within weeks. We are offering entry level packaging opportunities with our manufacturing partner in Fort Collins. These opportunities are Direct Hire but the initial screening and interview are held at Manpower.
    We're looking for career minded individuals with stable work history and desire to excel and grow with a local pharmaceutical company. As a Packaging Tech I, you will work stable overnight hours from 10:00p-6:30a Sunday - Thursday with scheduled Over Time every 3rd week on Friday. Candidates who like to work on their feet and have good attention to detail are ideal candidates for this exciting role in a clean room environment.
    Starting salary for this opportunity is $12.30 per hour with a shift differential of $2.00 per hour for 3rd shift.
    Pre-employment requirements are applicable, please apply today to learn more about this opportunity.

  • Location: McPherson
    Job Type : Contract
    Date: Wednesday, 01 March 2017
    Manpower has immediate openings in McPherson for production workers. These positions offer an opportunity to get your foot in the door with a dynamic employer.

    What we offer?
    *Entry level positions - no experience necessary
    *$10.75-$11.50 per hour
    *Steady Work Hours and Set Schedule
    *Multiple Shifts Available
    *Temporary to Hire Potential
    *Access to Manpower's online training and education programs

    What's the Job?
    *Perform light Inspection
    *Assist with manufacturing and packaging of sterile products.
    *Work with ink, solvents, heat, steam and liquids

    What you bring to the job?
    *Ability to stand for 12 hour shifts
    *Ability to lift 35-45 lbs. sporadically; 10-20 lbs. frequently
    *Pass a background check and drug screen

    Our client is looking for candidates who want to grow and be hired full time. They offer an excellent benefit package and extensive pay progression. Apply today for immediate consideration. If you know someone else who may be interested please share our job. We love referrals!
  • Location: Boulder
    Job Type : Contract
    Date: Tuesday, 28 February 2017
    Pharmaceutical Production Tech openings in Boulder, CO. These positions do require prior experience handling with organic solvents.

    $22-27/hour depending on prior related experience

    * Perform process manufacturing tasks including operation of small/large scale equipment, weighing, measuring, and monitoring raw and in-process materials to assure batches contain proper ingredients, quantities, and process output.
    * Prepare batches of solvents or other process ingredients as required
    * Identify and inform supervisor of equipment malfunctions or process outputs that do not meet expected outcomes. May perform troubleshooting of equipment to recommend solutions.
    * Fill out process documentation timely and accurately as required by SOPs.
    * Maintain cleanliness and neat work area

    * Knowledge and/or experience in Pharmaceutical process manufacturing
    * Proficiency with MS Office Suite for documentation purposes
    * Skills to perform basic math calculations (weigh materials, calculate percentages, convert units of measure etc.)
    * Stable work-history
    * Ability to use hand/power tool and overall mechanical aptitude
  • Location: Gurnee
    Job Type : Temporary
    Date: Tuesday, 28 February 2017
    Manpower is currently hiring a Quality Analyst for our client, one of world's leading Bioscience and Medical Products Company in Round Lake Illinois

    What's in it for you?
    Pay rate : $15.51 / hour
    Shift : 1st shift (Tuesday - Thursday) Part time
    Duration : 6 months


     Responsible for reviewing pertinent documents, records and reports such a Manufacturing Formulation Records (MFRs), Manufacturing batch Records (MBRs), etc. against Standard Operating Procedures (SOPs) for accuracy and compliance to procedures based on regulatory requirements and internal guidelines, etc.
     Identify areas of non-conformance and inform management via the drafting of Non-Conformance Reports (NCRs) as needed to be disposed (unilaterally accepted or rejected) by others. NCRs at this level are minor and involve no patient risk
     Administer and maintain relevant databases, preparing and issuing reports as defined by the area.
     Assist in external and internal audits by maintaining audit records, extracting data from databases and creating reports, collecting relevant data, etc.

    We find that candidates are most successful with the following:

     Strong interpersonal skills and great attention to detail are necessary.
     Must be a strong team player with good problem solving, and good verbal and written communication skills.
     Must be able to handle multiple projects concurrently, have computer experience and have knowledge of FDA Regulations,
     Application of Good Laboratory Practices and Application of Good Manufacturing Practices.
     Associate degree in business/scientific discipline and one to three years of relevant experience.
     Bachelor's degree in the life sciences and experience with a medical device/pharma or other similarly regulated industry preferred

    Stop your job search and apply today.

    We love referrals so please share our job with friends and family. Also, check out Manpower's career platform with tools and resources to prepare you for today and tomorrows' jobs at www.manpower.com/mypath
  • Location: Allentown
    Job Type : Temporary
    Date: Monday, 27 February 2017
    Currently looking for a Quality Assurance Technician to perform quality assurance responsibilities with our client, an Allentown-based pharmaceutical manufacturing site.

    Examples of Some Required Duties:
    * Performs inspection of manufacturing, packaging, and testing activities associated with the manufacturing of solid dose and liquid drug products
    * Sample raw materials and packaging components; Release controlled printed materials to packaging; Performs real-time batch record review; Performs clearance of processing rooms, equipment and materials; Swabs equipment and submits to laboratory; coordinates between laboratory, formulation, and production
    * Verifies and analyzes data entries on quality records using Analyze production data using of one or more of the seven basic Quality Tools (Cause-and-effect diagram, check sheet, control chart, histogram, Pareto chart, Scatter diagram, and Stratification)
    * Perform routine cGMP audits of warehouse and production areas; Monitors equipment/instrumentation; Review equipment/facility logbooks for competition and accuracy; Submit samples, as required, to Analytical Services for testing
    * Carefully oversee the details of their assigned tasks to ensure accurate and timely documentation of manufacturing and inspection activities ; Assists in the training of new/junior employees on GMP and Quality Assurance activities

    The ideal candidate will have:
    * High school diploma or equivalent plus 2-4 years QA experience (pharmaceutical industry preferred); or Bachelor of Science degree (science or engineering preferred) with no experience
    * American Society of Quality certification (CQT, CQI, CQA) preferred
    * Experience in pharmaceutical manufacturing floor environment is desirable
    * Experienced in writing reports and memos using standard business language, grammar, and punctuation
    * Working knowledge of business software packages, such as Word, Excel, and Access, and modern office equipment

    This position offers:
    - Located just minutes from center city Allentown with easy access from Rt. 22
    - Temp to permanent opportunity with 2nd shift schedule,
    - Hourly pay rate of $20-25 depending upon experience
    - Reputable employer with a 4.7 star rating (out of 5) on GlassDoor.com
    - Great benefits upon permanent hire, as well as advancement opportunities with a growing company
  • Location: Boulder
    Job Type : Contract
    Date: Sunday, 26 February 2017
    Pay: $35-40/hour

    Schedule: Monday to Friday from 7:30am to 4:30pm

    Preventative Maintenance: Assists in maintaining and continually improving a comprehensive calibration program. Utilizes scheduling software complete with historical files and specific reporting functions. Performs tasks and complex projects proficiently in the following types of calibration work (cGMP and non-cGMP): instrument, repair, instrument calibration, loop calibration, and instrument specification and selection. Works from verbal and written procedures and project scope packages to support production and development needs. Works independently in the numerous process areas, laboratories, and utility areas with minimal supervision.

    Troubleshoot, Corrective Maintenance & Modification: Assists in coordinating the repair, building, troubleshooting etc. on all instrumentation and electrical power issues. This includes ensuring that adequate procedures, manuals, training records, and other pertinent documentation exists and is available as needed. Assists management in assessing new instrument needs or modifications to existing systems. Provides feedback to all affected department when appropriate.

    Procurement & Spare Parts: Generates requisitions for materials, instruments, spare parts and tools required to perform assigned tasks. Contributes recommendations for improvements to parts, materials, and tools.

    Contractor Management: Oversees the work of independent contractors and ensures all projects specifications/requirements/codes are met while work is being performed on-site.

    Department Documentation: Assists in the continued updates and improvements to all metrology SOPs.

    Requirements: 5-7 years of prior experience in instrumentation maintenance, repair, and replacement, preferably in chemical/pharmaceutical manufacturing or related field. cGMP experience desired. Ability to use personal computer to organize and communicate needs and issues affecting department including experience with calibration scheduling software.

    Following Electrical support experience is required: maintenance on switchgear, panels, motors and motor drives, UPS units, troubleshooting wiring/control issues, Vessel Pressure transmitters, Temp transmitters, Flow transmitters, Weigh scales & cells