Home   Pharmaceuticals Jobs
  • Valid City, State or Zip Code: Malvern
    Job Type : Contract
    Date: Thursday, 27 February 2020
    The Packaging Technician is responsible for activities supporting the primary and secondary packaging, labelling and assembly, warehousing and shipping preparation of investigational drugs used in various clinical studies. Sign and date batch records for activities performed on all supplies prepared for clinical investigation and verify the work of other production staff members. Work is assigned and reviewed by the Packaging Supervisor, and/or Team Leaders. Instructions will be in the forms of written batch records as well as verbal instructions. Experience 1-3 years
  • Valid City, State or Zip Code: Malvern
    Job Type : Contract
    Date: Thursday, 27 February 2020
    Support all Warehousing/Distribution activities associated with shipping product

    domestically and worldwide, receiving of incoming goods, dispensing of materials to

    the Packaging Department, supporting the Annual Physical Inventory, supporting the

    Destruction Process and supporting all other Inventory Management activities

    (including but not limited to Forklift and other Power Equipment Operations, Offsite

    storage, General Maintenance of the Warehouse and all Inventory Management

    Systems, Document Management Systems and Training Systems requirements).

    · Shipping Order Entry - including but not limited to entering, verifying or

    troubleshooting all shipment information, maintaining site addresses, attaching

    required documents, maintaining appropriate shipping statuses and entering all

    Clinical Supplies Shipping information into the appropriate data bases.

    · Pre-shipping activities - including but not limited to managing all communication into

    the warehouse where a shipment is required, being the liaison between Distribution

    and Order Entry, managing the shipping schedule, printing all shipping orders and

    working directly with Distribution to assure all shipments are addressed in the time

    period required

    · Post-shipping activities - including but not limited to tracking each shipment,

    representing each stage of the shipment and its tracking information in the

    appropriate inventory management systems, from the time its leaves the facility

    through to delivery to the end-user, filing of all paperwork as well as maintaining the

    Controlled GMP Filing Area and pulling and reviewing shipping paperwork to assist in

    shipment related investigations

    · Continuous Improvement initiatives or project related activities needed for the

    Warehouse / Distribution department.
  • Valid City, State or Zip Code: Groton
    Job Type : Contract
    Date: Tuesday, 25 February 2020
    Seeking a motivated individual to support Groton IM's, GMP space, and associated activities on a daily basis. As a member of the IM team the candidate will be required to learn a wide variety of support activities and functions while supporting development, clinical, and commercial materials. This role will be required to follow GMP standards, and for assuring compliance with (Company) Standard Operating Procedures (SOPs), policies along with all applicable worldwide regulations and guidelines (e.g. FDA, DEA, TSA, MHRA).

    RESPONSIBILITIES
    In order of importance, list the primary responsibilities critical to the performance of the position. Please include actual tasks and/or essential responsibilities that highlight accountability and level of judgment required.
    General Responsibilities:
    * Complete GMP/quality inspections on incoming materials, to include but not limited to API's, Excipients, Raw Materials, Drug Substance, Controlled Substances, and Hazardous Materials.
    * Receive, sample, dispense, ship, manage and maintain all material types to support development, clinical, and commercial activities.
    * Manage, maintain, and support the disposal of retention samples.
    * Strict adherence to quality, GMP, safety and environmental standards is required.
    * Responsible for identifying, reporting and supporting the resolution of quality concerns, and at times contributing to the subsequent investigational reports.
    * Receipt of materials into multiple approved electronic inventory systems, becoming proficient working within these systems.
    * Performing electronic and physical inventory transactions for all materials.
    * Perform GMP warehouse infrastructure duties to include; warehouse management, cycle counts, stock rotation, transferring, picking, cleaning, destruction/waste management, segregation of materials, etc.
    * Subdividing and sampling of all material types, to include hazardous materials.
    * Responsible for the completion of all shipping functions.
    * Follow and understand applicable SOPs/procedures in relation to activities being complete.
    * Demonstrates sound understanding and advanced knowledge of practices/concepts of IM and a working knowledge of principles, practices, concepts and operations within other partner disciplines.
    * Must be adaptable and maintain flexibility in completing daily tasks in an ever changing work environment.
    * Proven ability to multitask, manage time and work load. Ability to escalate issues immediately.
    * Daily handling of controlled substances (CS) in accordance to state and federal regulations
    * Participating on teams as required (i.e. safety team, process improvement teams, procedure teams, project teams).

    Retention Sample Project - Related Duties:
    * Work fluently within Excel, GDMS, Peoplesoft M3, and other business related systems for the tracking and management of retain samples
    * Ability to work on a project team, and at times lead or drive work to completion, including delegating or working with other team members to ensure worked is completed on time.
    * Daily interaction with contract waste vendor to coordinate the inspection and disposal of retain samples
    * Experience working with and handling hazardous and dangerous compounds and understanding the safety risks associated with them.

    SKILLS
    * Experience with computers: databases, email, software, navigation of shared drives, search engines, word processing, spreadsheets
    * Ability to obtain the following certifications: Power Jack certification, Fork Lift, Raymond Lift, DOT/IATA regulations
    * Valid driver's license
  • Valid City, State or Zip Code: West Point
    Job Type : Contract
    Date: Monday, 24 February 2020
    What's in it for you?

    * Full time hours
    * Monday through Friday, 8:00am-5:00pm
    * Weekly Pay

    What is the job?

    * Assist 2 Associate Directors, 1 Sr. Admin. Associate and Quality and Tech Ops. Manager
    * Perform a variety of fundamental administrative/clerical tasks in a specific division/area
    * Compile records
    * Track and verify accuracy of data
    * Use computer to generate reports, tables, graphs and correspondence
    * Review resumes for clarity and detail and preparing them to send to hiring managers to review
    * Participate in project teams as dictated by business

    What you bring to the job?

    * Minimum of 4 years Administrative Assistant experience
    * At least 2 years of experience in a Human Resources role
    * Demonstrated capability in written and verbal communication
    * Proficiency in Microsoft Office products (Word, Excel, PowerPoint)
    * Must be able to pass a background check and drug test

    Stop your job search and apply today. Do you need more information? Contact our Recruiters at 610-313-1401. We love referrals, so please share our job with your family and friends. Start your path to a new career at Manpower!
  • Valid City, State or Zip Code: Allegan
    Job Type : Contract
    Date: Sunday, 23 February 2020
    JOB PURPOSE
    To ensure quality standards for packaging materials are met by inspecting, sampling, testing, reviewing and releasing incoming batches of packaging materials.

    Monday - Thursday 2nd Shift 2:00 pm - 12:00 am $16.00-$16.60/hour

    KNOWLEDGE, EXPERIENCE AND EDUCATION
    High school diploma or GED, with preference given to those with advanced education.
    Accuracy and attention to detail.
    Must possess an understanding of and ability to apply Current Good Manufacturing Practices (cGMPs).
    General computer knowledge in order to understand required programs used.
    General knowledge of testing and measuring equipment.
    Ability to work well with other departments.
    Ability to climb stepladder platforms for sampling purposes and the ability to lift up to 50 lbs.

    MAJOR DUTIES

    Major Duties / Responsibilities
    Pre-Print Inspection - Perform inspections on Cartons, Labels, inserts, etc., using computer software, approved Artwork, and industry standard color books to ensure samples meet the acceptable criteria
    Ensures documentation paperwork and case labels are accurate for incoming components. Contacts appropriate department for assistance when the needed information is either not present or is incorrect.
    Perform visual, dimensional, and functional-type testing on components per Package Engineering specification, Standard Operating Procedures, Standard Work Instructions, and Job Aids.
    Perform incoming inspection on Pre-print using Global Vision software, Pantone Formula Guide, and/or approved color chips.
    Reviews completed inspection forms and disposition components in SAP based on results.
    Ensures damaged or rejected cases are quarantined and Split Batch Request Form is filled out correctly.
    Ensures suspect components are held until authorization for release has been provided.
  • Valid City, State or Zip Code: Swiftwater
    Job Type : Contract
    Date: Tuesday, 18 February 2020
    Now Hiring! Quality Assurance Analyst in Swiftwater PA

    Do you want to do something meaningful? Do you want to help save lives? Manpower is currently seeking Quality Control Biochemists for a well known company that creates flu vaccines!

    What's in it for you:

    Full time hours
    Various Shifts (1st,2nd,3rd)
    $33-44 per hour based experience
    Fast paced - never boring

    What the job is:

    Conduct tests to determine quality of raw materials, bulk intermediate and finished products. May conduct stability sample tests. Calibrate, validate, or maintain laboratory equipment. Complete documentation needed to support testing procedures including data capture forms, equipment logbooks, or inventory forms. Monitor testing procedures to ensure that all tests are performed according to established item specifications, standard test methods, or protocols.

    Key Responsibilities:

    The individual must have expertise in chemistry testing. They should be able to follow testing instructions and schedule as assigned. The candidate should be able to understand the theory and technical components of the processes used within the test they are performing. The individual should have good oral and written skills with emphasis on Good Documentation Practices.

    What you bring to the job:

    BS or BA degree preferred.
    3+ years of relevant QA technical experience..
    Expertise in database testing in Microsoft SQL Server environments including designing and manipulating test data, validating stored procs, jobs, triggers and replication.
    Create clear, concise detail oriented test plans/cases.
    Ability to understand and create test plans from specifications or verbal communications.
    Liaison with development, project management, and customer support
    Industry experience in a cGMP/Quality environment preferred..
    Requires 20/20 vision- may be achieved with corrective lenses.

    Apply To Get In Touch or Learn More:
    Choose the option that is most convenient to you to get the conversation started.

    Step 1:
    · Register as a job seeker on www.manpower.com

    Step 2:
    · Click Apply to this advertisement
    · Email me at Austrilia.Portis@manpower.com
    · Call a Recruiter: 414-312-5203 ext. 1482
    · Text "Swiftwater QA" w/ Name & email to 414-982-1957
  • Valid City, State or Zip Code: Swiftwater
    Job Type : Contract
    Date: Monday, 10 February 2020
    Now Hiring! QC TECHNICIANS in Swiftwater PA

    Do you want to do something meaningful? Do you want to help save lives? Manpower is currently seeking Quality Control Biochemists for a well known company that creates flu vaccines!

    What's in it for you:

    Full time hours
    1st shift Tuesday to Saturday
    $18 to $20 per hour based experience
    Fast paced - never boring

    What the job is:

    This position will support the Quality Control Biochemistry team through wet chemistry testing. Requires general laboratory/testing and cGMP knowledge as well as analytical, organizational, interpersonal and computer skills.

    Key Responsibilities:

    The individual must have expertise in chemistry testing. They should be able to follow testing instructions and schedule as assigned. The candidate should be able to understand the theory and technical components of the processes used within the test they are performing. The individual should have good oral and written skills with emphasis on Good Documentation Practices.

    What you bring to the job:

    * Bachelor Degree in Chemistry/Biochemistry/Biological Science with 1-2 years of relevant work experience.
    * Industry experience in a cGMP/Quality environment preferred.
    * Previous Quality Control experience desired.
    * Exceptional attention to detail and strong writing skills are required.
    * Candidate should be familiar with cGMP guidelines.
    * Must be able to work off shift and in a team environment.
    * Requires 20/20 vision- may be achieved with corrective lenses.

    Apply To Get In Touch or Learn More:
    Choose the option that is most convenient to you to get the conversation started.

    Step 1:
    · Register as a job seeker on www.manpower.com

    Step 2:
    · Click Apply to this advertisement
    · Email me at Austrilia.Portis@manpower.com
    · Call a Recruiter: 414-312-5203 ext. 1482
    · Text "Swiftwater" to 414-982-1957 w/ Name & email
  • Valid City, State or Zip Code: Allegan
    Job Type : Contract
    Date: Thursday, 06 February 2020
    JOB PURPOSE
    To ensure quality standards for packaging materials are met by inspecting, sampling, testing, reviewing and releasing incoming batches of packaging materials.

    Monday - Thursday 2nd Shift 2:00 pm - 12:00 am $16.00-$16.60/hour

    KNOWLEDGE, EXPERIENCE AND EDUCATION
    High school diploma or GED, with preference given to those with advanced education.
    Accuracy and attention to detail.
    Must possess an understanding of and ability to apply Current Good Manufacturing Practices (cGMPs).
    General computer knowledge in order to understand required programs used.
    General knowledge of testing and measuring equipment.
    Ability to work well with other departments.
    Ability to climb stepladder platforms for sampling purposes and the ability to lift up to 50 lbs.

    MAJOR DUTIES

    Major Duties / Responsibilities
    Pre-Print Inspection - Perform inspections on Cartons, Labels, inserts, etc., using computer software, approved Artwork, and industry standard color books to ensure samples meet the acceptable criteria
    Ensures documentation paperwork and case labels are accurate for incoming components. Contacts appropriate department for assistance when the needed information is either not present or is incorrect.
    Perform visual, dimensional, and functional-type testing on components per Package Engineering specification, Standard Operating Procedures, Standard Work Instructions, and Job Aids.
    Perform incoming inspection on Pre-print using Global Vision software, Pantone Formula Guide, and/or approved color chips.
    Reviews completed inspection forms and disposition components in SAP based on results.
    Ensures damaged or rejected cases are quarantined and Split Batch Request Form is filled out correctly.
    Ensures suspect components are held until authorization for release has been provided.
  • Valid City, State or Zip Code: West Point
    Job Type : Contract
    Date: Wednesday, 05 February 2020
    What's in it for you?

    * Full Time Hours
    * 8:00am-5:00pm

    What is the job?

    * Support and manage Outlook calendars, reschedule calendar conflict and schedule meetings
    * Assist with onboarding new employees, contractors and summer interns
    * Prioritize workload
    * Schedule complex, multi-leg and international travel
    * Provide effective communication with all levels
    * Assisting 18 people to include making appointments, scheduling for 6 people, mainly travel and expenses

    What you bring to the job?

    * High School Diploma or equivalent required
    * Up to 3 years of experience as an Administrative Assistant
    * Advanced computer experience in MS Outlook, Word, Excel and PowerPoint)
    * Experience with COMET/SAP
    * Extraordinary attention to detail
    * High level of professionalism

    Stop your job search and apply today. Do you need more information? Contact our Recruiters at 610-313-1401. We love referrals, so please share our job with your family and friends. Start your path to a new career at Manpower!
  • Valid City, State or Zip Code: Westford
    Job Type : Contract
    Date: Wednesday, 05 February 2020
    Are you looking for a career? Manpower has immediate openings for Warehouse Associate Westford, MA

    What's in it for you?

    - Duration: Full time (1 year) Temp-to Hire
    - Pay rate:$15.13
    - Shift: 1st shift 5:00AM-3:30PM

    What is the job?
    This is a non-exempt position. This position is responsible for the production of high quality medical devices within a manufacturing cell. Working under close supervision, may perform a combination of assembly, repair, and test operations on pacemakers, implantable cardioverter defibrillators (ICDs), leads, and related medical device assemblies. Performs routine assignments according to specified and/or standardized procedures. Work is closely and continually reviewed. Ensure that relevant job documentation for cell operations and functions is accurate and up to date. Be able to clearly communicate ideas, problems and solutions to all levels of manufacturing management in both written and oral form. Maintain a positive attitude when interacting with internal customers and external customers such as tours. Follow safety guidelines and utilize appropriate safety devices when performing all operations. Participate in continuous improvement/quality initiatives in order to enhance production processes to achieve quality and profitability metrics. Maintain accurate records to ensure traveler and quality documents are accurate, all parts are traceable and quality issues can be addressed to assure the quality of all products. Demonstrates a basis understanding of Lean Manufacturing. Participate with the Manufacturing Supervisor/Manager in setting and monitoring individual goals and cell performance metrics that continuously seek to improve the quality of operations. Support all Divisional initiatives as identified by divisional management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements

    Must be possess:
    Ability to read, comprehend, and follow written procedures; understand and follow verbal instructions - Understanding of and ability to utilize electronic data collection systems and computer software packages. Ability to prioritize work by determining the sequencing and timing of different jobs based on precedence and importance. Ability to handle and maneuver small components and parts. Ability to make critical decisions and judgments with minimal supervision. High school degree or equivalent preferred.
    For more details you may also call 414-269-8731 ext 1837 and ask for Nate or send your resume at
    nathaniel.sevilla@manpower.com We love referrals so please share our job with family and friends.
  • Valid City, State or Zip Code: St. Paul
    Job Type : Contract
    Date: Wednesday, 05 February 2020
    Are you looking for a career? Manpower has immediate openings for Materials Coordinator in Saint Paul, MN

    What's in it for you?

    - Duration: Full time (1 year) Temp-to Hire
    - Pay rate:$14.63
    - Shift: 1st shift 5:00AM-1:30PM

    What is the job?
    Will be responsible for assembling heart valves in accordance with approved manufacturing procedures. Candidataes will Utilize small hand tools, calibrated
    instruments, measuring equipment, microscopes and test fixtures. Valve Specialists are responsible for ensuring the tissue, stent, and all compliant valve
    materials used in Tendyne's end product, successfully meet all planning based on design, testing, verification, validation for new and existing products,
    and support of team members.

    Must be possess:
    2-5 years experience in related field with sewing background
    Skills: Sewing skills; attention to detail and ability to do very detail work
    Education: HS diploma or GED

    For more details you may also call 414-269-8731 ext 1837 and ask for Nate or send your resume at
    nathaniel.sevilla@manpower.com We love referrals so please share our job with family and friends.
  • Valid City, State or Zip Code: Swiftwater
    Job Type : Contract
    Date: Tuesday, 04 February 2020
    Filling

    The Filling Department's role is to aseptically fill vaccines that are formulated through the Formulation Department. The Filling Department fills vials and syringes, which can include Flu, Adacel (diphtheria, tetanus acellular, and pertussis), and Menactra. The daily activities can include vial and syringe handling, loading, and movement. There is also extensive documentation, as well as following strict Standard Operating Procedures (SOP's), Standard Work Instructions (SWI) and FDA guidelines. Included in this department as well is extensive preparation, cleaning and sterilization. Filling requires extensive training in order to complete several tasks.


    Requirements:
    Must have a Life Science Degree
    · Must be able to write clear and concise documentation
    · Ability to follow Standard Operating Procedures and Standard Work Instructions
    · Each task requires within the Filling Department requires specific training. Each worker must be able to track their own training, and can only work on tasks they are qualified to perform
    · Able and willing to perform aseptic cleaning, which will require cleaning Standard Work Instructions for preparation of disinfection, lifting 2-4 gallons of water, stretching above height level to clean machines, and pulling/pushing small tanks filled with disinfection.
    · Must be able to transport pallets of syringes and vials using a pallet jack from staging area to filling area. The process involves lifting and bending of boxes weighing up to 25 pounds.
    .Basic computer skills
    Every employee must be able to work weekends, holidays and overtime if necessary. Everyone is scheduled two days off, but days off may not be consecutive and may vary from week to week (rotating schedule).
    Jewelry and makeup are not allowed on the floor. Perfume, hairspray, cologne, aftershave and/or any scents are not permitted. Long fingernails and nail polish are not allowed.
    The attire includes sterile scrubs and gowns, hairnets, beard covers, safety glasses and steel toe boots. There may be extended gowning for higher grade areas.

    Filling:
    Good documentation skills
    Some pharmaceutical experience
    Forklift experience
    Some manufacturing background.
  • Valid City, State or Zip Code: West Point
    Job Type : Contract
    Date: Monday, 03 February 2020
    What's in it for you?

    * Full Time Hours
    * Weekly Pay

    What is the job?

    * Performs all tasks related to clinical packaging while following appropriate health and safety guidelines
    * Ensures that each component or bulk material used in the packaging of a product is properly identified, not expired, weighed, verified throughout processing and corresponds to the written information on the work order before proceeding to the next step
    * Verifies before use that equipment calibration date has not been exceeded
    * Signs and dates utilization charts and all critical packaging steps in the work order documentation
    * Performs quality verifications and equipment challenge tests.

    What you bring to the job?

    * High School Diploma or equivalent required
    * Associate's or Bachelor's Degree in Science or Healthcare field preferred
    * 4-8 years of pharmaceutical packaging experience
    * Good written and verbal communication skills
    * Proficiency in Microsoft Office products (Word, Excel, PowerPoint)
    * High level of attention to detail
    * Must pass a background check and drug test

    Stop your job search and apply today. Do you need more information? Contact our Recruiters at 610-313-1401. We love referrals, so please share our job with your family and friends. Start your path to a new career at Manpower!
  • Valid City, State or Zip Code: Swiftwater
    Job Type : Contract
    Date: Monday, 03 February 2020
    Job Description
    Do you have a bachelors degree in life science or chemistry? Are you looking for a career opportunity in the Poconos? Manpower has immediate openings for High Level Pharmaceutical Production Associates on 1st Shift, 2nd Shift and 3rd Shift at Sanofi Pasteur in Swiftwater, PA. The position is a fast paced team environment with great career potential.
    What's in it for you?
    Full time hours
    1st Shift, 2nd Shift and 3rd Shift availability.
    Competitive Wages: $18/Hour starting.
    Option to take free college courses and skills training
    Paid training
    Performance bonus
    Overtime available
    What is the job?
    Actively working in positions relating to the production of vaccines.
    Maintaining a clean work environment.
    Able to work in a clean, sterile environment.
    Performing manual documentation and information retrieval.
    Ability to work on your feet for 8-12 hour shifts.
    What you bring to the job?
    Previous work experience (1-2 years)
    Great attitude and ability to work in a team
    Bachelors Degree in Life Science (Biology, biotechnology, chemical biotechnology, chemistry).
    Ability to pass a Background Check and Drug Screen
    Stop your job search and apply today. Create your profile at www.manpower.com. 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 tomorrow's jobs at www.manpower.com/mypath.
    Job Types: Full-time, Contract
    Salary: $18.50 to $20.00 /hour
    Application Questions