Metrologist, Quality Control
Akorn 2

Decatur, Illinois

Posted in Science and Research


This job has expired.

Job Info


The Quality Control Metrologist performs instrument qualifications and assists in instrument installation.

  • Responsible for the laboratory instrument qualifications, installation and decommission.
  • Create CCRs, Work Orders, Protocols, SOPs, related forms in support of instrument qualification, installations and decommissions.
  • Coordinate external vendor visits and support on-site visits in support of instrument qualification, installations and decommissions.
  • Coordinate with other departments in support of completing instrument qualification, installations and decommissions.
  • Perform instrument preventative maintenance (exchange consumables, flush out instruments, change out wash solutions). ICP periodic maintenance (cleaning out spray chamber, nembulizer, torch, cones, etc.)
  • Responsible for equipment/instrument shipping for external vendor qualification (pipettes, instrument standards and equipment).
  • Support document review for other department activities such as validation master plan.
  • Coordinate balance weight verification.
  • Draft memo’s in support instrument qualification, installation or decommission.
  • General laboratory maintenance via work order request.
  • Review laboratory contracts and negotiation of price.
  • Responsible for additional assigned laboratory duties such as maintaining an inventory of consumable supplies.
  • Responsible for instrument troubleshooting and corresponding with the vendor’s customer support.
  • Keep track of instrument gas levels and order as necessary.
  • Records entries in laboratory logbooks as necessary.
  • Generally works in agreeable conditions. May require extended periods of standing or sitting. Requires the ability to wear a respirator or breathing apparatus.
  • Performs work in accordance with general and specific safety precautions
  • Responsible for the peer review all instrument documentation to ensure compliance to SOP’s and cGMP’s.
  • Works in a fast paced, moderately stressful environment. Adherence to project deadlines is critical.
  • Initiates DCR’s to correct or clarify SOP’s .
  • Requires the ability to work with computers as well as proprietary software.
  • Responsible for maintaining confidentiality of work assignments.
  • Works on multiple projects in a concurrent manner on a routine basis.
  • Experienced with the operation and theory of the majority of instrumentation within Quality Control. Including the HPLC, GC, UV, AA, ICP, etc.
  • Able to perform maintenance on instrumentation such as replacement of consumable items such as
  • HPLC Replacement lamps, seals, etc.
  • AA Replacement and alignment of lamps and general system cleaning
  • GC replacement of syringe, Septa, Jets, Liners
    • Advanced trouble-shooting skills with the ability to recognize methodology deficiencies.
    • May perform additional audits on notebook write-ups and laboratory areas to ensure cGMP compliance/SOP.
    • Provides support for new employees for training and orientation.
    • Assists with investigation reports by testing or writing on an occasional basis.
    • Assists or creates deviation reports on an occasional basis.
    • Creates and revises QC laboratory SOP’s on a regular basis.
    • Has routine customer interaction.
    • Recommends activity which will promote laboratory efficiency within QC.
    • Assist with the implementation and training of new and revised SOP’s.


    Qualifications
    • BS degree in Chemistry required.
    • Minimum 2-5 years of industry experience involving analytical or wet chemistry test procedures in a Quality Control environment is preferred.
    • Requires superior writing skills.
    • Requires exceptional attention to detail with the ability to focus on current assignments. While Laboratory mistakes are unavoidable they must be kept to a minimum due to their ramifications.
    • Requires initiative and self-motivation works with moderate supervision in a detail-oriented manner.
    • Requires the ability to work on multiple projects in a concurrent manner.
    • Must possess the ability to work in an independent manner, as well as a group environment.
    • Satisfactory completes initial and annual training for cGMP and corporate operating procedures.


    Company Overview
    Who we are?

    Aside from being a pharmaceutical industry leader with deep roots in the eye care community, Akorn has proven through the years, to be a company of clear vision. A vision of what it takes to continually develop and evolve in order sustain our mission, which is to improve patients' lives through the quality, availability and affordability of our products. Along with developing and manufacturing branded and generic ophthalmics, Akorn manufactures injectable, oral liquid, optic, topical, inhalant, and animal health products. To learn more please visit our website at www.Akorn.com .

    Why choose us?

    Akorn employees are modern day superheroes! That might sound like an exaggeration; however, when you think of it, superheroes help those in need. That is exactly what we do here at Akorn. If you choose to work with us, you are not choosing to work an ordinary job. You are choosing to make an impact in this world. You are choosing to have a career with purpose. If you are seeking a rewarding opportunity where you can make a difference for others, then put on your cape and join the team!!

    What do we offer?
    • Competitive pay
    • Growth and development opportunities
    • Tuition Reimbursement
    • 3 weeks PTO + Personal Days
    • 9 company holidays
    • 401K match
    • Medical, Dental and Vision Benefit Options
    • 100% Paid Maternity Leave
    • Fast paced, family-oriented work environment
    • Wellness Program
    • Inclusive and diverse culture
    • Adoption Assistance
    • Flexible Spending Accounts


    EEO Statement
    Akorn, Inc. is an Equal Opportunity Employer and takes pride in maintaining a diverse environment. We do not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status.


    This job has expired.

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