Quality Control Chemist - cGMP

Full Time
Solon, OH 44139
Posted
Job description

MP Biomedicals is dedicated to giving scientists and researchers quality tools and superior service to aid them in their quest for ground-breaking discovery. We manufacture and sell more than 10,000 products and are one of the only companies in the industry to offer a comprehensive line of life science, fine chemical, and diagnostics products.

Working at MP Biomedicals

At MP Biomedicals, we are striving to make the world a better place. Whether our work has us developing innovative new products or supporting customers to keep their projects on track, our teams come together to help advance scientific discovery.

We foster an environment of collaboration and creativity, and value the importance of our team members' unique talents and contributions. Join MP Biomedicals today to advance your career and help make the world a better place.

Job Summary

The cGMP QC Chemist performs sampling and analytical testing on incoming materials from suppliers, and production samples for in-house manufactured products. This role ensures the identity, quality, and integrity of products manufactured and distributed by MP Biomedicals LLC, cGMP Division.

Responsibilities

  • Perform analytical testing that may include HPLC, GC, TGA, AA, Karl Fischer, FTIR, UV/VIS, optical rotation, TLC, melting point, loss on drying, pH, conductivity, density, and osmolality/osmolarity
  • Additional testing may include cell culture, DNA / RNA isolation, gel electrophoresis, Q-PCR, endotoxins, bioburden, and sterility
  • Perform and record all activities and results per cGMP
  • Perform analysis of data, including interpretation of spectra and test results
  • Support QA product investigations through additional testing or experiments
  • Participate in OOS investigations and retesting as needed
  • Troubleshoot instrument, test method, or product issues
  • Perform basic instrument maintenance and calibration
  • Assist in minor chemical spill response and cleanup activity
  • May participate in internal auditing
  • Other duties as assigned

Qualifications

  • BS/BA in Biology, Chemistry, or related field
  • 2 years of experience in cGMP analytical laboratory (pharmaceutical industry preferred)
  • Highly proficient with Microsoft Office products
  • Familiar with 21 CFR 210/211, 820, and/or ISO13485:2016
  • Familiar with USP/NF testing

In Addition to Very Competitive Wages, MP Biomedicals offers a comprehensive list of benefits including:

  • Childcare Credit
  • Employee Referral Program
  • Paid Vacation and Paid Time Off
  • 10 Paid Holidays Per Year
  • 401k with company matching contributions
  • Very competitive Healthcare Benefits
  • Life Insurance
  • Health Savings Account
  • Employee Assistance Program
  • Employee Discounts
  • Life Insurance
  • Opportunities develop personally and professionally
  • And so much moreā€¦.

Recruiters: Please note that MP Biomedicals does not seek or accept unsolicited resumes or offers of recruiting service associated with any published or unpublished employment opportunities. Any unsolicited information sent to MP Biomedicals will be considered as unencumbered and free from any fee or charge whatsoever. Only members of our Human Resources Team have the authority to engage or authorize recruiting services. At the present time, we are not looking to add to our approved partners list. Thank you for your cooperation.

Job Type: Full-time

Benefits:

  • 401(k)
  • 401(k) matching
  • Dental insurance
  • Employee assistance program
  • Employee discount
  • Health insurance
  • Health savings account
  • Life insurance
  • Paid time off
  • Professional development assistance
  • Referral program
  • Vision insurance

Schedule:

  • 8 hour shift

Ability to commute/relocate:

  • Solon, OH 44139: Reliably commute or planning to relocate before starting work (Required)

Experience:

  • quality control in cGMP facility: 1 year (Required)

Work Location: One location

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