Quality Analyst II 1
MilliporeSigma

Carlsbad, California

Posted in Science and Research


This job has expired.

Job Info


A career with MilliporeSigma is an ongoing journey of discovery: our 58,000 people are shaping how the world lives, works and plays through next generation advancements in Healthcare, Life Science and Electronics. For more than 350 years and across the world we have passionately pursued our curiosity to find novel and vibrant ways of enhancing the lives of others. MilliporeSigma is a business of Merck KGaA, Darmstadt, Germany.

Your role

As a Quality Analyst II, you will support the daily operations of the Quality Control Group activities which include performing a wide variety of analytical testing methods including raw material testing for raw materials and consumables performing analytical testing for in-process testing. The role will entail operating in a fast-paced, highly dynamic environment with multifunctional groups/departments, including both internal and external stakeholders as needed.

  • Support the daily operations of the Quality Control group to ensure raw materials, consumables, in-process testing is completed by the assigned deadline (i.e. pH, Osmolality, Chemical ID, HPLC, FTIR, Biochemical analysis, TOC, ELISAs, etc.)
  • Supports the daily operations of the Quality Control group to ensure lab is in a state of readiness for both testing and client audits.
  • Support SOP generation and revisions, item specification revisions, protocol generation, final report preparation, data summary, testing data trending, and other related documentation as needed
  • Promote a safety-first culture
  • Act as a potential resource of information for the junior analysts

Who You Are:

Basic Qualifications:
  • Bachelor's degree in Chemistry, Biology, or other Life Science discipline
  • 2+ years of analytical lab experience
  • 2+ years of experience in Quality Control
  • 2+ years of experience and knowledge in molecular, cell biology, and chemical assays (i.e., Virus titer assay, Immunoassay, HPLC, FTIR)

OR

  • Master's degree in Chemistry, Biology, or other Life Science discipline
  • 1+ years of experience in analytical lab
  • 2+ years of experience in Quality Control
  • 2+ years of experience and knowledge in molecular, cell biology and chemical assays (i.e., Virus titer assay, Immunoassay, HPLC, FTIR)

Preferred Qualifications:
  • 2+ years experience with cGMP, aseptic techniques
  • Experience with molecular and cell biology analytical test methods (i.e. qPCR, Potency assays, etc.)
  • CMO experience
  • Experience with project management, time management, and task prioritization
  • Understanding and knowledge of governmental regulatory guidelines relating to the manufacturing of biologics and pharmaceuticals
  • Experience in initiating, investigating, resolving, and completing event records within our controlled quality system TRACKWISE
  • Experience ensuring testing compliance with ISO, FDA, cGMP, EMA
  • Knowledge of Aseptic Technique and Gowning
RSRMS

What we offer: With us, there are always opportunities to break new ground. We empower you to fulfil your ambitions, and our diverse businesses offer various career moves to seek new horizons. We trust you with responsibility early on and support you to draw your own career map that is responsive to your aspirations and priorities in life. Join us and bring your curiosity to life!

Curious? Apply and find more information at https://jobs.vibrantm.com

The Company is an Equal Employment Opportunity employer. No employee or applicant for employment will be discriminated against on the basis of race, color, religion, age, sex, sexual orientation, national origin, ancestry, disability, military or veteran status, genetic information, gender identity, transgender status, marital status, or any other classification protected by applicable federal, state, or local law. This policy of Equal Employment Opportunity applies to all policies and programs relating to recruitment and hiring, promotion, compensation, benefits, discipline, termination, and all other terms and conditions of employment. Any applicant or employee who believes they have been discriminated against by the Company or anyone acting on behalf of the Company must report any concerns to their Human Resources Business Partner, Legal, or Compliance immediately. The Company will not retaliate against any individual because they made a good faith report of discrimination.

Job Requisition ID: 230460

Location: Carlsbad

Career Level: C - Professional (1-3 years)

Working time model: full-time


This job has expired.

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