Quality Control Microbiologist

Posted 2 Days Ago
Be an Early Applicant
87121, Albuquerque, NM, USA
In-Office
55K-65K Annually
Mid level
Food • Healthtech • Pharmaceutical • Manufacturing
The Role
Perform microbiological analyses and method development/validation for raw materials, intermediates, and finished products; operate and qualify lab instrumentation, review data, investigate non-conformances, update specifications, and support QA/QC processes within GMP/ pharmacopoeial requirements.
Summary Generated by Built In

Position Summary:

As a QC Microbiologist, you will be mainly responsible for conducting microbiological analyses for raw materials, intermediates, and finished product samples according to written procedures. This is a more experienced position requiring sound knowledge of quality control systems, methods, and procedures.

Position Responsibilities:
• Accountable for microbiological testing of raw materials, intermediates, and/or finished product samples as required by the procedure so that manufacturing activities are not impacted.
• Support routine Environmental Monitoring activities including room monitoring, utility monitoring, and allergen/protein testing.
• Owns the OOS process that pertains to microbiological testing and analysis.
• Reviews data and results of testing to ensure compliance to appropriate specifications.
• Assisting investigating non-conforming products and disposition.
• Assist with investigations and pertinent customer complaints and submit findings to QC/QA manager.
• Orders supplies and assigns expiry to incoming materials, tracks requisitions and reconciles against incoming materials.
• Writes and executes protocols for the qualification and re-qualification of new and current instrumentation as applicable.
• Troubleshoots instrumentation/test methods.
• Follows technology changes, recommends new technologies, purchase and implement if appropriate.
• Staying abreast of regulatory changes related to the industry.
• May serve as a technical resource relating to Microbiology within the department as well as cross functionally.
• Assisting as needed in all other aspects of the QC department.
• Other duties as assigned by the QC manager.

Qualifications

Skills & Requirements:
• 4+ years of relevant experience and a BS degree in Microbiology or equivalent.
• 2+ years of relevant experience and a MS.
• Prior experience in a manufacturing industry is preferred.
• Working knowledge of Good Manufacturing Practices (GMPs) and Good Laboratory Practices (GLPs) for testing pertaining to the Dietary Supplement environment is required.Proficiency in general Microbiology techniques such as plate streaking, aseptic technique, and interpretation of microbiological results.
• Working knowledge of pharmacopoeia and regulatory requirements for testing and validation pertaining to the dietary/herbal supplement industry is required.
• Investigation skills, report writing skills.
• Ability to work quickly and accurately in a production environment.
• Good verbal, written, and interpersonal communication skills.
• Proficiency in Microsoft Office applications.

Physical Demands & Working Conditions:
• Able to sit for long periods of time.
• Position will require some walking, standing and sitting.
• Some lifting of at least 50 pounds on occasion may be required.
 Vitality Works is committed to providing access, equal opportunity and reasonable accommodation for individuals with disabilities in employment, its services, programs, and activities. To request reasonable accommodation, please contact Human Resources.

Skills Required

  • BS degree in Chemistry (or equivalent) with 4+ years relevant experience
  • MS degree with 2+ years relevant experience (alternate qualification)
  • Experience with HPLC, HPTLC, UV-Vis, ICP-MS, and FT-IR instrumentation
  • Working knowledge of GMPs, GLPs, and pharmacopoeial/regulatory requirements (USP/EP/CMSP)
  • Method development, validation, and troubleshooting skills for analytical methods
  • Investigation and report writing skills for non-conformances and customer complaints
  • Proficiency in Microsoft Office applications
  • Ability to work accurately and meet quotas in a production laboratory environment
  • Prior manufacturing industry experience
  • Ability to lift at least 50 pounds occasionally
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The Company
HQ: Albuquerque, NM
350 Employees
Year Founded: 1982

What We Do

Vitality Works, Inc. is a contract manufacturer specializing in private label and custom manufacturing of high-quality herbal, vitamin, nutraceutical supplements, and essential oils, operating as an FDA-registered facility.

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