Quality Control Microbiologist

Vitality Works Inc; Albuquerque (NM); On-site; USD 65,000 - 85,000; Full time

Job summary

Vitality Works Inc. in Albuquerque, NM, is seeking an experienced QC Microbiologist to conduct microbiological analyses of raw materials, intermediates, and finished products under GMP/GLP.

You will develop and validate methods, maintain instrumentation, write protocols, and support investigations into non-conforming products. The role requires 4+ years in chemistry or related field, a BS in Chemistry, and familiarity with HPLC, HPTLC, UV-Vis, ICP-MS, FT-IR.

Qualifications

• Requires 4+ years of relevant experience with BS in Chemistry or related field.
• Must follow GMP/GLP and pharmacopoeial requirements in testing and validation.
• Ability to write, review, and update SOPs and procedures.
• Proficient in data analysis, report writing, and documentation control.
• Experience with instrument qualification and method development.

Responsibilities

• Perform microbiological analyses on raw materials, intermediates, and finished products.
• Develop, validate, and write methods for analytical testing.
• Qualify and troubleshoot instrumentation and test methods.
• Review data for compliance with specifications and protocols.
• Assist investigations of non-conforming products and customer complaints.
• Maintain reference materials and update specifications and databases.
• Assist in regulatory changes awareness and department duties.

Skills

HPLC

HPTLC

UV-Vis

ICP-MS

FT-IR

GMPs

GLPs

USP/EP knowledge

Investigation skills

Report writing

MS Office

Data interpretation

Communication skills

Education

BS in Chemistry

MS in Chemistry or related

Tools

HPLC

HPTLC

UV-Vis

ICP-MS

FT-IR

Job description

This is a more experienced position requiring sound knowledge of quality control systems, methods, and procedures. The QC Microbiologist will be responsible for conducting microbiological analyses for raw materials, intermediates, and finished product samples according to written procedures.Duties and Responsibilities include but are not limited to:Developing and writing methods for analysis of all raw materials, intermediates, and finished product samples as requiredAccountable for analytical testing of raw materials, intermediates, and/or finished product samples as required by the procedureReviews data and results of testing to ensure compliance to appropriate specifications and protocols.Writes and executes protocols for the qualification and re-qualification of new and current instrumentationTroubleshoots instrumentation/test methods.Updating specifications and other appropriate databases.Establish and validate test methods via internal testing and/or 3rd party approved analytical labs.Maintain a library of pertinent published reference material including monographs, books, studies, and compendia.Ensuring analytical methods are updated and documentedFollows technology changes, recommends new technologies, purchase and implement if appropriateAssisting investigating non-conforming products and disposition.Assist with investigations and pertinent customer complaints and submit findings to QC/QA manager.Staying abreast of regulatory changes related to the industry.Assisting as needed in all other aspects of the QC department.Other duties as assigned by the QA/QC manager.Knowledge, Skills, and Abilities:Knowledge of systems such as HPLC, HPTLC, UV-Vis, ICP-MS, and FT-IR.Understanding of Pharmacopoeial requirements and must be able to follow changes, implement changes, qualify methods.Understanding of USP/EP/CMSP and other pharmacopoeias as well as the change process.Working knowledge of GMPs, GLPs, phamacopoeial, and regulatory requirements for testing and validation pertaining to the dietary/herbal supplement industry is required.Investigation skills, report writing skillsAbility to work quickly and accurately in a production environment.Good verbal, written, and interpersonal communication skills.Proficiency in Microsoft Office applicationsPerformance Measurements:Attendance and promptnessMeeting quotas and goalsFollowing appropriate SOP’s and department proceduresMaking recommendations and continuous improvementsDependability & AccountabilityEducation & Experience:4+ years of relevant experience and a BS degree in Chemistry or equivalent2+ years of relevant experience and a MSPrior experience in a manufacturing industry is preferredPhysicalAble to sit for long periods of timePosition will require some walking, standing and sittingSome lifting of at least 50 pounds on occasion may be required