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Quality Specialist I - QOTF

Location Cincinnati, Ohio, United States of America Job Id R-01310725 Job Type Full time Category Quality & Regulatory Remote Fully Onsite
The Quality Difference at Thermo Fisher Scientific: What makes our quality teams unique is a shared passion for getting it done right the first time and working for the right reasons with our customers always in mind. Our team of Quality professionals understand our customers rely on the accuracy, safety, and effectiveness of our products and services that are improving lives around the world. When you join our team of quality professionals, you’ll collaborate on projects on a global scale while being encouraged to grow your skills and discover new career paths with us.
JOB DESCRIPTION

Work Schedule

12 hr shift/days

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Standing for full shift

Job Description

Summary:

Assists in the investigation and monitors Operations and Quality Operations departments to assure that FDA current Good Manufacturing Practices, company SOPs and product registrations are followed and maintained. Assists in the investigations of batches, preps, lots, equipment, and facilities as required per the Code of Federal Regulations. Assists the Operations and Quality Operations departments in satisfying all FDA requirements. This role will support CPI, Granulation, and Dispensing.

Shift:

Monday - Wednesday 6:00am - 6:30pm

Essential Functions:

  • Acts as a resource to operations teams and problem-solving groups and aids in resolution of problems.
  • Assists Operations and Quality Operations in implementing corrective action for process deviations, assisting with CAPA initiatives.
  • Conducts GMP inspections of facilities to assure compliance with the current GMP regulations.
  • Performs housekeeping inspections to assure Operations is maintaining work areas in an orderly and clean manner.
  • Assures that operators are following written instructions and methods and procedures via real-time record review.

Education:

  • High School Diploma/GED Required
  • Bachelors Degree in, Science or applicable field, preferred

Experience:

  • 3+ years of QA  experience required
  • 2+ year experience Manufacturing. Process Engineering, Engineering services and/or GMP environment preferred

Competencies:

  • Through knowledge of OSD manufacturing, including equipment and process understanding.
  • Excellent problem solving and writing skills.
  • Ability to work on multiple projects simultaneously, adaptable for a fast-paced fluid environment.
  • Strong attention to detail
  • Works well independently and leads collaboratively within team and cross-functionally.

Required:

Requires a basic understanding of the practices, principles, and theory of GMP Services

Physical Requirements:

Position requires ordinary ambulatory skills and physical coordination sufficient to move about office locations; ability to stand, walk, stoop, kneel, crouch periodically for prolonged periods of time; manipulation (lift, carry, move) of light to medium weights of 10-35 pound pounds; arm, hand and finger dexterity, including ability to grasp and type for prolonged periods of time; visual acuity to use a keyboard, computer monitor, operate equipment, and read materials for prolonged periods of time; ability to sit, reach with hands and arms, talk, and hear for prolonged periods of time.

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"Quality is everyone's responsibility. Right the first time should not be only a metric, but a lifestyle."


Elaine
Director, Regulatory Affairs,
Latin America, Specialty Diagnostics

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