BioReagents Formulator (A Shift)

4 Weeks ago • All levels

Job Summary

Job Description

The BioReagents Formulator will perform duties in compliance with the company's Quality System and regulatory requirements, including Good Manufacturing Practices (GMP) and Standard Operating Procedures. Responsibilities include operating production equipment, formulating wet and freeze-dried reagents, sub-assemblies, and finished goods, and maintaining cleanliness in formulation labs. The role involves assisting with in-process testing to ensure batch specifications are met and performing additional tasks as assigned by management. The position works under the immediate supervision of the Formulation Team Lead and reports to the Reagent Production Supervisor. Key skills required include proficiency in math, especially unit conversions, good communication, precise pipetting, attention to detail, and the ability to execute repetitive tasks consistently. Knowledge of PCR, RT-PCR, and fluorescence-based nucleic acid detection techniques is also beneficial.
Must have:
  • Compliance with company policy and quality system
  • Maintain records per regulatory requirements and GMP
  • Operate production equipment
  • Formulate reagents and sub-assemblies
  • Maintain clean formulation labs
  • Proficient in math and unit conversions
  • Good oral and written communication
  • Attention to detail for extended periods
  • Execute repetitive tasks with consistency
Good to have:
  • Two years of college coursework or 2+ years of relevant industry experience
  • Bachelor's degree in a biological science
  • 1+ years of scientific/laboratory experience
  • 1+ years of cGMP experience
  • Experience with pipetting/liquid handling
  • Experience with technical writing/reviewing
  • Familiarity with commonly used concepts, practices, and procedures including PCR, RT-PCR, and fluorescence-based nucleic acid detection techniques

Job Details

Description

Primary Duties:

  1. Perform all work in compliance with company policy and within the guidelines of BioFire Diagnostics’ Quality System.
  2. Maintains records in compliance with regulatory requirements, current Good Manufacturing Practices, and Standard Operating Procedures.
  3. Relies on pre-established written guidelines to perform job functions.
  4. Operates Production Equipment
  5. Responsible for wet and freeze-dried reagent formulations, sub-assemblies, and finished goods.
  6. Responsible for maintaining a clean environment of formulation labs and associated spaces.
  7. May assist with in-process testing to assure batches or lots meet specifications.
  8. Performs additional tasks as assigned by management.
  9. Works under immediate supervision of the BFDX Formulation Team Lead and reports to the BFDX Reagent Production Supervisor.
  10. Performs other duties as assigned.

Training and Education:

Minimum -Completed two years, or equivalent, of college coursework or 2+ years of work experience in an FDA/ISO regulated industry in lieu of education.
 

Preferred- Bachelor’s degree/4 year program with an emphasis on a biological science. 1+ years scientific/laboratory experience. 1+ years cGMP.

In lieu of degree: two years, or equivalent, of college coursework or 2+ years of work experience in an FDA/ISO regulated industry in lieu of education

Experience:

Preferred - Experience pipetting/liquid handling, technical writing/reviewing, detail-oriented work. Software (Word, Excel, Web browser).
 
Knowledge, Skills, Abilities:
Proficient in math, specifically unit conversions. Good oral/written communication, pipetting/liquid handling of multiple volumes. Maintain attention to detail for extended periods of time. Execute repetitive tasks and maintain high level of consistency over time.  Has knowledge of commonly used concepts, practices, and procedures including PCR, RT-PCR real-time PCR, and use of fluorescence based nucleic acid detection techniques.
 
Work Conditions:
 Ability to remain in stationary position, often standing, for prolonged periods.
 Ability to wear PPE correctly most of the day.
 Ability to adjust or move objects up to 50 pounds in all directions.

Please be aware that recruitment related scams are on the rise. Fraudulent job postings are being placed on other websites, and individuals posing as bioMérieux Talent Acquisition team members are reaching out via email or text message in an attempt to collect your personal and confidential information. In some cases, these scammers are also conducting bogus interviews prior to extending fraudulent offers of employment. Beware of individuals reaching out using general phone numbers and non-bioMerieux email domains (i.e. Hotmail.com, Gmail.com, Yahoo.com, etc.). If you are concerned that an interview experience or offer of employment might be a scam, please make sure you are searching for the posting on our careers site https://careers.biomerieux.com/ or contact us at recruitment@biomerieux.com.

BioMérieux Inc. and its affiliates are Equal Opportunity/Affirmative Action Employers. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veteran or disabled status, or genetic information. Please be advised that the receipt of satisfactory responses to reference requests and the provision of satisfactory proof of an applicant’s identity and legal authorization to work in the United States are required of all new hires. Any misrepresentation, falsification, or material omission may result in the failure to receive an offer, the retraction of an offer, or if already hired, dismissal. If you are a qualified individual with a disability, you may request a reasonable accommodation in BioMérieux’s or its affiliates’ application process by contacting us via telephone at (385) 770-1132, by email at recruitment@biomerieux.com, or by dialing 711 for access to Telecommunications Relay Services (TRS).

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