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QA Technician/Auditor
Talencia LLC Decatur, IL
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$95k-117k (estimate)
Full Time 1 Day Ago
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Talencia LLC is Hiring a QA Technician/Auditor Near Decatur, IL

Job Description

Job Description

POSITION DESCRIPTION
Position Title : QA Technician - Grand Department: Quality Assurance
Reports To: Senior Manager Quality Assurance - Operations

Work Location : Decatur, Illinois
Position Summary:
The QA Technician performs quality assurance duties to prevent or eliminate defects in products for sterile filling operations or in final inspection and packaging operations.
This individual must work in a detail-oriented, compliant manner in a high-stress environment where adherence to deadlines is critical.
The individual must display an exemplary level of integrity at all times.
Manage a workload of varying priorities while adhering to strict deadlines.
Essential Duties & Responsibilities:

  • Monitor the production process and ensure consistency of procedures.
  • Perform visual inspection of finished product.
  • Perform AQL testing of finished product.
  • Review in process documentation.
  • Audit manufacturing rooms for adherence to cGMP and SOPs Audit the maintenance of a clean and sanitary environment.
  • Review daily/weekly/monthly and bi-monthly logbook entries for completeness.
  • Review, approve and issue verified -clean green release stickers to operations.
  • Check machine settings.
  • Observe/mentor personnel on aseptic performance.
  • Perform line clearances and review documentation (circular charts, autoclave tapes etc.) to allow operations to initiate production (release to fill).
  • Obtain and maintain gown certification for clean room entry.

Education and Experience:

  • Associate\'s Degree or equivalent from a two-year college or technical school;
  • One year related experience and/or training; or equivalent combination of education and experience.

Job Prerequisites:

  • All full-time employees are required to work a 40-hour week.
  • At times, additional hours during the weekdays, evenings, and/or weekends will be required to complete tasks and meet deadlines.
  • All applicants must be able to meet the attendance standards.
  • Must have a complete knowledge of current Good Manufacturing Practices, United States Pharmacopeia, current Code of Federal Regulations (21 CFR parts 11, 210, 211, 820), and other FDA regulations and guidances.
  • Have general math skills: adding, subtracting, multiplication, division, and percentage calculation.
  • Ability to calculate figures and amounts such as discounts, interest, commissions, and proportions.
  • Able to use personal computer and standard office equipment such as fax and copy machines, calculators, and printers.
  • Aptitude to learn computer programs as needed (i.e. Microsoft Office Word, Excel) in addition to other business applications.
  • Strong verbal and written communication skills.
  • Resourceful and well organized.
  • Ability to read and interpret standard documents such as: procedure manuals, employee handbook, and job related publications.
  • Ability to write routine reports and correspondence.
  • Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists.
  • Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form.

Physical Demands, Mental Requirements, and Work Environment:

  • While performing the duties of this job, the employee is regularly required to sit, stand, walk, talk, and hear.
  • The employee is required to use hands to finger, handle, or feel.
  • Specific vision abilities required by this job include close vision for written work and PC use.

Mental Requirements :

  • Ability to write, read, and apply technical scientific writing, procedures, and quality policies.
  • Ability to work independently in an efficient and detail-oriented manner.
  • Ability to work on multiple projects and priorities in a concurrent manner.
  • Ability to work in an independent manner, as well as a group environment.
  • Ability to apply deductive reasoning and analytical thought to understand complicated issues.
  • Ability to receive instructions and follow work rules and company policies.
  • Ability to follow safety and security practices.
  • Ability to meet deadlines and effectively deal with a high level of office stress.
  • Ability to maintain confidentiality of work assignments and personnel issues.

Safety Requirements:

  • Safety glasses, close-toed shoes, and latex gloves are required in many areas within the facility
Client Description
Rising Pharma Holdings, INC is an industry leader in marketing and distributing innovative branded and multi-source prescription and over-the-counter pharmaceutical products. Our many commercial products cross a variety of therapeutic areas and multiple dosage forms. We have a robust emerging pipeline of pharmaceutical products through the development of Abbreviated New Drug Applications (ANDA) filed,or in the process of being filed,with the FDA. Rising is committed to providing our customers with high quality pharmaceuticals. Our products are manufactured in state-of-the-art, FDA approved facilities using quality assurance techniques that meet regulatory standards. Through our close partnerships with our customers throughout the United States, we ensure the safe and effective delivery of our products to the public. Our leading management team of industry experts is dedicated towards continued innovation in drug development, marketing and distribution.
Must Have
  • Minimum of 5-6yrs of Quality experience.
  • Minimum HS/GED required.
  • Associate degree preferred.
  • Specific vision abilities required by this job include close vision for written work and PC use.
  • Must be able to obtain and maintain gown certification for clean room entry.

Interview Process:

  • *Initial phone screening with HR to confirm relocation to the area, salary requirements, etc.
  • *Next, phone screening with Quality Control Leadership if the candidate is not in the area.
  • *Then on-site interview. Offer to be made.
  • *If a candidate is within driving distance, we can proceed to the on-site interview after the initial screening.

Benefits: Full benefit package offered; medical, dental, vision insurance, STD/LTD, 100% match to 401K up to 4%, PTO, 8 paid holidays, health savings plans, life insurance, and more.
Relocation Expenses: Would be on a case-by-case basis at this time.

Would need to review details/requests before making commitments.

Job Summary

JOB TYPE

Full Time

SALARY

$95k-117k (estimate)

POST DATE

06/30/2024

EXPIRATION DATE

07/15/2024

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