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Careers|CURIA
Grafton, WI | Full Time
$65k-84k (estimate)
2 Months Ago
Quality Control Specialist
Careers|CURIA Grafton, WI
$65k-84k (estimate)
Full Time 2 Months Ago
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Careers|CURIA is Hiring a Quality Control Specialist Near Grafton, WI

JOB SUMMARY:

The Quality Control Specialist is responsible for supporting the manufacturing department and external customers. Routine functions include, but are not limited to instrument calibrations, environmental monitoring, water sampling and testing, environmental microbial sampling, sample preparation, cleaning glassware, waste disposal, shipping and handling of materials, and sampling of materials. 

WE PROUDLY OFFER:

• Generous benefit options (eligible first day of employment) 
• Paid training, vacation and holidays (vacation accrual begins on first day of employment)
• Career advancement opportunities 
• Education reimbursement
• 401k program
• Learning platform
• And more! 

EDUCATION/EXPERIENCE:

  1. Demonstrated ability to learn.
  2. Demonstrated organizational skills.
  3. Ability to maintain effective time management skills when making decisions.
  4. Ability to work independently while meeting all deadlines.
  5. This position requires a high school degree and a minimum of 1-2 years of pharmaceutical experience or an equivalent combination of education and experience.
  6. Preferred: Experience working in cGMP or GLP pharmaceutical industry environment.

ESSENTIAL JOB DUTIES:

  1. Conducts daily instrument checks.
  2. Performs and maintains micro sampling, environmental monitoring, and water sampling and testing per Curia’s standard operating procedures.
  3. Performs and maintains particle count testing per Curia standard operating procedures.
  4. Prepare samples for outside testing when needed.
  5. Clean and store glassware
  6. Conduct raw material sampling and receipt.
  7. Responsible for waste disposal per Curia standard operating procedures.
  8. Assists with coordination of testing performed at outside testing labs, raw materials, etc.
  9. Receive and document receipt of reference standards, reagents and supplies.
  10. Maintains a detailed and accurate recording of all activities and results on paperwork following standard operating procedures.
  11. Support equipment upkeep.
  12. Prepare and order supplies, as necessary.
  13. Enter data into relevant data management systems.
  14. Perform tracking and trending of data as requested.
  15. Compile data and provide data summaries to management.
  16. Interact with other departments, sites, and contract labs.

KNOWLEDGE, SKILLS, AND ABILITIES

  1. Excellent verbal and written communication skills, including the ability to effectively present information and respond to questions from groups of managers and auditors.
  2. Ability to meet deadlines and work under pressure with limited supervision.
  3. Strong time management and organizational skills with the ability to multi-task and manage multiple projects independently.
  4. Ability to read and understand standard operating procedures, SDSs, procedure manuals, technical procedures, government regulations.
  5. Proficient use of computer software including Microsoft Office Suite
  6. Knowledgeable in FDA GMPs (21 CFR, 211, 820, and/or 600)

PHYSICAL REQUIREMENTS

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

While performing duties of this job, the employee is regularly required to talk and hear. The employee is frequently required to stand, walk, or sit, and use hands to handle or feel and reach with hands and arms. The employee must frequently lift, carry, or move medium weights up to 50 pounds. The employee must frequently move full drums and pallets using a drum cart and/or pallet jack. Ability to work wearing HazMat PPE and a respirator.

WORK ENVIRONMENT

The work environment characteristic described here are representative of those an employee encounters while performing essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

While performing the duties of this job, the employee is frequently exposed to fumes or airborne particles and toxic or caustic chemicals. The employee is occasionally exposed to wet and/or humid conditions, moving mechanical parts, moving mechanical parts, high, precarious places, risk of electrical shock, explosives, risk of radiation and vibration. The noise level in the work environment is usually moderate.

PAY RANGE:

Education, experience, location and tenure may be considered along with internal equity when job offers are extended.

All interested applicants must apply online. Please be aware of scammers. Curia will only send offer letters and requests for sensitive personal information from a curiaglobal.com email address. Curia is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Curia is an E-Verify employer.

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Job Summary

JOB TYPE

Full Time

SALARY

$65k-84k (estimate)

POST DATE

03/21/2024

EXPIRATION DATE

05/19/2024

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The job skills required for Quality Control Specialist include Quality Control, Microsoft Office, Written Communication, Time Management, Standard Operating Procedures, Organizational Skills, etc. Having related job skills and expertise will give you an advantage when applying to be a Quality Control Specialist. That makes you unique and can impact how much salary you can get paid. Below are job openings related to skills required by Quality Control Specialist. Select any job title you are interested in and start to search job requirements.

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If you are interested in becoming a Quality Control Specialist, you need to understand the job requirements and the detailed related responsibilities. Of course, a good educational background and an applicable major will also help in job hunting. Below are some tips on how to become a Quality Control Specialist for your reference.

Step 1: Understand the job description and responsibilities of an Accountant.

Quotes from people on Quality Control Specialist job description and responsibilities

Quality Assurance (QA) Specialist duties and responsibilities Providing management and control of the quality assurance processes Maintaining the quality of products.

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Quality control specialists work as part of a manufacturing team, maintaining records of defective materials and ensuring that defective parts are repaired, re-tested, or pulled from production.

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The quality control specialist may provide these reports to supervisors or plant managers to help them make decisions about manufacturing processes and practices.

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Quality control specialists need to possess a high level of attention to detail and familiarity with product specifications and expectations.

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Measure the quality of products using a pre-defined set of criteria.

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Step 2: Knowing the best tips for becoming an Accountant can help you explore the needs of the position and prepare for the job-related knowledge well ahead of time.

Career tips from people on Quality Control Specialist jobs

These roles require highly organized specialists with meticulous attention to detail.

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Knowledge of Quality Assurance and training principles.

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There are certain skills needed to become an effective quality control specialist.

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Monitor Critical Control Points.

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