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Quality Specialist I
The Position
Welcome to Greendale, Indiana! Greendale is one of two gummy technology development and manufacturing facilities in North America.
The site has the capability to manufacture traditional gelatin gummies as well as 100% plant-based pectin gummies for nutritional supplements and nutraceuticals.
With extensive development and manufacturing expertise and a wide range of flavors, shapes, sizes, and colors available, we can work with complex ingredients to help create engaging new products consumers will love.
The Quality Assurance Specialist I is responsible for auditing the products and processes at various points in the areas of production and packaging to ensure adherence to company quality standards.
The Quality Assurance Specialist I will communicate any deviations to management & assist the Quality Assurance team with special projects as required.
The regular working hours for this position are Monday - Thursday from 6 pm - 6 am. New Hires will be eligible for a Sign on Bonus of up to $1,000.
The Role
Conduct thorough and detailed quality audits of lines to ensure products meet established quality standards. Equipment verification including metal detector, x-ray, scales, etc.
Audit paperwork of operators to ensure they are meeting quality standards.
Report any deviations to QA Supervisor in complete appropriate details. Report any housekeeping issues that need attention.
Document all areas of non-compliance and ensure corrective action to eliminate them.
Work with Production and Packaging Managers, Supervisors, and hourly associates on daily issues and problems.
Utilize computer to enter and track result data.
Comply with SQF, Food Safety Plan (HACCP), Food Quality Plan (FQP) standards. Responsible for ensuring compliance to FDA and cGMP standards for Quality Control, including continuous training.
Responsible for ensuring Dietary Supplement’s Identity, Purity, Strength and Quality.
Participate in all necessary training is required to successfully perform job responsibilities.
Other duties as assigned.
The Candidate
High School Diploma. BS in Food Science or related major is preferred.
For business and safety reasons, must be able to communicate effectively verbally and in written English. Ability to communicate with all line level positions and management.
Knowledge of GMP and Quality systems.
The employee must be able to lift and / or move up to 50 pounds. While performing the duties of this job, the employee is required to use hands to finger, handle, or feel and is frequently required to stand, walk, reach with hands and arms, stoop, kneel, crouch, or crawl, and talk or hear.
The employee is required to sit, climb, or balance and taste or smell. The position requires a great deal of walking and standing, approximately 85%.
Why You Should Work At Catalent
Spearhead exciting and innovative projects
Fast-paced, dynamic environment
High visibility to members at all levels of the organization
152 hours of PTO 8 paid holidays
Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market.
Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.
Catalent is committed to the health and safety of its employees, visitors and the customers and patients we serve. As a result of the global pandemic, we have modified many of our recruitment and on-boarding processes to maintain everyone’s safety.
The Human Resources teams will communicate all necessary safety processes and procedures throughout each stage.
personal initiative. dynamic pace. meaningful work.
Visit to explore career opportunities.
Catalent is an Equal Opportunity Employer, including disability and veterans.
If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to .
This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.
S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.
Notice to Agency and Search Firm Representatives : Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and / or search firms for this job posting.
Resumes submitted to any Catalent employee by a third party agency and / or search firm without a valid written & signed search agreement, will become the sole property of Catalent.
No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.
Important Security Notice to U.S. Job Seekers :
Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media.
If you receive any such request, DO NOT respond it is a fraudulent request. Please forward such requests to for us to investigate with local authorities.
California Job Seekers can find our California Job Applicant Notice .
Last updated : 2024-05-31
Full Time
Pharmaceutical
$85k-102k (estimate)
04/06/2024
07/29/2024
catalent.com
SOMERSET, NJ
7,500 - 15,000
2007
Public
JOHN R CHIMINSKI
$3B - $5B
Pharmaceutical
Catalent is a provider of delivery, development and manufacturing solutions for drugs, biologics and consumer health products.
The job skills required for Quality specialist include Quality Assurance, Food Safety, Quality Control, Packaging, HACCP, Auditing, etc. Having related job skills and expertise will give you an advantage when applying to be a Quality 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 specialist. Select any job title you are interested in and start to search job requirements.
The following is the career advancement route for Quality specialist positions, which can be used as a reference in future career path planning. As a Quality specialist, it can be promoted into senior positions as a Quality Assurance Specialist IV that are expected to handle more key tasks, people in this role will get a higher salary paid than an ordinary Quality specialist. You can explore the career advancement for a Quality specialist below and select your interested title to get hiring information.
If you are interested in becoming a Quality 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 Specialist for your reference.
Step 1: Understand the job description and responsibilities of an Accountant.
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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 Specialist jobs
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Step 3: View the best colleges and universities for Quality Specialist.