Quality Specialist II WKD PM Job in Indiana (IN), Chemistry Career, Full Time Jobs in Catalent

We use cookies. Find out about cookies here. By continuing to browse this site you are agreeing to our use of cookies.
Close

Sign in

Create a candidate account

Create a candidate account

Create an employer account

Sign in to an existing account

Create a candidate account

Create an employer account

Sign in to an existing account

Forgot password

Forgot password

Sign in

Create a candidate account

Sign in

Create an employer account

Advanced search

Quality Specialist II WKD PM job in Greendale

Vacancy has expired

Sign in

Create a candidate account

Back to search results

Indiana (IN), Greendale

Job Code:	CATAUSR918077EXTERNALENUS_xTdtAFc8WFit
Employer:	Catalent
Category:	Chemistry
Job Type:	Full Time
Location
Country:	United States
State:	Indiana (IN)
City:	Greendale
Post Date:	03/27/2024
Description
Quality Assurance Specialist II 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 Specialist II 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. Communicate any deviations to management. The Quality Specialist II will assist the Quality Assurance team with special projects as required. Comply with SQF, Food Safety Plan (HACCP), Food Quality Plan (FQP) standards. Shift: Friday - Sunday 6 pm - 6 am The Role Monitor changeover activities and be able to resolve issues of varying complexity Conduct thorough and detailed quality audits ensure products meet established quality standards. Communicate any deviations to the appropriate parties promptly. Audit paperwork of operators to ensure they are meeting quality standards Conduct PCQI documentation review. Responsible for holding products that are not meeting company quality standards and provide the appropriate dispositions. 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 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. All other duties as assigned. The Candidate For business and safety reasons, must be able to communicate effectively verbally and in written English. This position requires BS in Food Science and/or related major or have High School diploma with 1 year experience in manufacturing and training - HACCP, PCQI, GFSI, cGMP. Ability to communicate with all line level positions and management Attention to detail Able to assert himself / herself effectively Strong problem solving skills Strong interpersonal skills are essential. Ability to develop cross functional and multinational relationships to support interaction with various internal customers. Strong analytical skills Ability to read and follow documents (Standard Operating Procedures and Test Methods) Knowledge of GMP and Quality systems Knowledge of spoken Spanish is a plus 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. 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 offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. 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 Catalent Careers 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 DisabilityAccommodations@catalent.com . 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 spam@catalent.com for us to investigate with local authorities. California Job Seekers can find our California Job Applicant Notice HERE .

ref: (CATAUSR918077EXTERNALENUS_xTdtAFc8WFit) 31 days ago

Back to search results

Featured jobs

MORE JOBS LIKE THOSE View more

Featured employers

Popular locations: New Jersey (NJ) (546) | North Carolina (NC) (178) | Pennsylvania (PA) (117) | California (CA) (70) | Massachusetts (MA) (55) | New Mexico (NM) (44) | New Hampshire (NH) (29) | Connecticut (CT) (25) | Remote (24) | Indiana (IN) (18)

Popular categories: Research and Development (184) | Clinical Research (83) | Regulatory Affairs (76) | Sales (70) | Manufacturing (62) | Biology (59) | Director Clinical Research (52) | Medical Communications (51) | Chemistry (47) | Engineering (39)

Popular jobs: Director (313) | Manager (263) | Associate Director (118) | Sales (84) | Project Management (36) | Account Manager (31) | Senior Specialist (25) | Automation Engineer (9) | Business Development (9) | Intern (9)