Experience Inc. Jobs

Quality Control Technician II

Position Summary:

Catalent is a global, high-growth, public company and a leading partner for the pharmaceutical industry in the development and manufacturing of new treatments for patients worldwide. Your talents, ideas, and passion are essential to our mission: to help people live better, healthier lives.

Catalent’s Kansas City facility is home to our Oral & Specialty Drug Delivery, Biologics Analytical Services and Clinical Supply Services businesses. The site provides a range of integrated services for oral solid dosage forms, from formulation development and analytical testing to clinical and commercial-scale manufacture. The Kansas City facility is a Center-of-Excellence for our Biologics Analytical Services business. Our talented team has over 25 years of experience providing analytical services for stand-alone and integrated biologics projects.

Catalent Pharma Solutions in Kansas City, MO is hiring a Quality Control (QC) Technician II. The QC Technician II performs tasks from detailed instructions and established procedures and ensures that all work is carried out in compliance with regulatory requirements, corporate policies, good manufacturing practices (cGMP) and standard operating procedures (SOPs). This individual will support the Sample Management Office for our Kansas City site.

This is a full-time hourly position: Monday – Friday, on 1st shift 8am-4pm.

Catalent is committed to a Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer, and Catalent employee.

The Role:

• Physically receive, count, label, and organize samples/standards for the purpose of further distribution. Activities include handling temperature recording devices (stopping, starting, and interpreting or providing data to clients), and performing registration activities for all samples and standards into the chain of custody software

• Communicate effectively with internal (project management, operations, and laboratory personnel) and external customers to facilitate efficient sample flow

• Obtain DEA clearance and participate in controlled substance inventory verification

• Execute assigned daily work plan or schedule as developed by the Team Lead and/or Group Leader and perform support activities for/on behalf of the Quality Control department

• Maintain high quality documentation in accordance with applicable regulatory guidance and site SOPs documenting work as appropriate within notebooks, forms, etc.

• Execute procedures or methods of increasing complexity with high quality and review own work to ensure accuracy and completeness. May perform review of peer's documentation for accuracy, thoroughness, and compliance with the ability to identify and remediate minor quality/compliance gaps during routine work

• Assist in the execution of efficiency/compliance improvement projects with guidance

• All other duties as assigned

The Candidate:

• High School Diploma/GED is required with a minimum of two years of experience in laboratory or pharmaceutical industry. We will also accept a Bachelor’s degree and no industry experience

• Must have familiarity with Microsoft Office (Word, Excel, Outlook, Teams, etc.), and experience with LIMS (Lab Information Management System) is preferred

• Mathematical and scientific reasoning ability is required, along with the ability to learn and retain technical information

• Requires the ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form

• Physical Requirements: On an average 8-hour day this position requires the ability to walk, sit and stand, use hands to handle or feel, reach with hands and arms at or above shoulder height and below waist height, climb or balance, stoop, kneel, crouch, or crawl; talk and hear, smell and lift up to 40 pounds. Specific vision requirements including reading of written documents, visual inspection of materials and use of computer monitor screen frequently. Able to occasionally work in cold storage conditions of 2-8°C and/or -20°C as needed and also work with respirator (P100, PAPR, etc.)

Why you should join Catalent:

• Defined career path and annual performance review and feedback process

• Diverse, inclusive culture

• Positive working environment focusing on continually improving processes to remain innovative

• Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives

• 152 Hours + 8 paid holidays

• Several Employee Resource Groups focusing on D&I

• Dynamic, fast-paced work environment

• Community engagement and green initiatives

• Generous 401K match

• Company match on donations to organizations

• Medical, dental and vision benefits effective day one of employment

• Tuition Reimbursement – Let us help you finish your degree or start a new degree!

• WellHub program to promote overall physical wellness

• Perkspot - offers exclusive or private discounts from approximately 900+ merchants in a wide array of categories

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.

personal initiative. dynamic pace. meaningful work.

Visit Catalent Careers (https://careers.catalent.com/us/en) 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 (https://cdn.catalent.com/files/legal/CCPA-Privacy-Notice-at-Collection-for-California-Employees-and-Applicants-English.pdf) .