Returns Associate II

Catalent•Kansas City, MO

7d•Onsite

About The Position

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 Returns Associate II. The Kansas City Clinical Supply Services Returns Associate II supports clinical trial projects through the processing of returned clinical trial medications that are returned by clinical research sites for destruction and ensuring that all work is carried out in compliance with regulatory requirements, good manufacturing practices (cGMP) and standard operating procedures (SOPs). Although the main focus is in Returned Goods and Destruction, this position will also support other areas of operation as needed and as requested in order to support the needs of the business.

Requirements

High School degree or equivalent
1-3 years of clinical trial Returned Goods Summaries/Destruction or related pharmaceutical operations experience preferred
Ability to work in a team environment
Self-motivated and proactive
Proven written and verbal communication skills
Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form
High attention to detail
Ability to work effectively to meet competing workplace demands
Basic computer skills – including, but not limited to e-mail, Microsoft Word & Excel, Internet Explorer

Nice To Haves

1-3 years of clinical trial Returned Goods Summaries/Destruction or related pharmaceutical operations experience preferred

Responsibilities

Follow safety and manual handling guidelines delineated in SOPs and MSDS
Process returned clinical trial medications as delineated in the Returned Goods Summaries/Destruction Plans to ensure processing instructions are followed in accordance with SOPs and client authorized requests
Follow safe handling procedures when utilizing manual lifting equipment to move material
Prepare and complete documentation in compliance with SOPs and cGMP
Reconcile returned clinical trial material and add to the appropriate inventory system
Ensure daily targeted productivity goals are achieved
Ensure a high quality standard work by reporting any deviations from the Returned Goods Summaries/Destruction instructions or SOP procedures to management
Work with the Senior Returns Operator to complete verification of material for destruction
Other duties as assigned

Benefits

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 of PTO + 8 paid holidays
Several Employee Resource Groups focusing on D&I
Dynamic, fast-paced work environment
Community engagement and green initiatives
Generous 401K match
Medical, dental and vision benefits effective day one of employment
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