This is an entry-level position created to support clinical trial projects through the packaging of clinical trial supplies. All activities performed will ensure that all work is carried out in compliance with regulatory requirements, good documentation practices (GDP), current good manufacturing practices (cGMP) and standard operating procedures (SOPs). This position reports to the Production Supervisor and may accept tasks issued from Room Leads and Team Leads.
Essential Functions:
Ensure that during all packaging operations the site’s safety, quality and compliance metrics are met or surpassed while meeting corporate and site standards and policies
Establish a strong working knowledge of cGMP, GDP, local site policies and regulatory requirements
Develop proficiency in packaging batch record execution in accordance with SOPs and regulatory requirements by ensuring that all entries into the batch record will be right the first time
Develop a Patient first customer focus mindset
Establish an understanding of clinical trials and how they relate back to the work performed in clinical packaging
Complete training and execute documentation in compliance with SOPs and GDP
Inspect drug product, components, and clinical labels for defects, blemishes or missing text prior to and during production
Develop a high aptitude for cleanliness in the work space
Label application to consistently follow all visual/written procedures
Clean associated packaging equipment and packaging room(s) in compliance with SOPs
Requirements:
High School degree or equivalent.
Proven written and verbal communication skills
Ability to work in a team environment
High attention to detail
Basic computer skills – including, but not limited to e-mail, Microsoft Word, Internet Explorer
Basic mathematical skill
Physical Requirements:
Must pass vision exam with 20/30 corrected vision for distance and 14/20 for near sighted
Able to distinguish all colors
May be required to operate a manual pallet jack
Position requires ability to spend extended periods of time in the following GMP environments:
Controlled Room Temperature 68 degrees F – 77 degrees F (15 degrees C – 25 degrees C)
Refrigerator 35 degrees F – 46 degrees F (2 degrees C – 8 degrees C)
#nowhiring
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Numbers & Facts
Location
Kansas City, MO
Skills
Biotech and Pharmaceuticalunmatched
Clinical Supportunmatched
Clinical Trialunmatched
Communication Skillsunmatched
Computer Skillsunmatched
Current Good Manufacturing Practice (cGMP)unmatched
Customer Relationsunmatched
Detail Orientedunmatched
Documentationunmatched
Drug Productsunmatched
GMP (Good Manufacturing Practices)unmatched
High School Diplomaunmatched
Mathematicsunmatched
Medical Productsunmatched
Microsoft Internet Explorer Browserunmatched
Microsoft Wordunmatched
Pallet Jackunmatched
Presentation/Verbal Skillsunmatched
Product Packagingunmatched
Production Managementunmatched
Quality Metricsunmatched
Regulatory Complianceunmatched
Regulatory Requirementsunmatched
Safety/Work Safetyunmatched
Standard Operating Procedures (SOP)unmatched
Team Lead/Managerunmatched
Team Playerunmatched
Writing Skillsunmatched
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