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$Not specified
Support laboratory logistics, manage inventory and compliance, and coordinate study supplies.
High school diploma, 2+ years in logistics or clinical supply, proficiency in MS Office, understanding of clinical supply processes, strong organizational skills.
## Key Role Overview As a Kit Production Coordinator (Lab Warehouse Order Picker) you will coordinate and perform logistics and kit production tasks to support laboratory studies at the Global Central Laboratory in West Chester Township, OH. The role focuses on inventory and clinical supply management — receiving, labeling, storing, distributing, tracking expirations, and ensuring compliance with SOPs and Gx. P/regulatory requirements. ## Key Responsibilities - Coordinates, supports, and performs logistics and administrative work to support the department. - Supports day-to-day operations of study drug, comparators and ancillaries management. - Oversee daily drug product/medical device receipt, ordering, storage, label printing and labeling activities. - Manage inventory, distribution, return drug accountability and destruction. - Ensure depot activities comply with company SOPs and client requirements. - Track inventories and expiration dates; issue monthly status reports. - Arrange purchases of additional supplies upon request. - Maintain accurate data in electronic management systems and updated PPD-owned metrics/indicator reports. - Complete ongoing training on regulations concerning clinical supplies, Gx. P and GMP activities. - Participate in and support department project teams and may serve as liaison cross-functionally. - Actively problem-solve logistics challenges and suggest solutions. ## Required Qualifications - High / Secondary school diploma or equivalent; relevant formal academic/vocational qualification. - Minimum 2 years of prior experience providing the knowledge, skills, and abilities to perform the job; equivalency by education/training may be considered. - Proficient in English (verbal and written). - Strong computer skills with solid understanding of Microsoft Project, Excel, and Word. - Proven understanding of the Clinical Supply process (manufacturing, handling, importing, shipping, exporting, auditing, labeling and packaging). - Strong organizational, planning, time management and analytical skills. - Strong customer service orientation and attention to detail; ability to work independently and in a team with moderate supervision. - Ability to follow proper channels of communication to voice concerns and suggestions. - Eligibility to work in the United States without sponsorship. - Ability to pass a comprehensive background check including drug screening. ## Preferred Qualifications - Technical certificate for technical positions (when applicable). - Experience with GMP activities and clinical supply regulations. - Experience coordinating logistics for moderate to complex studies or serving as a cross-functional liaison. ## Compensation & Benefits - Salary range: Not specified in the posting. - Benefits: Not specified in the posting; company references support for career development, reasonable accommodations, and standard corporate benefits. ## Additional Information - Work schedule: Standard (Mon - Fri); fully onsite at the Global Central Laboratory in West Chester Township, OH. - Relocation assistance is not provided; any relocation costs are the candidate's responsibility. - Physical requirements: Able to stand for typical working hours; lift and move objects of 15 to 40 pounds; perform under pressure and prioritize multiple projects. - Possible exposure to potentially hazardous elements, including infectious agents, and occasional exposure to fluctuating/extreme temperatures. - Accessibility/Disability accommodations available for the application process; contact 1-855-471-2255 for assistance. - Thermo Fisher Scientific is an Equal Opportunity Employer and provides reasonable accommodations for individuals with disabilities.
This job posting was last updated on 12/12/2025