Lead Label Specialist
Work Summary
Work Schedule: Monday to Friday 2:30pm - 11:30pm with training on first shift
100% based on-site in Kansas City
Catalent’s Kansas City (KCM) facility is a premier site for integrated drug development, manufacturing, and clinical supply services, supporting a wide range of pharmaceutical and biotech products. With cutting-edge technologies and a collaborative work environment, it offers exciting opportunities for professionals across all functions—from science and engineering to operations and logistics.
The Lead Label Specialist provides support to the Project Management Team, Operations Team and our customers by designing, printing and inspecting labels for use in clinical and commercial packaging and distribution.The Lead Label Specialist is tasked with overseeing all projects that run through Label Control while following the master schedule.Organization, leadership and strong attention to detail are a few of the required traits of this position.
The Role
Creation of GSA jobs, including the importing of verification data.
This role may also include performing the role of LSO for the KCM site. These additional responsibilities include: set up and modification of users; creation/modification of sites within GSA; creation/modification of Clients within GSA; and training local users among other responsibilities outlined per SOP.
Good Project manager, client and team rapport. Ability to communicate, educate and assist in all areas of label control.
Attend Kick off meetings and assist in ensuring that each kickoff meeting has representation. Set a standard of what is expected and assist in holding team accountable. Knowledgeable about campaigns and the requirements.
Organization and manage assigned projects with the ability to prioritize while assisting others in managing theirs. Utilize and be able to help others use WorkFront.
Assist with enforcing the master schedule with a commitment to hitting OTD. Prioritize self with a big picture of the team. Promote teamwork where necessary to accomplish tasks.
Provide regulatory audit and client audit support.
Other duties assigned.
The Candidate
High-school diploma or GED required
1+ years of clinical labelling experience or related pharmaceutical operations experience preferred
Knowledge regarding design control, documentation, risk management and processes such as FMEA, Design Verification, and URS is a plus.
Ability to communicate effectively with project managers, customers, and other personnel.
Supervisory skills and experience strongly recommended
High level of attention to detail.
Excellent documentation skills.
Strong problem solving and analytical skills.
Excellent written, verbal and interpersonal communication skills, including the ability to present information.
Demonstrate a willingness to share skills and information with others.
Demonstrated ability to read, write, and speak clear English.
Why you should join Catalent
Career growth with a clear path and regular performance reviews
Day-one benefits: medical, dental, vision
401(k) match, tuition reimbursement, and wellness perks
Paid time off: 152 hours + 8 holidays
Inclusive culture with Employee Resource Groups and community initiatives
Discounts from 900+ merchants via Perkspot
A mission-driven workplace where your work helps save lives
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 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.
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