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Compliance Specialist II

Catalent Pharma Solutions
Posted a day ago, valid for 20 days
Location

Kansas City, MO, US

Salary

Competitive

Contract type

Full Time

Paid Time Off
Tuition Reimbursement

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Sonic Summary

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  • Catalent is seeking a Compliance Specialist II for its Kansas City facility, focusing on cGMP compliance across various business units.
  • The role involves reviewing batch records, drafting standard operating procedures, and maintaining high-quality documentation to meet regulatory requirements.
  • Candidates are required to have a minimum of a High School Diploma and preferably some GMP experience, with the ability to lift up to 50 pounds.
  • This full-time position offers a Monday to Friday schedule from 8:00 am to 5:00 pm, and the salary is competitive, though not specified in the posting.
  • Catalent provides a defined career path, annual performance reviews, and comprehensive benefits including medical, dental, vision, and tuition reimbursement.

Compliance Specialist II

About Site

Catalent’s Kansas City facility is home to our Oral & Specialty Drug Delivery, Biologics Analytical Services and Clinical Supply Services businesses.

Position Summary

We have an opportunity for a Compliance Specialist II to join our team. In this role, you will support cGMP business units to ensure a high level of compliance. You will work under the direct guidance of a supervisor to ensure all documentation meets regulatory requirements, good manufacturing practices (cGMP), and standard operating procedures (SOPs). This position is key to maintaining quality and compliance across our operations.

Shift: Monday-Friday; 8:00am-5:00pm
Location: Kansas City, MO
100% Onsite

The Role

  • Review executed batch records and documentation to ensure conformance to cGMPs, SOPs, and other protocols.
  • Draft and review batch records for use by pharmaceutics and operations personnel.
  • Recommend batch record changes for continuous improvement per approved SOPs and collaborate with cGMP business units to resolve inconsistencies.
  • Draft standard operating procedures for processes used by pharmaceutics and operations personnel.
  • Complete all assigned training and follow training guidelines strictly.
  • Maintain high-quality manufacturing documentation in accordance with regulatory guidance and site SOPs.
  • Maintain readiness for on-site clients.
  • Perform spot-checks of experimental areas and assets, and track laboratory notebooks.
  • Track and trend batch record initiation, approvals, updates, and feedback after execution.
  • Perform all other duties as assigned.

The Candidate

Minimum Requirements

  • High School Diploma
  • Ability to lift up to 50 pounds

Preferred Skills & Background

  • GMP experience is preferred

Why You Should Join Catalent

  • Defined career path and annual performance review and feedback process
  • Diverse, inclusive culture
  • Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives
  • Competitive paid time off plus 8 paid holidays
  • Community engagement and green initiatives
  • Medical, dental, and vision benefits effective day one of employment
  • Tuition reimbursement

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.

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.




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By applying, a Catalent Pharma Solutions account will be created for you. Catalent Pharma Solutions's Privacy Policy and Terms & Conditions will apply.

SonicJobs' Terms & Conditions and Privacy Policy also apply.