Senior Technician, QC Aliquoting - Severn Maryland

Company: Disability Solutions
Location: Severn, Maryland
Posted On: 02/03/2025

Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually.The role:

• Respond to other department inquiries regarding status of aliquoting requests
• Preparation of labels and label vials for samples
• Reconstitution and aliquoting of samples
• Sample coordination and receipt from other departments for internal and external testing
• Ensure that suitable written records and work undertaken are kept in accord with cGMP and company procedures
• Receive Batch Records and Test Request forms from other departments
• Order and receive supplies for groups as necessary
• Execute document revisions
• Works closely with Manufacturing, Stability, and/or other teams, for scheduling of samples submission to the QC lab.-- May also interact with Project Managers on sample coordination.
• Ensure adequate stock of aliquoting supplies through forecasting of upcoming sample submission
• Assist with tracking sample receipt and chain of custody for internal and contract laboratory submission
• Execute assigned activities within GLIMS
• Work under general supervision to meet project goals
• Flexibility in following unique campaign requirements that may include off-hour and weekend work
• Assist with tracking internal / external testing as necessary
• Assist with QC reagent preparation as necessary
• Perform laboratory cleaning as part of routine work
• Assist with maintaining inventory of QC non-critical and critical reagents as necessary
• Other duties as assignedThe candidate:
  • High school diploma and 1 - 3 years' experience within biologics, biopharmaceuticals, or a regulated industry
  • Ability to produce results in a fast-paced environment to meet client deadlines under minimal supervision
  • Experience working in cGMP Quality Control
  • Previous laboratory sample handling, including pipetting, required
  • Strong attention to detail and strong organizational skills
  • Experience working in a Phase III / Commercial Manufacturing setting, preferred
  • Have the knowledge and ability to apply basic scientific and regulatory principles to solve operational and other routine quality tasks.The anticipated salary range for this position in Maryland is $47,600 to $65,450 plus an annual bonus target. The final salary offered to a successful candidate may vary, and will be dependent on several factors that may include but are not limited to: the type and length of experience within the job, type and length of experience within the industry, skillset, education, business needs, etc. Catalent is a multi-state employer, and this salary range may not reflect positions that work in other states.Why you should join Catalent:
    • Competitive medical benefits and 401K
    • 152 hours PTO + 8 Paid Holidays
    • Dynamic, fast-paced work environment
    • Opportunity to work on Continuous Improvement ProcessesCatalent 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 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 . 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 . More...

          

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