Sample Management Technician I

Catalent

Greenville (NC)

On-site

USD 42,000 - 55,000

Full time

14 days+
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Benefits offered by this job

Competitive PTO
Medical, dental, and vision benefits
Tuition reimbursement

Job summary

Catalent’s Greenville, North Carolina site is seeking a Sample Management Technician I to support sample handling in a GMP environment. You will manage stability samples, reference standards, controlled substances, and logistics for internal and external customers.

The role emphasizes following regulatory guidelines, maintaining accurate documentation, and supporting inventory and reconciliation processes. Onsite, Monday–Friday, 8:00am–5:00pm.

Qualifications

  • High School diploma or equivalent required; one year of applicable experience or completion of Grads2Work/BioWorks preferred.
  • Must be able to sit, stand, and walk regularly; lift over 30 lbs.
  • Must have access to manufacturing floor and office areas and operate standard office equipment.
  • Strong documentation and recordkeeping skills; attention to detail.

Responsibilities

  • Manage high-volume sample inventory with accurate tracking and organization.
  • Perform routine and precise use of analytical balances for weighing and prep.
  • Maintain thorough documentation including lab records and SOPs.
  • Ensure quality compliance through accurate recordkeeping and procedures.

Skills

Physical stamina

Education

High School diploma or equivalent
Grads2Work Program / BioWorks certificate

Tools

Analytical balances

Job description

About Site

Catalent’s Greenville, North Carolina site is a major oral solid dose development and manufacturing campus, delivering end‑to‑end, turnkey solutions from formulation development through commercial manufacturing and packaging. The site specializes in oral solid dosage forms, supported by integrated formulation expertise, comprehensive analytical services, and scalable manufacturing capabilities designed to support both commercial products and potent or targeted therapies, including orphan drugs. Backed by more than $100 million in recent investments, the Greenville operation features fit‑for‑scale infrastructure, potent handling capabilities, and a strong regulatory track record, making it a critical part of Catalent’s global network for advancing complex oral drug programs from development to market.

Sample Management Technician I Role

About Site

Catalent’s Greenville, North Carolina site is a major oral solid dose development and manufacturing campus, delivering end‑to‑end, turnkey solutions from formulation development through commercial manufacturing and packaging. The site specializes in oral solid dosage forms, supported by integrated formulation expertise, comprehensive analytical services, and scalable manufacturing capabilities designed to support both commercial products and potent or targeted therapies, including orphan drugs. Backed by more than $100 million in recent investments, the Greenville operation features fit‑for‑scale infrastructure, potent handling capabilities, and a strong regulatory track record, making it a critical part of Catalent’s global network for advancing complex oral drug programs from development to market.

Position Summary

We have an opportunity for a Sample Management Technician I to join our team. This entry-level role supports sample management in a Good Manufacturing Practice environment under general supervision. You will assist with stability, reference standards, controlled substances, and sample logistics for internal departments and external customers. The position involves following regulatory guidelines, maintaining accurate documentation, and supporting inventory and reconciliation processes.

Shift: Monday- Friday 8:00am-5:00pm

Location: Grenville, NC

100% Onsite

The Role

  • Manage high-volume sample inventory while ensuring accurate tracking and organization.
  • Perform routine and precise use of analytical balances for sample weighing and preparation.
  • Maintain comprehensive documentation, including laboratory records, inventory logs, and standard operating procedures.
  • Ensure compliance with quality standards through accurate recordkeeping and documentation practices.

The Candidate

Minimum Requirements

  • High School diploma or equivalent with a minimum of one year of applicable experience, or completion of Grads2Work Program, or BioWorks certificate program required.
  • Individual may be required to sit, stand, and walk regularly.
  • Ability to lift more than 30 lbs. unassisted.
  • Accessible to manufacturing floor and office staff and able to use required office equipment.
  • Specific vision requirements include reading written documents and frequent use of a computer monitor.
  • Other duties as assigned.

Preferred Skills & Background

  • Associate degree in a science or technology-related discipline.

Why You Should Join Catalent

  • Positive and fast-paced working environment focusing on continual improvement and innovation.
  • Competitive Paid Time Off plus 8 paid holidays.
  • Medical, dental, and vision benefits effective day one of employment.
  • Tuition Reimbursement to help you finish your degree or earn a new one.
  • Engaging site-based activities such as Music Bingo, Puppy Supply Donation Program, and seasonal events.
  • Employee Resource Groups promoting Diversity and Inclusion.
  • Green initiatives and community engagement programs including highway clean-up.
  • Defined career path with annual performance reviews and growth opportunities.
  • WellHub program promoting physical and mental wellness, including onsite fitness center.
  • Exclusive discounts through Perkspot from over 900 merchants.

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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