Senior Technician, QC Sample Management

Catalent; Harmans (MD); On-site; USD 47,000 - 66,000; Full time

Job summary

An established industry player is seeking a Senior Technician for QC Sample Management. In this pivotal role, you will be responsible for the receipt and coordination of samples for testing, ensuring compliance with cGMP standards. Your expertise will contribute to enhancing product quality and safety in a fast-paced environment. With opportunities for career growth and a commitment to continuous improvement, this position offers a chance to make a significant impact in the pharmaceutical and biotech sectors. Join a dedicated team focused on delivering life-saving products to patients worldwide.

Benefits

Competitive benefits

401K

PTO

Holidays

Opportunities for career growth

Qualifications

• 2-4 years of experience in a cGMP environment.
• Knowledge of GMP requirements for pharmaceuticals and biologics.

Responsibilities

• Receiving samples for QC testing and creating documentation.
• Coordinating testing with contract labs and managing inventories.
• Communicating updates and results effectively.

Skills

cGMP experience

Biologic sample coordination

Microsoft Excel

Microsoft Word

Attention to detail

Organizational skills

Communication skills

Education

High School Diploma

Job description

Join to apply for the Senior Technician, QC Sample Management role at Catalent.

The Sr. Technician, QC is responsible for receiving samples for QC testing, creating testing documentation, coordinating testing with contract labs, managing laboratory supply inventories, service contracts, and purchase requisitions. Responsibilities include sample receipt, chain of custody, verification of materials, data entry, and coordinating shipment of testing samples.

Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) dedicated to developing, manufacturing, and supplying products that improve lives. It supports product development, launch, and full lifecycle supply for pharma, biotech, and consumer health clients, with over 40 global sites and thousands of employees.

The role includes:

1. Sampling of raw materials according to established specifications.
2. Sample coordination and receipt for testing.
3. Coordination of testing with contract laboratories and reporting results.
4. Managing reference standards and reagents, including labeling and transfer.
5. Lab duties such as reconstitution and aliquoting of samples.
6. Scheduling QC testing and activities.
7. Follow-up on testing deadlines and trending results.
8. Collaborating with Manufacturing, Analytical Development, and Project Managers.
9. Communicating updates and results effectively.

Candidate requirements:

• HS Diploma with 2-4 years of experience in a cGMP environment.
• Biologic sample coordination experience preferred.
• Knowledge of GMP requirements for pharmaceuticals and biologics.
• Proficiency in Microsoft Excel and Word.
• Strong attention to detail, organization, and communication skills.

The salary range in Maryland is $47,600 - $65,450 plus bonus, dependent on experience and other factors.

Why join Catalent?

• Competitive benefits, 401K, PTO, and holidays.
• Fast-paced, dynamic environment.
• Opportunities for continuous improvement and career growth.

Join us in making a difference by helping bring life-saving products to patients worldwide. Catalent is an Equal Opportunity Employer and provides accommodations for applicants with disabilities.