Catalent, Inc.

pharmaceutical

ManufacturingTechnician(2ndShift)

$40–40k San Diego, California, United States FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Entry candidates.

The Brief

“Manufacturing Technician (2nd Shift) at Catalent, Inc.. Skills: cGMP manufacturing, process management, cross-functional coordination, vendor/stakeholder management, operational metrics, resource planning, continuous improvement. conducting Good Manufacturing Practices (cGMP) manufacturing of solid oral and liquid oral pharmaceutical dosage forms for Phase and Phase II clinical trials. production equipment set up”

What You'll Achieve.

deliver unparalleled service to our clients and quality drug products to the patients

Industry & Context.

pharmaceutical
Eligibility Requirements

ability to walk, sit and stand, use hands to handle or feel, reach with hands and arms at or above shoulder height and below waist height, climb or balance, stoop, kneel, crouch, or talk and hear, smell and lift up to 40 pounds, Specific vision requirements including reading of written documents, visual inspection of materials and use of computer monitor screen frequently, 100% on-site (San Diego), Monday-Friday from 2: 00 - 10: 30 PM

What They're Looking For.

Must Have

High School Diploma or GED equivalent is required

Nice to Have

Some GMP experience in pharmaceutical or medical device manufacturing a plus

What You'll Do.

conducting Good Manufacturing Practices (cGMP) manufacturing of solid oral and liquid oral pharmaceutical dosage forms for Phase and Phase II clinical trials

production equipment set up

weighing of materials

sieve and blending activities

coating and packaging

equipment and manufacturing suites for production

Packaging and labeling of manufactured products

Pre/postproduction cleaning of equipment

supplies and manufacturing area

Follow Standard Operating Procedures (SOPs) and production batch records

Responsible for accurate documentation in production batch records

assist engineering with equipment validations

preventative maintenance

and cleaning verifications

How You'll Work.

Team & Collaboration

key member of a multi-site mission to deliver unparalleled service to our clients and quality drug products to the patients

Full Job Description

**Manufacturing Technician I (2nd Shift)** **Position Summary:** * **Work Schedule:** Monday-Friday from 2:00 - 10:30 PM * 100% on-site (San Diego) Catalent, Inc. is a leading global Contract Development and Manufacturing Organization (CDMO), and Catalent’s San Diego facility focuses on early-stage development of small molecule and peptide drug candidates from the bench to the clinic. This facility offers an array of services that support oral and injectable dosage forms that include preformulation testing, formulation and analytical development, cGMP manufacturing and clinical packaging, labeling, and worldwide distribution. Our San Diego location is the home of our Catalent Spray Drying technologies with downstream roller compaction capabilities to support the needs of our client’s most challenging compounds. The Manufacturing Technician I will be responsible for conducting Good Manufacturing Practices (cGMP) manufacturing of solid oral and liquid oral pharmaceutical dosage forms for Phase I and Phase II clinical trials. Daily responsibilities will include production equipment set up, weighing of materials, sieve and blending activities, spray drying, milling, granulation, mixing, roller compaction, submitting samples, encapsulation, tableting, coating and packaging. You will be a key member of a multi-site mission to deliver unparalleled service to our clients and quality drug products to the patients. **The Role:** * Prepare materials, equipment and manufacturing suites for production * Conduct GMP manufacturing of solid oral and liquid oral dosage forms * Packaging and labeling of manufactured products * Pre/postproduction cleaning of equipment, supplies and manufacturing area * Follow Standard Operating Procedures (SOPs) and production batch records * Responsible for accurate documentation in production batch records * May also assist engineering with equipment validations, preventative maintenance, and cleaning verifications * Other duties as assigned **The C

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