Pharmaceutical Manufacturing Operator I

About the role

Work Schedule: Monday – Friday, 6:00AM – 2:30PM

Catalent is a leading provider of pharmaceutical manufacturing services. As a Pharmaceutical Manufacturing Operator I, you'll play a crucial role in transforming scientific advancements into life-saving treatments.

Responsibilities

• Ensure cGMP compliance, general good housekeeping, and inform senior technicians of work orders for processing rooms and equipment.
• Maintain 5S standards and keep the facility "tour ready" at all times.
• Support core group metrics and efficiency improvements by providing training updates and ensuring adherence to SOPs.
• Build proficiency with key business equipment and maintain high quality standards.
• Follow safety procedures, identify and communicate necessary adjustments for safety concerns, and ensure proper use of PPE.
• Operate safely in a dynamic environment, managing multiple tasks and complex operations.
• Wear PAPR and required gowns when necessary.
• Manage priorities and projects effectively, and work in a matrix organization.
• Stay updated on cGMP regulations and trends relevant to your responsibilities.

Requirements

• High school diploma or GED
• 0-3 years of experience in Pharma or cGMP manufacturing environment
• Equipment process and framework knowledge
• Basic computer skills
• Knowledge of cGMP, FDA, MHRA, and DEA guidelines
• Preferred: Solid Dosage manufacturing experience
• Ability to prioritize and manage multiple tasks
• Capable of managing priorities and projects effectively
• Experience in a matrix organization
• Current knowledge of cGMP regulations and trends

Qualifications

• High school diploma or GED
• 0-3 years of experience in Pharma or cGMP manufacturing environment
• Equipment process and framework knowledge
• Basic computer skills
• Knowledge of cGMP, FDA, MHRA, and DEA guidelines
• Preferred: Solid Dosage manufacturing experience
• Ability to prioritize and manage multiple tasks
• Capable of managing priorities and projects effectively
• Experience in a matrix organization
• Current knowledge of cGMP regulations and trends

Skills

• Equipment process and framework knowledge
• Basic computer skills
• Knowledge of cGMP, FDA, MHRA, and DEA guidelines
• Preferred: Solid Dosage manufacturing experience
• Ability to prioritize and manage multiple tasks
• Capable of managing priorities and projects effectively
• Experience in a matrix organization
• Current knowledge of cGMP regulations and trends

Benefits

• Day-one benefits: medical, dental, vision
• 401(k) match
• Tuition reimbursement
• Wellness perks
• Paid time off: 152 hours + 8 paid holidays
• Discounts from 900+ merchants via Perkspot
• Employee Resource Groups and community initiatives
• Discounts from 900+ merchants via Perkspot

Pay

Competitive compensation package

Schedule

Monday – Friday, 6:00AM – 2:30PM

Company Overview

Catalent is a global leader in drug development and delivery. We produce more than 70 billion doses annually and work with pharma, biopharma, and consumer health companies to bring life-saving and life-enhancing products to patients worldwide. Join us in making a difference!

Equal Opportunity Employer

Catalent is committed to a diverse and inclusive workforce. We are an equal opportunity employer and do not discriminate against applicants based on race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability.