Bosma Jobs

Operator I, Inspection/Packaging

Summary:

Catalent Biologics is a fast-growing business within Catalent Pharma Solutions focused on providing innovative technologies and solutions to help more and better biologic treatments get to patients. The business includes our proprietary GPEx cell line engineering platform, our new state-of-the-art biomanufacturing facility in Madison, WI, and our market leading biologics analytical services in Kansas City, MO and Research Triangle Park, NC, as well as SMARTag Antibody Drug Conjugate technology in Emeryville, CA. Leveraging our growing differentiated technology portfolio, world class manufacturing capability, and other integrated services across the Catalent network, Catalent Biologics is positioned to drive significant growth for Catalent.

Working for Catalent Biologics is an opportunity to join an entrepreneurial team. Catalent Biologics is making significant investments in people and capabilities. This is a unique opening to join a small, fast-growing business, backed by a global public company. People joining our team will have the opportunity for career development as our business continues to grow and expand. Catalent employees are helping to improve future patient outcomes by working on products that are designed to treat COVID-19, cancer, various autoimmune, fibrotic and blood disorders, HIV, diabetes, heart, and lung diseases as well as Alzheimer’s.

The Secondary Manufacturing department is responsible for the execution of clinical and commercial manufacturing in accordance with regulatory, site, and client requirements. Manufacturing cGMP production activities include manual, semi-automated and automated inspection, complex and bulk packaging. Further, manufacturing operations is tasked to utilize continuous improvement methodologies to realize process optimization, efficiency gains, and waste reduction to maximize capacity outputs.

The department is comprised of four distinct, but integrated, channels. Inspection, Packaging, Label Control, and Pit Crew. The Inspection and Packaging teams execute batch production processes in a cGMP environment, focusing on ‘right first time’ and on-time delivery. The Label Control team is responsible for receiving ready to execute batch records, kitting, and control of printed materials. The Pit Crew team is responsible for storage, movement, and staging of material and product.

The Role:

• Entry-level position with little or no prior relevant training or work experience

• Work is prescribed and completed with close supervision

• Duties are clearly defined, and methods and tasks are described in detail

• Safely operates basic equipment

• Supports cleaning and organizational efforts, including maintaining visual factory

• Required to read, understand, and follow GMP documents

• Participates in area continuous improvement activities

• Reports safety, quality concerns, and recommends improvements

• Demonstrates mathematical skills, including the ability to perform addition, subtraction, multiplication, division, and conversions

• Accurately count product via product count procedures

• Must be able to effectively palletize product and material per written specifications

Inspection

• Perform inspection techniques for manual visual inspection product families

• Perform inspection activities while sitting in a lighted booth for a 12-hour shift

• Perform inspection activities while operating in a Semi-Automated Syringe Inspection system and a Semi-Automated Vial Inspection System

• Perform inspection activities within a fully automated inspection process

Packaging

• Perform basic packaging activities by constructing secondary and tertiary containers for finished packaging products

• Must be able to stand for a 12-hour shift

• Must be able to perform manual packaging and labeling activities within complex packaging operations

Label Control

• Works autonomously OR with limited supervision within established procedures

• Required to read, understand, follow, and review GMP documents

• Demonstrates mathematical skills, including the ability to perform addition, subtraction, multiplication, division, and conversions

• Collaborates and communicates with support teams

• Utilize the assigned logbook to document workstation line clearances

• Ensures batch readiness by gathering materials and documents required for such activities

• High attention to detail due to criticality of labeling process

• Verification and inspection of printed labels

• Gather and Issue pre-printed material component

• Perform reconciliation/destruction and return of printed materials

The Candidate

• High School/GED

• 0-2 years of experience

• GMP experience preferred

P osition Benefits:

• 152 hours PTO & 8 Holidays

• Medical, Dental & Vision Benefits and 401k

• Tuition Reimbursement

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.

Catalent is committed to the health and safety of its employees, visitors and the customers and patients we serve. As a result of the global pandemic, we have modified many of our recruitment and on-boarding processes to maintain everyone’s safety. The Human Resources teams will communicate all necessary safety processes and procedures throughout each stage.

personal initiative. dynamic pace. meaningful work.

Visit Catalent Careers (https://careers.catalent.com/us/en) 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 (https://cdn.catalent.com/files/legal/CCPA-Privacy-Notice-at-Collection-for-California-Employees-and-Applicants-English.pdf) .