Pre-Production Associate

CATALENT CTS (SINGAPORE) PRIVATE LIMITED; Região Norte; On-site; BRL 194,000 - 259,000; Full time

Benefits offered by this job

Annual Salary

Job summary

Catalent is seeking a Pre-Production Associate for our Singapore site to coordinate packaging of clinical trial supplies, acting as the link between Project Management and Operations. You will plan pack designs, raise QIFs when designs deviate, and ensure GMP-compliant documentation.

Responsibilities include procuring packaging components, coordinating with PM on client docs, and setting up packaging configurations in the Global Scan Assembly system, with LPF and Batch Records managed via

Qualifications

• Experience in pharmaceutical packaging, production planning or GMP environments.
• Fluent in English, written and spoken.
• Strong attention to detail and ability to manage multiple projects.

Responsibilities

• Plan and prioritize Pre-Production packaging for clinical trial supplies.
• Create accurate Pack Designs and ensure GMP-compliant documentation.
• Procure packaging components from approved vendors to hit timelines.
• Coordinate with Project Management to secure client documentation (e.g., Label Approvals).
• Set up labels and packaging configurations in global systems (Label Printing, Global Scan Assembly).
• Prepare LPF and Batch Records documentation, automated via SupplyFlex and manual.

Skills

Pharma packaging

Project coordination

GMP knowledge

English fluency

Excel

JDE

SharePoint

Communication

Tools

Excel

JDE

SharePoint

Job description

Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives.

We are seeking to recruit a Pre-Production Associate for our Singapore site. The Pre Production Associate will be the main point of contact and the link between Project Management and Operations in all secondary packaging activities.

The Role

• Plan and prioritize the Pre-Production aspects of the packaging of clinical trial supplies, including:
• Creation of accurate Pack Designs that reflect the needs of the client and meet GMP requirements.
• Ensure appropriate QIF’s are raised in the event that final Pack Designs differ from the original contract.
• Procurement with approved vendors to purchase required packaging components, label stock and equipment in a timely manner to hit Production timelines
• Working closely with the Project Management team to ensure good understanding of the projects and that all client required documentation is received and approved in a timely manner e.g. Label Approvals
• Working with the Centre of Excellence for Label Printing (Catalent SCH) to organize the set-up of new labels within the label printing system and to set-up local label printing jobs
• Set-up of packaging configurations and packaging jobs within the Global Scan Assembly system
• Creation of accurate packaging and labeling documentation to meet the needs of both the client and regulatory GMP requirements including Label Print Forms (LPF’s) and Batch Records (automated via SupplyFlex and manual)

The Candidate

• Experience within pharmaceutical packaging, packaging design, production planning, supply chain, logistics or a GMP-regulated manufacturing environment would be advantageous
• Fluent in English, both written and spoken
• Critical thinker, problem solver, able to work in a fast paced environment
• High level attention to detail while managing multiple projects and/or priorities under tight deadlines is a must
• Strong computer skills are required – (including, but not limited to, SupplyFlex, Microsoft Excel, JDE, SharePoint and ability to quickly learn new systems/programs)
• Strong organizational skills are required
• Proven written, verbal, and interpersonal communication skills are required.
• Ability to work effectively and efficiently under pressure to meet competing workplace demands and appropriately prioritize is required
• Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form is required

Position Benefits

• Annual Salary

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.

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 @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.

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