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Catalent, Inc.

Pre-Production Associate

Posted 9 Days Ago
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In-Office
Singapore, SGP
Entry level
In-Office
Singapore, SGP
Entry level
Coordinates pre-production packaging activities for clinical trial supplies, serving as the link between Project Management and Operations. Responsibilities include creating GMP-compliant pack designs, procuring packaging components, coordinating label approvals and printing, configuring packaging jobs, and preparing labeling and batch documentation. The role requires strong organization, attention to detail, communication, computer proficiency, and the ability to manage multiple priorities in a fast-paced pharmaceutical manufacturing environment.
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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.

Visit Catalent Careers 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 [email protected]. 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 [email protected] for us to investigate with local authorities.

Catalent, Inc. Singapore, Singapore, SGP Office

Singapore, Singapore

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