Takeda
SecondaryPackagingTechnologist
Neural analysis suggests this role is
optimal for Mid+ candidates.
“Secondary Packaging Technologist at Takeda. Skills: process management, cross-functional coordination, vendor/stakeholder management, operational metrics, resource planning, continuous improvement. Carry out packaging and inspection operations. Manufacture product in compliance with procedures”
What You'll Achieve.
Achievement of the Key Performance Indicator targets; Actively participate in the achievement of the relevant KPI’s for your work centre
What They're Looking For.
Must Have
Minimum 1 year of experience in a pharmaceutical environment, Basic PC literacy essential, Ability to follow instructions accurately, Good documentation practice with attention to detail, Excellent attendance and punctuality
Nice to Have
preferably in a cGMP-compliant setting
What You'll Do.
Carry out packaging and inspection operations
Manufacture product in compliance with procedures
Complete all relevant checks
Maintain work place to a high degree of cGMP adherence
Ensure all relevant equipment is in calibration
Comply with all safety procedures
Assembly & Packaging of product
Ensure adequate stock levels of production consumables
Carry out visual inspection of finished product
Perform area clearance and verification
How You'll Work.
Team & Collaboration
Work closely with engineering to ensure timely resolution of downtime issues; Active participation in addressing processing/packaging issues in conjunction with other departments; Employee participation in cross functional training; Active participation in performance dialogues
Communication Scope
interpersonal and communication skills
Full Job Description
By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s [Privacy Notice](https://jobs.takeda.com/privacynotice) and [Terms of Use](https://www.takeda.com/terms-and-conditions/). I further attest that all information I submit in my employment application is true to the best of my knowledge. ## **Job Description** **JOB PURPOSE:** To carry out the packaging and inspection operations in the P2 Secondary Packaging area in accordance with cGMPs. **How You Will Contribute:** **Quality / Safety / 5S:** * Compliance with TILGC quality standards and cGMP pertaining to Production. * Manufacture of product in strict compliance with procedures and batch manufacturing records (BMR’s), incorporating cGMP and safety procedures. * Accurate and timely completion of all relevant checks as per Batch Records and ancillary paper documents. * Maintain an awareness of the focus areas for cGMP to ensure the correct attitudes and behaviours towards cGMP are maintained within your work centre. * Generation of relevant Standard Operating Procedures and Manufacturing Batch Records as required * Maintain your work place to a high degree of cGMP adherence with particular attention to the company 5S program. * Ensure all relevant equipment and in-process test equipment is in calibration. * Strict compliance with all safety procedures including the reporting of all accidents / near misses. * Full cooperation with all onsite safety initiatives. * To proactively ensure that all Health, Safety and Environmental responsibilities area carried out according to EHS regulations and plans. **Performance & Continuous Improvement:** * Maintain a flexible approach to the daily tasks assigned to you within your work centre. * Achievement of the Key Performance Indicator targets. * Strong willingness to learn / apply new tools / techniques. * Practical application of
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