Lonza
Specialist ,QC ( Sample Management)
Singapore · Work style not stated · Full time
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About the role
Description from the employer’s posting. Check the employer’s page for the current version.
- EmployerLonza
- LocationSingapore
- Work styleWork style not stated
- Employment typeFull time
- Employer posted
This role is responsible to coordinate and manage QC samples (receive, retain, shipment), manage and coordinate on-site / off-site archival of QC documents, coordinate equipment maintenance and revision of related operation procedure. Role is also required to coordinate with the other departments to ensure timely delivery of samples/results and equipment maintenance performed.
What you’ll get
An agile career and dynamic working culture in a global life sciences leader.
An inclusive and ethical workplace that values diversity and integrity.
Competitive compensation programs that recognize high performance.
Professional growth opportunities through cross-functional projects and global exposure.
Comprehensive medical insurance, with the option to enroll family members at partially subsidized premiums.
Company transport provided from designated MRT locations to and from the Tuas site.
Show full description
Access to Lonza’s full suite of employee benefits: www.lonza.com/careers/benefits
What you’ll do:
To manage QC samples (including receipt, storage, shipment and discard of samples).
Control and audit of retain samples (process and raw materials).
Coordination of Sample Logistics documentation and QC assay sheet issuance.
Manage and coordinate on-site/ off-site archival of QC documents.
Write, maintain, edit and review Standard Operating Procedures.
Write deviation and change request
Maintain data and records in compliance with regulatory requirements and Standard Operating Procedures.
Actively contributes to operational efficiency/continuous improvement initiatives.
Any other duties as assigned by your Supervisor/Manager.
What we’re looking for:
Degree/Diploma in a relevant Chemistry, Science field or Equivalent.
Relevant experience and accomplishment to dictate final position for which the candidate may qualify.
Well versed in cGMP regulations.
Knowledge of area specific responsibilities.
Good problem solving and analytical skills.
Good communication skills.
A key team player.
About Lonza
At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of.
Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board.
Ready to shape the future of life sciences? Apply now.
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At a glance
- Employment typeFull time
- Employer posted
- Added to ROLIVA
- Last checked