Associate Specialist, Quality Control
5 days ago
Job Description
THE OPPORTUNITY
Be part of the team that ensures sustainable products meet standard quality and are committed to delivering to customers worldwide
Based in Singapore , the regional hub for
Asia Pacific (AP)
and
top-ranked biopharmaceutical company on the Straits Times
and
Statista’s list of Best Employers in Singapore for three consecutive years (2020, 2021, 2023).
Join the premier biopharmaceutical company
that has been
in Singapore for more than 25 years and in AP for over 60 years.
Our Quality group ensures every single material inside our products is manufactured, processed, tested, packaged, stored, and distributed aligned with our incredibly high standards of quality and meets all regulatory requirements. Partnering across our internal manufacturing facilities, external contract manufacturers, and suppliers, we create an interdependent global manufacturing network committed to delivering a compliant, reliable supply to customers and patients on time, every time.
WHAT YOU WILL DO
The position of Associate Specialist in Value Stream (VSM) Laboratory will be responsible for ensuring and maintaining high standards of quality and compliance within our organization.
In this role, you will be responsible for all or a subset of the key responsibilities below:
Perform analytical testing of intermediates and finished drug substances/products according to approved procedures.
Participate in analytical method transfer/validation/verification, new product introduction, and equipment qualification.
Assist in conducting laboratory investigations and ensure effective implementation of related actions within the agreed timeframe.
Provide inputs for the development and revision of Analytical Standards, Standard Operating Procedures, Work Instructions, and other GMP documents.
Maintain proper laboratory housekeeping and ensure inspection readiness.
Execute quality and laboratory improvement initiatives and other special projects.
WHAT YOU MUST HAVE
Bachelor's Degree in Chemistry/Biochemistry with a minimum of 2 years of working experience.
Good writing and communication skills.
Demonstrated knowledge and understanding of cGMP, GLP, and associated regulatory expectations related to Analytical testing is preferred.
This is a career conversion programme under Workforce Singapore (WSG), and candidates must meet the following criteria and are open to the following conditions:
Singaporeans/Singapore PRs only.
PMETs/Mid-Careerists with no prior work experience in the Biopharma industry are welcomed to apply.
Open to a two years contract.
WHAT YOU CAN EXPECT
Limitless opportunities across various areas in Manufacturing; well-structured career path.
A state-of-the-art facility that delivers solutions to its customers worldwide.
We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. We are an equal opportunity employer, committed to fostering an inclusive and diverse workplace.
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