Company description: WuXi Biologics is a world-class biologics services provider (from discovery, through to commercialisation) with global clients in the biopharmaceutical and healthcare industries.
Our mission is to accelerate and transform discovery, development and manufacturing in the fast growing field of biologics to benefit patients worldwide.
The company has sites/offices in China, US, EU, Asia and Israel.
The company currently employs over 5,000 employees worldwide, and are providing services to over 200+ clients globally, including 13 of the top 20 biopharmaceutical companies.
Job description: As a QC Raw Materials Laboratory Technician, youll support the Laboratory Analysts and Senior Analysts with the maintenance of documentation systems within the QC department and the maintenance of laboratory systems, equipment, and testing preparation.
Organization Description WuXi Biologics is a premier provider of biologics services (from discovery to commercialization) with global customers in the biopharmaceutical and healthcare industries.
Were one of the world's top three contract development and manufacturing companies for biopharmaceuticals, we provide our clients with a world-leading open access technology platform.
We enable our clients to research, develop and manufacture drugs from the concept phase to commercial manufacturing.
Our mission is to accelerate and transform discovery, development, and manufacturing in the rapidly growing field of biologics to benefit patients worldwide.
We have sites/offices in China, the US, the EU, and Asia.
We currently employ over 10,000 people and provide services to more than 600 customers worldwide, including the top 20 biopharmaceutical companies.
Department Description As a QC Raw Materials Laboratory Technician, youll be joining an organization where people of all backgrounds and experiences are respected, and where we work together focused on changing lives.
In this role, youll be reporting to the QC Raw Materials and Compendial Senior Scientist.
Essential Duties and Responsibilities Following Good Manufacturing Practice requirements in all aspects of role.
Following lab procedures and standards.
Supporting QC Analysts for preparation of testing.
Maintaining the consumable and reagent levels.
Supporting Health and Safety walkthroughs and associated tasks.
Collation and entry of stock, inventory to LIMS (Laboratory Information System) as applicable.
Completes record of results as per good document practices when required.
Responsible for managing temperature records and escalation of any out of specifications or adverse trends.
Be responsible for arranging all QC documents to take effect and inform involved departments and document coordinators.
Be responsible for the regular review of QC documents, preparing the annual review plan, documentation distribution and notifying coordinators of each department.
Maintaining QC equipment in a validated GMP state, as per QC procedures.
Completing QC tasks as directed by QC management.
Recommends and implements revisions, corrections and changes to laboratory procedures, test equipment procedures and test methods when required.
Responsible for completing Training requirements in a timely manner.
Prepares for and participates in Regulatory and internal audits as directed.
All employees are responsible for minimising both the Environmental and Health & Safety effects of the work that they perform Operations within a GMP environment.
Responsible for supporting QC activities - equipment calibrations & verifications, equipment daily checks, inventory control, glassware, cleans and solution preparation.
Assisting in laboratory investigations as appropriate.
Supporting the QC Department on any additional tasks as per business needs.
Technical Competencies Excellent organizational skills, prioritizing abilities and work efficiently.?
Capable of planning ahead to ensure any problems are resolved promptly and accurately.?
Excellent communication and interpersonal skills.
Experience?
Experience in working as part of a team and as an individual contributor.
Strong communication skills.
Excellent attention to detail.
Performing work assignments accurately, timely and in a safe manner.
Previous experience in a Quality Control/GMP environment is an advantage Knowledge?
Knowledge / experience in the operation of GMP Pharmaceutical Sites would be an advantage.?
Qualifications?
Diploma / degree qualification is desirable.
Behavioural Competencies??
Excellent communication and interpersonal skills.
Ability to demonstrate troubleshooting and problem-solving skills.
Comfortable in a fast-paced working environment and able to adjust workload based upon changing priorities.
Flexible approach to work and a positive attitude will be a good fit within the team dynamic.
Demonstrate strong ethics in adhering to company procedures and policies, regulatory standards, and our customers expectations.
Collaborative and inclusive approach to work and your colleagues.?
Engage cross functionally in conjunction with a site-based team.?
As we extend our global reach, we need colleagues interested in change, in challenge, and in building a new future together.
Reach beyond yourself and discover your true potential!
If you have the ability to thrive in a dynamic and fast-paced environment and feel that the moment has come for you to be part of such an exciting journey towards accomplishing our vision -Any drug can be made, and any disease can be treated- dont miss out on this opportunity to join us and reach beyond yourself and discover your true potential.
Apply now!
Would you like to know more before you apply?
Please visit us ator contact us via WuXi Biologics is an equal opportunities employer.
Skills: GMP QC Documentation Laboratory Benefits: Bonus Canteen Life Assurance Paid Holidays Parking Pension VHI