Production Associate

Job description

3374562
Additional Cities

Singapore
Career Level

Experienced
Relocation Assistance

No
Business

GE Healthcare
Business Segment

Healthcare BioPharma
Function

Manufacturing
Country/Territory

Singapore
Postal Code

638034
Role Summary/Purpose

The production associate may have responsibilities including preparation and review of batch records, manufacturing, assembly, basic testing and packaging of products.
Essential Responsibilities

•Generate forms and documents for production job using Oracle and Master Control.
•Review GMP documents before submitting to production for use in production jobs.
•Review all completed batch records and forms from production to ensure compliance to cGMP
and GDP.
•Perform transaction of raw material and finish product in Oracle after completion of all completed
jobs.
•Manage and coordinate all administrative work relating to production e.g. OT form and production
KPI reporting.
•Reads and follows work procedures and schematics or receives verbal instructions regarding
duties to be performed
•Performs manufacturing/assembly operations and various tasks following procedures, bills of
materials, work instructions, and process aid sheets
•Maintains daily production output
•Follows all EHS and Quality policies and procedures
•May participate in quality control inspections
•Works with team lead, engineers, supervisors, and managers to improve quality and process
efficiency
•Other duties as assigned, and may be asked to be included in quality activities, training sessions,
and employee activity teams
•Comply with EHS regulations and policies

Quality Specific Goals:
1.Aware of and comply with the GEHC Quality Manual, Quality Management System, Quality
Management Policy, Quality Goals, and applicable laws and regulations as they apply to this job
type/position
2.Complete all planned Quality & Compliance training within the defined deadlines
3.Identify and report any quality or compliance concerns and take immediate corrective action as
required
4.Knowledge and understanding of production process, work instructions, documentation
configuration control, non-conforming & rework documentation requirements and operates within
them to ensure that a device conforms to it’s specification.
5.Aware of and comply with Calibration, Preventative Maintenance, Material Identification &
Segregation, and Good Documentation Practices, as associated with this job type/position
Qualifications/Requirements

•High School Diploma or local equivalent or 6 months of manufacturing experience
•Ability to communicate, receive and understand instructions regarding duties
to be performed
•Demonstrated ability to detail and quality-minded work habits
•Demonstrated ability to communicate with co-workers and leadership
•Proficient in Microsoft Words, Excel and PowerPoint
Desired Characteristics

•High School Diploma/GED or local equivalent
•2 or more years of related manufacturing and GMP experience
About Us

There is no other life sciences company quite like GE Healthcare Life Sciences. A $5 billion business with more than 11,000 individuals in over 100 countries, we are at work enabling a new era in medicine. For more than 60 years, GE Healthcare Life Sciences has globally supported the development and use of new therapies, helping accelerate the journey from biological understanding to clinical therapy. GE Healthcare Life Sciences works with cutting edge technology enabling and advancing the discovery, diagnosis and medical treatments of the present and the future. We are accelerating biology to cell therapy in ways no other company can.
Primary Country

Singapore
Primary State/Province

Central Singapore
Primary City

Singapore