Quality Specialist Trainee - Attach & Train program
Roche is hiring a Quality Specialist Trainee - Attach & Train program. Level rates it ; you can apply on Roche.
Level's read on this job
- On Level's scale, this role is Little AI ●○○○: aI is not part of the work.
- Tools and skills the posting cites include quality assurance, cgmp and batch review.
- Level classifies it as a junior role.
- Level lists 1,200+ other open roles at Roche.
AI in this role
Provide QA oversight for manufacturing operations to ensure medicinal products comply with global standards and regulations.
At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.
The Position
Purpose
- Provide QA oversight for RSTO to ensure that investigational medicinal products (IMPs) and commercial medicinal products are manufactured in accordance with global Roche, Pharmaceutical Quality System (PQS) and local site requirements.
- Responsible for escalation of quality issues following the criteria defined in current governing documents
- Support and/or perform routine “Make, Assess, Release” operations to meet targets and timelines
- Participate in the design and implementation of department and cross-functional initiatives
- To undertake additional responsibilities as required by Quality Management to meet business needs.
Key Responsibilities
Technical and Functional:
- Perform batch record, batch reports, logbook, cGMP documents and audit trail review to ensure quality of product, compliance to Roche requirements and on-time batch disposition per defined adherence to lead time
- Perform the following activities with QA oversight in accordance with Health Authority, Roche site and global PQS requirements:
- Provide guidance on categorization of unplanned events
- GMP area, Utilities and equipment release
- Review and approve discrepancies justification for resuming GMP processing.
- Execute Periodic Floor Walk
- Perform assigned tasks and manage competing priorities while meeting timelines to achieve company goals and department objectives
- Notify Senior Management of potential quality, regulatory and compliance issues
Safety, Health & Environment:
- Comply with all RSTO’s Safety, Health & Environmental (SHE) requirements, never put oneself and others at safety & health risks, and report any workplace accidents, near misses and hazards as soon as practicable.
- Observe all RSTO’s site security measures at all times, and report any suspicious characters/objects & damaged security mechanisms to Site Security immediately.
Lean Production System:
- Embody PT Lean Production System (LPS), while demonstrating a continuous improvement mindset and behaviors through the use and application of LPS tools for continuous improvement initiatives.
Qualifications
- Degree in Life Sciences or Engineering discipline or equivalent
- 1-3 years of related working experience for degree holders or equivalent holders with combination of education and relative work experience
- Related working experience in a biotech or pharmaceutical operating environment is a plus
- Good knowledge of cGMP and GDP relevant to the pharmaceutical industry
- Executes defined procedures well and shows progression in performing tasks independently
- Displays good level of problem solving ability and begins to offer suggestions on complex issues
- Ability to prioritise, plan and manage deliverables effectively
- Meticulous, systematic and of an analytical mind
- Good interpersonal, oral and written communication skills
- Proactive team player
- Flexible in work hours (including shift work) to meet business objectives
Who we are
A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.
Let’s build a healthier future, together.
Roche is an Equal Opportunity Employer.
How we rate this
Quality Specialist Trainee - Attach & Train program at Roche rates 0 out of 100 for how much of the daily work is AI. That makes it Little AI (AI Level 1 of 4). The level is about AI in the job, not seniority.
Little AI. AI is not part of the work.
- ●●●● Builds AI80 to 100
- ●●●○ Works on AI60 to 79
- ●●○○ Uses AI40 to 59
- ●○○○ Little AI0 to 39
Levels come from how often the tools, models and workflows of the role are named in the posting itself. Read the description and count the AI tools, models and workflows it names.
Prepare for this job
Built from this posting and from similar jobs on Level.
Skills and AI tools this role asks for
Questions you could be asked
- Tell me about a project where quality assurance was part of your work. What did you do?
- Tell me about a project where cgmp was part of your work. What did you do?
- Tell me about a project where batch review was part of your work. What did you do?
- Tell me about a project where compliance was part of your work. What did you do?
- Tell me about a project where lean production was part of your work. What did you do?
Adapt your resume
- List these exact terms on your resume: Quality Assurance, Cgmp, Batch Review, Compliance, and Lean Production. An applicant tracking system matches the wording, not the idea.
- Attach one line of real, concrete experience to at least one of them. A tool named with nothing behind it rarely survives a human read.
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