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Salary
$121k – $270k per year (Estimated)
Location
In office (Singapore)
Seniority
Staff · 5+ years exp
Employment
Full-Time
Overview
Company
Impact
Profile match
Roche is a Swiss healthcare group founded in Basel in 1896 and is unusual in operating two large divisions of comparable importance: prescription medicines and in vitro diagnostics. The pharmaceutical business is built on oncology, neurology, immunology, ophthalmology and haemophilia, with products such as Ocrevus, Hemlibra, Perjeta and Vabysmo, while the diagnostics division supplies laboratory analysers, molecular tests and sequencing systems to hospitals worldwide. The group owns the American biotechnology company Genentech outright and the Japanese firm Chugai in majority, is controlled by a family shareholder pool, and spends among the largest research budgets in the industry.

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

A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love.

That’s what makes us Roche.

The Opportunity

This position has overall accountability for hands-on, daily supervision of manufacturing operations and personnel while in full compliance with current Good Manufacturing Practices (cGMPs) and Roche’s corporate principles, quality policies and standards.

Key Responsibilities:

  • Work effectively within the management team to execute goals, objectives and tasks to achieve desired results.

  • Responsible for the hands-on, daily supervision of GMP manufacturing operations and personnel within the manufacturing site(s).

  • Responsible for all day to day operations in the GMP manufacturing suite, as assigned. Specific responsibilities will include:

    • Hands on supervision and support of manufacturing staff.

    • Create and revise batch records, standard operating procedures (SOPs) and other supporting documents in compliance with cGMP guidelines.

    • Timely review of completed manufacturing documentation (batch records, forms and logbooks etc.).

    • Schedule manufacturing staff to ensure manufacturing timelines are met.

    • Review production schedule and priorities to establish shift assignments.

    • Ensure required levels of safety, quality and productivity are met.

  • Provide assistance in problem solving of manufacturing process issues.

  • Timely reporting, investigation and resolution of manufacturing deviations.

  • Provide expertise in cross-functional coordination and issue resolution.

  • Coordinate equipment maintenance activities.

  • Make recommendations to management on matters relating to human resources, budget and department operations.

  • Has contact with internal personnel and outside representatives concerning scheduling of specific projects or contracts.

  • May be involved in conducting briefings and participating in meetings for internal and external representatives concerning immediate area of responsibility.

  • Lead cross-functional improvement initiatives and closure of audit commitments.

  • Participate in all aspects of personnel management (interviewing, training, coaching and developing).

Preferred

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 fostering and advocating a continuous improvement mindset and culture throughout the organization, by encouraging experimentation and learning.

Who You Are

  • Degree in Life Sciences or Engineering discipline (or equivalent)

  • Minimum 5 years of related working experience or equivalent holders with combination of education and related work experience

  • 3 or more years in managing teams in biotechnology or pharmaceutical operating environment is preferred

  • Knowledge of GMP systems and biologics production process

  • Good interpersonal and communication skills

  • Excellent leadership skills in team-based environment

  • Demonstrated advanced troubleshooting skills for resolution of process and equipment problems

  • Prepared to work on 12-hour shift schedule

  • Must be able to carry heavy loads of up to 25kg

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.

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