Manufacturing Supervisor

Job description

  Job facts

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

Key Responsibilities :

·  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.
·  Implement, enforce and take ownership on all RSTO’s Safety, Health & Environmental (SHE) requirements and initiatives within his/her areas of responsibilities.
·  Ensure all employees are competent and provided with the necessary tools and equipment to work safely and without health risks.
·  Responsible for the hands-on, daily supervision of GMP manufacturing operations and personnel within the manufacturing site(s).
·  Participate in all aspects of personnel management (interviewing, training, coaching and developing).
·  Responsible for all day to day operations in the GMP manufacturingsuite, as assigned. Specific responsibilities will include:
·  Hands on supervision and support of manufacturing staff.
·  Write and revise batch records, SOPs and solution preparation documents to ensure compliance to GMPs.
·  Timely review of completed manufacturing documentation (batch records, worksheets, solution docs., 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.
·  Work effectively within the management team to execute goals, objectives and tasks to achieve desired results.
·  Provide assistance in problem solving manufacturing process issues.
·  Timely reporting, investigation and resolution of manufacturing deviations.
·  Serve as lead trainer on manufacturing processes and all related equipment.
·  Provide cross-functional coordination and issue resolution.
·  Coordinate equipment maintenance activities

Qualifications

·  Degree/Diploma in Life Sciences or Engineering discipline (or equivalent).
·  Minimum 3 years of relevant industry experience. Preferably 2 years of supervisory experience in a cGMP manufacturing environment.
·  Knowledge of GMP systems
·  Good interpersonal and communication skills
·  Willingness to train extensively on Biologics production operations while on the job.
·  Excellent leadership skills in team based environment
·  Demonstrated ability to trouble shoot process and equipment problems with good problem solving skills
·  Prepared to work on 12-hour shift schedulle

Appointment to this position will be on local Singapore salary and benefits package.

Roche is an equal opportunity employer.
Manufacturing, Manufacturing > General Manufacturing

·  Who we are

At Roche, 94,000 people across 100 countries are pushing back the frontiers of healthcare. Working together, we’ve become one of the world’s leading research-focused healthcare groups. Our success is built on innovation, curiosity and diversity.

Roche is an equal opportunity employer.