Associate Technician, Operations (WDA)-1

MSD INTERNATIONAL GMBH (Singapore Branch); Singapore; On-site; SGD 40,000 - 60,000; Full time

Job summary

A leading biopharmaceutical company seeks an Associate Technician for a 2-year contract in Singapore. The role includes operating in a clean room, performing inspections, and supporting manufacturing processes for lifesaving cancer medications. Candidates should have a diploma along with 2-8 years of relevant industry experience and a good command of English. Opportunities for career growth and a collaborative work environment await successful candidates.

Benefits

Limitless opportunities in Pharmaceutical Manufacturing

Engaging team environment

State-of-the-art facility

Qualifications

• Min 2-8 years of experience in manufacturing preferred.
• Ability to support overtime as per business needs.
• Work non-shift hours.

Responsibilities

• Manufacture medicines in a clean room environment.
• Perform vials inspection and routine EM sampling.
• Complete batch documentation and maintain GMP compliance.

Skills

Knowledge of safety procedures/practices

Ability to work collaboratively in a team

Initiative and willingness to speak up

Good command of English

Education

Diploma or Technical School graduate in operations or relevant field

Tools

MES

SAP

GLIMS

Job description

Associate Technician, Operations (WDA) - 2 Years Contract

THE OPPORTUNITY

• Fantastic entry point into the world of sterile manufacturing! Join our team of technicians in Tuas who manufacture lifesaving cancer medications. The position is a 2 year WDA contract at Biotech facility.
• Based in Singapore, the regional hub for Asia Pacific (AP) and top-ranked biopharmaceutical company on The Straits Times and Statista’s list of Best Employers in Singapore for three consecutive years (2020, 2021, 2022).
• Join the premier biopharmaceutical company that has been in Singapore for more than 25 years and in AP for over 60 years.

WHAT YOU WILL DO

As a technician you will join one of the teams who manufacture our medicines. The environment that these teams work in is a clean room environment doing filling and inspection of sterile vials. We are proud of being a diverse organization with an even split of genders at a technician level within Biotech.

As part of the continual evolution of our operations, you will be joining our newly created Inspection & Support Team. The core responsibility of this team will be to perform the vials inspection and routine EM sampling. This team will work normal office hours (8am to 5pm, Monday to Friday) but is expected to step up to support the shift team on overtime if the business need arise.

The main shift team consist of approximately 10 people per shift working on a 24x7 shift pattern. The shift team focus on the operations related to filling of the vials which include Part Prep/ Autoclave, Formulation and Filling.

Expectations

Achieve Competency in the following:

• 1) Core Activities (Qualified in all 3 Core Activities)

• AVIM
• Manual Inspection
• Routine EM Sampling

• 2) Operating Modules (Optional but good to be qualified for at least 1 module)

• Parts Prep/ Autoclave
• Formulation
• Filling

• 3) Proficient in core systems (Perform independently)

• MES
• SAP
• GLIMS

• 4) Proficient all support activities (Perform independently)

• Cleaning & Sanitization
• Material Management
• Waste Management

• 5) MPS (Basic Knowledge)

• Standardized Work
• Problem Solving/ On-Point Problem Solving

Routine Operation

• Core Activities
  • Complete batch documentation as required including raising of exceptions in a DI compliant manner.
  • Perform in-process sampling on semi-finished drug products
  • Perform visual inspection, labeling and packaging on semi-finished drug products
  • Perform all tasks in accordance with the standard operating procedures and maintain strict compliance to GMP at all times.
  • Perform routine QC sampling and in-process testing of the product at various stages throughout manufacturing i.e bioburden sampling, water sampling
  • Perform cleaning and upkeep of the Grade C & D cleanrooms and production equipment.
• Other Support Activities
  • Setup and operate pharmaceutical production equipment including high-speed filling lines for sterile injectables, robotic technology, compounding panels and automatic CIP/SIP.
  • Dispense, formulate and fill active biological product batches as required to meet the production schedule.
  • Microbial sampling and swabbing of room and equipment.
  • Perform filter integrity testing using an automatic filter integrity test unit.
  • Preparation of equipment including loading and starting of sterilisation cycles in autoclaves.

Event, Atypical Investigations

• Report QN/deviations if any.
• Participate in SHE, Business Compliance, cGMP and compliance matters, where applicable.
• Responsible to escalates Operations issues to Lead Tech or Shift Manager when required

Continuous Improvement

• Responsible to participate in Kaizen events in pharm operations in accordance with Kaizen plans when assigned

WHAT YOU MUST HAVE

To be successful in this role, you will have:

• A Diploma or Technical School graduate with background in operations and maintenance or any relevant studies
• Work non-Shift hours
• Must be willing to support overtime according to business needs
• Min 2 -8 years of working experience preferably in manufacturing industry preferred depending on the level of the role you are applying.
• Good understanding of safety procedures/practices.
• Good command of English to be able to read and understand procedures, write simple comments, and communicate with team.
• Ability to work collaboratively in a team environment
• Take initiative and willing to speak up

WHAT YOU CAN EXPECT

• Limitless opportunities across various areas in Pharmaceutical Manufacturing.
• A state-of-the-art facility that delivers solution to its customers world-wide
• Highly engaging team that aims to innovate the future

Our Manufacturing & Supply Division is committed to be the most trusted supplier of biopharmaceuticals worldwide. Our facilities, along with our external contractors, suppliers, and partners, create an interdependent global manufacturing network that’s committed to delivering a high quality, reliable supply to customers and patients on time, every time.