Job Description

Associate Technician, Operations (WDA) - 2 Years Contract

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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 be 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 escalate Operations issues to Lead Tech or Shift Manager when required

Continuous Improvement

Responsible to participant 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.

Required Skills:

Accountability, Accountability, Autoclaves, Biological Manufacturing, Chemical Plant Operations, Computer Literacy, Environmental Controls, GMP Compliance, Good Manufacturing Practices (GMP), Healthcare Innovation, Human Factors, Manufacturing Operations, Mechanical Equipment Maintenance, Operations Management, Operations Support, Pharmaceutical Manufacturing, Pharmaceutical Packaging, Pharmaceutical Production, Pharmaceutical Quality Assurance, Production Scheduling, Regulatory Compliance, Safety, Health, Environment and Quality (SHEQ), Safety Awareness, Safety Procedures, Shift Work {+ 4 more}

Preferred Skills:

Current Employees apply HERE


Current Contingent Workers apply HERE

Search Firm Representatives Please Read Carefully

Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

Employee Status:

Intern/Co-op (Fixed Term)

Relocation:

VISA Sponsorship:

Travel Requirements:

Flexible Work Arrangements:

Not Applicable

Shift:

Valid Driving License:

Hazardous Material(s):

Job Posting End Date:

11/22/2025

A job posting is effective until 11:59:59PM on the day

BEFORE

the listed job posting end date. Please ensure you apply to a job posting no later than the day

BEFORE

the job posting end date.

Requisition ID:

R368015