Merck Gruppe - MSD Sharp & Dohme
Assoc Technician, Operations (WDA)
Merck Gruppe - MSD Sharp & Dohme, Rahway, New Jersey, us, 07065
Job Description
Assoc. Tech, Operations (WDA) 2 Year contract
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 two consecutive years (2020, 2021).
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 Routine Operation
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.
Perform routine QC sampling and in-process testing of the product at various stages throughout manufacturing i.e bioburden sampling, water sampling
Microbial sampling and swabbing of room and equipment.
Perform cleaning and upkeep of the Grade C & D cleanrooms and production equipment.
Perform filter integrity testing using an automatic filter integrity test unit.
Preparation of equipment including loading and starting of sterilisation cycles in autoclaves.
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.
Event, Atypical Investigations
Report QN/deviations if any.
Participate in SHE, Business Compliance, cGMP and compliance matters, where applicable.
Responsible to escalat…
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
Must be willing to work in 24x7 rotating shift pattern
Min 2 years of working experience preferably in manufacturing industry preferred
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
This is a Career Conversion Program(CCP for Advanced Biopharmaceuticals Manufacturing Professionals (Place-and-Train) under Workforce Singapore (WSG) and candidates must meet the following criteria and are open to the following conditions:
PMETs/Mid-Careerist with minimum 2 years of working experience
Singaporeans/PRs only
We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. We are an equal opportunity employer, committed to fostering an inclusive and diverse workplace.
Required Skills Accountability, Accountability, Autoclaves, Biomanufacturing, Chemical Plant Operations, Computer Literacy, Environmental Controls, GMP Compliance, Good Manufacturing Practices (GMP), Healthcare Innovation, Human Factors, Labeling Equipment, Labels, Manufacturing Operations, Operations Management, Operations Support, Pharmaceutical Manufacturing, Pharmaceutical Production, Pharmaceutical Quality Assurance, Production Scheduling, Product Testing, Regulatory Compliance, Regulatory Compliance Consulting, Safety, Health, Environment and Quality (SHEQ), Safety Awareness {+ 5 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)
Job Posting End Date: 01/30/2026
*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.
#J-18808-Ljbffr
Assoc. Tech, Operations (WDA) 2 Year contract
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 two consecutive years (2020, 2021).
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 Routine Operation
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.
Perform routine QC sampling and in-process testing of the product at various stages throughout manufacturing i.e bioburden sampling, water sampling
Microbial sampling and swabbing of room and equipment.
Perform cleaning and upkeep of the Grade C & D cleanrooms and production equipment.
Perform filter integrity testing using an automatic filter integrity test unit.
Preparation of equipment including loading and starting of sterilisation cycles in autoclaves.
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.
Event, Atypical Investigations
Report QN/deviations if any.
Participate in SHE, Business Compliance, cGMP and compliance matters, where applicable.
Responsible to escalat…
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
Must be willing to work in 24x7 rotating shift pattern
Min 2 years of working experience preferably in manufacturing industry preferred
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
This is a Career Conversion Program(CCP for Advanced Biopharmaceuticals Manufacturing Professionals (Place-and-Train) under Workforce Singapore (WSG) and candidates must meet the following criteria and are open to the following conditions:
PMETs/Mid-Careerist with minimum 2 years of working experience
Singaporeans/PRs only
We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. We are an equal opportunity employer, committed to fostering an inclusive and diverse workplace.
Required Skills Accountability, Accountability, Autoclaves, Biomanufacturing, Chemical Plant Operations, Computer Literacy, Environmental Controls, GMP Compliance, Good Manufacturing Practices (GMP), Healthcare Innovation, Human Factors, Labeling Equipment, Labels, Manufacturing Operations, Operations Management, Operations Support, Pharmaceutical Manufacturing, Pharmaceutical Production, Pharmaceutical Quality Assurance, Production Scheduling, Product Testing, Regulatory Compliance, Regulatory Compliance Consulting, Safety, Health, Environment and Quality (SHEQ), Safety Awareness {+ 5 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)
Job Posting End Date: 01/30/2026
*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.
#J-18808-Ljbffr