MSD
Job Description
POCS – Rahway: Technician, Operations (FLEx Sterile Filling Technician)
Level: O3
Job Family: Manuf/Operations
Senior Technician, Operations
Pharmaceutical Operations and Clinical Supply is seeking highly motivated individuals for R&D Operations roles in our Rahway, NJ, Formulation, Laboratory, and Experimentation (FLEx) Center to support drug product development and GMP clinical supply of sterile dosage forms. Positions will support development and clinical manufacturing and supply, as part of the FLEx‑Sterile team, specifically in Filling.
This position will be responsible for hands‑on processing activities that include sterile filling and lyophilization, and capping. There will be opportunity for technicians to cross‑train in other parts of the process including thaw, formulation, visual inspection, and sterile supply. These individuals are expected to partner with, and support formulation development colleagues in further understanding and knowledge capture of processes, which could include providing feedback on product and process development.
These roles require adherence to GMP procedures, strong attention to detail in completing GMP documentation, proficiency in electronic systems, and participation in continuous improvement projects. Positions may also support commissioning, qualification, and demonstration of new equipment and technologies. Successful candidates will collaborate closely with team members and partner groups including formulators, engineers, Quality, Safety, and Facilities management to drive overall success and performance of the area and clinical pipeline.
Key Responsibilities
Aseptic Processing:
Perform sterile filling operations in compliance with Good Manufacturing Practices (GMP) and Standard Operating Procedures (SOPs). Experience with operating isolator filling machines is required.
Aseptic experience:
Experience in working in Grade A environment is required, including aseptic qualification and performing environmental monitoring.
Isolator Operation:
Operate and maintain large complex isolators, ensuring optimal performance and adherence to safety protocols.
Documentation:
Maintain accurate records of inspection results and maintain accurate records of findings in an electronic system. Knowledge of PAS‑X is preferable.
GMP:
Follow established inspection batch records, protocols and quality standards to ensure compliance with industry regulations. Able to report any recurring issues or trends to management for further investigation.
Cleanroom Environment:
Able to gown and work in Grade C conditions, maintaining good aseptic cleanroom behaviors.
Collaboration:
Able to communicate clearly with team and work closely with other teams to ensure on time delivery.
Training and Compliance:
Assist in training new staff on sterile supply procedures and protocols, ensuring adherence to GMP standards.
Leadership:
Identify and escalates issues, perform basic troubleshooting, capture learnings to improve systems and processes. Organizes and prioritizes own work to meet shop floor priorities and identifies discrepancies in advance. Attends and actively participates in safety, quality, and process improvement initiatives to enhance flexibility, efficiency, and compliance.
Schedule Adherence:
Understands schedule adherence impact and communicates risk. Maintains a continuous improvement mindset and implements initiatives to increase efficiency or reduce risk to schedule adherence.
Compliance:
Identifies and addresses compliance, environmental, safety and process deviations as appropriate while notifying management. Able to redline SOPs for continuous improvement.
Investigations and Corrective Actions:
Supports investigations and implementation of corrective/preventative actions.
Positions are based in Rahway, NJ and 100% on-site.
Education Minimum Requirements
High School Diploma/GED, with at least 5 years in pharmaceutical manufacturing or processing.
OR Associates Degree in Science/Engineering related field with at least 3 years in pharmaceutical manufacturing.
OR Bachelors Degree in Engineering Technology or related field.
Required Experience and Skills
Relevant GMP Pharmaceutical experience, or equivalent (e.g. chemical, nuclear, military experience).
Demonstrated written and verbal communication skills.
Proficiency in computer systems and applications including but not limited to: Microsoft Office (Word, Excel and Outlook), Equipment HMI use, MODA, PAS‑X, SAP, Calibration/Maintenance Database Systems.
Must be willing and able to lift 50 lbs, bend, stoop, squat, crawl, twist, climb ladders, and don & wear cleanroom protective gowning including respirators.
Supports investigations and implementation of corrective/preventative actions.
Flexibility working overtime is a requirement in manufacturing.
Preferred Experience and Skills
Familiarity with regulatory requirements and Good Documentation Practices (GDP).
Experience with highly complex and state-of-the-art equipment, isolators, containment technology, aseptic filling using automated machinery, sterile manufacturing, SAP or other ERP systems.
Associates Degree in science or related field.
BioWork Certificate (working in an FDA or similar regulated industry).
Experience with automated systems (MES, SAP or similar).
Demonstrated troubleshooting / problem‑solving skills.
Demonstrated ability to identify and initiate process improvements.
Shift and Work Details First and second shift openings available.
Resident and Accommodation Information US and Puerto Rico Residents Only:
Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Click here if you need an accommodation during the application or hiring process.
San Francisco Residents Only:
We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance.
Los Angeles Residents Only:
We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance.
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 and Miscellaneous Employee Status: Regular
Relocation: Domestic
VISA Sponsorship: No
Travel Requirements: No Travel Required
Flexible Work Arrangements: Not Applicable
Shift: 1st - Day, 2nd - Evening
Valid Driving License: No
Hazardous Material(s): n/a
Job Posting End Date: 12/5/2025
U.S. Hybrid Work Model Effective September 5, 2023, employees in office‑based positions in the U.S. will be working a Hybrid work consisting of three total days on‑site per week, Monday - Thursday, although the specific days may vary by site or organization, with Friday designated as a remote‑working day, unless business critical tasks require an on‑site presence. This Hybrid work model does not apply to, and daily in‑person attendance is required for, field‑based positions; facility‑based, manufacturing‑based, or research‑based positions where the work to be performed is located at a Company site; positions covered by a collective‑bargaining agreement (unless the agreement provides for hybrid work); or any other position for which the Company has determined the job requirements cannot be reasonably met working remotely. Please note, this Hybrid work model guidance also does not apply to roles that have been designated as “remote”.
Equal Employment Opportunity Statement As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit: EEOC Know Your Rights EEOC GINA Supplement. We are proud to be a company that embraces the value of bringing together talented and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. Learn more about your rights, including under California, Colorado and other US State Acts.
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Level: O3
Job Family: Manuf/Operations
Senior Technician, Operations
Pharmaceutical Operations and Clinical Supply is seeking highly motivated individuals for R&D Operations roles in our Rahway, NJ, Formulation, Laboratory, and Experimentation (FLEx) Center to support drug product development and GMP clinical supply of sterile dosage forms. Positions will support development and clinical manufacturing and supply, as part of the FLEx‑Sterile team, specifically in Filling.
This position will be responsible for hands‑on processing activities that include sterile filling and lyophilization, and capping. There will be opportunity for technicians to cross‑train in other parts of the process including thaw, formulation, visual inspection, and sterile supply. These individuals are expected to partner with, and support formulation development colleagues in further understanding and knowledge capture of processes, which could include providing feedback on product and process development.
These roles require adherence to GMP procedures, strong attention to detail in completing GMP documentation, proficiency in electronic systems, and participation in continuous improvement projects. Positions may also support commissioning, qualification, and demonstration of new equipment and technologies. Successful candidates will collaborate closely with team members and partner groups including formulators, engineers, Quality, Safety, and Facilities management to drive overall success and performance of the area and clinical pipeline.
Key Responsibilities
Aseptic Processing:
Perform sterile filling operations in compliance with Good Manufacturing Practices (GMP) and Standard Operating Procedures (SOPs). Experience with operating isolator filling machines is required.
Aseptic experience:
Experience in working in Grade A environment is required, including aseptic qualification and performing environmental monitoring.
Isolator Operation:
Operate and maintain large complex isolators, ensuring optimal performance and adherence to safety protocols.
Documentation:
Maintain accurate records of inspection results and maintain accurate records of findings in an electronic system. Knowledge of PAS‑X is preferable.
GMP:
Follow established inspection batch records, protocols and quality standards to ensure compliance with industry regulations. Able to report any recurring issues or trends to management for further investigation.
Cleanroom Environment:
Able to gown and work in Grade C conditions, maintaining good aseptic cleanroom behaviors.
Collaboration:
Able to communicate clearly with team and work closely with other teams to ensure on time delivery.
Training and Compliance:
Assist in training new staff on sterile supply procedures and protocols, ensuring adherence to GMP standards.
Leadership:
Identify and escalates issues, perform basic troubleshooting, capture learnings to improve systems and processes. Organizes and prioritizes own work to meet shop floor priorities and identifies discrepancies in advance. Attends and actively participates in safety, quality, and process improvement initiatives to enhance flexibility, efficiency, and compliance.
Schedule Adherence:
Understands schedule adherence impact and communicates risk. Maintains a continuous improvement mindset and implements initiatives to increase efficiency or reduce risk to schedule adherence.
Compliance:
Identifies and addresses compliance, environmental, safety and process deviations as appropriate while notifying management. Able to redline SOPs for continuous improvement.
Investigations and Corrective Actions:
Supports investigations and implementation of corrective/preventative actions.
Positions are based in Rahway, NJ and 100% on-site.
Education Minimum Requirements
High School Diploma/GED, with at least 5 years in pharmaceutical manufacturing or processing.
OR Associates Degree in Science/Engineering related field with at least 3 years in pharmaceutical manufacturing.
OR Bachelors Degree in Engineering Technology or related field.
Required Experience and Skills
Relevant GMP Pharmaceutical experience, or equivalent (e.g. chemical, nuclear, military experience).
Demonstrated written and verbal communication skills.
Proficiency in computer systems and applications including but not limited to: Microsoft Office (Word, Excel and Outlook), Equipment HMI use, MODA, PAS‑X, SAP, Calibration/Maintenance Database Systems.
Must be willing and able to lift 50 lbs, bend, stoop, squat, crawl, twist, climb ladders, and don & wear cleanroom protective gowning including respirators.
Supports investigations and implementation of corrective/preventative actions.
Flexibility working overtime is a requirement in manufacturing.
Preferred Experience and Skills
Familiarity with regulatory requirements and Good Documentation Practices (GDP).
Experience with highly complex and state-of-the-art equipment, isolators, containment technology, aseptic filling using automated machinery, sterile manufacturing, SAP or other ERP systems.
Associates Degree in science or related field.
BioWork Certificate (working in an FDA or similar regulated industry).
Experience with automated systems (MES, SAP or similar).
Demonstrated troubleshooting / problem‑solving skills.
Demonstrated ability to identify and initiate process improvements.
Shift and Work Details First and second shift openings available.
Resident and Accommodation Information US and Puerto Rico Residents Only:
Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Click here if you need an accommodation during the application or hiring process.
San Francisco Residents Only:
We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance.
Los Angeles Residents Only:
We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance.
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 and Miscellaneous Employee Status: Regular
Relocation: Domestic
VISA Sponsorship: No
Travel Requirements: No Travel Required
Flexible Work Arrangements: Not Applicable
Shift: 1st - Day, 2nd - Evening
Valid Driving License: No
Hazardous Material(s): n/a
Job Posting End Date: 12/5/2025
U.S. Hybrid Work Model Effective September 5, 2023, employees in office‑based positions in the U.S. will be working a Hybrid work consisting of three total days on‑site per week, Monday - Thursday, although the specific days may vary by site or organization, with Friday designated as a remote‑working day, unless business critical tasks require an on‑site presence. This Hybrid work model does not apply to, and daily in‑person attendance is required for, field‑based positions; facility‑based, manufacturing‑based, or research‑based positions where the work to be performed is located at a Company site; positions covered by a collective‑bargaining agreement (unless the agreement provides for hybrid work); or any other position for which the Company has determined the job requirements cannot be reasonably met working remotely. Please note, this Hybrid work model guidance also does not apply to roles that have been designated as “remote”.
Equal Employment Opportunity Statement As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit: EEOC Know Your Rights EEOC GINA Supplement. We are proud to be a company that embraces the value of bringing together talented and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. Learn more about your rights, including under California, Colorado and other US State Acts.
#J-18808-Ljbffr