Sr. Technician, Shared Services Operations (Onsite)

HireLifeScience; Rahway (NJ); On-site; USD 68,000 - 107,000; Full time

Benefits offered by this job

401(k)

Job summary

Merck & Co., Inc. in Rahway, NJ seeks a Senior Technician, Operations to support R&D operations in the FLEx Center for sterile dosage forms, handling aseptic formulation, visual inspection, and GMP documentation.

You will work in Grade C environments, maintain equipment, manage inventory, and collaborate with formulators, engineers, QA, Safety, and Facilities to enable clinical supply. On-site, 1st shift with opportunities for cross-training and process improvements; requires high attention to

Qualifications

• GMP pharmaceutical manufacturing experience required.
• Able to lift 50 lbs and wear cleanroom gowning incl. respirators.
• Strong written and verbal communication skills.
• Proficiency with PAS‑X, SAP, and related systems.

Responsibilities

• Assemble sterile equipment per drawings for clinical development and manufacturing.
• Operate cleaning and sterilization equipment (autoclaves, washers, ovens).
• Receive and store sterile supplies maintaining inventory.
• Prepare and formulate sterile products in Grade A isolator and Grade C areas.
• Perform visual inspections of products and components for defects.
• Maintain meticulous records of processes and conditions.
• Follow GMP SOPs and participate in continuous improvement.
• Collaborate with formulators, engineers, QA, Safety, Facilities.
• Support training of new staff on sterile procedures and protocols.

Skills

Biopharmaceutical manufacturing

Equipment operations

GMP

Laboratory techniques

Quality control

Process development

Product inspections

Shift work

SOP

Education

High school diploma / GED with 5 years pharma

Associates degree in science/engineering

Bachelor’s degree in engineering technology

Tools

Microsoft Office (Word, Excel, Outlook)

PAS‑X

SAP

HMI / calibration database

Job description

Job Description

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 Manufacturing Shared Services which supports sterile supply, aseptic formulation and visual inspection.

This position will be responsible for hands‑on processing activities that include equipment assembly and disassembly, sterile processing, inventory management, open aseptic formulation in an isolator and closed formulation activities in a Grade C environment, and manual visual inspection of filled units (i.e. vials or syringes). There is also opportunity to cross‑train in other areas, such as filling. 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

• Assembly: Able to read, understand, and follow drawings to assemble sterile equipment to utilize in clinical development and manufacturing processes.---
• Sterilization Processes: Operate and maintain cleaning and sterilization equipment, including parts washers, dry heat ovens, and autoclaves.-
• Supply Management: Receive, inspect, and store sterile supplies and equipment, ensuring proper inventory levels and organization within the sterile supply area.-
• Sterile Formulation: Prepare and formulate sterile products according to established protocols and batch records, ensuring accuracy and compliance with GMP standards.- Able to perform closed formulation activities as well as open aseptic activities inside a Grade A isolator.- Experience with operating isolator machines and/or Grade A aseptic experience is required.-
• Visual Inspection: Perform visual inspections of products and components to identify defects, inconsistencies, and non-conformities.- Individual should be detailed and organized, and able to manage a large quantity of units.-
• Attention to Detail: Maintain meticulous records of formulation processes, including ingredient quantities, equipment used, and environmental conditions.-
• GMP Compliance: Follow all GMP guidelines and standard operating procedures (SOPs) to ensure the quality and safety of clinical production lots. Identifies and addresses compliance, environmental, safety, and process deviations as appropriate while notifying management.-
• Batch Adaptability: Quickly adapt to changes in batch procedures and production schedules, demonstrating flexibility and problem-solving skills.-
• Cleanroom Environment: Able to gown and work in Grade C conditions, maintaining good aseptic cleanroom behaviors-
• Documentation: Maintain accurate records of sterilization processes, inventory levels, and equipment logs in an electronic system.- Knowledge of PAS‑X is preferable.-
• Collaboration: Able to communicate clearly with team and work closely with other teams to ensure on time delivery of supplies.-
• Training and Compliance: Assist in training new staff on sterile supply procedures and protocols, ensuring adherence to GMP standards.-
• Leadership: Able to identify and escalation issues, perform basic troubleshooting, and capturing learnings to improve systems and processes. Organizes and prioritizes own work to meet shop floor priorities and identifies discrepancies in advance.- Also 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 initiates 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.-
• 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.-
• Demonstrated ability to work and communicate both independently and as a part of a team.-
• Flexibility working overtime is a requirement in manufacturing-

Preferred Experience and Skills

• Familiarity with regulatory requirements and Good Documentation Practices (GDP).---
• Experience with some of the following: 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.-

The salary range for this role is:

$68,000 - $107,000

This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee's position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs.

The successful candidate will be eligible for annual bonus and long‑term incentive, if applicable.

Benefits

• We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days.

Required Skills

• Biopharmaceutical Manufacturing
• Efficiency Improvements
• Equipment Operations
• Good Manufacturing Practices (GMP)
• Laboratory Techniques
• Manufacturing Quality Control
• Pharmaceutical Process Development
• Product Inspections
• Shift Work
• Standard Operating Procedure (SOP)

Preferred Skills

• Aseptics
• GMP Guidelines
• Sterile Manufacturing

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.

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

Regular

Relocation

Domestic

VISA Sponsorship

No

Travel Requirements

10%

Flexible Work Arrangements

Not Applicable

Shift

1st - Day

Valid Driving License

No

Hazardous Material(s)

n/a

Job Posting End Date

10/6/2026

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.

Requisition ID

R415978

Equal Employment Opportunity

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

Company Culture

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.

Legal Residency Statements

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.