Senior Operations Technician

MSD Malaysia; De Soto (KS); Hybrid; USD 59,000 - 93,000; Full time

Benefits offered by this job

Medical, dental, vision insurance

401(k) retirement benefits

Job summary

MSD is seeking a Senior Operations Technician for the De Soto, KS site to support antigen production operations. You will drive process work, sampling, documentation, material transfers and training to ensure schedules are met in a compliant manner.

The role emphasizes GMP, cGMP, deviation handling, change control, Lean Six Sigma, and continuous improvement, with a Monday–Friday shift 7:00 AM to 3:30 PM. Prior pharma manufacturing experience preferred.

Qualifications

• Pharmaceutical manufacturing experience required or preferred.
• Strong knowledge of GMP and documentation practices.
• Ability to work with cross-functional teams and meet deadlines.

Responsibilities

• Lead and coach team while applying lean and Six Sigma practices.
• Ensure compliance with safety, quality, and regulatory requirements.
• Support production scheduling and continuous improvement initiatives.

Skills

Aseptic Operations

CAPA Management

Change Controls

Change Management

GMP Compliance

Documentation

Production Scheduling

Manufacturing Processes

Master Batch Records

Equipment Setup

Information Systems

Quality Improvement

Education

BSc in Microbiology/ Biotechnology or related

High School Diploma + 3+ years pharma manufacturing

Tools

SAP

Job description

Job Description For over 130 years, we have pioneered groundbreaking science. Today, we are driven by continuous innovation to develop breakthrough medicines, vaccines and technology. Rooted in direct experience on the farm and in the clinic, we work hand in hand with our customers every step of the way. Our singular focus is to empower those who care for animals, helping them manage their vital responsibility with confidence. Because when it comes to animal health, no one sees it like we do. Our Manufacturing Operations teams are the people that make our products. We work in the manufacturing plants with a “Safety First, Quality Always” mindset striving for continuous improvement. We work in the local plant connected to our global manufacturing network to ensure the highest quality of raw materials, intermediates, and finished products.

We are recruiting for a Senior Operations Technician position. The Senior Operations Technician, in conjunction with the execution routine production activities, will primarily support the team by driving completion of process work, sampling, documentation, material transfers, and assisting with training. The Senior Operations Technician also supports continuous improvement, transfer of new products, and may assist with deviations and change management. The basic purpose of this position is to provide expert support for our Company Animal Health antigen production operations at our site in De Soto, Kansas. This position provides technical and operations support to ensure that manufacturing schedules are met in a compliant manner with safety, quality, and regulatory requirements.

Responsibilities include that antigen products specifications are met prior to release for compliance to product Outlines, United States Department of Agriculture 9 Code of Federal Regulations, and cGMP. The scope of support includes every manufacturing stage from raw materials through final antigen product.

Our current opening is for the following shift: Monday – Friday, 7:00 AM -3:30 PM

Responsibilities

• Models Company leadership principles and inclusive behaviors
• Provides coaching and supports skills development and process capabilities within their team
• Supports effective feedback and coaching within the team during the Performance Management cycle
• Providing appropriate task-based training
• Safety Compliance Demonstrates a strong compliance mind-set (EHS and Quality) and continuously sets a high standard for themselves and others
• Follows safe operating instructions for all tasks and equipment
• Ensures that the right tools and equipment specified for the task are available and utilized
• Ensures that the correct personal protective equipment required is available and utilized
• Follow up any reported defects or workplace hazards immediately
• Report all accidents, incidents and near misses within 24 hours and to participate in investigation and identification of effective corrective and preventative actions
• Quality Compliance On-time completion of Quality compliance tasks in relation to Deviation, CAPA and Change Control management.
• Quality Assurance including cGMP, RFT and good documentation practices and provides coaching to others.
• Change Manager and Stakeholder for change management activities within Production.
• Supports the update, review and approval of GMP documentation including, but not limited to: SOP’s | MD’s | Qualification Protocols | New product/product transfer documentation
• Productivity and Financial Supports the Daily, Weekly and Monthly schedule adherence of production activities within their department
• Build and maintain strong collaborations with different stakeholders throughout the Site Operations such as BTS, Engineering, Quality and R&D
• Supports the Manufacturing Operations Teams in creating a culture of continuous improvement and leads by example
• Representatives Manufacturing Operations in the execution of the project portfolio and improvement initiatives
• Supports initiatives for stabilizing and improving production processes
• Assures effective application of Lean Six Sigma, Project Management and Change Management Tools
• Supports Manufacturing Operations key productivity metrics by investigating and solving operations issues with appropriate techniques and skills
• Contributing to a data driven decision making process and visualizing problems, progress and results
• Recognizes and investigates opportunities for financial savings

Education Requirements

• High School Diploma plus three (3)+ years of experience working in a Pharmaceutical Manufacturing role
• BSc Degree in a relevant scientific discipline plus experience working within a Pharmaceutical Manufacturing role

Experience Requirements

• Strong knowledge of Good Manufacturing Practices demonstrated within applicable manufacturing environment
• Efficient and effective attention to detail, achieve consistent error‑free implementation of daily job assignments and complete documentation using Good Documentation Practices and be able to identify opportunities for process improvement and employ basic problem‑solving skill
• Principled verbal and written communications
• Follow and comply with Manufacturing Directions, Standard Operating Procedures, Company/Corporate/Regulatory Policies
• Demonstrate basic skills in effective time management to meet given deadlines and complete basic laboratory procedures
• Ability to work effectively with team members and show initiative to assist others on the team
• Proficient computer skills including Microsoft Word and Excel
• Experience using quality improvement tools and continuous improvement processes and site quality metrics
• Knowledge of system-controlled material usage through ERP environments such as SAP
• Preferred Experience: Degree in Microbiology, Biotechnology, Immunology or similar
• Experience working in a manufacturing environment and using large scale filtration and separation techniques
• Knowledge of aseptic processes used in manufacturing

Salary

• #MSJR The salary range for this role is: $59,100 - $93,000

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

• Aseptic Operations
• Aseptic Operations
• CAPA Management
• Change Controls
• Change Management
• Cleanroom Gouning
• Coaching
• Computer Literacy
• Corrective Action Management
• Deviation Management
• Documentation Preparation
• Document Management
• Equipment Set Up
• GMP Compliance
• GMP Documentation
• GMP Training
• Information Systems
• Manufacturing
• Manufacturing Processes
• Manufacturing Strategies
• Master Batch Records
• Operations Support
• Pharmaceutical Manufacturing
• Production Scheduling
• Product Transfers

Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities.

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

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

Employee Status: Regular Relocation: No relocation VISA Sponsorship: No Travel Requirements: No Travel Required Flexible Work Arrangements: Not Applicable Shift: 1st - Day Valid Driving License: No Hazardous Material(s): N/A Job Posting End Date: 08/26/2026