Technician, Operations-2

MSD; De Soto (KS); On-site; USD 49,000 - 77,000; Full time

Benefits offered by this job

Medical, dental, vision benefits

401(k) retirement plan

Paid holidays

Vacation and sick days

Job summary

MSD in De Soto, Kansas is seeking an Operations Technician to support antigen production operations on a Monday–Friday 1st shift, with occasional weekend/holiday work. You will drive process work, sampling, and documentation, ensuring schedules meet safety, quality, and regulatory requirements.

Ideal candidates have a high school diploma, with preferred BSc in a relevant science and experience in pharmaceutical manufacturing, GMP, and ERP systems like SAP.

Qualifications

• Strong knowledge of GMP in pharmaceutical manufacturing.
• Attention to detail with documentation accuracy.
• Ability to follow SOPs and manufacturing directions.

Responsibilities

• Operate within production schedules to support antigen manufacturing.
• Perform process work, sampling, and documentation tasks.
• Provide technical and operations support to ensure compliance with safety, quality and regulatory requirements.
• Follow QA/QC procedures and contribute to continuous improvement.
• Maintain proper use of equipment and PPE; report hazards and incidents promptly.

Skills

Analytical problem solving

Computer literacy

Data entry

Equipment maintenance

GMP documentation

Manufacturing documentation

Manufacturing operations

Manufacturing quality control

Media preparation

Process improvements

Regulatory compliance

Safety practices

SOP writing

Sterilizing equipment

SAP

Education

High School Diploma

BSc in a relevant science with experience

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 an Operations Technician position. The Operations Technician, in conjunction with the execution routine production activities, will support the team by driving completion of process work, sampling, documentation, and assisting with other initiatives.

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. Occasional weekend work or partial holiday shifts required.

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

Education Requirements

• Required | High School Diploma
• Preferred | 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

• Experience working in a manufacturing environment and using large scale filtration and separation techniques
• Knowledge of aseptic processes used in manufacturing

Required Skills

• Analytical Problem Solving
• Computer Literacy
• Data Entry
• Equipment Maintenance
• GMP Documentation
• Good Manufacturing Practices (GMP)
• Manufacturing Documentation
• Manufacturing Operations
• Manufacturing Quality Control
• Media Preparation
• Process Improvements
• Regulatory Compliance
• Safety Practices
• Standard Operating Procedure (SOP) Writing
• Sterilizing Equipment #MSJR

The salary range for this role is: $48,600 - $76,600. 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.

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.

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.

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.

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: 10/27/2026

Our company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where we have codified our legacy for over a century. Our success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.