Associate Technician, Operations

MSD; North East; On-site; GBP 32,000 - 50,000; Full time

Benefits offered by this job

Annual bonus

Long-term incentive

Medical, dental, vision benefits

401(k) retirement plan

Paid holidays and vacation

Job summary

MSD in Durham, NC, seeks a Manufacturing Operations associate to support production activities in material manufacture. You will perform manual and automated operations, maintain documentation for traceability, and keep equipment, materials, and workspace organized.

The role requires lifting 50 lbs and shift work (2-2-3), with possible weekends and nights. Preferred Bioworks certificate or related science degree.

Qualifications

• Demonstrated written and verbal communications skills.
• Proficiency with GMP gowning for required classifications as needed for role.
• Must be willing and able to lift 50 lbs.
• Must be willing to work shift schedules (2-2-3) which may include working every other weekend, night shift, and holidays.

Responsibilities

• Support production activities in the manufacture of material.
• Perform manual and automated operations, general maintenance and support functions necessary for production.
• Provide and/or author all documentation and clerical functions necessary to allow proper accountability and traceability of product.
• Maintain, inventory, and transport all required equipment, materials, supplies and products.
• Perform housekeeping and facility decontamination, and prepare equipment for use in production.
• Perform sampling/in-process testing supporting manufacturing and validation processes.
• Deliver samples and materials to laboratories, coordinating with Quality and Logistics.
• Maintain training status and participate in lean initiatives and safety trainings.

Skills

Written and verbal communication

GMP gowning proficiency

Able to lift 50 lbs

Shift work (2-2-3)

Regulatory awareness

Education

High School Diploma/GED

Bioworks Certificate

Job description

This opening is for all shifts.

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.

The Maurice R. Hilleman Center for Vaccine Manufacturing is located in Durham, NC. This state-of-the-art facility established in 2004, manufactures our Company lifesaving vaccines in bulk and finished forms.

Responsibilities may include but are not limited to:

• Support production activities in the manufacture of material.
• Working in conjunction with all appropriate personnel, performs manual and automated operations, general maintenance and support functions necessary for production.
• Provides and/or authors all documentation and clerical functions necessary to allow proper accountability and traceability of product.
• Maintains, inventories, and transports all required equipment, materials, supplies and products.
• Performs housekeeping in all work areas. Executes facility decontamination according to procedures. Maintains, cleans and prepares equipment used in production.
• Performs sampling/in-process testing supporting the manufacturing and validation process for current process.
• Provides timely delivery of sample and other materials as required to appropriate laboratories, coordinating with Quality and Logistics as required.
• Self-motivated to maintain own training status
• Attends and actively participates in HAZOPS, waste walkthroughs, 5S, kaizen events, or any other operations, lean six-sigma, quality, safety or environmental training/initiatives as required.

Education Minimum Requirement:

• High School Diploma/GED or higher

Required Experience and Skills:

• Demonstrated written and verbal communications skills
• Proficiency with GMP gowning for required classifications as needed for role
• Must be willing and able to lift 50 lbs
• Must be willing to work shift schedules (2-2-3) which may include working every other weekend, night shift, and holidays

Preferred Experience and Skills:

• Bioworks Certificate or Associates Degree in science or related field, in addition to minimum required experience and skills
• Experience with on-the-floor cGMP manufacturing and familiarity with regulatory requirements
• Demonstrated ability to work both independently and as a part of a team

Travel: 0%

#MSJR

The salary range for this role is: $43,100 - $67,800

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.

Required Skills:

• Accountability, Cleanroom Gowning, Computer Literacy, Good Manufacturing Practices (GMP), Manufacturing, Production Support, Safety Procedures, Working Independently, Written Communication

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:

• Employee Status: Regular
• Relocation: No relocation
• VISA Sponsorship: No
• Travel Requirements: No Travel Required
• Flexible Work Arrangements: Not Applicable
• Shift: Not Indicated
• Valid Driving License: No
• Hazardous Material(s): n/a

Job Posting End Date: 11/20/2026*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.