Job Description

Position Description

This position is designated Mon-Fri, dayshift, and will work 06:00am - 2:30pm as we transition into commercial production.

The Vaccine Manufacturing Facility Production Associate is an excellent opportunity for experienced individuals that are interested in working in vaccine production and manufacturing operations. The individual in this position will support the vaccine manufacturing process through hands on processing activities. Key responsibilities for the Production Associate include the execution of aseptic processing requirements, adherence to Good Manufacturing Practices, and working in a self-directed team environment to accomplish shift and departmental goals.

Responsibilities include, but are not limited to:

• Works collaboratively with all operations and support personnel, performing manual and automated processing of vaccine manufacturing equipment, performing general troubleshooting tasks, and supporting functions necessary for the production of vaccines.

• Executes all documentation and clerical functions necessary for proper accountability and traceability of product.

• Maintains, inventories, and transports all required processing equipment, materials, supplies, and products needed to support manufacturing.

• Operates various computer-controlled process support/process equipment (i.e. washers and autoclaves).

• Assists in troubleshooting of equipment.

• Performs housekeeping in all work areas. Executes facility sanitization and decontamination according to approved procedures.

• Completes in-process testing and inspections supporting the vaccine manufacturing, validation, and development processes as required.

• Identifies and addresses compliance, environmental, safety, and process deviations as appropriate and escalates to appropriate personnel.

• Maintains, cleans, and prepares equipment used in vaccine manufacturing process.

• Schedules and performs environmental monitoring during processing and records results in the computerized database system. Provides timely delivery of sample and other materials as required to appropriate laboratories, coordinating with Quality and Logistics as required.

• Attends and actively participates in safety & housekeeping, walkthroughs, 5S, kaizen events, or any other operations, lean six-sigma, quality, safety, or environmental training/initiatives as required.

• Serves on safety, quality, and other committees as required.

Education Minimum Requirement:

• High School Diploma or equivalent is required for this position. Prefer Bachelor's degree in Life Science or Engineering or Associate's degree in Life Science or Engineering with at least 2 years relevant experience

Required Experience and Skills:

• Previous experience in pharmaceuticals is a plus, or related experience in manufacturing

• Must be able to successfully gown into C/D graded spaces

• Must be willing and able to lift 50 lbs, bend, stoop, squat, crawl, twist, climb ladders, and wear a respirator

• Demonstrated verbal and written communication skills

• Must be able to demonstrate basic computer literacy (internet browsers, e-mail, word processing)

• Successful completion of TB titer and Chest X-ray are required.

The following experience is an advantage for an Associate Technician supporting our Production Support and Media operations:

Preferred Experience and Skills (General):

• Bachelor's degree in Life Science or Engineering

• Associate's degree in Life Science or Engineering

• BioWorks Certificate (working in an FDA regulated industry).

• Experience utilizing System Applications and Products in a manufacturing setting.

• Experience in the use of Electronic Batch Records

• Experience performing Environmental Monitoring and Sampling

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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".

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:

Relocation:

VISA Sponsorship:

Travel Requirements:

Flexible Work Arrangements:

Shift:

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Hazardous Material(s):

Job Posting End Date:

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Requisition ID:R318520