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  • Sr. Tech, Operations

    Merck (Wilson, NC)



    Apply Now

    Job Description

    Senior Technician, Operations

    **Position Overview** :

     

    The Senior Operations Technician will be a member of the Maintenance & Operations team within the Vaccines integrated process team for a start-up vaccine manufacturing facility in Wilson, NC. This person operates and assists coaches with managing final packaging & inspection equipment as part of an empowered work team. This position carries out our mission by assuring finished goods and services are of the highest quality, optimal cost, and delivered on schedule. The Senior Operations Technician routinely performs and leads line-specific duties including line check-in, batch management, in-process quality monitoring, equipment operation, work center cleaning, change-over and material movement with a high degree of accuracy and efficiency in accordance with established procedures. In addition to leading operations activities, the role will be accountable for enforcing EHS and GMP compliance within their area of assignment. This position will be an individual contributor and a lead member of the Operations team.

    Primary Responsibilities

    + Function as a role model in our team-based Employee Involvement culture, focusing on the effectiveness of operations and implementation of viable continuous improvement initiatives

    + Assists with the coordination of daily work schedules and effectively communicates daily customer service and performance targets

    + Assist coaches and operators with operational, mechanical, and technical activities that support our production standards, while enforcing GMPs and SOP adherence

    + Leads the charge to ensure standard work areas are in a constant state of compliance with respect to proper housekeeping, material segregation, and personal gowning, including required protective equipment

    + Team leader and trainer in the set up and adjust of production equipment, including single use mixer, filling, high-voltage leak detectors, labelers, cartoners, printers and other assemblies, as needed for optimal performance within qualified parameters

    + Assists in the development of training documents and procedures and provides training to ensure team members are qualified and proficient in production equipment and processes

    + Manages areas to ensure the maintenance of detailed records as it relates to equipment cleaning, set-up, and challenge documentation

    + Assists with managing the accuracy of critical information, and ensures the completion of required documentation for production processes to ensure optimal line performance

    + Assists coaches to ensures operational concerns are visible and solutions and/or continuous improvement actions are taken with an appropriate sense of urgency for appropriate resolution

    + Resolves and reports issues with product accountability and SAP system problems

    + Demonstrates a mechanical aptitude with the ability to troubleshoot equipment and process related occurrences

    + Responsible for problem solving and process improvement initiatives

    + Assists management with completing Tier 1 actions; escalates concerns to the Tier 2 process

    + Supports off-shifts and weekend work as required for this position

    Quality

    + Interacts with other departments to ensure all packaging operations are performed in accordance with current Good Manufacturing Practices (cGMP), site Standard Operating Procedures (SOPs) and Divisional policies and guidelines

    + Works with Quality, Maintenance, and Planning to identify and resolve quality issues/deviations; supports all investigations and corrective actions

    + Examine products to detect defects, product damage, or other visual quality problems

    + Troubleshoot and offer resolution and recommendation to coaches; appropriately gather and provide information for corrective actions

    + Provides guidance to others with documentation actions in the SAP PI sheets and paper records. Interacts with MMS (Materials Management Specialists) personnel to resolve component issues, including incoming quality concerns

    Safety

    + Conforms to established safety procedures in accordance with OSHA and other regulatory agencies

    + Recognizes, utilize, and enforces the use of safety equipment when/as needed

    + Champion for and actively takes accountability for personal safety as well as the safety of others

    + Identifies, reports, and documents unsafe acts/conditions, participates in the investigation of accidents/injuries/incidents and in developing corrective and preventative actions (CAPA)

    Equipment

    + Operates and trains others to use packaging & inspection equipment within qualified parameters; performs and documents equipment challenges per current procedures.

    + Demonstrates mechanical ability to troubleshoot, problem solve, and train others to recognize and solve equipment concerns as it relates to product jams and component problems

    + Identifies and effectively communicates equipment problems to assist maintenance technicians with troubleshooting and corrective repairs

    Financial

    + Contribute to achieving departmental financial goals by understanding, communicating, and controlling labor costs, component usage and material waste.

    + Works with the coach to determine root cause for line downtime that causes misses for SA (Schedule Adherence) and delivery

    Team | Individual Performance

    + Actively assist coaches in leading a team-based culture through team meetings and continuous improvement activities

    + Demonstrates a high degree of maturity, leadership, and personal integrity

    + Strictly adheres to all site policies on personal conduct and attendance

    + Collaborates and communications with peers and other employees at various levels throughout the organization; demonstrates leadership and conflict-resolution ability

    + Demonstrates a willingness to provide and receive constructive feedback in 360° performance review

    Reporting Relationships:

    + Solid line report to: Manager, Maintenance & Operations

    + Dotted line report to: N/A

    + Position(s) reporting to this position: N/A (individual contributor)

    Work Schedule:

    + 8-hours, 2nd shift

    Minimum Education Requirement

    + High School diploma or equivalent

    Required Experience and Skills

    + Three or more years of experience in a GMP manufacturing facility (aseptic GMP environment strongly preferred)

    + Demonstrated proactive leadership ability, peer training experience, and productivity improvement activity involvement

    + Demonstrated organizational and interpersonal skills with ability to influence and support others through a culture of inclusion, feedback, and empowerment

    + Must have excellent verbal and written communication skills

    + Ability to gown and work in an aseptic environment

    + Demonstrated ability to work with computerized and automated systems.

    + Willing to work irregular hours to support multi-shift operation on an as needed basis

    Preferred Experience and Skills

    + Associate's degree in business, Science, or Technology-based field and/or bio-pharma focused certificates such as Bio-works preferred.

    + Yellow Belt certified or Kata training

    + Experience with aseptic filling, visual inspection systems, CIP/SIP systems, packaging equipment and similar aseptic formulation and filling operations

    + Experience operating, maintaining, troubleshooting, and/or repairing industrial equipment

    + Experience working in a regulated environment (FDA, etc.) and basic knowledge of cGMPs as they apply to the vaccine/pharmaceutical industry

    + Experience in Continuous Improvement, Lean Manufacturing, Problem Solving, and/or Right First-Time methodologies

    + SAP / MES / electronic logbook basic knowledge from a production execution perspective

    + Outstanding communication skills both within direct team and across multiple shifts to ensure success of overall team

    + Effective and efficient computer skills with experience using SAP

    + Ability to support technical writing of documents such as standard operating procedures (SOPs) and work instructions (Wis)

    \#MSJR

    VETJOBS

    Current Employees apply HERE (https://wd5.myworkday.com/msd/d/task/1422$6687.htmld)

     

    Current Contingent Workers apply HERE (https://wd5.myworkday.com/msd/d/task/1422$4020.htmld)

    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. Please click here (https://survey.sogosurvey.com/r/aCdfqL) if you need an accommodation during the application or hiring process.

     

    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 (https://www.eeoc.gov/sites/default/files/2022-10/22-088\_EEOC\_KnowYourRights\_10\_20.pdf)

     

    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 (https://www.msdprivacy.com/us/en/CCPA-notice/)

     
     

    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:

    Regular

    Relocation:

    No relocation

    VISA Sponsorship:

    No

    Travel Requirements:

    No Travel Required

    Flexible Work Arrangements:

    Not Applicable

    Shift:

    2nd - Evening

    Valid Driving License:

    No

    Hazardous Material(s):

    N/A

    Required Skills:

    Aseptic Operations, Aseptic Operations, Biopharmaceuticals, Biopharmaceutics, Cleanroom Gowning, Computer Literacy, Customer Service Management, Equipment Maintenance, GMP Compliance, GMP Documentation, GMP Training, Machine Troubleshooting, Maintenance Processes, Maintenance Troubleshooting, Master Batch Records, Mechanical Troubleshooting, Packaging Processes, Pharmaceutical Manufacturing, Process Improvement Projects, Process Improvements, Production Scheduling, Production Standards, Safety Compliance, Standard Operating Procedure (SOP) Writing, Teamwork {+ 4 more}

    Preferred Skills:

    Job Posting End Date:

    06/19/2025

     

    *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:** R352440

     


    Apply Now



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