Merck Senior Technician in Durham, North Carolina
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 linked to our global manufacturing network to ensure the highest quality of raw materials, intermediates and finished products.
This is a day /night shift position, 12 hour ( 6:00 AM - 6:30 PM/6:00PM – 6:30 AM *) rotation (2-2-3). *
The Vaccine Manufacturing Facility Senior Production Technician is an excellent opportunity for highly trained individuals with expertise working in aseptic production and manufacturing operations. The individual in this position will promote the Vaccine manufacturing process through hands on processing activities. Key duties for the Senior Production Technician 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. The ideal candidate for this position has demonstrated the ability to manage their own work activities as well as act as a key contributor toward the success of the team through the use of their decision-making and problem-solving skills and their knowledge of aseptic manufacturing.
Responsibilities include, but are not limited to:
Works collaboratively with all operations, 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 trace ability of product.
Maintains, inventories, and transports all required processing equipment, materials, supplies and products.
Operates various computer-controlled process support/process equipment (i.e. washer, autoclave, vial filler, lyophilizer, capping/inspect machines, etc.).
Performs process troubleshooting while maintaining production schedule
Executes equipment setup/breakdown, operational, and equipment inspections, as required
Assists Maintenance, Instrumentation and Automation during troubleshooting of common faults/errors
Performs housekeeping in all work areas. Executes facility sanitization and decontamination according to approved procedures.
Completes in-process testing and inspections promoting 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.
Serves as the subject matter expert within the processing suite and trains new team members
*Education Minimum Requirement: *
- High School Diploma or equivalent
Required Experience and Skills:
At least two (2) years GMP manufacturing/processing experience, or a Bachelor’s degree in Life Science or Engineering
Must be willing to work 12-hour day/night shift (6:00 AM to 6:30 PM/6:00PM to 630AM) on a rotating 2-2-3 schedule. Note that this schedule does include working alternating weekends and holidays
Must be able to successfully pass and maintain aseptic gowning qualification. Aseptic gowning requires that all skin and hair be covered through wearing the following: beard/mustache cover, hair net, hood and facemask, goggles, jumpsuit, gloves and boots.
Must be willing and able to lift 50 lbs., bend, stoop, squat, crawl, twist, climb ladders, and wear a respirator
Must be willing to work various shifts
Computer literacy (internet browsers, e-mail, spreadsheets, word processing)
Experience with batch record execution, including good documentation practices
Preferred Experience and Skills:
Bachelor’s degree in Life Science or Engineering
Associate’s degree in Life Science or Engineering
BioWorks Certificate (working in an FDA regulated industry)
Certified Yellow Belt
Environmental Monitoring and Sampling
Proficiency in the use of SAP in a manufacturing setting
Execution of Electronic Batch Records
Our Manufacturing & Supply Division is dedicated to being the most trusted supplier of bio-pharmaceuticals worldwide. Our facilities, along with our external contractors, suppliers, and partners, create a reliable global manufacturing network that’s devoted to delivering a high quality, reliable supply to customers and patients on time, every time.
Who we are …
We are known as Merck & Co., Inc., Kenilworth, New Jersey, USA in the United States and Canada and MSD everywhere else. For more than a century, we have been inventing for life, bringing forward medicines and vaccines for many of the world's most challenging diseases. Today, our company continues to be at the forefront of research to deliver innovative health solutions and advance the prevention and treatment of diseases that threaten people and animals around the world.
What we look for …
In a world of rapid innovation, we seek brave Inventors who want to make an Impact in all aspects of our business, enabling breakthroughs that will affect generations to come. We encourage you to bring your disruptive thinking, collaborative spirit and diverse perspective to our organization. Together we will continue Inventing For Life, Impacting Lives while Inspiring Your Career Growth .
NOTICE FOR INTERNAL APPLICANTS
In accordance with Managers' Policy - Job Posting and Employee Placement, all employees subject to this policy are required to have a minimum of twelve (12) months of service in current position prior to applying for open positions.
If you have been offered a separation benefits package, but have not yet reached your separation date and are offered a position within the salary and geographical parameters as set forth in the Summary Plan Description (SPD) of your separation package, then you are no longer eligible for your separation benefits package. To discuss in more detail, please contact your HRBP or Talent Acquisition Advisor.
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OFCCP EEO Supplement at https://www.dol.gov/ofccp/regs/compliance/posters/pdf/OFCCPEEOSupplementFinalJRFQA508c.pdf
OFCCP Pay Transparency Rule at https://www.dol.gov/ofccp/pdf/pay-transp%20EnglishformattedESQA508c.pdf
We are an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations.
Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Kenilworth, NJ, USA, also known as Merck Sharp & Dohme Corp., Kenilworth, 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.
No Travel Required
Flexible Work Arrangements:
Valid Driving License:
Number of Openings:
Requisition ID: R83130
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