Job Details
Senior Technician, Operations (R127446)
Job Description
Our Manufacturing Operations teams are the people that make therapies for our patients. We work in the manufacturing plants with a “Safety First, Quality Always” mindset, striving for continuous improvement, and earn our right to produce. We work in local plants connected to our global manufacturing network supplying the highest quality of raw materials, intermediates, and finished products.
This role is within a capital project start-up in Durham, North Carolina. The new facility will include end-to-end processing of drug substance, drug product, including biotech culture growth, harvest, lyophilization, product inspection, utilities, and warehouse.
As the team finishes design and construction of the facility, the Lead Technician will play a critical role in supporting the Global Engineering Services team, partnering with internal stakeholders, and building the operations team who will take ownership of the facility. Members of the Operations team in this new and exciting facility will have the unique opportunity to give input in the design process, startup their areas, and lead the teams to full production.
Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity, and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement, and teamwork. As part of our global team, you’ll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.
Responsibilities
Project Support
Supports project team as operations expert through start-up, commissioning, qualification through licensure and ramp up of facility.
Author, review, and/or edit operations and technical documentation (Batch Records, SOPs, Job Aides, training, and engineering documents) to support project and future operations.
Identifies and addresses compliance, environmental, safety, and process deviations as appropriate while coordinating with appropriate personnel.
Actively participate in team meetings HAZOPS, waste walkthroughs, 5S, kaizen events, or any other operations, lean six-sigma, quality, safety or environmental training/initiatives as required.
Operational Expertise
Competent execution and ownership to meet production targets for area within responsibility including:
Attending and escalation of concerns or needs at daily huddles and as needed
Cleaning, setup, operation and troubleshooting of equipment and facilities
Maintenance and transportation of consumable and material inventories
Maintenance of excellent recordkeeping and housekeeping
Drives culture of continuous improvement. Implements and raises ideas to increase success of group
Participates on and/or performs activities to support technical and OPEX functions such as Kaizen events, ad-hoc sampling, or protocol execution.
Maintains detailed knowledge of equipment and processes.
Identifies and addresses compliance, environmental, safety, and process deviations as appropriate while notifying appropriate personnel.
Education Requirement
High School Diploma/GED or higher
Experience and Skills
Required
Minimum two years in GMP manufacturing/processing or a Bachelor’s degree in Life Science or Engineering
Effective written and verbal communications skills
Successfully pass and maintain aseptic gowning qualifications | 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
Computer literacy (internet browsers, e-mail, spreadsheets, word processing)
Able to lift 50 lbs., bend, stoop, squat, crawl, twist, climb ladders, and wear a respirator
Successful completion of TB blood test and Chest X-ray
Preferred
Associates Degree in science or related field
Biowork Certificate (working in an FDA or similar regulated industry)
Applicable mechanical and project management experience
Experience with automated systems (MES, SAP, DeltaV, or similar)
Experience with on-the-floor cGMP manufacturing and familiarity with regulatory requirements and Good Documentation Practices (GDP)
Demonstrated ability to work both independently and as a part of a team
The following experience is a significant advantage for a Senior Technician supporting Drug Product operations
Aseptic filling operations
Grade A isolator containment systems
Lyophilization
Visual inspection of product in glass vials including manual & automated techniques
Autoclaves, washers, and dry heat ovens
Travel
Up to 15% of the time
Shift and Hours
Position will initially be Monday to Friday, day shift
Willing to work various shift schedules as required when operations starts, expected in 2023
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 …
Imagine getting up in the morning for a job as important as helping to save and improve lives around the world. Here, you have that opportunity. You can put your empathy, creativity, digital mastery, or scientific genius to work in collaboration with a diverse group of colleagues who pursue and bring hope to countless people who are battling some of the most challenging diseases of our time. Our team is constantly evolving, so if you are among the intellectually curious, join us—and start making your impact today.
NOTICE FOR INTERNAL APPLICANTS
In accordance with [Register to View] 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. #BCGExp TechnicianDurham
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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.
Employee Status:
RegularRelocation:
No relocationVISA Sponsorship:
NoTravel Requirements:
10%Flexible Work Arrangements:
Not SpecifiedShift:
1st - DayValid Driving License:
NoHazardous Material(s):
Cleaning productsNumber of Openings:
2Requisition ID:R127446