Manufacturing Automation Specialist (Durham, NC)
Manufacturing Automation Specialist (Durham, NC)
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Job Description
Job Description
Our Engineers support internal and external manufacturing operations to remain operational continuously improve and innovate. With our extensive range of facilities and environments our Engineers have opportunities across many diverse areas including Biological Chemical Automation Capital Projects Maintenance Safety Process Development Technical Services Utilities and Validation.
Our company is expanding its global recombinant human papillomavirus (HPV) vaccine production network by investing $650 million and have added a 225000-square-foot building within the footprint of the Maurice R. Hilleman Center for Vaccine Manufacturing in Durham NC. The new facility is being used to produce the bulk active ingredient for the HPV vaccine comprised of fermentation microfiltration/ultrafiltration and chromatography steps.
Approximately 614000 people are diagnosed with certain HPV-related cancers each year. Our company manufactures the two HPV vaccines that are predominantly utilized to eradicate these cancers globally. In recent years countries around the world have enacted new or expanded HPV vaccination programs which has created an unprecedented increase in global demand. The manufacturing facility in Durham will play a critical role in the network of plants that produce life-saving medicines and vaccines including our HPV vaccines.
This Individual will provide leadership as the automation engineer for our companys vaccine Bulk Facility directly supporting Alum production. Responsible for problem resolution implementation of process control data collection techniques and troubleshooting in compliance with SDLC GMP safety and environmental regulations. Actively support participate and embrace an empowered team culture including significant interaction with manufacturing quality and engineering groups. Supports a large spectrum of sophisticated automated systems within Manufacturing Operations; providing multiple opportunities to learn new automation technologies and make a positive impact. Provides direct support to Automation Lead including leading cross functional teams and providing direct guidance to the Automation team. Also provides technical coverage on automated systems.
Primary Activities include but are not limited to:
Understands and supports allGood Manufacturing Practices (GMPs) safety and environmental regulations. Review and approve automation documents preventive maintenance and SOPs to ensure compliance withGood Manufacturing Practicesand safety.
Leads investigations of automation incidents and problems to prevent recurrence including the development and implementation of corrective actions.
Evaluates automated and information technology systems and develops strategies to optimize and ensure quality and stability of automation systems through future expansion replacement or upgrade.
Assists the Automation Lead in the training development motivation and assignments for employees and contractors.
Coordinates projects with staff group for timely implementation.
Uses technical knowledge to assure the efficient operation of variety of automated processing and information technology systems. Leads in installing and placing new equipment into operations. Develops solutions for automation problems.
Participates in audits and training programs in the area of responsibility.
Project coordination leadership and implementation of troubleshooting activities and change control.
Initiate and lead collaboration within the Operations Quality and Technical organizations to resolve complex problems.
On-floor support of manufacturing activities.
Identify and implement process/equipment improvements and manufacturing efficiencies.
Serves as liaison with corporate and divisional automation and IT groups.
Position Qualifications:
Education Minimum Requirement:
High School Diploma required.
Required Experience and Skills:
Minimum of 3 years of experience in process automation in a GMP environment.
Experience programming Emerson DeltaV.
Computer system validation and systems life-cycle development methodology experience required. Experience implementing and maintaining ALCOA principles.
Proven track record of analytical skills problem solving and attention to detail
Strong understanding of manufacturing principles/ processes and ability to translate manufacturing and business requirements into Automation/digital solution
Preferred Experience and Skills:
Experience in the following areas is desired: DeltaV Version 14 DeltaV Live SQL (basic querying) DeltaV SIS
Experience working with Information Technology teams.
Experience with regulatory audits and working knowledge of data integrity principles.
Understanding of Lean Manufacturing /Six Sigma methodology.
Strong leadership interpersonal and communication skills.
#eligibleforerp
MSJR
Current Employees apply HERE
Current Contingent Workers apply HERE
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 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 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:
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 anothers thinking and approach problems collectively.
Learn more about your rights including under California Colorado and other US State Acts
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 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.
The salary range for this role is
$85600.00 - $134800.00This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employees 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. More information about benefits is available at can apply for this role through (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting.
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:
RegularRelocation:
No relocationVISA Sponsorship:
NoTravel Requirements:
10%Flexible Work Arrangements:
HybridShift:
Not IndicatedValid Driving License:
NoHazardous Material(s):
N/ARequired Skills:
Applied Engineering Audit Management Automation Business Process Improvements Communication Data Management Emerson DeltaV GMP Environments Problem Management Quality ManagementPreferred Skills:
Job Posting End Date:
06/20/2025*A job posting is effective until 11:59:59PM on the day BEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
Required Experience:
Unclear Seniority
Employment Type
Full-Time
