Job Description
The Process Support Lab at the Durham site is seeking an Associate Specialist with strong interpersonal, communication, and collaboration skills responsible for lab-scale vaccine process development execution, technical transfer support, and post commercial process enhancements activities for multiple pipeline vaccine programs. The well-qualified candidate must have analytical, problem-solving, and communication skills. Furthermore, the candidate will be required to work in a fast-paced environment. Off-shift or weekend coverage may occasionally be required to support the technical team, based on project-specific assignments and/or the vaccine production schedule.
Key responsibilities may include but are not limited to:
Provide technical hands-on support in execution of lab-scale experiments in at least one of the following areas: buffer/media preparation, cell/tissue culture, particle isolation, or product lyophilization.
Execute bio-analytical assays for in-process and post-process samples (can include potency assays, metabolite analysis, moisture analysis, FTIR, SEM-EDS, UV/Vis, etc)
Perform particle isolation, microscope imaging, and particulate analysis using analytical equipment to determine origin of particulate submissions with quick turnaround to support manufacturing investigations at the site.
Assist in design and execution of lab experiments to support process characterization, commercial technology transfer, and qualification studies associated with the development and implementation of bulk processes, systems and facilities related to pipeline vaccine bulk products.
Execute experimental studies as needed for investigational, developmental, or continuous improvement projects for our Company's existing Durham vaccine products (investigational and/or developmental studies).
Troubleshoot equipment and assays as needed.
Ability to support off-shift or weekend work if needed.
Author and present experimental design proposals, technical reports and documents.
Compile process data and employ statistical tools for experimental analysis and process monitoring.
Actively participate on cross-functional manufacturing teams to advance project goals and deliverables related to vaccine processes.
Education Minimum Requirement:
Required Experience and Skills:
Preferred Experience and Skills:
Vaccine or biologics manufacturing within an aseptic, cGMP environment
Hands-on experience in large molecule manufacturing or bio-analytical assays.
Experience designing experiments and authoring technical documentation.
Solves Technical Problems Independently
Strong Attention to Detail
Ability to foster collaborative work environment
Demonstrated systematic problem-solving skills
Required Skills:
Adaptability, Adaptability, Applied Mathematics, Biochemical Assays, Cell Cultures, Cell Physiology, Chemical Engineering Fundamentals, Chemical Plant Operations, Data Analysis, Engineering Standards, Estimation and Planning, Fast-Paced Environments, Field Failure Analysis, Interpersonal Communication, Job Descriptions, Mammalian Cell Culture, Manufacturing Scale-Up, Oral Solid Dosage, Plan of Action and Milestones (POA&M), Primary Cell Culture, Problem Solving, Process Optimization, Professional Engineering, Site Supervision, Teamwork {+ 2 more}
Preferred Skills:
Current Employees apply HERE
Current Contingent Workers apply HERE
The salary range for this role is
$71,900.00 - $113,200.00
This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee’s 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 https://jobs.merck.com/us/en/compensation-and-benefits.
You can apply for this role through https://jobs.merck.com/us/en (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:
Regular
Relocation:
No relocation
VISA Sponsorship:
No
Travel Requirements:
10%
Flexible Work Arrangements:
Not Applicable
Shift:
1st - Day
Valid Driving License:
No
Hazardous Material(s):
N/A
Job Posting End Date:
07/28/2026
*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.
