Senior Specialist, Engineering

Merck & Co.

Omaha, NE

Apply

JOB DETAILS

SALARY

$117,000–$184,200 Per Year

SKILLS

Affirmative Action, Analysis Skills, Automation, Biochemistry, Bioengineering, Biological Processes, Biology, Biomolecules, Biotech and Pharmaceutical, Change Control, Chemical Engineering, Chemistry, Cross-Functional, Data Analysis, Documentation, Driver's License, EEO Regulations, Environmental Health, Experiment Design, Federal Contracts, GMP (Good Manufacturing Practices), Interpersonal Skills, Laboratory Operations, Leadership, Manufacturing, Manufacturing/Industrial Processes, Microbiology, Presentation/Verbal Skills, Problem Solving Skills, Process Development, Process Improvement, Process Manufacturing, Product Demonstration, Product Development, Product Testing, Project Development, Project Planning, Project Tracking, Project/Program Management, Protocol Design, Quality Control, Regulations, Regulatory Compliance, Research & Development (R&D), Resume Search, Risk Analysis, Root Cause Analysis, Safety Compliance, Safety/Work Safety, State Laws and Regulations, Statistics, Team Lead/Manager, Team Player, Technical Operations, Technical Support, Technical Writing, Testing, United States Department of Agriculture (USDA), Vaccination, Veterinary Medicine, Viruses, Willing to Travel, Writing Skills

LOCATION

Omaha, NE

POSTED

Today

Job Description

The function of Senior Specialist, Engineering at Bio Technology and Solutions (BTS) - Tech Hub will have a focus in Vaccine and Biologicals processes development for Manufacturing. BTS Tech Hub is responsible

for process development of production processes. Within a multidisciplinary environment you will cooperate with your colleagues at BTS, Manufacturing, Engineering, Quality and R&D. Your main field of attention is to provide all round technological support on Vaccine and Biologicals Manufacturing of new (R&D) products.

Primary Responsibilities

Leads and works independently as a team member on the development and scale up of processes or technologies of microbial, virus and cell cultivations, biomolecules concentration and purification and final formulation of veterinary vaccines and therapeutics.
Leads and works independently as a team member on the transfer of processes or technologies of microbial, virus and cell cultivations, biomolecules concentration and purification and final formulation of veterinary vaccines and therapeutics to the production lines.
Leads and works independently as a team member on the development of processes or technologies and its transfer to the production lines within the timelines set for this purpose, whereby these processes and technologies meet the requirements of the customer with regard to safety, quality, cost-efficiency, practical applicability and consistency.
Leads and works independently as a team member on technical investigations, validation and/or process improvement projects.
Examines issues from diverse perspectives (safety, compliance, automation, equipment, process and people) in order to best understand and resolve the root cause.
Whether or not in collaboration with team members from other departments (e.g. QC, Pharmaceutical Technical Support, R&D, Production or Analytical Technical Services) gives direction to scientifically based decisions within projects aimed at the improvement of products, solving problems or development of new products.
Implement development, introduction and/or testing of new technologies Collaborates and interfaces with R&D and Manufacturing and other departments to bring new products to market.
Leads large cross-functional teams and demonstrates working knowledge of current USDA regulatory guidelines and advanced technical knowledge.
Develops project charters and project plans and align with all sponsors and stakeholders.
Key capabilities include standard project management activities: development of timelines, use of project tracking tools, definition of deliverables, definition of roles and responsibilities, risk identification tracking and mitigation.
Coordinates and tracks team activities by leading or participating in core team meetings, communicates project risks and status to appropriate stakeholders and escalates issues to sponsors as needed in advance of deviation from project plans.
In concert with Commercialization, Quality, and Regulatory, support inspection readiness. Assures consistent application of standardized work, engineering and process tools
Conducts and design experimental protocols as needed using the Technical Operations lab facilities and/or production equipment at full scale.
Creates and updates technical and manufacturing documents necessary for investigations, process design/definition, engineering studies, process demonstrations, change control and validation.
Displays our Company leadership behaviors and demonstrate a high emotional intelligence
Effectively collaborates with peers on site and above site as required.
Contributes to international projects (Global Projects).
Interacts closely with fellow scientists from your own and other departments. If required with external collaboration partners.
Actively contributes to the improvement or acceleration of activities within the department, also in the field of Environment Health and Safety.
Trains and guides employees and / or trainees

Education Minimum Requirement

Bachelor degree in Biochemical Engineering, Biotechnology, Chemical Engineering, Biology, Biochemistry, Protein Chemistry, Microbiology +5 years' experience in vaccine/biopharmaceuticals Research and Development, Process Development and/or Biological manufacturing or closely related field (or Master degree + 3 years' experience or PhD in related field).

Required Experience and Skills

Excellent written and verbal communication
Excellent project management, documentation and writing
Excellent teamwork
Strong problem-solving skills and a hands-on approach to solving problems inclusive of diverse perspectives (e.g. safety, compliance)
Work together in multidisciplinary and international teams

Preferred Experience and Skills

Experience in bioprocess scale up and vaccine manufacturing
Working knowledge of USDA regulations
Knowledge of GMP requirements for manufacture and testing of biological products
Understanding of statistics and application to process monitoring and control
Molecular biology, replicon particles, cell cultivation

Required Skills:
Adaptability, Data Analysis, Interpersonal Relationships, Manufacturing Processes, Production Process Development, Project Management, Regulatory Compliance, Root Cause Analysis (RCA)

Preferred Skills:

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 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

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

The salary range for this role is
$117,000.00 - $184,200.00

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

You 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:
Regular

Relocation:
No relocation

VISA Sponsorship:
No

Travel Requirements:
10%

Flexible Work Arrangements:
Not Applicable

Shift:
1st - Day

Valid Driving License:
Yes

Hazardous Material(s):
Yes

Job Posting End Date:
06/1/2026
*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.

About the Company

Merck & Co.

Resume Resources

Free Resume Templates Free Resume Builder