Wilson, North Carolina, United States · On-site
$117k–$184k/yr
Job Description Position Summary Reporting to the Associate Director of PTO Engineering, the Senior Process/Project Engineer is responsible for providing technical support to Manufacturing Division–Wilson packaging opera…
Skills: Device Packaging, Equipment Qualification, Good Manufacturing Practices (GMP), Packaging Engineering, Packaging Operations
Rahway, New Jersey, United States · Hybrid
$191k–$300k/yr
Job Description Our Company has an exciting and growing CV, Resp, Metabolic and Neuro pipeline, reinforcing our position as a sustainable innovation engine for the coming decade. Our Global Market Access (GMAx) organizat…
Skills: Executive Presence, Global Market Access, Healthcare Reimbursement, Health Economics, Leadership
Rahway, New Jersey, United States · On-site
$96k–$151k/yr
Job Description The Pharmaceutical Analytical Sciences group has an opening for a second shift Specialist based in Rahway, NJ. Join us and experience our culture first-hand - one of strong ethics & integrity, diversified…
Skills: Analytical Instrumentation, Audit Support, Data Analysis, Experimentation, GMP Compliance
South San Francisco, California, United States · On-site
$131k–$207k/yr
Job Description The Cardiometabolic Disease (CMD) department at our company's Research Labs South San Francisco is seeking a highly innovative and technically rigorous Scientist/Senior Scientist with deep expertise in pr…
Skills: Cardiometabolic, Cardiovascular Diseases, Cardiovascular Surgery, In Vivo Animal Models, In Vivo Imaging
North Wales, Pennsylvania, United States · Remote OK
$79k–$125k/yr
Job Description As a Cardiovascular Disease Specialist, you will drive meaningful patient impact by leveraging our scientific expertise and serving as the primary contact for customers within your assigned territory. As …
Skills: Account Management, Business Planning, Cardiovascular Disease, Competitive Markets, Customer Engagement
Atlanta, Georgia, United States · Remote OK
$191k–$300k/yr
Job Description Oncology Customer Team Leader (District Sales Manager) – Atlanta, GA Grow and accelerate your career with our Oncology Sales organization and join a team that’s driven to make an impact on cancer patients…
Skills: Account Management, Customer Relationship Management (CRM), Oncology, Team Leadership
Rahway, New Jersey, United States · Hybrid
$96k–$151k/yr
Job Description Senior Specialist, New Product Introductions Job Description Our company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The dif…
Skills: Strategic Procurement, Supplier Management, Data Analytics, Cost Reduction, Risk Management
Millsboro, Delaware, United States · On-site
$96k–$151k/yr
Job Description For over 130 years, we have pioneered groundbreaking science. Today, we are driven by continuous innovation to develop breakthrough medicines, vaccines and technology. Rooted in direct experience on the f…
Skills: Aseptic Manufacturing, Biopharmaceutical Industry, Cell Cultures, cGMP Compliance, Data Analysis
London, England, United Kingdom · Hybrid
Job Description Vaccines Associate Marketer Our commercial business is continuously evolving to enable us to align the needs of our customers with the commercial opportunities we are working towards within the next 5 yea…
Skills: Brand Management, Creative Campaign Development, Data Analysis, Digital Marketing, Healthcare Marketing
Upper Gwynedd Township, Pennsylvania, United States · On-site
$173k–$273k/yr
Job Description Join Our Company’s Manufacturing Division as a Director/ Principal Scientist, Biologics Drug Substance Commercialization (BDSC). This senior leadership role is responsible for driving late-stage and comme…
Skills: Antibody Therapeutics, Biologics, Cell Cultures, Clinical Manufacturing, Commercialization
Unterschleißheim, Bavaria, Germany · On-site
Job Description Unsere Produktionsteams setzen sich aus den Menschen zusammen, die unsere Produkte effektiv herstellen. In unseren Produktionsstätten gilt stets die Devise „Safety First, Quality Always“ mit dem Ziel der …
Skills: Good Manufacturing Practices (GMP), Pharmaceutical Production, Quality Assurance, Quality Control, Safety Compliance
Boxmeer, North Brabant, Netherlands · On-site
Job Description Step into a role where creativity meets purpose, and your work contributes to better health and care for animals every day. Join us as a: Brand Manager (Companion Animals) Welcome to our team Our Dutch co…
Skills: Brand Management, Creative Campaign Development, Marketing Strategy Implementation, Market Research, Product Lifecycle Management
Brussels, Brussels-Capital, Belgium · On-site
Job Description Make an impact where data, digital and animal health come together. Help turn data into meaningful insights while enhancing digital customer experiences that truly make a difference. Join our Animal Healt…
Skills: Customer Relationship Management (CRM), Digital Marketing, Market Development, Pricing Strategies, Salesforce
Rahway, New Jersey, United States · Hybrid
$117k–$184k/yr
Job Description Senior Empower Technical Lead Join us and be part of our dedicated team that provides support for our Global Manufacturing Laboratories to improve efficiency and compliance while improving our CDS Platfor…
Skills: Applied Engineering, Asset Management, Biochemical Analysis, Chromatography, GMP Compliance
Rahway, New Jersey, United States · Hybrid
$96k–$151k/yr
Job Description Senior Specialist, New Product Introductions Job Description Our company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The dif…
Skills: Adaptability, Analytical Thinking, Benchmarking, Contract Management, Cost Reduction Initiatives
St. Paul, Minnesota, United States · Remote OK
$96k–$151k/yr
Job Description For over 130 years, we have pioneered groundbreaking science. Today, we are driven by continuous innovation to develop breakthrough medicines, vaccines and technology. Rooted in direct experience on the f…
Skills: Account Management, Adaptability, Inbound Phone Sales, Industry Knowledge, Interpersonal Relationships
Wilson, North Carolina, United States · On-site
$117k–$184k/yr
Job Description Position Summary Reporting to the Associate Director of PTO Engineering, the Senior Process/Project Engineer is responsible for providing technical support to Manufacturing Division–Wilson packaging opera…
Skills: Device Packaging, Equipment Qualification, Good Manufacturing Practices (GMP), Packaging Engineering, Packaging Operations
Hyderabad, Telangana, India · Hybrid
Job Description Material Management, Specialist Business Analyst The Opportunity Based in Hyderabad, join a global healthcare biopharma company and be part of a 130-year legacy of success backed by ethical integrity, for…
Skills: Asset Management, Benefits Management, Management System Development, Product Management, Requirements Management
Hyderabad, Telangana, India · Hybrid
Job Description Manager, Lab Execution System, Tester The Opportunity Based in Hyderabad, join a global healthcare biopharma company and be part of a 130-year legacy of success backed by ethical integrity, forward moment…
Skills: Agile Methodology, Business Analysis, Client Partnerships, Customer-Focused, Deliverables Management
Dunboyne, The Municipal District of Ratoath, Ireland · On-site
Job Description A fantastic and exciting opportunity has arisen for a Senior Manufacturing Biotech Associate. This role will involve working shift, on a 24/7 basis. This role is a site based position. The Senior Manufact…
Skills: Biopharmaceutical Manufacturing, Good Manufacturing Practices (GMP), Production Operations, Regulatory Compliance, Shift Work
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The Senior Specialist provides technical support for packaging and medical device assembly lines, focusing on the design, installation, and qualification of equipment. They serve as a subject matter expert to drive process improvements, lead technical projects, and ensure regulatory compliance.
Requires a Bachelor's degree in Engineering or Industrial Technology and at least 5 years of industrial experience within a GMP pharmaceutical environment. Candidates should possess strong analytical skills, mechanical aptitude, and experience with equipment qualification (IQ/OQ/PQ).
Position Summary
Reporting to the Associate Director of PTO Engineering, the Senior Process/Project Engineer is responsible for providing technical support to Manufacturing Division–Wilson packaging operations (including oral solid dose and bottle packaging lines) as well as medical device assembly lines.
This role involves planning, designing, and implementing technical projects while serving as a subject matter expert (SME) for assigned packaging lines and associated processes. The position requires strong technical expertise, project management capability, and knowledge of company standards, procedures, and practices.
Specify, procure, install, and qualify new packaging and medical device assembly equipment.
Provide ongoing technical support, performance monitoring, and troubleshooting for packaging and device assembly equipment.
Partner with site and above-site teams to support the transfer of new products and processes from R&D or other manufacturing sites to Wilson.
Independently or as part of a team, plan, design, and execute technical projects related to packaging and device assembly equipment and processes.
Lead or contribute to project sub-teams, ensuring effective communication and execution.
Drive implementation of new technologies and applications of existing systems.
Serve as the technical lead/SME for assigned packaging lines, providing recommendations and decision support.
Support scale-up and technology transfer of processes from pilot to commercial production, including:
Equipment design and qualification
Process demonstration and performance qualification
Process validation (including packaging systems)
Lead and support equipment qualification activities (IQ/OQ/PQ) and ensure adherence to validation standards.
Author and maintain technical documentation, including process descriptions and change controls.
Provide technical assistance to operations for equipment issues and in-line product support.
Lead root cause investigations and support resolution of equipment-related quality events.
Drive process improvements to enhance quality, efficiency, and productivity.
Evaluate data, conduct experiments, and develop scientifically sound justifications for process changes.
Support regulatory and quality activities, including site inspections, audits, and preparation of technical documentation (e.g., NDA supplements, FDA responses).
Ensure all activities comply with company policies, site procedures, safety, and regulatory requirements.
Maintain accurate and up-to-date process documentation and packaging process descriptions.
Review industry literature to identify new technologies and process improvements.
Support evaluation of materials, specifications, and methods for packaging and device assembly.
Provide technical guidance and training to less experienced team members.
Bachelor’s degree in Engineering or Industrial Technology (or related discipline)
Minimum of 5 years of relevant industrial experience
Experience working in a GMP pharmaceutical environment
Demonstrated leadership and teamwork skills
Strong analytical and problem-solving ability
Excellent oral and written communication skills
Ability to work effectively with limited supervision
Strong mechanical aptitude with the ability to troubleshoot equipment issues
Experience in the pharmaceutical industry
Experience with oral solid dose and bottle packaging systems
Project management experience
Experience with equipment qualification (IQ/OQ/PQ)
Familiarity with Lean Six Sigma tools and methodologies
Current Employees apply HERE
Current Contingent Workers apply HERE
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:
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.
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The salary range for this role is
$117,000.00 - $184,200.00This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An 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.
Travel Requirements:
10%*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.
At MSD, known as Merck & Co., Inc., Rahway, NJ, USA in the United States and Canada, we are unified around our purpose: We use the power of leading-edge science to save and improve lives around the world. For more than 130 years, we have brought hope to humanity through the development of important medicines and vaccines. We aspire to be the premier research-intensive biopharmaceutical company in the world – and today, we are at the forefront of research to deliver innovative health solutions that advance the prevention and treatment of diseases in people and animals. We foster a diverse and inclusive global workforce and operate responsibly every day to enable a safe, sustainable and healthy future for all people and communities. For more information, visit www.msd.com and connect with us on Facebook, Instagram, Twitter, and YouTube.
Offices: 90 E Scott Ave, Rahway, New Jersey 07065, US · 2000 Galloping Hill Road, Kenilworth, NJ 07033, US · Jalan Puteri 5/20, Puchong, Selangor 47100, MY · Clos du Lynx 5, Woluwe-Saint-Lambert, Brussels Region 1200, BE · Keilaranta 3, Espoo, Southern Finland 02150, FI
At MSD, known as Merck & Co., Inc., Rahway, NJ, USA in the United States and Canada, we are unified around our purpose: We use the power of leading-edge science to save and improve lives around the world. For more than 130 years, we have brought hope to humanity through the development of important medicines and vaccines. We aspire to be the premier research-intensive biopharmaceutical company in the world – and today, we are at the forefront of research to deliver innovative health solutions that advance the prevention and treatment of diseases in people and animals. We foster a diverse and inclusive global workforce and operate responsibly every day to enable a safe, sustainable and healthy future for all people and communities. For more information, visit www.msd.com and connect with us on Facebook, Instagram, Twitter, and YouTube.
Offices: 90 E Scott Ave, Rahway, New Jersey 07065, US · 2000 Galloping Hill Road, Kenilworth, NJ 07033, US · Jalan Puteri 5/20, Puchong, Selangor 47100, MY · Clos du Lynx 5, Woluwe-Saint-Lambert, Brussels Region 1200, BE · Keilaranta 3, Espoo, Southern Finland 02150, FI
