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Senior Process Associate Jobs (NOW HIRING)

Senior Process Operator

Zebulon, NC · On-site

$16.25 - $20.50/hr

As a Production Senior Process Operator , you will Operate, challenges and cleans equipment ... Works in coordination with other associates, assistants, and/or technicians to carry out daily job ...

Senior Process Engineer II

Ann Arbor, MI · On-site

$105.06K - $139.59K/yr

At Terumo we're working to build a healthier, happier society for our associates and the world. Our ... Job Summary The Senior Process Engineer II leads the development, improvement, and deployment of ...

Senior Process Engineer

Whitehall, MI

$98.90K - $127.90K/yr

Development focused --provides guidance and assistance to associates; helps others improve in their ... Design, document, and optimize manufacturing processes, incorporating AI analytics for efficiency ...

Senior Process Engineer

Whitehall, MI

$98.90K - $127.90K/yr

Development focused --provides guidance and assistance to associates; helps others improve in their ... Design, document, and optimize manufacturing processes, incorporating AI analytics for efficiency ...

Senior Process Engineer

Whitehall, MI

$98.90K - $127.90K/yr

Development focused --provides guidance and assistance to associates; helps others improve in their ... Design, document, and optimize manufacturing processes, incorporating AI analytics for efficiency ...

Senior Process Engineer

Whitehall, MI

$98.90K - $127.90K/yr

Development focused --provides guidance and assistance to associates; helps others improve in their ... Design, document, and optimize manufacturing processes, incorporating AI analytics for efficiency ...

Senior Process Designer

Scottsdale, AZ · On-site

$90K - $125K/yr

We are seeking a skilled Senior Process Designer to join our dynamic team. In this role, you will ... An Associate degree in engineering or architectural fields is a plus. * Proficiency working with ...

MACS Sr. Process Supervisor

Rahway, NJ · On-site

$105.60K - $136.50K/yr

The Process Supervisor position will report to the Associate Director, MACS Operations and will be a member of the MACS Operations Team at the Rahway, NJ facility. Responsibilities of the Senior ...

MACS Sr. Process Supervisor

Rahway, NJ

$105.60K - $136.50K/yr

The Process Supervisor position will report to the Associate Director, MACS Operations and will be a member of the MACS Operations Team at the Rahway, NJ facility. -Responsibilities of the Senior ...

Senior Process Designer

Scottsdale, AZ · On-site

$90K - $125K/yr

We are seeking a skilled Senior Process Designer to join our dynamic team. In this role, you will ... An Associate degree in engineering or architectural fields is a plus. * Proficiency working with ...

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Senior Process Associate information

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How much do senior process associate jobs pay per hour?

As of May 28, 2026, the average hourly pay for senior process associate in the United States is $18.43, according to ZipRecruiter salary data. Most workers in this role earn between $14.42 and $17.31 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Senior Process Associate, and why are they important?

To thrive as a Senior Process Associate, you need strong analytical abilities, attention to detail, and proficiency in business process management, typically supported by a bachelor’s degree in business or a related field. Familiarity with workflow automation tools, ERP systems, and possibly Six Sigma or Lean certifications is highly valued. Excellent communication, problem-solving, and time management skills help you collaborate effectively and drive process improvements. These skills ensure efficient operations, high-quality deliverables, and ongoing optimization in business processes.

What are some common challenges Senior Process Associates face when managing multiple projects simultaneously?

Senior Process Associates often juggle several projects at once, which can present challenges such as prioritizing tasks, managing tight deadlines, and ensuring consistent process quality. Effective time management and clear communication with team members and stakeholders are crucial to prevent bottlenecks and maintain workflow efficiency. Leveraging project management tools and regularly reviewing progress can help mitigate these challenges and support successful project delivery.

What is a Senior Process Associate?

A Senior Process Associate is a professional who specializes in managing, optimizing, and improving business processes within an organization. They often handle complex tasks, work with various departments to streamline workflows, and ensure processes are efficient and compliant with company standards. Senior Process Associates may also mentor junior staff, identify opportunities for automation, and contribute to process documentation and reporting. Their goal is to enhance productivity and support the organization's operational objectives.
More about Senior Process Associate jobs
What cities are hiring for Senior Process Associate jobs? Cities with the most Senior Process Associate job openings:
Who are the top companies hiring for Senior Process Associate jobs? The top employers for Senior Process Associate jobs are:
What states have the most Senior Process Associate jobs? States with the most job openings for Senior Process Associate jobs include:
Infographic showing various Senior Process Associate job openings in the United States as of May 2026, with employment types broken down into 86% Full Time, 7% Part Time, and 7% Contract. Highlights an 93% In-person, and 7% Remote job distribution, with an average salary of $38,334 per year, or $18.4 per hour.
Senior Process Operator

Senior Process Operator

GSK

Zebulon, NC • On-site

$16.25 - $20.50/hr

Full-time

Posted 8 days ago


GlaxoSmithKline rating

8.9

Company rating: 8.9 out of 10

Based on 19 frontline employees who took The Breakroom Quiz

8th of 70 rated pharmaceutical


Job description

As a Production Senior Process Operator, you will Operate, challenges and cleans equipment, according to appropriate to SOPs, JSAs, and batch documents to deliver high quality products manufactured in a safe way to fulfil the needs of the supply chain. Monitors equipment for excessive rejects. Performs all duties in accordance with regulatory and OSHA requirements. Ability to changeover and set up equipment to design specifications including performing all SAP changeover tasks. Identified as the SME for all systems interaction and operations and proficient at all SOPs, JSAs, and OSW for the relevant area documents. Leads the creation of standards/systems to increase business results.
Key Responsibilities:
  • Operates, challenges, replenishes consumable supplies, cleans equipment, and all the duties needed by the business in accordance with cGMPs, Batch Documentation, SOPs, ZSPs and JSAs as required and responsible for maintaining inspection readiness of area with minimal supervision.
  • Actively participates and owns monitoring equipment for excessive rejects/ stoppages and utilizes performance data to escalate any problems occurring in the area that affects product quality, safety and other aspects of line performance.
  • Trained in the GSK Production System standards (i.e., 5s, standard work, problem solving, Gemba, process confirmations, and performance management) towards the goal of Zero Accidents, Zero Defects, and Zero Waste.
  • Participates in performance management entry, steps 1-3 of problem solving, and performing/maintaining OSW and 5S.
  • Delivers against safety, quality, waste & performance objectives defined by strategy deployment and identifies and recommends areas for process improvement or alternative operating methods to increase efficiency.
  • Recognized as an expert on operations/process and possesses the ability to troubleshoot and resolve minor equipment production stoppages.
  • Operator possesses considerable knowledge of the job and is reliable and able to produce high quality and high quantity work.
  • Utilizes systems/applications required for job performance (i.e. DELTA, my Learning, Free Weigh, DISY, Active Plant, IP21, SAP basic transactions for meeting production supply, etc.).
  • Works in coordination with other associates, assistants, and/or technicians to carry out daily job responsibilities, including recognizing and assisting with troubleshooting technical issues and providing information to the next supervisory level.
  • Demonstrates the ability to describe the technological theory of operation, product flow through equipment, and able to identify the function and purpose of all sensors, limit switches, and proximity sensors.
  • Demonstrates the ability to conduct equipment set up changeovers and start of batch activities to the designed specifications without start up issues. Ability to certify on multiple technologies and flow to the work as needed by the business.

Why you?
Basic Qualifications:
We are looking for professionals with these minimum required skills to achieve our goals:
  • High School Diploma or GED
  • 5+ years experience in Production Operator role
  • 3+ years experience working at GSK
  • OJT certified in all work centers in packaging or the majority of work centers in manufacturing
  • Demonstrated performance in all Process Operator job roles

Preferred Qualifications:
We are looking for professionals with these required skills to achieve our goals:
  • Associate Degree or equivalent education
  • Basic reading, writing and mathematical skills
  • Basic computer skills and understanding and operational computer skills, MS Word, and MS Excel.
  • Ability to work accurately with figures and information
  • Ability to use and analyze data effectively
  • Must be mechanically inclined with the ability to learn the operation, read gauges and instrumentation, and any equipment related to the production of medical devices and/or pharmaceutical products
  • Strong attention to detail and ability to create and follow detailed documentation.
  • Ability to follow both written and verbal instruction.

Skills:
  • Basic reading, writing and mathematical skills
  • Advanced computer skills and understanding and operational computer skills, MS Word, and MS Excel
  • Ability to proficiently utilize basic hand tools
  • Ability to work accurately with figures and information
  • Must be mechanically inclined with the ability to learn the operation, read gauges and instrumentation, and any equipment related to the production of medical devices and/or pharmaceutical products

Traits:
  • Visual inspection and attention to detail
  • Strong attention to detail and ability to create and follow detailed documentation.
  • Ability to follow both written and verbal instruction.
  • Thorough understanding of Overall Equipment Effectiveness
  • Advanced computer skills (focused on MS Office) use software to analyze data & troubleshoot
  • Ability to work independently
  • Ability to train others on job related tasks
  • Ability to set up equipment to scale measurements without assistance
  • Competent at problem solving utilizing 6 step process that identifies root cause

Physical Job Requirements:
  • Ability to climb, kneel, stoop, balance, crawl, crouch, reach, sit, stand, walk, push, pull, grasp, feel, talk, hear, lift, and perform tasks as defined by the specific role.
  • Ability to work overtime as needed.
  • Must be able to wear gloves, eye protection, and protective clothing as required by the specific job role.
  • Must be able to handle up to 40 lbs. of materials
  • Must be able to work inside a manufacturing environment where there may be exposure to noise, moving mechanical parts, and various drug compounds as the specific role mandates.
  • Must be able to flow to the work as needed and operate at a high energy fast-paced environment
  • Ability to learn at a rapid pace to support training module expectations
  • Ability to work up to 12.5 hrs. in one shift

About the Zebulon Site
GSK's Zebulon site is a global supplier of Respiratory and Solid Dose medicines to patients around the globe and the largest GSK Pharmaceutical secondary manufacturing site in North America. The site is located less than 30 minutes from downtown Raleigh, Wendell, Knightdale, Rocky Mount and Wake Forest.
Key differentiators about GSK and Zebulon:
  • Our commitment to inclusion is seen as a critical advantage of ours
  • Our focus on cultivating a positive work environment that cares for our employees
  • Demonstrated opportunities for continued career growth driven by individual ambition
  • Leaders that care about their teams and growth of both individuals and the company
  • A priority focus on Safety and Quality
  • Clean and GMP compliant work environment
  • Onsite cafeteria
  • Onsite gym
  • Temperature-controlled
  • Licensed onsite Health & Wellness clinic

#Earlycareers
Work Environment
This role is **on-site** and requires physical activity throughout the shift. You'll work in a temperature-controlled manufacturing environment with protective gear provided. If you're looking for a role where you can grow your career and contribute to a team that values safety and quality, we encourage you to apply!
Inclusion
We value inclusion and encourage applications from people with different backgrounds, experiences and perspectives. We hire for skills and potential and support careers through training and mentorship.
How to apply
If this role fits your skills and goals, please apply now. Tell us briefly why you want to join and what you will bring to the team. We look forward to hearing from you.
Please visit GSK US Benefits Summary to learn more about the comprehensive benefits program GSK offers US employees.
Why GSK?
Uniting science, technology and talent to get ahead of disease together.
GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases - to impact health at scale.
People and patients around the world count on the medicines and vaccines we make, so we're committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.
If you require an accommodation or other assistance to apply for a job at GSK, please contact the appropriate Recruitment Staff by emailing us at - usrecruitment.adjustments@gsk.com
GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.
Important notice to Employment businesses/ Agencies
GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.
Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov/

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About GlaxoSmithKline

Sourced by ZipRecruiter

GlaxoSmithKline is a globally recognized pharmaceutical and healthcare company based in Philadelphia, PA, USA. Originated from a merger between Glaxo Wellcome and SmithKline Beecham in 2000, the company excels in the pharmaceutical industry and holds a leading position in making medicines, vaccines, and consumer healthcare products. GSK's mission is to improve the quality of human life by enabling people to do more, feel better, and live longer. They adhere to core values of transparency, integrity, respect for people, and patient-focus, reflecting in their endeavors to conduct research and deliver innovative healthcare solutions to patients and consumers worldwide.

Industry

Scientific research and development services

Company size

10,000+ Employees

Headquarters location

Philadelphia, PA, US