View All Jobs 112179

Specialist, Process Engineering - Oral Solid Dosage, Clinical Manufacturing (onsite)

Lead on-the-floor batch manufacturing to ensure safety and quality of clinical supplies
Rahway, New Jersey, United States
Junior
$87,300 – 137,400 USD / year
yesterday
USA Jobs

USA Jobs

Provides a centralized online platform for searching and applying to employment opportunities across the United States.

Specialist - Process Engineer

The Formulation, Laboratory, and Experimentation (FLEx) Center is a multi-modality (small molecule, biologics, vaccine) drug product development and clinical manufacturing facility in Rahway, New Jersey. The Non-Sterile Process Engineering team ensures right-first-time manufacture and delivery of high-quality drug products (spray-dried intermediates, tablets and capsules), leveraging pharmaceutical unit operations such as spray-drying, hot-melt extrusion, blending, roller compaction, encapsulation, compression, and film coating. We are part of our Company's research division, focused on development and clinical deliveries in a GMP pilot facility supporting partners in Oral Formulation Sciences and Pharmaceutical Commercialization Technology to enable faster delivery of new medicines to clinical trials.

The Non-Sterile (Oral Solids Dosage) team at the FLEx Center in Rahway is looking for Specialist - Process Engineer to lead clinical supply manufacturing with scientific rigor of processes, to ultimately enable flexibility and speed of our company's pipeline.

This person will:

  • Lead and strategically plan on-the-floor batch manufacturing to ensure safety and quality of clinical supplies to augment and accelerate our products.
  • Draft and execute GMP documentation including but not limited to batch records, equipment qualification and cleaning, change records and deviations.
  • Facilitate and support early process development by assisting in lab activities, and sharing knowledge transfer for scaling at pilot plant scale with relevant partners, via technical reports and presentations.
  • Build partnerships by developing and leveraging relationships within and across work groups of formulators, engineers, safety and quality representatives.
  • Foster a culture of collaboration, learning and innovation.

Required Experience and Skills:

  • Experience in executing in GMP manufacturing facilities.
  • Knowledge and experience in drug product processing.
  • Strong problem-solving skills and a direct involvement approach to problem solving
  • Desire and willingness to learn and contribute through independent problem-solving.
  • Experience in leading and supporting quality investigations and change management.

Education Minimum Requirements:

  • Bachelor of Science degree in Chemical Engineering, Biomedical Engineering, Chemistry, Pharmaceutical Sciences or related scientific field with a minimum of 2 years relevant experience, or a Master's degree with 1 year of relevant experience.

Preferred Experience and Skills:

  • Pharmaceutical development experience.
  • Experience with small molecule drug product manufacturing technologies, including: blending, granulation, compression, encapsulation, film coating, spray drying, and hot-melt extrusion.
  • Experience with Commissioning, Qualification and Validation
  • Experience with spray dried intermediates and/or hot melt extrusion

Schedule:

This role supports operational coverage across multiple shifts. Candidates must be willing and able to float between 1st and 2nd shift.

Work schedules for this role will vary based on the needs and timing of assigned campaigns. While standard working hours will apply most of the time, there may be occasions when you are required to work earlier, later, or extended hours to support campaign requirements. Reasonable notice of schedule changes will be provided whenever possible.

The salary range for this role is

$87,300.00 - $137,400.00

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.

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.

Requisition ID: R388867

+ Show Original Job Post
























Specialist, Process Engineering - Oral Solid Dosage, Clinical Manufacturing (onsite)
Rahway, New Jersey, United States
$87,300 – 137,400 USD / year
Engineering
About USA Jobs
Provides a centralized online platform for searching and applying to employment opportunities across the United States.