Scientist, Chemical Commercialization & Technical Operations:
Merck

PRO016675-en_US
Merck
Rahway New Jersey
Pharmaceutical
Description
Requisition ID: PRO016675

Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where Merck has codified its legacy for over a century. Merck’s success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.


Merck Manufacturing Division, MMD, is a team of dedicated, energetic individuals who are committed to being the most trusted supplier of pharmaceuticals and health products worldwide. Our facilities, along with our external contractors, suppliers, and partners, comprise an interdependent global manufacturing network that’s committed to delivering a compliant, reliable supply to customers and patients on time, every time, across the globe. 


The Chemical Commercialization Technology (CCT) department is seeking highly motivated individuals who are looking for an opportunity to work in a fast-paced job that provides a high degree of technical responsibility, mentoring, and leadership of internal and external work. This Scientist, Engineering (R2) leverages scientific and technical experience to: 

  • complete assigned late-stage API characterization projects
  • mentor junior staff within the CCT organization
  • embed World-Class Supply (WCS) needs in the API working group (API-WG) discussions during process development
  • lead or support internal and external development, pre-validation, and validation for a selection of portfolio projects

 The incumbent is expected to provide and/or develop scientific expertise in small molecule process characterization work by learning and utilizing QRM/QbD methodologies and tools around statistical design and analysis of experiments. Face-to-face mentoring is expected within laboratories at the Rahway, NJ site to develop junior staff. The role includes participation in one or more cross-divisional API working groups (API-WG) and the candidate will need to help influence the API-WG’s direction on Merck Manufacturing Division (MMD) specific needs. The candidate will also have the opportunity to manage development and validation activities at external suppliers largely remotely, with some travel expected (10 – 20%). Normal travel per campaign might include a kickoff trip and a separate multi-week period of on-site coverage, typically 1-3 times per year depending on steps and complexity. Support of Merck Research Laboratories (MRL) led filing work, early development work, and/or piloting is also likely. The role focuses on late-stage development, validation, and supply support. As the early-stage portfolio progresses to late-stage projects, the incumbent is expected to help drive current MRL-led characterization work more fully to CCT ownership, leadership and execution/management.

Qualifications

Education: 

  • Bachelors Degree or higher in Chemistry/Biochemistry, Chemical/Biochemical Engineering, or suitable equivalent

Required: 

  • Familiarity with product, process, or equipment development or technical support for commercial products in any relevant industry (food, pharma/medical devices, diagnostics, cosmetics, chemicals, petroleum, etc.).
  • Strong understanding of the science behind chemistry and/or chemical engineering.
  • Desire to perform both laboratory experimentation and remote/field support of scale-up and manufacturing.
  • Ability to work in the laboratories at the Rahway, New Jersey site with occasional domestic and international travel, if necessary.

Preferred: 

  • Relevant work experience in process development in any modality (e.g. small molecules, large molecules, vaccines, drug substance or drug product, etc.) or chemical development in a related industry, ideally with experience conducting one or more programs of statistically-design experimentation. 
  • Experience interfacing with internal and external partners executing manufacturing or development.
  • Familiarity with process scale-up, technology transfer, and boots-on-the-ground support while moving from laboratory to pilot plant/factory for new and existing products/processes or desire to learn.
  • Experience executing an experimental program or statistical data analysis to address issues of process design, robustness, or productivity for an existing product/process.
  • Familiarity with the concepts and application of GLP’s/cGMP’s ideally during Pharma drug substance / drug product development and production, e.g. in a pilot and/or factory setting or desire to learn.
  • Familiarity with QRM/QbD methodologies and tools around statistical design and analysis or desire to learn.

Your role at Merck is integral to helping the world meet new breakthroughs that affect generations to come, and we’re counting on your skills and inventiveness to help make meaningful contributions to global medical advancement. At Merck, we’re inventing for life. 

 

If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to staffingaadar@merck.com.

  

Search Firm Representatives Please Read Carefully: 

Merck & Co., Inc. is not accepting unsolicited assistance from search firms for this employment opportunity.  Please, no phone calls or emails.  All resumes submitted by search firms to any employee at Merck via email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck.  No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

 

Visa sponsorship is not available for this position.

 

For more information about personal rights under Equal Employment Opportunity, visit:

 

            EEOC Poster

            EEOC GINA Supplement 



Job: Process Engineering
Other Locations:
Employee Status: Regular
Travel: Yes, 15 % of the Time
Number of Openings:
Shift (if applicable):
Hazardous Materials:
Company Trade Name: Merck
Basic Qualifications
Requirement