Our Engineers support internal and external manufacturing operations remain operational, continuously improve and innovate. With our extensive range of facilities and environments, our Engineers have opportunities across many diverse areas including Biological, Chemical, Automation, Capital Projects, Maintenance, Safety, Process Development, Technical Services, Utilities and Validation.
Primary responsibilities are routine laboratory dissolution, assay/degradate, content uniformity, and identity testing and documentation in a Good Manufacturing Practice (GMP) laboratory. Additional responsibilities include entering data into Labware, drafting investigations, participating and leading root cause analysis, updating standard operating procedures, training and mentoring other analysts, troubleshooting instrumentation issues, and participation in the daily tier process. Testing equipment utilized include but are not limited to Ultraviolet (UV), High-Performance Liquid Chromatography (HPLC), Fourier Transform Infrared (FTIR), dissolution baths, & Karl Fisher, pH meter, conductivity meter, & Near Infrared (NIR).
Education Minimum Requirements
- Bachelor of Arts or Science (B.A./B.S) Degree (Science or Engineering)
Required Experience and Skills
- Minimum of 3 years of pharmaceutical industry experience
- Knowledge of continuous improvement principles.
- Experience operating routine laboratory equipment including but not limited to: HPLC, dissolution apparatus, FTIR, NIR, Karl Fisher, pH meter, conductivity meter, UV, etc.
- Knowledge of regulatory and cGMP principles.
Preferred Experience and Skills
- Utilizing Empower
- Utilizing Labware/ Laboratory Information Management System (LIMS)
- Execution of root cause analysis
- Background in technical writing including but not limited to: updating of standard operating procedures and writing quality notifications
- Knowledge of Tier processes
- Executing Sort, Set, Shine, Standardize and Sustain (5S) principles
Our Manufacturing & Supply Division is committed to be the most trusted supplier of bio-pharmaceuticals worldwide. Our facilities, along with our external contractors, suppliers, and partners, create an interdependent global manufacturing network that’s committed to delivering a high quality, reliable supply to customers and patients on time, every time.
Who we are …
Merck & Co., Inc., Kenilworth, New Jersey, USA is known as “Merck” in the United States, Canada & Puerto Rico. We are known as “MSD” in Europe, Middle East, Africa, Latin America & Asia Pacific. We are a global biopharmaceutical leader with a diverse portfolio of prescription medicines, oncology, vaccines and animal health products.
We are driven by our purpose to develop and deliver innovative products that save and improve lives. With 69,000 employees operating in more than 140 countries, we offer state of the art laboratories, plants and offices that are designed to Inspire our employees as we learn, develop and grow in our careers. We are proud of our 125 years of service to humanity and continue to be one of the world’s biggest investors in Research & Development.
What we look for …
In a world of rapid innovation, we seek brave Inventors who want to make an Impact in all aspects of our business, enabling breakthroughs that will affect generations to come. We encourage you to bring your disruptive thinking, collaborative spirit and diverse perspective to our organization. Together we will continue Inventing For Life, Impacting Lives while Inspiring Your Career Growth.
NOTICE FOR INTERNAL APPLICANTS
In accordance with Managers' Policy - Job Posting and Employee Placement, all employees subject to this policy are required to have a minimum of twelve (12) months of service in current position prior to applying for open positions.
If you have been offered a separation benefits package, but have not yet reached your separation date and are offered a position within the salary and geographical parameters as set forth in the Summary Plan Description (SPD) of your separation package, then you are no longer eligible for your separation benefits package. To discuss in more detail, please contact your HRBP or Talent Acquisition Advisor.
If you need an accommodation for the application process please email us at email@example.com
For more information about personal rights under Equal Employment Opportunity, visit:
We are an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations.
Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Kenilworth, NJ, USA, also known as Merck Sharp & Dohme Corp., Kenilworth, 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.
Flexible Work Arrangements:
1st - Day
Valid Driving License:
General lab testing and chemicals. Acids, bases, strong organic chemicals
Number of Openings: