Associate Specialist, Chemist - Quality Control
Compensation: $78,130.00 - $122,480.00 /year *
Employment Type: Full-Time
Industry: Scientific Research
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Are you looking for an exciting opportunity with a rapidly growing pharmaceutical manufacturer? If so, then this is the opportunity for you!
Our Quality Assurance group ensures every single material inside our products is manufactured, processed, tested, packaged, stored and distributed aligned with our incredibly high standards of quality and meets all regulatory requirements. Partnering across our internal manufacturing facilities, external contract manufacturers and suppliers we create an interdependent global manufacturing network committed to deliver a compliant, reliable supply to customers and patients on time, every time, across the globe.
+ Routine laboratory dissolution, assay/degradate, content uniformity, and identity testing and documentation in a Good Manufacturing Practice (GMP) laboratory
+ Labware data entry
+ Participating in investigation meetings and some drafting of investigations
+ Participating in root cause analysis, simple troubleshooting instrumentation issues, and participation in the daily tier process
+ Testing equipment utilized include but are not limited to UV, HPLC, FTIR, dissolution baths, & Karl Fisher, pH meter, conductivity meter, & NIR.
+ GMP documentation and a good team mindset
+ Bachelor's degree in Science, Engineering, or related discipline
**Required Experience and Skills:**
+ Knowledge of continuous improvement principles.
+ Academic or professional experience operating routine laboratory equipment including but not limited to: Karl Fisher, pH meter, conductivity meter, UV, etc.
+ Knowledge of regulatory and current GMP principles
**Preferred Experience and Skills:**
+ Operating laboratory equipment: HPLC, dissolution apparatus, FTIR, NIR, etc.
+ Utilizing Empower
+ Utilizing Labware/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
+ Experience executing 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 ...@merck.com
For more information about personal rights under Equal Employment Opportunity, visit:
EEOC Poster at
EEOC GINA Supplement? at
OFCCP EEO Supplement at
OFCCP Pay Transparency Rule at English_formattedESQA508c.pdf
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:**
**Number of Openings:**
**Requisition ID:** R43916
Associated topics: aseptic, bacteria, biomedical, dietician, healthcare, microbiological, nutrition, pharmacology, pharmacy, toxicologist
* The salary listed in the header is an estimate based on salary data for similar jobs in the same area. Salary or compensation data found in the job description is accurate.
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