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Fort Lee, New Jersey, United States · On-site
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Mahwah, New Jersey, United States · On-site
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Jersey City, New Jersey, United States · On-site
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Totowa, New Jersey, United States · On-site
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Mount Olive, New Jersey, United States · On-site
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Totowa, New Jersey, United States · Hybrid
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Rahway, New Jersey, United States · Hybrid
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Robbinsville, New Jersey, United States · On-site
$70k–$91k/yr
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Totowa, New Jersey, United States · On-site
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Trenton, New Jersey, United States · On-site
$76k–$109k/yr
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Paulsboro, New Jersey, United States · On-site
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Raritan, New Jersey, United States · Hybrid
$164k–$283k/yr
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Newark, New Jersey, United States · On-site
$100k–$125k/yr
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Newark, New Jersey, United States · On-site
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Middletown Township, New Jersey, United States · On-site
$128k–$192k/yr
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Chandler, Arizona, United States · Hybrid
$122k–$200k/yr
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Support GMP activities including release and stability testing for APIs and pharmaceutical formulations using analytical tools. Lead laboratory investigations, validate analytical methods, and collaborate with cross-functional teams to enable drug development.
Requires a Bachelor's degree with 3+ years of industry experience or a Master's degree with 1+ years of experience in Chemistry or Life Sciences. Must have experience with chromatography instrumentation and strong communication skills within a fast-paced laboratory environment.
GMP Senior Scientist, Pharmaceutical Analytical Sciences
The Pharmaceutical Analytical Sciences group has an opening for a Scientist based in Rahway, NJ. Join us and experience our culture first-hand - one of strong ethics & integrity, diversified experiences, exceptional science, and a resounding passion for improving human health through innovative drug delivery technologies and predictive analytical tools. As part of our global team, you will have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.
In your role as Scientist, you will be part of a GMP analytical team working on cross-functional scientific teams to enable novel small molecule, peptide, and oligonucleotide drug development through laboratory-based analytical characterization and statistical data analysis.
Support execution of Good Manufacturing Practices (GMP) activities such as release and stability testing to support development of active pharmaceutical ingredients (APIs), pharmaceutical formulations, and manufacturing processes using both traditional and advanced analytical tools.
Document the execution, procedure, results, and conclusions of experiments in a detailed and organized manner following SOPs and ALCOA principles.
Troubleshoot and investigate any challenges associated with the GMP testing through active collaboration with cross-functional project teams and/or Quality stakeholders.
Validate and implement analytical methods to support release and stability testing of clinical materials.
Perform data entry, data review, and author analytical reports or data summaries.
Directly contributes to experimental design, execution, and data interpretation for GMP project support.
Lead laboratory investigations and deviations including root cause analysis and identification of robust corrective and preventative actions.
Strong collaboration with Pharmaceutical Analytical Sciences colleagues as well as cross-functional partners such as Global Development Quality, Process Chemistry, and Pharmaceutical Operations.
Support compliance audit/inspection activities.
Bachelor of Science degree with, at least, 3 years relevant industry experience or
Master of Science degree with, at least, 1-year relevant industry experience.
Degree in Chemistry, Pharmaceutical Sciences, or other Life Sciences.
Experience working in a fast-paced analytical laboratory utilizing chromatography instrumentation.
Excellent written and oral communication skills.
Interpersonal skills, are necessary to qualify for this role.
Ability to work in a team environment with cross-functional interactions.
The ideal applicant would have hands-on experience in a GMP environment.
Advanced chromatographic separation science, spectroscopy analysis, dissolution testing, and other analytical techniques.
Experience with Empower, Electronic Notebooks and leading laboratory investigations is a plus.
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Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process.
As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:
We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively.
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The salary range for this role is
$117,000.00 - $184,200.00This 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 at https://jobs.merck.com/us/en/compensation-and-benefits.
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.
San Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance
Los Angeles Residents Only: We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance
Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, 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.
Travel Requirements:
10%*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
Requisition ID:R408307
At MSD, known as Merck & Co., Inc., Rahway, NJ, USA in the United States and Canada, we are unified around our purpose: We use the power of leading-edge science to save and improve lives around the world. For more than 130 years, we have brought hope to humanity through the development of important medicines and vaccines. We aspire to be the premier research-intensive biopharmaceutical company in the world – and today, we are at the forefront of research to deliver innovative health solutions that advance the prevention and treatment of diseases in people and animals. We foster a diverse and inclusive global workforce and operate responsibly every day to enable a safe, sustainable and healthy future for all people and communities. For more information, visit www.msd.com and connect with us on Facebook, Instagram, Twitter, and YouTube.
Offices: 90 E Scott Ave, Rahway, New Jersey 07065, US · 2000 Galloping Hill Road, Kenilworth, NJ 07033, US · Jalan Puteri 5/20, Puchong, Selangor 47100, MY · Clos du Lynx 5, Woluwe-Saint-Lambert, Brussels Region 1200, BE · Keilaranta 3, Espoo, Southern Finland 02150, FI
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