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Job Description The Small Molecule Analytical Research and Development (SMAR&D) group has an exciting opportunity for a Principal Scientist based in Rahway, NJ. Join us and experience our culture firsthand - 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. As a Principal Scientist, you will be part of a team developing innovative analytical methodologies for medicines based on small molecules, peptides, mRNA, oligonucleotides and bioconjugates. Our responsibilities range from early stage up to commercialization for both drug substance and a broad array of oral, sterile and combination products. You will also contribute towards regulatory submissions to enable clinical trials. Your main responsibilities will include: Driving our Company's Pipeline: * Leading analytical teams driving the development of drugs in our Company's pipeline, with a deep understanding of product development from early stage through commercialization. * Actively partnering with other functional areas to design scientific studies guiding product and process development. * Defining and implementing end-to-end analytical control strategies for clinical supplies under good manufacturing practices (including method development and validation as well as specification setting). * Authoring investigational new drug (IND), investigational medicinal product dossier (IMPD), and new drug application (NDA)/ worldwide marketing application (WMA) submission documents across the project development lifecycle, as well as responding to agency questions. Scientific Excellence and Regulatory Influence: * Promoting our Company's scientific excellence and regulatory influence through leadership in the scientific community. * Advancing and expanding analytical capabilities via the adoption and implementation of novel technologies for product and process characterization. * Challenging your teams to design and execute the experiments needed to influence programs with data-driven decisions. Leadership: * Mentoring and providing day-to-day oversight of junior analytical scientists. * Representing your team and/or department via presentations to governance committees and other internal audiences. * Partnering with director-level management to develop and execute scientific and enterprise strategies. * Proactively identifying and escalating program risks. * Fostering strong collaborations with internal stakeholders and external partners by actively engaging in two-way communication to build trusting relationships. * Applying a deep understanding of new product development and commercialization to analytical development challenges for small molecules, peptides, mRNA, oligonucleotides, and bioconjugates. Use conventional and novel technologies through active collaboration with cross functional project teams and external vendors. Qualifications Education Minimum Requirements ? Applicants must hold one of: ? * PhD Degree in Analytical Chemistry, Biochemistry, Pharmaceutical Sciences or related fields with at least 7 years of pharmaceutical industry experience?. * Master's Degree in Analytical Chemistry, Biochemistry, Pharmaceutical Sciences or related fields with at least 10 years of pharmaceutical industry experience. ? * Bachelor's Degree in Analytical Chemistry, Biochemistry, Pharmaceutical Sciences or related fields with at least 12 years of pharmaceutical industry experience. ? Required Experience and Skills A strong team player with excellent written and oral communication skills, as well as strong leadership and interpersonal skills are necessary to qualify for this role. Additional skills: * Possess deep technical expertise and strategic experience in analytical control strategy development and execution * Demonstrated ability to develop talent through good mentoring skills * Demonstrated ability for taking initiative, creativity, and innovation in problem solving * Ability to design, execute and/or direct the development and qualification of release, characterization, and stability assays for testing of clinical trial material and in support of product and process development * Strong technical problem solving ability * A proven record of external scientific engagement demonstrated by scientific publications and presentations. * Ability to work both independently for development of analytical methodologies and cross-functionally for successful transfer methods. Plan optimization and documentation to meet program deadlines. * Authoring and reviewing internal technical reports, sections of regulatory filings (e.g., IND, BLA) and external scientific publications. * Experience with matrix management and peer to peer coaching * Strong ability to deliver complex objectives under aggressive timelines in a rapidly changing environment. Preferred Experience and Skills ? While not required, experience in one or more of the following areas is preferred: ? * Hands-on chromatography (e.g., LC, GC) method development, analysis and troubleshooting. ? * Other advanced analytical techniques such as mass spectrometry or dissolution. ? * Experience in development and characterization of small and/or large molecules, mRNA, and/or antibody drug conjugates? * Established scientific reputation supported by publications and external presentations * Experience in high-throughput experimentation and data-rich experimentation, or data science #AR&D Required Skills: Accountability, Accountability, Analytical Chemistry, Analytical Method Development, Assay Development, Bioanalytical Analysis, Biochemistry, Biopharmaceuticals, Chromatographic Techniques, Clinical Judgment, Clinical Trials, Communication, Cross-Functional Teamwork, Dosage Forms, Ethical Compliance, Immunochemistry, Liquid Chromatography (LC), Matrix Management, Mentoring Staff, Messenger RNA, Method Validation, Personal Initiative, Pharmaceutical Management, Pharmacology, Product Development {+ 4 more} Preferred Skills: Current Employees apply HERE () Current Contingent Workers apply HERE () US and Puerto Rico Residents Only: 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: EEOC Know Your Rights () EEOC GINA Supplement? 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. Learn more about your rights, including under California, Colorado and other US State Acts () U.S. Hybrid Work Model Effective September 5, 2023, employees in office-based positions in the U.S. will be working a Hybrid work consisting of three total days on-site per week, Monday - Thursday, although the specific days may vary by site or organization, with Friday designated as a remote-working day, unless business critical tasks require an on-site presence.This Hybrid work model does not apply to, and daily in-person attendance is required for, field-based positions; facility-based, manufacturing-based, or research-based positions where the work to be performed is located at a Company site; positions covered by a collective-bargaining agreement (unless the agreement provides for hybrid work); or any other position for which the Company has determined the job requirements cannot be reasonably met working remotely. Please note, this Hybrid work model guidance also does not apply to roles that have been designated as "remote". The salary range for this role is $156,900.00 - $247,000.00 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 at . You can apply for this role through (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. Employee Status: Regular Relocation: VISA Sponsorship: Travel Requirements: Flexible Work Arrangements: Not Applicable Shift: Valid Driving License: Hazardous Material(s): Job Posting End Date: 03/31/2026 *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: R386716

GMP Lab Scientist- executing GMP testing for release and stability for oral solid dosage forms. The Merck Small Molecule Analytical Research and Development group has a temporary opening for a Scientist based in Rahway, NJ.

Job Description Job Title: Clinical Laboratory Technologist – Level V (Full-Time) Location: New York, NY 10029 Schedule Shift: Day Shift Days: Monday – Friday Time: 9:00 AM – 5:00 PM Hours per Week: 35 Compensation & Benefits Salary: $120,000 – $133,468 per year This is an excellent opportunity to work in a highly specialized clinical laboratory environment supporting advanced diagnostic services and patient care. Position Overview A healthcare organization in New York is seeking an experienced Clinical Laboratory Technologist – Level V to support and supervise operations within the Clinical Chemistry Laboratory. This role requires strong technical expertise and leadership skills to ensure high-quality laboratory testing, regulatory compliance, and efficient laboratory operations. The technologist will oversee testing personnel, maintain quality assurance standards, and ensure compliance with accreditation and regulatory guidelines. The ideal candidate will have significant experience in clinical chemistry laboratory supervision, quality control monitoring, and laboratory compliance standards. Key Responsibilities * Supervise laboratory testing personnel and ensure adherence to performance standards * Monitor quality control programs, instrument maintenance, and laboratory quality assurance procedures * Ensure compliance with laboratory SOPs, safety protocols, and regulatory requirements * Review laboratory test results and ensure accuracy before reporting * Manage proficiency testing programs and competency assessments * Train and orient laboratory staff and maintain competency standards * Maintain proper documentation and records in accordance with CLIA standards * Monitor laboratory equipment performance and testing accuracy * Track reagent inventory, expiration dates, and laboratory supplies * Ensure proper specimen handling across pre-analytic, analytic, and post-analytic phases * Coordinate staffing schedules and support daily laboratory workflow * Assist with hiring, training, and performance evaluations of laboratory personnel * Promote a safe, collaborative, and compliant laboratory environment Required Qualifications * Valid New York State license as a Clinical Laboratory Technologist, Cytotechnologist, or Histotechnologist issued by NYSED * Bachelor’s Degree in Chemical, Biological, Clinical Laboratory Science, or Medical Technology * Minimum 4 years of experience as a Clinical Laboratory Technologist qualifying for a regulatory or accreditation supervisory role * Clinical Chemistry laboratory supervisory experience required Preferred Qualifications * Medical Laboratory Scientist (MLS) certification from ASCP preferred Knowledge & Skills * Strong knowledge of laboratory medicine, workflows, regulatory requirements, and biosafety standards * Experience with Laboratory Information Systems (LIS) and laboratory middleware applications * Strong leadership and team management skills * Excellent communication, analytical, and problem-solving abilities * Ability to manage multiple priorities in a fast-paced clinical environment * Strong attention to detail and commitment to quality assurance For more details contact at or Call / Text at 516-862-1169. About Navitas Healthcare, LLC certified WBENC and one of the fastest-growing healthcare staffing firms in the US providing Medical, Clinical and Non-Clinical services to numerous hospitals. We offer the most competitive pay for every position we cater. We understand this is a partnership. You will not be blindsided and your salary will be discussed upfront.