
Job Information
Merck Sr. Director, Pharmacokinetics in Lower Gwynedd, Pennsylvania
Job Description
Description
Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity, and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement, and teamwork. As part of our global team, you’ll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.
The Department of Pharmacokinetics, Dynamics, Metabolism, and Bioanalytics (PDMB) at Spring House Innovation Park is seeking Senior Director to join our Company and lead a team of approximately 19 scientists to deliver bioanalytical solutions that enable and accelerate vaccine preclinical and clinical development. The Senior Director will report to the Executive Director of Early Development Vaccines and be part of the leadership team to design and executive a modernization effort to accelerate vaccine development. The primary role of the successful candidate will be to lead a team to support vaccine early development (Phase 1 and 2) and contribute to drug discovery and development teams within the Infectious Disease and Vaccines therapeutic areas via overseeing a broad portfolio of molecular and cell-mediate based assays. The successful candidate will be a scientific leader, with a passion for developing assays, delivering high quality data, and helping teams choose the right assays for data-driven decision making. A record of accomplishment of successful collaboration while working in cross-functional project teams is expected. The successful candidate will also have responsibility for mentoring, scientific supervision, and training scientists to become our future leaders.
Qualifications
Education :
- A Ph.D. degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or related area with 8+ years, a MD or MD/PhD or DVM/PhD (Dual Degree) with 3+ years, a MS degree with 10+ years, or BS degree with 14+ years of relevant experience
Required :
10+ years of experience in molecular, immunogenicity and cell-based assay development and optimization.
Actively working with staff to encourage and facilitate their personal and scientific development.
A strong aptitude for and previous experience in managing inclusive scientific teams and attracting, developing, and retaining diverse talent.
Maintaining a strong network internally and across the external academic and regulatory community is expected, as well as advancing a culture of scientific excellence and curiosity.
Setting future strategies and bringing new technologies into the regulated labs.
Responsible to partner with our Outsourcing team to provide scientific over-sight of at our Clinical Research Organizations (CROs) in collaboration with others to ensure data quality and accuracy is aligned with our company's expectations.
Has in-depth understanding of the drug discovery and/or development process and comprehensive knowledge of the principles and concepts of bioanalytical and/or vaccine clinical testing/regulatory filing.
Strong technical expertise in bioanalytical assay design, development, and execution in support of antiviral, antibacterial, cell and gene therapy, and/or vaccine discovery. Has advanced knowledge in multiplexed immunogenicity and cell based assays.
Candidate must be trained in GLP and GCLP requirements and must have experience working in a regulated laboratory environment.
Proven ability to lead the development of new, innovative approaches including experience in new assay technology evaluation and nurturing these technologies to garner health authority approval.
Established external scientific reputation (e.g. publication record, leadership in consortia, external presentations).
Preferred :
Experience with immunoassay platforms such as our Company, Luminex, ELISA, AphaLISA is a plus
Experience in cell-based functional assays to monitor immunogenicity.
Familiar with liquid handlers and other automation/robotic platforms for sample preparation and assay process.
Working knowledge and proponent of developing a strategy to utilize a standardization process to Data Analysis and strong supporter of using Design of experts to improve robustness in bioanalytical.
Current Employees apply HERE (https://wd5.myworkday.com/msd/d/task/1422$6687.htmld)
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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 (https://survey.sogosurvey.com/r/aCdfqL) if you need an accommodation during the application or hiring process.
We are an Equal Opportunity Employer, committed to fostering an inclusive and diverse workplace. All qualified applicants will receive consideration for employment without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status, or other applicable legally protected characteristics. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:
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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”.
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:
Domestic
VISA Sponsorship:
No
Travel Requirements:
10%
Flexible Work Arrangements:
Not Applicable
Shift:
Not Indicated
Valid Driving License:
No
Hazardous Material(s):
n/a
Job Posting End Date:
04/1/2025
*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: R340418
Merck
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