Associate Principal Scientist, Vaccine Analytical R&D Job in Pennsylvania (PA), Research and Development Career, Full Time Jobs in Merck & Co.
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Associate Principal Scientist, Vaccine Analytical R&D job in West Point

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Merck & Co. jobs
Pennsylvania (PA), West Point
Job Code:  MERCUSR291874ENUS
Employer:  Merck & Co.
Category:  Research and Development
Job Type:  Full Time

Location
Country:  United States
State:  Pennsylvania (PA)
City:  West Point
04/30/2024

Description
Job Description

We are seeking applicants for an Associate Principal Scientist position available at the West Point, Pennsylvania research facility.

The responsibilities of this role will be to lead and supervise a team of scientists to implement new-technologies, robotic systems, and-develop-automation-solutions to enable vaccine process development, formulation development, vaccine investigations, vaccine characterization, and method lifecycle-management.---•-

In this role, the individual must have strong analytical capabilities, ability to design, maintain, and implement robotic platform to support high-throughput and automated biochemical, immunological, and cell-based assays.- The individual should have in-depth knowledge of hardware, proven troubleshooting abilities and programming experience with robotic liquid handlers as well as scheduling software across a range of platforms (Tecan, Hamilton,-HighResBiosoutions).--The individual should have in-depth knowledge of immune based, virology, and cell-based assay to supporting bioprocess development.- Imaging and statistical analysis is considered a plus.

As part of this role, the individual will author and review CMC sections of regulatory submissions and associated source technical reports and risk assessment documents. Previous experience working in a regulated environment, training, and leading lab scientists, transferring and qualifying assays would also be directly applicable.•

The successful candidate must function well, both-independently-and-be able to collaborate in a fast-paced, integrated, multidisciplinary team environment with proven leadership-skills.-Applicants-must have effective organizational, multi-tasking, oral/written communications skills, show scientific leadership, and a desire to conduct research and-publish.--Additional-responsibilities include leading a small group of technical personal and providing guidance to other scientists, evaluating new technologies, drive innovations to influence trends in industry, and preparing technical documents to support regulatory submissions.- Evidence of strong cross-functional collaboration in bioprocess setting is also preferred.-

Education Minimum Requirement:-
  • A degree in Engineering,-chemistry/biochemistry/-or related field plus industry experience is required:- Ph.D. with a minimum of 4 years post-degree industry experience or M.S. with a minimum of 7 years or B.S. with a minimum of 10 years of experience in a related biotechnology field.

Required experience and skills:
  • In-depth knowledge and understanding of liquid handers, integrated robotic systems and software, and/or imaging methodology.
  • Proficiency in computer programming languages including Visual Basic, C#, MATLAB, Python and/or R.
  • Applied experience and knowledge with molecular biology, virology, and biochemistry techniques related to biologics or vaccines bioprocess.-
  • -In-depth knowledge of immune based, virology, and cell-based assay.
  • Experience training and leading junior scientists.-
  • Knowledge-of-requirements-in-supporting health authority filings.-
  • A strong team player with excellent oral and written communication skills; ability to work both independently for development of assays and cross-functionally for successful transfer of assays. Plan assay optimization and documentation to meet program deadlines.
  • Demonstrated scientific ability through publications and presentations in scientific conferences.

Preferred Experience and Skills:
  • Background in Analytical Methodologies and sound scientific understanding of Critical Quality Attributes/QbD/DOE principles as well as data analysis and statistics for setting specifications
  • Experience with qualification, validation, and transfer of assays to a GLP or regulated laboratory environment as listed in ICH Q2 and USP .
  • Ability to design, execute and/or direct development and qualification of release, characterization, and stability assays for testing of clinical trial material and in support of product and process development
  • Authoring and reviewing internal technical reports, sections of regulatory filings (e.g. IND, BLA) and external scientific publications.
  • Experience in representing analytical functional area on project teams.

#AR&D

#EligibleforERP

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.

Employees working in roles that the Company determines require routine collaboration with external stakeholders, such as customer-facing commercial, or research-based roles, will be expected to comply not only with Company policy but also with policies established by such external stakeholders (for example, a requirement to be vaccinated against COVID-19 in order to access a facility or meet with stakeholders). -Please understand that, as permitted by applicable law, if you have not been vaccinated against COVID-19 and an essential function of your job is to call on external stakeholders who require vaccination to enter their premises or engage in face-to-face meetings, then your employment may pose an undue burden to business operations, in which case you may not be offered employment, or your employment could be terminated. Please also note that, where permitted by applicable law, the Company reserves the right to require COVID-19 vaccinations for positions, such as in Global Employee Health, where the Company determines in its discretion that the nature of the role presents an increased risk of disease transmission.

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.

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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We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas 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, generally Tuesday, Wednesday and either Monday or 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".

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:
Yes

Travel Requirements:
No Travel Required

Flexible Work Arrangements:
Not Applicable

Shift:
1st - Day

Valid Driving License:

Hazardous Material(s):

Job Posting End Date:05/13/2024

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:R291874
ref: (MERCUSR291874ENUS)
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