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Join a forward-thinking company as a motivated scientist/engineer in the Bioprocess Drug Substance and Commercialization group. This exciting role involves executing process development for novel vaccine candidates and inline products. You will lead lab-scale experiments, collaborate with manufacturing teams, and author technical documents to support regulatory submissions. With a focus on innovation and excellence, this position offers a unique opportunity to contribute to the development of cutting-edge biopharmaceuticals in a hybrid work environment.
The Bioprocess Drug Substance and Commercialization (BDSC) group within our Manufacturing Division focuses on latestage process development technology transfer and inline support of vaccine seek a motivated scientist / engineer to work under technical direction of a group leader to support development and licensure of novel vaccine candidates and inline products.
In this role you will be responsible for :
Primary Responsibilities
Executing process development in large molecule downstream processing including labscale process development and optimization inprocess assay support and process scaleup / scaledown model development.
Leading the handson execution of labscale experiments and authoring associated technical reports and documents.
Collaborating with commercial manufacturing teams to support facility startup activities and provide onthefloor support for drug substance manufacturing.
Leading assignment execution against accelerated criticalpath timelines in a rightfirsttime manner.
Authoring and / or reviewing technical documents to support Process Performance Qualification (PPQ) and licensure.
Participate in and drive organizational excellence practices such as technical standards process platforms operational procedures
Bachelors Degree or higher in Chemical Engineering Chemistry Biology or comparable discipline with 3 years of experience.
Required Experience and Skills :
Relevant academic internship coop or professional experience in a laboratory setting.
Excellent oral and written communication skills.
Handson expertise with downstream unit operations (i.e. membrane filtration chromatography etc.) and process development for large molecules
Ability to understand and execute experiments independently in fulfillment of assigned program objectives in a manner that meets quality and timeline expectations
Welldeveloped organizational recordkeeping and problemsolving skills with an attention to detail
Preferred Experience and Skills :
Experience within or collaboration with analytical teams pilotscale and / or manufacturing environment.
Large molecule drug substance process development scaling (up and down) and technology transfer
Current Good Manufacturing Practice (cGMP) awareness or experience.
Experience authoring technical documentation in support of the following : process performance qualification risk assessment control strategy process comparability reports and / or regulatory submissions.
Communication of scientific information through oral presentations and written documents
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 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 anothers 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 officebased positions in the U.S. will be working a Hybrid work consisting of three total days onsite per week Monday Thursday although the specific days may vary by site or organization with Friday designated as a remoteworking day unless business critical tasks require an onsite Hybrid work model does not apply to and daily inperson attendance is required for fieldbased positions; facilitybased manufacturingbased or researchbased positions where the work to be performed is located at a Company site; positions covered by a collectivebargaining 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 Company is required to provide a reasonable estimate of the salary range for this job in certain states and cities within the United States. Final determinations with respect to salary will take into account a number of factors which may include but not be limited to the primary work location and the chosen candidates relevant skills experience and education.
Expected US salary range :
85600.00 $134800.00
Available benefits include bonus eligibility long term incentive if applicable health care and other insurance benefits (for employee and family) retirement benefits paid holidays vacation and sick days. A summary of benefits is listed here.
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 preexisting 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 :
Travel Requirements :
Flexible Work Arrangements :
Not Applicable
Shift : 1st Day
Valid Driving License :
n / a
Job Posting End Date :
05 / 9 / 2025
Key Skills
Laboratory Experience,Immunoassays,Machine Learning,Biochemistry,Assays,Research Experience,Spectroscopy,Research & Development,cGMP,Cell Culture,Molecular Biology,Data Analysis Skills
Employment Type : Full-Time
Experience : years
Vacancy : 1
Monthly Salary Salary : 85600 - 134800
Scientist Engineering • Rahway, New Jersey, USA