As a Principal Scientist you will have the opportunity to influence the future direction of our Company's Downstream Processing of Biologics. You will work with an immensely creative and ...
As a Principal Scientist you will have the opportunity to influence the future direction of our Company's Downstream Processing of Biologics. You will work with an immensely creative and ...
As a Principal Scientist you will have the opportunity to influence the future direction of our Company's Downstream Processing of Biologics. You will work with an immensely creative and ...
As a Principal Scientist you will have the opportunity to influence the future direction of our Company's Downstream Processing of Biologics. You will work with an immensely creative and ...
As a Principal Scientist you will have the opportunity to influence the future direction of our Company's Downstream Processing of Biologics. You will work with an immensely creative and ...
As a Principal Scientist you will have the opportunity to influence the future direction of our Company's Downstream Processing of Biologics. You will work with an immensely creative and ...
Downstream Process Development Associate - Gene Therapy Purification 3656143
San Diego, CA · On-site
$80 - $84.60/hr
Support continued development of downstream processing capabilities within a growing organization. Are you an experienced downstream process development professional ready to make an impact?
New
Quick apply
Downstream Process Development Associate - Gene Therapy Purification 3656143
San Diego, CA · On-site
$80 - $84.60/hr
Support continued development of downstream processing capabilities within a growing organization. Are you an experienced downstream process development professional ready to make an impact?
New
Associate Director/Director, Formulation & Downstream Process Development
San Diego, CA · On-site
$120K - $220K/yr
Stay current with advances in nanoparticle purification, LNP downstream processing, and scalable manufacturing technologies. * Provide scientific leadership for downstream process development ...
Associate Director/Director, Formulation & Downstream Process Development
San Diego, CA · On-site
$120K - $220K/yr
Stay current with advances in nanoparticle purification, LNP downstream processing, and scalable manufacturing technologies. * Provide scientific leadership for downstream process development ...
Stay current with advances in nanoparticle purification, LNP downstream processing, and scalable manufacturing technologies. * Provide scientific leadership for downstream process development ...
Stay current with advances in nanoparticle purification, LNP downstream processing, and scalable manufacturing technologies. * Provide scientific leadership for downstream process development ...
Downstream Process
Tustin, CA · On-site
Downstream Process Analytics Specialist Industry: Biopharmaceutical CDMO / Biologics Manufacturing Location: Irvine, CA (Onsite) Employment Type: Full-Time Schedule: MondayâFriday | Standard ...
Downstream Process
Tustin, CA · On-site
Downstream Process Analytics Specialist Industry: Biopharmaceutical CDMO / Biologics Manufacturing Location: Irvine, CA (Onsite) Employment Type: Full-Time Schedule: MondayâFriday | Standard ...
Technical Source is currently in search of a Downstream Process Engineer for our pharmaceutical client in the Raleigh-Durham-Chapel Hill Area. This is a long-term contract position that requires on ...
Quick apply
Technical Source is currently in search of a Downstream Process Engineer for our pharmaceutical client in the Raleigh-Durham-Chapel Hill Area. This is a long-term contract position that requires on ...
Scientist II, Downstream Viral Vector Process Development
Alameda, CA · On-site
$130 - $150/hr
Hands‑on experience with chromatography, filtration, TFF and other downstream processing techniques. * Strong analytical and problem‑solving skills, with the ability to interpret complex data ...
Scientist II, Downstream Viral Vector Process Development
Alameda, CA · On-site
$130 - $150/hr
Hands‑on experience with chromatography, filtration, TFF and other downstream processing techniques. * Strong analytical and problem‑solving skills, with the ability to interpret complex data ...
The successful candidate will drive scientific excellence in downstream processing (DSP)-including clarification, chromatography, TFF, sterile filtration and fill/finish-ensuring processes are robust ...
The successful candidate will drive scientific excellence in downstream processing (DSP)-including clarification, chromatography, TFF, sterile filtration and fill/finish-ensuring processes are robust ...
Scientist II, Downstream Viral Vector Process Development
Alameda, CA · On-site
$130K - $150K/yr
Hands-on experience with chromatography, filtration, TFF and other downstream processing techniques. * Strong analytical and problem-solving skills, with the ability to interpret complex data sets.
Quick apply
Scientist II, Downstream Viral Vector Process Development
Alameda, CA · On-site
$130K - $150K/yr
Hands-on experience with chromatography, filtration, TFF and other downstream processing techniques. * Strong analytical and problem-solving skills, with the ability to interpret complex data sets.
TITLE: Downstream Supervisor REPORTS TO: Manager, Manufacturing LOCATION: San Antonio, Texas (On ... Our work focuses on translating defined program goals into scalable manufacturing processes and ...
Quick apply
TITLE: Downstream Supervisor REPORTS TO: Manager, Manufacturing LOCATION: San Antonio, Texas (On ... Our work focuses on translating defined program goals into scalable manufacturing processes and ...
TITLE: Downstream Supervisor REPORTS TO: Manager, Manufacturing LOCATION: San Antonio, Texas (On ... Our work focuses on translating defined program goals into scalable manufacturing processes and ...
TITLE: Downstream Supervisor REPORTS TO: Manager, Manufacturing LOCATION: San Antonio, Texas (On ... Our work focuses on translating defined program goals into scalable manufacturing processes and ...
Scientist II, Downstream Viral Vector Process Development
Alameda, CA · On-site
$130K - $150K/yr
Hands-on experience with chromatography, filtration, TFF and other downstream processing techniques. * Strong analytical and problem-solving skills, with the ability to interpret complex data sets.
Scientist II, Downstream Viral Vector Process Development
Alameda, CA · On-site
$130K - $150K/yr
Hands-on experience with chromatography, filtration, TFF and other downstream processing techniques. * Strong analytical and problem-solving skills, with the ability to interpret complex data sets.
Downstream Supervisor REPORTS TO: Manager, Manufacturing LOCATION: San Antonio, Texas (On-site) The ... Our work focuses on translating defined program goals into scalable manufacturing processes and ...
Downstream Supervisor REPORTS TO: Manager, Manufacturing LOCATION: San Antonio, Texas (On-site) The ... Our work focuses on translating defined program goals into scalable manufacturing processes and ...
... processing. The individual will serve as a subject matter expert (SME) in downstream processes for outsourced drug-substance manufacturing, technology transfer, life cycle management, and global ...
... processing. The individual will serve as a subject matter expert (SME) in downstream processes for outsourced drug-substance manufacturing, technology transfer, life cycle management, and global ...
Description Do you enjoy developing downstream purification processes for microbial production of small molecules and metabolites? Do you want to apply your expertise in in downstream bioprocess ...
Description Do you enjoy developing downstream purification processes for microbial production of small molecules and metabolites? Do you want to apply your expertise in in downstream bioprocess ...
Hands-on experience with chromatography, filtration, TFF and other downstream processing techniques. * Strong analytical and problem-solving skills, with the ability to interpret complex data sets.
Hands-on experience with chromatography, filtration, TFF and other downstream processing techniques. * Strong analytical and problem-solving skills, with the ability to interpret complex data sets.
Engage customers peer-to-peer to support process development, optimization, and technology integration across downstream workflows. * Lead pre- and post-sales technical activities, including product ...
New
Engage customers peer-to-peer to support process development, optimization, and technology integration across downstream workflows. * Lead pre- and post-sales technical activities, including product ...
New
Director, Downstream Process Development Allakos Inc. is a clinical-stage company developing therapeutic antibodies for inhibitory receptors on the surface of immune effector cells involved in ...
Director, Downstream Process Development Allakos Inc. is a clinical-stage company developing therapeutic antibodies for inhibitory receptors on the surface of immune effector cells involved in ...
Downstream Processing information
See salary details
$13.46 - $15.47
2% of jobs
$15.47 - $17.48
9% of jobs
$17.48 - $19.49
13% of jobs
$19.77 is the 25th percentile. Wages below this are outliers.
$19.49 - $21.50
12% of jobs
$21.50 - $23.51
11% of jobs
The median wage is $24.05 / hr.
$23.51 - $25.52
16% of jobs
$27.46 is the 75th percentile. Wages above this are outliers.
$25.52 - $27.53
14% of jobs
$27.53 - $29.55
12% of jobs
$29.55 - $31.56
6% of jobs
$31.56 - $33.57
4% of jobs
$33.57 - $35.58
2% of jobs
$13
$24
$35
How much do downstream processing jobs pay per hour?
What is downstream processing?
A Downstream Processing (DSP) job involves purifying and recovering biomolecules, such as proteins or vaccines, after fermentation or cell culture. Professionals in this role use techniques like filtration, chromatography, and centrifugation to ensure product purity and quality. They work in industries like pharmaceuticals, biotechnology, and bioprocessing. Key responsibilities include optimizing purification processes, troubleshooting equipment, and ensuring compliance with regulatory standards.
What are the typical daily responsibilities of someone working in downstream processing?
In Downstream Processing, your daily activities often include operating and optimizing purification systems, conducting in-process testing, and meticulously documenting process parameters and results. You’ll collaborate closely with upstream teams, quality control labs, and engineering staff to troubleshoot and improve workflows. Managing equipment maintenance, adhering to safety and compliance standards, and actively participating in process development projects are also key facets of the job. This hands-on role is essential for ensuring the purity and consistency of biopharmaceutical products.
What are the key skills and qualifications needed to thrive in downstream processing, and why are they important?
To thrive in Downstream Processing, you typically need a background in biochemistry, chemical engineering, or a related field, along with experience in purification and separation techniques. Familiarity with technical tools such as chromatography systems, filtration units, and process control software, as well as cGMP certification, is often required. Strong attention to detail, problem-solving skills, and effective teamwork are valuable soft skills for this role. These competencies ensure efficient production, product quality, and compliance in highly regulated biopharmaceutical environments.
What does downstream processing involve?
What cities are hiring for Downstream Processing jobs?
Cities with the most Downstream Processing job openings:
What are the most commonly searched types of Downstream Processing jobs?
The most popular types of Downstream Processing jobs are:
What states have the most Downstream Processing jobs?
States with the most job openings for Downstream Processing jobs include:
What job categories do people searching Downstream Processing jobs look for?
The top searched job categories for Downstream Processing jobs are:
- Upstream Process Development Scientist
- Senior Scientist Downstream Process Development
- Downstream Process Development Scientist
- Senior Innovation Scientist
- Formulation Science
- Phd Drug Development Scientist
- Online International Pharmaceutical Scientist
- Remote Downstream Process Development Scientist
- Internship Colloidal
- Associate Process Development Scientist

Full-time
Medical, Dental, Vision, Retirement, PTO
Posted 19 days ago
Merck rating
8.0
Based on 51 frontline employees who took The Breakroom Quiz
43rd of 86 rated pharmaceutical
Job description
BPR&D within our Company's Research Laboratories is on a mission to rapidly deliver biotherapeutics to patients by efficiently developing innovative, robust manufacturing processes and technologies. To achieve this, we work closely with colleagues in Discovery, Pre-clinical, Early Development, Analytical, Formulation, and Commercial Manufacturing while providing an inclusive environment for all. Beyond process development for pipeline biologics, we innovate and build next generation biomanufacturing technologies. Examples include investments for development of continuous manufacturing, green and sustainable processes, and proprietary technology platforms. We actively publish and engage with the scientific community to influence the field.
As a Principal Scientist you will have the opportunity to influence the future direction of our Company's Downstream Processing of Biologics. You will work with an immensely creative and collaborative team of scientists and engineers to design purification processes while developing technical strategies related to downstream processing for drug candidates in early- and late-stage development.
Responsibilities include but are not limited to:
• As an impactful contributor, shape and realize innovation across the Biologics' pipeline, strategy, and science
• Advance the pipeline by collaborating with cross-functional teams, from Research & Manufacturing, in a fast-paced, multidisciplinary environment
• Participate in or lead 1) development of robust and scalable purification processes for biologics in different stages of clinical development, 2) process characterization and regulatory filings for successful commercialization
• Advance downstream processes by improving efficiency and cost effectiveness through research and innovation, while assessing technologies and industry best practices
• Collaborate with academia, industry, and vendors to drive development and early adoption of novel process technologies
• Contribute to strategic initiatives; partner with senior leaders to set overall project strategy, and guide teams towards its execution
• Conceptualize, plan, and execute projects with effective organizational, prioritization and problem-solving skills
• Stay abreast of scientific and regulatory landscape; actively present (premier conferences), publish (peer-reviewed journals) and patent
• Represent BPR&D as a downstream bioprocess expert in internal, cross-functional project teams and external conferences/consortia
• Mentor and actively share expertise; guide career development; build strong, collaborative teams
• Champion compliance and safety; promote a culture of inclusion
MINIMUM EDUCATION REQUIREMENTS:
Ph.D. with 6+ years, MS with 8+ years, or BS with 10+ years of industry experience and background in Chemical/Biochemical engineering, or a related field
REQUIRED EXPERIENCE, SKILLS, AND COMPETENCIES
• Strong fundamental knowledge and subject matter expertise in downstream processing of biologics, recent advances, and challenges in the field
• Expertise in independently conducting and directing the design, execution, analysis, and documentation of all stages of purification process development
• Track record of accomplishments in downstream bioprocessing with a history of peer-reviewed publications and presentations
• Knowledge of biologics CMC development
• Adaptability and agility to prioritize and deliver complex objectives, often on tight timelines, in a rapidly changing environment
• Experience and aptitude to lead, work, and collaborate in internal and external cross-functional, matrixed teams
• Action-oriented, mindset for creativity; ability to take initiative, innovate, iterate and problem-solve
• Demonstrated commitment to coach and mentor staff to maximize talent development and utilization
• Excellent interpersonal and communication skills
PREFERRED EXPERIENCE & SKILLS:
• Leadership of CMC development teams
• Continuous biomanufacturing integrated with process-analytical technologies
• High-throughput experimentation, automation, and process control
• Knowledge of protein expression, analytics, conjugation chemistry and formulation
• Biophysical, mechanistic and facility modeling; statistical analysis, data-science, machine learning, artificial intelligence
Required Skills:
Adaptability, Adaptability, Artificial Intelligence (AI), Biomanufacturing, Bioprocess Engineering, Career Development, Cell Culture Process Development, Cell Line Development, Combination Products, Data Analysis, Finite Element Analysis (FEA), Innovation, Innovative Thinking, Leadership Mentoring, Manufacturing Operations, Pharmaceutical Process Development, Prioritization, Process Characterization, Professional Collaboration, Professional Networking, Protein Expression, Publishing, Quality by Design, Regulatory Filings, Strategic Initiative {+ 2 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
The salary range for this role is
$173,200.00 - $272,600.00
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 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.
Employee Status:
Regular
Relocation:
Domestic
VISA Sponsorship:
Yes
Travel Requirements:
10%
Flexible Work Arrangements:
Not Applicable
Shift:
Not Indicated
Valid Driving License:
No
Hazardous Material(s):
n/a
Job Posting End Date:
10/1/2026
*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.
About Merck
Sourced by ZipRecruiter
Industry
Pharmaceutical product wholesalers and pharmaceutical and medicine manufacturing
Company size
10,000+ Employees
Headquarters location
Rahway, NJ, US