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Biotech Downstream Manager Jobs (NOW HIRING)

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Biotech Downstream Manager information

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$28.5K

$62.7K

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How much do biotech downstream manager jobs pay per year?

As of Sep 10, 2026, the average yearly pay for biotech downstream manager in the United States is $62,661.00, according to ZipRecruiter salary data. Most workers in this role earn between $45,000.00 and $69,000.00 per year, depending on experience, location, and employer.

What is a biotech downstream manager?

Biotech Downstream Managers are professionals responsible for overseeing the purification and processing of biological products after the initial production phase (upstream processing) in biotechnology manufacturing. They manage teams, optimize processes, ensure product quality, and maintain compliance with regulatory standards. Their role is crucial in ensuring that biologics such as proteins, antibodies, or vaccines are safely and efficiently purified for use in pharmaceuticals, research, or other applications. They often collaborate with upstream managers, quality assurance teams, and regulatory bodies to achieve production goals. Strong technical knowledge and leadership skills are essential for success in this role.

What are some common challenges a biotech downstream manager faces when scaling up purification processes from lab to production scale?

A Biotech Downstream Manager often encounters challenges such as maintaining product quality and yield when transitioning purification protocols from lab-scale to large-scale manufacturing. Issues can arise with equipment compatibility, process reproducibility, and increased risk of contamination. Strong collaboration with upstream teams, process engineers, and quality assurance is essential to troubleshoot and optimize each stage. Additionally, ensuring compliance with regulatory standards while meeting production timelines requires careful planning and attention to detail.

What are the key skills and qualifications needed to thrive as a biotech downstream manager, and why are they important?

To thrive as a Biotech Downstream Manager, you need expertise in bioprocess engineering, protein purification, and a solid background in biology or chemical engineering, often supported by a relevant degree and experience in biomanufacturing. Familiarity with chromatography systems, filtration technologies, GMP regulations, and process control software is essential. Strong leadership, problem-solving, and communication skills help in managing teams and troubleshooting complex processes. These skills ensure efficient and compliant production of high-quality biopharmaceutical products, directly impacting product success and regulatory approval.

What are popular job titles related to Biotech Downstream Manager jobs?

For Biotech Downstream Manager jobs, the most frequently searched job titles are:

Infographic showing various Biotech Downstream Manager job openings in the United States as of September 2026, with employment types broken down into 67% Full Time, and 33% Nights. Highlights an 67% In-person, and 33% Remote job distribution, with an average salary of $62,661 per year, or $30.1 per hour.

Manager - New Product Introduction (NPI) and Manufacturing Execution System (MES)

Thousand Oaks, CA โ€ข On-site

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 16 days ago


Key responsibilities

  • Manage a team responsible for the introduction of new products and advanced technologies into the plant, including electronic batch record development and management.

  • Coordinate with cross-functional teams to ensure successful implementation of new products, revised batch records, and technologies, while maintaining compliance and audit readiness.

  • Lead continuous improvement initiatives, including Lean Transformation and Operational Excellence, to enhance manufacturing processes and plant performance.


Job description

Career Category
Manufacturing
Job Description
Join Amgen's Mission of Serving Patients
At Amgen, if you feel like you're part of something bigger, it's because you are. Our shared mission-to serve patients living with serious illnesses-drives all that we do.
Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest diseases. With our focus on four therapeutic areas -Oncology, Inflammation, General Medicine, and Rare Disease- we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity-related conditions. As a member of the Amgen team, you'll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.
Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you'll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.
Manager-New Product Introduction (NPI) and Manufacturing Execution System (MES)
What you will do
Let's do this. Let's change the world. In this vital role you will act as the Downstream Manager for the New Product Introduction (NPI) and Manufacturing Execution Systems (MES) Team in B23 GMP Drug Substance Supply. This position is within Amgen Thousand Oaks (ATO) Manufacturing and Clinical Supply - Manufacturing Systems organization.
ATO B23 is a dynamic environment and an important launch point for Amgen's pipeline products. The GMP DSS plant manufactures drug substance for clinical trials through commercial production using both stainless steel and single-use equipment platforms. This NPI/MES team is a key communication and technical interface between the GMP manufacturing operations teams in the plant and Process Development, Drug Substance Technologies & Engineering, Supply Chain, Facilities & Engineering, and Quality.
Responsibilities:
  • Directly manage a team of Downstream NPI Specialists and MES Sr. Associates responsible for introduction of new products and/or advanced technologies into the plant, as well as Electronic Batch Record (EBR) development and management. Includes hiring, training, oversight, performance evaluations, and development.
  • Proactively assess team capabilities to meet the evolving drug substance clinical/commercial supply needs (ex. resources, platform technical understanding, cross-functional alignment).
  • Lead downstream area team meetings and drive alignment in business processes across the team.
  • Coordinate with PD, DSTE, Supply Chain, Planning, Facilities and Engineering, Quality, MES network, as well as Manufacturing for the introduction of new products, new/revised electronic batch records, and/or advanced technologies into the plant.
  • Champions Lean Transformation and OE initiatives, facilitates the drive towards continuous improvement in the plant and tracks progress on a plant level.
  • Collaborate with Regulatory and Quality partners to ensure compliance of team change control records/documents and respond to regulatory questions and/or audit findings.
  • Drive a culture of inspection readiness across the team by ensuring NPI and MES playbooks are kept up to date and supporting staff with audit or regulatory response strategy.

What we expect of you
We are all different, yet we all use our unique contributions to serve patients. The dedicated professional we seek is a collaborative partner with these qualifications.
Basic Qualifications:
  • Doctorate degree OR
  • Master's degree and 3 years of biotechnology operations experience OR
  • Bachelor's degree and 5 years of biotechnology operations experience OR
  • Associate's degree and 10 years of biotechnology operations experience

AND
In addition to meeting at least one of the above requirements, you must have experience directly managing people and/or leadership experience leading teams, projects, programs, or directing the allocation of resources. Your managerial experience may run concurrently with the required technical experience referenced above
Preferred Qualifications:
  • Degree in Chemical Engineering, Industrial Engineering, Biology or Biochemistry
  • Experience leading/managing a team of direct reports
  • Experience with PAS X, Werum software
  • Experience in GMP operations, including New Product Introduction (NPI)
  • Strong technical knowledge of drug substance processing (cell culture, harvest, chromatography, filtration, buffer compounding) and a broad understanding of related disciplinary areas in bioprocessing
  • Ability to organize, analyze and interpret technical data through trend analysis, forecasting, modeling, etc.
  • Ability to effectively communicate complex technical information with internal and external colleagues of varying organizational levels in both presentation and technical writing forms
  • Ability to coach, mentor and/or cross train colleagues within core technical areas
  • Background in lean manufacturing methodologies and operational excellence
  • Experience in cross functional Project Management

What you can expect from us
As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we'll support your journey every step of the way.
The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.
In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:
  • A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
  • A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
  • Stock-based long-term incentives
  • Award-winning time-off plans
  • Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.

Apply now and make a lasting impact with the Amgen team.
careers.amgen.com
In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.
Application deadline
Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.
Sponsorship
Sponsorship for this role is not guaranteed.
As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.
Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.
Salary Range
120,818.15USD -163,459.85 USD