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Biotech Process Development Jobs in Novi, MI (NOW HIRING)

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... In this vital role you will be part of a development and sustaining device engineering team that ...

About MMS MMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, and ... Write and edit clinical development documents, including but not limited to, clinical protocols ...

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Biotech Process Development information

See Novi, MI salary details

$17

$31

$46

How much do biotech process development jobs pay per hour?

As of Jun 26, 2026, the average hourly pay for biotech process development in Novi, MI is $31.60, according to ZipRecruiter salary data. Most workers in this role earn between $25.91 and $38.80 per hour, depending on experience, location, and employer.

What is biotech process development?

Biotech process development refers to the design, optimization, and scale-up of manufacturing processes used to produce biological products, such as pharmaceuticals, enzymes, or vaccines. Professionals in this field work to turn laboratory procedures into efficient, large-scale industrial processes that meet regulatory and quality standards. This often involves selecting suitable equipment, optimizing conditions, ensuring reproducibility, and troubleshooting production issues. The ultimate goal is to produce high-quality products safely, consistently, and cost-effectively.

What is the difference between Biotech Process Development vs Biotech Manufacturing Associate?

AspectBiotech Process DevelopmentBiotech Manufacturing Associate
Primary FocusDesigning, optimizing, and scaling up bioprocesses for product developmentExecuting manufacturing processes to produce biopharmaceuticals at scale
Work EnvironmentLaboratories and pilot plant facilitiesProduction floors and manufacturing plants
Required SkillsProcess design, lab techniques, troubleshootingEquipment operation, quality control, adherence to SOPs
Typical CredentialsBSc/MSc in Biotechnology, Chemical Engineering, or related fieldsBSc in Biotechnology, Biology, or related fields

While both roles are essential in biotech, Biotech Process Development focuses on creating and optimizing processes during product development, whereas Biotech Manufacturing Associates handle the day-to-day production to ensure consistent product quality at scale.

What are the key skills and qualifications needed to thrive in Biotech Process Development, and why are they important?

To excel in Biotech Process Development, you need a strong background in bioprocess engineering, molecular biology, and chemistry, typically supported by a degree in biotechnology or related fields. Familiarity with tools such as bioreactors, chromatography systems, and data analysis software, along with certifications in Good Manufacturing Practice (GMP), is highly valuable. Strong problem-solving skills, attention to detail, and effective teamwork distinguish top performers in this role. These competencies are crucial for optimizing processes, ensuring product quality, and driving innovation in the biotech industry.

What are some common challenges faced by professionals in Biotech Process Development, and how are they typically addressed?

Professionals in Biotech Process Development often encounter challenges related to scaling up processes from the laboratory to commercial production, ensuring product consistency, and meeting strict regulatory standards. Addressing these challenges typically involves close collaboration with cross-functional teams such as quality assurance, regulatory affairs, and manufacturing. Continuous process optimization, thorough documentation, and robust validation protocols are essential strategies to overcome these hurdles and ensure successful product development and commercialization.
What are popular job titles related to Biotech Process Development jobs in Novi, MI? For Biotech Process Development jobs in Novi, MI, the most frequently searched job titles are:
What job categories do people searching Biotech Process Development jobs in Novi, MI look for? The top searched job categories for Biotech Process Development jobs in Novi, MI are:
Associate Director, External Data Acquisition and Delivery

Associate Director, External Data Acquisition and Delivery

Regeneron Pharmaceuticals

Warren, MI

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 24 days ago


Regeneron rating

8.7

Company rating: 8.7 out of 10

Based on 42 frontline employees who took The Breakroom Quiz

13th of 73 rated pharmaceutical


Job description

Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health.

As an Associate Director, External Data Acquisition and Delivery (EDAD), you will provide strategic oversight and operational leadership for External Data Acquisition and Delivery activities across Regeneron's clinical trial portfolio and initiatives. You will ensure readiness of external data collection platforms, data conformance tools, reconciliation processes, and the delivery of high-quality, compliant external data from third-party vendors including laboratory, biomarker, Digital Health Technologies, imaging, ECG, PK, genomics, and specialty data. You will partner closely with Clinical Data Management, CROs, external vendors, and cross-functional partners to drive external data strategy, operational excellence, vendor oversight, digital transformation initiatives, and process improvements.

A Typical Day May Include:

  • Leading External Data Acquisition, integration, quality oversight, and delivery strategy across the clinical trial portfolio
  • Serving as a portfolio-level lead for external data quality and clinical-data operational strategy
  • Reviewing protocol requirements, vendor specifications, and operational data flows
  • Leading all aspects of development and maintenance of Data Transfer Specification (DTS) documents to ensure compliance with Regeneron standards and timelines
  • Providing expert mentorship on external data services including biomarker, eSource, eCOA, imaging, ECG, PK, genomics, and laboratory data
  • Driving external vendor oversight, onboarding, qualification, governance, and ongoing performance monitoring
  • Establishing and handling vendor KPIs, SLAs, and quality metrics
  • Governing reconciliation activities between EDC systems and vendor data platforms to ensure data integrity and consistency
  • Monitoring reconciliation metrics, discrepancy trends, and resolution timelines across studies
  • Collaborating with Database Development, Biostatistics, Study Data Managers, and external vendors to resolve complex data discrepancies
  • Leading process improvement initiatives, automation opportunities, and implementation of innovative external data solutions
  • Managing and developing a team of EDAD Managers, Specialists, and associates through coaching, mentoring, and performance management
  • Supporting SOP development, inspection readiness, audit activities, and regulatory compliance
  • Representing EDAD in leadership forums, governance committees, and technology discussions

This Role May Be For You If You Have:

  • Strong expertise managing multiple clinical external data types including biomarker, imaging, eCOA, ECG, PK, genomics, laboratory, and Digital Health Technology data
  • Advanced knowledge of external data reconciliation processes and EDC platforms such as Medidata Rave, Veeva, or Oracle Inform
  • Experience working with SAS, CSV, and XML data formats
  • Strong understanding of industry regulations including 21 CFR Part 11, ICH-GCP, and CDISC standards
  • Proven experience handling external vendor relationships and driving accountability for quality deliverables
  • Strong leadership, people management, coaching, and mentoring capabilities
  • Strategic thinking, creativity, problem-solving, and analytical skills
  • Strong project management and stakeholder management capabilities
  • Excellent verbal and written communication skills
  • Ability to work effectively in a fast-paced, matrixed, and global environment

To Be Considered For This Role, You Must Have:

  • Minimum 10+ years of experience in Clinical DataAcquisition/Managementwithin biotechnology, pharmaceutical, or healthcare industries
  • Minimum 4+ years of people management experience
  • Demonstrated experience overseeing external data reconciliation activities between EDC systems and vendor platforms
  • Experience driving process improvements and vendor oversight in supervised environments
  • Bachelor's degree in Science, Health, Mathematics, Computing, Information Systems, or a related field
  • Advanced degree preferred

Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.

Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter.


Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed onsite. Please speak with your recruiter and hiring manager for more information about onsite expectations for your role and location.


As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.


For jobs in Canada: this posting is for an existing position.


Salary Range (annually)

$154,800.00 - $252,800.00

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