... processes, and the delivery of high-quality, compliant external data from third-party vendors ... Leading all aspects of development and maintenance of Data Transfer Specification (DTS) documents ...
... processes, and the delivery of high-quality, compliant external data from third-party vendors ... Leading all aspects of development and maintenance of Data Transfer Specification (DTS) documents ...
Field Patient Access Director
Detroit, MI · On-site
$220K - $245K/yr
Key Responsibilities Field Team Leadership & Development * Lead, coach, and develop a high ... Identify opportunities for process improvement and lead initiatives that enhance operational ...
Field Patient Access Director
Detroit, MI · On-site
$220K - $245K/yr
Key Responsibilities Field Team Leadership & Development * Lead, coach, and develop a high ... Identify opportunities for process improvement and lead initiatives that enhance operational ...
Field Patient Access Director
Detroit, MI · On-site
$220K - $245K/yr
Key Responsibilities Field Team Leadership & Development * Lead, coach, and develop a high ... Identify opportunities for process improvement and lead initiatives that enhance operational ...
Field Patient Access Director
Detroit, MI · On-site
$220K - $245K/yr
Key Responsibilities Field Team Leadership & Development * Lead, coach, and develop a high ... Identify opportunities for process improvement and lead initiatives that enhance operational ...
... processes, and the delivery of high-quality, compliant external data from third-party vendors ... Leading all aspects of development and maintenance of Data Transfer Specification (DTS) documents ...
... processes, and the delivery of high-quality, compliant external data from third-party vendors ... Leading all aspects of development and maintenance of Data Transfer Specification (DTS) documents ...
To be considered a bachelor's degree with a minimum of 10 years of pharmaceutical/biotech industry ... Experience with device regulatory requirements and development processes for combination products ...
To be considered a bachelor's degree with a minimum of 10 years of pharmaceutical/biotech industry ... Experience with device regulatory requirements and development processes for combination products ...
Senior Mechanical Engineer
Ann Arbor, MI · Hybrid
$102K - $135K/yr
... Development Life Cycle process. You will work with a team of engineers and scientists to conceive, model, prototype, and test laboratory products in accordance with established requirements, goals ...
Senior Mechanical Engineer
Ann Arbor, MI · Hybrid
$102K - $135K/yr
... Development Life Cycle process. You will work with a team of engineers and scientists to conceive, model, prototype, and test laboratory products in accordance with established requirements, goals ...
... biotechnology, pharmaceutical or health related industry, including significant interaction with ... Understanding of the drug discovery and development process, regionally and globally. * Strong ...
... biotechnology, pharmaceutical or health related industry, including significant interaction with ... Understanding of the drug discovery and development process, regionally and globally. * Strong ...
By reducing processing time and improving efficiency, you enable users to achieve faster results ... Act as a bridge between data scientists and product development teams. You will translate user ...
By reducing processing time and improving efficiency, you enable users to achieve faster results ... Act as a bridge between data scientists and product development teams. You will translate user ...
Troubleshoot process & equipment problems promptly to minimize Manufacturing downtime. * Assemble ... Personal and Professional Development: Mentoring, leadership programs, internal seminar offerings ...
Troubleshoot process & equipment problems promptly to minimize Manufacturing downtime. * Assemble ... Personal and Professional Development: Mentoring, leadership programs, internal seminar offerings ...
Create service orders, update status, process parts orders, service invoicing, and creation of ... Personal and Professional Development: Mentoring, leadership programs, internal seminar offerings ...
New
Create service orders, update status, process parts orders, service invoicing, and creation of ... Personal and Professional Development: Mentoring, leadership programs, internal seminar offerings ...
New
... process analysis and design, requirements planning, business case development, analytics support ... biotech, healthcare delivery, insurance, regulatory, or policy). * Minimum 2 years of experience ...
... process analysis and design, requirements planning, business case development, analytics support ... biotech, healthcare delivery, insurance, regulatory, or policy). * Minimum 2 years of experience ...
Senior Mechanical Engineer
Ann Arbor, MI · Hybrid
$102K - $135K/yr
... Development Life Cycle process. You will work with a team of engineers and scientists to conceive, model, prototype, and test laboratory products in accordance with established requirements, goals ...
Senior Mechanical Engineer
Ann Arbor, MI · Hybrid
$102K - $135K/yr
... Development Life Cycle process. You will work with a team of engineers and scientists to conceive, model, prototype, and test laboratory products in accordance with established requirements, goals ...
Create service orders, update status, process parts orders, service invoicing, and creation of ... Personal and Professional Development: Mentoring, leadership programs, internal seminar offerings ...
New
Create service orders, update status, process parts orders, service invoicing, and creation of ... Personal and Professional Development: Mentoring, leadership programs, internal seminar offerings ...
New
The incumbent will lead or participate in process and methodology development for department goals ... biotechnology, pharmaceutical or health related industry, including some project and people ...
The incumbent will lead or participate in process and methodology development for department goals ... biotechnology, pharmaceutical or health related industry, including some project and people ...
Engineer II
Detroit, MI · On-site
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 ...
Engineer II
Detroit, MI · On-site
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 ...
Senior Medical Writer (Remote)
Canton, MI · On-site +1
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 ...
Senior Medical Writer (Remote)
Canton, MI · On-site +1
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 ...
Troubleshoot process & equipment problems promptly to minimize Manufacturing downtime. * Assemble ... Personal and Professional Development: Mentoring, leadership programs, internal seminar offerings ...
Troubleshoot process & equipment problems promptly to minimize Manufacturing downtime. * Assemble ... Personal and Professional Development: Mentoring, leadership programs, internal seminar offerings ...
Senior Medical Writer (Remote)
Canton, MI · On-site
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 ...
Quick apply
Senior Medical Writer (Remote)
Canton, MI · On-site
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 ...
Monthly review and processing of production order settlements. * Monthly / Quarterly adjusting ... Personal and Professional Development: Mentoring, leadership programs, internal seminar offerings ...
Monthly review and processing of production order settlements. * Monthly / Quarterly adjusting ... Personal and Professional Development: Mentoring, leadership programs, internal seminar offerings ...
... process-based experience in Life Science * Excellent communication and negotiation skills ... Personal and Professional Development: Mentoring, leadership programs, internal seminar offerings ...
... process-based experience in Life Science * Excellent communication and negotiation skills ... Personal and Professional Development: Mentoring, leadership programs, internal seminar offerings ...
Biotech Process Development information
See Novi, MI salary details
$17.82 - $20.42
3% of jobs
$20.42 - $23.02
6% of jobs
$23.02 - $25.63
12% of jobs
$26.07 is the 25th percentile. Wages below this are outliers.
$25.63 - $28.23
23% of jobs
The median wage is $29.25 / hr.
$28.23 - $30.84
15% of jobs
$30.84 - $33.44
15% of jobs
$34.52 is the 75th percentile. Wages above this are outliers.
$33.44 - $36.04
3% of jobs
$36.04 - $38.65
3% of jobs
$38.65 - $41.25
6% of jobs
$41.25 - $43.85
3% of jobs
$43.85 - $46.46
11% of jobs
$17
$31
$46
How much do biotech process development jobs pay per hour?
What is biotech process development?
What is the difference between Biotech Process Development vs Biotech Manufacturing Associate?
| Aspect | Biotech Process Development | Biotech Manufacturing Associate |
|---|---|---|
| Primary Focus | Designing, optimizing, and scaling up bioprocesses for product development | Executing manufacturing processes to produce biopharmaceuticals at scale |
| Work Environment | Laboratories and pilot plant facilities | Production floors and manufacturing plants |
| Required Skills | Process design, lab techniques, troubleshooting | Equipment operation, quality control, adherence to SOPs |
| Typical Credentials | BSc/MSc in Biotechnology, Chemical Engineering, or related fields | BSc 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?
What are some common challenges faced by professionals in Biotech Process Development, and how are they typically addressed?
Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Posted 24 days ago
Regeneron rating
8.7
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 - $252,800.00What Regeneron employees say
Pay
Benefits
Hours and flexibility
Workplace
Get the full story on Breakroom
About Regeneron
Sourced by ZipRecruiter
Industry
Biotechnology research and development
Company size
5,001 - 10,000 Employees
Headquarters location
Tarrytown, NY, US
Year founded
1988