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Master In Biotechnology Jobs in Deerfield, IL (NOW HIRING)

Tempus

Director, (GCP) Quality Assurance

Chicago, IL · On-site

Conduct audits, including Internal, Investigator Site and Trial Master File. * Host and support ... Preferred * 5+ years of experience in a Leadership role at a CRO, biotech, or pharma company. * 10+ ...

Tempus

Director, (GCP) Quality Assurance

Chicago, IL · On-site +1

Conduct audits, including Internal, Investigator Site and Trial Master File. * Host and support ... Preferred * 5+ years of experience in a Leadership role at a CRO, biotech, or pharma company. * 10+ ...

AbbVie

Senior Training Manager - Oncology

Mettawa, IL · On-site

Master's Degree is preferred * 5+ years of pharmaceutical/biotech industry experience * Training, Marketing or Sales experience in the pharmaceutical/biotech industry preferred * Knowledge of ...

AbbVie

Senior Training Manager - Oncology

Mettawa, IL · On-site +1

$124K/yr

Master's Degree is preferred * 5+ years of pharmaceutical/biotech industry experience * Training, Marketing or Sales experience in the pharmaceutical/biotech industry preferred * Knowledge of ...

Tempus

Director, (GCP) Quality Assurance

Chicago, IL · On-site

$160 - $200/hr

Conduct audits, including Internal, Investigator Site and Trial Master File. * Host and support ... Preferred 5+ years of experience in a Leadership role at a CRO, biotech, or pharma company. * 10+ ...

AbbVie

Senior Training Manager - Oncology

Mettawa, IL · On-site

Master's Degree is preferred * 5+ years of pharmaceutical/biotech industry experience * Training, Marketing or Sales experience in the pharmaceutical/biotech industry preferred * Knowledge of ...

Perkins & Will

Lab Planner

Chicago, IL · On-site

$90K - $120K/yr

... biotech, or other emerging technical facilities. * Provides technical planning expertise and ... Bachelor's degree in Architecture required * Master's degree * Requires 5 plus year's progressive ...

Perkins and Will

Lab Planner

Chicago, IL · On-site

$90K - $120K/yr

... biotech, or other emerging technical facilities. * Provides technical planning expertise and ... Bachelor's degree in Architecture required * Master's degree * Requires 5 plus year's progressive ...

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Master In Biotechnology information

What is a master in biotechnology?

A Master in Biotechnology is a graduate-level degree program focused on the advanced study of biological processes and the use of technology to manipulate living organisms for applications in medicine, agriculture, and industry. Students learn about molecular biology, genetics, bioinformatics, and laboratory techniques, as well as how to apply these skills to develop new products and solutions. This degree prepares graduates for careers in research, pharmaceuticals, healthcare, environmental management, and biotechnology companies, or for further study at the doctoral level.

What are typical career paths for a master in biotechnology, and how can they progress within the industry?

Graduates with a Master in Biotechnology can pursue diverse career paths, such as research scientist, quality control analyst, regulatory affairs specialist, or roles in product development and project management. Advancement often involves taking on leadership responsibilities, such as managing teams or projects, or specializing further in areas like bioinformatics or clinical research. Many professionals also transition into roles in biotech startups, pharmaceuticals, or government agencies, and may further their expertise through certifications or a doctoral degree. Networking, continuous skill development, and staying updated with industry trends are key to progressing within the biotechnology sector.

What are the key skills and qualifications needed to thrive as a master in biotechnology, and why are they important?

To thrive as a Master in Biotechnology, you need advanced knowledge in molecular biology, genetics, and laboratory techniques, typically supported by a master's degree in biotechnology or a related field. Familiarity with bioinformatics tools, PCR, and laboratory information management systems (LIMS) is essential, and certifications in laboratory safety can be advantageous. Strong problem-solving, critical thinking, and teamwork skills distinguish top professionals in this field. These competencies enable effective research, innovation, and collaboration in the rapidly evolving biotech industry.

What is the difference between Master In Biotechnology vs Biotechnology Research Associate?

CriteriaMaster In BiotechnologyBiotechnology Research Associate
Required CredentialsMaster's degree in Biotechnology or related fieldBachelor's or Master's degree in Biotechnology or related field
Work EnvironmentLaboratories, research facilities, academic institutionsLaboratories, biotech companies, research organizations
Employer & Industry UsageAcademic, research, biotech industryBiotech companies, research labs, pharmaceutical firms
Common Search & ComparisonYesYes

The Master In Biotechnology typically prepares individuals for advanced roles in research, development, and academia, requiring a master's degree. A Biotechnology Research Associate usually holds a bachelor's or master's degree and works directly in research projects within biotech companies or labs. While both roles involve laboratory work and research, the Master's degree often leads to more senior or specialized positions.

Is a Master in Biotechnology a good career?

A Master in Biotechnology prepares individuals for careers in research, development, and quality control within biotech, pharmaceutical, and healthcare industries. It offers opportunities in laboratory work, product development, and regulatory roles, often requiring skills in molecular biology, data analysis, and laboratory techniques. The field is growing due to advances in medical research and biomanufacturing, making it a viable career path for those interested in science and innovation.

What can I do with a master in biotechnology?

A master in biotechnology prepares individuals for roles such as research scientist, bioprocess engineer, quality control analyst, or laboratory manager in industries like pharmaceuticals, healthcare, agriculture, and environmental science. Graduates often work with laboratory techniques, data analysis, and regulatory compliance, and may pursue certifications or further specialization to advance their careers.

What job categories do people searching Master In Biotechnology jobs in Deerfield, IL look for?

The top searched job categories for Master In Biotechnology jobs in Deerfield, IL are:

What cities near Deerfield, IL are hiring for Master In Biotechnology jobs?

Cities near Deerfield, IL with the most Master In Biotechnology job openings:

Master In Biotechnology jobs near you
Infographic showing various Master In Biotechnology job openings in Deerfield, IL as of June 2026, with employment types broken down into 96% Part Time, and 4% Temporary. Highlights an 72% Physical, 3% Hybrid, and 25% Remote job distribution.

Senior Director, Analytical Research

AbbVie

North Chicago, IL • On-site

$206K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 7 days ago

AbbVie rating

8.6

Company rating: 8.6 out of 10

Based on 101 frontline employees who took The Breakroom Quiz

15th of 86 rated pharmaceutical

Job description

Company Description
About AbbVie
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.
Job Description
The Senior Director will be responsible for leading the Synthetic Molecule (SM) Analytical R&D organization in Lake County supporting AbbVie's innovative and unique early stage pipeline which includes small molecule, peptides, ADCs (antibody-drug conjugates), APCs (antibody-peptide conjugates), LNP (Lipid Nanoparticle), and future modalities paired with formulation development support for conventional (e.g. OSD, injectables) and complex formulations (e.g. Long Acting Injectables, co-formulations).
This individual will lead the organization to develop industry-leading analytical methods, analytical characterization packages, and control strategies to advance the manufacturing, purification, formulation, and process development for drug intermediates, Drug Substance and Drug Products from Discovery Research through late-stage clinical development. The Senior Director will advance fundamental understanding of novel synthetic modalities and their degradation mechanisms during manufacturing, shelf-life, distribution, and administration. He/she will partner cross-functionally to drive robust drug substance and drug product manufacturing processes and formulation selection by providing key analytical data and insights.
The Senior Director will ensure that all analytical deliverables are achieved within set timelines, budgets, and regulatory frameworks, while seamlessly integrating analytical and program strategies into broader business objectives. He/she will drive top-tier analytical method development and validation strategies, implementation of new technologies, and automation. The Senior Director will establish collaborative and productive working relationships with key partner organizations to define successful process development strategies for drug intermediate, drug substance, drug product and novel drug delivery development. He/she will effectively manage Discovery Research and Operations interfaces to ensure seamless transition of research programs into clinical development and technology transfers to commercial manufacturing and testing sites. He/she will also partner with global Analytical R&D peer organizations working to advance similar Synthetic modalities to benchmark strategies and technologies and leverage analytical best practices.
Responsibilities:
  • Provide leadership and talent development for > 50 highly skilled analytical and pharmaceutical scientists at the AbbVie Abbott Park, North Chicago, and Ludwigshafen Germany sites
  • Define and communicate industry-leading analytical strategies for complex modalities
  • Responsible for development, validation and transfer of analytical methods aligned with global strategies
  • Establish industry-leading analytical characterization capabilities to support process development, formulation design and comparability
  • Drive fundamental understanding of CQAs, degradation mechanisms and product/excipient interactions
  • Manage departmental budget, analytical laboratories and equipment
  • Balance resources, resolve issues and achieve target timing for pipeline projects and key strategic initiatives
  • Drive technical excellence and innovations in science that improve the capabilities and productivity of the organization.
  • Work collaboratively across R&D and Operations to align and influence a broad range of development strategies that directly support drug development programs.
  • Manage and develop scientific talent across multiple disciplines and/or projects to address current and future business needs.
  • Ensure scientific excellence and foster functional, scientific, and professional development of staff.
  • Identify, evaluate, and propose both internal and external collaborations to drive scientific innovation and shared learning.
  • Accountable for compliance with Environmental Health and Safety regulations for the group.
  • Solves difficult and highly complex technical issues in an evolving regulatory climate.

Qualifications
  • PhD with at least 15 years of relevant pharma/biotech industry experience or master's degree with at least 20 years of pharma/biotech experience.
  • Proven experience leading an Analytical development organization with a range of experience levels and scientific disciplines
  • Demonstrated record of success leading strategic initiatives and new technology evaluation/implementation
  • Strong oral and written communication skills.
  • Experience motivating and maintaining positive morale of highly skilled technical individuals and teams in an environment where compliance with standard procedures is required.
  • Solid understanding of the various scientific disciplines needed for therapeutic development (including analytical, drug substance development, drug product development, combination product development, manufacturing, QA, supply chain, regulatory).
  • Strong negotiating, influencing, and leadership skills
  • Entrepreneurial thinker capable of driving innovative ideas and making smart business decisions.

Team size: 50+
Number of programs supported: 20+
Recent additional responsibilities: peptides, LNP
Additional Information
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
  • The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
  • We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
  • This job is eligible to participate in our long-term incentive programs.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company's sole and absolute discretion, consistent with applicable law.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
https://www.abbvie.com/join-us/reasonable-accommodations.html

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About AbbVie

Sourced by ZipRecruiter

AbbVie's mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas: immunology, oncology, neuroscience, eye care, virology, women's health, and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube, and LinkedIn.

Industry

Scientific research and development services

Company size

10,000+ Employees

Headquarters location

North Chicago, IL, US

Year founded

2013

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