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Master In Biotechnology Jobs in Virginia (NOW HIRING)

Turner & Townsend

Senior Scheduler - CQV

Richmond, VA · On-site

Develop, monitor and update owners' Project Integrated Master Schedule (IMS).  * Establish the ... Experience in biotech, pharmaceutical, or life sciences facility construction is required ...

Emcor UK

Executive Administrator to the CEO

Sterling, VA · On-site

$85K - $100K/yr

... biotech, healthcare, commercial, transportation, and technology companies, as well as many ... Maintain all company business and master electrician licenses. Ensure they are kept current

EMCOR Group Inc

Dynalectric Company

Dulles, VA · On-site

$85K - $100K/yr

... in the company's organization, coordination, and maintenance ... Maintain all company business and master electrician licenses. Ensure they are kept current

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Master In Biotechnology information

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.

What can I do with a master of biotechnology?

A Master in Biotechnology prepares graduates for roles such as research scientist, bioprocess engineer, quality control analyst, or laboratory manager in industries like pharmaceuticals, agriculture, and healthcare. It often involves skills in laboratory techniques, data analysis, and regulatory compliance, with opportunities in research and development, manufacturing, or clinical settings.

What jobs can I get after an MSc in biotechnology?

An MSc in biotechnology qualifies graduates for roles such as research scientist, quality control analyst, bioprocess engineer, clinical research associate, and laboratory technician. These positions often require knowledge of laboratory techniques, data analysis, and familiarity with biotech tools and regulations.

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 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 careers can I get with a masters in biotechnology?

A master's in biotechnology prepares individuals for careers such as research scientist, bioprocess engineer, quality control analyst, or regulatory affairs specialist. These roles often require knowledge of laboratory techniques, data analysis, and familiarity with biotech tools and regulations.

What are 5 careers in biotechnology?

Five common careers in biotechnology include research scientist, bioprocess engineer, quality control analyst, clinical research associate, and regulatory affairs specialist. These roles often require knowledge of laboratory techniques, data analysis, and familiarity with industry regulations. Biotechnology professionals work in labs, manufacturing facilities, and regulatory agencies to develop and improve products like medicines, vaccines, and agricultural solutions.

What are some typical career paths for professionals with 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.
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Infographic showing various Master In Biotechnology job openings in Virginia as of July 2026, with employment types broken down into 50% Locum Tenens, 3% Internship, 35% Full Time, 5% Part Time, 1% Contract, and 6% Summer. Highlights an 74% Physical, 3% Hybrid, and 23% Remote job distribution.

Senior Scheduler - CQV

Turner & Townsend

Richmond, VA • On-site

Full-time

Posted 13 days ago

Job description

Company Description
Turner & Townsend is a global professional services company with over 22,000 people in more than 60 countries.
Working with our clients across real estate, infrastructure, energy and natural resources, we transform together delivering outcomes that improve people's lives. Working in partnership makes it possible to deliver the world's most impactful projects and programmes as we turn challenge into opportunity and complexity into success.
Our capabilities include programme, project, cost, asset and commercial management, controls and performance, procurement and supply chain, net zero and digital solutions.
We are majority-owned by CBRE Group, Inc., the world's largest commercial real estate services and investment firm, with our partners holding a significant minority interest. Turner & Townsend and CBRE work together to provide clients with the premier programme, project and cost management offering in markets around the world.
Job Description
Turner & Townsend is seeking an experienced Senior CQV Scheduler to join our team to support scheduling as a project controls function on a large-scale project. The ideal individual will have a proven track record of successfully delivering construction project control services.
Responsibilities:
  • Develop, monitor and update owners' Project Integrated Master Schedule (IMS).
  • Establish the schedule management program and deliverables to be used on large scale capital programs.
  • Interface with project stakeholders as trusted advisors to provide guidance and recommendations for the project.
  • Prepare baseline schedules and schedule basis documents for approval by project teams.
  • Conduct schedule of resource loading and leveling.
  • Consolidate contractors schedule to incorporate into IMS.
  • Assess impacts on the critical path and near-critical activities and report to the project team.
  • Monitor schedule deviations and variances and assist in the development of alternative methods for corrective action.
  • Apply EVM methodology to measure project progress.
  • Review schedules with project team members on a regular basis to ensure that accurate and timely data is incorporated into the schedule.
  • Prepare and provide schedule progress reports, trending charts, and schedule analysis on a periodic basis.
  • Maintain record of scope changes, trends and variances that potentially affect schedule performance.
  • Assure the credibility of the information contained in the schedule.
  • Maintain liaison with clients and other consultants at all projects stages.
  • SOX control responsibilities may be part of this role, which are to be adhered to where applicable.

Project/Program specifications:
  • Develop and manage detailed CQV (Commissioning, Qualification, and Validation) schedules for complex life sciences construction projects, ensuring alignment with project milestones and regulatory requirements.
  • Collaborate with cross-functional teams including engineering, construction, and quality to integrate CQV activities into overall project timelines.
  • Monitor progress of CQV tasks, identify potential delays, and proactively implement mitigation strategies to keep projects on track.
  • Utilize scheduling tools such as Primavera P6 or MS Project to create and maintain accurate schedules and reports.
  • Support resource planning and allocation for CQV activities across multiple concurrent projects.
  • Ensure compliance with GMP (Good Manufacturing Practices) and other regulatory standards throughout the CQV lifecycle.
  • Provide regular updates and reports to project stakeholders, highlighting key risks, dependencies, and progress metrics.
  • Experience in biotech, pharmaceutical, or life sciences facility construction is required; familiarity with cleanroom environments and process equipment is a plus.

Qualifications
  • Bachelor's degree in construction management, cost management, quantity surveying, engineering or field related to construction.
  • Minimum 5-7 years of applicable experience.
  • Direct experience working on teams within a complex matrix environment.
  • Expertise using Primavera P6.
  • Excellent communication skills.

Additional Information
*On-site presence and requirements may change depending on our clients' needs.*
Our inspired people share our vision and mission. We provide a great place to work, where each person has the opportunity and voice to affect change.
We want our people to succeed both in work and life. To support this we promote a healthy, productive and flexible working environment that respects work-life balance.
Turner & Townsend is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees and actively encourage applications from all sectors of the community.
Please find out more about us at www.turnerandtownsend.com/
Turner & Townsend does not accept any speculative or unsolicited CV's that have been sent to our internal recruitment team or hiring managers from agencies outside of our preferred supplier list or that have not followed due process. Any speculative or unsolicited CV's will be treated as a direct application.
All your information will be kept confidential according to EEO guidelines.
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It is strictly against Turner & Townsend policy for candidates to pay any fee in relation to our recruitment process. No recruitment agency working with Turner & Townsend will ask candidates to pay a fee at any time.
Any unsolicited resumes/CVs submitted through our website or to Turner & Townsend personal e-mail accounts, are considered property of Turner & Townsend and are not subject to payment of agency fees. In order to be an authorised Recruitment Agency/Search Firm for Turner & Townsend, there must be a formal written agreement in place and the agency must be invited, by the Recruitment Team, to submit candidates for review.

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