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Program Biotech Jobs in Arizona (NOW HIRING)

Validation Engineer

Tucson, AZ · On-site

$35 - $40/hr

Leading biotechnology company (Tucson, AZ 85755 - Onsite) * W2 Employment, Group Medical, Dental, Vision, Life, Retirement Savings Program, PSL * 40 hours/week, 12 Month Assignment A leading ...

Validation Engineer

Tucson, AZ · On-site

$35 - $40/hr

Leading biotechnology company (Tucson, AZ 85755 - Onsite) * W2 Employment, Group Medical, Dental, Vision, Life, Retirement Savings Program, PSL * 40 hours/week, 12 Month Assignment A leading ...

Inizio Engage has a long-standing partnership with a leading biotechnology organization across ... Recognition programs, contests, and company-wide awards * Exceptional, collaborative culture * Best ...

Inizio Engage has a long-standing partnership with a leading biotechnology organization across ... Recognition programs, contests, and company-wide awards * Exceptional, collaborative culture * Best ...

Inizio Engage has a long-standing partnership with a leading biotechnology organization across ... Recognition programs, contests, and company-wide awards * Exceptional, collaborative culture * Best ...

Remote Contact Center Representative

Phoenix, AZ · Remote

$17.50 - $22.75/hr

Inizio has a long-standing partnership with a leading Biotechnology company, across Commercial ... Recognition programs, contests, and company-wide awards * Exceptional, collaborative culture * Best ...

Citizen COMPANY OVERVIEW Hyperion Biotechnology, Inc. has been providing services to federal ... programs. Hyperion is an equal opportunity employer and does not discriminate in hiring or ...

Citizen COMPANY OVERVIEW Hyperion Biotechnology, Inc. has been providing services to federal ... programs. Hyperion is an equal opportunity employer and does not discriminate in hiring or ...

Fabricator

Tolleson, AZ · On-site

$18 - $23.25/hr

... biotechnology, and data centers. At Exyte, you will be part of a global community of challenge ... Paid Volunteer Time Off, Above & Beyond Recognition, Birthday Recognition, Wellness Program with ...

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Program Biotech information

What is a Program Biotech?

A Program Biotech is a professional who manages and coordinates biotechnology projects or programs within an organization. They oversee research and development activities, ensure compliance with regulations, manage budgets, and facilitate collaboration between scientists, engineers, and other stakeholders. Their role is crucial in bringing biotech innovations from concept to market by ensuring projects stay on schedule and meet organizational goals.

What is the difference between Program Biotech vs Laboratory Technician?

AspectProgram BiotechLaboratory Technician
Required CredentialsBiotech degree or certification, specialized trainingAssociate degree or certification in laboratory sciences
Work EnvironmentResearch labs, biotech companies, pharmaceutical firmsClinical, research, or industrial labs
Employer & Industry UsageBiotech firms, research institutions, pharma companiesHospitals, research labs, manufacturing plants
Common Search & ComparisonYesNo

Program Biotech professionals focus on research, development, and overseeing biotech projects, often requiring advanced degrees and specialized training. Laboratory Technicians perform routine lab tests and support research or manufacturing processes, typically with an associate degree. While both roles work in lab environments within the biotech and healthcare industries, Program Biotech roles are more research-oriented, whereas Laboratory Technicians handle day-to-day testing and sample analysis.

What are some common challenges faced by Program Biotech professionals when managing cross-functional teams?

Program Biotech professionals often coordinate projects that involve diverse teams, including research scientists, regulatory specialists, and business development staff. One key challenge is ensuring clear communication and alignment among team members with varying backgrounds and priorities. Additionally, balancing project timelines with regulatory requirements and scientific uncertainties can require strong problem-solving skills. Being proactive in facilitating collaboration and adapting to shifting project goals are essential for success in this role.

What are the key skills and qualifications needed to thrive as a Program Biotech professional, and why are they important?

To excel as a Program Biotech professional, you need a solid background in life sciences, project management, and regulatory knowledge, often supported by an advanced degree in biotechnology or a related field. Familiarity with laboratory information management systems (LIMS), project management software, and compliance frameworks like GLP or GMP is common. Strong leadership, problem-solving abilities, and effective communication are crucial soft skills for coordinating multidisciplinary teams. These skills and qualifications are essential to drive innovation, ensure regulatory compliance, and achieve successful outcomes in complex biotech projects.
What are popular job titles related to Program Biotech jobs in Arizona? For Program Biotech jobs in Arizona, the most frequently searched job titles are:
What cities in Arizona are hiring for Program Biotech jobs? Cities in Arizona with the most Program Biotech job openings:
Manufacturing & Process Transfer Specialist - Biotech/Diagnostics

Manufacturing & Process Transfer Specialist - Biotech/Diagnostics

Sharp Decisions

Tucson, AZ • On-site

$30 - $32/hr

Other

Posted yesterday


Job description

Manufacturing & Process Transfer Specialist – Biotech/Diagnostics

Pay - $30.00-$32.00/hr on W2

Onsite - Tucson, AZ 85755

Contract of 12 months with possible extension



THE OPPORTUNITY

The Technical Transfer Specialist supports the introduction of new assays, reagents, and bulk materials for tissue diagnostics into manufacturing processes. This role ensures the seamless integration of new products from Development into Operations, focusing on manufacturability, quality, cost, and schedule. You will leverage technical knowledge, project management skills, and lean manufacturing principles to support efficient, scalable, and compliant manufacturing practices.


REQUIRED QUALIFICATIONS

--Bachelor's or Master's degree in a Life Sciences (Biology, Chemistry, Biochemistry, Physiology, etc.) or Engineering (Biomedical/Chemical) discipline.

--Minimum of 1 year of directly relevant work experience, preferably within the pharmaceutical, biotechnology, or medical devices industry.

--Experience operating in a GMP/regulated environment

--Basic knowledge of Lean principles. Familiarity with Six Sigma methodologies is a plus.

--Excellent stakeholder management, communication, and project coordination skills.

--Proven ability to strictly follow standard operating procedures (SOPs), operational procedures (OPs), and quality protocols, ensuring compliance and data integrity.

--Strong teamwork ethic and exceptional interpersonal skills, with the ability to effectively collaborate across multiple functions, anticipate team needs, and navigate a matrix organization.

-Basic Technical Problem-Solving: Candidates must have indirect or academic experience in troubleshooting, technical projects, or lab work (e.g., from college courses, a masters program, or tutoring). Direct industry experience is not required.

-Collaboration & Independence: Candidates must work well with different teams and be capable of managing their own daily tasks independently after initial onboarding and training.

-Strong Professional Communication: Candidates must have great interpersonal skills, know how to self-manage their workload, and be comfortable escalating issues when needed.

-Curiosity & Eagerness to Learn: Well suited candidates should display a growth mindset, a strong willingness to learn, and the confidence to ask questions (e.g., a great fit for a recent grad or someone transitioning from a technician role).


KEY RESPONSIBILITIES

Technical Transfer (70%)

--Execute product design transfer tasks from late-stage development through commercial launch.

--Coordinate process transfers from R&D to manufacturing sites (local or external) and track project milestones.

--Collaborate cross-functionally with Operations, Development, Regulatory, and Project teams to align on manufacturability, quality, and cost objectives.

--Document and integrate end-to-end manufacturing requirements and best practices, including scalability considerations, into transfer projects.

--Utilize project management methodologies to execute transfer activities, troubleshoot issues, and support the evaluation of new tools and technologies.

--Support process validation readiness by gathering necessary documentation and collaborating with Validation Engineers.

--Actively participate in training and mentorship to develop technical excellence within the design transfer team.


Quality, Safety, and Compliance (15%)

--Ensure all processes are conducted safely and adhere strictly to current Good Manufacturing Practices (cGMP), local, international, and (MQMS) standards.

Assist in audit readiness by collecting and organizing documentation, and supporting non-compliance events (e.g., NCR investigations and corrective actions).

--Keep updated with relevant regulations to maintain company compliance.


Continuous Improvement (15%)

--Learn and apply basic Lean principles and problem-solving methodologies (e.g., Five Whys, Fishbone diagrams) to identify and eliminate process inefficiencies.

--Use statistical tools and software (e.g., Minitab) to analyze process data, minimize risk, and generate actionable plans for improvements.

--Develop and maintain standardized procedures and documentation for processes.


Knowledge, Skills, and Abilities

--Foundational knowledge in applying scientific methods and principles to process transfer tasks, focusing on learning how to document and incorporate basic design and manufacturing elements while supporting a design for manufacturability approach.

--Basic understanding of the end-to-end production process for assays and reagents (formulation, filling, and packaging).

--Advanced technical writing skills to produce reports and documents.

--Excellent stakeholder management, communication, and project coordination skills are required.

--Strong organizational, critical thinking, and problem-solving abilities, with the capacity to manage multiple low-complexity assignments and meet project deadlines.

--Proven ability to strictly follow standard operating procedures (SOPs), operational procedures (OPs), and quality protocols, ensuring compliance and data integrity.

--Strong teamwork ethic and exceptional interpersonal skills, with the ability to effectively collaborate across multiple functions, anticipate team needs, and navigate a matrix organization.

--Strong organizational, critical thinking, and problem-solving abilities, with the capacity to manage multiple low-complexity assignments and meet project deadlines.