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Program Biotech Jobs in Georgia (NOW HIRING)

VERO BIOTECH INC

Senior Quality Engineer

Atlanta, GA

$85K - $115K/yr

Stability Program Studies * Human Factors * Supports new product development teams to assure product quality is achieved through proper design, testing, and Engineering and Quality specifications

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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 Georgia? For Program Biotech jobs in Georgia, the most frequently searched job titles are:
What job categories do people searching Program Biotech jobs in Georgia look for? The top searched job categories for Program Biotech jobs in Georgia are:
Program Biotech jobs near you
Senior Quality Engineer

Senior Quality Engineer

VERO BIOTECH INC

Atlanta, GA

$85K - $115K/yr

Full-time

Posted 14 days ago

Job description

Responsible for product quality through proper design and implementation of appropriate procedures and specifications, as well as finished goods quality.

Essential Duties and Responsibilities

  • Authors, executes and reports on qualification/validations in the following areas:
    • Equipment Qualifications
    • Facility Qualifications
    • Software Validation
    • Computer System Validation
    • Test Method Validations
    • Stability Program Studies
    • Human Factors
  • Supports new product development teams to assure product quality is achieved through proper design, testing, and Engineering and Quality specifications
  • Assists in risk management program, assesses FMEA updates and controls
  • Reviews/develops engineering test/qualification protocols, where required, to assure product/design changes are properly validated prior to release
  • Supports process validation activities.
  • Communicates and carries Quality Engineering philosophy to other internal groups
  • Assures compliance to documentation procedures
  • Reviews change requests
  • Performs process capability analysis and assists in design of experiment activities
  • Interfaces with Product and R&D Engineering groups on design and specification-related issues as well as for approvals, as required.
  • Works closely with Quality System personnel to assure compliance with quality system requirements.
  • Performs other duties and responsibilities, as required
  • Bachelor’s Degree in technical field and minimum 2 years related experience for Quality Engineer or 4 years for Sr. Quality Engineer; Master’s Degree Preferred
  • Strong knowledge of pharmaceutical manufacturing processes, computer and equipment validation, GMPs, and product/process validation.
  • Test Method Validations
  • Stability Program Studies
  • ASQ Certification preferred.
  • Knowledge of quality engineering principles.
  • Ability to analyze component and final product processes to improve overall efficiency and quality..
  • Thorough knowledge of GMP, CFR, and factors impacting compliance.
  • Knowledge of and ability to utilize statistic in evaluation of data.
  • Thorough knowledge of FDA regulations
  • Experience with laboratory environment, equipment, and safety procedures.
  • Commitment to excellence and high standards
  • Excellent verbal and written communications skills in English
  • Ability to manage priorities and workflow
  • Versatility, flexibility, and a willingness to work within constantly changing priorities with enthusiasm
  • Acute attention to detail
  • Demonstrated ability to plan and organize projects
  • Ability to work independently and as member of various teams and committees
  • Proven ability to handle multiple projects and meet deadlines
  • Ability to develop clear, concise, and timely oral and written reports.

Supervisory Responsibilities

  • N/A

Competencies

  • Analytical--Synthesizes complex or diverse information; Collects and researches data; Uses intuition and experience to complement data; Designs workflows and procedures.
  • Problem Solving--Identifies and resolves problems in a timely manner; Gathers and analyzes information skillfully; Develops alternative solutions; Works well in group problem solving situations; Uses reason even when dealing with emotional topics
  • Change Management—Develops workable implementation plans; Communicates changes effectively; Builds commitment and overcomes resistance; Prepares and supports those affected by change; Monitors transition and evaluates results
  • Quality Management--Looks for ways to improve and promote quality; Demonstrates accuracy and thoroughness.

Physical Demands and Work Environment

  • Ability to lift/move up to 50 pounds

Apply