PharmEng Technology

Validation Engineer

PharmEng Technology  •  Sanford, NC (Onsite)  •  8 days ago
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Job Description

Job Title: Validation Engineer Lyophilization Specialist

Location: Sanford, NC (Long-Term Contract)

About the Role:
We are seeking an experienced Validation Engineer specializing in lyophilization processes and equipment. The ideal candidate will lead validation activities, ensuring compliance with regulatory standards while supporting manufacturing excellence in a pharmaceutical or biotech setting.

Key Responsibilities:

  • Develop and execute validation protocols for lyophilization equipment and processes.
  • Perform Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) for lyophilizers.
  • Create, review, and maintain validation documentation, including protocols, reports, and risk assessments.
  • Conduct validation testing to meet regulatory and industry compliance standards.
  • Collaborate with cross-functional teams, including Quality Assurance, Regulatory Affairs, and Manufacturing.
  • Address validation issues and implement corrective and preventive actions (CAPA).
  • Stay updated on industry trends and regulatory changes related to lyophilization and validation.
  • Participate in audits concerning validation processes.
  • Provide training and guidance on validation protocols and best practices.

Qualifications:

  • Bachelors degree in Engineering, Life Sciences, or a related field.
  • Extensive experience in lyophilization validation within the pharmaceutical or biotech industry.
  • Strong understanding of GMP and regulatory requirements for equipment validation.
  • Excellent analytical and problem-solving skills.
  • Outstanding communication and team collaboration abilities.

Preferred Skills:

  • Experience with computerized system validation (CSV).
  • Familiarity with validation software tools.
  • Certification in validation engineering or related disciplines.
  • Knowledge of Lean or Six Sigma methodologies.

Apply Now:
If you are a detail-oriented Validation Engineer with expertise in lyophilization, we encourage you to apply and contribute to cutting-edge pharmaceutical advancements. This is a unique opportunity to work on impactful projects in a dynamic and innovative environment.

PharmEng Technology

About PharmEng Technology

PharmEng Technology, now part of Efor Group, leader in Compliance Engineering, is a leading provider of technical services and solutions to the pharmaceutical, biotechnology, and healthcare industries. With over 25 years of experience, we specialize in Commissioning, Qualification, and Validation (CQV) services for facilities, utilities, equipment, and processes.

As part of Efor’s global network of 3,000 experts across 12 countries, we are better equipped than ever to deliver innovative and comprehensive solutions tailored to the unique needs of clients worldwide. This integration strengthens our ability to combine global expertise with local proximity, positioning PharmEng as a strategic partner for the industry’s most prominent players.

Our team of highly skilled professionals brings a wealth of industry expertise and knowledge to every project, ensuring that our clients receive the highest quality services and solutions. We pride ourselves on our ability to provide flexible, innovative, and cost-effective solutions that meet our clients' unique challenges.

At PharmEng Technology by Efor, we are committed to delivering excellence in everything we do. We work closely with our clients to understand their goals and objectives, developing customized solutions that deliver measurable results. Our focus on quality, safety, and compliance ensures that our clients can trust us to meet their most critical needs.

Specialties: PharmEng Technology specializes in the planning, design, construction, and validation of Health Care, Laboratory, API Pharmaceutical, and Biotechnology facilities and equipment, including computer systems. We provide professional services that meet both regulatory and business demands, following current Good Manufacturing Practices (cGMP), Good Engineering Practices (GEP), and Good Laboratory Practices (GLP).

Industry
Chemicals & Materials
Company Size
201-500 employees
Headquarters
Toronto, CA
Year Founded
Unknown
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