Commissioning Qualification Validation Engineer

3 weeks ago

india PSC Biotech Full time
Job Description
PSC Biotech provides the life sciences with essential services to ensure that health care products are developed, manufactured, and distributed to the highest standards, in compliance with all applicable regulatory requirements.
Our goal is to skyrocket our clients’ success, and you can be a part of our team’s achievements. Employing a global team of skilled professionals and experts that span across strategically located offices in North America, Europe, Asia-Pacific and the Middle East, we are proud of the roles we have fulfilled to help our clients achieve success.
The Experience
With operations spanning the globe and featuring a multi-cultural team, PSC Biotech® is passionate about bringing the best and brightest together in an effort to form something truly special. When you make the decision to join our team, you will be offered the ability to feel inspired in your career, explore your professional passions, and work alongside a group of people who will value and nurture your talents.
We are firm believers in coaching and developing the next generation of industry leaders and influencers. As such, you will not only be offered compensation and benefits structure that rewards you, but also be provided with the tools that will help you grow and learn.
At PSC Biotech®, it’s about more than just a job—it’s about your career and your future.
Your Role

We are looking for a Commissioning, Qualification, and Validation (CQV) Engineer . The CQV Professional would work alongside a talented PSC Biotech Team in an exciting, developing, and diverse biotechnology landscape.                                                                                                                                          
  • Commission, qualify, and validate, GxP facilities, equipment, and utilities in assigned projects.
  • Responsible for protocol writing and execution - Draft, execute, review, and approve validation documentation ensuring the documentation meets cGMP requirements, regulatory requirements, and quality standards.
  • Draft and execute validation documentation such as:
  • Validation Project & Master Plans
  • Requirement Specifications (URS, DS, FS)
  • IQ and OQ Test Scripts
  • IQ/OQ/PQ Protocols
  • Validation Summary Report
  • Initiate and coordinate risk analyses, design reviews, and execute FAT/SAT, IQ, OQ, and PQ.
  • Conduct preventative maintenance and perform risk assessments.
  • Recommended process improvements where needed ensuring compliance with industry standards.
  • Establish validation standards and develop performance testing and quality control measures.
  • Execute process equipment and clean room validation.
  • Clearly communicate all progress, updates, and action steps for assigned projects. Collaborate with multiple departments on assigned project activities and deliverables.
  • Additional duties as assigned.

Requirements
  • Bachelor's Degree in a relevant science or engineering field, or equivalent years of hands-on experience.
  • 3+ years’ experience in the biotechnology and pharmaceutical industries with a minimum of 2 years relevant experience performing CQV activities within GMP environment.
  • Sound industry knowledge, project proficiency, and autonomy expected.
  • Experienced in CQV of facility/utility/equipment, including PW, HVAC and process or laboratory equipment, etc.
  • Understands current risk-based validation approaches.
  • Experience in authoring, revising, reviewing, and completing controlled documents for validation projects.
  • Experience with system impact assessment and risk assessment.
  • Good knowledge of the code of GMP and PIC/S code.
  • Previous experience in the Life Sciences Industry is required.
  • Previous experience in GxP Industries are required.
  • Must be adaptable, customer service oriented, have a positive attitude.
  • Excellent organizational skills.
  • High attention to detail.
  • Must have strong written and verbal communication skills.

Requirements
Bachelor's Degree in a relevant science or engineering field, or equivalent hands-on experience. 3+ years of experience in the biotechnology and pharmaceutical industries with a minimum of 2 years of relevant experience performing CQV activities within GMP environment. Sound industry knowledge, project proficiency, and autonomy expected. Experienced in validation of facilities/utilities/equipment, including cleaning validation and IQ/OQ/PQ of equipment. Strong understanding of current risk-based validation approaches. Experienced in authoring, revising, reviewing, and completing controlled documents for validation projects. Experienced with risk assessments. Excellent organizational skills. High attention to detail. Strong written and verbal communication skills. Strong knowledge of the code of GMP and PIC/S code. Must be adaptable, customer service oriented, and have a positive attitude. #LI-MS2

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