Validation Consultant

Mid-level
Emeryville, 🇺🇸 United States
Quality assurance

Zifo is hiring! We are looking to add a Validation Consultant to our Quality & Compliance team. This person will be responsible for validation strategy and planning, executing and qualification of computer systems and/or analytical instruments in accordance with applicable policies procedures and regulatory requirements.

**This role requires 2-3 days per week on-site in Emeryville, CA**

Responsibilities :

· Define validation Strategy for computerized systems and/or analytical instruments utilized in GxP Space

· Create Validation deliverables such as Validation Plan, Test Protocols, Traceability matrix and execution of protocols

Conduct user review meetings. Lead discussions with Quality Assurance and Compliance groups

· Conduct Risk Assessments. Develop and maintain policies and procedures

· Effectively communicate the validation activities and deliverables to the project team, customer stake holders and global team within Zifo

· Act as a liaison between Zifo remote teams and customers in US & Canada

· Participate in internal initiatives around Computer Systems Validation

Requirements

Required Qualifications:

· Bachelor or Master’s degree in Life Sciences or Computer Sciences

· 5-7+ years’ experience with Computer Systems Validation within the pharmaceutical industry is required for this role

· Strong knowledge of GxP Requirements, GLP and GMP regulations, 21 CFR part 11 requirements

· Experience with laboratory or GxP systems validation like ELN, LIMS, QMS etc.

Successful Zifo-ites are:

· Independent, Self-Motivated & Results driven

· Willing & able to quickly acquire new Technical Skills & Business Principles

· A critical thinker who possesses logical reasoning

· Curious and always looking for creative solutions to complex problems

Benefits

About Zifo:

CURIOSITY DRIVEN, SCIENCE FOCUSED, EMPLOYEE BUILT. Our culture is unlike any other, one where we debate, challenge ourselves, and interact with all alike. We are a curious bunch, characterized by our passion to learn and spirit of teamwork. Zifo is a global R&D solutions provider focused on the industries of Pharma, Biotech, Manufacturing QC, Medical Devices, specialty chemicals and other research-based organizations. Our team’s knowledge of science and expertise in technology help Zifo better serve our customers around the globe, including 7 of the Top 10 Biopharma companies.

We look for Science – Biotechnology, Pharmaceutical Technology, Biomedical Engineering, Microbiology etc. We possess scientific and technical knowledge and bear professional and personal goals. While we have a “no doors” policy to promote free access within, we do have a tough door to walk in. We search with a two-point agenda – technical competency and cultural adaptability.

We offer a competitive compensation package including accrued vacation, medical, dental, vision, 401k with company matching, life insurance, and flexible spending accounts.

If you share these sentiments and are prepared for the atypical, then Zifo is your calling!

Zifo is an equal opportunity employer, and we value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

 

Zifo

Zifo

Zifo is a global scientific informatics service provider working across research, development, manufacturing, and clinical domains.

Biotechnology
Clinical Trials
Consulting
Healthcare
Laboratory Services
Research
Technology

LinkedIn

🏭Information Technology & Services
🎂2008
1.9K
38.6K

Updated  

Other jobs at Zifo

 

 

 

 

 

 

 

 

View all Zifo jobs

Why OmniJobs?

  • Rare & hidden jobs
  • New jobs every day
  • No expired job posts
  • All jobs in English

Receive emails about similar jobs

Get alerts to your inbox about new open jobs that are similar to this one.

🇺🇸 United States
Quality assurance

No spam. No ads. Unsubscribe anytime.

Similar jobs