Zifo is looking for a Senior Change Control Analyst/Lead to join their team of laboratory IT (lab computing, Lab IT systems, QA, Validation) professionals.
**This role will require a 100% on-site presence in Albany, NY.**
**This role is not eligible for relocation assistance**
Responsibilities:
- Create and support review of validation life cycle documents for Analytical Instrument Qualification and computerized systems
- Experience in validation of analytical instrument systems (e.g. benchtop analytical systems - spectroscopy, chromatography, protein analyzers, next gen sequencers, PCRs etc.)
- Consult clients on data integrity requirements in Analytical Instruments and perform verification of DI in the systems
- Author validation life cycle documents for client’s review and approval
- Route drafted documents for review
- Route reviewed documents for workflow approval
- Request approval workflows to Doc Control
- Execute approved protocols in GxP facility
- Understand SDLC process and SDLC methodology such as agile etc.
- Work with global team in delivering validation project deliverables
- Manage change controls necessary for project life cycle through process compliance and interface with Quality Assurance change control area
- Author change control documents for client review and approval
Qualifications:
- Bachelor’s/ master’s degree or equivalent in a scientific or health care field.
- 8-10 years of experience as a Senior Change Control / Validation Analyst in the pharmaceutical /Life sciences industry preferred.
A successful Zifo-ite is:
- 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
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.
What We Do
Did you know that the saying ‘Curiosity killed the cat’ actually ends with ‘but satisfaction brought it back’? We suspect that the shortened version is the doing of grown-ups suppressing the innately curious child inside them!
For us at Zifo, we take curiosity as unbounded - it is a celebrated value. Curiosity does wonderful things - drive exploration, accelerate learning, inspire better solutions, lead to innovation, drive conversations. We believe that the scientific community’s most important duty to the world is to stay curious. And this is what we do at Zifo.
We have a global presence of over 1000 employees spread across our offices in US, UK, France, Germany, Switzerland, Japan, China, Canada, Singapore & India.
We offer services in areas such as Scientific Informatics, Lab Informatics, Clinical Biometrics, Regulatory Compliance including Computer System Validation and Genome Informatics across 20+ countries. Our customers include 7 of the Top 10 global Bio-pharma companies.
We are listed as 'Technology Fast 50' by Deloitte for 9 consecutive years (2012-2020) and as one of the 'Best Places to Work' for the past five years.
We strive to stay curious, day in and day out. Asking the right questions, and listening to provide the right solutions.
Write to us at [email protected].
