Process Validation in Pharma Environment
$25-50 USD / godzinę
What we need is professionals with processes validation background. Validation in pharma environment, how to write protocols, tests, validations plans in a GxP regulated environment
Validation Lead Skillset:
· Direct computer system validation (CSV) experience
· Use of quality center or electronic protocol/requirements systems (i.e. TIMS)
· Strong written/verbal communication skills
· Understanding of managing changes to validated systems in a regulated environment
Key Deliverables in Validation Role:
· Capable of leveraging technical knowledge/experience to apply in redlining URS, FRS, DS documents as a starting point for SMEs
· Comfortable managing their own work with little direction/oversight
· Able to take information from project team, PM, and readily apply to work
· Able to understand the deep NN process (local & corporate) requirements such that work is driven by requirements, not necessarily the way it’s always been done
· Set’s best practice with simplicity mindset
· Capable of multi-tasking
Numer ID Projektu: #18033589
O projekcie
15 freelancerów złożyło ofertę na średnią kwotę $43/godzinę w tym projekcie
Hi, topacademicse will give you best work in Validation in pharma environment about how to write protocols, tests, validations plans in a GxP regulated environment. kindly discuss details regards Rashid.
I excel in the fields of technical writing and content management projects. I have spent the past five years providing IBM, and a multitude of companies ranging greatly in size, with high quality, innovative technical Więcej
I believe that my experience and skill in this background will prove to be of great help to you. Contact me to discuss more on the details
Past experience in validation. PMP certified project manager, MBA, business analyst, market researcher,writer, proficient in the field of business plans, presentations, SEO, social media, Adwords project management, p Więcej
14 years of Pharmaceutical product Development and technical transfer of validation, CPV,critical process parameters. experience in writing technical protocol,validation protocol.
Hello, Greetings... I am a Computer system validation expert. I have 6 years experience in validation project. I have worked with many pharma MNC like Cipla Ltd, Torrent Pharmaceutical Ltd, Strides Shasun, Parsa Więcej
I am a pharmacist on sabbatical who has also moonlighted as a writer for almost ten years (writing for various online publications). I have both a healthcare background and writing/editing experience. Thank you for you Więcej
Hello I have experience of more than 10 years working as QA Manager in Pharmaceutical industry. You can see my CV on my Linkedin (ivanamilanovic7)
Hands on experience in preparation of protocols &reports for IQ, OQ, PQ & RQ, other validation deliverable (URS, Gap Assessment, Risk Assessment, Compliance Report, Tractability Matrix, Summary report and interim repor Więcej