We Are Hiring: CQV Associate

Incepbio Hiring for CQV Associate

Organization Overview:

Incepbio is a leading pharma consulting company offering specialized solutions for the pharmaceutical industry. With over 50 years of combined experience, their team of experts provides a wide range of services, including Commissioning, Qualification, Validation, Calibration, Automation, Computer System Validation, Compliance, and more. Incepbio tailors solutions to meet each client’s unique needs, working closely with them to navigate industry challenges and achieve their goals. Committed to long-term relationships and exceptional results, Incepbio serves both start-ups and large corporations, maintaining many FDA-approved clients who trust them for reliable consulting services in the competitive pharma market.

Job Location Options:

Bangalore 🏙️

Hyderabad 🌆

Vizag 🏞️

Pune 🏢

Goa 🏖️

Indore 🏛️

📜 Qualifications Required:

Bachelor of Science (B.Sc.) in Biotechnology 🎓

Master of Science (M.Sc.) in Biotechnology 🎓

Bachelor of Technology (B.Tech.) in Biotechnology 🎓

💼 Experience Required:

6 to 8 years in the Pharma industry 🏥

🌐 Industry:

Pharmaceutical industry 💊

📌 Key Requirements:

1.Regulatory Knowledge 📜

2.Familiarity with regulatory requirements and industrial standards 🏗️.

3.Must understand and comply with guidelines critical for ensuring quality and safety in the pharmaceutical sector.

4.Validation Protocol Expertise 🔍

5.Hands-on experience with e-Validation or ValGenesis systems.

6.Proficiency in developing and executing validation protocols to ensure compliance and safety 🛡️.

7.Documentation Skills 📝

8.Strong focus on documentation as per Good Documentation Practice (GDP) principles.

9.Ability to maintain and manage records systematically to ensure traceability and accountability 📂.

10.Protocol Adherence 🔒

11.Strict adherence to validation protocols.

12.Commitment to producing reliable results by following every step meticulously and accurately .

13.Problem-Solving Skills 🛠️

14.Skill in analyzing issues that may arise in the validation process.

15.Capable of identifying root causes of problems and implementing effective solutions swiftly 💡.

16.Qualification and Validation Experience ⚙️

Hands-on experience in qualifying and validating a wide range of equipment:

Process Equipment 🏭

Process Gases 💨

Clean Utility 🧼

Cold Storage Equipment ❄️

📧 How to Apply:

Email: Send your resume to careers@incepbio.com 📩.

Website: Visit www.incepbio.com 🌐.

Contact: Reach out via phone at +91 9741738323 📞.

This CQV Associate position at IncepBio provides an exciting opportunity to work across various locations in India. This role is perfect for professionals with a biotechnology background and experience in the pharmaceutical sector, specifically in validation processes and documentation practices.

If you have a keen eye for detail, strong problem-solving abilities, and a solid understanding of regulatory standards, this position is a great fit. You’ll be contributing to ensuring the highest standards in pharmaceutical manufacturing through meticulous validation and qualification procedures.