Validation Engineer
Pharmaceutical and Medicine ManufacturingSalary Range for Validation Engineer in Pharmaceutical and Medicine Manufacturing
The salary range for a Validation Engineer in the Pharmaceutical and Medicine Manufacturing industry typically varies based on factors such as experience, qualifications, and location. However, the average salary range for a Validation Engineer in this field is approximately $65,000 to $100,000 per year.Sample Job Description for Validation Engineer in Pharmaceutical and Medicine Manufacturing Industry
Job Description:
A Validation Engineer In The Pharmaceutical And Medicine Manufacturing Industry Plays A Crucial Role In Ensuring That All Processes And Equipment Used In The Manufacturing And Production Of Pharmaceutical Products Are Operating Effectively And In Compliance With Industry Regulations. Their Primary Objective Is To Validate And Verify The Systems And Processes Involved In Manufacturing Medicines, Ensuring Their Safety, Efficacy, And Quality.Job Requirements:
1. Bachelor'S Degree In Engineering Or A Related Field. 2. Prior Experience In The Pharmaceutical Or Medical Device Industry Is Preferred. 3. Strong Knowledge Of Regulatory Guidelines And Requirements, Such As Fda Regulations. 4. Proficiency In Validation Protocols, Procedures, And Equipment Qualification. 5. Excellent Analytical And Problem-Solving Skills. 6. Attention To Detail And Ability To Work With Precision. 7. Strong Communication And Interpersonal Skills. 8. Ability To Work Collaboratively In Cross-Functional Teams. 9. Familiarity With Current Good Manufacturing Practices (Cgmp) Is Essential. 10. Knowledge Of Risk Assessment And Validation Documentation.Job Responsibilities:
1. Develop Validation Protocols, Including Installation Qualification (Iq), Operational Qualification (Oq), And Performance Qualification (Pq). 2. Execute Validation Activities, Ensuring Compliance With Regulatory Requirements. 3. Perform Risk Assessments And Develop Strategies To Mitigate Potential Risks. 4. Collaborate With Cross-Functional Teams To Ensure Alignment And Compliance With Validation Requirements. 5. Conduct Equipment Qualifications And Requalification As Necessary. 6. Analyze Validation Data And Prepare Reports Summarizing The Results. 7. Assist In The Development And Implementation Of Validation Strategies And Procedures. 8. Stay Updated With Industry Trends And Regulatory Changes Related To Validation. 9. Participate In Internal And External Audits And Inspections. 10. Provide Training And Guidance To Team Members On Validation Processes.Top 10 Employers for Validation Engineer in Pharmaceutical and Medicine Manufacturing:
1. Pfizer Inc. (HQ: New York, USA) - Website: www.pfizer.com 2. Johnson & Johnson (HQ: New Jersey, USA) - Website: www.jnj.com 3. Novartis International AG (HQ: Basel, Switzerland) - Website: www.novartis.com 4. Roche Holding AG (HQ: Basel, Switzerland) - Website: www.roche.com 5. Merck & Co., Inc. (HQ: New Jersey, USA) - Website: www.merck.com 6. GlaxoSmithKline plc (HQ: London, UK) - Website: www.gsk.com 7. AstraZeneca (HQ: Cambridge, UK) - Website: www.astrazeneca.com 8. Sanofi (HQ: Paris, France) - Website: www.sanofi.com 9. Eli Lilly and Company (HQ: Indiana, USA) - Website: www.lilly.com 10. Amgen Inc. (HQ: California, USA) - Website: www.amgen.comCareer Path for Validation Engineer in Pharmaceutical and Medicine Manufacturing:
1. Entry-level Position: Validation Technician - Recommended experience: 1-2 years 2. Intermediate Position: Validation Specialist - Recommended experience: 3-5 years 3. Advanced Position: Senior Validation Engineer - Recommended experience: 6-8 years 4. Expert Position: Validation Manager - Recommended experience: 8+ yearsTop 5 Countries by Validation Engineer in Pharmaceutical and Medicine Manufacturing:
1. United States 2. Switzerland 3. Germany 4. United Kingdom 5. FranceTop 5 Countries with Established Pharmaceutical and Medicine Manufacturing:
1. United States 2. Switzerland 3. Germany 4. United Kingdom 5. JapanLet's make a difference
Enhance collaboration to streamline business processes at scale and improve operational efficiency and transparency.