Bachem

Sr / Principal Validation Engineer

Bachem • $103K — $166K *
Vista, CA 92084In-Person
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in science discipline (chemistry, biochemistry, organic chemistry, biology, microbiology, chemical engineering or equivalent)
  • Master's degree in a science-related field is preferred
  • 5+ years of Commissioning, Qualification and Validation (CQV) experience in a GMP/GDP environment
  • Proven experience in planning, writing, and executing qualification protocols (IQ, OQ, PQ)
  • Experience in validation and monitoring of pharmaceutical utility systems
  • Knowledge of Lean Six Sigma methods for technical problem analysis
  • Understanding of GMP for Active Pharmaceutical Ingredients per ICH Q7

Responsibilities

  • Develop cleaning validation strategies and acceptance criteria
  • Lead cross-functional teams to ensure timely qualification and validation deliverables
  • Write and execute validation protocols and final reports
  • Conduct and document investigations related to validation studies
  • Perform periodic re-validation and re-qualification activities
  • Optimize operations based on validation studies and recommendations
  • Ensure compliance with cGMP and safety procedures

Benefits

  • Comprehensive Medical/Dental/Vision coverage
  • 401(k) plan with employer contribution
  • Paid vacation, personal, and sick days
  • Annual performance bonus
  • Generous benefits package
Full Job Description
A brief overview

The Sr. / Principal Validation Engineer fulfills a critical role in GMP operations, supporting cleaning validation activities for API and PMO manufacturing, and the qualification of equipment, facilities, utilities. This position will work in close cooperation with Manufacturing, Engineering, and other functional areas to plan and perform validation activities under the Quality Engineering scope of work. This individual must also monitor facility / utility validated systems, plan, write and execute validation/ qualification protocols, reports, and other technical documents, as well as conduct related investigations

What you will do

  • Develop strategy, establish acceptance criteria, generate, execute cleaning validation protocols and reports
  • Perform, coordinate, execute and analyze cleaning recovery studies.
  • Lead cross-functional project teams to address issues and ensure on-time completion of all qualification / validation deliverables.
  • Provide qualification / validation guidance and strategy during project planning and development phases. Train, coach and mentor Quality Engineer I and II.
  • Write validation protocols and final reports, test methods, standard operating procedures, and technical reports.
  • Planning, writing, and executing qualification protocols (DQ, IQ, OQ, PQ) and reports.
  • Independently conduct and document investigations related to validation studies.
  • Based on validation studies, evaluate and make recommendations for improvements to operations, processes and methods.
  • Accountable for the accuracy and validity of testing results
  • Support and assist with l inspections and audits.
  • Perform other related duties as assigned.
  • Plan and perform required periodic re-validation / re-qualification activities
  • Work and communicate with different associates within the company to ensure timely completion of assigned tasks and projects.
  • Adherence to cGMP and safety procedures and contribute to GMP systems improvements.


Qualifications

  • Bachelor's degree in science discipline (chemistry, biochemistry, organic chemistry, biology, microbiology, chemical engineering or equivalent)
  • Master's degree in science related field (engineering, chemistry, biology or equivalent). (preferred)
  • 5+ years of Commissioning, Qualification and Validation (CQV) experience in a GMP/GDP environment
  • Experience with planning, writing and executing qualification protocols (IQ, OQ, PQ) and reports
  • Experience with validation / monitoring of critical pharmaceutical utility systems, including purified water, nitrogen systems and cold storage units
  • Experience with planning and execution of cleaning validation of production lab glassware and equipment including performance of validation studies, writing validation protocols and reports and other technical documents, as well as conducting validation related investigations (preferred)
  • Experience with developing coupon spike and recovery studies for cleaning validation
  • Experience with Lean Six Sigma methods: root cause analysis, failure mode analysis and analyzing / organizing complex technical problems
  • Understanding of cleaning validation requirements for pharmaceutical industry
  • Knowledge of and ability to perform MAC calculation for APIs
  • Understanding of GMP for Active Pharmaceutical Ingredients per ICH Q7.
  • Knowledge of the chemical composition, structure, and properties of substances and of the chemical processes and transformations they undergo, including use of chemicals and their interactions, danger signs, production techniques, and disposal methods.
  • General lab instrumentation knowledge and operation experience.
  • Capable of working methodically and adhering to rules and regulations.


Base salary range:

Sr Engineer: $103,939 - $142,916

Principal Engineer: $120,875 - $166,204

Placement of new hires in these wage ranges is based on several factors including education, skill sets, experience, and training.

Total Rewards

We offer all Team Members a total rewards package including competitive pay, annual performance bonus, a generous benefit package with comprehensive Medical/Dental/Vision coverage, 401(k) plan with employer contribution, and paid vacation, personal and sick days.

About Bachem

Bachem is a Swiss biochemical company that provides services to the pharmaceutical and biotechnology industries. The company specializes in the development of innovative, efficient manufacturing processes and the reliable production of peptide-based active pharmaceutical ingredients. Bachem has a global presence with headquarters in Switzerland and subsidiaries in Europe, the US, and Asia. The company was founded in 1971 and has since become a leading supplier of peptides worldwide. Bachem's products are used in the treatment of diseases such as diabetes, cancer, and cardiovascular diseases.
Learn more about Bachem
Size
1,200 employees
Industry

Similar Jobs

More Jobs at Bachem

More Pharmaceuticals & Biotech Jobs

Find similar Sr / Principal Validation Engineer jobs: