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Senior Process Engineer (Consultant)

Location: Los Angeles, CA

Job Description

About Azzur:
Our employees are fueled by an entrepreneurial spirit and the desire to make a difference in the lives of our customers, coworkers and our partners. If you’re ready to put in the work, take personal responsibility and test the limits of what’s possible, we’re ready to provide the reward.

Do What You Love


At Azzur Group, it is our purpose to foster a culture that attracts and enables individuals with unique abilities and passions to reach both their life and career goals.  We take crucial steps to ensure that each employee is fulfilled both in and out of the office.
In addition to our purpose, we have a set of core values that we live and breathe each day. Every benefit offered here at Azzur is designed to uphold our 5 core values; Integrity, Putting Others First, Having the Courage to Take Action, Taking Personal Responsibility and Having Fun. 
It is our mission to serve our communities, build positive and established relationships, create a healthy and fun work environment, ensure each employee and their families are healthy and thriving, grow each employee professionally with one of our customized training programs and keep a clear and open line of communication.
We are an equal opportunity employer and promote diverse culture, ethnicity, gender and age in our workplace. We believe that promoting diversity plays an important role in developing top quality talent, fostering greater innovation and creativity, and enhancing our relationships with customers and the communities in which we operate.
If philanthropy, long lasting relationships, a clear career path forward and a positive, transparent and fun company culture are something you are looking for in your next role, Azzur is the place for you.
 
Ideal Qualities:
Ideal candidates will exhibit, or have the willingness to develop, the following qualities:
  • Strategic thinker with strong analytical skills who can translate client needs into actionable value-added projects/results
  • Understands the competitive landscape of the medical device, pharmaceutical, and biotechnology industry
  • Willing to work hands on, assist with building client libraries, learn from a mentor and become a mentor for others. 
  • Understands worldwide regulations and phase appropriate applications
  • Draws insights from projects and supplemental research to help drive new and existing growth. 
  • Ensures activities are efficient, optimized, and client-centric. 
  • Highly motivated and organized, solutions oriented leader
  • Curious and adaptable - has the ability to transform knowledge into actionable activities
  • Able to produce results in a fast paced, collaborative environment   
 
Essential Duties and Responsibilities
Azzur personnel are expected to live up to our core values at all times and exhibit a high level of integrity and personal responsibility, especially when interacting with our valued clients. The following is a short list of the typical responsibilities and deliverables of any given project.  The level of knowledge expected will be commensurate with level of incoming experience.
 
 
  • Develop engineering deliverables including: Process Flow Diagrams, P&IDs, System Specifications, and Functional Specifications
  • Implement system modifications under cGMP change control
  • Develop and execute Site and Factory Acceptance Tests (S/FAT), commissioning protocols, and qualification protocols
  • Develop robust calibration and preventative maintenance plans
  • Lead investigations into system deviations and implement corrective actions and preventative actions
  • Assist lead engineers in development and implementation of programs related to system qualification, asset management, project execution, and Good Engineering Practices
  • Stay current with biopharmaceutical industry best practices and technologies
  • Interface with various roles and departments to accomplish project goals
  • Develop, evaluate, and implement engineering solutions to complex problems
 
Qualifications
 
  • BS in Engineering, Science or equivalent technical degree
  • 7+ years’ experience in a regulated, manufacturing environment within the biotechnology, pharmaceutical or medical device industry
  • Experience in pharmaceutical manufacturing, engineering, plant expansions and all phases of validation
  • Experienced in the design, construction and start up (inception through routine operation) of cGMP compliant facilities for the manufacture of biopharmaceutical and food products including the development of quality systems, commissioning/validation, and process design/optimization
  • Experience in the areas of design documentation (URS, FS, DS and other engineering specifications) Validation (IQ, OQ, PQ, PV, CV, CSV, etc.), Quality Systems (Change Control, Non-Conformances, Requalification, etc), and Process Excellence Methodologies (Six-Sigma, Lean, etc.).
  • Excellent written and verbal communication skills; excellent technical writing skills
  • Strong interpersonal skills and the ability to work in a team environment
  • Ability to work effectively in a fast-paced multitasking environment
  • Strong working knowledge of FDA and cGMP regulations and documentation practices
  • Proficient in Microsoft Word, Excel, PowerPoint
  • Ability to work for multiple clients throughout the region
 
 
Perks of Working at Azzur West
 
  • Medical, Dental and Vision
  • Competitive 401K plan
  • Wellness reimbursement program
  • Volunteer Paid Time Off
  • Flexible Paid Vacation Time
  • Employee Recognition Program
  • Diversity and Inclusion Initiatives
  • Training and Mentorship Opportunities
 
Find us on social media 
Instagram for our California regions: Azzur_LA, Azzur_SD and Azzur_SF
View our culture video in Youtube: https://www.youtube.com/watch?v=GPNjmsDu0LY


Apply Now
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